000D00	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Excitation energies from ground-state density-functionals by means of generator coordinates</title><author><name sortKey="Orestes, E" uniqKey="Orestes E">E. Orestes</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Física e Química, Instituto de Química de São Carlos, Universidade de São Paulo, Caixa Postal 780</s1><s2>13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369</s1><s2>SP 13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silva, A B F" uniqKey="Da Silva A">A. B. F. Da Silva</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Física e Química, Instituto de Química de São Carlos, Universidade de São Paulo, Caixa Postal 780</s1><s2>13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Capelle, K" uniqKey="Capelle K">K. Capelle</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369</s1><s2>SP 13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0323136</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0323136 INIST</idno><idno type="RBID">Pascal:09-0323136</idno><idno type="wicri:Area/Main/Corpus">001C79</idno></publicationStmt><seriesStmt><idno type="ISSN">1463-9076</idno><title level="j" type="abbreviated">PCCP, Phys. chem. chem. phys. : (Print)</title><title level="j" type="main">PCCP. Physical chemistry chemical physics : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Density functional</term><term>Density functional method</term><term>Equation</term><term>Excited state</term><term>Ground state</term><term>Ions</term><term>Potential</term><term>Test method</term><term>Theoretical study</term><term>Time dependence</term><term>Transition energy</term><term>Variational principle</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Energie transition</term><term>Etat fondamental</term><term>Fonctionnelle densité</term><term>Dépendance du temps</term><term>Méthode fonctionnelle densité</term><term>Etude théorique</term><term>Principe variationnel</term><term>Equation</term><term>Méthode essai</term><term>Etat excité</term><term>Ion</term><term>Potentiel</term><term>3115E</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The generator-coordinate method is a flexible and powerful reformulation of the variational principle. Here we show that by introducing a generator coordinate in the Kohn-Sham equation of density-functional theory, excitation energies can be obtained from ground-state density functionals. As a viability test, the method is applied to ground-state energies and various types of excited-state energies of atoms and ions from the He and the Li isoelectronic series. Results are compared to a variety of alternative DFT-based approaches to excited states, in particular time-dependent density-functional theory with exact and approximate potentials.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1463-9076</s0></fA01><fA03 i2="1"><s0>PCCP, Phys. chem. chem. phys. : (Print)</s0></fA03><fA05><s2>11</s2></fA05><fA06><s2>22</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Excitation energies from ground-state density-functionals by means of generator coordinates</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Time-Dependent Density-Functional Theory</s1></fA09><fA11 i1="01" i2="1"><s1>ORESTES (E.)</s1></fA11><fA11 i1="02" i2="1"><s1>DA SILVA (A. B. F.)</s1></fA11><fA11 i1="03" i2="1"><s1>CAPELLE (K.)</s1></fA11><fA12 i1="01" i2="1"><s1>RUBIO (Angel)</s1><s9>limin.</s9></fA12><fA12 i1="02" i2="1"><s1>MARQUES (Miguel)</s1><s9>limin.</s9></fA12><fA14 i1="01"><s1>Departamento de Física e Química, Instituto de Química de São Carlos, Universidade de São Paulo, Caixa Postal 780</s1><s2>13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369</s1><s2>SP 13560-970, São Carlos</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>Universidad del País Vasco</s1><s2>Bilbao</s2><s3>ESP</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>CSIC-UPV/EHU, ETSF and DIPC</s1><s2>San Sebatian</s2><s3>ESP</s3><sZ>1 aut.</sZ></fA15><fA15 i1="03"><s1>Université Claude Bernard and CNRS</s1><s2>Lyon</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>4564-4569</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26801</s2><s5>354000188583410160</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>24 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0323136</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>PCCP. Physical chemistry chemical physics : (Print)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The generator-coordinate method is a flexible and powerful reformulation of the variational principle. Here we show that by introducing a generator coordinate in the Kohn-Sham equation of density-functional theory, excitation energies can be obtained from ground-state density functionals. As a viability test, the method is applied to ground-state energies and various types of excited-state energies of atoms and ions from the He and the Li isoelectronic series. Results are compared to a variety of alternative DFT-based approaches to excited states, in particular time-dependent density-functional theory with exact and approximate potentials.</s0></fC01><fC02 i1="01" i2="X"><s0>001C01</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Energie transition</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Transition energy</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Energía transición</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Etat fondamental</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Ground state</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Estado fundamental</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Fonctionnelle densité</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Density functional</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Funciónal densidad</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Dépendance du temps</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Time dependence</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Dependencia del tiempo</s0><s5>04</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Méthode fonctionnelle densité</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Density functional method</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Etude théorique</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Theoretical study</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Estudio teórico</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Principe variationnel</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Variational principle</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Principio variacional</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Equation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Equation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Ecuación</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Méthode essai</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Test method</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Método ensayo</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Etat excité</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Excited state</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estado excitado</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Ion</s0><s2>NA</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Ions</s0><s2>NA</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Ión</s0><s2>NA</s2><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Potentiel</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Potential</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Potencial</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>3115E</s0><s4>INC</s4><s5>32</s5></fC03><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0323136 INIST</NO><ET>Excitation energies from ground-state density-functionals by means of generator coordinates</ET><AU>ORESTES (E.); DA SILVA (A. B. F.); CAPELLE (K.); RUBIO (Angel); MARQUES (Miguel)</AU><AF>Departamento de Física e Química, Instituto de Química de São Carlos, Universidade de São Paulo, Caixa Postal 780/13560-970, São Carlos/Brésil (1 aut., 2 aut.); Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369/SP 13560-970, São Carlos/Brésil (1 aut., 3 aut.); Universidad del País Vasco/Bilbao/Espagne (1 aut.); CSIC-UPV/EHU, ETSF and DIPC/San Sebatian/Espagne (1 aut.); Université Claude Bernard and CNRS/Lyon/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>PCCP. Physical chemistry chemical physics : (Print); ISSN 1463-9076; Royaume-Uni; Da. 2009; Vol. 11; No. 22; Pp. 4564-4569; Bibl. 24 ref.</SO><LA>Anglais</LA><EA>The generator-coordinate method is a flexible and powerful reformulation of the variational principle. Here we show that by introducing a generator coordinate in the Kohn-Sham equation of density-functional theory, excitation energies can be obtained from ground-state density functionals. As a viability test, the method is applied to ground-state energies and various types of excited-state energies of atoms and ions from the He and the Li isoelectronic series. Results are compared to a variety of alternative DFT-based approaches to excited states, in particular time-dependent density-functional theory with exact and approximate potentials.</EA><CC>001C01</CC><FD>Energie transition; Etat fondamental; Fonctionnelle densité; Dépendance du temps; Méthode fonctionnelle densité; Etude théorique; Principe variationnel; Equation; Méthode essai; Etat excité; Ion; Potentiel; 3115E</FD><ED>Transition energy; Ground state; Density functional; Time dependence; Density functional method; Theoretical study; Variational principle; Equation; Test method; Excited state; Ions; Potential</ED><SD>Energía transición; Estado fundamental; Funciónal densidad; Dependencia del tiempo; Estudio teórico; Principio variacional; Ecuación; Método ensayo; Estado excitado; Ión; Potencial</SD><LO>INIST-26801.354000188583410160</LO><ID>09-0323136</ID></server></inist></record>
000D01	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Physical signatures of discontinuities of the time-dependent exchange-correlation potential</title><author><name sortKey="Vieira, Daniel" uniqKey="Vieira D">Daniel Vieira</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, São Carlos</s1><s2>São Paulo, 13560-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Department of Physics and Astronomy, University of Missouri</s1><s2>Columbia, Missouri, 65211</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Capelle, K" uniqKey="Capelle K">K. Capelle</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, São Carlos</s1><s2>São Paulo, 13560-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ullrich, C A" uniqKey="Ullrich C">C. A. Ullrich</name><affiliation><inist:fA14 i1="02"><s1>Department of Physics and Astronomy, University of Missouri</s1><s2>Columbia, Missouri, 65211</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0323144</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0323144 INIST</idno><idno type="RBID">Pascal:09-0323144</idno><idno type="wicri:Area/Main/Corpus">001C78</idno></publicationStmt><seriesStmt><idno type="ISSN">1463-9076</idno><title level="j" type="abbreviated">PCCP, Phys. chem. chem. phys. : (Print)</title><title level="j" type="main">PCCP. Physical chemistry chemical physics : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adiabatic approximation</term><term>Charge transfer</term><term>Confinement</term><term>Correlation</term><term>Density functional method</term><term>Dissociation</term><term>Electron loss</term><term>Exchange potential</term><term>Ionization</term><term>Local density approximation</term><term>Models</term><term>Particle number</term><term>Quantum system</term><term>Quantum well</term><term>Real time</term><term>Simulation</term><term>Theoretical study</term><term>Time dependence</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Potentiel échange</term><term>Corrélation</term><term>Dépendance du temps</term><term>Méthode fonctionnelle densité</term><term>Etude théorique</term><term>Nombre particule</term><term>Confinement</term><term>Approximation adiabatique</term><term>Approximation densité locale</term><term>Perte électron</term><term>Modèle</term><term>Puits quantique</term><term>Système quantique</term><term>Temps réel</term><term>Simulation</term><term>Dissociation</term><term>Ionisation</term><term>Transfert charge</term><term>3115E</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The exact exchange-correlation (XC) potential in time-dependent density-functional theory (TDDFT) is known to develop steps and discontinuities upon change of the particle number in spatially confined regions or isolated subsystems. We demonstrate that the self-interaction corrected adiabatic local-density approximation for the XC potential has this property, using the example of electron loss of a model quantum well system. We then study the influence of the XC potential discontinuity in a real-time simulation of a dissociation process of an asymmetric double quantum well system, and show that it dramatically affects the population of the resulting isolated single quantum wells. This indicates the importance of a proper account of the discontinuities in TDDFT descriptions of ionization, dissociation or charge transfer processes.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1463-9076</s0></fA01><fA03 i2="1"><s0>PCCP, Phys. chem. chem. phys. : (Print)</s0></fA03><fA05><s2>11</s2></fA05><fA06><s2>22</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Physical signatures of discontinuities of the time-dependent exchange-correlation potential</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Time-Dependent Density-Functional Theory</s1></fA09><fA11 i1="01" i2="1"><s1>VIEIRA (Daniel)</s1></fA11><fA11 i1="02" i2="1"><s1>CAPELLE (K.)</s1></fA11><fA11 i1="03" i2="1"><s1>ULLRICH (C. A.)</s1></fA11><fA12 i1="01" i2="1"><s1>RUBIO (Angel)</s1><s9>limin.</s9></fA12><fA12 i1="02" i2="1"><s1>MARQUES (Miguel)</s1><s9>limin.</s9></fA12><fA14 i1="01"><s1>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, São Carlos</s1><s2>São Paulo, 13560-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Physics and Astronomy, University of Missouri</s1><s2>Columbia, Missouri, 65211</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>Universidad del País Vasco</s1><s2>Bilbao</s2><s3>ESP</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>CSIC-UPV/EHU, ETSF and DIPC</s1><s2>San Sebatian</s2><s3>ESP</s3><sZ>1 aut.</sZ></fA15><fA15 i1="03"><s1>Université Claude Bernard and CNRS</s1><s2>Lyon</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>4647-4654</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26801</s2><s5>354000188583410260</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>35 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0323144</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>PCCP. Physical chemistry chemical physics : (Print)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The exact exchange-correlation (XC) potential in time-dependent density-functional theory (TDDFT) is known to develop steps and discontinuities upon change of the particle number in spatially confined regions or isolated subsystems. We demonstrate that the self-interaction corrected adiabatic local-density approximation for the XC potential has this property, using the example of electron loss of a model quantum well system. We then study the influence of the XC potential discontinuity in a real-time simulation of a dissociation process of an asymmetric double quantum well system, and show that it dramatically affects the population of the resulting isolated single quantum wells. This indicates the importance of a proper account of the discontinuities in TDDFT descriptions of ionization, dissociation or charge transfer processes.</s0></fC01><fC02 i1="01" i2="X"><s0>001C01</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Potentiel échange</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Exchange potential</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Potencial intercambio</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Corrélation</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Correlation</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Correlación</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Dépendance du temps</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Time dependence</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Dependencia del tiempo</s0><s5>03</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Méthode fonctionnelle densité</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Density functional method</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Etude théorique</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Theoretical study</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Estudio teórico</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Nombre particule</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Particle number</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Número partícula</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Confinement</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Confinement</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Confinamiento</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Approximation adiabatique</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Adiabatic approximation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Aproximación adiabática</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Approximation densité locale</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Local density approximation</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Aproximación densidad local</s0><s5>09</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Perte électron</s0><s5>10</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Electron loss</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Modèle</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Models</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Modelo</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Puits quantique</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Quantum well</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Pozo cuántico</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Système quantique</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Quantum system</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Sistema cuántico</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Temps réel</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Real time</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Tiempo real</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Simulation</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Simulation</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Simulación</s0><s5>15</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Dissociation</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Dissociation</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Disociación</s0><s5>16</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Ionisation</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Ionization</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Ionización</s0><s5>17</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Transfert charge</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Charge transfer</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Transferencia carga</s0><s5>18</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>3115E</s0><s4>INC</s4><s5>32</s5></fC03><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0323144 INIST</NO><ET>Physical signatures of discontinuities of the time-dependent exchange-correlation potential</ET><AU>VIEIRA (Daniel); CAPELLE (K.); ULLRICH (C. A.); RUBIO (Angel); MARQUES (Miguel)</AU><AF>Departamento de Física e Informática, Instituto de Física de São Carlos, Universidade de São Paulo, Caixa Postal 369, São Carlos/São Paulo, 13560-970/Brésil (1 aut., 2 aut.); Department of Physics and Astronomy, University of Missouri/Columbia, Missouri, 65211/Etats-Unis (1 aut., 3 aut.); Universidad del País Vasco/Bilbao/Espagne (1 aut.); CSIC-UPV/EHU, ETSF and DIPC/San Sebatian/Espagne (1 aut.); Université Claude Bernard and CNRS/Lyon/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>PCCP. Physical chemistry chemical physics : (Print); ISSN 1463-9076; Royaume-Uni; Da. 2009; Vol. 11; No. 22; Pp. 4647-4654; Bibl. 35 ref.</SO><LA>Anglais</LA><EA>The exact exchange-correlation (XC) potential in time-dependent density-functional theory (TDDFT) is known to develop steps and discontinuities upon change of the particle number in spatially confined regions or isolated subsystems. We demonstrate that the self-interaction corrected adiabatic local-density approximation for the XC potential has this property, using the example of electron loss of a model quantum well system. We then study the influence of the XC potential discontinuity in a real-time simulation of a dissociation process of an asymmetric double quantum well system, and show that it dramatically affects the population of the resulting isolated single quantum wells. This indicates the importance of a proper account of the discontinuities in TDDFT descriptions of ionization, dissociation or charge transfer processes.</EA><CC>001C01</CC><FD>Potentiel échange; Corrélation; Dépendance du temps; Méthode fonctionnelle densité; Etude théorique; Nombre particule; Confinement; Approximation adiabatique; Approximation densité locale; Perte électron; Modèle; Puits quantique; Système quantique; Temps réel; Simulation; Dissociation; Ionisation; Transfert charge; 3115E</FD><ED>Exchange potential; Correlation; Time dependence; Density functional method; Theoretical study; Particle number; Confinement; Adiabatic approximation; Local density approximation; Electron loss; Models; Quantum well; Quantum system; Real time; Simulation; Dissociation; Ionization; Charge transfer</ED><SD>Potencial intercambio; Correlación; Dependencia del tiempo; Estudio teórico; Número partícula; Confinamiento; Aproximación adiabática; Aproximación densidad local; Modelo; Pozo cuántico; Sistema cuántico; Tiempo real; Simulación; Disociación; Ionización; Transferencia carga</SD><LO>INIST-26801.354000188583410260</LO><ID>09-0323144</ID></server></inist></record>
000D02	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Naturalist transgressions in Europe and Latin America</title><author><name sortKey="Swarnakar, Sudha" uniqKey="Swarnakar S">Sudha Swarnakar</name><affiliation><inist:fA14 i1="01"><s1>State Universisty of Paraíba</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Motta Oliveira, Paulo" uniqKey="Motta Oliveira P">Paulo Motta Oliveira</name><affiliation><inist:fA14 i1="02"><s1>University of Sao Paulo</s1><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Acouisto, Joseph" uniqKey="Acouisto J">Joseph Acouisto</name><affiliation><inist:fA14 i1="03"><s1>University of Vermont</s1><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mendes, I Leonardo" uniqKey="Mendes I">I. Leonardo Mendes</name><affiliation><inist:fA14 i1="04"><s1>State University of Rio de Janeiro</s1><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bulhoes, Marcelo" uniqKey="Bulhoes M">Marcelo Bulhoes</name><affiliation><inist:fA14 i1="05"><s1>Université d'État Paulista</s1><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Santos, Ana Clara" uniqKey="Santos A">Ana Clara Santos</name></author><author><name sortKey="Batalha, Maria Cristina" uniqKey="Batalha M">Maria Cristina Batalha</name><affiliation><inist:fA14 i1="06"><s1>Université de l'État de Rio de Janeiro</s1><s3>BRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Luna Silva, Claudia" uniqKey="Luna Silva C">Claudia Luna Silva</name><affiliation><inist:fA14 i1="07"><s1>Universidad Federal de Rio de Janeiro</s1><s3>BRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Helena, Lucia" uniqKey="Helena L">Lucia Helena</name><affiliation><inist:fA14 i1="08"><s1>Université Fédérale Fluminense</s1><s3>FRA</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0324339</idno><date when="2006">2006</date><idno type="stanalyst">FRANCIS 09-0324339 INIST</idno><idno type="RBID">Francis:09-0324339</idno><idno type="wicri:Area/Main/Corpus">001F98</idno></publicationStmt><seriesStmt><idno type="ISSN">1021-5417</idno><title level="j" type="abbreviated">Excavatio : (San Rafael)</title><title level="j" type="main">Excavatio : (San Rafael)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Castelo Branco (C.)</term><term>Century 19-20</term><term>Comparative literature</term><term>France</term><term>Naturalism</term><term>Portugal</term><term>Rodrigues (N.)</term><term>Sexuality</term><term>Theater</term><term>Zola (E.)</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Naturalisme</term><term>Zola (E.)</term><term>Brésil</term><term>Castelo Branco (C.)</term><term>Portugal</term><term>France</term><term>Sexualité</term><term>Rodrigues (N.)</term><term>Théâtre</term><term>Siècle 19-20</term><term>Littérature comparée</term><term>Jorge Amado</term><term>Paul Bonnetain</term><term>Esteban Echevarria</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1021-5417</s0></fA01><fA03 i2="1"><s0>Excavatio : (San Rafael)</s0></fA03><fA05><s2>21</s2></fA05><fA06><s2>1-2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Naturalist transgressions in Europe and Latin America</s1></fA08><fA11 i1="01" i2="1"><s1>SWARNAKAR (Sudha)</s1></fA11><fA11 i1="02" i2="1"><s1>MOTTA OLIVEIRA (Paulo)</s1></fA11><fA11 i1="03" i2="1"><s1>ACOUISTO (Joseph)</s1></fA11><fA11 i1="04" i2="1"><s1>MENDES (I. Leonardo)</s1></fA11><fA11 i1="05" i2="1"><s1>BULHOES (Marcelo)</s1></fA11><fA11 i1="06" i2="1"><s1>SANTOS (Ana Clara)</s1></fA11><fA11 i1="07" i2="1"><s1>BATALHA (Maria Cristina)</s1></fA11><fA11 i1="08" i2="1"><s1>LUNA SILVA (Claudia)</s1></fA11><fA11 i1="09" i2="1"><s1>HELENA (Lucia)</s1></fA11><fA14 i1="01"><s1>State Universisty of Paraíba</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>University of Sao Paulo</s1><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>University of Vermont</s1><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>State University of Rio de Janeiro</s1><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Université d'État Paulista</s1><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Université de l'État de Rio de Janeiro</s1><s3>BRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>Universidad Federal de Rio de Janeiro</s1><s3>BRA</s3><sZ>8 aut.</sZ></fA14><fA14 i1="08"><s1>Université Fédérale Fluminense</s1><s3>FRA</s3><sZ>9 aut.</sZ></fA14><fA20><s1>1-105</s1></fA20><fA21><s1>2006</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27688</s2><s5>354000162507720010</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA47 i1="01" i2="1"><s0>09-0324339</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Excavatio : (San Rafael)</s0></fA64><fA66 i1="01"><s0>CAN</s0></fA66><fA68 i1="01" i2="1" l="FRE"><s1>Transgressions naturalistes en Europe et en Amérique latine</s1></fA68><fC02 i1="01" i2="I"><s0>52328</s0><s1>II</s1></fC02><fC02 i1="02" i2="I"><s0>523</s0></fC02><fC03 i1="01" i2="I" l="FRE"><s0>Naturalisme</s0><s5>01</s5></fC03><fC03 i1="01" i2="I" l="ENG"><s0>Naturalism</s0><s5>01</s5></fC03><fC03 i1="02" i2="I" l="FRE"><s0>Zola (E.)</s0><s2>NF</s2><s2>FA</s2><s5>02</s5></fC03><fC03 i1="02" i2="I" l="ENG"><s0>Zola (E.)</s0><s2>NF</s2><s2>FA</s2><s5>02</s5></fC03><fC03 i1="03" i2="I" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>03</s5></fC03><fC03 i1="03" i2="I" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>03</s5></fC03><fC03 i1="04" i2="I" l="FRE"><s0>Castelo Branco (C.)</s0><s2>NF</s2><s2>FA</s2><s5>04</s5></fC03><fC03 i1="04" i2="I" l="ENG"><s0>Castelo Branco (C.)</s0><s2>NF</s2><s2>FA</s2><s5>04</s5></fC03><fC03 i1="05" i2="I" l="FRE"><s0>Portugal</s0><s2>NG</s2><s5>05</s5></fC03><fC03 i1="05" i2="I" l="ENG"><s0>Portugal</s0><s2>NG</s2><s5>05</s5></fC03><fC03 i1="06" i2="I" l="FRE"><s0>France</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="I" l="ENG"><s0>France</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="07" i2="I" l="FRE"><s0>Sexualité</s0><s5>07</s5></fC03><fC03 i1="07" i2="I" l="ENG"><s0>Sexuality</s0><s5>07</s5></fC03><fC03 i1="08" i2="I" l="FRE"><s0>Rodrigues (N.)</s0><s2>NF</s2><s2>FA</s2><s5>08</s5></fC03><fC03 i1="08" i2="I" l="ENG"><s0>Rodrigues (N.)</s0><s2>NF</s2><s2>FA</s2><s5>08</s5></fC03><fC03 i1="09" i2="I" l="FRE"><s0>Théâtre</s0><s5>09</s5></fC03><fC03 i1="09" i2="I" l="ENG"><s0>Theater</s0><s5>09</s5></fC03><fC03 i1="10" i2="I" l="FRE"><s0>Siècle 19-20</s0><s2>ND</s2><s5>10</s5></fC03><fC03 i1="10" i2="I" l="ENG"><s0>Century 19-20</s0><s2>ND</s2><s5>10</s5></fC03><fC03 i1="11" i2="I" l="FRE"><s0>Littérature comparée</s0><s5>11</s5></fC03><fC03 i1="11" i2="I" l="ENG"><s0>Comparative literature</s0><s5>11</s5></fC03><fC03 i1="12" i2="I" l="FRE"><s0>Jorge Amado</s0><s4>INC</s4><s5>31</s5></fC03><fC03 i1="13" i2="I" l="FRE"><s0>Paul Bonnetain</s0><s4>INC</s4><s5>32</s5></fC03><fC03 i1="14" i2="I" l="FRE"><s0>Esteban Echevarria</s0><s4>INC</s4><s5>33</s5></fC03><fN21><s1>236</s1></fN21></pA></standard><server><NO>FRANCIS 09-0324339 INIST</NO><FT>(Transgressions naturalistes en Europe et en Amérique latine)</FT><ET>Naturalist transgressions in Europe and Latin America</ET><AU>SWARNAKAR (Sudha); MOTTA OLIVEIRA (Paulo); ACOUISTO (Joseph); MENDES (I. Leonardo); BULHOES (Marcelo); SANTOS (Ana Clara); BATALHA (Maria Cristina); LUNA SILVA (Claudia); HELENA (Lucia)</AU><AF>State Universisty of Paraíba/Brésil (1 aut.); University of Sao Paulo/Brésil (2 aut.); University of Vermont/France (3 aut.); State University of Rio de Janeiro/Brésil (4 aut.); Université d'État Paulista/France (5 aut.); Université de l'État de Rio de Janeiro/Brésil (7 aut.); Universidad Federal de Rio de Janeiro/Brésil (8 aut.); Université Fédérale Fluminense/France (9 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Excavatio : (San Rafael); ISSN 1021-5417; Canada; Da. 2006; Vol. 21; No. 1-2; Pp. 1-105</SO><LA>Anglais</LA><CC>52328; 523</CC><FD>Naturalisme; Zola (E.); Brésil; Castelo Branco (C.); Portugal; France; Sexualité; Rodrigues (N.); Théâtre; Siècle 19-20; Littérature comparée; Jorge Amado; Paul Bonnetain; Esteban Echevarria</FD><ED>Naturalism; Zola (E.); Brazil; Castelo Branco (C.); Portugal; France; Sexuality; Rodrigues (N.); Theater; Century 19-20; Comparative literature</ED><LO>INIST-27688.354000162507720010</LO><ID>09-0324339</ID></server></inist></record>
000D03	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Screening naturalism : Problematics of film adaptation</title><author><name sortKey="Baguley, David" uniqKey="Baguley D">David Baguley</name><affiliation><inist:fA14 i1="01"><s1>Durham University</s1><s3>USA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wolter, Jennifer" uniqKey="Wolter J">Jennifer Wolter</name><affiliation><inist:fA14 i1="02"><s1>Grand Valley State University</s1><s3>USA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cummins, Laurel" uniqKey="Cummins L">Laurel Cummins</name><affiliation><inist:fA14 i1="03"><s1>Bronx Community College</s1><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Griffiths, Kate" uniqKey="Griffiths K">Kate Griffiths</name><affiliation><inist:fA14 i1="04"><s1>University of Wales</s1><s2>Bangor</s2><s3>GBR</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schaffner, Isabelle" uniqKey="Schaffner I">Isabelle Schaffner</name><affiliation><inist:fA14 i1="05"><s1>École Polytechnique de Paris</s1><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Carvalhao Buescu, Helena" uniqKey="Carvalhao Buescu H">Helena Carvalhao Buescu</name><affiliation><inist:fA14 i1="06"><s1>University of Lisbon</s1><s3>PRT</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Figueiredo, Monica" uniqKey="Figueiredo M">Monica Figueiredo</name><affiliation><inist:fA14 i1="07"><s1>Université Fédérale de Rio de Janeiro</s1><s3>BRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0324341</idno><date when="2006">2006</date><idno type="stanalyst">FRANCIS 09-0324341 INIST</idno><idno type="RBID">Francis:09-0324341</idno><idno type="wicri:Area/Main/Corpus">001F97</idno></publicationStmt><seriesStmt><idno type="ISSN">1021-5417</idno><title level="j" type="abbreviated">Excavatio : (San Rafael)</title><title level="j" type="main">Excavatio : (San Rafael)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aesthetics</term><term>Century 19-20</term><term>Cinematographic adaptation</term><term>France</term><term>Naturalism</term><term>Portugal</term><term>Zola (E.)</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>France</term><term>Siècle 19-20</term><term>Naturalisme</term><term>Zola (E.)</term><term>Adaptation cinématographique</term><term>Portugal</term><term>Esthétique</term><term>La Bête humaine</term><term>Jean Renoir</term><term>Fritz Lang</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1021-5417</s0></fA01><fA03 i2="1"><s0>Excavatio : (San Rafael)</s0></fA03><fA05><s2>21</s2></fA05><fA06><s2>1-2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Screening naturalism : Problematics of film adaptation</s1></fA08><fA11 i1="01" i2="1"><s1>BAGULEY (David)</s1></fA11><fA11 i1="02" i2="1"><s1>WOLTER (Jennifer)</s1></fA11><fA11 i1="03" i2="1"><s1>CUMMINS (Laurel)</s1></fA11><fA11 i1="04" i2="1"><s1>GRIFFITHS (Kate)</s1></fA11><fA11 i1="05" i2="1"><s1>SCHAFFNER (Isabelle)</s1></fA11><fA11 i1="06" i2="1"><s1>CARVALHAO BUESCU (Helena)</s1></fA11><fA11 i1="07" i2="1"><s1>FIGUEIREDO (Monica)</s1></fA11><fA14 i1="01"><s1>Durham University</s1><s3>USA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Grand Valley State University</s1><s3>USA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Bronx Community College</s1><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>University of Wales</s1><s2>Bangor</s2><s3>GBR</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>École Polytechnique de Paris</s1><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>University of Lisbon</s1><s3>PRT</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Université Fédérale de Rio de Janeiro</s1><s3>BRA</s3><sZ>7 aut.</sZ></fA14><fA20><s1>198-283</s1></fA20><fA21><s1>2006</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27688</s2><s5>354000162507720030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA47 i1="01" i2="1"><s0>09-0324341</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Excavatio : (San Rafael)</s0></fA64><fA66 i1="01"><s0>CAN</s0></fA66><fC02 i1="01" i2="I"><s0>523182</s0><s1>III</s1></fC02><fC02 i1="02" i2="I"><s0>523</s0></fC02><fC03 i1="01" i2="I" l="FRE"><s0>France</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="I" l="ENG"><s0>France</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="02" i2="I" l="FRE"><s0>Siècle 19-20</s0><s2>ND</s2><s5>02</s5></fC03><fC03 i1="02" i2="I" l="ENG"><s0>Century 19-20</s0><s2>ND</s2><s5>02</s5></fC03><fC03 i1="03" i2="I" l="FRE"><s0>Naturalisme</s0><s5>03</s5></fC03><fC03 i1="03" i2="I" l="ENG"><s0>Naturalism</s0><s5>03</s5></fC03><fC03 i1="04" i2="I" l="FRE"><s0>Zola (E.)</s0><s2>NF</s2><s2>FA</s2><s5>04</s5></fC03><fC03 i1="04" i2="I" l="ENG"><s0>Zola (E.)</s0><s2>NF</s2><s2>FA</s2><s5>04</s5></fC03><fC03 i1="05" i2="I" l="FRE"><s0>Adaptation cinématographique</s0><s5>05</s5></fC03><fC03 i1="05" i2="I" l="ENG"><s0>Cinematographic adaptation</s0><s5>05</s5></fC03><fC03 i1="06" i2="I" l="FRE"><s0>Portugal</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="I" l="ENG"><s0>Portugal</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="07" i2="I" l="FRE"><s0>Esthétique</s0><s5>07</s5></fC03><fC03 i1="07" i2="I" l="ENG"><s0>Aesthetics</s0><s5>07</s5></fC03><fC03 i1="08" i2="I" l="FRE"><s0>La Bête humaine</s0><s4>INC</s4><s5>31</s5></fC03><fC03 i1="09" i2="I" l="FRE"><s0>Jean Renoir</s0><s4>INC</s4><s5>32</s5></fC03><fC03 i1="10" i2="I" l="FRE"><s0>Fritz Lang</s0><s4>INC</s4><s5>33</s5></fC03><fN21><s1>236</s1></fN21></pA></standard><server><NO>FRANCIS 09-0324341 INIST</NO><ET>Screening naturalism : Problematics of film adaptation</ET><AU>BAGULEY (David); WOLTER (Jennifer); CUMMINS (Laurel); GRIFFITHS (Kate); SCHAFFNER (Isabelle); CARVALHAO BUESCU (Helena); FIGUEIREDO (Monica)</AU><AF>Durham University/Etats-Unis (1 aut.); Grand Valley State University/Etats-Unis (2 aut.); Bronx Community College/Etats-Unis (3 aut.); University of Wales/Bangor/Royaume-Uni (4 aut.); École Polytechnique de Paris/France (5 aut.); University of Lisbon/Portugal (6 aut.); Université Fédérale de Rio de Janeiro/Brésil (7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Excavatio : (San Rafael); ISSN 1021-5417; Canada; Da. 2006; Vol. 21; No. 1-2; Pp. 198-283</SO><LA>Anglais</LA><CC>523182; 523</CC><FD>France; Siècle 19-20; Naturalisme; Zola (E.); Adaptation cinématographique; Portugal; Esthétique; La Bête humaine; Jean Renoir; Fritz Lang</FD><ED>France; Century 19-20; Naturalism; Zola (E.); Cinematographic adaptation; Portugal; Aesthetics</ED><LO>INIST-27688.354000162507720030</LO><ID>09-0324341</ID></server></inist></record>
000D04	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Dasatinib in the Treatment of Chronic Myeloid Leukemia in Accelerated Phase After Imatinib Failure: The START A Trial</title><author><name sortKey="Apperley, Jane F" uniqKey="Apperley J">Jane F. Apperley</name><affiliation><inist:fA14 i1="01"><s1>From the Hammersmith Hospital, Imperial College</s1><s2>London</s2><s3>GBR</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>University of Texas M. D. Anderson Cancer Center</s1><s2>Houston, TX</s2><s3>USA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>St Mary's Hospital, the Catholic University of Korea</s1><s2>Seoul</s2><s3>KOR</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Chonnam National University</s1><s2>Hwasun-gun, Jeollanam-do</s2><s3>KOR</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>Clinical Research Center, Centre Hospitalier Universitaire de Poitiers</s1><s2>Poitiers</s2><s3>FRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="06"><s1>Weill Medical College of Cornell University, New York Presbyterian Hospital</s1><s2>New York, NY</s2><s3>USA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>S Orsola-Malpighi University Hospital</s1><s2>Bologna</s2><s3>ITA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="08"><s1>Ospedale S. Eugenio</s1><s2>Rome</s2><s3>ITA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="09"><s1>British Hospital of Buenos Aires</s1><s3>ARG</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="10"><s1>Medizinische Fakultät Mannheim, Universität Heidelberg</s1><s2>Mannheim</s2><s3>DEU</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="11"><s1>University Hospital</s1><s2>Basel</s2><s3>CHE</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="12"><s1>Universidade Estadual De Campinas</s1><s2>Campinas</s2><s3>BRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="13"><s1>University of Chicago</s1><s2>Chicago, IL</s2><s3>USA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="14"><s1>Princess Margaret Hospital</s1><s2>Toronto, Ontario</s2><s3>CAN</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="15"><s1>Emory University School of Medicine</s1><s2>Atlanta, GA</s2><s3>USA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="16"><s1>Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="17"><s1>University of Adelaide</s1><s2>Adelaide</s2><s3>AUS</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="18"><s1>Bristol-Myers Squibb</s1><s2>Wallingford, CT</s2><s3>USA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="19"><s1>Dana-Farber Cancer Institute</s1><s2>Boston, MA</s2><s3>USA</s3></inist:fA14></affiliation></author><author><name sortKey="Cortes, Jorge E" uniqKey="Cortes J">Jorge E. Cortes</name></author><author><name sortKey="Kim, Dong Wook" uniqKey="Kim D">Dong-Wook Kim</name></author><author><name sortKey="Roy, Lydia" uniqKey="Roy L">Lydia Roy</name></author><author><name sortKey="Roboz, Gail J" uniqKey="Roboz G">Gail J. Roboz</name></author><author><name sortKey="Rosti, Gianantonio" uniqKey="Rosti G">Gianantonio Rosti</name></author><author><name sortKey="Bullorsky, Eduardo O" uniqKey="Bullorsky E">Eduardo O. Bullorsky</name></author><author><name sortKey="Abruzzese, Elisabetta" uniqKey="Abruzzese E">Elisabetta Abruzzese</name></author><author><name sortKey="Hochhaus, Andreas" uniqKey="Hochhaus A">Andreas Hochhaus</name></author><author><name sortKey="Heim, Dominik" uniqKey="Heim D">Dominik Heim</name></author><author><name sortKey="De Souza, Carmino A" uniqKey="De Souza C">Carmino A. De Souza</name></author><author><name sortKey="Larson, Richard A" uniqKey="Larson R">Richard A. Larson</name></author><author><name sortKey="Lipton, Jeffrey H" uniqKey="Lipton J">Jeffrey H. Lipton</name></author><author><name sortKey="Khoury, H Jean" uniqKey="Khoury H">H. Jean Khoury</name></author><author><name sortKey="Kim, Hyeoung Joon" uniqKey="Kim H">Hyeoung-Joon Kim</name></author><author><name sortKey="Sillaber, Christian" uniqKey="Sillaber C">Christian Sillaber</name></author><author><name sortKey="Hughes, Timothy P" uniqKey="Hughes T">Timothy P. Hughes</name></author><author><name sortKey="Erben, Philipp" uniqKey="Erben P">Philipp Erben</name></author><author><name sortKey="Van Tornout, Jan" uniqKey="Van Tornout J">Jan Van Tornout</name></author><author><name sortKey="Stone, Richard M" uniqKey="Stone R">Richard M. Stone</name></author></titleStmt><publicationStmt><idno type="inist">09-0326540</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0326540 INIST</idno><idno type="RBID">Pascal:09-0326540</idno><idno type="wicri:Area/Main/Corpus">001C77</idno></publicationStmt><seriesStmt><idno type="ISSN">0732-183X</idno><title level="j" type="abbreviated">J. clin. oncol.</title><title level="j" type="main">Journal of clinical oncology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antineoplastic agent</term><term>Cancerology</term><term>Chronic myelogenous leukemia</term><term>Clinical trial</term><term>Dasatinib</term><term>Enzyme inhibitor</term><term>Imatinib</term><term>Protein-tyrosine kinase</term><term>Treatment</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dasatinib</term><term>Anticancéreux</term><term>Traitement</term><term>Imatinib</term><term>Leucémie myéloïde chronique</term><term>Protein-tyrosine kinase</term><term>Inhibiteur enzyme</term><term>Essai clinique</term><term>Cancérologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Purpose Patients with chronic myelogenous leukemia in accelerated phase (CML-AP) that is resistant or intolerant to imatinib have limited therapeutic options. Dasatinib, a potent inhibitor of BCR-ABL and SRC-family kinases, has efficacy in patients with CML-AP who have experienced treatment failure with imatinib. We now report follow-up data from the full patient cohort of 174 patients enrolled onto a phase II trial to provide a more complete assessment of the efficacy and safety of dasatinib in this population. Patients and Methods Patients with imatinib-resistant (n = 161) or -intolerant (n = 13) CML-AP received dasatinib 70 mg orally twice daily. Results At a median follow-up of 14.1 months (treatment duration, 0.1 to 21.7 months), major and complete hematologic responses were attained by 64% and 45% of patients, respectively, and major and complete cytogenetic responses were achieved in 39% and 32% of patients, respectively. Responses were achieved irrespective of imatinib status (resistant or intolerant), prior stem-cell transplantation, or the presence of prior BCR-ABL mutation. The 12-month progression-free survival and overall survival rates were 66% and 82%, respectively. Dasatinib was generally well tolerated; the most frequent nonhematologic severe treatment-related adverse event was diarrhea (52%; grade 3 to 4, 8%). Cytopenias were common, including grade 3 to 4 neutropenia (76%) and thrombocytopenia (82%). Pleural effusion occurred in 27% of patients (grade 3 to 4, 5%). Conclusion Dasatinib is effective in patients with CML-AP after imatinib treatment failure.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0732-183X</s0></fA01><fA03 i2="1"><s0>J. clin. oncol.</s0></fA03><fA05><s2>27</s2></fA05><fA06><s2>21</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Dasatinib in the Treatment of Chronic Myeloid Leukemia in Accelerated Phase After Imatinib Failure: The START A Trial</s1></fA08><fA11 i1="01" i2="1"><s1>APPERLEY (Jane F.)</s1></fA11><fA11 i1="02" i2="1"><s1>CORTES (Jorge E.)</s1></fA11><fA11 i1="03" i2="1"><s1>KIM (Dong-Wook)</s1></fA11><fA11 i1="04" i2="1"><s1>ROY (Lydia)</s1></fA11><fA11 i1="05" i2="1"><s1>ROBOZ (Gail J.)</s1></fA11><fA11 i1="06" i2="1"><s1>ROSTI (Gianantonio)</s1></fA11><fA11 i1="07" i2="1"><s1>BULLORSKY (Eduardo O.)</s1></fA11><fA11 i1="08" i2="1"><s1>ABRUZZESE (Elisabetta)</s1></fA11><fA11 i1="09" i2="1"><s1>HOCHHAUS (Andreas)</s1></fA11><fA11 i1="10" i2="1"><s1>HEIM (Dominik)</s1></fA11><fA11 i1="11" i2="1"><s1>DE SOUZA (Carmino A.)</s1></fA11><fA11 i1="12" i2="1"><s1>LARSON (Richard A.)</s1></fA11><fA11 i1="13" i2="1"><s1>LIPTON (Jeffrey H.)</s1></fA11><fA11 i1="14" i2="1"><s1>KHOURY (H. Jean)</s1></fA11><fA11 i1="15" i2="1"><s1>KIM (Hyeoung-Joon)</s1></fA11><fA11 i1="16" i2="1"><s1>SILLABER (Christian)</s1></fA11><fA11 i1="17" i2="1"><s1>HUGHES (Timothy P.)</s1></fA11><fA11 i1="18" i2="1"><s1>ERBEN (Philipp)</s1></fA11><fA11 i1="19" i2="1"><s1>VAN TORNOUT (Jan)</s1></fA11><fA11 i1="20" i2="1"><s1>STONE (Richard M.)</s1></fA11><fA14 i1="01"><s1>From the Hammersmith Hospital, Imperial College</s1><s2>London</s2><s3>GBR</s3></fA14><fA14 i1="02"><s1>University of Texas M. D. Anderson Cancer Center</s1><s2>Houston, TX</s2><s3>USA</s3></fA14><fA14 i1="03"><s1>St Mary's Hospital, the Catholic University of Korea</s1><s2>Seoul</s2><s3>KOR</s3></fA14><fA14 i1="04"><s1>Chonnam National University</s1><s2>Hwasun-gun, Jeollanam-do</s2><s3>KOR</s3></fA14><fA14 i1="05"><s1>Clinical Research Center, Centre Hospitalier Universitaire de Poitiers</s1><s2>Poitiers</s2><s3>FRA</s3></fA14><fA14 i1="06"><s1>Weill Medical College of Cornell University, New York Presbyterian Hospital</s1><s2>New York, NY</s2><s3>USA</s3></fA14><fA14 i1="07"><s1>S Orsola-Malpighi University Hospital</s1><s2>Bologna</s2><s3>ITA</s3></fA14><fA14 i1="08"><s1>Ospedale S. Eugenio</s1><s2>Rome</s2><s3>ITA</s3></fA14><fA14 i1="09"><s1>British Hospital of Buenos Aires</s1><s3>ARG</s3></fA14><fA14 i1="10"><s1>Medizinische Fakultät Mannheim, Universität Heidelberg</s1><s2>Mannheim</s2><s3>DEU</s3></fA14><fA14 i1="11"><s1>University Hospital</s1><s2>Basel</s2><s3>CHE</s3></fA14><fA14 i1="12"><s1>Universidade Estadual De Campinas</s1><s2>Campinas</s2><s3>BRA</s3></fA14><fA14 i1="13"><s1>University of Chicago</s1><s2>Chicago, IL</s2><s3>USA</s3></fA14><fA14 i1="14"><s1>Princess Margaret Hospital</s1><s2>Toronto, Ontario</s2><s3>CAN</s3></fA14><fA14 i1="15"><s1>Emory University School of Medicine</s1><s2>Atlanta, GA</s2><s3>USA</s3></fA14><fA14 i1="16"><s1>Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3></fA14><fA14 i1="17"><s1>University of Adelaide</s1><s2>Adelaide</s2><s3>AUS</s3></fA14><fA14 i1="18"><s1>Bristol-Myers Squibb</s1><s2>Wallingford, CT</s2><s3>USA</s3></fA14><fA14 i1="19"><s1>Dana-Farber Cancer Institute</s1><s2>Boston, MA</s2><s3>USA</s3></fA14><fA20><s1>3472-3479</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20094</s2><s5>354000187519420120</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>30 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0326540</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of clinical oncology</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Purpose Patients with chronic myelogenous leukemia in accelerated phase (CML-AP) that is resistant or intolerant to imatinib have limited therapeutic options. Dasatinib, a potent inhibitor of BCR-ABL and SRC-family kinases, has efficacy in patients with CML-AP who have experienced treatment failure with imatinib. We now report follow-up data from the full patient cohort of 174 patients enrolled onto a phase II trial to provide a more complete assessment of the efficacy and safety of dasatinib in this population. Patients and Methods Patients with imatinib-resistant (n = 161) or -intolerant (n = 13) CML-AP received dasatinib 70 mg orally twice daily. Results At a median follow-up of 14.1 months (treatment duration, 0.1 to 21.7 months), major and complete hematologic responses were attained by 64% and 45% of patients, respectively, and major and complete cytogenetic responses were achieved in 39% and 32% of patients, respectively. Responses were achieved irrespective of imatinib status (resistant or intolerant), prior stem-cell transplantation, or the presence of prior BCR-ABL mutation. The 12-month progression-free survival and overall survival rates were 66% and 82%, respectively. Dasatinib was generally well tolerated; the most frequent nonhematologic severe treatment-related adverse event was diarrhea (52%; grade 3 to 4, 8%). Cytopenias were common, including grade 3 to 4 neutropenia (76%) and thrombocytopenia (82%). Pleural effusion occurred in 27% of patients (grade 3 to 4, 5%). Conclusion Dasatinib is effective in patients with CML-AP after imatinib treatment failure.</s0></fC01><fC02 i1="01" i2="X"><s0>002B04</s0></fC02><fC02 i1="02" i2="X"><s0>002B19B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Anticancéreux</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Antineoplastic agent</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Anticanceroso</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Traitement</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Treatment</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Tratamiento</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Leucémie myéloïde chronique</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Chronic myelogenous leukemia</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Leucemia mieloidea crónica</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Inhibiteur enzyme</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Enzyme inhibitor</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Inhibidor enzima</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Essai clinique</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Clinical trial</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Ensayo clínico</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Cancérologie</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Cancerology</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Cancerología</s0><s5>11</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Inhibiteur de la tyrosine kinase</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Tyrosine kinase inhibitor</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Inhibidor tyrosine kinase</s0><s5>37</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Inhibiteur multikinase</s0><s5>38</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Multikinase inhibitor</s0><s5>38</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>inhibidor multicinasa</s0><s5>38</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Hémopathie maligne</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Malignant hemopathy</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Hemopatía maligna</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Syndrome myéloprolifératif</s0><s5>40</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Myeloproliferative syndrome</s0><s5>40</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Mieloproliferativo síndrome</s0><s5>40</s5></fC07><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0326540 INIST</NO><ET>Dasatinib in the Treatment of Chronic Myeloid Leukemia in Accelerated Phase After Imatinib Failure: The START A Trial</ET><AU>APPERLEY (Jane F.); CORTES (Jorge E.); KIM (Dong-Wook); ROY (Lydia); ROBOZ (Gail J.); ROSTI (Gianantonio); BULLORSKY (Eduardo O.); ABRUZZESE (Elisabetta); HOCHHAUS (Andreas); HEIM (Dominik); DE SOUZA (Carmino A.); LARSON (Richard A.); LIPTON (Jeffrey H.); KHOURY (H. Jean); KIM (Hyeoung-Joon); SILLABER (Christian); HUGHES (Timothy P.); ERBEN (Philipp); VAN TORNOUT (Jan); STONE (Richard M.)</AU><AF>From the Hammersmith Hospital, Imperial College/London/Royaume-Uni; University of Texas M. D. Anderson Cancer Center/Houston, TX/Etats-Unis; St Mary's Hospital, the Catholic University of Korea/Seoul/Corée, République de; Chonnam National University/Hwasun-gun, Jeollanam-do/Corée, République de; Clinical Research Center, Centre Hospitalier Universitaire de Poitiers/Poitiers/France; Weill Medical College of Cornell University, New York Presbyterian Hospital/New York, NY/Etats-Unis; S Orsola-Malpighi University Hospital/Bologna/Italie; Ospedale S. Eugenio/Rome/Italie; British Hospital of Buenos Aires/Argentine; Medizinische Fakultät Mannheim, Universität Heidelberg/Mannheim/Allemagne; University Hospital/Basel/Suisse; Universidade Estadual De Campinas/Campinas/Brésil; University of Chicago/Chicago, IL/Etats-Unis; Princess Margaret Hospital/Toronto, Ontario/Canada; Emory University School of Medicine/Atlanta, GA/Etats-Unis; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna/Vienna/Autriche; University of Adelaide/Adelaide/Australie; Bristol-Myers Squibb/Wallingford, CT/Etats-Unis; Dana-Farber Cancer Institute/Boston, MA/Etats-Unis</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of clinical oncology; ISSN 0732-183X; Etats-Unis; Da. 2009; Vol. 27; No. 21; Pp. 3472-3479; Bibl. 30 ref.</SO><LA>Anglais</LA><EA>Purpose Patients with chronic myelogenous leukemia in accelerated phase (CML-AP) that is resistant or intolerant to imatinib have limited therapeutic options. Dasatinib, a potent inhibitor of BCR-ABL and SRC-family kinases, has efficacy in patients with CML-AP who have experienced treatment failure with imatinib. We now report follow-up data from the full patient cohort of 174 patients enrolled onto a phase II trial to provide a more complete assessment of the efficacy and safety of dasatinib in this population. Patients and Methods Patients with imatinib-resistant (n = 161) or -intolerant (n = 13) CML-AP received dasatinib 70 mg orally twice daily. Results At a median follow-up of 14.1 months (treatment duration, 0.1 to 21.7 months), major and complete hematologic responses were attained by 64% and 45% of patients, respectively, and major and complete cytogenetic responses were achieved in 39% and 32% of patients, respectively. Responses were achieved irrespective of imatinib status (resistant or intolerant), prior stem-cell transplantation, or the presence of prior BCR-ABL mutation. The 12-month progression-free survival and overall survival rates were 66% and 82%, respectively. Dasatinib was generally well tolerated; the most frequent nonhematologic severe treatment-related adverse event was diarrhea (52%; grade 3 to 4, 8%). Cytopenias were common, including grade 3 to 4 neutropenia (76%) and thrombocytopenia (82%). Pleural effusion occurred in 27% of patients (grade 3 to 4, 5%). Conclusion Dasatinib is effective in patients with CML-AP after imatinib treatment failure.</EA><CC>002B04; 002B19B</CC><FD>Dasatinib; Anticancéreux; Traitement; Imatinib; Leucémie myéloïde chronique; Protein-tyrosine kinase; Inhibiteur enzyme; Essai clinique; Cancérologie</FD><FG>Transferases; Enzyme; Inhibiteur de la tyrosine kinase; Inhibiteur multikinase; Hémopathie maligne; Cancer; Syndrome myéloprolifératif</FG><ED>Dasatinib; Antineoplastic agent; Treatment; Imatinib; Chronic myelogenous leukemia; Protein-tyrosine kinase; Enzyme inhibitor; Clinical trial; Cancerology</ED><EG>Transferases; Enzyme; Tyrosine kinase inhibitor; Multikinase inhibitor; Malignant hemopathy; Cancer; Myeloproliferative syndrome</EG><SD>Dasatinib; Anticanceroso; Tratamiento; Imatinib; Leucemia mieloidea crónica; Protein-tyrosine kinase; Inhibidor enzima; Ensayo clínico; Cancerología</SD><LO>INIST-20094.354000187519420120</LO><ID>09-0326540</ID></server></inist></record>
000D05	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Assessing the stocks of the primary snappers caught in Northeastern Brazilian reef systems. 1: Traditional modelling approaches</title><author><name sortKey="Fredou, Thierry" uniqKey="Fredou T">Thierry Fredou</name><affiliation><inist:fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ferreira, Beatrice P" uniqKey="Ferreira B">Beatrice P. Ferreira</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Letourneur, Yves" uniqKey="Letourneur Y">Yves Letourneur</name><affiliation><inist:fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0327680</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0327680 INIST</idno><idno type="RBID">Pascal:09-0327680</idno><idno type="wicri:Area/Main/Corpus">001C76</idno></publicationStmt><seriesStmt><idno type="ISSN">0165-7836</idno><title level="j" type="abbreviated">Fish. res.</title><title level="j" type="main">Fisheries research</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Artisanal fishing</term><term>Brazil</term><term>Fishery</term><term>Marine environment</term><term>Modeling</term><term>Reef</term><term>Stock</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Stock</term><term>Brésil</term><term>Récif</term><term>Modélisation</term><term>Pêcherie</term><term>Milieu marin</term><term>Pagrus auratus</term><term>Lutjanus</term><term>Pêche artisanale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Traditional stock assessment models were used to describe the current status of Lutjanus analis, L. chrysurus, L. jocu, L synagris, and L. vivanus stocks off the coast of Northeast Brazil. The yield per recruit model, cohort analysis models (length-based cohort analysis (LCA), pseudo-cohort virtual population analysis (VPA), and real cohort VPA), and Thompson and Bell predictive model were used. The results showed LCA accumulates biases from pseudo-cohort VPA along with a high degree of sensitivity ofgrowth parameters, whose determination is problematic and may not be adequate for many other reef species. Although the real cohort VPA based on short time series may also be limited, this method was determined to be the most appropriate within the traditional methods applied for the assessment of reef fish. However, the VPA model heavily depends on the accuracy of landing data and discards estimation and estimated natural mortality (M), so caution should be applied when using such models. The conservative fishing mortality index F<sub>0.1</sub> was found to be the most adapted index when the uncertainty of parameter estimation and model limitations were considered. Consequently, a drastic reduction of 80-90% of the current fishing effort is recommended. Despite the VPA and Thompson and Bell model limitations, these models can provide insight into species/fishery dynamics and can also be utilised to analyse the effects of changes in fishing level on catches. In addition, the trends presented in this study are confirmed in a companion paper using more complex models.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0165-7836</s0></fA01><fA02 i1="01"><s0>FISRDJ</s0></fA02><fA03 i2="1"><s0>Fish. res.</s0></fA03><fA05><s2>99</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Assessing the stocks of the primary snappers caught in Northeastern Brazilian reef systems. 1: Traditional modelling approaches</s1></fA08><fA11 i1="01" i2="1"><s1>FREDOU (Thierry)</s1></fA11><fA11 i1="02" i2="1"><s1>FERREIRA (Beatrice P.)</s1></fA11><fA11 i1="03" i2="1"><s1>LETOURNEUR (Yves)</s1></fA11><fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA20><s1>90-96</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>19360</s2><s5>354000172424300040</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0327680</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Fisheries research</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>Traditional stock assessment models were used to describe the current status of Lutjanus analis, L. chrysurus, L. jocu, L synagris, and L. vivanus stocks off the coast of Northeast Brazil. The yield per recruit model, cohort analysis models (length-based cohort analysis (LCA), pseudo-cohort virtual population analysis (VPA), and real cohort VPA), and Thompson and Bell predictive model were used. The results showed LCA accumulates biases from pseudo-cohort VPA along with a high degree of sensitivity ofgrowth parameters, whose determination is problematic and may not be adequate for many other reef species. Although the real cohort VPA based on short time series may also be limited, this method was determined to be the most appropriate within the traditional methods applied for the assessment of reef fish. However, the VPA model heavily depends on the accuracy of landing data and discards estimation and estimated natural mortality (M), so caution should be applied when using such models. The conservative fishing mortality index F<sub>0.1</sub> was found to be the most adapted index when the uncertainty of parameter estimation and model limitations were considered. Consequently, a drastic reduction of 80-90% of the current fishing effort is recommended. Despite the VPA and Thompson and Bell model limitations, these models can provide insight into species/fishery dynamics and can also be utilised to analyse the effects of changes in fishing level on catches. In addition, the trends presented in this study are confirmed in a companion paper using more complex models.</s0></fC01><fC02 i1="01" i2="X"><s0>002A14D03</s0></fC02><fC02 i1="02" i2="X"><s0>002A14A02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Stock</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Stock</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Existencias</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Récif</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Reef</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Arrecife</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Modélisation</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Modeling</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Modelización</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Pêcherie</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Fishery</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Pesquería</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Milieu marin</s0><s5>23</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Marine environment</s0><s5>23</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Medio marino</s0><s5>23</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Pagrus auratus</s0><s4>INC</s4><s5>64</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Lutjanus</s0><s4>INC</s4><s5>65</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Pêche artisanale</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Artisanal fishing</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Pesca artesanal</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Sparidae</s0><s4>INC</s4><s5>70</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Lutjanidae</s0><s4>INC</s4><s5>71</s5></fC07><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0327680 INIST</NO><ET>Assessing the stocks of the primary snappers caught in Northeastern Brazilian reef systems. 1: Traditional modelling approaches</ET><AU>FREDOU (Thierry); FERREIRA (Beatrice P.); LETOURNEUR (Yves)</AU><AF>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540/13288 Marseille/France (1 aut., 3 aut.); Departamento de Oceanografia, Universidade Federal de Pernambuco/Recife, Pernambuco 50739-540/Brésil (1 aut., 2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Fisheries research; ISSN 0165-7836; Coden FISRDJ; Pays-Bas; Da. 2009; Vol. 99; No. 2; Pp. 90-96; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Traditional stock assessment models were used to describe the current status of Lutjanus analis, L. chrysurus, L. jocu, L synagris, and L. vivanus stocks off the coast of Northeast Brazil. The yield per recruit model, cohort analysis models (length-based cohort analysis (LCA), pseudo-cohort virtual population analysis (VPA), and real cohort VPA), and Thompson and Bell predictive model were used. The results showed LCA accumulates biases from pseudo-cohort VPA along with a high degree of sensitivity ofgrowth parameters, whose determination is problematic and may not be adequate for many other reef species. Although the real cohort VPA based on short time series may also be limited, this method was determined to be the most appropriate within the traditional methods applied for the assessment of reef fish. However, the VPA model heavily depends on the accuracy of landing data and discards estimation and estimated natural mortality (M), so caution should be applied when using such models. The conservative fishing mortality index F<sub>0.1</sub> was found to be the most adapted index when the uncertainty of parameter estimation and model limitations were considered. Consequently, a drastic reduction of 80-90% of the current fishing effort is recommended. Despite the VPA and Thompson and Bell model limitations, these models can provide insight into species/fishery dynamics and can also be utilised to analyse the effects of changes in fishing level on catches. In addition, the trends presented in this study are confirmed in a companion paper using more complex models.</EA><CC>002A14D03; 002A14A02</CC><FD>Stock; Brésil; Récif; Modélisation; Pêcherie; Milieu marin; Pagrus auratus; Lutjanus; Pêche artisanale</FD><FG>Amérique du Sud; Amérique; Pisces; Vertebrata; Sparidae; Lutjanidae</FG><ED>Stock; Brazil; Reef; Modeling; Fishery; Marine environment; Artisanal fishing</ED><EG>South America; America; Pisces; Vertebrata</EG><SD>Existencias; Brasil; Arrecife; Modelización; Pesquería; Medio marino; Pesca artesanal</SD><LO>INIST-19360.354000172424300040</LO><ID>09-0327680</ID></server></inist></record>
000D06	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Assessing the stocks of the primary snappers caught in Northeastern Brazilian Reef Systems. 2-A multi-fleet age-structured approach</title><author><name sortKey="Fredou, Thierry" uniqKey="Fredou T">Thierry Fredou</name><affiliation><inist:fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ferreira, Beatrice P" uniqKey="Ferreira B">Beatrice P. Ferreira</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Letourneur, Yves" uniqKey="Letourneur Y">Yves Letourneur</name><affiliation><inist:fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0327685</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0327685 INIST</idno><idno type="RBID">Pascal:09-0327685</idno><idno type="wicri:Area/Main/Corpus">001C75</idno></publicationStmt><seriesStmt><idno type="ISSN">0165-7836</idno><title level="j" type="abbreviated">Fish. res.</title><title level="j" type="main">Fisheries research</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Age</term><term>Artisanal fishing</term><term>Brazil</term><term>Fishery</term><term>Fleet</term><term>Interaction</term><term>Marine environment</term><term>Reef</term><term>Stock</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Stock</term><term>Brésil</term><term>Récif</term><term>Flotte</term><term>Age</term><term>Interaction</term><term>Pêcherie</term><term>Milieu marin</term><term>Pagrus auratus</term><term>Lutjanus</term><term>Pêche artisanale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This study investigates the exploitation of Lutjanus analis, Lutjanus chrysurus, Lutjanus jocu and Lutjanus synagris from multiple gear types in Northeast Brazil using models allowing for technological interactions. The spatial distribution of species and fleets have played an important role in the Northeastern Brazilian artisanal fishery. The results of a predictive model by Thompson and Bell, along with a catch-at-age model, clearly showed that different fleets had distinct effects on snapper stocks. The fishery mortality (F) from small-scale fleets ('Jangada' and 'Paquete') was higher for coastal species such as L. synagris that are typically found in these areas. Conversely, L. jocu, that inhabits deeper waters, was most affected by motorised and sailing boats. Snappers were exploited differently at each of their life history stages. 'Paquetes' mainly exploited juveniles, whereas boats caught larger individuals farther from the coast. As a consequence, effort control through fleet regulation seems to be much more applicable in a tropical context than traditional catch control. Further modelling studies and management options relevant to the Northeast Brazil fishery are discussed.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0165-7836</s0></fA01><fA02 i1="01"><s0>FISRDJ</s0></fA02><fA03 i2="1"><s0>Fish. res.</s0></fA03><fA05><s2>99</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Assessing the stocks of the primary snappers caught in Northeastern Brazilian Reef Systems. 2-A multi-fleet age-structured approach</s1></fA08><fA11 i1="01" i2="1"><s1>FREDOU (Thierry)</s1></fA11><fA11 i1="02" i2="1"><s1>FERREIRA (Beatrice P.)</s1></fA11><fA11 i1="03" i2="1"><s1>LETOURNEUR (Yves)</s1></fA11><fA14 i1="01"><s1>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540</s1><s2>13288 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Oceanografia, Universidade Federal de Pernambuco</s1><s2>Recife, Pernambuco 50739-540</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA20><s1>97-105</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>19360</s2><s5>354000172424300050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0327685</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Fisheries research</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>This study investigates the exploitation of Lutjanus analis, Lutjanus chrysurus, Lutjanus jocu and Lutjanus synagris from multiple gear types in Northeast Brazil using models allowing for technological interactions. The spatial distribution of species and fleets have played an important role in the Northeastern Brazilian artisanal fishery. The results of a predictive model by Thompson and Bell, along with a catch-at-age model, clearly showed that different fleets had distinct effects on snapper stocks. The fishery mortality (F) from small-scale fleets ('Jangada' and 'Paquete') was higher for coastal species such as L. synagris that are typically found in these areas. Conversely, L. jocu, that inhabits deeper waters, was most affected by motorised and sailing boats. Snappers were exploited differently at each of their life history stages. 'Paquetes' mainly exploited juveniles, whereas boats caught larger individuals farther from the coast. As a consequence, effort control through fleet regulation seems to be much more applicable in a tropical context than traditional catch control. Further modelling studies and management options relevant to the Northeast Brazil fishery are discussed.</s0></fC01><fC02 i1="01" i2="X"><s0>002A14D03</s0></fC02><fC02 i1="02" i2="X"><s0>002A15B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Stock</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Stock</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Existencias</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Récif</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Reef</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Arrecife</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Flotte</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Fleet</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Age</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Age</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Edad</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Interaction</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Interaction</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Interacción</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Pêcherie</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Fishery</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Pesquería</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Milieu marin</s0><s5>23</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Marine environment</s0><s5>23</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Medio marino</s0><s5>23</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Pagrus auratus</s0><s4>INC</s4><s5>64</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Lutjanus</s0><s4>INC</s4><s5>65</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Pêche artisanale</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Artisanal fishing</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Pesca artesanal</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Pisces</s0><s2>NS</s2><s5>29</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Sparidae</s0><s4>INC</s4><s5>70</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Lutjanidae</s0><s4>INC</s4><s5>71</s5></fC07><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0327685 INIST</NO><ET>Assessing the stocks of the primary snappers caught in Northeastern Brazilian Reef Systems. 2-A multi-fleet age-structured approach</ET><AU>FREDOU (Thierry); FERREIRA (Beatrice P.); LETOURNEUR (Yves)</AU><AF>Université de la Méditerranée, Centre d'Océanologie de Marseille, UMR CNRS 6540/13288 Marseille/France (1 aut., 3 aut.); Departamento de Oceanografia, Universidade Federal de Pernambuco/Recife, Pernambuco 50739-540/Brésil (1 aut., 2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Fisheries research; ISSN 0165-7836; Coden FISRDJ; Pays-Bas; Da. 2009; Vol. 99; No. 2; Pp. 97-105; Bibl. 1/4 p.</SO><LA>Anglais</LA><EA>This study investigates the exploitation of Lutjanus analis, Lutjanus chrysurus, Lutjanus jocu and Lutjanus synagris from multiple gear types in Northeast Brazil using models allowing for technological interactions. The spatial distribution of species and fleets have played an important role in the Northeastern Brazilian artisanal fishery. The results of a predictive model by Thompson and Bell, along with a catch-at-age model, clearly showed that different fleets had distinct effects on snapper stocks. The fishery mortality (F) from small-scale fleets ('Jangada' and 'Paquete') was higher for coastal species such as L. synagris that are typically found in these areas. Conversely, L. jocu, that inhabits deeper waters, was most affected by motorised and sailing boats. Snappers were exploited differently at each of their life history stages. 'Paquetes' mainly exploited juveniles, whereas boats caught larger individuals farther from the coast. As a consequence, effort control through fleet regulation seems to be much more applicable in a tropical context than traditional catch control. Further modelling studies and management options relevant to the Northeast Brazil fishery are discussed.</EA><CC>002A14D03; 002A15B</CC><FD>Stock; Brésil; Récif; Flotte; Age; Interaction; Pêcherie; Milieu marin; Pagrus auratus; Lutjanus; Pêche artisanale</FD><FG>Amérique du Sud; Amérique; Pisces; Vertebrata; Sparidae; Lutjanidae</FG><ED>Stock; Brazil; Reef; Fleet; Age; Interaction; Fishery; Marine environment; Artisanal fishing</ED><EG>South America; America; Pisces; Vertebrata</EG><SD>Existencias; Brasil; Arrecife; Edad; Interacción; Pesquería; Medio marino; Pesca artesanal</SD><LO>INIST-19360.354000172424300050</LO><ID>09-0327685</ID></server></inist></record>
000D07	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Combining silica-based adsorbents and SPME fibers in the extraction of the volatiles of beer : an exploratory study</title><author><name sortKey="Biazon, Cesar Luis" uniqKey="Biazon C">César Luis Biazon</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500</s1><s2>Porto Alegre 91501-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brambilla, Rodrigo" uniqKey="Brambilla R">Rodrigo Brambilla</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500</s1><s2>Porto Alegre 91501-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rigacci, Arnaud" uniqKey="Rigacci A">Arnaud Rigacci</name><affiliation><inist:fA14 i1="02"><s1>École des Mines de Paris, Center for Energy and Processes (CENERG), BP 207</s1><s2>06904 Sophia-Antipolis</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pizzolato, Tania M" uniqKey="Pizzolato T">Tania M. Pizzolato</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500</s1><s2>Porto Alegre 91501-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dos Santos, Joao H Z" uniqKey="Dos Santos J">Joao H. Z. Dos Santos</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500</s1><s2>Porto Alegre 91501-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0328894</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0328894 INIST</idno><idno type="RBID">Pascal:09-0328894</idno><idno type="wicri:Area/Main/Corpus">001C74</idno></publicationStmt><seriesStmt><idno type="ISSN">1618-2642</idno><title level="j" type="main">Analytical and bioanalytical chemistry</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adsorption</term><term>Aerogel</term><term>Alcohol</term><term>Alkyl</term><term>Chemical enrichment</term><term>Headspace</term><term>Microanalysis</term><term>Sample preparation</term><term>Silica</term><term>Solid phase microextraction</term><term>Sorption</term><term>Ultrasound</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Adsorption</term><term>Microanalyse</term><term>Microextraction phase solide</term><term>Préparation échantillon</term><term>Sorption</term><term>Enrichissement chimique</term><term>Espace tête</term><term>Ultrason</term><term>Silice</term><term>Alcool</term><term>Aérogel</term><term>Alkyle</term><term>Acétique acide ester éthyle</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A series of silica-based materials were employed as sorbents within solid-phase microextraction vials. The aim of the study was to evaluate the effect of an additional phase on the distribution of the volatile and less volatile analytes. The adsorption of six probe molecules, namely isoamyl acetate, ethyl hexanoate (ethyl caproate), phenylethyl alcohol, ethyl octanoate (ethyl caprilate), 2-phenylethyl acetate, and ethyl decanoate, was monitored by detecting the desorbed amount on a DVD-CAR-PDMS fiber from Pilsen beer. The microextraction process involved the presence of different silica-based phases produced via different methods: xerogel produced by hydrolytic and non-hydrolytic routes, aerogel, pyrogenic, and precipitated silica. The resulting data are discussed in correlation with sorbent texture properties (specific area and pore diameter). The modification of silica with alkyl groups also affects the preconcentrated amount of the target molecules in the headspace. The presence of sorbents was shown to affect the analyte signal more than the addition of NaCl or the use of ultrasound.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="2"><s0>1618-2642</s0></fA01><fA05><s2>394</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Combining silica-based adsorbents and SPME fibers in the extraction of the volatiles of beer : an exploratory study</s1></fA08><fA11 i1="01" i2="1"><s1>BIAZON (César Luis)</s1></fA11><fA11 i1="02" i2="1"><s1>BRAMBILLA (Rodrigo)</s1></fA11><fA11 i1="03" i2="1"><s1>RIGACCI (Arnaud)</s1></fA11><fA11 i1="04" i2="1"><s1>PIZZOLATO (Tania M.)</s1></fA11><fA11 i1="05" i2="1"><s1>DOS SANTOS (Joao H. Z.)</s1></fA11><fA14 i1="01"><s1>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500</s1><s2>Porto Alegre 91501-970</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>École des Mines de Paris, Center for Energy and Processes (CENERG), BP 207</s1><s2>06904 Sophia-Antipolis</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>549-556</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>853</s2><s5>354000186104030180</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>25 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0328894</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="2"><s0>Analytical and bioanalytical chemistry</s0></fA64><fA66 i1="01"><s0>DEU</s0></fA66><fC01 i1="01" l="ENG"><s0>A series of silica-based materials were employed as sorbents within solid-phase microextraction vials. The aim of the study was to evaluate the effect of an additional phase on the distribution of the volatile and less volatile analytes. The adsorption of six probe molecules, namely isoamyl acetate, ethyl hexanoate (ethyl caproate), phenylethyl alcohol, ethyl octanoate (ethyl caprilate), 2-phenylethyl acetate, and ethyl decanoate, was monitored by detecting the desorbed amount on a DVD-CAR-PDMS fiber from Pilsen beer. The microextraction process involved the presence of different silica-based phases produced via different methods: xerogel produced by hydrolytic and non-hydrolytic routes, aerogel, pyrogenic, and precipitated silica. The resulting data are discussed in correlation with sorbent texture properties (specific area and pore diameter). The modification of silica with alkyl groups also affects the preconcentrated amount of the target molecules in the headspace. The presence of sorbents was shown to affect the analyte signal more than the addition of NaCl or the use of ultrasound.</s0></fC01><fC02 i1="01" i2="X"><s0>001C04</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Adsorption</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Adsorption</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Adsorción</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Microanalyse</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Microanalysis</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Microanálisis</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Microextraction phase solide</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Solid phase microextraction</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Microextracción fase sólida</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Préparation échantillon</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Sample preparation</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Preparación muestreo</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Sorption</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Sorption</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Sorción</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Enrichissement chimique</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Chemical enrichment</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Enriquecimiento químico</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Espace tête</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Headspace</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Espacio cabeza</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Ultrason</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Ultrasound</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Ultrasonido</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Silice</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Silica</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Sílice</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Alcool</s0><s5>16</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Alcohol</s0><s5>16</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Alcohol</s0><s5>16</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Aérogel</s0><s5>17</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Aerogel</s0><s5>17</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Aerógel</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Alkyle</s0><s5>18</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Alkyl</s0><s5>18</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Alquilo</s0><s5>18</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Acétique acide ester éthyle</s0><s4>INC</s4><s5>32</s5></fC03><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0328894 INIST</NO><ET>Combining silica-based adsorbents and SPME fibers in the extraction of the volatiles of beer : an exploratory study</ET><AU>BIAZON (César Luis); BRAMBILLA (Rodrigo); RIGACCI (Arnaud); PIZZOLATO (Tania M.); DOS SANTOS (Joao H. Z.)</AU><AF>Instituto de Química, UFRGS, Av. Bento Gonçalves, 9500/Porto Alegre 91501-970/Brésil (1 aut., 2 aut., 4 aut., 5 aut.); École des Mines de Paris, Center for Energy and Processes (CENERG), BP 207/06904 Sophia-Antipolis/France (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Analytical and bioanalytical chemistry; ISSN 1618-2642; Allemagne; Da. 2009; Vol. 394; No. 2; Pp. 549-556; Bibl. 25 ref.</SO><LA>Anglais</LA><EA>A series of silica-based materials were employed as sorbents within solid-phase microextraction vials. The aim of the study was to evaluate the effect of an additional phase on the distribution of the volatile and less volatile analytes. The adsorption of six probe molecules, namely isoamyl acetate, ethyl hexanoate (ethyl caproate), phenylethyl alcohol, ethyl octanoate (ethyl caprilate), 2-phenylethyl acetate, and ethyl decanoate, was monitored by detecting the desorbed amount on a DVD-CAR-PDMS fiber from Pilsen beer. The microextraction process involved the presence of different silica-based phases produced via different methods: xerogel produced by hydrolytic and non-hydrolytic routes, aerogel, pyrogenic, and precipitated silica. The resulting data are discussed in correlation with sorbent texture properties (specific area and pore diameter). The modification of silica with alkyl groups also affects the preconcentrated amount of the target molecules in the headspace. The presence of sorbents was shown to affect the analyte signal more than the addition of NaCl or the use of ultrasound.</EA><CC>001C04</CC><FD>Adsorption; Microanalyse; Microextraction phase solide; Préparation échantillon; Sorption; Enrichissement chimique; Espace tête; Ultrason; Silice; Alcool; Aérogel; Alkyle; Acétique acide ester éthyle</FD><ED>Adsorption; Microanalysis; Solid phase microextraction; Sample preparation; Sorption; Chemical enrichment; Headspace; Ultrasound; Silica; Alcohol; Aerogel; Alkyl</ED><SD>Adsorción; Microanálisis; Microextracción fase sólida; Preparación muestreo; Sorción; Enriquecimiento químico; Espacio cabeza; Ultrasonido; Sílice; Alcohol; Aerógel; Alquilo</SD><LO>INIST-853.354000186104030180</LO><ID>09-0328894</ID></server></inist></record>
000D08	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Neonatal minimally invasive surgery for congenital diaphragmatic hernias: a multicenter study using thoracoscopy or laparoscopy</title><author><name sortKey="Gomes Ferreira, Cindy" uniqKey="Gomes Ferreira C">Cindy Gomes Ferreira</name><affiliation><inist:fA14 i1="01"><s1>Departement of Pediatric Surgery, University Hospital, Pôle Mère-Enfant - Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Avenue Molière</s1><s2>67100 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Reinberg, Olivier" uniqKey="Reinberg O">Olivier Reinberg</name><affiliation><inist:fA14 i1="02"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Universitaire Vaudois</s1><s2>1011 Lausanne</s2><s3>CHE</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Becmeur, Francois" uniqKey="Becmeur F">François Becmeur</name><affiliation><inist:fA14 i1="01"><s1>Departement of Pediatric Surgery, University Hospital, Pôle Mère-Enfant - Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Avenue Molière</s1><s2>67100 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Allal, Hossein" uniqKey="Allal H">Hossein Allal</name><affiliation><inist:fA14 i1="03"><s1>Departement of Pediatric Surgery, University Hospital, Hôpital Lapeyronie, 275, Avenue Doyen Gaston Giraud</s1><s2>34295 Montpellier</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Lagausie, Pascal" uniqKey="De Lagausie P">Pascal De Lagausie</name><affiliation><inist:fA14 i1="04"><s1>Departement of Pediatric Surgery, University Hospital, Hôpital La Timone, Hôpitaux de Marseille, 264, rue Saint Pierre</s1><s2>13385 Marseille</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lardy, Hubert" uniqKey="Lardy H">Hubert Lardy</name><affiliation><inist:fA14 i1="05"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Gatien de Clocheville, 49, Boulevard Beranger</s1><s2>97044 Tours</s2><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Philippe, Paul" uniqKey="Philippe P">Paul Philippe</name><affiliation><inist:fA14 i1="06"><s1>Departement of Pediatric Surgery, University Hospital, Clinique Pédiatrique, Centre Hospitalier du Luxembourg, 4, rue Ernest Barblé</s1><s2>1210 Luxembourg</s2><s3>LUX</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lopez, Manuel" uniqKey="Lopez M">Manuel Lopez</name><affiliation><inist:fA14 i1="07"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Saint Etienne</s1><s2>42055 Saint Etienne</s2><s3>FRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Varlet, Francois" uniqKey="Varlet F">François Varlet</name><affiliation><inist:fA14 i1="07"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Saint Etienne</s1><s2>42055 Saint Etienne</s2><s3>FRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Podevin, Guillaume" uniqKey="Podevin G">Guillaume Podevin</name><affiliation><inist:fA14 i1="08"><s1>Departement of Pediatric Surgery, University Hospital, Põle Mère-Enfant, Centre Hospitalier Universitaire Hõtel Dieu</s1><s2>44093 Nantes</s2><s3>FRA</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schleef, J Rgen" uniqKey="Schleef J">J Rgen Schleef</name><affiliation><inist:fA14 i1="09"><s1>Departement of Pediatric Surgery, University Hospital, Children's Hospital of Trieste, IRCCS Bo Garafolo, Via dell' Istria 65/1</s1><s2>34137 Trieste</s2><s3>ITA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schlobach, Max" uniqKey="Schlobach M">Max Schlobach</name><affiliation><inist:fA14 i1="10"><s1>Departement of Pediatric Surgery, University Hospital, Hospital Felicio Rocho, Avenida do Contorno</s1><s2>9530 Belo Horizonte</s2><s3>BRA</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0329289</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0329289 INIST</idno><idno type="RBID">Pascal:09-0329289</idno><idno type="wicri:Area/Main/Corpus">001C73</idno></publicationStmt><seriesStmt><idno type="ISSN">0930-2794</idno><title level="j" type="abbreviated">Surg. endosc.</title><title level="j" type="main">Surgical endoscopy</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Congenital</term><term>Diaphragmatic hernia</term><term>Endoscopic surgery</term><term>Endoscopy</term><term>Laparoscopy</term><term>Medicine</term><term>Minimally invasive surgery</term><term>Multicenter study</term><term>Newborn</term><term>Thoracoscopy</term><term>Treatment</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Chirurgie miniinvasive</term><term>Thoracoscopie</term><term>Endoscopie</term><term>Nouveau né</term><term>Congénital</term><term>Etude multicentrique</term><term>Laparoscopie</term><term>Médecine</term><term>Chirurgie endoscopique</term><term>Traitement</term><term>Hernie diaphragmatique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background Minimally invasive surgery (MIS) for late-presenting congenital diaphragmatic hernia (CDH) has been described previously, but few neonatal cases of CDH have been reported. This study aimed to report the multicenter experience of these rare cases and to compare the laparoscopic and thoracoscopic approaches. Methods Using MIS procedures, 30 patients (16 boys and 14 girls) from nine centers underwent surgery for CDH within the first month of life, 26 before day 5. Only one patient had associated malformations. There were 10 pre-term patients (32-36 weeks of gestational age). Their weight at birth ranged from 1,800 to 3,800 g, with three patients weighing less than 2,600 g. Of the 30 patients, 18 were intubated at birth. Results The MIS procedures were performed in 18 cases by a thoracoscopic approach and in 12 cases by a laparoscopic approach. No severe complication was observed. For 20 patients, reduction of the intrathoracic contents was achieved easily with 15 thoracoscopies and 5 laparoscopies. In six cases, the reduction was difficult, proving to be impossible for the four remaining patients: one treated with thoracoscopy and three with laparoscopy. The reasons for the inability to reduce the thoracic contents were difficulty of liver mobilization (1 left CDH and 2 right CDH) and the presence of a dilated stomach in the thorax. Reductions were easier for cases of wide diaphragmatic defects using thoracoscopy. There were 10 conversions (5 laparoscopies and 5 thoracoscopies). The reported reasons for conversion were inability to reduce (n = 4), need for a patch (n = 5), lack of adequate vision (n = 4), narrow working space (n = 1), associated bowel malrotation (n = 1), and an anesthetic problem (n = 1). Five defects were too large for direct closure and had to be closed with a patch. Four required conversion, with one performed through video-assisted thoracic surgery. The recurrences were detected after two primer thoracoscopic closures, one of which was managed by successful reoperation using thoracoscopy. Conclusions In the neonatal period, CDH can be safely closed using MIS procedures. The overall success rate in this study was 67%. The indication for MIS is not related to weeks of gestational age, to weight at birth (if &#62;2,600 g), or to the extent of the immediate neonatal care. Patients with no associated anomaly who are hemodynamically stabilized can benefit from MIS procedures. Reduction of the herniated organs is easier using thoracoscopy. Right CDH, liver lobe herniation, and the need for a patch closure are the most frequent reasons for conversion.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0930-2794</s0></fA01><fA02 i1="01"><s0>SUREEX</s0></fA02><fA03 i2="1"><s0>Surg. endosc.</s0></fA03><fA05><s2>23</s2></fA05><fA06><s2>7</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Neonatal minimally invasive surgery for congenital diaphragmatic hernias: a multicenter study using thoracoscopy or laparoscopy</s1></fA08><fA11 i1="01" i2="1"><s1>GOMES FERREIRA (Cindy)</s1></fA11><fA11 i1="02" i2="1"><s1>REINBERG (Olivier)</s1></fA11><fA11 i1="03" i2="1"><s1>BECMEUR (François)</s1></fA11><fA11 i1="04" i2="1"><s1>ALLAL (Hossein)</s1></fA11><fA11 i1="05" i2="1"><s1>DE LAGAUSIE (Pascal)</s1></fA11><fA11 i1="06" i2="1"><s1>LARDY (Hubert)</s1></fA11><fA11 i1="07" i2="1"><s1>PHILIPPE (Paul)</s1></fA11><fA11 i1="08" i2="1"><s1>LOPEZ (Manuel)</s1></fA11><fA11 i1="09" i2="1"><s1>VARLET (François)</s1></fA11><fA11 i1="10" i2="1"><s1>PODEVIN (Guillaume)</s1></fA11><fA11 i1="11" i2="1"><s1>SCHLEEF (Jürgen)</s1></fA11><fA11 i1="12" i2="1"><s1>SCHLOBACH (Max)</s1></fA11><fA14 i1="01"><s1>Departement of Pediatric Surgery, University Hospital, Pôle Mère-Enfant - Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Avenue Molière</s1><s2>67100 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Universitaire Vaudois</s1><s2>1011 Lausanne</s2><s3>CHE</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Departement of Pediatric Surgery, University Hospital, Hôpital Lapeyronie, 275, Avenue Doyen Gaston Giraud</s1><s2>34295 Montpellier</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Departement of Pediatric Surgery, University Hospital, Hôpital La Timone, Hôpitaux de Marseille, 264, rue Saint Pierre</s1><s2>13385 Marseille</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Gatien de Clocheville, 49, Boulevard Beranger</s1><s2>97044 Tours</s2><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="06"><s1>Departement of Pediatric Surgery, University Hospital, Clinique Pédiatrique, Centre Hospitalier du Luxembourg, 4, rue Ernest Barblé</s1><s2>1210 Luxembourg</s2><s3>LUX</s3><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Saint Etienne</s1><s2>42055 Saint Etienne</s2><s3>FRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="08"><s1>Departement of Pediatric Surgery, University Hospital, Põle Mère-Enfant, Centre Hospitalier Universitaire Hõtel Dieu</s1><s2>44093 Nantes</s2><s3>FRA</s3><sZ>10 aut.</sZ></fA14><fA14 i1="09"><s1>Departement of Pediatric Surgery, University Hospital, Children's Hospital of Trieste, IRCCS Bo Garafolo, Via dell' Istria 65/1</s1><s2>34137 Trieste</s2><s3>ITA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="10"><s1>Departement of Pediatric Surgery, University Hospital, Hospital Felicio Rocho, Avenida do Contorno</s1><s2>9530 Belo Horizonte</s2><s3>BRA</s3><sZ>12 aut.</sZ></fA14><fA20><s1>1650-1659</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>21220</s2><s5>354000172414320440</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>13 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0329289</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Surgical endoscopy</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Background Minimally invasive surgery (MIS) for late-presenting congenital diaphragmatic hernia (CDH) has been described previously, but few neonatal cases of CDH have been reported. This study aimed to report the multicenter experience of these rare cases and to compare the laparoscopic and thoracoscopic approaches. Methods Using MIS procedures, 30 patients (16 boys and 14 girls) from nine centers underwent surgery for CDH within the first month of life, 26 before day 5. Only one patient had associated malformations. There were 10 pre-term patients (32-36 weeks of gestational age). Their weight at birth ranged from 1,800 to 3,800 g, with three patients weighing less than 2,600 g. Of the 30 patients, 18 were intubated at birth. Results The MIS procedures were performed in 18 cases by a thoracoscopic approach and in 12 cases by a laparoscopic approach. No severe complication was observed. For 20 patients, reduction of the intrathoracic contents was achieved easily with 15 thoracoscopies and 5 laparoscopies. In six cases, the reduction was difficult, proving to be impossible for the four remaining patients: one treated with thoracoscopy and three with laparoscopy. The reasons for the inability to reduce the thoracic contents were difficulty of liver mobilization (1 left CDH and 2 right CDH) and the presence of a dilated stomach in the thorax. Reductions were easier for cases of wide diaphragmatic defects using thoracoscopy. There were 10 conversions (5 laparoscopies and 5 thoracoscopies). The reported reasons for conversion were inability to reduce (n = 4), need for a patch (n = 5), lack of adequate vision (n = 4), narrow working space (n = 1), associated bowel malrotation (n = 1), and an anesthetic problem (n = 1). Five defects were too large for direct closure and had to be closed with a patch. Four required conversion, with one performed through video-assisted thoracic surgery. The recurrences were detected after two primer thoracoscopic closures, one of which was managed by successful reoperation using thoracoscopy. Conclusions In the neonatal period, CDH can be safely closed using MIS procedures. The overall success rate in this study was 67%. The indication for MIS is not related to weeks of gestational age, to weight at birth (if &#62;2,600 g), or to the extent of the immediate neonatal care. Patients with no associated anomaly who are hemodynamically stabilized can benefit from MIS procedures. Reduction of the herniated organs is easier using thoracoscopy. Right CDH, liver lobe herniation, and the need for a patch closure are the most frequent reasons for conversion.</s0></fC01><fC02 i1="01" i2="X"><s0>002B01</s0></fC02><fC02 i1="02" i2="X"><s0>002B24E03</s0></fC02><fC02 i1="03" i2="X"><s0>002B24E06</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Chirurgie miniinvasive</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Minimally invasive surgery</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Cirugía mini invasiva</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Thoracoscopie</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Thoracoscopy</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Toracoscopía</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Endoscopie</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Endoscopy</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Endoscopía</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Nouveau né</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Newborn</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Recién nacido</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Congénital</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Congenital</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Congénito</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Etude multicentrique</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Multicenter study</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Estudio multicéntrico</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Laparoscopie</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Laparoscopy</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Laparoscopia</s0><s5>13</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Médecine</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Medicine</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Medicina</s0><s5>14</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Chirurgie endoscopique</s0><s5>30</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Endoscopic surgery</s0><s5>30</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Cirugía endoscópica</s0><s5>30</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Traitement</s0><s5>31</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Treatment</s0><s5>31</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Tratamiento</s0><s5>31</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Hernie diaphragmatique</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Diaphragmatic hernia</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Hernia diafragmática</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Homme</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Human</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Hombre</s0></fC07><fN21><s1>236</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0329289 INIST</NO><ET>Neonatal minimally invasive surgery for congenital diaphragmatic hernias: a multicenter study using thoracoscopy or laparoscopy</ET><AU>GOMES FERREIRA (Cindy); REINBERG (Olivier); BECMEUR (François); ALLAL (Hossein); DE LAGAUSIE (Pascal); LARDY (Hubert); PHILIPPE (Paul); LOPEZ (Manuel); VARLET (François); PODEVIN (Guillaume); SCHLEEF (Jürgen); SCHLOBACH (Max)</AU><AF>Departement of Pediatric Surgery, University Hospital, Pôle Mère-Enfant - Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Avenue Molière/67100 Strasbourg/France (1 aut., 3 aut.); Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Universitaire Vaudois/1011 Lausanne/Suisse (2 aut.); Departement of Pediatric Surgery, University Hospital, Hôpital Lapeyronie, 275, Avenue Doyen Gaston Giraud/34295 Montpellier/France (4 aut.); Departement of Pediatric Surgery, University Hospital, Hôpital La Timone, Hôpitaux de Marseille, 264, rue Saint Pierre/13385 Marseille/France (5 aut.); Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Gatien de Clocheville, 49, Boulevard Beranger/97044 Tours/France (6 aut.); Departement of Pediatric Surgery, University Hospital, Clinique Pédiatrique, Centre Hospitalier du Luxembourg, 4, rue Ernest Barblé/1210 Luxembourg/Luxembourg (7 aut.); Departement of Pediatric Surgery, University Hospital, Centre Hospitalier Saint Etienne/42055 Saint Etienne/France (8 aut., 9 aut.); Departement of Pediatric Surgery, University Hospital, Põle Mère-Enfant, Centre Hospitalier Universitaire Hõtel Dieu/44093 Nantes/France (10 aut.); Departement of Pediatric Surgery, University Hospital, Children's Hospital of Trieste, IRCCS Bo Garafolo, Via dell' Istria 65/1/34137 Trieste/Italie (11 aut.); Departement of Pediatric Surgery, University Hospital, Hospital Felicio Rocho, Avenida do Contorno/9530 Belo Horizonte/Brésil (12 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Surgical endoscopy; ISSN 0930-2794; Coden SUREEX; Etats-Unis; Da. 2009; Vol. 23; No. 7; Pp. 1650-1659; Bibl. 13 ref.</SO><LA>Anglais</LA><EA>Background Minimally invasive surgery (MIS) for late-presenting congenital diaphragmatic hernia (CDH) has been described previously, but few neonatal cases of CDH have been reported. This study aimed to report the multicenter experience of these rare cases and to compare the laparoscopic and thoracoscopic approaches. Methods Using MIS procedures, 30 patients (16 boys and 14 girls) from nine centers underwent surgery for CDH within the first month of life, 26 before day 5. Only one patient had associated malformations. There were 10 pre-term patients (32-36 weeks of gestational age). Their weight at birth ranged from 1,800 to 3,800 g, with three patients weighing less than 2,600 g. Of the 30 patients, 18 were intubated at birth. Results The MIS procedures were performed in 18 cases by a thoracoscopic approach and in 12 cases by a laparoscopic approach. No severe complication was observed. For 20 patients, reduction of the intrathoracic contents was achieved easily with 15 thoracoscopies and 5 laparoscopies. In six cases, the reduction was difficult, proving to be impossible for the four remaining patients: one treated with thoracoscopy and three with laparoscopy. The reasons for the inability to reduce the thoracic contents were difficulty of liver mobilization (1 left CDH and 2 right CDH) and the presence of a dilated stomach in the thorax. Reductions were easier for cases of wide diaphragmatic defects using thoracoscopy. There were 10 conversions (5 laparoscopies and 5 thoracoscopies). The reported reasons for conversion were inability to reduce (n = 4), need for a patch (n = 5), lack of adequate vision (n = 4), narrow working space (n = 1), associated bowel malrotation (n = 1), and an anesthetic problem (n = 1). Five defects were too large for direct closure and had to be closed with a patch. Four required conversion, with one performed through video-assisted thoracic surgery. The recurrences were detected after two primer thoracoscopic closures, one of which was managed by successful reoperation using thoracoscopy. Conclusions In the neonatal period, CDH can be safely closed using MIS procedures. The overall success rate in this study was 67%. The indication for MIS is not related to weeks of gestational age, to weight at birth (if &#62;2,600 g), or to the extent of the immediate neonatal care. Patients with no associated anomaly who are hemodynamically stabilized can benefit from MIS procedures. Reduction of the herniated organs is easier using thoracoscopy. Right CDH, liver lobe herniation, and the need for a patch closure are the most frequent reasons for conversion.</EA><CC>002B01; 002B24E03; 002B24E06</CC><FD>Chirurgie miniinvasive; Thoracoscopie; Endoscopie; Nouveau né; Congénital; Etude multicentrique; Laparoscopie; Médecine; Chirurgie endoscopique; Traitement; Hernie diaphragmatique</FD><FG>Homme</FG><ED>Minimally invasive surgery; Thoracoscopy; Endoscopy; Newborn; Congenital; Multicenter study; Laparoscopy; Medicine; Endoscopic surgery; Treatment; Diaphragmatic hernia</ED><EG>Human</EG><SD>Cirugía mini invasiva; Toracoscopía; Endoscopía; Recién nacido; Congénito; Estudio multicéntrico; Laparoscopia; Medicina; Cirugía endoscópica; Tratamiento; Hernia diafragmática</SD><LO>INIST-21220.354000172414320440</LO><ID>09-0329289</ID></server></inist></record>
000D09	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Speckle photo electromotive force in CdTe:V and CdTe:Ge for measurement of vibration with large amplitude</title><author><name sortKey="Dos Santos, T O" uniqKey="Dos Santos T">T. O. Dos Santos</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Física &#34;Gleb-Wataghin&#34;, UNICAMP</s1><s2>13083-970 Campinas, São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Frejlich, J" uniqKey="Frejlich J">J. Frejlich</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Física &#34;Gleb-Wataghin&#34;, UNICAMP</s1><s2>13083-970 Campinas, São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Launay, J C" uniqKey="Launay J">J. C. Launay</name><affiliation><inist:fA14 i1="03"><s1>ICMCB, CNRS, Université Bordeaux 1</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Shcherbin, K" uniqKey="Shcherbin K">K. Shcherbin</name><affiliation><inist:fA14 i1="02"><s1>Institute of Physics, National Academy of Sciences, Prospekt Nauki 46</s1><s2>03028 Kiev</s2><s3>UKR</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0332456</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0332456 INIST</idno><idno type="RBID">Pascal:09-0332456</idno><idno type="wicri:Area/Main/Corpus">001C72</idno></publicationStmt><seriesStmt><idno type="ISSN">0946-2171</idno><title level="j" type="abbreviated">Appl. phys., B Lasers opt. : (Print)</title><title level="j" type="main">Applied physics. B, Lasers and optics : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Binary compounds</term><term>Cadmium Tellurides</term><term>Doped materials</term><term>Electromotive force</term><term>Germanium additions</term><term>Measuring methods</term><term>Nonlinear optics</term><term>Photorefractive effect</term><term>Speckles</term><term>Vanadium additions</term><term>Vibration measurement</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Speckle</term><term>Mesure vibration</term><term>Optique non linéaire</term><term>Méthode mesure</term><term>Composé binaire</term><term>Addition vanadium</term><term>Cadmium Tellurure</term><term>Addition germanium</term><term>Matériau dopé</term><term>Force électromotrice</term><term>Effet photoréfractif</term><term>CdTe:V</term><term>CdTe:Ge</term><term>4230M</term><term>4265H</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The photo-electromotive force induced by a speckle pattern vibrating with large amplitude in photorefractive CdTe:V and CdTe:Ge is experimentally studied. This technique is shown to be suitable for transversal amplitude vibration measurement as well as for material response time and associated conductivity characterization. Experiments were carried out with 532 and 1064 nm wavelength illumination over a wide vibration frequency range. The results are in good agreement with a previously reported theoretical model. The studied doped crystals exhibit peculiar different features that are described and discussed.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0946-2171</s0></fA01><fA03 i2="1"><s0>Appl. phys., B Lasers opt. : (Print)</s0></fA03><fA05><s2>95</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Speckle photo electromotive force in CdTe:V and CdTe:Ge for measurement of vibration with large amplitude</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Photorefractive Materials, Effects, and Devices: Control of Light and Matter</s1></fA09><fA11 i1="01" i2="1"><s1>DOS SANTOS (T. O.)</s1></fA11><fA11 i1="02" i2="1"><s1>FREJLICH (J.)</s1></fA11><fA11 i1="03" i2="1"><s1>LAUNAY (J. C.)</s1></fA11><fA11 i1="04" i2="1"><s1>SHCHERBIN (K.)</s1></fA11><fA12 i1="01" i2="1"><s1>BUSSE (Karsten)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>DENZ (Cornelia)</s1><s9>ed.</s9></fA12><fA12 i1="03" i2="1"><s1>KROLILOWSKI (Wieslaw)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Instituto de Física &#34;Gleb-Wataghin&#34;, UNICAMP</s1><s2>13083-970 Campinas, São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Institute of Physics, National Academy of Sciences, Prospekt Nauki 46</s1><s2>03028 Kiev</s2><s3>UKR</s3><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>ICMCB, CNRS, Université Bordeaux 1</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>Institute of Physics, University of Bonn, Wegelerstr. 8</s1><s2>53115 Bonn</s2><s3>DEU</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Institute of Applied Physics, University of Münster, Correnstr. 2</s1><s2>48149 Münster</s2><s3>DEU</s3><sZ>2 aut.</sZ></fA15><fA15 i1="03"><s1>Laser Physics Centre, Australian National University, John Carver Building, 58C</s1><s2>Canberra, ACT 0200</s2><s3>AUS</s3><sZ>3 aut.</sZ></fA15><fA20><s1>627-632</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>16194B</s2><s5>354000186284390340</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>16 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0332456</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied physics. B, Lasers and optics : (Print)</s0></fA64><fA66 i1="01"><s0>DEU</s0></fA66><fC01 i1="01" l="ENG"><s0>The photo-electromotive force induced by a speckle pattern vibrating with large amplitude in photorefractive CdTe:V and CdTe:Ge is experimentally studied. This technique is shown to be suitable for transversal amplitude vibration measurement as well as for material response time and associated conductivity characterization. Experiments were carried out with 532 and 1064 nm wavelength illumination over a wide vibration frequency range. The results are in good agreement with a previously reported theoretical model. The studied doped crystals exhibit peculiar different features that are described and discussed.</s0></fC01><fC02 i1="01" i2="3"><s0>001B40B30M</s0></fC02><fC02 i1="02" i2="3"><s0>001B40B65H</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Speckle</s0><s5>03</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Speckles</s0><s5>03</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Mesure vibration</s0><s5>04</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Vibration measurement</s0><s5>04</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Optique non linéaire</s0><s5>17</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Nonlinear optics</s0><s5>17</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Méthode mesure</s0><s5>30</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Measuring methods</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Composé binaire</s0><s5>50</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Binary compounds</s0><s5>50</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Addition vanadium</s0><s5>51</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Vanadium additions</s0><s5>51</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Cadmium Tellurure</s0><s2>NC</s2><s2>NA</s2><s5>52</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Cadmium Tellurides</s0><s2>NC</s2><s2>NA</s2><s5>52</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Addition germanium</s0><s5>53</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Germanium additions</s0><s5>53</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Matériau dopé</s0><s5>54</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Doped materials</s0><s5>54</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Force électromotrice</s0><s5>61</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Electromotive force</s0><s5>61</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Effet photoréfractif</s0><s5>62</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Photorefractive effect</s0><s5>62</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>CdTe:V</s0><s4>INC</s4><s5>71</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>CdTe:Ge</s0><s4>INC</s4><s5>72</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>4230M</s0><s4>INC</s4><s5>91</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>4265H</s0><s4>INC</s4><s5>92</s5></fC03><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0332456 INIST</NO><ET>Speckle photo electromotive force in CdTe:V and CdTe:Ge for measurement of vibration with large amplitude</ET><AU>DOS SANTOS (T. O.); FREJLICH (J.); LAUNAY (J. C.); SHCHERBIN (K.); BUSSE (Karsten); DENZ (Cornelia); KROLILOWSKI (Wieslaw)</AU><AF>Instituto de Física &#34;Gleb-Wataghin&#34;, UNICAMP/13083-970 Campinas, São Paulo/Brésil (1 aut., 2 aut.); Institute of Physics, National Academy of Sciences, Prospekt Nauki 46/03028 Kiev/Ukraine (4 aut.); ICMCB, CNRS, Université Bordeaux 1/Bordeaux/France (3 aut.); Institute of Physics, University of Bonn, Wegelerstr. 8/53115 Bonn/Allemagne (1 aut.); Institute of Applied Physics, University of Münster, Correnstr. 2/48149 Münster/Allemagne (2 aut.); Laser Physics Centre, Australian National University, John Carver Building, 58C/Canberra, ACT 0200/Australie (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Applied physics. B, Lasers and optics : (Print); ISSN 0946-2171; Allemagne; Da. 2009; Vol. 95; No. 3; Pp. 627-632; Bibl. 16 ref.</SO><LA>Anglais</LA><EA>The photo-electromotive force induced by a speckle pattern vibrating with large amplitude in photorefractive CdTe:V and CdTe:Ge is experimentally studied. This technique is shown to be suitable for transversal amplitude vibration measurement as well as for material response time and associated conductivity characterization. Experiments were carried out with 532 and 1064 nm wavelength illumination over a wide vibration frequency range. The results are in good agreement with a previously reported theoretical model. The studied doped crystals exhibit peculiar different features that are described and discussed.</EA><CC>001B40B30M; 001B40B65H</CC><FD>Speckle; Mesure vibration; Optique non linéaire; Méthode mesure; Composé binaire; Addition vanadium; Cadmium Tellurure; Addition germanium; Matériau dopé; Force électromotrice; Effet photoréfractif; CdTe:V; CdTe:Ge; 4230M; 4265H</FD><ED>Speckles; Vibration measurement; Nonlinear optics; Measuring methods; Binary compounds; Vanadium additions; Cadmium Tellurides; Germanium additions; Doped materials; Electromotive force; Photorefractive effect</ED><LO>INIST-16194B.354000186284390340</LO><ID>09-0332456</ID></server></inist></record>
000D10	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Effect of severe thermal treatment on spruce and beech wood lignins</title><author><name sortKey="Rousset, Patrick" uniqKey="Rousset P">Patrick Rousset</name><affiliation><inist:fA14 i1="01"><s1>UPR42 -Biomass Energy Unit, CIRAD/LPF-SFB</s1><s2>Brasilia DF, 708 18-900</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lapierre, Catherine" uniqKey="Lapierre C">Catherine Lapierre</name><affiliation><inist:fA14 i1="02"><s1>UMR-Chimie Biologique AgroParisTech/INRA, AgroParisTech Centre de Grignon</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pollet, Brigitte" uniqKey="Pollet B">Brigitte Pollet</name><affiliation><inist:fA14 i1="02"><s1>UMR-Chimie Biologique AgroParisTech/INRA, AgroParisTech Centre de Grignon</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Quirino, Waldir" uniqKey="Quirino W">Waldir Quirino</name><affiliation><inist:fA14 i1="03"><s1>Biomass Energy Research Unit, LPF-SFB</s1><s2>Brasilia DF, 70818-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Perre, Patrick" uniqKey="Perre P">Patrick Perre</name><affiliation><inist:fA14 i1="04"><s1>LERMAB, UMR1093, INRA, ENGREF, 14 rue Girardet</s1><s2>54042 Nancy</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0332567</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0332567 INIST</idno><idno type="RBID">Pascal:09-0332567</idno><idno type="wicri:Area/Main/Corpus">001C71</idno></publicationStmt><seriesStmt><idno type="ISSN">1286-4560</idno><title level="j" type="abbreviated">Ann. for. sci.</title><title level="j" type="main">Annals of forest science</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cellulose</term><term>Condensation</term><term>Ether</term><term>Fagus</term><term>Forestry</term><term>Genetic linkage</term><term>Guaiacyl unit</term><term>Hardwood</term><term>Heat treatment</term><term>Hemicellulose</term><term>Lignin</term><term>Monomer</term><term>Picea</term><term>Reactivity</term><term>Softwood</term><term>Syringyl unit</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Traitement thermique</term><term>Bois feuillu</term><term>Foresterie</term><term>Réactivité</term><term>Monomère</term><term>Liaison génétique</term><term>Condensation</term><term>Bois résineux</term><term>Picea</term><term>Fagus</term><term>Lignine</term><term>Cellulose</term><term>Hémicellulose</term><term>Ether</term><term>Unité syringyle</term><term>Unité guaiacyle</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">• La structure, la proportion et le mode de montage de la lignine, des celluloses et des hémicelluloses ont eu des effets marqués sur les mécanismes de la réaction au cours du traitement thermique et, par conséquent, ont eu une forte influence sur la qualité du produit final. L'effet des conditions de traitement, y compris des conditions sévères (jusqu'à 553 K) et la durée du traitement (jusqu'à 8 h) sur la structure de lignines de l'épicéa et du hêtre ont été étudiés. • La teneur en lignine a été déterminée par la méthode Klason et la structure de la lignine a été évaluée par thioacidolyse. • Les résultats ont mis en évidence la forte réactivité des lignines de l'épicéa et du hêtre vis-à-vis des traitements thermiques sévères. La sensibilité des différentes unités syringyl (S) et guaiacyl (G) vis-à-vis du traitement thermique est confirmée par comparaison des données obtenues avec les échantillons du hêtre et de l'épicéa. Le traitement le plus sévère (280 °C) du bois d'épicéa a induit un enrichissement spectaculaire en lignine ainsi que la quasi-disparition des unités de la lignine G, alors qu'un traitement plus modéré a sensiblement modifié la structure de la lignine par des réactions de dégradation qui affectent les p-hydroxyphényl (H ) et les unités de lignine G. • La thioacidolyse a révélé que le traitement thermique induit l'apparition de structures de vinyl éthers dans la lignine de l'épicéa. La diminution de production de la G et S thioacidolyses monomères reflète la disparition progressive des unités de lignine G et S impliquées seulement dans des liaisons β-O-4 et la formation de linkages de condensation en proportions de la sévérité du traitement. Dans des conditions difficiles, les unités S liées β-O-4 sont plus dégradées que leurs homologues G.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1286-4560</s0></fA01><fA03 i2="1"><s0>Ann. for. sci.</s0></fA03><fA05><s2>66</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Effect of severe thermal treatment on spruce and beech wood lignins</s1></fA08><fA11 i1="01" i2="1"><s1>ROUSSET (Patrick)</s1></fA11><fA11 i1="02" i2="1"><s1>LAPIERRE (Catherine)</s1></fA11><fA11 i1="03" i2="1"><s1>POLLET (Brigitte)</s1></fA11><fA11 i1="04" i2="1"><s1>QUIRINO (Waldir)</s1></fA11><fA11 i1="05" i2="1"><s1>PERRE (Patrick)</s1></fA11><fA14 i1="01"><s1>UPR42 -Biomass Energy Unit, CIRAD/LPF-SFB</s1><s2>Brasilia DF, 708 18-900</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>UMR-Chimie Biologique AgroParisTech/INRA, AgroParisTech Centre de Grignon</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Biomass Energy Research Unit, LPF-SFB</s1><s2>Brasilia DF, 70818-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>LERMAB, UMR1093, INRA, ENGREF, 14 rue Girardet</s1><s2>54042 Nancy</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA20><s2>110p1-110p8</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>959</s2><s5>354000186485100100</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0332567</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Annals of forest science</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>• La structure, la proportion et le mode de montage de la lignine, des celluloses et des hémicelluloses ont eu des effets marqués sur les mécanismes de la réaction au cours du traitement thermique et, par conséquent, ont eu une forte influence sur la qualité du produit final. L'effet des conditions de traitement, y compris des conditions sévères (jusqu'à 553 K) et la durée du traitement (jusqu'à 8 h) sur la structure de lignines de l'épicéa et du hêtre ont été étudiés. • La teneur en lignine a été déterminée par la méthode Klason et la structure de la lignine a été évaluée par thioacidolyse. • Les résultats ont mis en évidence la forte réactivité des lignines de l'épicéa et du hêtre vis-à-vis des traitements thermiques sévères. La sensibilité des différentes unités syringyl (S) et guaiacyl (G) vis-à-vis du traitement thermique est confirmée par comparaison des données obtenues avec les échantillons du hêtre et de l'épicéa. Le traitement le plus sévère (280 °C) du bois d'épicéa a induit un enrichissement spectaculaire en lignine ainsi que la quasi-disparition des unités de la lignine G, alors qu'un traitement plus modéré a sensiblement modifié la structure de la lignine par des réactions de dégradation qui affectent les p-hydroxyphényl (H ) et les unités de lignine G. • La thioacidolyse a révélé que le traitement thermique induit l'apparition de structures de vinyl éthers dans la lignine de l'épicéa. La diminution de production de la G et S thioacidolyses monomères reflète la disparition progressive des unités de lignine G et S impliquées seulement dans des liaisons β-O-4 et la formation de linkages de condensation en proportions de la sévérité du traitement. Dans des conditions difficiles, les unités S liées β-O-4 sont plus dégradées que leurs homologues G.</s0></fC01><fC02 i1="01" i2="X"><s0>002A33</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Traitement thermique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Heat treatment</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Tratamiento térmico</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Bois feuillu</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Hardwood</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Madera de frondosas</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Foresterie</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Forestry</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Ciencias forestales</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Réactivité</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Reactivity</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Reactividad</s0><s5>04</s5></fC03><fC03 i1="05" 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l="SPA"><s0>Picea</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Fagus</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Fagus</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Fagus</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Lignine</s0><s5>15</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Lignin</s0><s5>15</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Lignina</s0><s5>15</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Cellulose</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Cellulose</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Celulosa</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Hémicellulose</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Hemicellulose</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Hemicelulosa</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Ether</s0><s2>FX</s2><s5>18</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Ether</s0><s2>FX</s2><s5>18</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Eter</s0><s2>FX</s2><s5>18</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Unité syringyle</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Syringyl unit</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Unité guaiacyle</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Guaiacyl unit</s0><s4>CD</s4><s5>97</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Fagaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Arbre</s0><s5>31</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Tree</s0><s5>31</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Arbol</s0><s5>31</s5></fC07><fN21><s1>243</s1></fN21></pA></standard><server><NO>PASCAL 09-0332567 INIST</NO><ET>Effect of severe thermal treatment on spruce and beech wood lignins</ET><AU>ROUSSET (Patrick); LAPIERRE (Catherine); POLLET (Brigitte); QUIRINO (Waldir); PERRE (Patrick)</AU><AF>UPR42 -Biomass Energy Unit, CIRAD/LPF-SFB/Brasilia DF, 708 18-900/Brésil (1 aut.); UMR-Chimie Biologique AgroParisTech/INRA, AgroParisTech Centre de Grignon/78850 Thiverval-Grignon/France (2 aut., 3 aut.); Biomass Energy Research Unit, LPF-SFB/Brasilia DF, 70818-900/Brésil (4 aut.); LERMAB, UMR1093, INRA, ENGREF, 14 rue Girardet/54042 Nancy/France (5 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Annals of forest science; ISSN 1286-4560; France; Da. 2009; Vol. 66; No. 1; 110p1-110p8; Abs. français; Bibl. 3/4 p.</SO><LA>Anglais</LA><FA>• La structure, la proportion et le mode de montage de la lignine, des celluloses et des hémicelluloses ont eu des effets marqués sur les mécanismes de la réaction au cours du traitement thermique et, par conséquent, ont eu une forte influence sur la qualité du produit final. L'effet des conditions de traitement, y compris des conditions sévères (jusqu'à 553 K) et la durée du traitement (jusqu'à 8 h) sur la structure de lignines de l'épicéa et du hêtre ont été étudiés. • La teneur en lignine a été déterminée par la méthode Klason et la structure de la lignine a été évaluée par thioacidolyse. • Les résultats ont mis en évidence la forte réactivité des lignines de l'épicéa et du hêtre vis-à-vis des traitements thermiques sévères. La sensibilité des différentes unités syringyl (S) et guaiacyl (G) vis-à-vis du traitement thermique est confirmée par comparaison des données obtenues avec les échantillons du hêtre et de l'épicéa. Le traitement le plus sévère (280 °C) du bois d'épicéa a induit un enrichissement spectaculaire en lignine ainsi que la quasi-disparition des unités de la lignine G, alors qu'un traitement plus modéré a sensiblement modifié la structure de la lignine par des réactions de dégradation qui affectent les p-hydroxyphényl (H ) et les unités de lignine G. • La thioacidolyse a révélé que le traitement thermique induit l'apparition de structures de vinyl éthers dans la lignine de l'épicéa. La diminution de production de la G et S thioacidolyses monomères reflète la disparition progressive des unités de lignine G et S impliquées seulement dans des liaisons β-O-4 et la formation de linkages de condensation en proportions de la sévérité du traitement. Dans des conditions difficiles, les unités S liées β-O-4 sont plus dégradées que leurs homologues G.</FA><CC>002A33</CC><FD>Traitement thermique; Bois feuillu; Foresterie; Réactivité; Monomère; Liaison génétique; Condensation; Bois résineux; Picea; Fagus; Lignine; Cellulose; Hémicellulose; Ether; Unité syringyle; Unité guaiacyle</FD><FG>Coniferales; Gymnospermae; Spermatophyta; Fagaceae; Dicotyledones; Angiospermae; Arbre</FG><ED>Heat treatment; Hardwood; Forestry; Reactivity; Monomer; Genetic linkage; Condensation; Softwood; Picea; Fagus; Lignin; Cellulose; Hemicellulose; Ether; Syringyl unit; Guaiacyl unit</ED><EG>Coniferales; Gymnospermae; Spermatophyta; Fagaceae; Dicotyledones; Angiospermae; Tree</EG><SD>Tratamiento térmico; Madera de frondosas; Ciencias forestales; Reactividad; Monómero; Ligamiento genético; Condensación; Madera de coníferas; Picea; Fagus; Lignina; Celulosa; Hemicelulosa; Eter</SD><LO>INIST-959.354000186485100100</LO><ID>09-0332567</ID></server></inist></record>
000D11	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Effect of a health claim and personal characteristics on consumer acceptance of fruit juices with different concentrations of açaí (Euterpe oleracea Mart.)</title><author><name sortKey="Sabbe, Sara" uniqKey="Sabbe S">Sara Sabbe</name><affiliation><inist:fA14 i1="01"><s1>Department of Plant Production, Laboratory of Tropical and Subtropical Agronomy and Ethnobotany, Ghent University, Coupure Links 653</s1><s2>9000 Gent</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Verbeke, Wim" uniqKey="Verbeke W">Wim Verbeke</name><affiliation><inist:fA14 i1="02"><s1>Department of Agricultural Economics, Ghent University, Coupure Links 653</s1><s2>9000 Gent</s2><s3>BEL</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Deliza, Rosires" uniqKey="Deliza R">Rosires Deliza</name><affiliation><inist:fA14 i1="03"><s1>Embrapa Labex, Avenue d'Agropolis</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>INRA - UMR 1129 FLAVIC</s1><s2>21000 Dijon</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Matta, Virginia" uniqKey="Matta V">Virginia Matta</name><affiliation><inist:fA14 i1="05"><s1>Embrapa Food Technology, Avenida das Américas, CEP 23020-470</s1><s2>Rio de Janeiro-RJ 29501</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Van Damme, Patrick" uniqKey="Van Damme P">Patrick Van Damme</name><affiliation><inist:fA14 i1="01"><s1>Department of Plant Production, Laboratory of Tropical and Subtropical Agronomy and Ethnobotany, Ghent University, Coupure Links 653</s1><s2>9000 Gent</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0333496</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0333496 INIST</idno><idno type="RBID">Pascal:09-0333496</idno><idno type="wicri:Area/Main/Corpus">001C70</idno><idno type="stanalyst">FRANCIS 09-0333496 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">0195-6663</idno><title level="j" type="abbreviated">Appetite : (Print)</title><title level="j" type="main">Appetite : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acceptance</term><term>Attitude</term><term>Concentration</term><term>Consumer</term><term>Feeding behavior</term><term>Fruit juice</term><term>Information</term><term>Nutrition</term><term>Psychology</term><term>Psychopathology</term><term>Public health</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Santé publique</term><term>Consommateur</term><term>Acceptation</term><term>Jus fruit</term><term>Concentration</term><term>Information</term><term>Attitude</term><term>Nutrition</term><term>Psychologie</term><term>Psychopathologie</term><term>Comportement alimentaire</term><term>Acceptabilité</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This study evaluates the effect of a health claim and personal characteristics on the acceptance of two unfamiliar açaí fruit juices that have a low (40% açaí) versus a high (4% açaí) a priori overall liking. Hedonic and sensory measures as well as health- and nutrition-related attribute perceptions and purchase intention were rated before and after health information was presented. Differences in information effects due to interactions with juice type, consumer background attitudes and sociodemographics were investigated. Providing health information yielded a positive, though rather small increase, in overall liking, perceived healthiness and perceived nutritional value of both juices, as well as in their purchase intention. Sensory experiences remained predominant in the acceptance of the fruit juices, although the health claim had a stronger effect on the perceived healthiness and nutritional value of the least-liked juice. Background attitudes and socio-demographic characteristics influenced consumers' acceptance of both unfamiliar fruit juices. Health-oriented consumers were more likely to compromise on taste for an eventual health benefit, though they still preferred the best tasting juice. Consumers with a high food neophobia reported a lower liking for both unfamiliar fruit juices. Older respondents and women were more likely to accept fruit juices that claim a particular health benefit.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0195-6663</s0></fA01><fA02 i1="01"><s0>APPTD4</s0></fA02><fA03 i2="1"><s0>Appetite : (Print)</s0></fA03><fA05><s2>53</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Effect of a health claim and personal characteristics on consumer acceptance of fruit juices with different concentrations of açaí (Euterpe oleracea Mart.)</s1></fA08><fA11 i1="01" i2="1"><s1>SABBE (Sara)</s1></fA11><fA11 i1="02" i2="1"><s1>VERBEKE (Wim)</s1></fA11><fA11 i1="03" i2="1"><s1>DELIZA (Rosires)</s1></fA11><fA11 i1="04" i2="1"><s1>MATTA (Virginia)</s1></fA11><fA11 i1="05" i2="1"><s1>VAN DAMME (Patrick)</s1></fA11><fA14 i1="01"><s1>Department of Plant Production, Laboratory of Tropical and Subtropical Agronomy and Ethnobotany, Ghent University, Coupure Links 653</s1><s2>9000 Gent</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Agricultural Economics, Ghent University, Coupure Links 653</s1><s2>9000 Gent</s2><s3>BEL</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Embrapa Labex, Avenue d'Agropolis</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>INRA - UMR 1129 FLAVIC</s1><s2>21000 Dijon</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="05"><s1>Embrapa Food Technology, Avenida das Américas, CEP 23020-470</s1><s2>Rio de Janeiro-RJ 29501</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA20><s1>84-92</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>18770</s2><s5>354000170838830110</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0333496</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Appetite : (Print)</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>This study evaluates the effect of a health claim and personal characteristics on the acceptance of two unfamiliar açaí fruit juices that have a low (40% açaí) versus a high (4% açaí) a priori overall liking. Hedonic and sensory measures as well as health- and nutrition-related attribute perceptions and purchase intention were rated before and after health information was presented. Differences in information effects due to interactions with juice type, consumer background attitudes and sociodemographics were investigated. Providing health information yielded a positive, though rather small increase, in overall liking, perceived healthiness and perceived nutritional value of both juices, as well as in their purchase intention. Sensory experiences remained predominant in the acceptance of the fruit juices, although the health claim had a stronger effect on the perceived healthiness and nutritional value of the least-liked juice. Background attitudes and socio-demographic characteristics influenced consumers' acceptance of both unfamiliar fruit juices. Health-oriented consumers were more likely to compromise on taste for an eventual health benefit, though they still preferred the best tasting juice. Consumers with a high food neophobia reported a lower liking for both unfamiliar fruit juices. Older respondents and women were more likely to accept fruit juices that claim a particular health benefit.</s0></fC01><fC02 i1="01" i2="X"><s0>002A16E</s0></fC02><fC02 i1="02" i2="X"><s0>002A26</s0></fC02><fC02 i1="03" i2="X"><s0>002B22</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Santé publique</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Public health</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Salud pública</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Consommateur</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Consumer</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Consumidor</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Acceptation</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Acceptance</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Aceptación</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Jus fruit</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Fruit juice</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Jugo fruta</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Concentration</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Concentration</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Concentración</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Information</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Information</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Información</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Attitude</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Attitude</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Actitud</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Nutrition</s0><s5>12</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Nutrition</s0><s5>12</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Nutrición</s0><s5>12</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Psychologie</s0><s5>17</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Psychology</s0><s5>17</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Psicología</s0><s5>17</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Psychopathologie</s0><s5>18</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Psychopathology</s0><s5>18</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Psicopatología</s0><s5>18</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Comportement alimentaire</s0><s5>25</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Feeding behavior</s0><s5>25</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Conducta alimenticia</s0><s5>25</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Acceptabilité</s0><s4>INC</s4><s5>86</s5></fC03><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0333496 INIST</NO><ET>Effect of a health claim and personal characteristics on consumer acceptance of fruit juices with different concentrations of açaí (Euterpe oleracea Mart.)</ET><AU>SABBE (Sara); VERBEKE (Wim); DELIZA (Rosires); MATTA (Virginia); VAN DAMME (Patrick)</AU><AF>Department of Plant Production, Laboratory of Tropical and Subtropical Agronomy and Ethnobotany, Ghent University, Coupure Links 653/9000 Gent/Belgique (1 aut., 5 aut.); Department of Agricultural Economics, Ghent University, Coupure Links 653/9000 Gent/Belgique (2 aut.); Embrapa Labex, Avenue d'Agropolis/34394 Montpellier/France (3 aut.); INRA - UMR 1129 FLAVIC/21000 Dijon/France (3 aut.); Embrapa Food Technology, Avenida das Américas, CEP 23020-470/Rio de Janeiro-RJ 29501/Brésil (4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Appetite : (Print); ISSN 0195-6663; Coden APPTD4; Pays-Bas; Da. 2009; Vol. 53; No. 1; Pp. 84-92; Bibl. 1 p.</SO><LA>Anglais</LA><EA>This study evaluates the effect of a health claim and personal characteristics on the acceptance of two unfamiliar açaí fruit juices that have a low (40% açaí) versus a high (4% açaí) a priori overall liking. Hedonic and sensory measures as well as health- and nutrition-related attribute perceptions and purchase intention were rated before and after health information was presented. Differences in information effects due to interactions with juice type, consumer background attitudes and sociodemographics were investigated. Providing health information yielded a positive, though rather small increase, in overall liking, perceived healthiness and perceived nutritional value of both juices, as well as in their purchase intention. Sensory experiences remained predominant in the acceptance of the fruit juices, although the health claim had a stronger effect on the perceived healthiness and nutritional value of the least-liked juice. Background attitudes and socio-demographic characteristics influenced consumers' acceptance of both unfamiliar fruit juices. Health-oriented consumers were more likely to compromise on taste for an eventual health benefit, though they still preferred the best tasting juice. Consumers with a high food neophobia reported a lower liking for both unfamiliar fruit juices. Older respondents and women were more likely to accept fruit juices that claim a particular health benefit.</EA><CC>002A16E; 002A26; 002B22</CC><FD>Santé publique; Consommateur; Acceptation; Jus fruit; Concentration; Information; Attitude; Nutrition; Psychologie; Psychopathologie; Comportement alimentaire; Acceptabilité</FD><ED>Public health; Consumer; Acceptance; Fruit juice; Concentration; Information; Attitude; Nutrition; Psychology; Psychopathology; Feeding behavior</ED><SD>Salud pública; Consumidor; Aceptación; Jugo fruta; Concentración; Información; Actitud; Nutrición; Psicología; Psicopatología; Conducta alimenticia</SD><LO>INIST-18770.354000170838830110</LO><ID>09-0333496</ID></server></inist></record>
000D12	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Improving hydrological information acquisition from DEM processing in floodplains</title><author><name sortKey="Getirana, Augusto C V" uniqKey="Getirana A">Augusto C. V. Getirana</name><affiliation><inist:fA14 i1="01"><s1>Programa de Engenharia Civil, COPPE-Universidade Fédéral do Rio de Janeiro, CP 68506</s1><s2>CEP 21945-970, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université de Toulouse 3, LMTG, CNRS, UMR5563, UR154, IRD</s1><s2>31400 Toulouse</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bonnet, Marie Paule" uniqKey="Bonnet M">Marie-Paule Bonnet</name><affiliation><inist:fA14 i1="02"><s1>Université de Toulouse 3, LMTG, CNRS, UMR5563, UR154, IRD</s1><s2>31400 Toulouse</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rotunno Filho, Otto C" uniqKey="Rotunno Filho O">Otto C. Rotunno Filho</name><affiliation><inist:fA14 i1="01"><s1>Programa de Engenharia Civil, COPPE-Universidade Fédéral do Rio de Janeiro, CP 68506</s1><s2>CEP 21945-970, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mansur, Webe J" uniqKey="Mansur W">Webe J. Mansur</name><affiliation><inist:fA14 i1="01"><s1>Programa de Engenharia Civil, COPPE-Universidade Fédéral do Rio de Janeiro, CP 68506</s1><s2>CEP 21945-970, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0334222</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0334222 INIST</idno><idno type="RBID">Pascal:09-0334222</idno><idno type="wicri:Area/Main/Corpus">001C69</idno></publicationStmt><seriesStmt><idno type="ISSN">0885-6087</idno><title level="j" type="abbreviated">Hydrol. process.</title><title level="j" type="main">Hydrological processes</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amazon River</term><term>Brazil</term><term>channels</term><term>classification</term><term>digital elevation models</term><term>drainage</term><term>drainage basins</term><term>drainage patterns</term><term>floodplains</term><term>imagery</term><term>maps</term><term>new methods</term><term>satellites</term><term>spatial distribution</term><term>streams</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Plaine inondable</term><term>Modèle numérique élévation</term><term>Drainage</term><term>Réseau hydrographique</term><term>Cours eau</term><term>Carte</term><term>Bassin versant</term><term>Méthode nouvelle</term><term>Imagerie</term><term>Chenal</term><term>Distribution spatiale</term><term>Satellite</term><term>Classification</term><term>Brésil</term><term>Rivière Amazone</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Extraction of hydrological information from digital elevation models (DEMs) is a required step when conducting any spatially distributed hydrological modelling. In particular, automated methods are proposed to extract the drainage structure from the DEM. However, a realistic river network is not always derived from conventional DEM processing methods. Indeed, inaccuracy occurs in flat areas corresponding to floodplains. In these areas, additional sources of information are required to extract the correct drainage direction from the DEM. In this study, it is demonstrated that traditional approaches of DEM-preprocessing such as the commonly known 'stream burning' fail to provide correct maps of drainage directions and catchment areas when the extension of flat areas is large. A new method is proposed to take advantage of available imagery data. This method is based on a 'double DEM burning' process: DEM is first burned in the main rivers using the channel network, and then in the floodplain using the spatial distribution of floodplains provided by classified satellite images. In this sense, the method has been referred to as the floodplain burning approach (or simply FB approach). Spatial distribution of floodplains is derived from a multitemporal SAR image classification. A system of equations is used to vary the elevation offset required to be 'burnt' in each cell representing the floodplain, according to the minimal distance from the channel network, which is calculated by a distance transformation. The FB approach was applied to a sub-basin located within the larger Amazon River basin. The region is characterized by large floodplain extensions. Basin delineation maps derived from the new method were compared with those obtained from the traditional stream burning method and highlighted more realistic results.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0885-6087</s0></fA01><fA02 i1="01"><s0>HYPRE3</s0></fA02><fA03 i2="1"><s0>Hydrol. process.</s0></fA03><fA05><s2>23</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Improving hydrological information acquisition from DEM processing in floodplains</s1></fA08><fA11 i1="01" i2="1"><s1>GETIRANA (Augusto C. V.)</s1></fA11><fA11 i1="02" i2="1"><s1>BONNET (Marie-Paule)</s1></fA11><fA11 i1="03" i2="1"><s1>ROTUNNO FILHO (Otto C.)</s1></fA11><fA11 i1="04" i2="1"><s1>MANSUR (Webe J.)</s1></fA11><fA14 i1="01"><s1>Programa de Engenharia Civil, COPPE-Universidade Fédéral do Rio de Janeiro, CP 68506</s1><s2>CEP 21945-970, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Université de Toulouse 3, LMTG, CNRS, UMR5563, UR154, IRD</s1><s2>31400 Toulouse</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA20><s1>502-514</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>21671</s2><s5>354000184137090130</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0334222</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Hydrological processes</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Extraction of hydrological information from digital elevation models (DEMs) is a required step when conducting any spatially distributed hydrological modelling. In particular, automated methods are proposed to extract the drainage structure from the DEM. However, a realistic river network is not always derived from conventional DEM processing methods. Indeed, inaccuracy occurs in flat areas corresponding to floodplains. In these areas, additional sources of information are required to extract the correct drainage direction from the DEM. In this study, it is demonstrated that traditional approaches of DEM-preprocessing such as the commonly known 'stream burning' fail to provide correct maps of drainage directions and catchment areas when the extension of flat areas is large. A new method is proposed to take advantage of available imagery data. This method is based on a 'double DEM burning' process: DEM is first burned in the main rivers using the channel network, and then in the floodplain using the spatial distribution of floodplains provided by classified satellite images. In this sense, the method has been referred to as the floodplain burning approach (or simply FB approach). Spatial distribution of floodplains is derived from a multitemporal SAR image classification. A system of equations is used to vary the elevation offset required to be 'burnt' in each cell representing the floodplain, according to the minimal distance from the channel network, which is calculated by a distance transformation. The FB approach was applied to a sub-basin located within the larger Amazon River basin. The region is characterized by large floodplain extensions. Basin delineation maps derived from the new method were compared with those obtained from the traditional stream burning method and highlighted more realistic results.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01N01</s0></fC02><fC02 i1="02" i2="2"><s0>001E01J02</s0></fC02><fC02 i1="03" i2="2"><s0>226A01</s0></fC02><fC02 i1="04" i2="2"><s0>224B02</s0></fC02><fC03 i1="01" i2="2" l="FRE"><s0>Plaine inondable</s0><s5>01</s5></fC03><fC03 i1="01" i2="2" l="ENG"><s0>floodplains</s0><s5>01</s5></fC03><fC03 i1="01" i2="2" l="SPA"><s0>Llano inundable</s0><s5>01</s5></fC03><fC03 i1="02" i2="2" l="FRE"><s0>Modèle numérique élévation</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="ENG"><s0>digital elevation models</s0><s5>02</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Drainage</s0><s5>04</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>drainage</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="FRE"><s0>Réseau hydrographique</s0><s5>05</s5></fC03><fC03 i1="04" i2="2" l="ENG"><s0>drainage patterns</s0><s5>05</s5></fC03><fC03 i1="04" i2="2" l="SPA"><s0>Red hidrográfica</s0><s5>05</s5></fC03><fC03 i1="05" i2="2" l="FRE"><s0>Cours eau</s0><s5>07</s5></fC03><fC03 i1="05" i2="2" l="ENG"><s0>streams</s0><s5>07</s5></fC03><fC03 i1="05" i2="2" l="SPA"><s0>Curso agua</s0><s5>07</s5></fC03><fC03 i1="06" i2="2" l="FRE"><s0>Carte</s0><s5>08</s5></fC03><fC03 i1="06" i2="2" l="ENG"><s0>maps</s0><s5>08</s5></fC03><fC03 i1="06" i2="2" l="SPA"><s0>Mapa</s0><s5>08</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Bassin versant</s0><s5>09</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>drainage basins</s0><s5>09</s5></fC03><fC03 i1="07" i2="2" l="SPA"><s0>Cuenca</s0><s5>09</s5></fC03><fC03 i1="08" i2="2" l="FRE"><s0>Méthode nouvelle</s0><s5>11</s5></fC03><fC03 i1="08" i2="2" l="ENG"><s0>new methods</s0><s5>11</s5></fC03><fC03 i1="08" i2="2" l="SPA"><s0>Método nuevo</s0><s5>11</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Imagerie</s0><s5>12</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>imagery</s0><s5>12</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Imaginería</s0><s5>12</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Chenal</s0><s5>13</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>channels</s0><s5>13</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Canal</s0><s5>13</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Distribution spatiale</s0><s5>14</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>spatial distribution</s0><s5>14</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Distribución espacial</s0><s5>14</s5></fC03><fC03 i1="12" i2="2" l="FRE"><s0>Satellite</s0><s5>15</s5></fC03><fC03 i1="12" i2="2" l="ENG"><s0>satellites</s0><s5>15</s5></fC03><fC03 i1="12" i2="2" l="SPA"><s0>Satélite</s0><s5>15</s5></fC03><fC03 i1="13" i2="2" l="FRE"><s0>Classification</s0><s5>17</s5></fC03><fC03 i1="13" i2="2" l="ENG"><s0>classification</s0><s5>17</s5></fC03><fC03 i1="13" i2="2" l="SPA"><s0>Clasificación</s0><s5>17</s5></fC03><fC03 i1="14" i2="2" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="14" i2="2" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="14" i2="2" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="15" i2="2" l="FRE"><s0>Rivière Amazone</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="15" i2="2" l="ENG"><s0>Amazon River</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="15" i2="2" l="SPA"><s0>Río Amazona</s0><s2>NG</s2><s5>62</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fN21><s1>243</s1></fN21></pA></standard><server><NO>PASCAL 09-0334222 INIST</NO><ET>Improving hydrological information acquisition from DEM processing in floodplains</ET><AU>GETIRANA (Augusto C. V.); BONNET (Marie-Paule); ROTUNNO FILHO (Otto C.); MANSUR (Webe J.)</AU><AF>Programa de Engenharia Civil, COPPE-Universidade Fédéral do Rio de Janeiro, CP 68506/CEP 21945-970, Rio de Janeiro, RJ/Brésil (1 aut., 3 aut., 4 aut.); Université de Toulouse 3, LMTG, CNRS, UMR5563, UR154, IRD/31400 Toulouse/France (1 aut., 2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Hydrological processes; ISSN 0885-6087; Coden HYPRE3; Royaume-Uni; Da. 2009; Vol. 23; No. 3; Pp. 502-514; Bibl. 1 p.1/4</SO><LA>Anglais</LA><EA>Extraction of hydrological information from digital elevation models (DEMs) is a required step when conducting any spatially distributed hydrological modelling. In particular, automated methods are proposed to extract the drainage structure from the DEM. However, a realistic river network is not always derived from conventional DEM processing methods. Indeed, inaccuracy occurs in flat areas corresponding to floodplains. In these areas, additional sources of information are required to extract the correct drainage direction from the DEM. In this study, it is demonstrated that traditional approaches of DEM-preprocessing such as the commonly known 'stream burning' fail to provide correct maps of drainage directions and catchment areas when the extension of flat areas is large. A new method is proposed to take advantage of available imagery data. This method is based on a 'double DEM burning' process: DEM is first burned in the main rivers using the channel network, and then in the floodplain using the spatial distribution of floodplains provided by classified satellite images. In this sense, the method has been referred to as the floodplain burning approach (or simply FB approach). Spatial distribution of floodplains is derived from a multitemporal SAR image classification. A system of equations is used to vary the elevation offset required to be 'burnt' in each cell representing the floodplain, according to the minimal distance from the channel network, which is calculated by a distance transformation. The FB approach was applied to a sub-basin located within the larger Amazon River basin. The region is characterized by large floodplain extensions. Basin delineation maps derived from the new method were compared with those obtained from the traditional stream burning method and highlighted more realistic results.</EA><CC>001E01N01; 001E01J02; 226A01; 224B02</CC><FD>Plaine inondable; Modèle numérique élévation; Drainage; Réseau hydrographique; Cours eau; Carte; Bassin versant; Méthode nouvelle; Imagerie; Chenal; Distribution spatiale; Satellite; Classification; Brésil; Rivière Amazone</FD><FG>Amérique du Sud</FG><ED>floodplains; digital elevation models; drainage; drainage patterns; streams; maps; drainage basins; new methods; imagery; channels; spatial distribution; satellites; classification; Brazil; Amazon River</ED><EG>South America</EG><SD>Llano inundable; Red hidrográfica; Curso agua; Mapa; Cuenca; Método nuevo; Imaginería; Canal; Distribución espacial; Satélite; Clasificación; Brasil; Río Amazona</SD><LO>INIST-21671.354000184137090130</LO><ID>09-0334222</ID></server></inist></record>
000D13	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Lactococcus lactis Expressing either Staphylococcus aureus Fibronectin-Binding Protein A or Listeria monocytogenes Internalin A Can Efficiently Internalize and Deliver DNA in Human Epithelial Cells</title><author><name sortKey="Innocentin, Silvia" uniqKey="Innocentin S">Silvia Innocentin</name><affiliation><inist:fA14 i1="01"><s1>Unité de Virologie et Immunologie Moléculaires, UR892 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Guimaraes, Valeria" uniqKey="Guimaraes V">Valeria Guimaraes</name><affiliation><inist:fA14 i1="01"><s1>Unité de Virologie et Immunologie Moléculaires, UR892 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Miyoshi, Anderson" uniqKey="Miyoshi A">Anderson Miyoshi</name><affiliation><inist:fA14 i1="02"><s1>Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG-ICB)</s1><s2>Belo Horizonte-MG</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Azevedo, Vasco" uniqKey="Azevedo V">Vasco Azevedo</name><affiliation><inist:fA14 i1="02"><s1>Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG-ICB)</s1><s2>Belo Horizonte-MG</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Langella, Philippe" uniqKey="Langella P">Philippe Langella</name><affiliation><inist:fA14 i1="03"><s1>Unité d'Ecologie et Physiologie du Système Digestif, UR910 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chatel, Jean Marc" uniqKey="Chatel J">Jean-Marc Chatel</name><affiliation><inist:fA14 i1="03"><s1>Unité d'Ecologie et Physiologie du Système Digestif, UR910 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lefevre, Francois" uniqKey="Lefevre F">François Lefevre</name><affiliation><inist:fA14 i1="01"><s1>Unité de Virologie et Immunologie Moléculaires, UR892 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0334787</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0334787 INIST</idno><idno type="RBID">Pascal:09-0334787</idno><idno type="wicri:Area/Main/Corpus">001C68</idno></publicationStmt><seriesStmt><idno type="ISSN">0099-2240</idno><title level="j" type="abbreviated">Appl. environ. microbiol. : (Print)</title><title level="j" type="main">Applied and environmental microbiology : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Binding protein</term><term>DNA</term><term>Epithelial cell</term><term>Fibronectin</term><term>Human</term><term>Lactococcus lactis</term><term>Listeria monocytogenes</term><term>Staphylococcus aureus</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Lactococcus lactis</term><term>Staphylococcus aureus</term><term>Fibronectine</term><term>Protéine liaison</term><term>Listeria monocytogenes</term><term>DNA</term><term>Homme</term><term>Cellule épithéliale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lactococci are noninvasive bacteria frequently used as protein delivery vectors and, more recently, as in vitro and in vivo DNA delivery vehicles. We previously showed that a functional eukaryotic enhanced green fluorescent protein (eGFP) expression plasmid vector was delivered in epithelial cells by Lactococcus lactis producing Listeria monocytogenes internalin A (L. lactis InlA<sup>+</sup>), but this strategy is limited in vivo to transgenic mice and guinea pigs. In this study, we compare the internalization ability of L. lactis InlA<sup>+</sup> and L. lactis producing either the fibronectin-binding protein A of Staphylococcus aureus (L. lactis FnBPA+<sup>)</sup> or its fibronectin binding domains C and D (L. lactis CD<sup>+</sup>). L. lactis FnBPA<sup>+</sup> and L. lactis InlA<sup>+</sup> showed comparable internalization rates in Caco-2 cells, while the internalization rate observed with L. lactis CD<sup>+</sup> was lower. As visualized by conventional and confocal fluorescence microscopy, large clusters of L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were present in the cytoplasm of Caco-2 cells after internalization. Moreover, the internalization rates of Lactobacillus acidophilus NCFM and of an NCFM mutant strain with the gene coding for the fibronectin-binding protein (fbpA) inactivated were also evaluated in Caco-2 cells. Similar low internalization rates were observed for both wild-type L. acidophilus NCFM and the fbpA mutant, suggesting that commensal fibronectin binding proteins have a role in adhesion but not in invasion. L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were then used to deliver a eukaryotic eGFP expression plasmid in Caco-2 cells: flow cytometry analysis showed that the highest percentage of green fluorescent Caco-2 cells was observed after coculture with either L. lactis FnBPA<sup>+</sup> or L. lactis InlA<sup>+</sup>. Analysis of the in vivo efficiency of these invasive recombinant strains is currently in progress to validate their potential as DNA vaccine delivery vehicles.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0099-2240</s0></fA01><fA02 i1="01"><s0>AEMIDF</s0></fA02><fA03 i2="1"><s0>Appl. environ. microbiol. : (Print)</s0></fA03><fA05><s2>75</s2></fA05><fA06><s2>14</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Lactococcus lactis Expressing either Staphylococcus aureus Fibronectin-Binding Protein A or Listeria monocytogenes Internalin A Can Efficiently Internalize and Deliver DNA in Human Epithelial Cells</s1></fA08><fA11 i1="01" i2="1"><s1>INNOCENTIN (Silvia)</s1></fA11><fA11 i1="02" i2="1"><s1>GUIMARAES (Valeria)</s1></fA11><fA11 i1="03" i2="1"><s1>MIYOSHI (Anderson)</s1></fA11><fA11 i1="04" i2="1"><s1>AZEVEDO (Vasco)</s1></fA11><fA11 i1="05" i2="1"><s1>LANGELLA (Philippe)</s1></fA11><fA11 i1="06" i2="1"><s1>CHATEL (Jean-Marc)</s1></fA11><fA11 i1="07" i2="1"><s1>LEFEVRE (François)</s1></fA11><fA14 i1="01"><s1>Unité de Virologie et Immunologie Moléculaires, UR892 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG-ICB)</s1><s2>Belo Horizonte-MG</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>Unité d'Ecologie et Physiologie du Système Digestif, UR910 INRA, Domaine de Vilvert</s1><s2>78352 Jouy en Josas</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA20><s1>4870-4878</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>7195</s2><s5>354000172464310240</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>31 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0334787</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied and environmental microbiology : (Print)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Lactococci are noninvasive bacteria frequently used as protein delivery vectors and, more recently, as in vitro and in vivo DNA delivery vehicles. We previously showed that a functional eukaryotic enhanced green fluorescent protein (eGFP) expression plasmid vector was delivered in epithelial cells by Lactococcus lactis producing Listeria monocytogenes internalin A (L. lactis InlA<sup>+</sup>), but this strategy is limited in vivo to transgenic mice and guinea pigs. In this study, we compare the internalization ability of L. lactis InlA<sup>+</sup> and L. lactis producing either the fibronectin-binding protein A of Staphylococcus aureus (L. lactis FnBPA+<sup>)</sup> or its fibronectin binding domains C and D (L. lactis CD<sup>+</sup>). L. lactis FnBPA<sup>+</sup> and L. lactis InlA<sup>+</sup> showed comparable internalization rates in Caco-2 cells, while the internalization rate observed with L. lactis CD<sup>+</sup> was lower. As visualized by conventional and confocal fluorescence microscopy, large clusters of L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were present in the cytoplasm of Caco-2 cells after internalization. Moreover, the internalization rates of Lactobacillus acidophilus NCFM and of an NCFM mutant strain with the gene coding for the fibronectin-binding protein (fbpA) inactivated were also evaluated in Caco-2 cells. Similar low internalization rates were observed for both wild-type L. acidophilus NCFM and the fbpA mutant, suggesting that commensal fibronectin binding proteins have a role in adhesion but not in invasion. L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were then used to deliver a eukaryotic eGFP expression plasmid in Caco-2 cells: flow cytometry analysis showed that the highest percentage of green fluorescent Caco-2 cells was observed after coculture with either L. lactis FnBPA<sup>+</sup> or L. lactis InlA<sup>+</sup>. Analysis of the in vivo efficiency of these invasive recombinant strains is currently in progress to validate their potential as DNA vaccine delivery vehicles.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Lactococcus lactis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Lactococcus lactis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Lactococcus lactis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Staphylococcus aureus</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Staphylococcus aureus</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Staphylococcus aureus</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Fibronectine</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Fibronectin</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Fibronectina</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Protéine liaison</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Binding protein</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Proteína enlace</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Listeria monocytogenes</s0><s2>NS</s2><s5>12</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Listeria monocytogenes</s0><s2>NS</s2><s5>12</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Listeria monocytogenes</s0><s2>NS</s2><s5>12</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>DNA</s0><s5>19</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>DNA</s0><s5>19</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>DNA</s0><s5>19</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Homme</s0><s5>20</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Human</s0><s5>20</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Hombre</s0><s5>20</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Cellule épithéliale</s0><s5>21</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Epithelial cell</s0><s5>21</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Célula epitelial</s0><s5>21</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Streptococcaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Streptococcaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Streptococcaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Micrococcaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Micrococcaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Micrococcaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Bactérie lactique</s0><s5>23</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Lactic acid bacteria</s0><s5>23</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Bacteria láctica</s0><s5>23</s5></fC07><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0334787 INIST</NO><ET>Lactococcus lactis Expressing either Staphylococcus aureus Fibronectin-Binding Protein A or Listeria monocytogenes Internalin A Can Efficiently Internalize and Deliver DNA in Human Epithelial Cells</ET><AU>INNOCENTIN (Silvia); GUIMARAES (Valeria); MIYOSHI (Anderson); AZEVEDO (Vasco); LANGELLA (Philippe); CHATEL (Jean-Marc); LEFEVRE (François)</AU><AF>Unité de Virologie et Immunologie Moléculaires, UR892 INRA, Domaine de Vilvert/78352 Jouy en Josas/France (1 aut., 2 aut., 7 aut.); Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG-ICB)/Belo Horizonte-MG/Brésil (3 aut., 4 aut.); Unité d'Ecologie et Physiologie du Système Digestif, UR910 INRA, Domaine de Vilvert/78352 Jouy en Josas/France (5 aut., 6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Applied and environmental microbiology : (Print); ISSN 0099-2240; Coden AEMIDF; Etats-Unis; Da. 2009; Vol. 75; No. 14; Pp. 4870-4878; Bibl. 31 ref.</SO><LA>Anglais</LA><EA>Lactococci are noninvasive bacteria frequently used as protein delivery vectors and, more recently, as in vitro and in vivo DNA delivery vehicles. We previously showed that a functional eukaryotic enhanced green fluorescent protein (eGFP) expression plasmid vector was delivered in epithelial cells by Lactococcus lactis producing Listeria monocytogenes internalin A (L. lactis InlA<sup>+</sup>), but this strategy is limited in vivo to transgenic mice and guinea pigs. In this study, we compare the internalization ability of L. lactis InlA<sup>+</sup> and L. lactis producing either the fibronectin-binding protein A of Staphylococcus aureus (L. lactis FnBPA+<sup>)</sup> or its fibronectin binding domains C and D (L. lactis CD<sup>+</sup>). L. lactis FnBPA<sup>+</sup> and L. lactis InlA<sup>+</sup> showed comparable internalization rates in Caco-2 cells, while the internalization rate observed with L. lactis CD<sup>+</sup> was lower. As visualized by conventional and confocal fluorescence microscopy, large clusters of L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were present in the cytoplasm of Caco-2 cells after internalization. Moreover, the internalization rates of Lactobacillus acidophilus NCFM and of an NCFM mutant strain with the gene coding for the fibronectin-binding protein (fbpA) inactivated were also evaluated in Caco-2 cells. Similar low internalization rates were observed for both wild-type L. acidophilus NCFM and the fbpA mutant, suggesting that commensal fibronectin binding proteins have a role in adhesion but not in invasion. L. lactis FnBPA<sup>+</sup>, L. lactis CD<sup>+</sup>, and L. lactis InlA<sup>+</sup> were then used to deliver a eukaryotic eGFP expression plasmid in Caco-2 cells: flow cytometry analysis showed that the highest percentage of green fluorescent Caco-2 cells was observed after coculture with either L. lactis FnBPA<sup>+</sup> or L. lactis InlA<sup>+</sup>. Analysis of the in vivo efficiency of these invasive recombinant strains is currently in progress to validate their potential as DNA vaccine delivery vehicles.</EA><CC>002A05</CC><FD>Lactococcus lactis; Staphylococcus aureus; Fibronectine; Protéine liaison; Listeria monocytogenes; DNA; Homme; Cellule épithéliale</FD><FG>Streptococcaceae; Micrococcales; Bactérie; Micrococcaceae; Bactérie lactique</FG><ED>Lactococcus lactis; Staphylococcus aureus; Fibronectin; Binding protein; Listeria monocytogenes; DNA; Human; Epithelial cell</ED><EG>Streptococcaceae; Micrococcales; Bacteria; Micrococcaceae; Lactic acid bacteria</EG><SD>Lactococcus lactis; Staphylococcus aureus; Fibronectina; Proteína enlace; Listeria monocytogenes; DNA; Hombre; Célula epitelial</SD><LO>INIST-7195.354000172464310240</LO><ID>09-0334787</ID></server></inist></record>
000D14	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">A Public Policy Approach to Local Models of HIV/AIDS Control in Brazil</title><author><name sortKey="Le Loup, Guillaume" uniqKey="Le Loup G">Guillaume Le Loup</name><affiliation><inist:fA14 i1="01"><s1>Paris Hospital and Institut National de la Santé et la Recherche Medicale UMRS 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Pierre et Marie Curie</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Assis, Andreia" uniqKey="De Assis A">Andreia De Assis</name><affiliation><inist:fA14 i1="03"><s1>Fundaçao Getulio Vargas</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Costa Couto, Maria Helena" uniqKey="Costa Couto M">Maria-Helena Costa-Couto</name><affiliation><inist:fA14 i1="04"><s1>Instituto de Medicina Social, universidade Estadual de Rio de Janeiro. Jean-Claude Thoenig is emeritus of Centre National de la Recherche Scientifique</s1><s2>Paris</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Thoenig, Jean Claude" uniqKey="Thoenig J">Jean-Claude Thoenig</name><affiliation><inist:fA14 i1="01"><s1>Paris Hospital and Institut National de la Santé et la Recherche Medicale UMRS 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Pierre et Marie Curie</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fleury, Sonia" uniqKey="Fleury S">Sonia Fleury</name><affiliation><inist:fA14 i1="03"><s1>Fundaçao Getulio Vargas</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Camargo, Kenneth Jr" uniqKey="De Camargo K">Kenneth Jr De Camargo</name><affiliation><inist:fA14 i1="04"><s1>Instituto de Medicina Social, universidade Estadual de Rio de Janeiro. Jean-Claude Thoenig is emeritus of Centre National de la Recherche Scientifique</s1><s2>Paris</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Larouze, Bernard" uniqKey="Larouze B">Bernard Larouze</name><affiliation><inist:fA14 i1="01"><s1>Paris Hospital and Institut National de la Santé et la Recherche Medicale UMRS 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Pierre et Marie Curie</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0335032</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0335032 INIST</idno><idno type="RBID">Pascal:09-0335032</idno><idno type="wicri:Area/Main/Corpus">001C67</idno></publicationStmt><seriesStmt><idno type="ISSN">0090-0036</idno><title level="j" type="abbreviated">Am. j. publ. health : (1971)</title><title level="j" type="main">American journal of public health : (1971)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>AIDS</term><term>Brazil</term><term>Check</term><term>Human</term><term>Models</term><term>Political aspect</term><term>Public health</term><term>Surveillance</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Aspect politique</term><term>Modèle</term><term>SIDA</term><term>Surveillance</term><term>Contrôle</term><term>Brésil</term><term>Santé publique</term><term>Homme</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Objectives. We investigated involvement and cooperation patterns of local Brazilian AIDS program actors and the consequences of these patterns for program implementation and sustainability. Methods. We performed a public policy analysis (documentary analysis, direct observation, semistructured interviews of health service and nongovernmental organization [NGO] actors) in 5 towns in 2 states, São Paulo and Pará. Results. Patterns suggested 3 models. In model 1, local government, NGOs, and primary health care services were involved in AIDS programs with satisfactory response to new epidemiological trends but a risk that HIV/AIDS would become low priority. In model 2, mainly because of NGO activism, HIV/AIDS remained an exceptional issue, with limited responses to new epidemiological trends and program sustainability undermined by political instability. In model 3, involvement of public agencies and NGOs was limited, with inadequate response to epidemiological trends and poor mobilization threatening program sustainability. Conclusions, Within a common national AIDS policy framework, the degree of involvement and cooperation between public and NGO actors deeply impacts population coverage and program sustainability. Specific processes are required to maintain actor mobilization without isolating AIDS programs.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0090-0036</s0></fA01><fA02 i1="01"><s0>AJPEAG</s0></fA02><fA03 i2="1"><s0>Am. j. publ. health : (1971)</s0></fA03><fA05><s2>99</s2></fA05><fA06><s2>6</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>A Public Policy Approach to Local Models of HIV/AIDS Control in Brazil</s1></fA08><fA11 i1="01" i2="1"><s1>LE LOUP (Guillaume)</s1></fA11><fA11 i1="02" i2="1"><s1>DE ASSIS (Andreia)</s1></fA11><fA11 i1="03" i2="1"><s1>COSTA-COUTO (Maria-Helena)</s1></fA11><fA11 i1="04" i2="1"><s1>THOENIG (Jean-Claude)</s1></fA11><fA11 i1="05" i2="1"><s1>FLEURY (Sonia)</s1></fA11><fA11 i1="06" i2="1"><s1>DE CAMARGO (Kenneth JR)</s1></fA11><fA11 i1="07" i2="1"><s1>LAROUZE (Bernard)</s1></fA11><fA14 i1="01"><s1>Paris Hospital and Institut National de la Santé et la Recherche Medicale UMRS 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Université Pierre et Marie Curie</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Fundaçao Getulio Vargas</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Instituto de Medicina Social, universidade Estadual de Rio de Janeiro. Jean-Claude Thoenig is emeritus of Centre National de la Recherche Scientifique</s1><s2>Paris</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></fA14><fA20><s1>1108-1115</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2009</s2><s5>354000188478490260</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>39 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0335032</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>American journal of public health : (1971)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Objectives. We investigated involvement and cooperation patterns of local Brazilian AIDS program actors and the consequences of these patterns for program implementation and sustainability. Methods. We performed a public policy analysis (documentary analysis, direct observation, semistructured interviews of health service and nongovernmental organization [NGO] actors) in 5 towns in 2 states, São Paulo and Pará. Results. Patterns suggested 3 models. In model 1, local government, NGOs, and primary health care services were involved in AIDS programs with satisfactory response to new epidemiological trends but a risk that HIV/AIDS would become low priority. In model 2, mainly because of NGO activism, HIV/AIDS remained an exceptional issue, with limited responses to new epidemiological trends and program sustainability undermined by political instability. In model 3, involvement of public agencies and NGOs was limited, with inadequate response to epidemiological trends and poor mobilization threatening program sustainability. Conclusions, Within a common national AIDS policy framework, the degree of involvement and cooperation between public and NGO actors deeply impacts population coverage and program sustainability. Specific processes are required to maintain actor mobilization without isolating AIDS programs.</s0></fC01><fC02 i1="01" i2="X"><s0>002B30A11</s0></fC02><fC02 i1="02" i2="X"><s0>002B05C02D</s0></fC02><fC02 i1="03" i2="X"><s0>002B06D01</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Aspect politique</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Political aspect</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Aspecto político</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Modèle</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Models</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Modelo</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>SIDA</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>AIDS</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>SIDA</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Surveillance</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Surveillance</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Vigilancia</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Contrôle</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Check</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Control</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Santé publique</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Public health</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Salud pública</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Homme</s0><s5>25</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Human</s0><s5>25</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Hombre</s0><s5>25</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Virose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Viral disease</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Virosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Immunodéficit</s0><s5>37</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Immune deficiency</s0><s5>37</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Inmunodeficiencia</s0><s5>37</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Immunopathologie</s0><s5>39</s5></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Immunopathology</s0><s5>39</s5></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Inmunopatología</s0><s5>39</s5></fC07><fN21><s1>243</s1></fN21></pA></standard><server><NO>PASCAL 09-0335032 INIST</NO><ET>A Public Policy Approach to Local Models of HIV/AIDS Control in Brazil</ET><AU>LE LOUP (Guillaume); DE ASSIS (Andreia); COSTA-COUTO (Maria-Helena); THOENIG (Jean-Claude); FLEURY (Sonia); DE CAMARGO (Kenneth JR); LAROUZE (Bernard)</AU><AF>Paris Hospital and Institut National de la Santé et la Recherche Medicale UMRS 707/Paris/France (1 aut., 4 aut., 7 aut.); Université Pierre et Marie Curie/Paris/France (1 aut., 4 aut., 7 aut.); Fundaçao Getulio Vargas/Rio de Janeiro/Brésil (2 aut., 5 aut.); Instituto de Medicina Social, universidade Estadual de Rio de Janeiro. Jean-Claude Thoenig is emeritus of Centre National de la Recherche Scientifique/Paris/France (3 aut., 6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>American journal of public health : (1971); ISSN 0090-0036; Coden AJPEAG; Etats-Unis; Da. 2009; Vol. 99; No. 6; Pp. 1108-1115; Bibl. 39 ref.</SO><LA>Anglais</LA><EA>Objectives. We investigated involvement and cooperation patterns of local Brazilian AIDS program actors and the consequences of these patterns for program implementation and sustainability. Methods. We performed a public policy analysis (documentary analysis, direct observation, semistructured interviews of health service and nongovernmental organization [NGO] actors) in 5 towns in 2 states, São Paulo and Pará. Results. Patterns suggested 3 models. In model 1, local government, NGOs, and primary health care services were involved in AIDS programs with satisfactory response to new epidemiological trends but a risk that HIV/AIDS would become low priority. In model 2, mainly because of NGO activism, HIV/AIDS remained an exceptional issue, with limited responses to new epidemiological trends and program sustainability undermined by political instability. In model 3, involvement of public agencies and NGOs was limited, with inadequate response to epidemiological trends and poor mobilization threatening program sustainability. Conclusions, Within a common national AIDS policy framework, the degree of involvement and cooperation between public and NGO actors deeply impacts population coverage and program sustainability. Specific processes are required to maintain actor mobilization without isolating AIDS programs.</EA><CC>002B30A11; 002B05C02D; 002B06D01</CC><FD>Aspect politique; Modèle; SIDA; Surveillance; Contrôle; Brésil; Santé publique; Homme</FD><FG>Virose; Infection; Amérique du Sud; Amérique; Immunodéficit; Immunopathologie</FG><ED>Political aspect; Models; AIDS; Surveillance; Check; Brazil; Public health; Human</ED><EG>Viral disease; Infection; South America; America; Immune deficiency; Immunopathology</EG><SD>Aspecto político; Modelo; SIDA; Vigilancia; Control; Brasil; Salud pública; Hombre</SD><LO>INIST-2009.354000188478490260</LO><ID>09-0335032</ID></server></inist></record>
000D15	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Epidemiology of tuberculosis in the Americas: the Stop TB strategy and the Millennium Development Goals</title><author><name sortKey="Ramon Pardo, R" uniqKey="Ramon Pardo R">R. Ramon-Pardo</name><affiliation><inist:fA14 i1="01"><s1>Communicable Diseases Project, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Del Granado, M" uniqKey="Del Granado M">M. Del Granado</name><affiliation><inist:fA14 i1="02"><s1>Regional TB Program, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gerger, A" uniqKey="Gerger A">A. Gerger</name><affiliation><inist:fA14 i1="03"><s1>Health Analysis Project, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Canela Soler, J" uniqKey="Canela Soler J">J. Canela Soler</name><affiliation><inist:fA14 i1="03"><s1>Health Analysis Project, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Universidad de Barcelona</s1><s2>Barcelona</s2><s3>ESP</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mir, M" uniqKey="Mir M">M. Mir</name><affiliation><inist:fA14 i1="02"><s1>Regional TB Program, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>School of Public Health and Health Services, George Washington University</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Armengol, R" uniqKey="Armengol R">R. Armengol</name><affiliation><inist:fA14 i1="06"><s1>Tuberculosis Control and Prevention, International Union Against Tuberculosis and Lung Disease</s1><s2>Paris</s2><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lopez Olarte, R A" uniqKey="Lopez Olarte R">R. A. Lopez Olarte</name><affiliation><inist:fA14 i1="02"><s1>Regional TB Program, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rodriguez, R" uniqKey="Rodriguez R">R. Rodriguez</name><affiliation><inist:fA14 i1="07"><s1>TB Program, PAHO</s1><s2>Brasilia</s2><s3>BRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0335097</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0335097 INIST</idno><idno type="RBID">Pascal:09-0335097</idno><idno type="wicri:Area/Main/Corpus">001C66</idno></publicationStmt><seriesStmt><idno type="ISSN">1027-3719</idno><title level="j" type="abbreviated">Int. j. tuberc. lung dis.</title><title level="j" type="main">International journal of tuberculosis and lung disease</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>America</term><term>Development</term><term>Disease</term><term>Epidemiology</term><term>Pneumology</term><term>Respiratory disease</term><term>Sanitary program</term><term>Strategy</term><term>Tuberculosis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Tuberculose</term><term>Pathologie de l'appareil respiratoire</term><term>Epidémiologie</term><term>Amérique</term><term>Stratégie</term><term>Développement</term><term>Maladie</term><term>Programme sanitaire</term><term>Pneumologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">CONTEXTE: La tuberculose (TB), une maladie qui peut être prévenue et guérie, reste une menace majeure pour la santé publique dans les régions les plus pauvres des Amériques. Depuis 1993, la stratégie DOTS a été mise en œuvre pour lutter contre la TB dans la région, et depuis 2006 également la nouvelle stratégie Stop TB, qui insiste sur l'extension d'une stratégie DOTS de haute qualité. OBJECTIFS: Décrire l'épidémiologie de la TB dans la région des Amériques entre 1994 et 2005 afin d'analyser les progrès et les perspectives de lutte antituberculeuse en ce qui concerne la réalisation de l'Objectif 6 des MDG d'ici 2015. MÉTHODES: On a collationné dans les bases de données de l'Organisation mondiale de la Santé (OMS) entre 1994 et 2005 les taux d'incidence, de mortalité et de prévalence de la TB, ainsi que la couverture par DOTS et les taux de succès du traitement couvert par DOTS. R É S U LTATS: La couverture par DOTS et les taux de succès du traitement DOTS ont augmenté régulièrement entre 1994 et 2005. En 2005, 88% de la population a été couvert par DOTS et un taux de réussite de 80% a été observé à la fin de 2004. Les taux d'incidence, de prévalence et de mortalité de la TB ont également diminué de façon régulière entre 1994 et ce jour, mais ils varient en fonction des différents scénarios. CONCLUSIONS: A l'exception de quelques pays, une réduction ultérieure de l'incidence, de la prévalence et des décès de la TB est possible d'ici 2015. Une large mise en œuvre du DOTS doit être maintenue pour arriver aux cibles de l'OMS et atteindre les objectifs des MDG.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1027-3719</s0></fA01><fA03 i2="1"><s0>Int. j. tuberc. lung dis.</s0></fA03><fA05><s2>13</s2></fA05><fA06><s2>8</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Epidemiology of tuberculosis in the Americas: the Stop TB strategy and the Millennium Development Goals</s1></fA08><fA11 i1="01" i2="1"><s1>RAMON-PARDO (R.)</s1></fA11><fA11 i1="02" i2="1"><s1>DEL GRANADO (M.)</s1></fA11><fA11 i1="03" i2="1"><s1>GERGER (A.)</s1></fA11><fA11 i1="04" i2="1"><s1>CANELA SOLER (J.)</s1></fA11><fA11 i1="05" i2="1"><s1>MIR (M.)</s1></fA11><fA11 i1="06" i2="1"><s1>ARMENGOL (R.)</s1></fA11><fA11 i1="07" i2="1"><s1>LOPEZ OLARTE (R. A.)</s1></fA11><fA11 i1="08" i2="1"><s1>RODRIGUEZ (R.)</s1></fA11><fA14 i1="01"><s1>Communicable Diseases Project, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Regional TB Program, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Health Analysis Project, Pan American Health Organization (PAHO)</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Universidad de Barcelona</s1><s2>Barcelona</s2><s3>ESP</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>School of Public Health and Health Services, George Washington University</s1><s2>Washington, DC</s2><s3>USA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Tuberculosis Control and Prevention, International Union Against Tuberculosis and Lung Disease</s1><s2>Paris</s2><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>TB Program, PAHO</s1><s2>Brasilia</s2><s3>BRA</s3><sZ>8 aut.</sZ></fA14><fA20><s1>969-975</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA24 i1="02"><s0>spa</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>26450</s2><s5>354000170839740080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>27 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0335097</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of tuberculosis and lung disease</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>CONTEXTE: La tuberculose (TB), une maladie qui peut être prévenue et guérie, reste une menace majeure pour la santé publique dans les régions les plus pauvres des Amériques. Depuis 1993, la stratégie DOTS a été mise en œuvre pour lutter contre la TB dans la région, et depuis 2006 également la nouvelle stratégie Stop TB, qui insiste sur l'extension d'une stratégie DOTS de haute qualité. OBJECTIFS: Décrire l'épidémiologie de la TB dans la région des Amériques entre 1994 et 2005 afin d'analyser les progrès et les perspectives de lutte antituberculeuse en ce qui concerne la réalisation de l'Objectif 6 des MDG d'ici 2015. MÉTHODES: On a collationné dans les bases de données de l'Organisation mondiale de la Santé (OMS) entre 1994 et 2005 les taux d'incidence, de mortalité et de prévalence de la TB, ainsi que la couverture par DOTS et les taux de succès du traitement couvert par DOTS. R É S U LTATS: La couverture par DOTS et les taux de succès du traitement DOTS ont augmenté régulièrement entre 1994 et 2005. En 2005, 88% de la population a été couvert par DOTS et un taux de réussite de 80% a été observé à la fin de 2004. Les taux d'incidence, de prévalence et de mortalité de la TB ont également diminué de façon régulière entre 1994 et ce jour, mais ils varient en fonction des différents scénarios. CONCLUSIONS: A l'exception de quelques pays, une réduction ultérieure de l'incidence, de la prévalence et des décès de la TB est possible d'ici 2015. Une large mise en œuvre du DOTS doit être maintenue pour arriver aux cibles de l'OMS et atteindre les objectifs des MDG.</s0></fC01><fC02 i1="01" i2="X"><s0>002B11D</s0></fC02><fC02 i1="02" i2="X"><s0>002B05B02O</s0></fC02><fC02 i1="03" i2="X"><s0>002B30A01C</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Tuberculose</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Epidémiologie</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Epidemiology</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Epidemiología</s0><s5>09</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>America</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>America</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Stratégie</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Strategy</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Estrategia</s0><s5>11</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Développement</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Development</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Desarrollo</s0><s5>12</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Maladie</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Disease</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Enfermedad</s0><s5>13</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Programme sanitaire</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Sanitary program</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Programa sanitario</s0><s5>14</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Pneumologie</s0><s5>15</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Pneumology</s0><s5>15</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Neumología</s0><s5>15</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Mycobactériose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Mycobacterial infection</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Micobacteriosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Infección</s0></fC07><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0335097 INIST</NO><ET>Epidemiology of tuberculosis in the Americas: the Stop TB strategy and the Millennium Development Goals</ET><AU>RAMON-PARDO (R.); DEL GRANADO (M.); GERGER (A.); CANELA SOLER (J.); MIR (M.); ARMENGOL (R.); LOPEZ OLARTE (R. A.); RODRIGUEZ (R.)</AU><AF>Communicable Diseases Project, Pan American Health Organization (PAHO)/Washington, DC/Etats-Unis (1 aut.); Regional TB Program, Pan American Health Organization (PAHO)/Washington, DC/Etats-Unis (2 aut., 5 aut., 7 aut.); Health Analysis Project, Pan American Health Organization (PAHO)/Washington, DC/Etats-Unis (3 aut., 4 aut.); Universidad de Barcelona/Barcelona/Espagne (4 aut.); School of Public Health and Health Services, George Washington University/Washington, DC/Etats-Unis (5 aut.); Tuberculosis Control and Prevention, International Union Against Tuberculosis and Lung Disease/Paris/France (6 aut.); TB Program, PAHO/Brasilia/Brésil (8 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of tuberculosis and lung disease; ISSN 1027-3719; France; Da. 2009; Vol. 13; No. 8; Pp. 969-975; Abs. français/espagnol; Bibl. 27 ref.</SO><LA>Anglais</LA><FA>CONTEXTE: La tuberculose (TB), une maladie qui peut être prévenue et guérie, reste une menace majeure pour la santé publique dans les régions les plus pauvres des Amériques. Depuis 1993, la stratégie DOTS a été mise en œuvre pour lutter contre la TB dans la région, et depuis 2006 également la nouvelle stratégie Stop TB, qui insiste sur l'extension d'une stratégie DOTS de haute qualité. OBJECTIFS: Décrire l'épidémiologie de la TB dans la région des Amériques entre 1994 et 2005 afin d'analyser les progrès et les perspectives de lutte antituberculeuse en ce qui concerne la réalisation de l'Objectif 6 des MDG d'ici 2015. MÉTHODES: On a collationné dans les bases de données de l'Organisation mondiale de la Santé (OMS) entre 1994 et 2005 les taux d'incidence, de mortalité et de prévalence de la TB, ainsi que la couverture par DOTS et les taux de succès du traitement couvert par DOTS. R É S U LTATS: La couverture par DOTS et les taux de succès du traitement DOTS ont augmenté régulièrement entre 1994 et 2005. En 2005, 88% de la population a été couvert par DOTS et un taux de réussite de 80% a été observé à la fin de 2004. Les taux d'incidence, de prévalence et de mortalité de la TB ont également diminué de façon régulière entre 1994 et ce jour, mais ils varient en fonction des différents scénarios. CONCLUSIONS: A l'exception de quelques pays, une réduction ultérieure de l'incidence, de la prévalence et des décès de la TB est possible d'ici 2015. Une large mise en œuvre du DOTS doit être maintenue pour arriver aux cibles de l'OMS et atteindre les objectifs des MDG.</FA><CC>002B11D; 002B05B02O; 002B30A01C</CC><FD>Tuberculose; Pathologie de l'appareil respiratoire; Epidémiologie; Amérique; Stratégie; Développement; Maladie; Programme sanitaire; Pneumologie</FD><FG>Mycobactériose; Bactériose; Infection</FG><ED>Tuberculosis; Respiratory disease; Epidemiology; America; Strategy; Development; Disease; Sanitary program; Pneumology</ED><EG>Mycobacterial infection; Bacteriosis; Infection</EG><SD>Tuberculosis; Aparato respiratorio patología; Epidemiología; America; Estrategia; Desarrollo; Enfermedad; Programa sanitario; Neumología</SD><LO>INIST-26450.354000170839740080</LO><ID>09-0335097</ID></server></inist></record>
000D16	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">Les Cervidae (Mammalia, Artiodactyla) du Pléistocène supérieur-Holocène ancien de la région du Parc National Serra da Capivara (Piauf, Brésil)</title><author><name sortKey="Guerin, Claude" uniqKey="Guerin C">Claude Guerin</name><affiliation><inist:fA14 i1="01"><s1>UFR des sciences de la Terre, UMR-CNRS 5125 « paléoenvironnements et pciléobiosphere », université Claude-Bernard Lyon-1, campus de la Doua, bâtiment Géode, 43, boulevard du 11-Novembre</s1><s2>69622 Villeurbanne</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Fundação Museu do Homem Americano, Sào Raimundo Nonato</s1><s2>Piauí</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Faure, Martine" uniqKey="Faure M">Martine Faure</name><affiliation><inist:fA14 i1="01"><s1>UFR des sciences de la Terre, UMR-CNRS 5125 « paléoenvironnements et pciléobiosphere », université Claude-Bernard Lyon-1, campus de la Doua, bâtiment Géode, 43, boulevard du 11-Novembre</s1><s2>69622 Villeurbanne</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Fundação Museu do Homem Americano, Sào Raimundo Nonato</s1><s2>Piauí</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Université Lumière Lyon 1, 7, rue Raulin</s1><s2>69007 Lyon</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0335351</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0335351 INIST</idno><idno type="RBID">Pascal:09-0335351</idno><idno type="wicri:Area/Main/Corpus">001C65</idno></publicationStmt><seriesStmt><idno type="ISSN">0016-6995</idno><title level="j" type="abbreviated">Geobios : (Lyon)</title><title level="j" type="main">Geobios : (Lyon)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Cervidae</term><term>Piaui Brazil</term><term>biometry</term><term>biostratigraphy</term><term>bones</term><term>jaws</term><term>lower Holocene</term><term>national parks</term><term>teeth</term><term>upper Pleistocene</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cervidae</term><term>Pléistocène sup</term><term>Holocène inf</term><term>Parc national</term><term>Dent</term><term>Ossement</term><term>Biométrie</term><term>Biostratigraphie</term><term>Mâchoire</term><term>Brésil</term><term>Piaui</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The Upper Pleistocene/Lower Holocene fossil-bearing sites of the Serra da Capivara National Park Region have yielded three cervid species: Mazama gouazoubira, M. americana and Blastocerus dichotomus, all currently living in South America, the two first in the region. A grand total of more than one hundred remains demonstrates the presence of Mazama gouazoubira in seven sites, mainly the Toca das Moendas, the Toca do Serrote do Artur, the Toca da Cima dos Pilão. This small species shows, since the Upper Pleistocene, a conspicuous tendency to reduce the average dimensions of its teeth and long bones. From the taller M. americana, only a dozen of remains were found in four sites, mainly the Sitio do Meio. In ail of these it is sympatric with M. gouazoubira. It differs from this last one by its cheek teeth and its limb bones size and proportions. The oldest site  where the species is known is Tarija (Bolivia, Middle Pleistocene) and it does not show any significant changes in size and proportions between recent and fossil samples. Sixteen remains of the large B. dichotomus were found in five sites, mainly the Toca das Moendas and the Toca da Barra do Antonião. The species is a rare fossil, but is frequently figured in the rock art painting of the region, where it is presently unknown.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0016-6995</s0></fA01><fA03 i2="1"><s0>Geobios : (Lyon)</s0></fA03><fA05><s2>42</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="FRE"><s1>Les Cervidae (Mammalia, Artiodactyla) du Pléistocène supérieur-Holocène ancien de la région du Parc National Serra da Capivara (Piauf, Brésil)</s1></fA08><fA11 i1="01" i2="1"><s1>GUERIN (Claude)</s1></fA11><fA11 i1="02" i2="1"><s1>FAURE (Martine)</s1></fA11><fA14 i1="01"><s1>UFR des sciences de la Terre, UMR-CNRS 5125 « paléoenvironnements et pciléobiosphere », université Claude-Bernard Lyon-1, campus de la Doua, bâtiment Géode, 43, boulevard du 11-Novembre</s1><s2>69622 Villeurbanne</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Fundação Museu do Homem Americano, Sào Raimundo Nonato</s1><s2>Piauí</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Université Lumière Lyon 1, 7, rue Raulin</s1><s2>69007 Lyon</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>169-195</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>14199</s2><s5>354000187058640030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.3/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0335351</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Geobios : (Lyon)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA68 i1="01" i2="1" l="ENG"><s1>The Cervidae (Mammalia, Artiodactyla) of the Upper Pleistocene/Lower Holocene deposits of the Serra da Capivara National Park Region (Piauì, Brazil)</s1></fA68><fC01 i1="01" l="ENG"><s0>The Upper Pleistocene/Lower Holocene fossil-bearing sites of the Serra da Capivara National Park Region have yielded three cervid species: Mazama gouazoubira, M. americana and Blastocerus dichotomus, all currently living in South America, the two first in the region. A grand total of more than one hundred remains demonstrates the presence of Mazama gouazoubira in seven sites, mainly the Toca das Moendas, the Toca do Serrote do Artur, the Toca da Cima dos Pilão. This small species shows, since the Upper Pleistocene, a conspicuous tendency to reduce the average dimensions of its teeth and long bones. From the taller M. americana, only a dozen of remains were found in four sites, mainly the Sitio do Meio. In ail of these it is sympatric with M. gouazoubira. It differs from this last one by its cheek teeth and its limb bones size and proportions. The oldest site  where the species is known is Tarija (Bolivia, Middle Pleistocene) and it does not show any significant changes in size and proportions between recent and fossil samples. Sixteen remains of the large B. dichotomus were found in five sites, mainly the Toca das Moendas and the Toca da Barra do Antonião. The species is a rare fossil, but is frequently figured in the rock art painting of the region, where it is presently unknown.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01Q04</s0></fC02><fC02 i1="02" i2="2"><s0>001E01P02</s0></fC02><fC02 i1="03" i2="2"><s0>227A04</s0></fC02><fC02 i1="04" i2="2"><s0>226C02</s0></fC02><fC03 i1="01" i2="2" l="FRE"><s0>Cervidae</s0><s2>NY</s2><s5>01</s5></fC03><fC03 i1="01" i2="2" l="ENG"><s0>Cervidae</s0><s2>NY</s2><s5>01</s5></fC03><fC03 i1="01" i2="2" l="SPA"><s0>Cervidae</s0><s2>NY</s2><s5>01</s5></fC03><fC03 i1="02" i2="2" l="FRE"><s0>Pléistocène sup</s0><s2>NX</s2><s5>04</s5></fC03><fC03 i1="02" i2="2" l="ENG"><s0>upper Pleistocene</s0><s2>NX</s2><s5>04</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Holocène inf</s0><s2>NX</s2><s5>05</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>lower Holocene</s0><s2>NX</s2><s5>05</s5></fC03><fC03 i1="03" i2="2" l="SPA"><s0>Holoceno inf</s0><s2>NX</s2><s5>05</s5></fC03><fC03 i1="04" i2="2" l="FRE"><s0>Parc national</s0><s5>06</s5></fC03><fC03 i1="04" i2="2" l="ENG"><s0>national parks</s0><s5>06</s5></fC03><fC03 i1="05" i2="2" l="FRE"><s0>Dent</s0><s5>08</s5></fC03><fC03 i1="05" i2="2" l="ENG"><s0>teeth</s0><s5>08</s5></fC03><fC03 i1="05" i2="2" l="SPA"><s0>Diente</s0><s5>08</s5></fC03><fC03 i1="06" i2="2" l="FRE"><s0>Ossement</s0><s5>09</s5></fC03><fC03 i1="06" i2="2" l="ENG"><s0>bones</s0><s5>09</s5></fC03><fC03 i1="06" i2="2" l="SPA"><s0>Osamenta</s0><s5>09</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Biométrie</s0><s5>11</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>biometry</s0><s5>11</s5></fC03><fC03 i1="07" i2="2" l="SPA"><s0>Biometría</s0><s5>11</s5></fC03><fC03 i1="08" i2="2" l="FRE"><s0>Biostratigraphie</s0><s5>12</s5></fC03><fC03 i1="08" i2="2" l="ENG"><s0>biostratigraphy</s0><s5>12</s5></fC03><fC03 i1="08" i2="2" l="SPA"><s0>Bioestratigrafía</s0><s5>12</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Mâchoire</s0><s5>13</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>jaws</s0><s5>13</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Maxilar</s0><s5>13</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Piaui</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>Piaui Brazil</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Piaui</s0><s2>NG</s2><s5>62</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Ruminantia</s0><s2>NY</s2></fC07><fC07 i1="01" i2="2" l="ENG"><s0>Ruminantia</s0><s2>NY</s2></fC07><fC07 i1="02" i2="2" l="FRE"><s0>Artiodactyla</s0><s2>NY</s2></fC07><fC07 i1="02" i2="2" l="ENG"><s0>Artiodactyla</s0><s2>NY</s2></fC07><fC07 i1="02" i2="2" l="SPA"><s0>Artiodactyla</s0><s2>NY</s2></fC07><fC07 i1="03" i2="2" l="FRE"><s0>Eutheria</s0><s2>NY</s2></fC07><fC07 i1="03" i2="2" l="ENG"><s0>Eutheria</s0><s2>NY</s2></fC07><fC07 i1="04" i2="2" l="FRE"><s0>Theria</s0><s2>NY</s2></fC07><fC07 i1="04" i2="2" l="ENG"><s0>Theria</s0><s2>NY</s2></fC07><fC07 i1="05" i2="2" l="FRE"><s0>Mammalia</s0><s2>NY</s2></fC07><fC07 i1="05" i2="2" l="ENG"><s0>Mammalia</s0><s2>NY</s2></fC07><fC07 i1="05" i2="2" l="SPA"><s0>Mammalia</s0><s2>NY</s2></fC07><fC07 i1="06" i2="2" l="FRE"><s0>Tetrapoda</s0><s2>NY</s2></fC07><fC07 i1="06" i2="2" l="ENG"><s0>Tetrapoda</s0><s2>NY</s2></fC07><fC07 i1="06" i2="2" l="SPA"><s0>Tetrapoda</s0><s2>NY</s2></fC07><fC07 i1="07" i2="2" l="FRE"><s0>Vertebrata</s0><s2>NY</s2></fC07><fC07 i1="07" i2="2" l="ENG"><s0>Vertebrata</s0><s2>NY</s2></fC07><fC07 i1="07" i2="2" l="SPA"><s0>Vertebrata</s0><s2>NY</s2></fC07><fC07 i1="08" i2="2" l="FRE"><s0>Chordata</s0></fC07><fC07 i1="08" i2="2" l="ENG"><s0>Chordata</s0></fC07><fC07 i1="08" i2="2" l="SPA"><s0>Chordata</s0></fC07><fC07 i1="09" i2="2" l="FRE"><s0>Pléistocène</s0><s2>NX</s2></fC07><fC07 i1="09" i2="2" l="ENG"><s0>Pleistocene</s0><s2>NX</s2></fC07><fC07 i1="10" i2="2" l="FRE"><s0>Quaternaire</s0><s2>NX</s2></fC07><fC07 i1="10" i2="2" l="ENG"><s0>Quaternary</s0><s2>NX</s2></fC07><fC07 i1="10" i2="2" l="SPA"><s0>Cuaternario</s0><s2>NX</s2></fC07><fC07 i1="11" i2="2" l="FRE"><s0>Cénozoïque</s0><s2>NX</s2></fC07><fC07 i1="11" i2="2" l="ENG"><s0>Cenozoic</s0><s2>NX</s2></fC07><fC07 i1="11" i2="2" l="SPA"><s0>Cenozoico</s0><s2>NX</s2></fC07><fC07 i1="12" i2="2" l="FRE"><s0>Phanérozoïque</s0><s2>NX</s2></fC07><fC07 i1="12" i2="2" l="ENG"><s0>Phanerozoic</s0><s2>NX</s2></fC07><fC07 i1="12" i2="2" l="SPA"><s0>Fanerozoico</s0><s2>NX</s2></fC07><fC07 i1="13" i2="2" l="FRE"><s0>Holocène</s0><s2>NX</s2></fC07><fC07 i1="13" i2="2" l="ENG"><s0>Holocene</s0><s2>NX</s2></fC07><fC07 i1="13" i2="2" l="SPA"><s0>Holoceno</s0><s2>NX</s2></fC07><fC07 i1="14" i2="2" l="FRE"><s0>Quaternaire sup</s0><s2>NX</s2></fC07><fC07 i1="14" i2="2" l="ENG"><s0>upper Quaternary</s0><s2>NX</s2></fC07><fC07 i1="14" i2="2" l="SPA"><s0>Cuaternario sup</s0><s2>NX</s2></fC07><fC07 i1="15" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="15" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="15" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fN21><s1>243</s1></fN21></pA></standard><server><NO>PASCAL 09-0335351 INIST</NO><FT>Les Cervidae (Mammalia, Artiodactyla) du Pléistocène supérieur-Holocène ancien de la région du Parc National Serra da Capivara (Piauf, Brésil)</FT><ET>(The Cervidae (Mammalia, Artiodactyla) of the Upper Pleistocene/Lower Holocene deposits of the Serra da Capivara National Park Region (Piauì, Brazil))</ET><AU>GUERIN (Claude); FAURE (Martine)</AU><AF>UFR des sciences de la Terre, UMR-CNRS 5125 « paléoenvironnements et pciléobiosphere », université Claude-Bernard Lyon-1, campus de la Doua, bâtiment Géode, 43, boulevard du 11-Novembre/69622 Villeurbanne/France (1 aut., 2 aut.); Fundação Museu do Homem Americano, Sào Raimundo Nonato/Piauí/Brésil (1 aut., 2 aut.); Université Lumière Lyon 1, 7, rue Raulin/69007 Lyon/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Geobios : (Lyon); ISSN 0016-6995; France; Da. 2009; Vol. 42; No. 2; Pp. 169-195; Abs. anglais; Bibl. 1 p.3/4</SO><LA>Français</LA><EA>The Upper Pleistocene/Lower Holocene fossil-bearing sites of the Serra da Capivara National Park Region have yielded three cervid species: Mazama gouazoubira, M. americana and Blastocerus dichotomus, all currently living in South America, the two first in the region. A grand total of more than one hundred remains demonstrates the presence of Mazama gouazoubira in seven sites, mainly the Toca das Moendas, the Toca do Serrote do Artur, the Toca da Cima dos Pilão. This small species shows, since the Upper Pleistocene, a conspicuous tendency to reduce the average dimensions of its teeth and long bones. From the taller M. americana, only a dozen of remains were found in four sites, mainly the Sitio do Meio. In ail of these it is sympatric with M. gouazoubira. It differs from this last one by its cheek teeth and its limb bones size and proportions. The oldest site  where the species is known is Tarija (Bolivia, Middle Pleistocene) and it does not show any significant changes in size and proportions between recent and fossil samples. Sixteen remains of the large B. dichotomus were found in five sites, mainly the Toca das Moendas and the Toca da Barra do Antonião. The species is a rare fossil, but is frequently figured in the rock art painting of the region, where it is presently unknown.</EA><CC>001E01Q04; 001E01P02; 227A04; 226C02</CC><FD>Cervidae; Pléistocène sup; Holocène inf; Parc national; Dent; Ossement; Biométrie; Biostratigraphie; Mâchoire; Brésil; Piaui</FD><FG>Ruminantia; Artiodactyla; Eutheria; Theria; Mammalia; Tetrapoda; Vertebrata; Chordata; Pléistocène; Quaternaire; Cénozoïque; Phanérozoïque; Holocène; Quaternaire sup; Amérique du Sud</FG><ED>Cervidae; upper Pleistocene; lower Holocene; national parks; teeth; bones; biometry; biostratigraphy; jaws; Brazil; Piaui Brazil</ED><EG>Ruminantia; Artiodactyla; Eutheria; Theria; Mammalia; Tetrapoda; Vertebrata; Chordata; Pleistocene; Quaternary; Cenozoic; Phanerozoic; Holocene; upper Quaternary; South America</EG><SD>Cervidae; Holoceno inf; Diente; Osamenta; Biometría; Bioestratigrafía; Maxilar; Brasil; Piaui</SD><LO>INIST-14199.354000187058640030</LO><ID>09-0335351</ID></server></inist></record>
000D17	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Mutational Analysis of CLC-5, Cofilin and CLC-4 in Patients with Dent's Disease</title><author><name>FIONA WU</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Reed, Anita A C" uniqKey="Reed A">Anita A. C. Reed</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Williams, Sian E" uniqKey="Williams S">Sian E. Williams</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Loh, Nellie Y" uniqKey="Loh N">Nellie Y. Loh</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lippiat, Jonathan D" uniqKey="Lippiat J">Jonathan D. Lippiat</name><affiliation><inist:fA14 i1="02"><s1>Department of Physiology, University of Oxford</s1><s2>Oxford</s2><s3>GBR</s3><sZ>5 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Institute of Membrane and Systems Biology, Faculty of Biological Sciences, University of Leeds</s1><s2>Leeds</s2><s3>GBR</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Christie, Paul T" uniqKey="Christie P">Paul T. Christie</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Large, Oliver" uniqKey="Large O">Oliver Large</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bettinelli, Alberto" uniqKey="Bettinelli A">Alberto Bettinelli</name><affiliation><inist:fA14 i1="06"><s1>Unité Operative Pediatria, Ospidale Mandic</s1><s2>Merate</s2><s3>ITA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dillon, Michael J" uniqKey="Dillon M">Michael J. Dillon</name><affiliation><inist:fA14 i1="04"><s1>Department of Nephrology, Great Ormond St Hospital for Children</s1><s2>London</s2><s3>GBR</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Goldraich, Noemia P" uniqKey="Goldraich N">Noemia P. Goldraich</name><affiliation><inist:fA14 i1="07"><s1>Pediatric Nephrology Unit, Hospital de Clinicas de Porto Alegre, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hoppe, Bernd" uniqKey="Hoppe B">Bernd Hoppe</name><affiliation><inist:fA14 i1="08"><s1>Division of Pediatric Nephrology, Department of Pediatrics, University Hospital Cologne</s1><s2>Cologne</s2><s3>DEU</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lhotta, Karl" uniqKey="Lhotta K">Karl Lhotta</name><affiliation><inist:fA14 i1="09"><s1>Academic Teaching Hospital Feldkirch</s1><s2>Feldkirch</s2><s3>AUT</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Loirat, Chantal" uniqKey="Loirat C">Chantal Loirat</name><affiliation><inist:fA14 i1="11"><s1>Department of Pediatric Nephrology, Hospital Robert Debre</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Malik, Rayaz" uniqKey="Malik R">Rayaz Malik</name><affiliation><inist:fA14 i1="05"><s1>Academic Department of Medicine, Manchester Royal Infirmary</s1><s2>Manchester</s2><s3>GBR</s3><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Morel, Delphine" uniqKey="Morel D">Delphine Morel</name><affiliation><inist:fA14 i1="12"><s1>Department of Nephrology, Groupe Hospitalier Pellegrin</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kotanko, Peter" uniqKey="Kotanko P">Peter Kotanko</name><affiliation><inist:fA14 i1="10"><s1>Department of Clinical Medicine, Krankenhaus der Barmherzigen Brüder</s1><s2>Graz</s2><s3>AUT</s3><sZ>16 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Roussel, Bernard" uniqKey="Roussel B">Bernard Roussel</name><affiliation><inist:fA14 i1="13"><s1>Nephrologie Pediatrique, American Memorial Hospital, Centre Hospitalier Universitaire Reims</s1><s2>Reims</s2><s3>FRA</s3><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rubinger, Dvora" uniqKey="Rubinger D">Dvora Rubinger</name><affiliation><inist:fA14 i1="14"><s1>Nephrology Department, Hadassah-Hebrew University Medical Centre, Ein-Kerem Campus</s1><s2>Jerusalem</s2><s3>ISR</s3><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schrander Stumpel, Connie" uniqKey="Schrander Stumpel C">Connie Schrander-Stumpel</name><affiliation><inist:fA14 i1="15"><s1>Department of Clinical Genetics, University Hospital Maastricht and Research Institute for Growth and Development, University of Maastricht</s1><s2>Maastricht</s2><s3>NLD</s3><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Serdaroglu, Erkin" uniqKey="Serdaroglu E">Erkin Serdaroglu</name><affiliation><inist:fA14 i1="16"><s1>Department of Pediatric Nephrology, Ege University Medical School</s1><s2>Izmir</s2><s3>TUR</s3><sZ>20 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nesbit, M Andrew" uniqKey="Nesbit M">M. Andrew Nesbit</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ashcroft, Frances" uniqKey="Ashcroft F">Frances Ashcroft</name><affiliation><inist:fA14 i1="02"><s1>Department of Physiology, University of Oxford</s1><s2>Oxford</s2><s3>GBR</s3><sZ>5 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Thakker, Rajesh V" uniqKey="Thakker R">Rajesh V. Thakker</name><affiliation><inist:fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0337198</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0337198 INIST</idno><idno type="RBID">Pascal:09-0337198</idno><idno type="wicri:Area/Main/Corpus">001C64</idno></publicationStmt><seriesStmt><idno type="ISSN">1660-8151</idno><title level="j" type="abbreviated">Nephron j.</title><title level="j" type="main">The Nephron journals</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cofilin</term><term>Dent disease</term><term>Genetics</term><term>Human</term><term>Mutation</term><term>Nephrology</term><term>OCRL1 gene</term><term>Urology</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Mutation</term><term>Génétique</term><term>Homme</term><term>Néphrologie</term><term>Urologie</term><term>Cofiline</term><term>Maladie de Dent</term><term>Gène OCRL1</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background/Aims: Dent's disease is caused by mutations in the chloride/proton antiporter, CLC-5, or oculo-cerebro-renal-syndrome-of-Lowe (OCRL1) genes. Methods: Eighteen probands with Dent's disease were investigated for mutations in CLC-5 and two of its interacting proteins, CLC-4 and cofilin. Wild-type and mutant CLC-5s were assessed in kidney cells. Urinary calcium excretion following an oral calcium challenge was studied in one family. Results: Seven different CLC-5 mutations consisting of two nonsense mutations (Arg347Stop and Arg718Stop), two missense mutations (Ser244Leu and Arg516Trp), one intron 3 donor splice site mutation, one deletion-insertion (nt930delTCinsA) and an in-frame deletion (523delVal) were identified in 8 patients. In the remaining 10 patients, DNA sequence abnormalities were not detected in the coding regions of CLC-4 or cofilin, and were independently excluded for OCRL1. Patients with CLC-5 mutations were phenotypically similar to those without. The donor splice site CLC-5 mutation resulted in exon 3 skipping. Electrophysiology demonstrated that the 523delVal CLC-5 mutation abolished CLC-5-mediated chloride conductance. Sixty percent of women with the CLC-5 deletion-insertion had nephrolithiasis, although calcium excretion before and after oral calcium challenge was similar to that in unaffected females. Conclusions: Three novel CLC-5 mutations were identified, and mutations in OCRL1, CLC-4 and cofilin excluded in causing Dent's disease in this patient cohort.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1660-8151</s0></fA01><fA03 i2="1"><s0>Nephron j.</s0></fA03><fA05><s2>112</s2></fA05><fA06><s2>4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Mutational Analysis of CLC-5, Cofilin and CLC-4 in Patients with Dent's Disease</s1></fA08><fA11 i1="01" i2="1"><s1>FIONA WU</s1></fA11><fA11 i1="02" i2="1"><s1>REED (Anita A. C.)</s1></fA11><fA11 i1="03" i2="1"><s1>WILLIAMS (Sian E.)</s1></fA11><fA11 i1="04" i2="1"><s1>LOH (Nellie Y.)</s1></fA11><fA11 i1="05" i2="1"><s1>LIPPIAT (Jonathan D.)</s1></fA11><fA11 i1="06" i2="1"><s1>CHRISTIE (Paul T.)</s1></fA11><fA11 i1="07" i2="1"><s1>LARGE (Oliver)</s1></fA11><fA11 i1="08" i2="1"><s1>BETTINELLI (Alberto)</s1></fA11><fA11 i1="09" i2="1"><s1>DILLON (Michael J.)</s1></fA11><fA11 i1="10" i2="1"><s1>GOLDRAICH (Noemia P.)</s1></fA11><fA11 i1="11" i2="1"><s1>HOPPE (Bernd)</s1></fA11><fA11 i1="12" i2="1"><s1>LHOTTA (Karl)</s1></fA11><fA11 i1="13" i2="1"><s1>LOIRAT (Chantal)</s1></fA11><fA11 i1="14" i2="1"><s1>MALIK (Rayaz)</s1></fA11><fA11 i1="15" i2="1"><s1>MOREL (Delphine)</s1></fA11><fA11 i1="16" i2="1"><s1>KOTANKO (Peter)</s1></fA11><fA11 i1="17" i2="1"><s1>ROUSSEL (Bernard)</s1></fA11><fA11 i1="18" i2="1"><s1>RUBINGER (Dvora)</s1></fA11><fA11 i1="19" i2="1"><s1>SCHRANDER-STUMPEL (Connie)</s1></fA11><fA11 i1="20" i2="1"><s1>SERDAROGLU (Erkin)</s1></fA11><fA11 i1="21" i2="1"><s1>NESBIT (M. Andrew)</s1></fA11><fA11 i1="22" i2="1"><s1>ASHCROFT (Frances)</s1></fA11><fA11 i1="23" i2="1"><s1>THAKKER (Rajesh V.)</s1></fA11><fA14 i1="01"><s1>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism</s1><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>21 aut.</sZ><sZ>23 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Physiology, University of Oxford</s1><s2>Oxford</s2><s3>GBR</s3><sZ>5 aut.</sZ><sZ>22 aut.</sZ></fA14><fA14 i1="03"><s1>Institute of Membrane and Systems Biology, Faculty of Biological Sciences, University of Leeds</s1><s2>Leeds</s2><s3>GBR</s3><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Department of Nephrology, Great Ormond St Hospital for Children</s1><s2>London</s2><s3>GBR</s3><sZ>9 aut.</sZ></fA14><fA14 i1="05"><s1>Academic Department of Medicine, Manchester Royal Infirmary</s1><s2>Manchester</s2><s3>GBR</s3><sZ>14 aut.</sZ></fA14><fA14 i1="06"><s1>Unité Operative Pediatria, Ospidale Mandic</s1><s2>Merate</s2><s3>ITA</s3><sZ>8 aut.</sZ></fA14><fA14 i1="07"><s1>Pediatric Nephrology Unit, Hospital de Clinicas de Porto Alegre, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>10 aut.</sZ></fA14><fA14 i1="08"><s1>Division of Pediatric Nephrology, Department of Pediatrics, University Hospital Cologne</s1><s2>Cologne</s2><s3>DEU</s3><sZ>11 aut.</sZ></fA14><fA14 i1="09"><s1>Academic Teaching Hospital Feldkirch</s1><s2>Feldkirch</s2><s3>AUT</s3><sZ>12 aut.</sZ></fA14><fA14 i1="10"><s1>Department of Clinical Medicine, Krankenhaus der Barmherzigen Brüder</s1><s2>Graz</s2><s3>AUT</s3><sZ>16 aut.</sZ></fA14><fA14 i1="11"><s1>Department of Pediatric Nephrology, Hospital Robert Debre</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ></fA14><fA14 i1="12"><s1>Department of Nephrology, Groupe Hospitalier Pellegrin</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>15 aut.</sZ></fA14><fA14 i1="13"><s1>Nephrologie Pediatrique, American Memorial Hospital, Centre Hospitalier Universitaire Reims</s1><s2>Reims</s2><s3>FRA</s3><sZ>17 aut.</sZ></fA14><fA14 i1="14"><s1>Nephrology Department, Hadassah-Hebrew University Medical Centre, Ein-Kerem Campus</s1><s2>Jerusalem</s2><s3>ISR</s3><sZ>18 aut.</sZ></fA14><fA14 i1="15"><s1>Department of Clinical Genetics, University Hospital Maastricht and Research Institute for Growth and Development, University of Maastricht</s1><s2>Maastricht</s2><s3>NLD</s3><sZ>19 aut.</sZ></fA14><fA14 i1="16"><s1>Department of Pediatric Nephrology, Ege University Medical School</s1><s2>Izmir</s2><s3>TUR</s3><sZ>20 aut.</sZ></fA14><fA20><s2>p53-p62</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>11890</s2><s5>354000172498720120</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>42 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0337198</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>The Nephron journals</s0></fA64><fA66 i1="01"><s0>CHE</s0></fA66><fC01 i1="01" l="ENG"><s0>Background/Aims: Dent's disease is caused by mutations in the chloride/proton antiporter, CLC-5, or oculo-cerebro-renal-syndrome-of-Lowe (OCRL1) genes. Methods: Eighteen probands with Dent's disease were investigated for mutations in CLC-5 and two of its interacting proteins, CLC-4 and cofilin. Wild-type and mutant CLC-5s were assessed in kidney cells. Urinary calcium excretion following an oral calcium challenge was studied in one family. Results: Seven different CLC-5 mutations consisting of two nonsense mutations (Arg347Stop and Arg718Stop), two missense mutations (Ser244Leu and Arg516Trp), one intron 3 donor splice site mutation, one deletion-insertion (nt930delTCinsA) and an in-frame deletion (523delVal) were identified in 8 patients. In the remaining 10 patients, DNA sequence abnormalities were not detected in the coding regions of CLC-4 or cofilin, and were independently excluded for OCRL1. Patients with CLC-5 mutations were phenotypically similar to those without. The donor splice site CLC-5 mutation resulted in exon 3 skipping. Electrophysiology demonstrated that the 523delVal CLC-5 mutation abolished CLC-5-mediated chloride conductance. Sixty percent of women with the CLC-5 deletion-insertion had nephrolithiasis, although calcium excretion before and after oral calcium challenge was similar to that in unaffected females. Conclusions: Three novel CLC-5 mutations were identified, and mutations in OCRL1, CLC-4 and cofilin excluded in causing Dent's disease in this patient cohort.</s0></fC01><fC02 i1="01" i2="X"><s0>002B14</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Mutation</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Mutation</s0><s5>02</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Mutación</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Génétique</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Genetics</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Genética</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Homme</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Human</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Hombre</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Néphrologie</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Nephrology</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Nefrología</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Urologie</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Urology</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Urología</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Cofiline</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Cofilin</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Maladie de Dent</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Dent disease</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Enfermedad de Dent</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Gène OCRL1</s0><s4>CD</s4><s5>98</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>OCRL1 gene</s0><s4>CD</s4><s5>98</s5></fC03><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0337198 INIST</NO><ET>Mutational Analysis of CLC-5, Cofilin and CLC-4 in Patients with Dent's Disease</ET><AU>FIONA WU; REED (Anita A. C.); WILLIAMS (Sian E.); LOH (Nellie Y.); LIPPIAT (Jonathan D.); CHRISTIE (Paul T.); LARGE (Oliver); BETTINELLI (Alberto); DILLON (Michael J.); GOLDRAICH (Noemia P.); HOPPE (Bernd); LHOTTA (Karl); LOIRAT (Chantal); MALIK (Rayaz); MOREL (Delphine); KOTANKO (Peter); ROUSSEL (Bernard); RUBINGER (Dvora); SCHRANDER-STUMPEL (Connie); SERDAROGLU (Erkin); NESBIT (M. Andrew); ASHCROFT (Frances); THAKKER (Rajesh V.)</AU><AF>Nuffield Department of Clinical Medicine, Academic Endocrine Unit, University of Oxford, and Churchill Hospital, Oxford Centre for Diabetes, Endocrinology and Metabolism/Royaume-Uni (1 aut., 2 aut., 3 aut., 4 aut., 6 aut., 7 aut., 21 aut., 23 aut.); Department of Physiology, University of Oxford/Oxford/Royaume-Uni (5 aut., 22 aut.); Institute of Membrane and Systems Biology, Faculty of Biological Sciences, University of Leeds/Leeds/Royaume-Uni (5 aut.); Department of Nephrology, Great Ormond St Hospital for Children/London/Royaume-Uni (9 aut.); Academic Department of Medicine, Manchester Royal Infirmary/Manchester/Royaume-Uni (14 aut.); Unité Operative Pediatria, Ospidale Mandic/Merate/Italie (8 aut.); Pediatric Nephrology Unit, Hospital de Clinicas de Porto Alegre, Universidade Federal do Rio Grande do Sul/Porto Alegre/Brésil (10 aut.); Division of Pediatric Nephrology, Department of Pediatrics, University Hospital Cologne/Cologne/Allemagne (11 aut.); Academic Teaching Hospital Feldkirch/Feldkirch/Autriche (12 aut.); Department of Clinical Medicine, Krankenhaus der Barmherzigen Brüder/Graz/Autriche (16 aut.); Department of Pediatric Nephrology, Hospital Robert Debre/Paris/France (13 aut.); Department of Nephrology, Groupe Hospitalier Pellegrin/Bordeaux/France (15 aut.); Nephrologie Pediatrique, American Memorial Hospital, Centre Hospitalier Universitaire Reims/Reims/France (17 aut.); Nephrology Department, Hadassah-Hebrew University Medical Centre, Ein-Kerem Campus/Jerusalem/Israël (18 aut.); Department of Clinical Genetics, University Hospital Maastricht and Research Institute for Growth and Development, University of Maastricht/Maastricht/Pays-Bas (19 aut.); Department of Pediatric Nephrology, Ege University Medical School/Izmir/Turquie (20 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>The Nephron journals; ISSN 1660-8151; Suisse; Da. 2009; Vol. 112; No. 4; p53-p62; Bibl. 42 ref.</SO><LA>Anglais</LA><EA>Background/Aims: Dent's disease is caused by mutations in the chloride/proton antiporter, CLC-5, or oculo-cerebro-renal-syndrome-of-Lowe (OCRL1) genes. Methods: Eighteen probands with Dent's disease were investigated for mutations in CLC-5 and two of its interacting proteins, CLC-4 and cofilin. Wild-type and mutant CLC-5s were assessed in kidney cells. Urinary calcium excretion following an oral calcium challenge was studied in one family. Results: Seven different CLC-5 mutations consisting of two nonsense mutations (Arg347Stop and Arg718Stop), two missense mutations (Ser244Leu and Arg516Trp), one intron 3 donor splice site mutation, one deletion-insertion (nt930delTCinsA) and an in-frame deletion (523delVal) were identified in 8 patients. In the remaining 10 patients, DNA sequence abnormalities were not detected in the coding regions of CLC-4 or cofilin, and were independently excluded for OCRL1. Patients with CLC-5 mutations were phenotypically similar to those without. The donor splice site CLC-5 mutation resulted in exon 3 skipping. Electrophysiology demonstrated that the 523delVal CLC-5 mutation abolished CLC-5-mediated chloride conductance. Sixty percent of women with the CLC-5 deletion-insertion had nephrolithiasis, although calcium excretion before and after oral calcium challenge was similar to that in unaffected females. Conclusions: Three novel CLC-5 mutations were identified, and mutations in OCRL1, CLC-4 and cofilin excluded in causing Dent's disease in this patient cohort.</EA><CC>002B14</CC><FD>Mutation; Génétique; Homme; Néphrologie; Urologie; Cofiline; Maladie de Dent; Gène OCRL1</FD><ED>Mutation; Genetics; Human; Nephrology; Urology; Cofilin; Dent disease; OCRL1 gene</ED><SD>Mutación; Genética; Hombre; Nefrología; Urología; Enfermedad de Dent</SD><LO>INIST-11890.354000172498720120</LO><ID>09-0337198</ID></server></inist></record>
000D18	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Perceived exertion threshold: Comparison with ventilatory thresholds and critical power</title><author><name sortKey="Nakamura, F Y" uniqKey="Nakamura F">F. Y. Nakamura</name><affiliation><inist:fA14 i1="01"><s1>Universidade Estadual de Londrina</s1><s2>Londrina, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Okuno, N M" uniqKey="Okuno N">N. M. Okuno</name><affiliation><inist:fA14 i1="01"><s1>Universidade Estadual de Londrina</s1><s2>Londrina, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Perandini, L A B" uniqKey="Perandini L">L. A. B. Perandini</name><affiliation><inist:fA14 i1="01"><s1>Universidade Estadual de Londrina</s1><s2>Londrina, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Oliveira, F R" uniqKey="De Oliveira F">F. R. De Oliveira</name><affiliation><inist:fA14 i1="02"><s1>Universidade Federal de Lavras</s1><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Buchheit, M" uniqKey="Buchheit M">M. Buchheit</name><affiliation><inist:fA14 i1="03"><s1>Picardie Jules Verne University</s1><s2>Amiens</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Simoes, H G" uniqKey="Simoes H">H. G. Simoes</name><affiliation><inist:fA14 i1="04"><s1>Universidade Católica de Brasília</s1><s2>Brasília, DF</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0338612</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0338612 INIST</idno><idno type="RBID">Pascal:09-0338612</idno><idno type="wicri:Area/Main/Corpus">001C63</idno></publicationStmt><seriesStmt><idno type="ISSN">0765-1597</idno><title level="j" type="abbreviated">Sci. sports</title><title level="j" type="main">Science &#38; sports</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aerobe</term><term>Comparative study</term><term>Human</term><term>Oxygen consumption</term><term>Power</term><term>Sport</term><term>Threshold</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Seuil</term><term>Etude comparative</term><term>Puissance</term><term>Aérobie</term><term>Consommation oxygène</term><term>Homme</term><term>Sport</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Objectifs. - Le but de cette étude était de démontrer la validité du seuil de pénibilité perçue à l'effort (PET) à partir de relations avec des repères physiologiques caractérisant la capacité aérobie, obtenus lors de tests incrémentés et à intensité constante. Méthodes. - Onze étudiants masculins ont effectué 1) un test incrémenté pour déterminer le premier (VT<sub>1</sub>) et second (VT<sub>2</sub>) seuil ventilatoire, la consommation maximale d'oxygène ( V<sub>O2max</sub>) et la puissance maximale aérobie (MAP) ; 2) quatre exercices rectangulaires pour l'estimation de la puissance critique (CP) et de PET. Résultats. - La consommation d'oxygène (V<sub>O2</sub>) à VT<sub>1 </sub>et VT<sub>2</sub> était 22,9±4,2 et 35.8±4,7 ml/kg par minute, respectivement. La MAP et V<sub>O2max</sub> moyenne était 267 ± 34 W et 40,3 ± 6,3 ml/kg par minute, respectivement. PET (146±31 W) et CP (146±33 W) n'étaient pas significativement différents, et étaient tout deux entre VT<sub>1</sub> (121±28 W) et VT<sub>2</sub> (228±36 W). La corrélation entre PET et CP, exprimés de manière relative au poids de corps, était significative (p 0,01, r=0,84). Les corrélations entre PET et la V<sub>O2</sub> relative à VT<sub>1</sub> (r=0,76), VT<sub>2</sub> (r=0,72) et V<sub>O2max</sub> (r=0,73) étaient significatives (p &#60; 0,05). Conclusion. - PET n'était pas significativement différent de CP et présentait des corrélations significatives avec VT<sub>1</sub>, VT<sub>2</sub> et V<sub>O2max</sub> obtenues lors du test incrémental. Cela suggère la validité de PET comme une mesure indirecte des capacités aérobies.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0765-1597</s0></fA01><fA02 i1="01"><s0>SCSPED</s0></fA02><fA03 i2="1"><s0>Sci. sports</s0></fA03><fA05><s2>24</s2></fA05><fA06><s2>3-4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Perceived exertion threshold: Comparison with ventilatory thresholds and critical power</s1></fA08><fA11 i1="01" i2="1"><s1>NAKAMURA (F. Y.)</s1></fA11><fA11 i1="02" i2="1"><s1>OKUNO (N. M.)</s1></fA11><fA11 i1="03" i2="1"><s1>PERANDINI (L. A. B.)</s1></fA11><fA11 i1="04" i2="1"><s1>DE OLIVEIRA (F. R.)</s1></fA11><fA11 i1="05" i2="1"><s1>BUCHHEIT (M.)</s1></fA11><fA11 i1="06" i2="1"><s1>SIMOES (H. G.)</s1></fA11><fA14 i1="01"><s1>Universidade Estadual de Londrina</s1><s2>Londrina, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>Universidade Federal de Lavras</s1><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>Picardie Jules Verne University</s1><s2>Amiens</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Universidade Católica de Brasília</s1><s2>Brasília, DF</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>196-201</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>21171</s2><s5>354000170839090120</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>36 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0338612</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Science &#38; sports</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>Objectifs. - Le but de cette étude était de démontrer la validité du seuil de pénibilité perçue à l'effort (PET) à partir de relations avec des repères physiologiques caractérisant la capacité aérobie, obtenus lors de tests incrémentés et à intensité constante. Méthodes. - Onze étudiants masculins ont effectué 1) un test incrémenté pour déterminer le premier (VT<sub>1</sub>) et second (VT<sub>2</sub>) seuil ventilatoire, la consommation maximale d'oxygène ( V<sub>O2max</sub>) et la puissance maximale aérobie (MAP) ; 2) quatre exercices rectangulaires pour l'estimation de la puissance critique (CP) et de PET. Résultats. - La consommation d'oxygène (V<sub>O2</sub>) à VT<sub>1 </sub>et VT<sub>2</sub> était 22,9±4,2 et 35.8±4,7 ml/kg par minute, respectivement. La MAP et V<sub>O2max</sub> moyenne était 267 ± 34 W et 40,3 ± 6,3 ml/kg par minute, respectivement. PET (146±31 W) et CP (146±33 W) n'étaient pas significativement différents, et étaient tout deux entre VT<sub>1</sub> (121±28 W) et VT<sub>2</sub> (228±36 W). La corrélation entre PET et CP, exprimés de manière relative au poids de corps, était significative (p 0,01, r=0,84). Les corrélations entre PET et la V<sub>O2</sub> relative à VT<sub>1</sub> (r=0,76), VT<sub>2</sub> (r=0,72) et V<sub>O2max</sub> (r=0,73) étaient significatives (p &#60; 0,05). Conclusion. - PET n'était pas significativement différent de CP et présentait des corrélations significatives avec VT<sub>1</sub>, VT<sub>2</sub> et V<sub>O2max</sub> obtenues lors du test incrémental. Cela suggère la validité de PET comme une mesure indirecte des capacités aérobies.</s0></fC01><fC02 i1="01" i2="X"><s0>002A24</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Seuil</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Threshold</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Umbral</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Etude comparative</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Comparative study</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Estudio comparativo</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Puissance</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Power</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Potencia</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Aérobie</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Aerobe</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Aerobio</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Consommation oxygène</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Oxygen consumption</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Consumo oxígeno</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Homme</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Human</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Hombre</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Sport</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Sport</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Deporte</s0><s5>07</s5></fC03><fN21><s1>243</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0338612 INIST</NO><ET>Perceived exertion threshold: Comparison with ventilatory thresholds and critical power</ET><AU>NAKAMURA (F. Y.); OKUNO (N. M.); PERANDINI (L. A. B.); DE OLIVEIRA (F. R.); BUCHHEIT (M.); SIMOES (H. G.)</AU><AF>Universidade Estadual de Londrina/Londrina, PR/Brésil (1 aut., 2 aut., 3 aut.); Universidade Federal de Lavras/Brésil (4 aut.); Picardie Jules Verne University/Amiens/France (5 aut.); Universidade Católica de Brasília/Brasília, DF/Brésil (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Science &#38; sports; ISSN 0765-1597; Coden SCSPED; France; Da. 2009; Vol. 24; No. 3-4; Pp. 196-201; Abs. français; Bibl. 36 ref.</SO><LA>Anglais</LA><FA>Objectifs. - Le but de cette étude était de démontrer la validité du seuil de pénibilité perçue à l'effort (PET) à partir de relations avec des repères physiologiques caractérisant la capacité aérobie, obtenus lors de tests incrémentés et à intensité constante. Méthodes. - Onze étudiants masculins ont effectué 1) un test incrémenté pour déterminer le premier (VT<sub>1</sub>) et second (VT<sub>2</sub>) seuil ventilatoire, la consommation maximale d'oxygène ( V<sub>O2max</sub>) et la puissance maximale aérobie (MAP) ; 2) quatre exercices rectangulaires pour l'estimation de la puissance critique (CP) et de PET. Résultats. - La consommation d'oxygène (V<sub>O2</sub>) à VT<sub>1 </sub>et VT<sub>2</sub> était 22,9±4,2 et 35.8±4,7 ml/kg par minute, respectivement. La MAP et V<sub>O2max</sub> moyenne était 267 ± 34 W et 40,3 ± 6,3 ml/kg par minute, respectivement. PET (146±31 W) et CP (146±33 W) n'étaient pas significativement différents, et étaient tout deux entre VT<sub>1</sub> (121±28 W) et VT<sub>2</sub> (228±36 W). La corrélation entre PET et CP, exprimés de manière relative au poids de corps, était significative (p 0,01, r=0,84). Les corrélations entre PET et la V<sub>O2</sub> relative à VT<sub>1</sub> (r=0,76), VT<sub>2</sub> (r=0,72) et V<sub>O2max</sub> (r=0,73) étaient significatives (p &#60; 0,05). Conclusion. - PET n'était pas significativement différent de CP et présentait des corrélations significatives avec VT<sub>1</sub>, VT<sub>2</sub> et V<sub>O2max</sub> obtenues lors du test incrémental. Cela suggère la validité de PET comme une mesure indirecte des capacités aérobies.</FA><CC>002A24</CC><FD>Seuil; Etude comparative; Puissance; Aérobie; Consommation oxygène; Homme; Sport</FD><ED>Threshold; Comparative study; Power; Aerobe; Oxygen consumption; Human; Sport</ED><SD>Umbral; Estudio comparativo; Potencia; Aerobio; Consumo oxígeno; Hombre; Deporte</SD><LO>INIST-21171.354000170839090120</LO><ID>09-0338612</ID></server></inist></record>
000D19	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Understanding the genesis of ultramafic soils and catena dynamics in Niquelândia, Brazil</title><author><name sortKey="Garnier, J" uniqKey="Garnier J">J. Garnier</name><affiliation><inist:fA14 i1="01"><s1>UMR 8148 IDES, Univ. Paris Sud 11, CNRS</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Quantin, C" uniqKey="Quantin C">C. Quantin</name><affiliation><inist:fA14 i1="01"><s1>UMR 8148 IDES, Univ. Paris Sud 11, CNRS</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Guimaraes, E" uniqKey="Guimaraes E">E. Guimaraes</name><affiliation><inist:fA14 i1="02"><s1>UnB, IG/GMP-ICC Centro, Campus Universitario Darcy Ribeiro</s1><s2>70919-970, Brasilia-DF</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Garg, V K" uniqKey="Garg V">V. K. Garg</name><affiliation><inist:fA14 i1="03"><s1>UnB, IF-ICC Centro, Campus Universitário Darcy Ribeiro</s1><s2>70910-970, Brasília-DF</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Martins, E S" uniqKey="Martins E">E. S. Martins</name><affiliation><inist:fA14 i1="05"><s1>UMR 137, IRD, Univ. Paris VI and XII, SupAgro, Bâtiment 12, 2 place Viala</s1><s2>34060 Montpellier</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Becquer, T" uniqKey="Becquer T">T. Becquer</name><affiliation><inist:fA14 i1="04"><s1>Embrapa Cerrados, BR 020, km 18, rodovia Brasília/Fortateza, CP 08223</s1><s2>CEP 73301-970, Planaltina-DF</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>UMR 137, IRD, Univ. Paris VI and XII, SupAgro, Bâtiment 12, 2 place Viala</s1><s2>34060 Montpellier</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0343631</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0343631 INIST</idno><idno type="RBID">Pascal:09-0343631</idno><idno type="wicri:Area/Main/Corpus">001C62</idno></publicationStmt><seriesStmt><idno type="ISSN">0016-7061</idno><title level="j" type="abbreviated">Geoderma : (Amst.)</title><title level="j" type="main">Geoderma : (Amsterdam)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Goias Brazil</term><term>Iron oxide</term><term>Mossbauer spectra</term><term>Soil solution</term><term>X-ray diffraction</term><term>catenas</term><term>chromite</term><term>chromium</term><term>garnierite</term><term>magnetite</term><term>outcrops</term><term>oxidation</term><term>pedogenesis</term><term>secondary minerals</term><term>smectite</term><term>soil parent materials</term><term>tracers</term><term>tropical zone</term><term>ultramafics</term><term>weathering</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Pédogenèse</term><term>Zonéographie sol</term><term>Roche mère sol</term><term>Chrome</term><term>Roche ultramafique</term><term>Altération météorique</term><term>Zone tropicale</term><term>Diffraction RX</term><term>Affleurement</term><term>Spectre Mössbauer</term><term>Chromite</term><term>Magnetite</term><term>Minéral secondaire</term><term>Oxyde de fer</term><term>Smectite</term><term>Garnierite</term><term>Solution édaphique</term><term>Oxydation</term><term>Traceur</term><term>Brésil</term><term>Goias</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This study focuses on the fate of chromium during ultramafic weathering under tropical conditions. Three soils were studied along a characteristic catena on the ultramafic outcrop of Niquelândia, Brazil. In these soils, the Cr-bearing minerals are inherited chromites (15.4-26.8 wt.% Cr) and magnetites (0.4-4.8 wt.% Cr) and secondary minerals such as iron oxides (0-2 wt.% Cr) or Ni-smectites (0-6.8 wt.% Cr). Indeed, during weathering, Cr liberated from primary minerals can first be incorporated into Ni-smectites (garnierite) or Fe oxides. As the weathering continues, smectites become unstable and Cr liberated into the soil solution, and incorporates in Fe oxides. In this oxidized environment, Fe and Mn are oxidized and oxides can incorporate elements like Cr, Ni and Al. Two types of chromites were distinguished, i.e. a vein type (VC) and a rock type (RC) according to their composition. Chromites could be used as tracer of pedogenesis processes due to the distinct composition ofVC and RC types. They allow us to show that the upper part of some soil profile results exclusively from colluvial processes, and the lower part of the profile results from the ultramafic bedrock weathering. The chromite tracer allows us to propose a model of the catena evolution.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0016-7061</s0></fA01><fA02 i1="01"><s0>GEDMAB</s0></fA02><fA03 i2="1"><s0>Geoderma : (Amst.)</s0></fA03><fA05><s2>151</s2></fA05><fA06><s2>3-4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Understanding the genesis of ultramafic soils and catena dynamics in Niquelândia, Brazil</s1></fA08><fA11 i1="01" i2="1"><s1>GARNIER (J.)</s1></fA11><fA11 i1="02" i2="1"><s1>QUANTIN (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>GUIMARAES (E.)</s1></fA11><fA11 i1="04" i2="1"><s1>GARG (V. K.)</s1></fA11><fA11 i1="05" i2="1"><s1>MARTINS (E. S.)</s1></fA11><fA11 i1="06" i2="1"><s1>BECQUER (T.)</s1></fA11><fA14 i1="01"><s1>UMR 8148 IDES, Univ. Paris Sud 11, CNRS</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>UnB, IG/GMP-ICC Centro, Campus Universitario Darcy Ribeiro</s1><s2>70919-970, Brasilia-DF</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>UnB, IF-ICC Centro, Campus Universitário Darcy Ribeiro</s1><s2>70910-970, Brasília-DF</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Embrapa Cerrados, BR 020, km 18, rodovia Brasília/Fortateza, CP 08223</s1><s2>CEP 73301-970, Planaltina-DF</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="05"><s1>UMR 137, IRD, Univ. Paris VI and XII, SupAgro, Bâtiment 12, 2 place Viala</s1><s2>34060 Montpellier</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA20><s1>204-214</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>3607</s2><s5>354000187503650170</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0343631</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Geoderma : (Amsterdam)</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>This study focuses on the fate of chromium during ultramafic weathering under tropical conditions. Three soils were studied along a characteristic catena on the ultramafic outcrop of Niquelândia, Brazil. In these soils, the Cr-bearing minerals are inherited chromites (15.4-26.8 wt.% Cr) and magnetites (0.4-4.8 wt.% Cr) and secondary minerals such as iron oxides (0-2 wt.% Cr) or Ni-smectites (0-6.8 wt.% Cr). Indeed, during weathering, Cr liberated from primary minerals can first be incorporated into Ni-smectites (garnierite) or Fe oxides. As the weathering continues, smectites become unstable and Cr liberated into the soil solution, and incorporates in Fe oxides. In this oxidized environment, Fe and Mn are oxidized and oxides can incorporate elements like Cr, Ni and Al. Two types of chromites were distinguished, i.e. a vein type (VC) and a rock type (RC) according to their composition. Chromites could be used as tracer of pedogenesis processes due to the distinct composition ofVC and RC types. They allow us to show that the upper part of some soil profile results exclusively from colluvial processes, and the lower part of the profile results from the ultramafic bedrock weathering. The chromite tracer allows us to propose a model of the catena evolution.</s0></fC01><fC02 i1="01" i2="X"><s0>002A32</s0></fC02><fC02 i1="02" i2="2"><s0>001E01P03</s0></fC02><fC02 i1="03" i2="2"><s0>001E01B03</s0></fC02><fC02 i1="04" i2="2"><s0>226C03</s0></fC02><fC02 i1="05" i2="2"><s0>220B03</s0></fC02><fC03 i1="01" i2="2" l="FRE"><s0>Pédogenèse</s0><s5>01</s5></fC03><fC03 i1="01" i2="2" l="ENG"><s0>pedogenesis</s0><s5>01</s5></fC03><fC03 i1="01" i2="2" l="SPA"><s0>Pedogénesis</s0><s5>01</s5></fC03><fC03 i1="02" i2="2" l="FRE"><s0>Zonéographie sol</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="ENG"><s0>catenas</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="SPA"><s0>Zoneografía suelo</s0><s5>02</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Roche mère sol</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>soil parent materials</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="SPA"><s0>Roca madre suelo</s0><s5>03</s5></fC03><fC03 i1="04" i2="2" l="FRE"><s0>Chrome</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="ENG"><s0>chromium</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="SPA"><s0>Cromo</s0><s5>04</s5></fC03><fC03 i1="05" i2="2" l="FRE"><s0>Roche ultramafique</s0><s2>NV</s2><s5>05</s5></fC03><fC03 i1="05" i2="2" l="ENG"><s0>ultramafics</s0><s2>NV</s2><s5>05</s5></fC03><fC03 i1="06" i2="2" l="FRE"><s0>Altération météorique</s0><s5>06</s5></fC03><fC03 i1="06" i2="2" l="ENG"><s0>weathering</s0><s5>06</s5></fC03><fC03 i1="06" i2="2" l="SPA"><s0>Alteración meteórica</s0><s5>06</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Zone tropicale</s0><s5>07</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>tropical zone</s0><s5>07</s5></fC03><fC03 i1="07" i2="2" l="SPA"><s0>Zona tropical</s0><s5>07</s5></fC03><fC03 i1="08" i2="2" l="FRE"><s0>Diffraction RX</s0><s5>08</s5></fC03><fC03 i1="08" i2="2" l="ENG"><s0>X-ray diffraction</s0><s5>08</s5></fC03><fC03 i1="08" i2="2" l="SPA"><s0>Difracción RX</s0><s5>08</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Affleurement</s0><s5>09</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>outcrops</s0><s5>09</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Afloramiento</s0><s5>09</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Spectre Mössbauer</s0><s5>10</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>Mossbauer spectra</s0><s5>10</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Espectro Mossbauer</s0><s5>10</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Chromite</s0><s2>NZ</s2><s5>11</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>chromite</s0><s2>NZ</s2><s5>11</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Cromito</s0><s2>NZ</s2><s5>11</s5></fC03><fC03 i1="12" i2="2" l="FRE"><s0>Magnetite</s0><s2>NZ</s2><s5>12</s5></fC03><fC03 i1="12" i2="2" l="ENG"><s0>magnetite</s0><s2>NZ</s2><s5>12</s5></fC03><fC03 i1="12" i2="2" l="SPA"><s0>Magnetita</s0><s2>NZ</s2><s5>12</s5></fC03><fC03 i1="13" i2="2" l="FRE"><s0>Minéral secondaire</s0><s5>13</s5></fC03><fC03 i1="13" i2="2" l="ENG"><s0>secondary minerals</s0><s5>13</s5></fC03><fC03 i1="13" i2="2" l="SPA"><s0>Mineral secundario</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Oxyde de fer</s0><s5>15</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Iron oxide</s0><s5>15</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Hierro óxido</s0><s5>15</s5></fC03><fC03 i1="15" i2="2" l="FRE"><s0>Smectite</s0><s2>NZ</s2><s5>16</s5></fC03><fC03 i1="15" i2="2" l="ENG"><s0>smectite</s0><s2>NZ</s2><s5>16</s5></fC03><fC03 i1="15" i2="2" l="SPA"><s0>Esmectita</s0><s2>NZ</s2><s5>16</s5></fC03><fC03 i1="16" i2="2" l="FRE"><s0>Garnierite</s0><s2>NZ</s2><s5>18</s5></fC03><fC03 i1="16" i2="2" l="ENG"><s0>garnierite</s0><s2>NZ</s2><s5>18</s5></fC03><fC03 i1="16" i2="2" l="SPA"><s0>Garnierita</s0><s2>NZ</s2><s5>18</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Solution édaphique</s0><s5>19</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Soil solution</s0><s5>19</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Solución suelo</s0><s5>19</s5></fC03><fC03 i1="18" i2="2" l="FRE"><s0>Oxydation</s0><s5>20</s5></fC03><fC03 i1="18" i2="2" l="ENG"><s0>oxidation</s0><s5>20</s5></fC03><fC03 i1="18" i2="2" l="SPA"><s0>Oxidación</s0><s5>20</s5></fC03><fC03 i1="19" i2="2" l="FRE"><s0>Traceur</s0><s5>25</s5></fC03><fC03 i1="19" i2="2" l="ENG"><s0>tracers</s0><s5>25</s5></fC03><fC03 i1="19" i2="2" l="SPA"><s0>Trazador</s0><s5>25</s5></fC03><fC03 i1="20" i2="2" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="20" i2="2" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="20" i2="2" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>61</s5></fC03><fC03 i1="21" i2="2" l="FRE"><s0>Goias</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="21" i2="2" l="ENG"><s0>Goias Brazil</s0><s2>NG</s2><s5>62</s5></fC03><fC03 i1="21" i2="2" l="SPA"><s0>Goias</s0><s2>NG</s2><s5>62</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Roche plutonique</s0><s2>NV</s2></fC07><fC07 i1="01" i2="2" l="ENG"><s0>plutonic rocks</s0><s2>NV</s2></fC07><fC07 i1="01" i2="2" l="SPA"><s0>Roca granuda</s0><s2>NV</s2></fC07><fC07 i1="02" i2="2" l="FRE"><s0>Roche ignée</s0><s2>NV</s2></fC07><fC07 i1="02" i2="2" l="ENG"><s0>igneous rocks</s0><s2>NV</s2></fC07><fC07 i1="02" i2="2" l="SPA"><s0>Roca ignea</s0><s2>NV</s2></fC07><fC07 i1="03" i2="2" l="FRE"><s0>Spinelle</s0><s2>NZ</s2></fC07><fC07 i1="03" i2="2" l="ENG"><s0>spinel</s0><s2>NZ</s2></fC07><fC07 i1="03" i2="2" l="SPA"><s0>Espinela</s0><s2>NZ</s2></fC07><fC07 i1="04" i2="2" l="FRE"><s0>Oxyde</s0><s2>NZ</s2></fC07><fC07 i1="04" i2="2" l="ENG"><s0>oxides</s0><s2>NZ</s2></fC07><fC07 i1="04" i2="2" l="SPA"><s0>Óxido</s0><s2>NZ</s2></fC07><fC07 i1="05" i2="2" l="FRE"><s0>Argile minéral</s0><s2>NZ</s2></fC07><fC07 i1="05" i2="2" l="ENG"><s0>clay minerals</s0><s2>NZ</s2></fC07><fC07 i1="05" i2="2" l="SPA"><s0>Arcilla mineral</s0><s2>NZ</s2></fC07><fC07 i1="06" i2="2" l="FRE"><s0>Phyllosilicate</s0><s2>NZ</s2></fC07><fC07 i1="06" i2="2" l="ENG"><s0>sheet silicates</s0><s2>NZ</s2></fC07><fC07 i1="06" i2="2" l="SPA"><s0>Filosilicato</s0><s2>NZ</s2></fC07><fC07 i1="07" i2="2" l="FRE"><s0>Silicate</s0><s2>NZ</s2></fC07><fC07 i1="07" i2="2" l="ENG"><s0>silicates</s0><s2>NZ</s2></fC07><fC07 i1="07" i2="2" l="SPA"><s0>Silicato</s0><s2>NZ</s2></fC07><fC07 i1="08" i2="2" l="FRE"><s0>Serpentine</s0><s2>NZ</s2></fC07><fC07 i1="08" i2="2" l="ENG"><s0>serpentine</s0><s2>NZ</s2></fC07><fC07 i1="08" i2="2" l="SPA"><s0>Serpentina</s0><s2>NZ</s2></fC07><fC07 i1="09" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="09" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="09" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fN21><s1>250</s1></fN21></pA></standard><server><NO>PASCAL 09-0343631 INIST</NO><ET>Understanding the genesis of ultramafic soils and catena dynamics in Niquelândia, Brazil</ET><AU>GARNIER (J.); QUANTIN (C.); GUIMARAES (E.); GARG (V. K.); MARTINS (E. S.); BECQUER (T.)</AU><AF>UMR 8148 IDES, Univ. Paris Sud 11, CNRS/91405 Orsay/France (1 aut., 2 aut.); UnB, IG/GMP-ICC Centro, Campus Universitario Darcy Ribeiro/70919-970, Brasilia-DF/Brésil (3 aut.); UnB, IF-ICC Centro, Campus Universitário Darcy Ribeiro/70910-970, Brasília-DF/Brésil (4 aut.); Embrapa Cerrados, BR 020, km 18, rodovia Brasília/Fortateza, CP 08223/CEP 73301-970, Planaltina-DF/Brésil (6 aut.); UMR 137, IRD, Univ. Paris VI and XII, SupAgro, Bâtiment 12, 2 place Viala/34060 Montpellier/France (5 aut., 6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Geoderma : (Amsterdam); ISSN 0016-7061; Coden GEDMAB; Pays-Bas; Da. 2009; Vol. 151; No. 3-4; Pp. 204-214; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>This study focuses on the fate of chromium during ultramafic weathering under tropical conditions. Three soils were studied along a characteristic catena on the ultramafic outcrop of Niquelândia, Brazil. In these soils, the Cr-bearing minerals are inherited chromites (15.4-26.8 wt.% Cr) and magnetites (0.4-4.8 wt.% Cr) and secondary minerals such as iron oxides (0-2 wt.% Cr) or Ni-smectites (0-6.8 wt.% Cr). Indeed, during weathering, Cr liberated from primary minerals can first be incorporated into Ni-smectites (garnierite) or Fe oxides. As the weathering continues, smectites become unstable and Cr liberated into the soil solution, and incorporates in Fe oxides. In this oxidized environment, Fe and Mn are oxidized and oxides can incorporate elements like Cr, Ni and Al. Two types of chromites were distinguished, i.e. a vein type (VC) and a rock type (RC) according to their composition. Chromites could be used as tracer of pedogenesis processes due to the distinct composition ofVC and RC types. They allow us to show that the upper part of some soil profile results exclusively from colluvial processes, and the lower part of the profile results from the ultramafic bedrock weathering. The chromite tracer allows us to propose a model of the catena evolution.</EA><CC>002A32; 001E01P03; 001E01B03; 226C03; 220B03</CC><FD>Pédogenèse; Zonéographie sol; Roche mère sol; Chrome; Roche ultramafique; Altération météorique; Zone tropicale; Diffraction RX; Affleurement; Spectre Mössbauer; Chromite; Magnetite; Minéral secondaire; Oxyde de fer; Smectite; Garnierite; Solution édaphique; Oxydation; Traceur; Brésil; Goias</FD><FG>Roche plutonique; Roche ignée; Spinelle; Oxyde; Argile minéral; Phyllosilicate; Silicate; Serpentine; Amérique du Sud</FG><ED>pedogenesis; catenas; soil parent materials; chromium; ultramafics; weathering; tropical zone; X-ray diffraction; outcrops; Mossbauer spectra; chromite; magnetite; secondary minerals; Iron oxide; smectite; garnierite; Soil solution; oxidation; tracers; Brazil; Goias Brazil</ED><EG>plutonic rocks; igneous rocks; spinel; oxides; clay minerals; sheet silicates; silicates; serpentine; South America</EG><SD>Pedogénesis; Zoneografía suelo; Roca madre suelo; Cromo; Alteración meteórica; Zona tropical; Difracción RX; Afloramiento; Espectro Mossbauer; Cromito; Magnetita; Mineral secundario; Hierro óxido; Esmectita; Garnierita; Solución suelo; Oxidación; Trazador; Brasil; Goias</SD><LO>INIST-3607.354000187503650170</LO><ID>09-0343631</ID></server></inist></record>
000D20	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Monitoring water level in large trans-boundary ungauged basins with altimetry: the example of ENVISAT over the Amazon basin</title><author><name sortKey="Seyler, Frederique" uniqKey="Seyler F">Frederique Seyler</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement (IRD), Unité Espace</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Calmant, Stephane" uniqKey="Calmant S">Stephane Calmant</name><affiliation><inist:fA14 i1="02"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire d'Etudes en Géophysique et Océanographie Spatiales (LEGOS)</s1><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silva, Joecila" uniqKey="Da Silva J">Joecila Da Silva</name><affiliation><inist:fA14 i1="03"><s1>Univ. Federal de Rio de Janiero</s1><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Filizola, Naziano" uniqKey="Filizola N">Naziano Filizola</name><affiliation><inist:fA14 i1="04"><s1>Univ. do Estado de Amazonas</s1><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Roux, Emmanuel" uniqKey="Roux E">Emmanuel Roux</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement (IRD), Unité Espace</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cochonneau, Gerard" uniqKey="Cochonneau G">Gerard Cochonneau</name><affiliation><inist:fA14 i1="05"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire des Mécanismes et Transfert en Géologie (LMTG)</s1><s3>FRA</s3><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vauchel, Philippe" uniqKey="Vauchel P">Philippe Vauchel</name><affiliation><inist:fA14 i1="05"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire des Mécanismes et Transfert en Géologie (LMTG)</s1><s3>FRA</s3><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bonnet, Marie Paule" uniqKey="Bonnet M">Marie-Paule Bonnet</name><affiliation><inist:fA14 i1="05"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire des Mécanismes et Transfert en Géologie (LMTG)</s1><s3>FRA</s3><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0343966</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0343966 INIST</idno><idno type="RBID">Pascal:09-0343966</idno><idno type="wicri:Area/Main/Corpus">001C61</idno></publicationStmt><seriesStmt><idno type="ISSN">0277-786X</idno><title level="j" type="abbreviated">Proc. SPIE Int. Soc. Opt. Eng.</title><title level="j" type="main">Proceedings of SPIE, the International Society for Optical Engineering</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amazon Basin</term><term>Bolivia</term><term>Peru</term><term>Space remote sensing</term><term>altimetry</term><term>changes of level</term><term>floodplains</term><term>hydrology</term><term>meanders</term><term>monitoring</term><term>radar methods</term><term>tributaries</term><term>wetlands</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Bassin Amazone</term><term>Altimétrie</term><term>Télédétection spatiale</term><term>Surveillance</term><term>Hydrologie</term><term>Variation niveau</term><term>Plaine inondable</term><term>Zone humide</term><term>Méthode radar</term><term>Bolivie</term><term>Pérou</term><term>Affluent</term><term>Méandre</term><term>ENVISAT</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Brasil and Bolivia have water plans projects on the Beni-Madeira river, a major tributary of the Amazon. There are four main tributaries to the Rio Madeira: the Guapore, the Mamore and the Beni rivers into the Bolivian territory, and the Madre de Dios River crossing the North of Bolivia, coming from Peru. Most parts of these rivers are very far from the Andean capital cities of Bolivia and Peru, unreachable for long periods of time. Very few gauging stations are in operation, either for the Bolivian or the Peruvian part, most of them being located at the Andes piedmont or near the confluence at the Brazilian border as they form the Madeira river. This situation is exemplary of large transboundary basins in the tropical part of the world. We have computed 39 water level time series using ENVISAT altimetry data over the four tributaries of the Madeira and the Madeira itself. We present a preliminary study mostly conducted onto the Guapore river, in order to assess the quality of these time series for a variety of situations, but mostly narrow and meandering riverbeds. Comparison between water levels variation in the mainstream and within the inundations plains and lakes are drawn. We conclude by the perspectives offered by the combined use of radar altimetry and SAR imagery for the global monitoring of water resources, in large tropical transboundary basins.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0277-786X</s0></fA01><fA02 i1="01"><s0>PSISDG</s0></fA02><fA03 i2="1"><s0>Proc. SPIE Int. Soc. Opt. Eng.</s0></fA03><fA05><s2>7150</s2></fA05><fA08 i1="01" i2="1" l="ENG"><s1>Monitoring water level in large trans-boundary ungauged basins with altimetry: the example of ENVISAT over the Amazon basin</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Remote sensing of inland, coastal, and oceanic waters : 18-21 November 2008, Noumea, New Caledonia</s1></fA09><fA11 i1="01" i2="1"><s1>SEYLER (Frederique)</s1></fA11><fA11 i1="02" i2="1"><s1>CALMANT (Stephane)</s1></fA11><fA11 i1="03" i2="1"><s1>DA SILVA (Joecila)</s1></fA11><fA11 i1="04" i2="1"><s1>FILIZOLA (Naziano)</s1></fA11><fA11 i1="05" i2="1"><s1>ROUX (Emmanuel)</s1></fA11><fA11 i1="06" i2="1"><s1>COCHONNEAU (Gerard)</s1></fA11><fA11 i1="07" i2="1"><s1>VAUCHEL (Philippe)</s1></fA11><fA11 i1="08" i2="1"><s1>BONNET (Marie-Paule)</s1></fA11><fA12 i1="01" i2="1"><s1>FROUIN (Robert)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Institut de Recherche pour le Développement (IRD), Unité Espace</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire d'Etudes en Géophysique et Océanographie Spatiales (LEGOS)</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Univ. Federal de Rio de Janiero</s1><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Univ. do Estado de Amazonas</s1><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Univ. Toulouse 3 (France), IRD, Laboratoire des Mécanismes et Transfert en Géologie (LMTG)</s1><s3>FRA</s3><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA18 i1="01" i2="1"><s1>Society of Photo-optical Instrumentation Engineers</s1><s3>USA</s3><s9>org-cong.</s9></fA18><fA20><s2>715017.1-715017.17</s2></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA25 i1="01"><s1>SPIE</s1><s2>Bellingham, Wash.</s2></fA25><fA26 i1="01"><s0>9780819473929</s0></fA26><fA43 i1="01"><s1>INIST</s1><s2>21760</s2><s5>354000172946470290</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>24 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0343966</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Proceedings of SPIE, the International Society for Optical Engineering</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Brasil and Bolivia have water plans projects on the Beni-Madeira river, a major tributary of the Amazon. There are four main tributaries to the Rio Madeira: the Guapore, the Mamore and the Beni rivers into the Bolivian territory, and the Madre de Dios River crossing the North of Bolivia, coming from Peru. Most parts of these rivers are very far from the Andean capital cities of Bolivia and Peru, unreachable for long periods of time. Very few gauging stations are in operation, either for the Bolivian or the Peruvian part, most of them being located at the Andes piedmont or near the confluence at the Brazilian border as they form the Madeira river. This situation is exemplary of large transboundary basins in the tropical part of the world. We have computed 39 water level time series using ENVISAT altimetry data over the four tributaries of the Madeira and the Madeira itself. We present a preliminary study mostly conducted onto the Guapore river, in order to assess the quality of these time series for a variety of situations, but mostly narrow and meandering riverbeds. Comparison between water levels variation in the mainstream and within the inundations plains and lakes are drawn. We conclude by the perspectives offered by the combined use of radar altimetry and SAR imagery for the global monitoring of water resources, in large tropical transboundary basins.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01M04</s0></fC02><fC02 i1="02" i2="2"><s0>001E01O04</s0></fC02><fC02 i1="03" i2="2"><s0>001E01N01</s0></fC02><fC02 i1="04" i2="2"><s0>225B04</s0></fC02><fC02 i1="05" i2="2"><s0>226B04</s0></fC02><fC02 i1="06" i2="2"><s0>226A01</s0></fC02><fC03 i1="01" i2="2" l="FRE"><s0>Bassin Amazone</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="2" l="ENG"><s0>Amazon Basin</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="2" l="SPA"><s0>Cuenca Amazonas</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="02" i2="2" l="FRE"><s0>Altimétrie</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="ENG"><s0>altimetry</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="SPA"><s0>Altimetría</s0><s5>02</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Télédétection spatiale</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>Space remote sensing</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="SPA"><s0>Teledetección espacial</s0><s5>03</s5></fC03><fC03 i1="04" i2="2" l="FRE"><s0>Surveillance</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="ENG"><s0>monitoring</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="SPA"><s0>Vigilancia</s0><s5>04</s5></fC03><fC03 i1="05" i2="2" l="FRE"><s0>Hydrologie</s0><s5>05</s5></fC03><fC03 i1="05" i2="2" l="ENG"><s0>hydrology</s0><s5>05</s5></fC03><fC03 i1="06" i2="2" l="FRE"><s0>Variation niveau</s0><s5>06</s5></fC03><fC03 i1="06" i2="2" l="ENG"><s0>changes of level</s0><s5>06</s5></fC03><fC03 i1="06" i2="2" l="SPA"><s0>Variación nivel</s0><s5>06</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Plaine inondable</s0><s5>07</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>floodplains</s0><s5>07</s5></fC03><fC03 i1="07" i2="2" l="SPA"><s0>Llano inundable</s0><s5>07</s5></fC03><fC03 i1="08" i2="2" l="FRE"><s0>Zone humide</s0><s5>08</s5></fC03><fC03 i1="08" i2="2" l="ENG"><s0>wetlands</s0><s5>08</s5></fC03><fC03 i1="08" i2="2" l="SPA"><s0>Terreno húmedo</s0><s5>08</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Méthode radar</s0><s5>09</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>radar methods</s0><s5>09</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Radar</s0><s5>09</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Bolivie</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>Bolivia</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Bolivia</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Pérou</s0><s2>NG</s2><s5>11</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>Peru</s0><s2>NG</s2><s5>11</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Perú</s0><s2>NG</s2><s5>11</s5></fC03><fC03 i1="12" i2="2" l="FRE"><s0>Affluent</s0><s5>12</s5></fC03><fC03 i1="12" i2="2" l="ENG"><s0>tributaries</s0><s5>12</s5></fC03><fC03 i1="13" i2="2" l="FRE"><s0>Méandre</s0><s5>14</s5></fC03><fC03 i1="13" i2="2" l="ENG"><s0>meanders</s0><s5>14</s5></fC03><fC03 i1="13" i2="2" l="SPA"><s0>Meandro</s0><s5>14</s5></fC03><fC03 i1="14" i2="2" l="FRE"><s0>ENVISAT</s0><s4>INC</s4><s5>52</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fN21><s1>250</s1></fN21><fN44 i1="01"><s1>PSI</s1></fN44><fN82><s1>PSI</s1></fN82></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Remote sensing of inland, coastal, and oceanic waters</s1><s3>Noumea FRA</s3><s4>2008</s4></fA30></pR></standard><server><NO>PASCAL 09-0343966 INIST</NO><ET>Monitoring water level in large trans-boundary ungauged basins with altimetry: the example of ENVISAT over the Amazon basin</ET><AU>SEYLER (Frederique); CALMANT (Stephane); DA SILVA (Joecila); FILIZOLA (Naziano); ROUX (Emmanuel); COCHONNEAU (Gerard); VAUCHEL (Philippe); BONNET (Marie-Paule); FROUIN (Robert)</AU><AF>Institut de Recherche pour le Développement (IRD), Unité Espace/France (1 aut., 5 aut.); Univ. Toulouse 3 (France), IRD, Laboratoire d'Etudes en Géophysique et Océanographie Spatiales (LEGOS)/France (2 aut.); Univ. Federal de Rio de Janiero/Brésil (3 aut.); Univ. do Estado de Amazonas/Brésil (4 aut.); Univ. Toulouse 3 (France), IRD, Laboratoire des Mécanismes et Transfert en Géologie (LMTG)/France (6 aut., 7 aut., 8 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Proceedings of SPIE, the International Society for Optical Engineering; ISSN 0277-786X; Coden PSISDG; Etats-Unis; Da. 2008; Vol. 7150; 715017.1-715017.17; Bibl. 24 ref.</SO><LA>Anglais</LA><EA>Brasil and Bolivia have water plans projects on the Beni-Madeira river, a major tributary of the Amazon. There are four main tributaries to the Rio Madeira: the Guapore, the Mamore and the Beni rivers into the Bolivian territory, and the Madre de Dios River crossing the North of Bolivia, coming from Peru. Most parts of these rivers are very far from the Andean capital cities of Bolivia and Peru, unreachable for long periods of time. Very few gauging stations are in operation, either for the Bolivian or the Peruvian part, most of them being located at the Andes piedmont or near the confluence at the Brazilian border as they form the Madeira river. This situation is exemplary of large transboundary basins in the tropical part of the world. We have computed 39 water level time series using ENVISAT altimetry data over the four tributaries of the Madeira and the Madeira itself. We present a preliminary study mostly conducted onto the Guapore river, in order to assess the quality of these time series for a variety of situations, but mostly narrow and meandering riverbeds. Comparison between water levels variation in the mainstream and within the inundations plains and lakes are drawn. We conclude by the perspectives offered by the combined use of radar altimetry and SAR imagery for the global monitoring of water resources, in large tropical transboundary basins.</EA><CC>001E01M04; 001E01O04; 001E01N01; 225B04; 226B04; 226A01</CC><FD>Bassin Amazone; Altimétrie; Télédétection spatiale; Surveillance; Hydrologie; Variation niveau; Plaine inondable; Zone humide; Méthode radar; Bolivie; Pérou; Affluent; Méandre; ENVISAT</FD><FG>Amérique du Sud</FG><ED>Amazon Basin; altimetry; Space remote sensing; monitoring; hydrology; changes of level; floodplains; wetlands; radar methods; Bolivia; Peru; tributaries; meanders</ED><EG>South America</EG><SD>Cuenca Amazonas; Altimetría; Teledetección espacial; Vigilancia; Variación nivel; Llano inundable; Terreno húmedo; Radar; Bolivia; Perú; Meandro</SD><LO>INIST-21760.354000172946470290</LO><ID>09-0343966</ID></server></inist></record>
000D21	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">High-Affinity Copper Transport and Snq2 Export Permease of Saccharomyces cerevisiae Modulate Cytotoxicity of PR-10 from Theobroma cacao</title><author><name sortKey="Pungartnik, Cristina" uniqKey="Pungartnik C">Cristina Pungartnik</name><affiliation><inist:fA14 i1="01"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia de Fungos, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silva, Aline Clara" uniqKey="Da Silva A">Aline Clara Da Silva</name><affiliation><inist:fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Melo, Sarah Alves" uniqKey="De Melo S">Sarah Alves De Melo</name><affiliation><inist:fA14 i1="01"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia de Fungos, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Peres Gramacho, Karina" uniqKey="Peres Gramacho K">Karina Peres Gramacho</name><affiliation><inist:fA14 i1="03"><s1>CEPLAC/CEPEC, Cocoa Research Center</s1><s2>45600-970 Itabuna-BA</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Mattos Cascardo, J Lio Cezar" uniqKey="De Mattos Cascardo J">J Lio Cézar De Mattos Cascardo</name><affiliation><inist:fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brendel, Martin" uniqKey="Brendel M">Martin Brendel</name><affiliation><inist:fA14 i1="01"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia de Fungos, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Micheli, Fabienne" uniqKey="Micheli F">Fabienne Micheli</name><affiliation><inist:fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>CIRAD, UMR DAP, Avenue Agropolis TA96/03</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silva Gesteira, Abelmon" uniqKey="Da Silva Gesteira A">Abelmon Da Silva Gesteira</name><affiliation><inist:fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0344557</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0344557 INIST</idno><idno type="RBID">Pascal:09-0344557</idno><idno type="wicri:Area/Main/Corpus">001C60</idno></publicationStmt><seriesStmt><idno type="ISSN">0894-0282</idno><title level="j" type="abbreviated">Mol. plant-microb. interact.</title><title level="j" type="main">Molecular plant-microbe interactions</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cytotoxicity</term><term>Microbiology</term><term>Permease</term><term>Saccharomyces cerevisiae</term><term>Theobroma cacao</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Saccharomyces cerevisiae</term><term>Theobroma cacao</term><term>Cytotoxicité</term><term>Microbiologie</term><term>Permease</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A pathogenesis-related (PR) protein from Theobroma cacao (TcPR-10) was identified from a cacao-Moniliophthora perniciosa interaction cDNA library. Nucleotide and amino acid sequences showed homology with other PR-10 proteins having P loop motif and Betv1 domain. Recombinant TcPR-10 showed in vitro and in vivo ribonuclease activity, and antifungal activity against the basidiomycete cacao pathogen M. perniciosa and the yeast Saccharomyces cerevisiae. Fluorescein isothiocyanate-labeled TcPR-10 was internalized by M. perniciosa hyphae and S. cerevisiae cells and inhibited growth of both fungi. Energy and temperature-dependent internalization of the TcPR-10 suggested an active importation into the fungal cells. Chronical exposure to TcPR-10 of 29 yeast mutants with single gene defects in DNA repair, general membrane transport, metal transport, and antioxidant defenses was tested. Two yeast mutants were hyperresistant compared with their respective isogenic wild type: ctr3Δ mutant, lacking the high-affinity plasma membrane copper transporter and mac1Δ, the copper-sensing transcription factor involved in regulation of high-affinity copper transport. Acute exposure of exponentially growing yeast cells revealed that TcPR-10 resistance is also enhanced in the Snq2 export permease-lacking mutant which has reduced intracellular presence of TcPR-10.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0894-0282</s0></fA01><fA02 i1="01"><s0>MPMIEL</s0></fA02><fA03 i2="1"><s0>Mol. plant-microb. interact.</s0></fA03><fA05><s2>22</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>High-Affinity Copper Transport and Snq2 Export Permease of Saccharomyces cerevisiae Modulate Cytotoxicity of PR-10 from Theobroma cacao</s1></fA08><fA11 i1="01" i2="1"><s1>PUNGARTNIK (Cristina)</s1></fA11><fA11 i1="02" i2="1"><s1>DA SILVA (Aline Clara)</s1></fA11><fA11 i1="03" i2="1"><s1>DE MELO (Sarah Alves)</s1></fA11><fA11 i1="04" i2="1"><s1>PERES GRAMACHO (Karina)</s1></fA11><fA11 i1="05" i2="1"><s1>DE MATTOS CASCARDO (Júlio Cézar)</s1></fA11><fA11 i1="06" i2="1"><s1>BRENDEL (Martin)</s1></fA11><fA11 i1="07" i2="1"><s1>MICHELI (Fabienne)</s1></fA11><fA11 i1="08" i2="1"><s1>DA SILVA GESTEIRA (Abelmon)</s1></fA11><fA14 i1="01"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia de Fungos, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16</s1><s2>45650-000 Ilhéus-BA</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="03"><s1>CEPLAC/CEPEC, Cocoa Research Center</s1><s2>45600-970 Itabuna-BA</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>CIRAD, UMR DAP, Avenue Agropolis TA96/03</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA20><s1>39-51</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>21598</s2><s5>354000172509120040</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/2</s0></fA45><fA47 i1="01" i2="1"><s0>09-0344557</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Molecular plant-microbe interactions</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>A pathogenesis-related (PR) protein from Theobroma cacao (TcPR-10) was identified from a cacao-Moniliophthora perniciosa interaction cDNA library. Nucleotide and amino acid sequences showed homology with other PR-10 proteins having P loop motif and Betv1 domain. Recombinant TcPR-10 showed in vitro and in vivo ribonuclease activity, and antifungal activity against the basidiomycete cacao pathogen M. perniciosa and the yeast Saccharomyces cerevisiae. Fluorescein isothiocyanate-labeled TcPR-10 was internalized by M. perniciosa hyphae and S. cerevisiae cells and inhibited growth of both fungi. Energy and temperature-dependent internalization of the TcPR-10 suggested an active importation into the fungal cells. Chronical exposure to TcPR-10 of 29 yeast mutants with single gene defects in DNA repair, general membrane transport, metal transport, and antioxidant defenses was tested. Two yeast mutants were hyperresistant compared with their respective isogenic wild type: ctr3Δ mutant, lacking the high-affinity plasma membrane copper transporter and mac1Δ, the copper-sensing transcription factor involved in regulation of high-affinity copper transport. Acute exposure of exponentially growing yeast cells revealed that TcPR-10 resistance is also enhanced in the Snq2 export permease-lacking mutant which has reduced intracellular presence of TcPR-10.</s0></fC01><fC02 i1="01" i2="X"><s0>002A34G</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Saccharomyces cerevisiae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Saccharomyces cerevisiae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Saccharomyces cerevisiae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Theobroma cacao</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Theobroma cacao</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Theobroma cacao</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Cytotoxicité</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Cytotoxicity</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Citotoxicidad</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Microbiologie</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Microbiology</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Microbiología</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Permease</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Permease</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Permease</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Ascomycota</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Ascomycota</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Ascomycota</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Fungi</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Fungi</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Fungi</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Sterculiaceae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Sterculiaceae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Sterculiaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Plante stimulante</s0><s5>13</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Stimulant plant</s0><s5>13</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Planta estimulante</s0><s5>13</s5></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Levure</s0><s5>16</s5></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Yeast</s0><s5>16</s5></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Levadura</s0><s5>16</s5></fC07><fN21><s1>250</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0344557 INIST</NO><ET>High-Affinity Copper Transport and Snq2 Export Permease of Saccharomyces cerevisiae Modulate Cytotoxicity of PR-10 from Theobroma cacao</ET><AU>PUNGARTNIK (Cristina); DA SILVA (Aline Clara); DE MELO (Sarah Alves); PERES GRAMACHO (Karina); DE MATTOS CASCARDO (Júlio Cézar); BRENDEL (Martin); MICHELI (Fabienne); DA SILVA GESTEIRA (Abelmon)</AU><AF>UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia de Fungos, Rodovia Ilhéus-Itabuna, km 16/45650-000 Ilhéus-BA/Brésil (1 aut., 3 aut., 6 aut.); UESC, Centro de Biotecnologia e Genética, Laboratório de Biologia Molecular, Rodovia Ilhéus-Itabuna, km 16/45650-000 Ilhéus-BA/Brésil (2 aut., 3 aut., 5 aut., 7 aut., 8 aut.); CEPLAC/CEPEC, Cocoa Research Center/45600-970 Itabuna-BA/Brésil (4 aut.); CIRAD, UMR DAP, Avenue Agropolis TA96/03/34398 Montpellier/France (7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Molecular plant-microbe interactions; ISSN 0894-0282; Coden MPMIEL; Etats-Unis; Da. 2009; Vol. 22; No. 1; Pp. 39-51; Bibl. 1 p.1/2</SO><LA>Anglais</LA><EA>A pathogenesis-related (PR) protein from Theobroma cacao (TcPR-10) was identified from a cacao-Moniliophthora perniciosa interaction cDNA library. Nucleotide and amino acid sequences showed homology with other PR-10 proteins having P loop motif and Betv1 domain. Recombinant TcPR-10 showed in vitro and in vivo ribonuclease activity, and antifungal activity against the basidiomycete cacao pathogen M. perniciosa and the yeast Saccharomyces cerevisiae. Fluorescein isothiocyanate-labeled TcPR-10 was internalized by M. perniciosa hyphae and S. cerevisiae cells and inhibited growth of both fungi. Energy and temperature-dependent internalization of the TcPR-10 suggested an active importation into the fungal cells. Chronical exposure to TcPR-10 of 29 yeast mutants with single gene defects in DNA repair, general membrane transport, metal transport, and antioxidant defenses was tested. Two yeast mutants were hyperresistant compared with their respective isogenic wild type: ctr3Δ mutant, lacking the high-affinity plasma membrane copper transporter and mac1Δ, the copper-sensing transcription factor involved in regulation of high-affinity copper transport. Acute exposure of exponentially growing yeast cells revealed that TcPR-10 resistance is also enhanced in the Snq2 export permease-lacking mutant which has reduced intracellular presence of TcPR-10.</EA><CC>002A34G</CC><FD>Saccharomyces cerevisiae; Theobroma cacao; Cytotoxicité; Microbiologie; Permease</FD><FG>Ascomycota; Fungi; Sterculiaceae; Dicotyledones; Angiospermae; Spermatophyta; Plante stimulante; Levure</FG><ED>Saccharomyces cerevisiae; Theobroma cacao; Cytotoxicity; Microbiology; Permease</ED><EG>Ascomycota; Fungi; Sterculiaceae; Dicotyledones; Angiospermae; Spermatophyta; Stimulant plant; Yeast</EG><SD>Saccharomyces cerevisiae; Theobroma cacao; Citotoxicidad; Microbiología; Permease</SD><LO>INIST-21598.354000172509120040</LO><ID>09-0344557</ID></server></inist></record>
000D22	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Magnetization reversal in bulk and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> perovskite</title><author><name sortKey="Pena, O" uniqKey="Pena O">O. Pena</name><affiliation><inist:fA14 i1="01"><s1>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes</s1><s2>35042 Rennes</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Guilloux Viry, M" uniqKey="Guilloux Viry M">M. Guilloux-Viry</name><affiliation><inist:fA14 i1="01"><s1>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes</s1><s2>35042 Rennes</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Antunes, A B" uniqKey="Antunes A">A. B. Antunes</name><affiliation><inist:fA14 i1="01"><s1>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes</s1><s2>35042 Rennes</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>GEMA, Centro Universitário FEEVALE</s1><s2>Novo Hamburgo, RS</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name>WEI PENG</name><affiliation><inist:fA14 i1="01"><s1>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes</s1><s2>35042 Rennes</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name>YANWEI MA</name><affiliation><inist:fA14 i1="03"><s1>Applied Superconductivity Laboratory, Institute of Electrical Engineering, CAS</s1><s2>Beijing</s2><s3>CHN</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name>ZHAOSHUN GAO</name><affiliation><inist:fA14 i1="03"><s1>Applied Superconductivity Laboratory, Institute of Electrical Engineering, CAS</s1><s2>Beijing</s2><s3>CHN</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Moure, C" uniqKey="Moure C">C. Moure</name><affiliation><inist:fA14 i1="04"><s1>Electrocerámicas, Instituto de Cerámica y Vidrio, CSIC</s1><s2>Madrid</s2><s3>ESP</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0344987</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0344987 INIST</idno><idno type="RBID">Pascal:09-0344987</idno><idno type="wicri:Area/Main/Corpus">001C59</idno></publicationStmt><seriesStmt><idno type="ISSN">0304-8853</idno><title level="j" type="abbreviated">J. magn. magn. mater.</title><title level="j" type="main">Journal of magnetism and magnetic materials</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cobalt Erbium Manganese Oxides Mixed</term><term>Epitaxial layers</term><term>Exchange interactions</term><term>Ferrimagnetic materials</term><term>Magnetic hysteresis</term><term>Magnetic properties</term><term>Magnetic thin films</term><term>Magnetization</term><term>Magnetization reversal</term><term>Perovskites</term><term>Pulsed laser deposition</term><term>Scanning electron microscopy</term><term>Solid state reaction</term><term>Spin reversal</term><term>Sublattices</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Inversion aimantation</term><term>Propriété magnétique</term><term>Microscopie électronique balayage</term><term>Dépôt laser pulsé</term><term>Réaction état solide</term><term>Renversement spin</term><term>Sous réseau</term><term>Interaction échange</term><term>Hystérésis magnétique</term><term>Aimantation</term><term>Cobalt Erbium Manganèse Oxyde Mixte</term><term>Matériau ferrimagnétique</term><term>Perovskites</term><term>Couche épitaxique</term><term>Couche mince magnétique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We present herein a comparison of the magnetic properties of bulk ceramics and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> compound. Epitaxial thin films were deposited onto (100) SrTiO<sub>3</sub> substrates by pulsed-laser ablation while bulk ceramics were prepared by solid state reaction. When cooling under low applied fields, a spin reversal is observed in both thin film and bulk due to the competition between two magnetic sublattices (Co/Mn and Er) coupled by a negative exchange interaction. Original features are observed in the M(H) loops for bulk materials: abrupt jumps at 4T due to a reorientation of domains, while in the low field region, the increasing and decreasing branches of the magnetization intersect each other. In the thin film, the ordering temperature increased from 69 to 75 K, and the ZFC anomaly (AF transition) became sharper, compared to the bulk specimen. The oxygen content and the microstructure are crucial to observe the intersection of the magnetization branches.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0304-8853</s0></fA01><fA02 i1="01"><s0>JMMMDC</s0></fA02><fA03 i2="1"><s0>J. magn. magn. mater.</s0></fA03><fA05><s2>321</s2></fA05><fA06><s2>11</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Magnetization reversal in bulk and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> perovskite</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Selected papers from the E-MRS Spring Meeting 2008. Symposium F.: Multiferroics and Magnetoelectrics Materials, May 26-30, 2008, Strasbourg, France</s1></fA09><fA11 i1="01" i2="1"><s1>PENA (O.)</s1></fA11><fA11 i1="02" i2="1"><s1>GUILLOUX-VIRY (M.)</s1></fA11><fA11 i1="03" i2="1"><s1>ANTUNES (A. B.)</s1></fA11><fA11 i1="04" i2="1"><s1>WEI PENG</s1></fA11><fA11 i1="05" i2="1"><s1>YANWEI MA</s1></fA11><fA11 i1="06" i2="1"><s1>ZHAOSHUN GAO</s1></fA11><fA11 i1="07" i2="1"><s1>MOURE (C.)</s1></fA11><fA12 i1="01" i2="1"><s1>DUBOURDIEU (Catherine)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>PRELLIER (Wilfrid)</s1><s9>ed.</s9></fA12><fA12 i1="03" i2="1"><s1>MATHUR (Neil)</s1><s9>ed.</s9></fA12><fA12 i1="04" i2="1"><s1>PIGNOLET (Alain)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes</s1><s2>35042 Rennes</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>GEMA, Centro Universitário FEEVALE</s1><s2>Novo Hamburgo, RS</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Applied Superconductivity Laboratory, Institute of Electrical Engineering, CAS</s1><s2>Beijing</s2><s3>CHN</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="04"><s1>Electrocerámicas, Instituto de Cerámica y Vidrio, CSIC</s1><s2>Madrid</s2><s3>ESP</s3><sZ>7 aut.</sZ></fA14><fA15 i1="01"><s1>LMGP-Grenoble</s1><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Laboratoire CRISMAT-Caen</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA15 i1="03"><s1>University of Cambridge</s1><s2>Cambridge</s2><s3>GBR</s3><sZ>3 aut.</sZ></fA15><fA15 i1="04"><s1>INRS - Université du Québec</s1><s2>Varennes</s2><s3>CAN</s3><sZ>4 aut.</sZ></fA15><fA20><s1>1723-1726</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>17230</s2><s5>354000187889280090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>17 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0344987</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of magnetism and magnetic materials</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>We present herein a comparison of the magnetic properties of bulk ceramics and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> compound. Epitaxial thin films were deposited onto (100) SrTiO<sub>3</sub> substrates by pulsed-laser ablation while bulk ceramics were prepared by solid state reaction. When cooling under low applied fields, a spin reversal is observed in both thin film and bulk due to the competition between two magnetic sublattices (Co/Mn and Er) coupled by a negative exchange interaction. Original features are observed in the M(H) loops for bulk materials: abrupt jumps at 4T due to a reorientation of domains, while in the low field region, the increasing and decreasing branches of the magnetization intersect each other. In the thin film, the ordering temperature increased from 69 to 75 K, and the ZFC anomaly (AF transition) became sharper, compared to the bulk specimen. The oxygen content and the microstructure are crucial to observe the intersection of the magnetization branches.</s0></fC01><fC02 i1="01" i2="3"><s0>001B70E70A</s0></fC02><fC02 i1="02" i2="3"><s0>001B70E60E</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Inversion aimantation</s0><s5>02</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Magnetization reversal</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Propriété magnétique</s0><s5>03</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Magnetic properties</s0><s5>03</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Microscopie électronique balayage</s0><s5>04</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Scanning electron microscopy</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Dépôt laser pulsé</s0><s5>05</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Pulsed laser deposition</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Réaction état solide</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Solid state reaction</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Reacción estado sólido</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Renversement spin</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Spin reversal</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Inversión espín</s0><s5>09</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Sous réseau</s0><s5>10</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Sublattices</s0><s5>10</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Interaction échange</s0><s5>11</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Exchange interactions</s0><s5>11</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Hystérésis magnétique</s0><s5>12</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Magnetic hysteresis</s0><s5>12</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Aimantation</s0><s5>13</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Magnetization</s0><s5>13</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Cobalt Erbium Manganèse Oxyde Mixte</s0><s2>NC</s2><s2>NA</s2><s5>14</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Cobalt Erbium Manganese Oxides Mixed</s0><s2>NC</s2><s2>NA</s2><s5>14</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Mixto</s0><s2>NC</s2><s2>NA</s2><s5>14</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Matériau ferrimagnétique</s0><s5>16</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Ferrimagnetic materials</s0><s5>16</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Perovskites</s0><s5>17</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Perovskites</s0><s5>17</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Couche épitaxique</s0><s5>18</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Epitaxial layers</s0><s5>18</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>Couche mince magnétique</s0><s5>21</s5></fC03><fC03 i1="15" i2="3" l="ENG"><s0>Magnetic thin films</s0><s5>21</s5></fC03><fN21><s1>250</s1></fN21></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Symposium F.: Multiferroics and Magnetoelectrics Materials</s1><s3>Strasbourg FRA</s3><s4>2008-05-26</s4></fA30></pR></standard><server><NO>PASCAL 09-0344987 INIST</NO><ET>Magnetization reversal in bulk and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> perovskite</ET><AU>PENA (O.); GUILLOUX-VIRY (M.); ANTUNES (A. B.); WEI PENG; YANWEI MA; ZHAOSHUN GAO; MOURE (C.); DUBOURDIEU (Catherine); PRELLIER (Wilfrid); MATHUR (Neil); PIGNOLET (Alain)</AU><AF>Sciences Chimiques, UMR 6226, Université de Rennes 1, Rennes/35042 Rennes/France (1 aut., 2 aut., 3 aut., 4 aut.); GEMA, Centro Universitário FEEVALE/Novo Hamburgo, RS/Brésil (3 aut.); Applied Superconductivity Laboratory, Institute of Electrical Engineering, CAS/Beijing/Chine (5 aut., 6 aut.); Electrocerámicas, Instituto de Cerámica y Vidrio, CSIC/Madrid/Espagne (7 aut.); LMGP-Grenoble/France (1 aut.); Laboratoire CRISMAT-Caen/France (2 aut.); University of Cambridge/Cambridge/Royaume-Uni (3 aut.); INRS - Université du Québec/Varennes/Canada (4 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Journal of magnetism and magnetic materials; ISSN 0304-8853; Coden JMMMDC; Pays-Bas; Da. 2009; Vol. 321; No. 11; Pp. 1723-1726; Bibl. 17 ref.</SO><LA>Anglais</LA><EA>We present herein a comparison of the magnetic properties of bulk ceramics and thin films of the ferrimagnetic ErCo<sub>0.50</sub>Mn<sub>0.50</sub>O<sub>3</sub> compound. Epitaxial thin films were deposited onto (100) SrTiO<sub>3</sub> substrates by pulsed-laser ablation while bulk ceramics were prepared by solid state reaction. When cooling under low applied fields, a spin reversal is observed in both thin film and bulk due to the competition between two magnetic sublattices (Co/Mn and Er) coupled by a negative exchange interaction. Original features are observed in the M(H) loops for bulk materials: abrupt jumps at 4T due to a reorientation of domains, while in the low field region, the increasing and decreasing branches of the magnetization intersect each other. In the thin film, the ordering temperature increased from 69 to 75 K, and the ZFC anomaly (AF transition) became sharper, compared to the bulk specimen. The oxygen content and the microstructure are crucial to observe the intersection of the magnetization branches.</EA><CC>001B70E70A; 001B70E60E</CC><FD>Inversion aimantation; Propriété magnétique; Microscopie électronique balayage; Dépôt laser pulsé; Réaction état solide; Renversement spin; Sous réseau; Interaction échange; Hystérésis magnétique; Aimantation; Cobalt Erbium Manganèse Oxyde Mixte; Matériau ferrimagnétique; Perovskites; Couche épitaxique; Couche mince magnétique</FD><ED>Magnetization reversal; Magnetic properties; Scanning electron microscopy; Pulsed laser deposition; Solid state reaction; Spin reversal; Sublattices; Exchange interactions; Magnetic hysteresis; Magnetization; Cobalt Erbium Manganese Oxides Mixed; Ferrimagnetic materials; Perovskites; Epitaxial layers; Magnetic thin films</ED><SD>Reacción estado sólido; Inversión espín; Mixto</SD><LO>INIST-17230.354000187889280090</LO><ID>09-0344987</ID></server></inist></record>
000D23	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">CNONa and <sup>12</sup>C/<sup>13</sup>C in giant stars of 10 open clusters</title><author><name sortKey="Smiljanic, R" uniqKey="Smiljanic R">R. Smiljanic</name><affiliation><inist:fA14 i1="01"><s1>Universidade de São Paulo, IAG, Rua do Matao 1226, Cidade Universitária</s1><s2>05508-090, São Paulo, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gauderon, R" uniqKey="Gauderon R">R. Gauderon</name><affiliation><inist:fA14 i1="02"><s1>Laboratoire d'astrophysique, École Polytechnique Fédérale de Lausanne (EPFL), Observatoire de Sauverny</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="North, P" uniqKey="North P">P. North</name><affiliation><inist:fA14 i1="02"><s1>Laboratoire d'astrophysique, École Polytechnique Fédérale de Lausanne (EPFL), Observatoire de Sauverny</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Barbuy, B" uniqKey="Barbuy B">B. Barbuy</name><affiliation><inist:fA14 i1="01"><s1>Universidade de São Paulo, IAG, Rua do Matao 1226, Cidade Universitária</s1><s2>05508-090, São Paulo, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Charbonnel, C" uniqKey="Charbonnel C">C. Charbonnel</name><affiliation><inist:fA14 i1="03"><s1>Geneva Observatory, University of Geneva, Chemin des Maillettes 51</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>5 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>LATT, CNRS UMR 5572, Université de Toulouse, 14 avenue Edouard Belin</s1><s2>31400 Toulouse</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mowlavi, N" uniqKey="Mowlavi N">N. Mowlavi</name><affiliation><inist:fA14 i1="05"><s1>Observatoire de Genève, Integral Science Data Center, Chemin d'Ecogia 16</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0345964</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0345964 INIST</idno><idno type="RBID">Pascal:09-0345964</idno><idno type="wicri:Area/Main/Corpus">001C58</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Asymptotic giant branch</term><term>Atmosphere model</term><term>Convection</term><term>Correlations</term><term>Equivalent width</term><term>Giant stars</term><term>Low-mass stars</term><term>Metallicity</term><term>Mixing</term><term>Mixing process</term><term>Open clusters</term><term>Red giant stars</term><term>Signal-to-noise ratio</term><term>Star clusters</term><term>Stellar abundance</term><term>Stellar evolution</term><term>Stellar mass</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Etoile géante</term><term>Amas ouvert</term><term>Etoile faible masse</term><term>Métallicité</term><term>Mélangeage</term><term>Abondance stellaire</term><term>Convection</term><term>Géante rouge</term><term>Branche géante asymptotique</term><term>Corrélation</term><term>Masse stellaire</term><term>Modèle atmosphère</term><term>Rapport signal bruit</term><term>Largeur équivalente</term><term>Processus mélangeant</term><term>Evolution stellaire</term><term>Amas stellaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Context. Evolved low-mass stars (0.8 ≤ M/M<sub>◦.</sub> ≤ 2.5) of a wide range of metallicity bear signatures of a non-standard mixing event in their surface abundances of Li, C, and N, and in their <sup>12</sup>C/<sup>13</sup>C ratio. A Na overabundance has also been reported in some giants of open clusters but remains controversial. The cause of the extra-mixing has been attributed to thermohaline convection that should take place after the RGB bump for low-mass stars and on the early-AGB for more massive objects. Aims. To track the occurrence of this process over a wide mass range, we derive in a homogeneous way the abundances of C, N, O, and Na, as well as the <sup>12</sup>C/<sup>13</sup>C ratio in a sample of 31 giants of 10 open clusters with turn-off masses from 1.7 to 3.1 M<sub>◦.</sub>. The sample includes red giants, clump giants, and early-AGB stars. We study the observational behavior of the abundances as well as the possible correlations between different elements and between the chemical abundances and stellar mass. Methods. A model atmosphere analysis is conducted using high signal-to-noise ratio, high-resolution FEROS and EMMI spectra. We derive atmospheric parameters using Fe and Fe II lines. We calculate abundances for Na, C, N, and O, as well as the <sup>12</sup>C/<sup>13</sup>C ratio using spectral synthesis. For the elements Mg, Ca, Si, Sc, Ti, V, Cr, Co, and Ni, abundances are derived using equivalent widths. Results. A group of first ascent red giants with M/M<sub>◦.</sub> ≤ 2.5 exhibits lower [N/C] ratios than those measured in clump giants of the same mass range, suggesting an additional increase in the [N/C] ratio after the first dredge-up. The sodium abundances corrected from NLTE are found to be about solar. [Na/Fe] shows a slight increase of 0.10 dex as a function of stellar mass in the 1.8 to 3.2 M<sub>◦.</sub> range covered by our sample, in agreement with standard first dredge-up predictions. Our results do not support previous claims of sodium overabundances as high as +0.60 dex. An anti-correlation between <sup>12</sup>C/<sup>13</sup>C and turn-off mass is identified and interpreted as being caused by a post-bump thermohaline mixing. Moreover, we find low <sup>12</sup>C/<sup>13</sup>C ratios in a few intermediate-mass early-AGB stars, confirming that an extra-mixing process also operates in stars that do not experienced the RGB bump. In this case, the extra-mixing possibly acts on the early-AGB, in agreement with theoretical expectations for thermohaline mixing.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>502</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>CNONa and <sup>12</sup>C/<sup>13</sup>C in giant stars of 10 open clusters</s1></fA08><fA11 i1="01" i2="1"><s1>SMILJANIC (R.)</s1></fA11><fA11 i1="02" i2="1"><s1>GAUDERON (R.)</s1></fA11><fA11 i1="03" i2="1"><s1>NORTH (P.)</s1></fA11><fA11 i1="04" i2="1"><s1>BARBUY (B.)</s1></fA11><fA11 i1="05" i2="1"><s1>CHARBONNEL (C.)</s1></fA11><fA11 i1="06" i2="1"><s1>MOWLAVI (N.)</s1></fA11><fA14 i1="01"><s1>Universidade de São Paulo, IAG, Rua do Matao 1226, Cidade Universitária</s1><s2>05508-090, São Paulo, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Laboratoire d'astrophysique, École Polytechnique Fédérale de Lausanne (EPFL), Observatoire de Sauverny</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Geneva Observatory, University of Geneva, Chemin des Maillettes 51</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>LATT, CNRS UMR 5572, Université de Toulouse, 14 avenue Edouard Belin</s1><s2>31400 Toulouse</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Observatoire de Genève, Integral Science Data Center, Chemin d'Ecogia 16</s1><s2>1290 Versoix</s2><s3>CHE</s3><sZ>6 aut.</sZ></fA14><fA20><s1>267-282</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000170870170240</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0345964</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Context. Evolved low-mass stars (0.8 ≤ M/M<sub>◦.</sub> ≤ 2.5) of a wide range of metallicity bear signatures of a non-standard mixing event in their surface abundances of Li, C, and N, and in their <sup>12</sup>C/<sup>13</sup>C ratio. A Na overabundance has also been reported in some giants of open clusters but remains controversial. The cause of the extra-mixing has been attributed to thermohaline convection that should take place after the RGB bump for low-mass stars and on the early-AGB for more massive objects. Aims. To track the occurrence of this process over a wide mass range, we derive in a homogeneous way the abundances of C, N, O, and Na, as well as the <sup>12</sup>C/<sup>13</sup>C ratio in a sample of 31 giants of 10 open clusters with turn-off masses from 1.7 to 3.1 M<sub>◦.</sub>. The sample includes red giants, clump giants, and early-AGB stars. We study the observational behavior of the abundances as well as the possible correlations between different elements and between the chemical abundances and stellar mass. Methods. A model atmosphere analysis is conducted using high signal-to-noise ratio, high-resolution FEROS and EMMI spectra. We derive atmospheric parameters using Fe and Fe II lines. We calculate abundances for Na, C, N, and O, as well as the <sup>12</sup>C/<sup>13</sup>C ratio using spectral synthesis. For the elements Mg, Ca, Si, Sc, Ti, V, Cr, Co, and Ni, abundances are derived using equivalent widths. Results. A group of first ascent red giants with M/M<sub>◦.</sub> ≤ 2.5 exhibits lower [N/C] ratios than those measured in clump giants of the same mass range, suggesting an additional increase in the [N/C] ratio after the first dredge-up. The sodium abundances corrected from NLTE are found to be about solar. [Na/Fe] shows a slight increase of 0.10 dex as a function of stellar mass in the 1.8 to 3.2 M<sub>◦.</sub> range covered by our sample, in agreement with standard first dredge-up predictions. Our results do not support previous claims of sodium overabundances as high as +0.60 dex. An anti-correlation between <sup>12</sup>C/<sup>13</sup>C and turn-off mass is identified and interpreted as being caused by a post-bump thermohaline mixing. Moreover, we find low <sup>12</sup>C/<sup>13</sup>C ratios in a few intermediate-mass early-AGB stars, confirming that an extra-mixing process also operates in stars that do not experienced the RGB bump. In this case, the extra-mixing possibly acts on the early-AGB, in agreement with theoretical expectations for thermohaline mixing.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Etoile géante</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Giant stars</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Amas ouvert</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Open clusters</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Etoile faible masse</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Low-mass stars</s0><s5>28</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Métallicité</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Metallicity</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Metalicidad</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Mélangeage</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Mixing</s0><s5>30</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Abondance stellaire</s0><s5>31</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Stellar abundance</s0><s5>31</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Abundancia estelar</s0><s5>31</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Convection</s0><s5>32</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Convection</s0><s5>32</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Géante rouge</s0><s5>33</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Red giant stars</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Branche géante asymptotique</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Asymptotic giant branch</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Rama gigante asintótica</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Corrélation</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Correlations</s0><s5>35</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Masse stellaire</s0><s5>36</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Stellar mass</s0><s5>36</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Modèle atmosphère</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Atmosphere model</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Modelo atmósfera</s0><s5>37</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Rapport signal bruit</s0><s5>38</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Signal-to-noise ratio</s0><s5>38</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Largeur équivalente</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Equivalent width</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Anchura equivalente</s0><s5>39</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Processus mélangeant</s0><s5>40</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Mixing process</s0><s5>40</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Proceso mezclante</s0><s5>40</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Evolution stellaire</s0><s5>41</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Stellar evolution</s0><s5>41</s5></fC03><fC03 i1="17" i2="3" l="FRE"><s0>Amas stellaire</s0><s5>42</s5></fC03><fC03 i1="17" i2="3" l="ENG"><s0>Star clusters</s0><s5>42</s5></fC03><fN21><s1>250</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0345964 INIST</NO><ET>CNONa and <sup>12</sup>C/<sup>13</sup>C in giant stars of 10 open clusters</ET><AU>SMILJANIC (R.); GAUDERON (R.); NORTH (P.); BARBUY (B.); CHARBONNEL (C.); MOWLAVI (N.)</AU><AF>Universidade de São Paulo, IAG, Rua do Matao 1226, Cidade Universitária/05508-090, São Paulo, SP/Brésil (1 aut., 4 aut.); Laboratoire d'astrophysique, École Polytechnique Fédérale de Lausanne (EPFL), Observatoire de Sauverny/1290 Versoix/Suisse (2 aut., 3 aut.); Geneva Observatory, University of Geneva, Chemin des Maillettes 51/1290 Versoix/Suisse (5 aut.); LATT, CNRS UMR 5572, Université de Toulouse, 14 avenue Edouard Belin/31400 Toulouse/France (5 aut.); Observatoire de Genève, Integral Science Data Center, Chemin d'Ecogia 16/1290 Versoix/Suisse (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 502; No. 1; Pp. 267-282; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Context. Evolved low-mass stars (0.8 ≤ M/M<sub>◦.</sub> ≤ 2.5) of a wide range of metallicity bear signatures of a non-standard mixing event in their surface abundances of Li, C, and N, and in their <sup>12</sup>C/<sup>13</sup>C ratio. A Na overabundance has also been reported in some giants of open clusters but remains controversial. The cause of the extra-mixing has been attributed to thermohaline convection that should take place after the RGB bump for low-mass stars and on the early-AGB for more massive objects. Aims. To track the occurrence of this process over a wide mass range, we derive in a homogeneous way the abundances of C, N, O, and Na, as well as the <sup>12</sup>C/<sup>13</sup>C ratio in a sample of 31 giants of 10 open clusters with turn-off masses from 1.7 to 3.1 M<sub>◦.</sub>. The sample includes red giants, clump giants, and early-AGB stars. We study the observational behavior of the abundances as well as the possible correlations between different elements and between the chemical abundances and stellar mass. Methods. A model atmosphere analysis is conducted using high signal-to-noise ratio, high-resolution FEROS and EMMI spectra. We derive atmospheric parameters using Fe and Fe II lines. We calculate abundances for Na, C, N, and O, as well as the <sup>12</sup>C/<sup>13</sup>C ratio using spectral synthesis. For the elements Mg, Ca, Si, Sc, Ti, V, Cr, Co, and Ni, abundances are derived using equivalent widths. Results. A group of first ascent red giants with M/M<sub>◦.</sub> ≤ 2.5 exhibits lower [N/C] ratios than those measured in clump giants of the same mass range, suggesting an additional increase in the [N/C] ratio after the first dredge-up. The sodium abundances corrected from NLTE are found to be about solar. [Na/Fe] shows a slight increase of 0.10 dex as a function of stellar mass in the 1.8 to 3.2 M<sub>◦.</sub> range covered by our sample, in agreement with standard first dredge-up predictions. Our results do not support previous claims of sodium overabundances as high as +0.60 dex. An anti-correlation between <sup>12</sup>C/<sup>13</sup>C and turn-off mass is identified and interpreted as being caused by a post-bump thermohaline mixing. Moreover, we find low <sup>12</sup>C/<sup>13</sup>C ratios in a few intermediate-mass early-AGB stars, confirming that an extra-mixing process also operates in stars that do not experienced the RGB bump. In this case, the extra-mixing possibly acts on the early-AGB, in agreement with theoretical expectations for thermohaline mixing.</EA><CC>001E03</CC><FD>Etoile géante; Amas ouvert; Etoile faible masse; Métallicité; Mélangeage; Abondance stellaire; Convection; Géante rouge; Branche géante asymptotique; Corrélation; Masse stellaire; Modèle atmosphère; Rapport signal bruit; Largeur équivalente; Processus mélangeant; Evolution stellaire; Amas stellaire</FD><ED>Giant stars; Open clusters; Low-mass stars; Metallicity; Mixing; Stellar abundance; Convection; Red giant stars; Asymptotic giant branch; Correlations; Stellar mass; Atmosphere model; Signal-to-noise ratio; Equivalent width; Mixing process; Stellar evolution; Star clusters</ED><SD>Metalicidad; Abundancia estelar; Rama gigante asintótica; Modelo atmósfera; Anchura equivalente; Proceso mezclante</SD><LO>INIST-14176.354000170870170240</LO><ID>09-0345964</ID></server></inist></record>
000D24	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">POLITIQUES D'INFORMATION FACE AUX NOUVEAUX PARADIGMES: LES NOUVELLES TECHNOLOGIES DE L'INFORMATION ET DE LA COMMUNICATION ET LES CONTENUS CULTURELS</title><author><name sortKey="Pinheiro Aun, Marta" uniqKey="Pinheiro Aun M">Marta Pinheiro Aun</name><affiliation><inist:fA14 i1="01"><s1>Information Escola Ciência da Informação Universidade Federal de Minas Gerais</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0348018</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0348018 INIST</idno><idno type="RBID">Pascal:09-0348018</idno><idno type="wicri:Area/Main/Corpus">001C57</idno><idno type="stanalyst">FRANCIS 09-0348018 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">1635-6187</idno><title level="j" type="main">Collection Perspectives Villes et Territoires</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Communication</term><term>Information communication technology</term><term>Information policy</term><term>Information science</term><term>Information society</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Technologie information communication</term><term>Politique information</term><term>Science information</term><term>Communication</term><term>Société information</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Le développement des technologies de l'information et de la communication a transformé toute l'activité humaine, individuelle et collective, ce qui nous oblige à repenser les politiques d'information donc, les processus de construction précédemment liés au développement de la science et la technologie. Ces dernières ont fait naître récemment une confrontation interdisciplinaire. Elle nous conduit à une discussion nécessaire et urgente en Science de l'Information, sur les relations entre l'État, les technologies et la culture. Cette communication, se focalisant sur la formation à la compétence informationnelle, nécessaire à la participation à la société de l'information, vise à mettre au jour les limites du processus en cours de la construction des nouvelles politiques d'information et de son importance comme champ de recherche en Science de l'information. Cette recherche met en relief cinq points de discussion: le changement structurel de l'État et le rôle de l'économie mondiale ; la convergence des technologies de l'information et de la communication et son influence sur le processus de construction de politiques d'information ; les différentiels culturels de l'information et leur expression dans les politiques de contenu ; l'occasion d'inclusion ou le risque d'exclusion dans la Société de l'Information et finalement, le nouveau format des politiques d'information.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1635-6187</s0></fA01><fA05><s2>n.19</s2></fA05><fA08 i1="01" i2="1" l="FRE"><s1>POLITIQUES D'INFORMATION FACE AUX NOUVEAUX PARADIGMES: LES NOUVELLES TECHNOLOGIES DE L'INFORMATION ET DE LA COMMUNICATION ET LES CONTENUS CULTURELS</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité</s1></fA09><fA11 i1="01" i2="1"><s1>PINHEIRO AUN (Marta)</s1></fA11><fA12 i1="01" i2="1"><s1>VOLANT (Christiane)</s1><s9>dir. publ.</s9></fA12><fA14 i1="01"><s1>Information Escola Ciência da Informação Universidade Federal de Minas Gerais</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA18 i1="01" i2="1"><s1>Centre d'étude du débat public et des médiations</s1><s2>Tours</s2><s3>FRA</s3><s9>org-cong.</s9></fA18><fA20><s1>201-214</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA25 i1="01"><s1>Presses universitaires F. Rabelais</s1><s2>Tours</s2></fA25><fA26 i1="01"><s0>978-2-86906-239-9</s0></fA26><fA43 i1="01"><s1>INIST</s1><s2>Y 39288</s2><s5>354000182452750150</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/2</s0></fA45><fA47 i1="01" i2="1"><s0>09-0348018</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="2"><s0>Collection Perspectives Villes et Territoires</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>Le développement des technologies de l'information et de la communication a transformé toute l'activité humaine, individuelle et collective, ce qui nous oblige à repenser les politiques d'information donc, les processus de construction précédemment liés au développement de la science et la technologie. Ces dernières ont fait naître récemment une confrontation interdisciplinaire. Elle nous conduit à une discussion nécessaire et urgente en Science de l'Information, sur les relations entre l'État, les technologies et la culture. Cette communication, se focalisant sur la formation à la compétence informationnelle, nécessaire à la participation à la société de l'information, vise à mettre au jour les limites du processus en cours de la construction des nouvelles politiques d'information et de son importance comme champ de recherche en Science de l'information. Cette recherche met en relief cinq points de discussion: le changement structurel de l'État et le rôle de l'économie mondiale ; la convergence des technologies de l'information et de la communication et son influence sur le processus de construction de politiques d'information ; les différentiels culturels de l'information et leur expression dans les politiques de contenu ; l'occasion d'inclusion ou le risque d'exclusion dans la Société de l'Information et finalement, le nouveau format des politiques d'information.</s0></fC01><fC02 i1="01" i2="X"><s0>001A01A03</s0></fC02><fC02 i1="02" i2="X"><s0>001A01A06A</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Technologie information communication</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Information communication technology</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Nueva tecnología información comunicación</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Politique information</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Information policy</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Política información</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Science information</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Information science</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Ciencia información</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Communication</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Communication</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Comunicación</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Société information</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Information society</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Sociedad información</s0><s5>08</s5></fC03><fN21><s1>250</s1></fN21></pA><pR><fA30 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité. Colloque international</s1><s3>Tours FRA</s3><s4>2006-04-06</s4></fA30></pR></standard><server><NO>PASCAL 09-0348018 INIST</NO><FT>POLITIQUES D'INFORMATION FACE AUX NOUVEAUX PARADIGMES: LES NOUVELLES TECHNOLOGIES DE L'INFORMATION ET DE LA COMMUNICATION ET LES CONTENUS CULTURELS</FT><AU>PINHEIRO AUN (Marta); VOLANT (Christiane)</AU><AF>Information Escola Ciência da Informação Universidade Federal de Minas Gerais/Brésil (1 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Collection Perspectives Villes et Territoires; ISSN 1635-6187; France; Da. 2008; Vol. n.19; Pp. 201-214; Abs. anglais; Bibl. 1 p.1/2</SO><LA>Français</LA><FA>Le développement des technologies de l'information et de la communication a transformé toute l'activité humaine, individuelle et collective, ce qui nous oblige à repenser les politiques d'information donc, les processus de construction précédemment liés au développement de la science et la technologie. Ces dernières ont fait naître récemment une confrontation interdisciplinaire. Elle nous conduit à une discussion nécessaire et urgente en Science de l'Information, sur les relations entre l'État, les technologies et la culture. Cette communication, se focalisant sur la formation à la compétence informationnelle, nécessaire à la participation à la société de l'information, vise à mettre au jour les limites du processus en cours de la construction des nouvelles politiques d'information et de son importance comme champ de recherche en Science de l'information. Cette recherche met en relief cinq points de discussion: le changement structurel de l'État et le rôle de l'économie mondiale ; la convergence des technologies de l'information et de la communication et son influence sur le processus de construction de politiques d'information ; les différentiels culturels de l'information et leur expression dans les politiques de contenu ; l'occasion d'inclusion ou le risque d'exclusion dans la Société de l'Information et finalement, le nouveau format des politiques d'information.</FA><CC>001A01A03; 001A01A06A</CC><FD>Technologie information communication; Politique information; Science information; Communication; Société information</FD><ED>Information communication technology; Information policy; Information science; Communication; Information society</ED><SD>Nueva tecnología información comunicación; Política información; Ciencia información; Comunicación; Sociedad información</SD><LO>INIST-Y 39288.354000182452750150</LO><ID>09-0348018</ID></server></inist></record>
000D25	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">LA RECHERCHE EN SCIENCES DE L'INFORMATION AU BRÉSIL: MARQUES INSTITUTIONNELLES, SCÉNARIOS ET PERSPECTIVES</title><author><name sortKey="Maria Marteleto, Regina" uniqKey="Maria Marteleto R">Regina Maria Marteleto</name><affiliation><inist:fA14 i1="01"><s1>CNPq - Conseil National de Développement Scientifique et Technique et ANCIB - Association Nationale de Recherche et Post-Graduation en Sciences de l'Information</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0348032</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0348032 INIST</idno><idno type="RBID">Pascal:09-0348032</idno><idno type="wicri:Area/Main/Corpus">001C56</idno><idno type="stanalyst">FRANCIS 09-0348032 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">1635-6187</idno><title level="j" type="main">Collection Perspectives Villes et Territoires</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Formation</term><term>Higher education</term><term>Information policy</term><term>Information science</term><term>Scientific research</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Brésil</term><term>Recherche scientifique</term><term>Science information</term><term>Enseignement supérieur</term><term>Formation</term><term>Politique information</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1635-6187</s0></fA01><fA05><s2>n.19</s2></fA05><fA08 i1="01" i2="1" l="FRE"><s1>LA RECHERCHE EN SCIENCES DE L'INFORMATION AU BRÉSIL: MARQUES INSTITUTIONNELLES, SCÉNARIOS ET PERSPECTIVES</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité</s1></fA09><fA11 i1="01" i2="1"><s1>MARIA MARTELETO (Regina)</s1></fA11><fA12 i1="01" i2="1"><s1>VOLANT (Christiane)</s1><s9>dir. publ.</s9></fA12><fA14 i1="01"><s1>CNPq - Conseil National de Développement Scientifique et Technique et ANCIB - Association Nationale de Recherche et Post-Graduation en Sciences de l'Information</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA18 i1="01" i2="1"><s1>Centre d'étude du débat public et des médiations</s1><s2>Tours</s2><s3>FRA</s3><s9>org-cong.</s9></fA18><fA20><s1>31-48</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA25 i1="01"><s1>Presses universitaires F. Rabelais</s1><s2>Tours</s2></fA25><fA26 i1="01"><s0>978-2-86906-239-9</s0></fA26><fA43 i1="01"><s1>INIST</s1><s2>Y 39288</s2><s5>354000182452750020</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0348032</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="2"><s0>Collection Perspectives Villes et Territoires</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC02 i1="01" i2="X"><s0>001A01A04</s0></fC02><fC02 i1="02" i2="X"><s0>001A01A06A</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Recherche scientifique</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Scientific research</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Investigación científica</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Science information</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Information science</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Ciencia información</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Enseignement supérieur</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Higher education</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Enseñanza superior</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Formation</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Formation</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Formación</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Politique information</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Information policy</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Política información</s0><s5>08</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>250</s1></fN21></pA><pR><fA30 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité. Colloque international</s1><s3>Tours FRA</s3><s4>2006-04-06</s4></fA30></pR></standard><server><NO>PASCAL 09-0348032 INIST</NO><FT>LA RECHERCHE EN SCIENCES DE L'INFORMATION AU BRÉSIL: MARQUES INSTITUTIONNELLES, SCÉNARIOS ET PERSPECTIVES</FT><AU>MARIA MARTELETO (Regina); VOLANT (Christiane)</AU><AF>CNPq - Conseil National de Développement Scientifique et Technique et ANCIB - Association Nationale de Recherche et Post-Graduation en Sciences de l'Information/Brésil (1 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Collection Perspectives Villes et Territoires; ISSN 1635-6187; France; Da. 2008; Vol. n.19; Pp. 31-48; Bibl. 1 p.</SO><LA>Français</LA><CC>001A01A04; 001A01A06A</CC><FD>Brésil; Recherche scientifique; Science information; Enseignement supérieur; Formation; Politique information</FD><FG>Amérique du Sud; Amérique</FG><ED>Brazil; Scientific research; Information science; Higher education; Formation; Information policy</ED><EG>South America; America</EG><SD>Brasil; Investigación científica; Ciencia información; Enseñanza superior; Formación; Política información</SD><LO>INIST-Y 39288.354000182452750020</LO><ID>09-0348032</ID></server></inist></record>
000D26	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">INFORMATION ET IDENTITÉ DANS LA PRODUCTION DE LA CONNAISSANCE: REPRÉSENTATION MÉTAPHORIQUE DANS UN RÉSEAU DE RECHERCHE</title><author><name sortKey="Dill Orrico, Evelyn Goyannes" uniqKey="Dill Orrico E">Evelyn Goyannes Dill Orrico</name><affiliation><inist:fA14 i1="01"><s1>Information IBICT/UFRJ Universidade Federal do Estado do Rio de Janeiro - UNIRIO Professeur Adjoint</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Correia De Olvieira, Carmen" uniqKey="Correia De Olvieira C">Carmen Correia De Olvieira</name><affiliation><inist:fA14 i1="02"><s1>Information IBICT/UFF Universidade Federal do Estado do Rio de Janeiro - UNIRIO Assistant administratif / Chercheuse du Groupe de recherche Mémoire et Discours</s1><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0348037</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0348037 INIST</idno><idno type="RBID">Pascal:09-0348037</idno><idno type="wicri:Area/Main/Corpus">001C55</idno><idno type="stanalyst">FRANCIS 09-0348037 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">1635-6187</idno><title level="j" type="main">Collection Perspectives Villes et Territoires</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Case study</term><term>Discourse analysis</term><term>Information communication technology</term><term>Information representation</term><term>Metaphor</term><term>Network</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Analyse discours</term><term>Métaphore</term><term>Technologie information communication</term><term>Etude cas</term><term>Représentation information</term><term>Réseau</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">De nos jours, les nouvelles technologies rendent viables des situations ambivalentes car, permettant l'usage de langages naturels, elles permettent aussi la communication entre des cultures assez distinctes, apportant toute sorte de difficultés pour les échanges informationnels, puisque le taux de rappel est très élevé dans les systèmes non-spécialisés de récupération d'information. Le contact avec des communautés culturelles différentes présuppose l'interaction avec les identités établies et basées sur la mémoire des acteurs sociaux impliqués. Partant de la présupposition théorique que la métaphore est une forme de représentation propre à la condition humaine, cette communication, dont la base empirique est une étude de cas, est focalisée sur la gestion de l'information et propose une discussion théorique sur la représentation et la quête d'information, spécialement tournée vers des groupes spécifiques structurés en réseau, en considérant l'identité du groupe comme élément orienteur du « faire » académique. Ce travail, basé sur des entrevues avec des membres de groupes de recherche, et les résultats obtenus jusqu'à présent indiquent la présence de métaphores partagées qui, si elles sont appliquées aux moteurs de recherche, peuvent augmenter la précision dans la récupération de l'information.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1635-6187</s0></fA01><fA05><s2>n.19</s2></fA05><fA08 i1="01" i2="1" l="FRE"><s1>INFORMATION ET IDENTITÉ DANS LA PRODUCTION DE LA CONNAISSANCE: REPRÉSENTATION MÉTAPHORIQUE DANS UN RÉSEAU DE RECHERCHE</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité</s1></fA09><fA11 i1="01" i2="1"><s1>DILL ORRICO (Evelyn Goyannes)</s1></fA11><fA11 i1="02" i2="1"><s1>CORREIA DE OLVIEIRA (Carmen)</s1></fA11><fA12 i1="01" i2="1"><s1>VOLANT (Christiane)</s1><s9>dir. publ.</s9></fA12><fA14 i1="01"><s1>Information IBICT/UFRJ Universidade Federal do Estado do Rio de Janeiro - UNIRIO Professeur Adjoint</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Information IBICT/UFF Universidade Federal do Estado do Rio de Janeiro - UNIRIO Assistant administratif / Chercheuse du Groupe de recherche Mémoire et Discours</s1><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA18 i1="01" i2="1"><s1>Centre d'étude du débat public et des médiations</s1><s2>Tours</s2><s3>FRA</s3><s9>org-cong.</s9></fA18><fA20><s1>263-279</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA25 i1="01"><s1>Presses universitaires F. Rabelais</s1><s2>Tours</s2></fA25><fA26 i1="01"><s0>978-2-86906-239-9</s0></fA26><fA43 i1="01"><s1>INIST</s1><s2>Y 39288</s2><s5>354000182452750190</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0348037</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="2"><s0>Collection Perspectives Villes et Territoires</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>De nos jours, les nouvelles technologies rendent viables des situations ambivalentes car, permettant l'usage de langages naturels, elles permettent aussi la communication entre des cultures assez distinctes, apportant toute sorte de difficultés pour les échanges informationnels, puisque le taux de rappel est très élevé dans les systèmes non-spécialisés de récupération d'information. Le contact avec des communautés culturelles différentes présuppose l'interaction avec les identités établies et basées sur la mémoire des acteurs sociaux impliqués. Partant de la présupposition théorique que la métaphore est une forme de représentation propre à la condition humaine, cette communication, dont la base empirique est une étude de cas, est focalisée sur la gestion de l'information et propose une discussion théorique sur la représentation et la quête d'information, spécialement tournée vers des groupes spécifiques structurés en réseau, en considérant l'identité du groupe comme élément orienteur du « faire » académique. Ce travail, basé sur des entrevues avec des membres de groupes de recherche, et les résultats obtenus jusqu'à présent indiquent la présence de métaphores partagées qui, si elles sont appliquées aux moteurs de recherche, peuvent augmenter la précision dans la récupération de l'information.</s0></fC01><fC02 i1="01" i2="X"><s0>001A01E02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Analyse discours</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Discourse analysis</s0><s5>04</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Análisis de contenido</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Métaphore</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Metaphor</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Metáfora</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Technologie information communication</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Information communication technology</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Nueva tecnología información comunicación</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Etude cas</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Case study</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Estudio caso</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Représentation information</s0><s2>563</s2><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Information representation</s0><s2>563</s2><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Representación de las informaciones</s0><s2>563</s2><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Réseau</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Network</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Red</s0><s5>09</s5></fC03><fN21><s1>250</s1></fN21></pA><pR><fA30 i1="01" i2="1" l="FRE"><s1>L'information dans les organisations : dynamique et complexité. Colloque international</s1><s3>Tours FRA</s3><s4>2006-04-06</s4></fA30></pR></standard><server><NO>PASCAL 09-0348037 INIST</NO><FT>INFORMATION ET IDENTITÉ DANS LA PRODUCTION DE LA CONNAISSANCE: REPRÉSENTATION MÉTAPHORIQUE DANS UN RÉSEAU DE RECHERCHE</FT><AU>DILL ORRICO (Evelyn Goyannes); CORREIA DE OLVIEIRA (Carmen); VOLANT (Christiane)</AU><AF>Information IBICT/UFRJ Universidade Federal do Estado do Rio de Janeiro - UNIRIO Professeur Adjoint/Brésil (1 aut.); Information IBICT/UFF Universidade Federal do Estado do Rio de Janeiro - UNIRIO Assistant administratif / Chercheuse du Groupe de recherche Mémoire et Discours/Brésil (2 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Collection Perspectives Villes et Territoires; ISSN 1635-6187; France; Da. 2008; Vol. n.19; Pp. 263-279; Abs. anglais; Bibl. 1/2 p.</SO><LA>Français</LA><FA>De nos jours, les nouvelles technologies rendent viables des situations ambivalentes car, permettant l'usage de langages naturels, elles permettent aussi la communication entre des cultures assez distinctes, apportant toute sorte de difficultés pour les échanges informationnels, puisque le taux de rappel est très élevé dans les systèmes non-spécialisés de récupération d'information. Le contact avec des communautés culturelles différentes présuppose l'interaction avec les identités établies et basées sur la mémoire des acteurs sociaux impliqués. Partant de la présupposition théorique que la métaphore est une forme de représentation propre à la condition humaine, cette communication, dont la base empirique est une étude de cas, est focalisée sur la gestion de l'information et propose une discussion théorique sur la représentation et la quête d'information, spécialement tournée vers des groupes spécifiques structurés en réseau, en considérant l'identité du groupe comme élément orienteur du « faire » académique. Ce travail, basé sur des entrevues avec des membres de groupes de recherche, et les résultats obtenus jusqu'à présent indiquent la présence de métaphores partagées qui, si elles sont appliquées aux moteurs de recherche, peuvent augmenter la précision dans la récupération de l'information.</FA><CC>001A01E02</CC><FD>Analyse discours; Métaphore; Technologie information communication; Etude cas; Représentation information; Réseau</FD><ED>Discourse analysis; Metaphor; Information communication technology; Case study; Information representation; Network</ED><SD>Análisis de contenido; Metáfora; Nueva tecnología información comunicación; Estudio caso; Representación de las informaciones; Red</SD><LO>INIST-Y 39288.354000182452750190</LO><ID>09-0348037</ID></server></inist></record>
000D27	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Sequence Diversity of the Factor H Binding Protein Vaccine Candidate in Epidemiologically Relevant Strains of Serogroup B Neisseria meningitidis</title><author><name sortKey="Murphy, Ellen" uniqKey="Murphy E">Ellen Murphy</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Andrew, Lubomira" uniqKey="Andrew L">Lubomira Andrew</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lee, Kwok Leung" uniqKey="Lee K">Kwok-Leung Lee</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dilts, Deborah A" uniqKey="Dilts D">Deborah A. Dilts</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nunez, Lorna" uniqKey="Nunez L">Lorna Nunez</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fink, Pamela S" uniqKey="Fink P">Pamela S. Fink</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ambrose, Karita" uniqKey="Ambrose K">Karita Ambrose</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Borrow, Ray" uniqKey="Borrow R">Ray Borrow</name><affiliation><inist:fA14 i1="04"><s1>Health Protection Agency, Manchester Royal Infirmary</s1><s2>Manchester</s2><s3>GBR</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Findlow, Jamie" uniqKey="Findlow J">Jamie Findlow</name><affiliation><inist:fA14 i1="04"><s1>Health Protection Agency, Manchester Royal Infirmary</s1><s2>Manchester</s2><s3>GBR</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Taha, Muhamed Kheir" uniqKey="Taha M">Muhamed-Kheir Taha</name><affiliation><inist:fA14 i1="05"><s1>Institut Pasteur, Invasive Bacterial Infections Unit</s1><s2>Paris</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Deghmane, Ala Eddine" uniqKey="Deghmane A">Ala-Eddine Deghmane</name><affiliation><inist:fA14 i1="05"><s1>Institut Pasteur, Invasive Bacterial Infections Unit</s1><s2>Paris</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Friz, Paula" uniqKey="Friz P">Paula Friz</name><affiliation><inist:fA14 i1="06"><s1>National Institute of Public Health</s1><s2>Prague</s2><s3>CZE</s3><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Musilek, Martin" uniqKey="Musilek M">Martin Musilek</name><affiliation><inist:fA14 i1="06"><s1>National Institute of Public Health</s1><s2>Prague</s2><s3>CZE</s3><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kalmusova, Jitka" uniqKey="Kalmusova J">Jitka Kalmusova</name><affiliation><inist:fA14 i1="06"><s1>National Institute of Public Health</s1><s2>Prague</s2><s3>CZE</s3><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Caugant, Dominique A" uniqKey="Caugant D">Dominique A. Caugant</name><affiliation><inist:fA14 i1="07"><s1>Norwegian Institute of Public Health</s1><s2>Oslo</s2><s3>NOR</s3><sZ>15 aut.</sZ><sZ>16 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Alvestad, Torill" uniqKey="Alvestad T">Torill Alvestad</name><affiliation><inist:fA14 i1="07"><s1>Norwegian Institute of Public Health</s1><s2>Oslo</s2><s3>NOR</s3><sZ>15 aut.</sZ><sZ>16 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mayer, Leonard W" uniqKey="Mayer L">Leonard W. Mayer</name><affiliation><inist:fA14 i1="02"><s1>Centers for Disease Control and Prevention</s1><s3>USA</s3><sZ>17 aut.</sZ><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sacchi, Claudio T" uniqKey="Sacchi C">Claudio T. Sacchi</name><affiliation><inist:fA14 i1="02"><s1>Centers for Disease Control and Prevention</s1><s3>USA</s3><sZ>17 aut.</sZ><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="08"><s1>Instituto Adolfo Lutz</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name>XIN WANG</name><affiliation><inist:fA14 i1="02"><s1>Centers for Disease Control and Prevention</s1><s3>USA</s3><sZ>17 aut.</sZ><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Martin, Diana" uniqKey="Martin D">Diana Martin</name><affiliation><inist:fA14 i1="09"><s1>Institute of Environmental Science and Research</s1><s2>Porirua</s2><s3>NZL</s3><sZ>20 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Von Gottberg, Anne" uniqKey="Von Gottberg A">Anne Von Gottberg</name><affiliation><inist:fA14 i1="10"><s1>Respiratory and Meningeal Pathogens Research Unit, National Institute for Communicable Diseases</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Du Plessis, Mignon" uniqKey="Du Plessis M">Mignon Du Plessis</name><affiliation><inist:fA14 i1="10"><s1>Respiratory and Meningeal Pathogens Research Unit, National Institute for Communicable Diseases</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Klugman, Keith P" uniqKey="Klugman K">Keith P. Klugman</name><affiliation><inist:fA14 i1="03"><s1>Rollins School of Public Health, Emory University</s1><s2>Atlanta, Georgia</s2><s3>USA</s3><sZ>23 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="10"><s1>Respiratory and Meningeal Pathogens Research Unit, National Institute for Communicable Diseases</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Anderson, Annaliesa S" uniqKey="Anderson A">Annaliesa S. Anderson</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jansen, Kathrin U" uniqKey="Jansen K">Kathrin U. Jansen</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Zlotnick, Gary W" uniqKey="Zlotnick G">Gary W. Zlotnick</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hoiseth, Susan K" uniqKey="Hoiseth S">Susan K. Hoiseth</name><affiliation><inist:fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0349081</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0349081 INIST</idno><idno type="RBID">Pascal:09-0349081</idno><idno type="wicri:Area/Main/Corpus">001C54</idno></publicationStmt><seriesStmt><idno type="ISSN">0022-1899</idno><title level="j" type="abbreviated">J. infect. dis.</title><title level="j" type="main">The Journal of infectious diseases</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Binding protein</term><term>Infection</term><term>Microbiology</term><term>Neisseria meningitidis</term><term>Vaccine strain</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Neisseria meningitidis</term><term>Protéine liaison</term><term>Souche vaccinale</term><term>Microbiologie</term><term>Infection</term><term>Facteur H</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background. Recombinant forms of Neisseria meningitidis human factor H binding protein (fHBP) are undergoing clinical trials in candidate vaccines against invasive meningococcal serogroup B disease. We report an extensive survey and phylogenetic analysis of the diversity of fhbp genes and predicted protein sequences in invasive clinical isolates obtained in the period 2000-2006. Methods. Nucleotide sequences of fhbp genes were obtained from 1837 invasive N. meningitidis serogroup B (MnB) strains from the United States, Europe, New Zealand, and South Africa. Multilocus sequence typing (MLST) analysis was performed on a subset of the strains. Results. Every strain contained the fhbp gene. All sequences fell into 1 of 2 subfamilies (A or B), with 60%-75% amino acid identity between subfamilies and at least 83% identity within each subfamily. One fHBP sequence may have arisen via inter-subfamily recombination. Subfamily B sequences were found in 70% of the isolates, and subfamily A sequences were found in 30%. Multiple fHBP variants were detected in each of the common MLST clonal complexes. All major MLST complexes include strains in both subfamily A and subfamily B. Conclusions. The diversity of strains observed underscores the importance of studying the distribution of the vaccine antigen itself rather than relying on common epidemiological surrogates such as MLST.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0022-1899</s0></fA01><fA02 i1="01"><s0>JIDIAQ</s0></fA02><fA03 i2="1"><s0>J. infect. dis.</s0></fA03><fA05><s2>200</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Sequence Diversity of the Factor H Binding Protein Vaccine Candidate in Epidemiologically Relevant Strains of Serogroup B Neisseria meningitidis</s1></fA08><fA11 i1="01" i2="1"><s1>MURPHY (Ellen)</s1></fA11><fA11 i1="02" i2="1"><s1>ANDREW (Lubomira)</s1></fA11><fA11 i1="03" i2="1"><s1>LEE (Kwok-Leung)</s1></fA11><fA11 i1="04" i2="1"><s1>DILTS (Deborah A.)</s1></fA11><fA11 i1="05" i2="1"><s1>NUNEZ (Lorna)</s1></fA11><fA11 i1="06" i2="1"><s1>FINK (Pamela S.)</s1></fA11><fA11 i1="07" i2="1"><s1>AMBROSE (Karita)</s1></fA11><fA11 i1="08" i2="1"><s1>BORROW (Ray)</s1></fA11><fA11 i1="09" i2="1"><s1>FINDLOW (Jamie)</s1></fA11><fA11 i1="10" i2="1"><s1>TAHA (Muhamed-Kheir)</s1></fA11><fA11 i1="11" i2="1"><s1>DEGHMANE (Ala-Eddine)</s1></fA11><fA11 i1="12" i2="1"><s1>FRIZ (Paula)</s1></fA11><fA11 i1="13" i2="1"><s1>MUSILEK (Martin)</s1></fA11><fA11 i1="14" i2="1"><s1>KALMUSOVA (Jitka)</s1></fA11><fA11 i1="15" i2="1"><s1>CAUGANT (Dominique A.)</s1></fA11><fA11 i1="16" i2="1"><s1>ALVESTAD (Torill)</s1></fA11><fA11 i1="17" i2="1"><s1>MAYER (Leonard W.)</s1></fA11><fA11 i1="18" i2="1"><s1>SACCHI (Claudio T.)</s1></fA11><fA11 i1="19" i2="1"><s1>XIN WANG</s1></fA11><fA11 i1="20" i2="1"><s1>MARTIN (Diana)</s1></fA11><fA11 i1="21" i2="1"><s1>VON GOTTBERG (Anne)</s1></fA11><fA11 i1="22" i2="1"><s1>DU PLESSIS (Mignon)</s1></fA11><fA11 i1="23" i2="1"><s1>KLUGMAN (Keith P.)</s1></fA11><fA11 i1="24" i2="1"><s1>ANDERSON (Annaliesa S.)</s1></fA11><fA11 i1="25" i2="1"><s1>JANSEN (Kathrin U.)</s1></fA11><fA11 i1="26" i2="1"><s1>ZLOTNICK (Gary W.)</s1></fA11><fA11 i1="27" i2="1"><s1>HOISETH (Susan K.)</s1></fA11><fA14 i1="01"><s1>Wyeth Vaccines Research</s1><s2>Pearl River, New York</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></fA14><fA14 i1="02"><s1>Centers for Disease Control and Prevention</s1><s3>USA</s3><sZ>17 aut.</sZ><sZ>18 aut.</sZ><sZ>19 aut.</sZ></fA14><fA14 i1="03"><s1>Rollins School of Public Health, Emory University</s1><s2>Atlanta, Georgia</s2><s3>USA</s3><sZ>23 aut.</sZ></fA14><fA14 i1="04"><s1>Health Protection Agency, Manchester Royal Infirmary</s1><s2>Manchester</s2><s3>GBR</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="05"><s1>Institut Pasteur, Invasive Bacterial Infections Unit</s1><s2>Paris</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="06"><s1>National Institute of Public Health</s1><s2>Prague</s2><s3>CZE</s3><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ></fA14><fA14 i1="07"><s1>Norwegian Institute of Public Health</s1><s2>Oslo</s2><s3>NOR</s3><sZ>15 aut.</sZ><sZ>16 aut.</sZ></fA14><fA14 i1="08"><s1>Instituto Adolfo Lutz</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>18 aut.</sZ></fA14><fA14 i1="09"><s1>Institute of Environmental Science and Research</s1><s2>Porirua</s2><s3>NZL</s3><sZ>20 aut.</sZ></fA14><fA14 i1="10"><s1>Respiratory and Meningeal Pathogens Research Unit, National Institute for Communicable Diseases</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></fA14><fA20><s1>379-389</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2052</s2><s5>354000170912740090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>40 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0349081</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>The Journal of infectious diseases</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Background. Recombinant forms of Neisseria meningitidis human factor H binding protein (fHBP) are undergoing clinical trials in candidate vaccines against invasive meningococcal serogroup B disease. We report an extensive survey and phylogenetic analysis of the diversity of fhbp genes and predicted protein sequences in invasive clinical isolates obtained in the period 2000-2006. Methods. Nucleotide sequences of fhbp genes were obtained from 1837 invasive N. meningitidis serogroup B (MnB) strains from the United States, Europe, New Zealand, and South Africa. Multilocus sequence typing (MLST) analysis was performed on a subset of the strains. Results. Every strain contained the fhbp gene. All sequences fell into 1 of 2 subfamilies (A or B), with 60%-75% amino acid identity between subfamilies and at least 83% identity within each subfamily. One fHBP sequence may have arisen via inter-subfamily recombination. Subfamily B sequences were found in 70% of the isolates, and subfamily A sequences were found in 30%. Multiple fHBP variants were detected in each of the common MLST clonal complexes. All major MLST complexes include strains in both subfamily A and subfamily B. Conclusions. The diversity of strains observed underscores the importance of studying the distribution of the vaccine antigen itself rather than relying on common epidemiological surrogates such as MLST.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05B15</s0></fC02><fC02 i1="02" i2="X"><s0>002B05</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Protéine liaison</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Binding protein</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Proteína enlace</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Souche vaccinale</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Vaccine strain</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Cepa de vacuna</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Microbiologie</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Microbiology</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Microbiología</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Infection</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Infection</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Infección</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Facteur H</s0><s4>INC</s4><s5>79</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0349081 INIST</NO><ET>Sequence Diversity of the Factor H Binding Protein Vaccine Candidate in Epidemiologically Relevant Strains of Serogroup B Neisseria meningitidis</ET><AU>MURPHY (Ellen); ANDREW (Lubomira); LEE (Kwok-Leung); DILTS (Deborah A.); NUNEZ (Lorna); FINK (Pamela S.); AMBROSE (Karita); BORROW (Ray); FINDLOW (Jamie); TAHA (Muhamed-Kheir); DEGHMANE (Ala-Eddine); FRIZ (Paula); MUSILEK (Martin); KALMUSOVA (Jitka); CAUGANT (Dominique A.); ALVESTAD (Torill); MAYER (Leonard W.); SACCHI (Claudio T.); XIN WANG; MARTIN (Diana); VON GOTTBERG (Anne); DU PLESSIS (Mignon); KLUGMAN (Keith P.); ANDERSON (Annaliesa S.); JANSEN (Kathrin U.); ZLOTNICK (Gary W.); HOISETH (Susan K.)</AU><AF>Wyeth Vaccines Research/Pearl River, New York/Etats-Unis (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 24 aut., 25 aut., 26 aut., 27 aut.); Centers for Disease Control and Prevention/Etats-Unis (17 aut., 18 aut., 19 aut.); Rollins School of Public Health, Emory University/Atlanta, Georgia/Etats-Unis (23 aut.); Health Protection Agency, Manchester Royal Infirmary/Manchester/Royaume-Uni (8 aut., 9 aut.); Institut Pasteur, Invasive Bacterial Infections Unit/Paris/France (10 aut., 11 aut.); National Institute of Public Health/Prague/Tchèque, République (12 aut., 13 aut., 14 aut.); Norwegian Institute of Public Health/Oslo/Norvège (15 aut., 16 aut.); Instituto Adolfo Lutz/Sao Paulo/Brésil (18 aut.); Institute of Environmental Science and Research/Porirua/Nouvelle-Zélande (20 aut.); Respiratory and Meningeal Pathogens Research Unit, National Institute for Communicable Diseases/Johannesburg/Afrique du Sud (21 aut., 22 aut., 23 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>The Journal of infectious diseases; ISSN 0022-1899; Coden JIDIAQ; Etats-Unis; Da. 2009; Vol. 200; No. 3; Pp. 379-389; Bibl. 40 ref.</SO><LA>Anglais</LA><EA>Background. Recombinant forms of Neisseria meningitidis human factor H binding protein (fHBP) are undergoing clinical trials in candidate vaccines against invasive meningococcal serogroup B disease. We report an extensive survey and phylogenetic analysis of the diversity of fhbp genes and predicted protein sequences in invasive clinical isolates obtained in the period 2000-2006. Methods. Nucleotide sequences of fhbp genes were obtained from 1837 invasive N. meningitidis serogroup B (MnB) strains from the United States, Europe, New Zealand, and South Africa. Multilocus sequence typing (MLST) analysis was performed on a subset of the strains. Results. Every strain contained the fhbp gene. All sequences fell into 1 of 2 subfamilies (A or B), with 60%-75% amino acid identity between subfamilies and at least 83% identity within each subfamily. One fHBP sequence may have arisen via inter-subfamily recombination. Subfamily B sequences were found in 70% of the isolates, and subfamily A sequences were found in 30%. Multiple fHBP variants were detected in each of the common MLST clonal complexes. All major MLST complexes include strains in both subfamily A and subfamily B. Conclusions. The diversity of strains observed underscores the importance of studying the distribution of the vaccine antigen itself rather than relying on common epidemiological surrogates such as MLST.</EA><CC>002A05B15; 002B05</CC><FD>Neisseria meningitidis; Protéine liaison; Souche vaccinale; Microbiologie; Infection; Facteur H</FD><FG>Neisseriaceae; Micrococcales; Bactérie</FG><ED>Neisseria meningitidis; Binding protein; Vaccine strain; Microbiology; Infection</ED><EG>Neisseriaceae; Micrococcales; Bacteria</EG><SD>Neisseria meningitidis; Proteína enlace; Cepa de vacuna; Microbiología; Infección</SD><LO>INIST-2052.354000170912740090</LO><ID>09-0349081</ID></server></inist></record>
000D28	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Lipectomy as a new approach to secondary procedure superficialization of direct autogenous forearm radial-cephalic arteriovenous accesses for hemodialysis</title><author><name sortKey="Bourquelot, Pierre" uniqKey="Bourquelot P">Pierre Bourquelot</name><affiliation><inist:fA14 i1="01"><s1>Clinique Jouvenet</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Centre Hospitalier Univcrsitaire La Pitié-Salpétrière</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Clinique Arago</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>Dialysis Access Specialists, LLC, Interventional Nephrology</s1><s2>Miami</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="06"><s1>Centro Hospitalar Setúbal E.P.E.</s1><s2>Setúbal</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>Centre Médico-Chirurgical Ambroise Paré</s1><s2>Neuilly sur Seine</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bijan Tawakol, Jan" uniqKey="Bijan Tawakol J">Jan Bijan Tawakol</name></author><author><name sortKey="Gaudric, Julien" uniqKey="Gaudric J">Julien Gaudric</name><affiliation><inist:fA14 i1="02"><s1>Centre Hospitalier Univcrsitaire La Pitié-Salpétrière</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Natario, Ana" uniqKey="Natario A">Ana Natario</name></author><author><name sortKey="Franco, Gilbert" uniqKey="Franco G">Gilbert Franco</name><affiliation><inist:fA14 i1="03"><s1>Clinique Arago</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Turmel Rodrigues, Luc" uniqKey="Turmel Rodrigues L">Luc Turmel-Rodrigues</name></author><author><name sortKey="Van Laere, Olivier" uniqKey="Van Laere O">Olivier Van Laere</name><affiliation><inist:fA14 i1="01"><s1>Clinique Jouvenet</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Centre Hospitalier Univcrsitaire La Pitié-Salpétrière</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Clinique Arago</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0350014</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0350014 INIST</idno><idno type="RBID">Pascal:09-0350014</idno><idno type="wicri:Area/Main/Corpus">001C53</idno></publicationStmt><seriesStmt><idno type="ISSN">0741-5214</idno><title level="j" type="abbreviated">J. vasc. surg.</title><title level="j" type="main">Journal of vascular surgery</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cardiovascular disease</term><term>Hemodialysis</term><term>Surgery</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Pathologie de l'appareil circulatoire</term><term>Hémodialyse</term><term>Chirurgie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background: The depth of veins can discourage surgeons from creating radial-cephalic arteriovenous accesses for hemodialysis in obese patients. Elevation and tunneled transposition are the two techniques that have been described to superficialize these veins and make them accessible for cannulation. Unfortunately, such manipulation of veins has potential drawbacks. We report lipectomy, a new technique that removes subcutaneous fat and does not mobilize the vein. Methods: This single-center prospective study included 49 consecutive patients (17 men, 32 women) who underwent second-stage lipectomy after creation of a radial-cephalic fistula. Mean patient age was 54 years, 36% had diabetes, and the mean body mass index was 31 ± 5.6 kg/m<sup>2</sup>. Subcutaneous fatty tissues were removed after two transverse skin incisions under regional anesthesia and preventive hemostasis. Cannulation was first allowed 1 month later, after clinical and color duplex ultrasound evaluation. Technical success was defined as the ability to remove the fat and to palpate the patent vein immediately under the skin at the end of the operation. Clinical success was defined as the ability to perform at least three consecutive dialysis sessions with two needles. All patients were checked systematically every 6 months by the surgeon. Results: Technical and clinical success rates were 96% (47 of 49) and 94% (46 of 49), respectively. Mean vein depth decreased from 8 ± 2 to 3 ± 1 mm according to duplex ultrasound imaging. The mean vein diameter increased from 6 ± 1 to 8 ± 2 mm. In one patient, vein tortuosity that was overlooked required conventional repeat tunneling. One extensive hematoma resulted in loss of the fistula. One patient died before the fistula could be used. Primary patency rates were 71% ± 7% and 63% ± 8% at 1 and 3 years, respectively, and secondary patency rates were 98% ± 2% and 88% ± 7%. Delayed complications were treated by surgery (n = 7) or by endovascular procedures (n = 10). Conclusion: Lipectomy is a safe, effective, and durable approach to make deep arterialized forearm veins accessible for routine cannulation for hemodialysis in obese patients. It might even be hypothesized that incident obese dialysis patients will eventually have the highest proportion of radial-cephalic fistulas because they often have distal veins that have been preserved by their fat from previous attempts at cannulation for blood sampling or infusion.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0741-5214</s0></fA01><fA02 i1="01"><s0>JVSUES</s0></fA02><fA03 i2="1"><s0>J. vasc. surg.</s0></fA03><fA05><s2>50</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Lipectomy as a new approach to secondary procedure superficialization of direct autogenous forearm radial-cephalic arteriovenous accesses for hemodialysis</s1></fA08><fA11 i1="01" i2="1"><s1>BOURQUELOT (Pierre)</s1></fA11><fA11 i1="02" i2="1"><s1>BIJAN TAWAKOL (Jan)</s1></fA11><fA11 i1="03" i2="1"><s1>GAUDRIC (Julien)</s1></fA11><fA11 i1="04" i2="1"><s1>NATARIO (Ana)</s1></fA11><fA11 i1="05" i2="1"><s1>FRANCO (Gilbert)</s1></fA11><fA11 i1="06" i2="1"><s1>TURMEL-RODRIGUES (Luc)</s1></fA11><fA11 i1="07" i2="1"><s1>VAN LAERE (Olivier)</s1></fA11><fA14 i1="01"><s1>Clinique Jouvenet</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Centre Hospitalier Univcrsitaire La Pitié-Salpétrière</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Clinique Arago</s1><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="04"><s1>Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3></fA14><fA14 i1="05"><s1>Dialysis Access Specialists, LLC, Interventional Nephrology</s1><s2>Miami</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="06"><s1>Centro Hospitalar Setúbal E.P.E.</s1><s2>Setúbal</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>Centre Médico-Chirurgical Ambroise Paré</s1><s2>Neuilly sur Seine</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></fA14><fA20><s1>369-374</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20352</s2><s5>354000170906070200</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>19 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0350014</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of vascular surgery</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Background: The depth of veins can discourage surgeons from creating radial-cephalic arteriovenous accesses for hemodialysis in obese patients. Elevation and tunneled transposition are the two techniques that have been described to superficialize these veins and make them accessible for cannulation. Unfortunately, such manipulation of veins has potential drawbacks. We report lipectomy, a new technique that removes subcutaneous fat and does not mobilize the vein. Methods: This single-center prospective study included 49 consecutive patients (17 men, 32 women) who underwent second-stage lipectomy after creation of a radial-cephalic fistula. Mean patient age was 54 years, 36% had diabetes, and the mean body mass index was 31 ± 5.6 kg/m<sup>2</sup>. Subcutaneous fatty tissues were removed after two transverse skin incisions under regional anesthesia and preventive hemostasis. Cannulation was first allowed 1 month later, after clinical and color duplex ultrasound evaluation. Technical success was defined as the ability to remove the fat and to palpate the patent vein immediately under the skin at the end of the operation. Clinical success was defined as the ability to perform at least three consecutive dialysis sessions with two needles. All patients were checked systematically every 6 months by the surgeon. Results: Technical and clinical success rates were 96% (47 of 49) and 94% (46 of 49), respectively. Mean vein depth decreased from 8 ± 2 to 3 ± 1 mm according to duplex ultrasound imaging. The mean vein diameter increased from 6 ± 1 to 8 ± 2 mm. In one patient, vein tortuosity that was overlooked required conventional repeat tunneling. One extensive hematoma resulted in loss of the fistula. One patient died before the fistula could be used. Primary patency rates were 71% ± 7% and 63% ± 8% at 1 and 3 years, respectively, and secondary patency rates were 98% ± 2% and 88% ± 7%. Delayed complications were treated by surgery (n = 7) or by endovascular procedures (n = 10). Conclusion: Lipectomy is a safe, effective, and durable approach to make deep arterialized forearm veins accessible for routine cannulation for hemodialysis in obese patients. It might even be hypothesized that incident obese dialysis patients will eventually have the highest proportion of radial-cephalic fistulas because they often have distal veins that have been preserved by their fat from previous attempts at cannulation for blood sampling or infusion.</s0></fC01><fC02 i1="01" i2="X"><s0>002B25F</s0></fC02><fC02 i1="02" i2="X"><s0>002B27B03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil circulatoire</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Cardiovascular disease</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Hémodialyse</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Hemodialysis</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Hemodiálisis</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Chirurgie</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Surgery</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Cirugía</s0><s5>10</s5></fC03><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0350014 INIST</NO><ET>Lipectomy as a new approach to secondary procedure superficialization of direct autogenous forearm radial-cephalic arteriovenous accesses for hemodialysis</ET><AU>BOURQUELOT (Pierre); BIJAN TAWAKOL (Jan); GAUDRIC (Julien); NATARIO (Ana); FRANCO (Gilbert); TURMEL-RODRIGUES (Luc); VAN LAERE (Olivier)</AU><AF>Clinique Jouvenet/France (1 aut., 7 aut.); Centre Hospitalier Univcrsitaire La Pitié-Salpétrière/France (1 aut., 3 aut., 7 aut.); Clinique Arago/France (1 aut., 5 aut., 7 aut.); Hôpital Européen Georges Pompidou/Paris/France; Dialysis Access Specialists, LLC, Interventional Nephrology/Miami/Etats-Unis (1 aut., 2 aut., 7 aut.); Centro Hospitalar Setúbal E.P.E./Setúbal/Brésil (1 aut., 4 aut., 7 aut.); Centre Médico-Chirurgical Ambroise Paré/Neuilly sur Seine/France (1 aut., 6 aut., 7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of vascular surgery; ISSN 0741-5214; Coden JVSUES; Etats-Unis; Da. 2009; Vol. 50; No. 2; Pp. 369-374; Bibl. 19 ref.</SO><LA>Anglais</LA><EA>Background: The depth of veins can discourage surgeons from creating radial-cephalic arteriovenous accesses for hemodialysis in obese patients. Elevation and tunneled transposition are the two techniques that have been described to superficialize these veins and make them accessible for cannulation. Unfortunately, such manipulation of veins has potential drawbacks. We report lipectomy, a new technique that removes subcutaneous fat and does not mobilize the vein. Methods: This single-center prospective study included 49 consecutive patients (17 men, 32 women) who underwent second-stage lipectomy after creation of a radial-cephalic fistula. Mean patient age was 54 years, 36% had diabetes, and the mean body mass index was 31 ± 5.6 kg/m<sup>2</sup>. Subcutaneous fatty tissues were removed after two transverse skin incisions under regional anesthesia and preventive hemostasis. Cannulation was first allowed 1 month later, after clinical and color duplex ultrasound evaluation. Technical success was defined as the ability to remove the fat and to palpate the patent vein immediately under the skin at the end of the operation. Clinical success was defined as the ability to perform at least three consecutive dialysis sessions with two needles. All patients were checked systematically every 6 months by the surgeon. Results: Technical and clinical success rates were 96% (47 of 49) and 94% (46 of 49), respectively. Mean vein depth decreased from 8 ± 2 to 3 ± 1 mm according to duplex ultrasound imaging. The mean vein diameter increased from 6 ± 1 to 8 ± 2 mm. In one patient, vein tortuosity that was overlooked required conventional repeat tunneling. One extensive hematoma resulted in loss of the fistula. One patient died before the fistula could be used. Primary patency rates were 71% ± 7% and 63% ± 8% at 1 and 3 years, respectively, and secondary patency rates were 98% ± 2% and 88% ± 7%. Delayed complications were treated by surgery (n = 7) or by endovascular procedures (n = 10). Conclusion: Lipectomy is a safe, effective, and durable approach to make deep arterialized forearm veins accessible for routine cannulation for hemodialysis in obese patients. It might even be hypothesized that incident obese dialysis patients will eventually have the highest proportion of radial-cephalic fistulas because they often have distal veins that have been preserved by their fat from previous attempts at cannulation for blood sampling or infusion.</EA><CC>002B25F; 002B27B03</CC><FD>Pathologie de l'appareil circulatoire; Hémodialyse; Chirurgie</FD><ED>Cardiovascular disease; Hemodialysis; Surgery</ED><SD>Aparato circulatorio patología; Hemodiálisis; Cirugía</SD><LO>INIST-20352.354000170906070200</LO><ID>09-0350014</ID></server></inist></record>
000D29	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Ozonation of azo dyes (Orange II and Acid Red 27) in saline media</title><author><name sortKey="Silva, Alessandra C" uniqKey="Silva A">Alessandra C. Silva</name><affiliation><inist:fA14 i1="01"><s1>Chemical Engineering Program, COPPE, Federal University of Rio de Janeiro, Av. Noracio Macedo, 2030, P.O. Box, 68502</s1><s2>CEP 21941-972, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Stephane Pic, Jean" uniqKey="Stephane Pic J">Jean Stephane Pic</name><affiliation><inist:fA14 i1="02"><s1>Institut National des Sciences Appliquées. INSA-GPE-LIPE</s1><s2>Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sant Anna, Geraldo L Jr" uniqKey="Sant Anna G">Geraldo L. Jr Sant Anna</name><affiliation><inist:fA14 i1="01"><s1>Chemical Engineering Program, COPPE, Federal University of Rio de Janeiro, Av. Noracio Macedo, 2030, P.O. Box, 68502</s1><s2>CEP 21941-972, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dezotti, Marcia" uniqKey="Dezotti M">Marcia Dezotti</name><affiliation><inist:fA14 i1="01"><s1>Chemical Engineering Program, COPPE, Federal University of Rio de Janeiro, Av. Noracio Macedo, 2030, P.O. Box, 68502</s1><s2>CEP 21941-972, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0350280</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0350280 INIST</idno><idno type="RBID">Pascal:09-0350280</idno><idno type="wicri:Area/Main/Corpus">001C52</idno></publicationStmt><seriesStmt><idno type="ISSN">0304-3894</idno><title level="j" type="abbreviated">J. hazard. mater.</title><title level="j" type="main">Journal of hazardous materials</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Azo dye</term><term>Biodegradation</term><term>Bubble column</term><term>Color</term><term>Degradation product</term><term>Discoloration</term><term>Kinetics</term><term>Mineralization</term><term>Operating conditions</term><term>Ozone</term><term>Ozonization</term><term>Physicochemical purification</term><term>Pollutant behavior</term><term>Rate constant</term><term>Reactor</term><term>Respirometry</term><term>Surveillance</term><term>pH</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Ozonation</term><term>Colorant azoïque</term><term>Surveillance</term><term>Colonne bulle</term><term>Réacteur</term><term>pH</term><term>Ozone</term><term>Constante vitesse</term><term>Cinétique</term><term>Décoloration</term><term>Condition opératoire</term><term>Couleur</term><term>Minéralisation</term><term>Dégradation biologique</term><term>Respirométrie</term><term>Produit dégradation</term><term>Epuration physicochimique</term><term>Devenir polluant</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Ozonation of two azo dyes was investigated in a monitored bench scale bubble column reactor (8.5-L), varying liquid media salt content (0, 1, 40 and 100 gL<sup>-1</sup>, NaCl). In experiments with Orange II pH was varied (5, 7.5 and 9) but ozonation of Acid Red 27 was performed at pH 7.5. Ozone self-decomposition rate-constant increased with salt concentration. Color removal was very effective and fast achieved under all experimental conditions. For the two azo dyes tested, more than 98% of color intensity was removed in 30-min ozonation assays. However, only partial mineralization of azo dyes (45%-Orange II; 20%-Acid Red 27) was attained in such experiments. The degree of mineralization (TOC removal) was negatively affected by salt concentration. Biodegradation assays conducted by respirometry revealed the inhibitory effect of dye degradation products formed during ozonation.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0304-3894</s0></fA01><fA02 i1="01"><s0>JHMAD9</s0></fA02><fA03 i2="1"><s0>J. hazard. mater.</s0></fA03><fA05><s2>169</s2></fA05><fA06><s2>1-3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Ozonation of azo dyes (Orange II and Acid Red 27) in saline media</s1></fA08><fA11 i1="01" i2="1"><s1>SILVA (Alessandra C.)</s1></fA11><fA11 i1="02" i2="1"><s1>STEPHANE PIC (Jean)</s1></fA11><fA11 i1="03" i2="1"><s1>SANT'ANNA (Geraldo L. JR)</s1></fA11><fA11 i1="04" i2="1"><s1>DEZOTTI (Marcia)</s1></fA11><fA14 i1="01"><s1>Chemical Engineering Program, COPPE, Federal University of Rio de Janeiro, Av. Noracio Macedo, 2030, P.O. Box, 68502</s1><s2>CEP 21941-972, Rio de Janeiro, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Institut National des Sciences Appliquées. INSA-GPE-LIPE</s1><s2>Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>965-971</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>15708</s2><s5>354000170933201340</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>36 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0350280</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of hazardous materials</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>Ozonation of two azo dyes was investigated in a monitored bench scale bubble column reactor (8.5-L), varying liquid media salt content (0, 1, 40 and 100 gL<sup>-1</sup>, NaCl). In experiments with Orange II pH was varied (5, 7.5 and 9) but ozonation of Acid Red 27 was performed at pH 7.5. Ozone self-decomposition rate-constant increased with salt concentration. Color removal was very effective and fast achieved under all experimental conditions. For the two azo dyes tested, more than 98% of color intensity was removed in 30-min ozonation assays. However, only partial mineralization of azo dyes (45%-Orange II; 20%-Acid Red 27) was attained in such experiments. The degree of mineralization (TOC removal) was negatively affected by salt concentration. Biodegradation assays conducted by respirometry revealed the inhibitory effect of dye degradation products formed during ozonation.</s0></fC01><fC02 i1="01" i2="X"><s0>001D16</s0></fC02><fC02 i1="02" i2="X"><s0>001D07H</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Ozonation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Ozonization</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Ozonización</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Colorant azoïque</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Azo dye</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Colorante azoico</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Surveillance</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Surveillance</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Vigilancia</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Colonne bulle</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Bubble column</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Columna burbuja</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Réacteur</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Reactor</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Reactor</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>pH</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>pH</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>pH</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Ozone</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Ozone</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Ozono</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Constante vitesse</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Rate constant</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Constante velocidad</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Cinétique</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Kinetics</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Cinética</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Décoloration</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Discoloration</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Decoloración</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Condition opératoire</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Operating conditions</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Condición operatoria</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Couleur</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Color</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Color</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Minéralisation</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Mineralization</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Mineralización</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Dégradation biologique</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Biodegradation</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Degradación biológica</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Respirométrie</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Respirometry</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Respirometría</s0><s5>15</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Produit dégradation</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Degradation product</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Producto degradación</s0><s5>16</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Epuration physicochimique</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Physicochemical purification</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Depuración fisicoquímica</s0><s5>17</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Devenir polluant</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Pollutant behavior</s0><s5>18</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Evolución contaminante</s0><s5>18</s5></fC03><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0350280 INIST</NO><ET>Ozonation of azo dyes (Orange II and Acid Red 27) in saline media</ET><AU>SILVA (Alessandra C.); STEPHANE PIC (Jean); SANT'ANNA (Geraldo L. JR); DEZOTTI (Marcia)</AU><AF>Chemical Engineering Program, COPPE, Federal University of Rio de Janeiro, Av. Noracio Macedo, 2030, P.O. Box, 68502/CEP 21941-972, Rio de Janeiro, RJ/Brésil (1 aut., 3 aut., 4 aut.); Institut National des Sciences Appliquées. INSA-GPE-LIPE/Toulouse/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of hazardous materials; ISSN 0304-3894; Coden JHMAD9; Pays-Bas; Da. 2009; Vol. 169; No. 1-3; Pp. 965-971; Bibl. 36 ref.</SO><LA>Anglais</LA><EA>Ozonation of two azo dyes was investigated in a monitored bench scale bubble column reactor (8.5-L), varying liquid media salt content (0, 1, 40 and 100 gL<sup>-1</sup>, NaCl). In experiments with Orange II pH was varied (5, 7.5 and 9) but ozonation of Acid Red 27 was performed at pH 7.5. Ozone self-decomposition rate-constant increased with salt concentration. Color removal was very effective and fast achieved under all experimental conditions. For the two azo dyes tested, more than 98% of color intensity was removed in 30-min ozonation assays. However, only partial mineralization of azo dyes (45%-Orange II; 20%-Acid Red 27) was attained in such experiments. The degree of mineralization (TOC removal) was negatively affected by salt concentration. Biodegradation assays conducted by respirometry revealed the inhibitory effect of dye degradation products formed during ozonation.</EA><CC>001D16; 001D07H</CC><FD>Ozonation; Colorant azoïque; Surveillance; Colonne bulle; Réacteur; pH; Ozone; Constante vitesse; Cinétique; Décoloration; Condition opératoire; Couleur; Minéralisation; Dégradation biologique; Respirométrie; Produit dégradation; Epuration physicochimique; Devenir polluant</FD><ED>Ozonization; Azo dye; Surveillance; Bubble column; Reactor; pH; Ozone; Rate constant; Kinetics; Discoloration; Operating conditions; Color; Mineralization; Biodegradation; Respirometry; Degradation product; Physicochemical purification; Pollutant behavior</ED><SD>Ozonización; Colorante azoico; Vigilancia; Columna burbuja; Reactor; pH; Ozono; Constante velocidad; Cinética; Decoloración; Condición operatoria; Color; Mineralización; Degradación biológica; Respirometría; Producto degradación; Depuración fisicoquímica; Evolución contaminante</SD><LO>INIST-15708.354000170933201340</LO><ID>09-0350280</ID></server></inist></record>
000D30	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Space-time adaptive multiresolution methods for hyperbolic conservation laws: Applications to compressible Euler equations</title><author><name sortKey="Domingues, Margarete O" uniqKey="Domingues M">Margarete O. Domingues</name><affiliation><inist:fA14 i1="01"><s1>Laboratório Associado de Computação e Matemática Aplicada (LAC). Cordenaçào dos Laboratórios Associados (CTE), Instituto Nacional de Pesquisas Espaciais (INPE), Av. dos Astronautas, 1758</s1><s2>12227-010 Sào José dos Campos</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Laboratoire de Modélisation en Mécanique Procédés Propres (M2P2). CNRS and Universités d'Aix-Marseille, 38, rue Frédéric Joliot-Curie</s1><s2>13451 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gomes, Sonia M" uniqKey="Gomes S">Sônia M. Gomes</name><affiliation><inist:fA14 i1="02"><s1>Universidade Estadual de Campinas, IMECC, Caixa Postal 6065</s1><s2>13083-970 Campinas SP</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Roussel, Olivier" uniqKey="Roussel O">Olivier Roussel</name><affiliation><inist:fA14 i1="04"><s1>Institut für Tedinische Chemie und Polymerchemie (TCP). Universität Karlsruhe (TH). Kaiserstr. 12</s1><s2>76128 Karlsruhe</s2><s3>DEU</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schneider, Kai" uniqKey="Schneider K">Kai Schneider</name><affiliation><inist:fA14 i1="03"><s1>Laboratoire de Modélisation en Mécanique Procédés Propres (M2P2). CNRS and Universités d'Aix-Marseille, 38, rue Frédéric Joliot-Curie</s1><s2>13451 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>Centre de Mathématiques et d'Informatique (CMI), Université de Provence. 39, rue Frédéric Joliot-Curie</s1><s2>13453 Marseille</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0352756</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0352756 INIST</idno><idno type="RBID">Pascal:09-0352756</idno><idno type="wicri:Area/Main/Corpus">001C51</idno></publicationStmt><seriesStmt><idno type="ISSN">0168-9274</idno><title level="j" type="abbreviated">Appl. numer. math.</title><title level="j" type="main">Applied numerical mathematics</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adaptive method</term><term>Applied mathematics</term><term>Conservation law</term><term>Discretization method</term><term>Error estimation</term><term>Euler equation</term><term>Finite volume method</term><term>Grid pattern</term><term>Numerical analysis</term><term>Numerical stability</term><term>Runge Kutta method</term><term>Truncation</term><term>Truncation error</term><term>Two-dimensional calculations</term><term>Wavelet transformation</term><term>Wavelets</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Transformation ondelette</term><term>Méthode adaptative</term><term>Loi conservation</term><term>Equation Euler</term><term>Méthode volume fini</term><term>Méthode discrétisation</term><term>Maillage</term><term>Ondelette</term><term>Stabilité numérique</term><term>Estimation erreur</term><term>Erreur troncature</term><term>Troncature</term><term>Méthode Runge Kutta</term><term>Calcul 2 dimensions</term><term>Mathématiques appliquées</term><term>Analyse numérique</term><term>35L65</term><term>42C40</term><term>65T60</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Adaptive strategies in space and time allow considerable speed-up of finite volume schemes for conservation laws, while controlling the accuracy of the discretization. In this paper, a multiresolution technique for finite volume schemes with explicit time discretization is presented. An adaptive grid is introduced by suitable thresholding of the wavelet coefficients, which maintains the accuracy of the finite volume scheme of the regular grid. Further speed-up is obtained by local scale-dependent time stepping, i.e., on large scales larger time steps can be used without violating the stability condition of the explicit scheme. Furthermore, an estimation of the truncation error in time, using embedded Runge-Kutta type schemes, guarantees a control of the time step for a given precision. The accuracy and efficiency of the fully adaptive method is illustrated with applications for compressible Euler equations in one and two space dimensions.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0168-9274</s0></fA01><fA02 i1="01"><s0>ANMAEL</s0></fA02><fA03 i2="1"><s0>Appl. numer. math.</s0></fA03><fA05><s2>59</s2></fA05><fA06><s2>9</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Space-time adaptive multiresolution methods for hyperbolic conservation laws: Applications to compressible Euler equations</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Second Chilean Workshop on Numerical Analysis of Partial Differential Equations (WONAPDE 2007)</s1></fA09><fA11 i1="01" i2="1"><s1>DOMINGUES (Margarete O.)</s1></fA11><fA11 i1="02" i2="1"><s1>GOMES (Sônia M.)</s1></fA11><fA11 i1="03" i2="1"><s1>ROUSSEL (Olivier)</s1></fA11><fA11 i1="04" i2="1"><s1>SCHNEIDER (Kai)</s1></fA11><fA12 i1="01" i2="1"><s1>BÜRGER (Raimund)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>RODRIGUEZ (Rodolfo)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Laboratório Associado de Computação e Matemática Aplicada (LAC). Cordenaçào dos Laboratórios Associados (CTE), Instituto Nacional de Pesquisas Espaciais (INPE), Av. dos Astronautas, 1758</s1><s2>12227-010 Sào José dos Campos</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Universidade Estadual de Campinas, IMECC, Caixa Postal 6065</s1><s2>13083-970 Campinas SP</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratoire de Modélisation en Mécanique Procédés Propres (M2P2). CNRS and Universités d'Aix-Marseille, 38, rue Frédéric Joliot-Curie</s1><s2>13451 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Institut für Tedinische Chemie und Polymerchemie (TCP). Universität Karlsruhe (TH). Kaiserstr. 12</s1><s2>76128 Karlsruhe</s2><s3>DEU</s3><sZ>3 aut.</sZ></fA14><fA14 i1="05"><s1>Centre de Mathématiques et d'Informatique (CMI), Université de Provence. 39, rue Frédéric Joliot-Curie</s1><s2>13453 Marseille</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA15 i1="01"><s1>Universidad de Conception</s1><s3>CHL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA15><fA20><s1>2303-2321</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20860</s2><s5>354000187100130170</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>45 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0352756</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied numerical mathematics</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>Adaptive strategies in space and time allow considerable speed-up of finite volume schemes for conservation laws, while controlling the accuracy of the discretization. In this paper, a multiresolution technique for finite volume schemes with explicit time discretization is presented. An adaptive grid is introduced by suitable thresholding of the wavelet coefficients, which maintains the accuracy of the finite volume scheme of the regular grid. Further speed-up is obtained by local scale-dependent time stepping, i.e., on large scales larger time steps can be used without violating the stability condition of the explicit scheme. Furthermore, an estimation of the truncation error in time, using embedded Runge-Kutta type schemes, guarantees a control of the time step for a given precision. The accuracy and efficiency of the fully adaptive method is illustrated with applications for compressible Euler equations in one and two space dimensions.</s0></fC01><fC02 i1="01" i2="X"><s0>001A02I01O</s0></fC02><fC02 i1="02" i2="X"><s0>001A02E08</s0></fC02><fC02 i1="03" i2="X"><s0>001A02E12</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Transformation ondelette</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Wavelet transformation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Transformación ondita</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Méthode adaptative</s0><s5>17</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Adaptive method</s0><s5>17</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Método adaptativo</s0><s5>17</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Loi conservation</s0><s5>18</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Conservation law</s0><s5>18</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Ley conservación</s0><s5>18</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Equation Euler</s0><s5>19</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Euler equation</s0><s5>19</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Ecuación Euler</s0><s5>19</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Méthode volume fini</s0><s5>20</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Finite volume method</s0><s5>20</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Método volumen finito</s0><s5>20</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Méthode discrétisation</s0><s5>21</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Discretization method</s0><s5>21</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Método discretización</s0><s5>21</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Maillage</s0><s5>22</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Grid pattern</s0><s5>22</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Celdarada</s0><s5>22</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Ondelette</s0><s5>23</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Wavelets</s0><s5>23</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Stabilité numérique</s0><s5>24</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Numerical stability</s0><s5>24</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Estabilidad numérica</s0><s5>24</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Estimation erreur</s0><s5>25</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Error estimation</s0><s5>25</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estimación error</s0><s5>25</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Erreur troncature</s0><s5>26</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Truncation error</s0><s5>26</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Error truncamiento</s0><s5>26</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Troncature</s0><s5>27</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Truncation</s0><s5>27</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Truncamiento</s0><s5>27</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Méthode Runge Kutta</s0><s5>28</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Runge Kutta method</s0><s5>28</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Método Runge Kutta</s0><s5>28</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Calcul 2 dimensions</s0><s5>29</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Two-dimensional calculations</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Mathématiques appliquées</s0><s5>30</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Applied mathematics</s0><s5>30</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Matemáticas aplicadas</s0><s5>30</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Analyse numérique</s0><s5>31</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Numerical analysis</s0><s5>31</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Análisis numérico</s0><s5>31</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>35L65</s0><s4>INC</s4><s5>70</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>42C40</s0><s4>INC</s4><s5>71</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>65T60</s0><s4>INC</s4><s5>72</s5></fC03><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Chilean Workshop on Numerical Analysis of Partial Differential Equations (WONAPDE 2007)</s1><s2>2</s2><s3>Concepción CHL</s3><s4>2007-01-16</s4></fA30></pR></standard><server><NO>PASCAL 09-0352756 INIST</NO><ET>Space-time adaptive multiresolution methods for hyperbolic conservation laws: Applications to compressible Euler equations</ET><AU>DOMINGUES (Margarete O.); GOMES (Sônia M.); ROUSSEL (Olivier); SCHNEIDER (Kai); BÜRGER (Raimund); RODRIGUEZ (Rodolfo)</AU><AF>Laboratório Associado de Computação e Matemática Aplicada (LAC). Cordenaçào dos Laboratórios Associados (CTE), Instituto Nacional de Pesquisas Espaciais (INPE), Av. dos Astronautas, 1758/12227-010 Sào José dos Campos/Brésil (1 aut.); Universidade Estadual de Campinas, IMECC, Caixa Postal 6065/13083-970 Campinas SP/Brésil (2 aut.); Laboratoire de Modélisation en Mécanique Procédés Propres (M2P2). CNRS and Universités d'Aix-Marseille, 38, rue Frédéric Joliot-Curie/13451 Marseille/France (1 aut., 4 aut.); Institut für Tedinische Chemie und Polymerchemie (TCP). Universität Karlsruhe (TH). Kaiserstr. 12/76128 Karlsruhe/Allemagne (3 aut.); Centre de Mathématiques et d'Informatique (CMI), Université de Provence. 39, rue Frédéric Joliot-Curie/13453 Marseille/France (4 aut.); Universidad de Conception/Chili (1 aut., 2 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Applied numerical mathematics; ISSN 0168-9274; Coden ANMAEL; Pays-Bas; Da. 2009; Vol. 59; No. 9; Pp. 2303-2321; Bibl. 45 ref.</SO><LA>Anglais</LA><EA>Adaptive strategies in space and time allow considerable speed-up of finite volume schemes for conservation laws, while controlling the accuracy of the discretization. In this paper, a multiresolution technique for finite volume schemes with explicit time discretization is presented. An adaptive grid is introduced by suitable thresholding of the wavelet coefficients, which maintains the accuracy of the finite volume scheme of the regular grid. Further speed-up is obtained by local scale-dependent time stepping, i.e., on large scales larger time steps can be used without violating the stability condition of the explicit scheme. Furthermore, an estimation of the truncation error in time, using embedded Runge-Kutta type schemes, guarantees a control of the time step for a given precision. The accuracy and efficiency of the fully adaptive method is illustrated with applications for compressible Euler equations in one and two space dimensions.</EA><CC>001A02I01O; 001A02E08; 001A02E12</CC><FD>Transformation ondelette; Méthode adaptative; Loi conservation; Equation Euler; Méthode volume fini; Méthode discrétisation; Maillage; Ondelette; Stabilité numérique; Estimation erreur; Erreur troncature; Troncature; Méthode Runge Kutta; Calcul 2 dimensions; Mathématiques appliquées; Analyse numérique; 35L65; 42C40; 65T60</FD><ED>Wavelet transformation; Adaptive method; Conservation law; Euler equation; Finite volume method; Discretization method; Grid pattern; Wavelets; Numerical stability; Error estimation; Truncation error; Truncation; Runge Kutta method; Two-dimensional calculations; Applied mathematics; Numerical analysis</ED><SD>Transformación ondita; Método adaptativo; Ley conservación; Ecuación Euler; Método volumen finito; Método discretización; Celdarada; Estabilidad numérica; Estimación error; Error truncamiento; Truncamiento; Método Runge Kutta; Matemáticas aplicadas; Análisis numérico</SD><LO>INIST-20860.354000187100130170</LO><ID>09-0352756</ID></server></inist></record>
000D31	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Learning How to Extract Rotation-Invariant and Scale-Invariant Features from Texture Images</title><author><name sortKey="Montoya Zegarra, Javier A" uniqKey="Montoya Zegarra J">Javier A. Montoya-Zegarra</name><affiliation><inist:fA14 i1="01"><s1>Computer Engineering Department, Faculty of Engineering, San Pablo Catholic University, Av. Salaverry 301</s1><s2>Vallecito, Arequipa</s2><s3>PER</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Papa, Joao Paulo" uniqKey="Papa J">Joao Paulo Papa</name><affiliation><inist:fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Leite, Neucimar J" uniqKey="Leite N">Neucimar J. Leite</name><affiliation><inist:fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silva Torres, Ricardo" uniqKey="Da Silva Torres R">Ricardo Da Silva Torres</name><affiliation><inist:fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Falcao, Alexandre X" uniqKey="Falcao A">Alexandre X. Falcao</name><affiliation><inist:fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0353167</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0353167 INIST</idno><idno type="RBID">Pascal:09-0353167</idno><idno type="wicri:Area/Main/Corpus">001C50</idno></publicationStmt><seriesStmt><idno type="ISSN">1687-6172</idno><title level="j" type="abbreviated">EURASIP J. Adv.  Signal Process. : (Print)</title><title level="j" type="main">EURASIP Journal on Advances in Signal Processing : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Automatic classification</term><term>Content analysis</term><term>Feature extraction</term><term>Image quality</term><term>Learning</term><term>Rotational invariance</term><term>Scale invariance</term><term>Signal classification</term><term>Signal distortion</term><term>Signal processing</term><term>State of the art</term><term>Texture</term><term>Texture analysis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Apprentissage</term><term>Invariance rotationnelle</term><term>Invariance échelle</term><term>Texture</term><term>Extraction caractéristique</term><term>Analyse texture</term><term>Distorsion signal</term><term>Qualité image</term><term>Classification automatique</term><term>Etat actuel</term><term>Traitement signal</term><term>Analyse contenu</term><term>Classification signal</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Learning how to extract texture features from noncontrolled environments characterized by distorted images is a still-open task. By using a new rotation-invariant and scale-invariant image descriptor based on steerable pyramid decomposition, and a novel multiclass recognition method based on optimum-path forest, a new texture recognition system is proposed. By combining the discriminating power of our image descriptor and classifier, our system uses small-size feature vectors to characterize texture images without compromising overall classification rates. State-of-the-art recognition results are further presented on the Brodatz data set. High classification rates demonstrate the superiority of the proposed system.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1687-6172</s0></fA01><fA03 i2="1"><s0>EURASIP J. Adv.  Signal Process. : (Print)</s0></fA03><fA05><s2>2008</s2></fA05><fA06><s2>18</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Learning How to Extract Rotation-Invariant and Scale-Invariant Features from Texture Images</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Machine Learning in Image Processing</s1></fA09><fA11 i1="01" i2="1"><s1>MONTOYA-ZEGARRA (Javier A.)</s1></fA11><fA11 i1="02" i2="1"><s1>PAPA (Joao Paulo)</s1></fA11><fA11 i1="03" i2="1"><s1>LEITE (Neucimar J.)</s1></fA11><fA11 i1="04" i2="1"><s1>DA SILVA TORRES (Ricardo)</s1></fA11><fA11 i1="05" i2="1"><s1>FALCAO (Alexandre X.)</s1></fA11><fA12 i1="01" i2="1"><s1>LEZORAY (Olivier)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>CHARRIER (Christophe)</s1><s9>ed.</s9></fA12><fA12 i1="03" i2="1"><s1>CARDOT (Hubert)</s1><s9>ed.</s9></fA12><fA12 i1="04" i2="1"><s1>LEFEVRE (Sébastien)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Computer Engineering Department, Faculty of Engineering, San Pablo Catholic University, Av. Salaverry 301</s1><s2>Vallecito, Arequipa</s2><s3>PER</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Institute of Computing, The State University of Campinas</s1><s2>13083-970 Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA15 i1="01"><s1>GREYC, UMR CNRS 6072, ENSICAEN, Université de Caen Basse-Normandie, 6 Boulevard du Maréchal Juin</s1><s2>14050 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA15><fA15 i1="02"><s1>Pattern Recognition and Image analysis Team, Computer Science Laboratory (LI), Université François Rabelais de Tours, 64 avenue Jean Portalis</s1><s2>37200 Tours</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA15><fA15 i1="03"><s1>Models Images Vision (MIV) Team, Image Sciences, Computer Sciences and Remote Sensing Laboratory (LSIIT), Université Louis Pasteur de Strasbourg, Pôle API, Bd. Brant, BP 10413</s1><s2>67412 Illkirch</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA15><fA20><s2>J1-J15</s2></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27499</s2><s5>354000188381030100</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>53 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0353167</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>EURASIP Journal on Advances in Signal Processing : (Print)</s0></fA64><fA66 i1="01"><s0>EGY</s0></fA66><fC01 i1="01" l="ENG"><s0>Learning how to extract texture features from noncontrolled environments characterized by distorted images is a still-open task. By using a new rotation-invariant and scale-invariant image descriptor based on steerable pyramid decomposition, and a novel multiclass recognition method based on optimum-path forest, a new texture recognition system is proposed. By combining the discriminating power of our image descriptor and classifier, our system uses small-size feature vectors to characterize texture images without compromising overall classification rates. State-of-the-art recognition results are further presented on the Brodatz data set. High classification rates demonstrate the superiority of the proposed system.</s0></fC01><fC02 i1="01" i2="X"><s0>001D04A04A2</s0></fC02><fC02 i1="02" i2="X"><s0>001D04A05D</s0></fC02><fC02 i1="03" i2="X"><s0>001D04A04A1</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Apprentissage</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Learning</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Aprendizaje</s0><s5>01</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Invariance rotationnelle</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Rotational invariance</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Invariance échelle</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Scale invariance</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Invarianza escala</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Texture</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Texture</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Textura</s0><s5>04</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Extraction caractéristique</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Feature extraction</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Analyse texture</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Texture analysis</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Análisis textura</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Distorsion signal</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Signal distortion</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Distorsión señal</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Qualité image</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Image quality</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Calidad imagen</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Classification automatique</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Automatic classification</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Clasificación automática</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Etat actuel</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>State of the art</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estado actual</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Traitement signal</s0><s5>31</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Signal processing</s0><s5>31</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Procesamiento señal</s0><s5>31</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Analyse contenu</s0><s5>32</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Content analysis</s0><s5>32</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Análisis contenido</s0><s5>32</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Classification signal</s0><s5>33</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Signal classification</s0><s5>33</s5></fC03><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0353167 INIST</NO><ET>Learning How to Extract Rotation-Invariant and Scale-Invariant Features from Texture Images</ET><AU>MONTOYA-ZEGARRA (Javier A.); PAPA (Joao Paulo); LEITE (Neucimar J.); DA SILVA TORRES (Ricardo); FALCAO (Alexandre X.); LEZORAY (Olivier); CHARRIER (Christophe); CARDOT (Hubert); LEFEVRE (Sébastien)</AU><AF>Computer Engineering Department, Faculty of Engineering, San Pablo Catholic University, Av. Salaverry 301/Vallecito, Arequipa/Pérou (1 aut.); Institute of Computing, The State University of Campinas/13083-970 Campinas, SP/Brésil (1 aut., 2 aut., 3 aut., 4 aut., 5 aut.); GREYC, UMR CNRS 6072, ENSICAEN, Université de Caen Basse-Normandie, 6 Boulevard du Maréchal Juin/14050 Caen/France (1 aut., 2 aut.); Pattern Recognition and Image analysis Team, Computer Science Laboratory (LI), Université François Rabelais de Tours, 64 avenue Jean Portalis/37200 Tours/France (3 aut.); Models Images Vision (MIV) Team, Image Sciences, Computer Sciences and Remote Sensing Laboratory (LSIIT), Université Louis Pasteur de Strasbourg, Pôle API, Bd. Brant, BP 10413/67412 Illkirch/France (4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>EURASIP Journal on Advances in Signal Processing : (Print); ISSN 1687-6172; Egypte; Da. 2008; Vol. 2008; No. 18; J1-J15; Bibl. 53 ref.</SO><LA>Anglais</LA><EA>Learning how to extract texture features from noncontrolled environments characterized by distorted images is a still-open task. By using a new rotation-invariant and scale-invariant image descriptor based on steerable pyramid decomposition, and a novel multiclass recognition method based on optimum-path forest, a new texture recognition system is proposed. By combining the discriminating power of our image descriptor and classifier, our system uses small-size feature vectors to characterize texture images without compromising overall classification rates. State-of-the-art recognition results are further presented on the Brodatz data set. High classification rates demonstrate the superiority of the proposed system.</EA><CC>001D04A04A2; 001D04A05D; 001D04A04A1</CC><FD>Apprentissage; Invariance rotationnelle; Invariance échelle; Texture; Extraction caractéristique; Analyse texture; Distorsion signal; Qualité image; Classification automatique; Etat actuel; Traitement signal; Analyse contenu; Classification signal</FD><ED>Learning; Rotational invariance; Scale invariance; Texture; Feature extraction; Texture analysis; Signal distortion; Image quality; Automatic classification; State of the art; Signal processing; Content analysis; Signal classification</ED><SD>Aprendizaje; Invarianza escala; Textura; Análisis textura; Distorsión señal; Calidad imagen; Clasificación automática; Estado actual; Procesamiento señal; Análisis contenido</SD><LO>INIST-27499.354000188381030100</LO><ID>09-0353167</ID></server></inist></record>
000D32	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">eNOS Activation Induced by a Polyphenol-Rich Grape Skin Extract in Porcine Coronary Arteries</title><author><name sortKey="Vanesca Frota Madeira, Socorro" uniqKey="Vanesca Frota Madeira S">Socorro Vanesca Frota Madeira</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Department of Pharmacology, IBRAG-CB State University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Auger, Cyril" uniqKey="Auger C">Cyril Auger</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Anselm, Eric" uniqKey="Anselm E">Eric Anselm</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chataigneau, Marta" uniqKey="Chataigneau M">Marta Chataigneau</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chataigneau, Thierry" uniqKey="Chataigneau T">Thierry Chataigneau</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Soares De Moura, Roberto" uniqKey="Soares De Moura R">Roberto Soares De Moura</name><affiliation><inist:fA14 i1="02"><s1>Department of Pharmacology, IBRAG-CB State University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schini Kerth, Valerie B" uniqKey="Schini Kerth V">Valérie B. Schini-Kerth</name><affiliation><inist:fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0354190</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0354190 INIST</idno><idno type="RBID">Pascal:09-0354190</idno><idno type="wicri:Area/Main/Corpus">001C49</idno></publicationStmt><seriesStmt><idno type="ISSN">1018-1172</idno><title level="j" type="abbreviated">J. vasc. res.</title><title level="j" type="main">Journal of vascular research</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Activation</term><term>Circulatory system</term><term>Coronary artery</term><term>Endothelium</term><term>Kinase</term><term>Mammalia</term><term>Nitric oxide</term><term>Phosphoinositide</term><term>Pig</term><term>Polyphenol</term><term>Skin</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Activation</term><term>Polyphénol</term><term>Peau</term><term>Artère coronaire</term><term>Inositophospholipide</term><term>Kinase</term><term>Monoxyde d'azote</term><term>Endothélium</term><term>Appareil circulatoire</term><term>Mammalia</term><term>Porc</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background/Aims: Drinking red wine is associated with a decreased mortality from coronary heart diseases. This study examined whether polyphenols contained in a grape skin extract (GSE) triggered the endothelial formation of nitric oxide (NO) and investigated the underlying mechanism. Methods: Vascular reactivity was assessed in organ chambers using porcine coronary artery rings in the presence of indomethacin (a cyclooxygenase inhibitor) and charybdotoxin plus apamin (inhibitors ofendothelium-derived hyper-polarizing factor-mediated responses).The phosphorylation level of Src, Akt and endothelial NO synthase (eNOS) were assessed by Western blot analysis, and the formation of reactive oxygen species (ROS) was investigated using dihydro-ethidine and dichlorodihydrofluorescein. Results: GSE-induced endothelium-dependent relaxations were abolished by N<sup>G</sup>-nitro-L-arginine (an eNOS inhibitor) and ODQ (a soluble guanylyl cyclase inhibitor), and they were reduced by MnTMPyP, polyethyleneglycol catalase, PP2 (an inhibitor of Src kinase) and wortmannin (an inhibitor of phosphoinositide 3-kinase). GSE caused phosphorylation of Src, which was prevented by MnTMPyP. It also caused phosphorylation of Akt and eNOS, which were prevented by MnTMPyP, polyethyleneglycol catalase, PP2, wortmannin and LY294002. GSE elicited the formation of ROS in native and cultured endothelial cells, which was prevented by MnTMPyP. Conclusions: GSE causes endothelium-dependent NO-mediated relaxations of coronary arteries. This effect involves the intracellular formation of ROS in endothelial cells leading to the Src kinase/phosphoinositide 3-kinase/Akt-dependent phosphorylation of eNOS.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1018-1172</s0></fA01><fA03 i2="1"><s0>J. vasc. res.</s0></fA03><fA05><s2>46</s2></fA05><fA06><s2>5</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>eNOS Activation Induced by a Polyphenol-Rich Grape Skin Extract in Porcine Coronary Arteries</s1></fA08><fA11 i1="01" i2="1"><s1>VANESCA FROTA MADEIRA (Socorro)</s1></fA11><fA11 i1="02" i2="1"><s1>AUGER (Cyril)</s1></fA11><fA11 i1="03" i2="1"><s1>ANSELM (Eric)</s1></fA11><fA11 i1="04" i2="1"><s1>CHATAIGNEAU (Marta)</s1></fA11><fA11 i1="05" i2="1"><s1>CHATAIGNEAU (Thierry)</s1></fA11><fA11 i1="06" i2="1"><s1>SOARES DE MOURA (Roberto)</s1></fA11><fA11 i1="07" i2="1"><s1>SCHINI-KERTH (Valérie B.)</s1></fA11><fA14 i1="01"><s1>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur</s1><s2>Illkirch</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Pharmacology, IBRAG-CB State University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></fA14><fA20><s1>406-416</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>11498</s2><s5>354000172566120030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>44 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0354190</s0></fA47><fA60><s1>P</s1><s3>PR</s3></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of vascular research</s0></fA64><fA66 i1="01"><s0>CHE</s0></fA66><fC01 i1="01" l="ENG"><s0>Background/Aims: Drinking red wine is associated with a decreased mortality from coronary heart diseases. This study examined whether polyphenols contained in a grape skin extract (GSE) triggered the endothelial formation of nitric oxide (NO) and investigated the underlying mechanism. Methods: Vascular reactivity was assessed in organ chambers using porcine coronary artery rings in the presence of indomethacin (a cyclooxygenase inhibitor) and charybdotoxin plus apamin (inhibitors ofendothelium-derived hyper-polarizing factor-mediated responses).The phosphorylation level of Src, Akt and endothelial NO synthase (eNOS) were assessed by Western blot analysis, and the formation of reactive oxygen species (ROS) was investigated using dihydro-ethidine and dichlorodihydrofluorescein. Results: GSE-induced endothelium-dependent relaxations were abolished by N<sup>G</sup>-nitro-L-arginine (an eNOS inhibitor) and ODQ (a soluble guanylyl cyclase inhibitor), and they were reduced by MnTMPyP, polyethyleneglycol catalase, PP2 (an inhibitor of Src kinase) and wortmannin (an inhibitor of phosphoinositide 3-kinase). GSE caused phosphorylation of Src, which was prevented by MnTMPyP. It also caused phosphorylation of Akt and eNOS, which were prevented by MnTMPyP, polyethyleneglycol catalase, PP2, wortmannin and LY294002. GSE elicited the formation of ROS in native and cultured endothelial cells, which was prevented by MnTMPyP. Conclusions: GSE causes endothelium-dependent NO-mediated relaxations of coronary arteries. This effect involves the intracellular formation of ROS in endothelial cells leading to the Src kinase/phosphoinositide 3-kinase/Akt-dependent phosphorylation of eNOS.</s0></fC01><fC02 i1="01" i2="X"><s0>002A22</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Activation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Activation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Activación</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Polyphénol</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Polyphenol</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Polifenol</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Peau</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Skin</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Piel</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Artère coronaire</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Coronary artery</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Arteria coronaria</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Inositophospholipide</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Phosphoinositide</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Inositofosfolípido</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Kinase</s0><s2>FE</s2><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Monoxyde d'azote</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Nitric oxide</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Nitrógeno monóxido</s0><s2>NK</s2><s2>FX</s2><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Endothélium</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Endothelium</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Endotelio</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Appareil circulatoire</s0><s5>10</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Circulatory system</s0><s5>10</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Aparato circulatorio</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Mammalia</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Mammalia</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Mammalia</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Porc</s0><s5>54</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Pig</s0><s5>54</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Cerdo</s0><s5>54</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Phénols</s0><s2>FX</s2><s5>20</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Phenols</s0><s2>FX</s2><s5>20</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Fenoles</s0><s2>FX</s2><s5>20</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Artiodactyla</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Artiodactyla</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Artiodactyla</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Ungulata</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Ungulata</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Ungulata</s0><s2>NS</s2></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0354190 INIST</NO><ET>eNOS Activation Induced by a Polyphenol-Rich Grape Skin Extract in Porcine Coronary Arteries</ET><AU>VANESCA FROTA MADEIRA (Socorro); AUGER (Cyril); ANSELM (Eric); CHATAIGNEAU (Marta); CHATAIGNEAU (Thierry); SOARES DE MOURA (Roberto); SCHINI-KERTH (Valérie B.)</AU><AF>UMR CNRS 7175, Pharmacologie et Physico-Chimie, Faculté de Pharmacie, Université Louis Pasteur/Illkirch/France (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 7 aut.); Department of Pharmacology, IBRAG-CB State University of Rio de Janeiro/Rio de Janeiro/Brésil (1 aut., 6 aut.)</AF><DT>Publication en série; Papier de recherche; Niveau analytique</DT><SO>Journal of vascular research; ISSN 1018-1172; Suisse; Da. 2009; Vol. 46; No. 5; Pp. 406-416; Bibl. 44 ref.</SO><LA>Anglais</LA><EA>Background/Aims: Drinking red wine is associated with a decreased mortality from coronary heart diseases. This study examined whether polyphenols contained in a grape skin extract (GSE) triggered the endothelial formation of nitric oxide (NO) and investigated the underlying mechanism. Methods: Vascular reactivity was assessed in organ chambers using porcine coronary artery rings in the presence of indomethacin (a cyclooxygenase inhibitor) and charybdotoxin plus apamin (inhibitors ofendothelium-derived hyper-polarizing factor-mediated responses).The phosphorylation level of Src, Akt and endothelial NO synthase (eNOS) were assessed by Western blot analysis, and the formation of reactive oxygen species (ROS) was investigated using dihydro-ethidine and dichlorodihydrofluorescein. Results: GSE-induced endothelium-dependent relaxations were abolished by N<sup>G</sup>-nitro-L-arginine (an eNOS inhibitor) and ODQ (a soluble guanylyl cyclase inhibitor), and they were reduced by MnTMPyP, polyethyleneglycol catalase, PP2 (an inhibitor of Src kinase) and wortmannin (an inhibitor of phosphoinositide 3-kinase). GSE caused phosphorylation of Src, which was prevented by MnTMPyP. It also caused phosphorylation of Akt and eNOS, which were prevented by MnTMPyP, polyethyleneglycol catalase, PP2, wortmannin and LY294002. GSE elicited the formation of ROS in native and cultured endothelial cells, which was prevented by MnTMPyP. Conclusions: GSE causes endothelium-dependent NO-mediated relaxations of coronary arteries. This effect involves the intracellular formation of ROS in endothelial cells leading to the Src kinase/phosphoinositide 3-kinase/Akt-dependent phosphorylation of eNOS.</EA><CC>002A22</CC><FD>Activation; Polyphénol; Peau; Artère coronaire; Inositophospholipide; Kinase; Monoxyde d'azote; Endothélium; Appareil circulatoire; Mammalia; Porc</FD><FG>Transferases; Enzyme; Vertebrata; Phénols; Artiodactyla; Ungulata</FG><ED>Activation; Polyphenol; Skin; Coronary artery; Phosphoinositide; Kinase; Nitric oxide; Endothelium; Circulatory system; Mammalia; Pig</ED><EG>Transferases; Enzyme; Vertebrata; Phenols; Artiodactyla; Ungulata</EG><SD>Activación; Polifenol; Piel; Arteria coronaria; Inositofosfolípido; Kinase; Nitrógeno monóxido; Endotelio; Aparato circulatorio; Mammalia; Cerdo</SD><LO>INIST-11498.354000172566120030</LO><ID>09-0354190</ID></server></inist></record>
000D33	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Analgesic properties of S100A9 C-terminal domain: a mechanism dependent on calcium channel inhibition</title><author><name sortKey="Squarzoni Dale, Camila" uniqKey="Squarzoni Dale C">Camila Squarzoni Dale</name><affiliation><inist:fA14 i1="01"><s1>INSERM, U563, Centre de Physiopathologie de Toulouse Purpan</s1><s2>Toulouse 31 300</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Toulouse III Paul Sabatier</s1><s2>Toulouse 31000</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Altier, Christophe" uniqKey="Altier C">Christophe Altier</name><affiliation><inist:fA14 i1="03"><s1>Department of Physiology and Biophysics Hotchkiss Brain Institute, University of Calgary</s1><s2>Calgary, AB T2N 4N1</s2><s3>CAN</s3><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cenac, Nicolas" uniqKey="Cenac N">Nicolas Cenac</name><affiliation><inist:fA14 i1="01"><s1>INSERM, U563, Centre de Physiopathologie de Toulouse Purpan</s1><s2>Toulouse 31 300</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Toulouse III Paul Sabatier</s1><s2>Toulouse 31000</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Giorgi, Renata" uniqKey="Giorgi R">Renata Giorgi</name><affiliation><inist:fA14 i1="04"><s1>Laboratory of Pathophysiolog,y. Butantan Institute</s1><s2>São Paulo, SP 05505-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Aparecida Juliano, Maria" uniqKey="Aparecida Juliano M">Maria Aparecida Juliano</name><affiliation><inist:fA14 i1="05"><s1>Department of Biophysics, Pharmacology Institute, Federal University of São Paulo</s1><s2>São Paulo, SP 04044-020</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Juliano, Luiz" uniqKey="Juliano L">Luiz Juliano</name><affiliation><inist:fA14 i1="05"><s1>Department of Biophysics, Pharmacology Institute, Federal University of São Paulo</s1><s2>São Paulo, SP 04044-020</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Zamponi, Gerald W" uniqKey="Zamponi G">Gerald W. Zamponi</name><affiliation><inist:fA14 i1="03"><s1>Department of Physiology and Biophysics Hotchkiss Brain Institute, University of Calgary</s1><s2>Calgary, AB T2N 4N1</s2><s3>CAN</s3><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vergnolle, Nathalie" uniqKey="Vergnolle N">Nathalie Vergnolle</name><affiliation><inist:fA14 i1="01"><s1>INSERM, U563, Centre de Physiopathologie de Toulouse Purpan</s1><s2>Toulouse 31 300</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Université Toulouse III Paul Sabatier</s1><s2>Toulouse 31000</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="06"><s1>Department of Pharmacology and Therapeutics, University of Calgary</s1><s2>AB T2N4N1</s2><s3>CAN</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0356132</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0356132 INIST</idno><idno type="RBID">Pascal:09-0356132</idno><idno type="wicri:Area/Main/Corpus">001C48</idno></publicationStmt><seriesStmt><idno type="ISSN">0767-3981</idno><title level="j" type="abbreviated">Fundam. clin. pharmacol.</title><title level="j" type="main">Fundamental &#38; clinical pharmacology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Analgesia</term><term>Analgesic</term><term>C terminal-Sequence</term><term>Calcium</term><term>Calgranulin B</term><term>Inflammation</term><term>Inhibitor</term><term>Ionic channel</term><term>Mechanism of action</term><term>N-type calcium channel</term><term>Neuron</term><term>Spinal ganglion</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Analgésique</term><term>Séquence C terminale</term><term>Mécanisme action</term><term>Canal ionique</term><term>Calcium</term><term>Inhibiteur</term><term>Analgésie</term><term>Ganglion spinal</term><term>Neurone</term><term>Inflammation</term><term>Canal calcique N</term><term>Calgranuline B</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Calcium-binding protein S100A9 and its C-terminus peptide (mS100A9p) are anti-inflammatory and induce antinociception in rodents. We investigated the mechanisms involved in this effect, and whether they depend or not on the anti-inflammatory properties of mS100A9p. In mice, mS100A9p inhibited thermal and mechanical hyperalgesia and allodynia induced by either carrageenan or formalin, without interfering with paw edema. mS100A9p also inhibited myeloperoxidase activity (MPO), a marker of granulocyte infiltration, induced by carrageenan, but increased MPO after formalin intraplantar injection. The in vivo analgesic properties of mS100A9p were independent of opioid receptor activation. Calcium flux into dorsal root ganglia neurons induced by KCl was inhibited by mS100A9p, suggesting that this protein is able to inhibit signaling, in sensory neurons. The inhibitory effects of mS100A9p on primary afferent signaling were neither due to intracellular calcium store inhibition nor to calcium chelating properties. However, mS100A9p was able to inhibit calcium currents carried by transiently expressed N-type, but not L-type calcium channels, as demonstrated both by gene transfection techniques and electrophysiology. These data demonstrate that mS100A9p interferes with mechanisms involved in nociception, hyperalgesia and calcium signaling in sensory neurons, modulating primary afferent nociceptive signal by inhibiting activation of N-type voltage operated calcium channels.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0767-3981</s0></fA01><fA02 i1="01"><s0>FCPHEZ</s0></fA02><fA03 i2="1"><s0>Fundam. clin. pharmacol.</s0></fA03><fA05><s2>23</s2></fA05><fA06><s2>4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Analgesic properties of S100A9 C-terminal domain: a mechanism dependent on calcium channel inhibition</s1></fA08><fA11 i1="01" i2="1"><s1>SQUARZONI DALE (Camila)</s1></fA11><fA11 i1="02" i2="1"><s1>ALTIER (Christophe)</s1></fA11><fA11 i1="03" i2="1"><s1>CENAC (Nicolas)</s1></fA11><fA11 i1="04" i2="1"><s1>GIORGI (Renata)</s1></fA11><fA11 i1="05" i2="1"><s1>APARECIDA JULIANO (Maria)</s1></fA11><fA11 i1="06" i2="1"><s1>JULIANO (Luiz)</s1></fA11><fA11 i1="07" i2="1"><s1>ZAMPONI (Gerald W.)</s1></fA11><fA11 i1="08" i2="1"><s1>VERGNOLLE (Nathalie)</s1></fA11><fA14 i1="01"><s1>INSERM, U563, Centre de Physiopathologie de Toulouse Purpan</s1><s2>Toulouse 31 300</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="02"><s1>Université Toulouse III Paul Sabatier</s1><s2>Toulouse 31000</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="03"><s1>Department of Physiology and Biophysics Hotchkiss Brain Institute, University of Calgary</s1><s2>Calgary, AB T2N 4N1</s2><s3>CAN</s3><sZ>2 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="04"><s1>Laboratory of Pathophysiolog,y. Butantan Institute</s1><s2>São Paulo, SP 05505-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Department of Biophysics, Pharmacology Institute, Federal University of São Paulo</s1><s2>São Paulo, SP 04044-020</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="06"><s1>Department of Pharmacology and Therapeutics, University of Calgary</s1><s2>AB T2N4N1</s2><s3>CAN</s3><sZ>8 aut.</sZ></fA14><fA20><s1>427-438</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14711</s2><s5>354000172550280060</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>44 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0356132</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Fundamental &#38; clinical pharmacology</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Calcium-binding protein S100A9 and its C-terminus peptide (mS100A9p) are anti-inflammatory and induce antinociception in rodents. We investigated the mechanisms involved in this effect, and whether they depend or not on the anti-inflammatory properties of mS100A9p. In mice, mS100A9p inhibited thermal and mechanical hyperalgesia and allodynia induced by either carrageenan or formalin, without interfering with paw edema. mS100A9p also inhibited myeloperoxidase activity (MPO), a marker of granulocyte infiltration, induced by carrageenan, but increased MPO after formalin intraplantar injection. The in vivo analgesic properties of mS100A9p were independent of opioid receptor activation. Calcium flux into dorsal root ganglia neurons induced by KCl was inhibited by mS100A9p, suggesting that this protein is able to inhibit signaling, in sensory neurons. The inhibitory effects of mS100A9p on primary afferent signaling were neither due to intracellular calcium store inhibition nor to calcium chelating properties. However, mS100A9p was able to inhibit calcium currents carried by transiently expressed N-type, but not L-type calcium channels, as demonstrated both by gene transfection techniques and electrophysiology. These data demonstrate that mS100A9p interferes with mechanisms involved in nociception, hyperalgesia and calcium signaling in sensory neurons, modulating primary afferent nociceptive signal by inhibiting activation of N-type voltage operated calcium channels.</s0></fC01><fC02 i1="01" i2="X"><s0>002B02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Analgésique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Analgesic</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Analgésico</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Séquence C terminale</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>C terminal-Sequence</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Secuencia C terminal</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Mécanisme action</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Mechanism of action</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Mecanismo acción</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Canal ionique</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Ionic channel</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Canal iónico</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Calcium</s0><s2>NC</s2><s2>FR</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Calcium</s0><s2>NC</s2><s2>FR</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Calcio</s0><s2>NC</s2><s2>FR</s2><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Inhibiteur</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Inhibitor</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Inhibidor</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Analgésie</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Analgesia</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Analgesia</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Ganglion spinal</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Spinal ganglion</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Ganglio espinal</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Neurone</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Neuron</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Neurona</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Inflammation</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Inflammation</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Inflamación</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Canal calcique N</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>N-type calcium channel</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Canal calcio tipo N</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Calgranuline B</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Calgranulin B</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Elément minéral</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Inorganic element</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Elemento inorgánico</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Moelle épinière</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Spinal cord</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Médula espinal</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Système nerveux central</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Central nervous system</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Sistema nervioso central</s0><s5>39</s5></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0356132 INIST</NO><ET>Analgesic properties of S100A9 C-terminal domain: a mechanism dependent on calcium channel inhibition</ET><AU>SQUARZONI DALE (Camila); ALTIER (Christophe); CENAC (Nicolas); GIORGI (Renata); APARECIDA JULIANO (Maria); JULIANO (Luiz); ZAMPONI (Gerald W.); VERGNOLLE (Nathalie)</AU><AF>INSERM, U563, Centre de Physiopathologie de Toulouse Purpan/Toulouse 31 300/France (1 aut., 3 aut., 8 aut.); Université Toulouse III Paul Sabatier/Toulouse 31000/France (1 aut., 3 aut., 8 aut.); Department of Physiology and Biophysics Hotchkiss Brain Institute, University of Calgary/Calgary, AB T2N 4N1/Canada (2 aut., 7 aut.); Laboratory of Pathophysiolog,y. Butantan Institute/São Paulo, SP 05505-900/Brésil (4 aut.); Department of Biophysics, Pharmacology Institute, Federal University of São Paulo/São Paulo, SP 04044-020/Brésil (5 aut., 6 aut.); Department of Pharmacology and Therapeutics, University of Calgary/AB T2N4N1/Canada (8 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Fundamental &#38; clinical pharmacology; ISSN 0767-3981; Coden FCPHEZ; Royaume-Uni; Da. 2009; Vol. 23; No. 4; Pp. 427-438; Bibl. 44 ref.</SO><LA>Anglais</LA><EA>Calcium-binding protein S100A9 and its C-terminus peptide (mS100A9p) are anti-inflammatory and induce antinociception in rodents. We investigated the mechanisms involved in this effect, and whether they depend or not on the anti-inflammatory properties of mS100A9p. In mice, mS100A9p inhibited thermal and mechanical hyperalgesia and allodynia induced by either carrageenan or formalin, without interfering with paw edema. mS100A9p also inhibited myeloperoxidase activity (MPO), a marker of granulocyte infiltration, induced by carrageenan, but increased MPO after formalin intraplantar injection. The in vivo analgesic properties of mS100A9p were independent of opioid receptor activation. Calcium flux into dorsal root ganglia neurons induced by KCl was inhibited by mS100A9p, suggesting that this protein is able to inhibit signaling, in sensory neurons. The inhibitory effects of mS100A9p on primary afferent signaling were neither due to intracellular calcium store inhibition nor to calcium chelating properties. However, mS100A9p was able to inhibit calcium currents carried by transiently expressed N-type, but not L-type calcium channels, as demonstrated both by gene transfection techniques and electrophysiology. These data demonstrate that mS100A9p interferes with mechanisms involved in nociception, hyperalgesia and calcium signaling in sensory neurons, modulating primary afferent nociceptive signal by inhibiting activation of N-type voltage operated calcium channels.</EA><CC>002B02</CC><FD>Analgésique; Séquence C terminale; Mécanisme action; Canal ionique; Calcium; Inhibiteur; Analgésie; Ganglion spinal; Neurone; Inflammation; Canal calcique N; Calgranuline B</FD><FG>Elément minéral; Moelle épinière; Système nerveux central</FG><ED>Analgesic; C terminal-Sequence; Mechanism of action; Ionic channel; Calcium; Inhibitor; Analgesia; Spinal ganglion; Neuron; Inflammation; N-type calcium channel; Calgranulin B</ED><EG>Inorganic element; Spinal cord; Central nervous system</EG><SD>Analgésico; Secuencia C terminal; Mecanismo acción; Canal iónico; Calcio; Inhibidor; Analgesia; Ganglio espinal; Neurona; Inflamación; Canal calcio tipo N</SD><LO>INIST-14711.354000172550280060</LO><ID>09-0356132</ID></server></inist></record>
000D34	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Trypanosoma cruzi: adaptation to its vectors and its hosts</title><author><name sortKey="Noireau, Francois" uniqKey="Noireau F">François Noireau</name><affiliation><inist:fA14 i1="01"><s1>UR 016, Institut de Recherche pour le Développement (IRD)</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Facultad de Medicina, Universidad Mayor San Simón</s1><s2>Cochabamba</s2><s3>BOL</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Diosque, Patricio" uniqKey="Diosque P">Patricio Diosque</name><affiliation><inist:fA14 i1="03"><s1>Unidad de Epidemiología Molecular, Instituto de Patologia Experimental, Facultad de Ciencias de la Salud, Universidad Nacional de Salta</s1><s2>Salta</s2><s3>ARG</s3><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)</s1><s3>ARG</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jansen, Ana Maria" uniqKey="Jansen A">Ana Maria Jansen</name><affiliation><inist:fA14 i1="05"><s1>Laboratório de Biologia de Tripanosomatideos, Instituto Oswaldo Cruz, Av. Brasil 4365, PO Box 926</s1><s2>Rio de Janeiro, 21040-360, RJ</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0356331</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0356331 INIST</idno><idno type="RBID">Pascal:09-0356331</idno><idno type="wicri:Area/Main/Corpus">001C47</idno></publicationStmt><seriesStmt><idno type="ISSN">0928-4249</idno><title level="j" type="abbreviated">Vet. res. : (Print)</title><title level="j" type="main">Veterinary research : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adaptation</term><term>Mammalia</term><term>Microbiology</term><term>Transmission</term><term>Trypanosoma cruzi</term><term>Vector</term><term>Veterinary</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Trypanosoma cruzi</term><term>Mammalia</term><term>Adaptation</term><term>Vecteur</term><term>Transmission</term><term>Microbiologie</term><term>Vétérinaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">American trypanosomiasis is a parasitic zoonosis that occurs throughout Latin America. The etiological agent, Trypanosoma cruzi, is able to infect almost all tissues of its mammalian hosts and spreads in the environment in multifarious transmission cycles that may or not be connected. This biological plasticity, which is probably the result of the considerable heterogeneity of the taxon, exemplifies a successful adaptation of a parasite resulting in distinct outcomes of infection and a complex epidemiological pattern. In the 1990s, most endemic countries strengthened national control programs to interrupt the transmission of this parasite to humans. However, many obstacles remain to the effective control of the disease. Current knowledge of the different components involved in elaborate system that is American trypanosomiasis (the protozoan parasite T. cruzi, vectors Triatominae and the many reservoirs of infection), as well as the interactions existing within the system, is still incomplete. The Triatominae probably evolve from predatory reduvids in response to the availability of vertebrate food source. However, the basic mechanisms of adaptation of some of them to artificial ecotopes remain poorly understood. Nevertheless, these adaptations seem to be associated with a behavioral plasticity, a reduction in the genetic repertoire and increasing developmental instability.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0928-4249</s0></fA01><fA03 i2="1"><s0>Vet. res. : (Print)</s0></fA03><fA05><s2>40</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Trypanosoma cruzi: adaptation to its vectors and its hosts</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Adaptative strategies of vector-borne pathogens to vectorial transmission</s1></fA09><fA11 i1="01" i2="1"><s1>NOIREAU (François)</s1></fA11><fA11 i1="02" i2="1"><s1>DIOSQUE (Patricio)</s1></fA11><fA11 i1="03" i2="1"><s1>JANSEN (Ana Maria)</s1></fA11><fA12 i1="01" i2="1"><s1>CHOMEL (Bruno B.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>UR 016, Institut de Recherche pour le Développement (IRD)</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Facultad de Medicina, Universidad Mayor San Simón</s1><s2>Cochabamba</s2><s3>BOL</s3><sZ>1 aut.</sZ></fA14><fA14 i1="03"><s1>Unidad de Epidemiología Molecular, Instituto de Patologia Experimental, Facultad de Ciencias de la Salud, Universidad Nacional de Salta</s1><s2>Salta</s2><s3>ARG</s3><sZ>2 aut.</sZ></fA14><fA14 i1="04"><s1>Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)</s1><s3>ARG</s3><sZ>2 aut.</sZ></fA14><fA14 i1="05"><s1>Laboratório de Biologia de Tripanosomatideos, Instituto Oswaldo Cruz, Av. Brasil 4365, PO Box 926</s1><s2>Rio de Janeiro, 21040-360, RJ</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>UC Davis</s1><s3>USA</s3><sZ>1 aut.</sZ></fA15><fA20><s2>2008009.1-2008009.23</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14119</s2><s5>354000188361800050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>123 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0356331</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Veterinary research : (Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>American trypanosomiasis is a parasitic zoonosis that occurs throughout Latin America. The etiological agent, Trypanosoma cruzi, is able to infect almost all tissues of its mammalian hosts and spreads in the environment in multifarious transmission cycles that may or not be connected. This biological plasticity, which is probably the result of the considerable heterogeneity of the taxon, exemplifies a successful adaptation of a parasite resulting in distinct outcomes of infection and a complex epidemiological pattern. In the 1990s, most endemic countries strengthened national control programs to interrupt the transmission of this parasite to humans. However, many obstacles remain to the effective control of the disease. Current knowledge of the different components involved in elaborate system that is American trypanosomiasis (the protozoan parasite T. cruzi, vectors Triatominae and the many reservoirs of infection), as well as the interactions existing within the system, is still incomplete. The Triatominae probably evolve from predatory reduvids in response to the availability of vertebrate food source. However, the basic mechanisms of adaptation of some of them to artificial ecotopes remain poorly understood. Nevertheless, these adaptations seem to be associated with a behavioral plasticity, a reduction in the genetic repertoire and increasing developmental instability.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05</s0></fC02><fC02 i1="02" i2="X"><s0>002A11D</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Trypanosoma cruzi</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Trypanosoma cruzi</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Trypanosoma cruzi</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Mammalia</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Mammalia</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Mammalia</s0><s2>NS</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Adaptation</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Adaptation</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Adaptación</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Vecteur</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Vector</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Vector</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Transmission</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Transmission</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Transmisión</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Microbiologie</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Microbiology</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Microbiología</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Vétérinaire</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Veterinary</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Veterinario</s0><s5>09</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Kinetoplastida</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Kinetoplastida</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Kinetoplastida</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Protozoa</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Protozoa</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Protozoa</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Vertebrata</s0><s2>NS</s2></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0356331 INIST</NO><ET>Trypanosoma cruzi: adaptation to its vectors and its hosts</ET><AU>NOIREAU (François); DIOSQUE (Patricio); JANSEN (Ana Maria); CHOMEL (Bruno B.)</AU><AF>UR 016, Institut de Recherche pour le Développement (IRD)/Montpellier/France (1 aut.); Facultad de Medicina, Universidad Mayor San Simón/Cochabamba/Bolivie (1 aut.); Unidad de Epidemiología Molecular, Instituto de Patologia Experimental, Facultad de Ciencias de la Salud, Universidad Nacional de Salta/Salta/Argentine (2 aut.); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET)/Argentine (2 aut.); Laboratório de Biologia de Tripanosomatideos, Instituto Oswaldo Cruz, Av. Brasil 4365, PO Box 926/Rio de Janeiro, 21040-360, RJ/Brésil (3 aut.); UC Davis/Etats-Unis (1 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Veterinary research : (Print); ISSN 0928-4249; France; Da. 2009; Vol. 40; No. 2; 2008009.1-2008009.23; Bibl. 123 ref.</SO><LA>Anglais</LA><EA>American trypanosomiasis is a parasitic zoonosis that occurs throughout Latin America. The etiological agent, Trypanosoma cruzi, is able to infect almost all tissues of its mammalian hosts and spreads in the environment in multifarious transmission cycles that may or not be connected. This biological plasticity, which is probably the result of the considerable heterogeneity of the taxon, exemplifies a successful adaptation of a parasite resulting in distinct outcomes of infection and a complex epidemiological pattern. In the 1990s, most endemic countries strengthened national control programs to interrupt the transmission of this parasite to humans. However, many obstacles remain to the effective control of the disease. Current knowledge of the different components involved in elaborate system that is American trypanosomiasis (the protozoan parasite T. cruzi, vectors Triatominae and the many reservoirs of infection), as well as the interactions existing within the system, is still incomplete. The Triatominae probably evolve from predatory reduvids in response to the availability of vertebrate food source. However, the basic mechanisms of adaptation of some of them to artificial ecotopes remain poorly understood. Nevertheless, these adaptations seem to be associated with a behavioral plasticity, a reduction in the genetic repertoire and increasing developmental instability.</EA><CC>002A05; 002A11D</CC><FD>Trypanosoma cruzi; Mammalia; Adaptation; Vecteur; Transmission; Microbiologie; Vétérinaire</FD><FG>Kinetoplastida; Protozoa; Vertebrata</FG><ED>Trypanosoma cruzi; Mammalia; Adaptation; Vector; Transmission; Microbiology; Veterinary</ED><EG>Kinetoplastida; Protozoa; Vertebrata</EG><SD>Trypanosoma cruzi; Mammalia; Adaptación; Vector; Transmisión; Microbiología; Veterinario</SD><LO>INIST-14119.354000188361800050</LO><ID>09-0356331</ID></server></inist></record>
000D35	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Fast-track rehabilitation for lung cancer lobectomy: a five-year experience</title><author><name sortKey="Das Neves Pereira, Joa Carlos" uniqKey="Das Neves Pereira J">Joa-Carlos Das-Neves-Pereira</name><affiliation><inist:fA14 i1="02"><s1>Thoracic Surgery Department of Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Thoracic Surgery Department of Sao Paulo University Medical School General Hospital</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bagan, Patrick" uniqKey="Bagan P">Patrick Bagan</name><affiliation><inist:fA14 i1="02"><s1>Thoracic Surgery Department of Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Coimbra Israel, Ana Paula" uniqKey="Coimbra Israel A">Ana-Paula Coimbra-Israel</name><affiliation><inist:fA14 i1="01"><s1>Thoracic Surgery Service of Brazilian Institute for Cancer Control (IBCC)</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Grimaillof Junior, Antonio" uniqKey="Grimaillof Junior A">Antonio Grimaillof-Junior</name><affiliation><inist:fA14 i1="01"><s1>Thoracic Surgery Service of Brazilian Institute for Cancer Control (IBCC)</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cesar Lopez, Gillian" uniqKey="Cesar Lopez G">Gillian Cesar-Lopez</name><affiliation><inist:fA14 i1="01"><s1>Thoracic Surgery Service of Brazilian Institute for Cancer Control (IBCC)</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Milanez De Campos, Joseribas" uniqKey="Milanez De Campos J">Joséribas Milanez-De-Campos</name><affiliation><inist:fA14 i1="03"><s1>Thoracic Surgery Department of Sao Paulo University Medical School General Hospital</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Riquet, Marc" uniqKey="Riquet M">Marc Riquet</name><affiliation><inist:fA14 i1="02"><s1>Thoracic Surgery Department of Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Biscegli Jatene, Fabio" uniqKey="Biscegli Jatene F">Fabio Biscegli-Jatene</name><affiliation><inist:fA14 i1="03"><s1>Thoracic Surgery Department of Sao Paulo University Medical School General Hospital</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0358790</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0358790 INIST</idno><idno type="RBID">Pascal:09-0358790</idno><idno type="wicri:Area/Main/Corpus">001C46</idno></publicationStmt><seriesStmt><idno type="ISSN">1010-7940</idno><title level="j" type="abbreviated">Eur. j. cardio-thorac. surg.</title><title level="j" type="main">European journal of cardio-thoracic surgery</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cardiology</term><term>Circulatory system</term><term>Experience</term><term>Lobectomy</term><term>Lung cancer</term><term>Pneumology</term><term>Recovery</term><term>Rehabilitation</term><term>Rehabilitation(human)</term><term>Surgery</term><term>Treatment</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cancer du poumon</term><term>Réhabilitation</term><term>Réadaptation</term><term>Lobectomie</term><term>Expérience</term><term>Récupération</term><term>Chirurgie</term><term>Appareil circulatoire</term><term>Cardiologie</term><term>Pneumologie</term><term>Traitement</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Objective: Fast-track rehabilitation is a group of simple measures that reduces morbidity, postoperative complication and accelerates postoperative rehabilitation reducing hospital stay. It can be applied to lung cancer lobectomy. Fast-track rehabilitation cornerstones are: minimally invasive surgical techniques using video-assisted and muscle sparring incisions, normovolemia, normothermia, good oxygenation, euglicemia, no unnecessary antibiotics, epidural patient-controlled analgesia, systemic opiods-free analgesia, early ambulation and oral feeding. Our objective is to describe a five-year experience with fast-track rehabilitation for lung cancer lobectomy. Patients and methods: A retrospective non-controlled study including 109 consecutive patients submitted to fast-track rehabilitation in the postoperative care of lung cancer lobectomy was performed. Only collaborative patients who could receive double-lumen intubation, epidural catheters with patient-controlled analgesia, who had Karnofsky index of 100, previous normal feeding and ambulation, absence of morbid obesity, diabetes or asthma, were eligible. Postoperative oral feeding and aggressive ambulation started as soon as possible. Results: Immediate postoperative extubation even in the operation room was possible in 107 patients and oral feeding and ambulation were possible before the first hour in 101 patients. Six patients could not receive early oral feeding or ambulate due to hypnosis secondary to preoperative long effect benzodiazepines. Two patients could not ambulate immediately due to epidural catheter misplacement with important postoperative pain. Ninety-nine discharges occurred at the second postoperative day, four of them with a chest tube connected to a Heimlich valve due to air leak. No complication of early feeding and ambulation was observed. Postoperative hypnosis due to long duration benzodiazepines or pain does not allow early oral feeding or ambulation. Avoiding long duration preoperative benzodiazepines, immediate postoperative extubation, regional thoracic PCA and early oral feeding and ambulation were related to a lesser frequency of complication and a shorter hospital stay. Conclusion: Fast-track rehabilitation for lung cancer lobectomies can be safely performed in a selected group of patients if a motivated multidisciplinary group of professionals is available and seems to reduce postoperative complication and hospital stay.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1010-7940</s0></fA01><fA02 i1="01"><s0>EJCSE7</s0></fA02><fA03 i2="1"><s0>Eur. j. cardio-thorac. surg.</s0></fA03><fA05><s2>36</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Fast-track rehabilitation for lung cancer lobectomy: a five-year experience</s1></fA08><fA11 i1="01" i2="1"><s1>DAS-NEVES-PEREIRA (Joa-Carlos)</s1></fA11><fA11 i1="02" i2="1"><s1>BAGAN (Patrick)</s1></fA11><fA11 i1="03" i2="1"><s1>COIMBRA-ISRAEL (Ana-Paula)</s1></fA11><fA11 i1="04" i2="1"><s1>GRIMAILLOF-JUNIOR (Antonio)</s1></fA11><fA11 i1="05" i2="1"><s1>CESAR-LOPEZ (Gillian)</s1></fA11><fA11 i1="06" i2="1"><s1>MILANEZ-DE-CAMPOS (Joséribas)</s1></fA11><fA11 i1="07" i2="1"><s1>RIQUET (Marc)</s1></fA11><fA11 i1="08" i2="1"><s1>BISCEGLI-JATENE (Fabio)</s1></fA11><fA14 i1="01"><s1>Thoracic Surgery Service of Brazilian Institute for Cancer Control (IBCC)</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Thoracic Surgery Department of Hôpital Européen Georges Pompidou</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Thoracic Surgery Department of Sao Paulo University Medical School General Hospital</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ></fA14><fA20><s1>383-392</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>21307</s2><s5>354000187543340260</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>19 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0358790</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European journal of cardio-thoracic surgery</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>Objective: Fast-track rehabilitation is a group of simple measures that reduces morbidity, postoperative complication and accelerates postoperative rehabilitation reducing hospital stay. It can be applied to lung cancer lobectomy. Fast-track rehabilitation cornerstones are: minimally invasive surgical techniques using video-assisted and muscle sparring incisions, normovolemia, normothermia, good oxygenation, euglicemia, no unnecessary antibiotics, epidural patient-controlled analgesia, systemic opiods-free analgesia, early ambulation and oral feeding. Our objective is to describe a five-year experience with fast-track rehabilitation for lung cancer lobectomy. Patients and methods: A retrospective non-controlled study including 109 consecutive patients submitted to fast-track rehabilitation in the postoperative care of lung cancer lobectomy was performed. Only collaborative patients who could receive double-lumen intubation, epidural catheters with patient-controlled analgesia, who had Karnofsky index of 100, previous normal feeding and ambulation, absence of morbid obesity, diabetes or asthma, were eligible. Postoperative oral feeding and aggressive ambulation started as soon as possible. Results: Immediate postoperative extubation even in the operation room was possible in 107 patients and oral feeding and ambulation were possible before the first hour in 101 patients. Six patients could not receive early oral feeding or ambulate due to hypnosis secondary to preoperative long effect benzodiazepines. Two patients could not ambulate immediately due to epidural catheter misplacement with important postoperative pain. Ninety-nine discharges occurred at the second postoperative day, four of them with a chest tube connected to a Heimlich valve due to air leak. No complication of early feeding and ambulation was observed. Postoperative hypnosis due to long duration benzodiazepines or pain does not allow early oral feeding or ambulation. Avoiding long duration preoperative benzodiazepines, immediate postoperative extubation, regional thoracic PCA and early oral feeding and ambulation were related to a lesser frequency of complication and a shorter hospital stay. Conclusion: Fast-track rehabilitation for lung cancer lobectomies can be safely performed in a selected group of patients if a motivated multidisciplinary group of professionals is available and seems to reduce postoperative complication and hospital stay.</s0></fC01><fC02 i1="01" i2="X"><s0>002B11A</s0></fC02><fC02 i1="02" i2="X"><s0>002B12</s0></fC02><fC02 i1="03" i2="X"><s0>002B25E</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Cancer du poumon</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Lung cancer</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Cáncer del pulmón</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Réhabilitation</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Rehabilitation</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Rehabilitación</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Réadaptation</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Rehabilitation(human)</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Readaptación</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Lobectomie</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Lobectomy</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Lobectomía</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Expérience</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Experience</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Experiencia</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Récupération</s0><s5>13</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Recovery</s0><s5>13</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Recuperación</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Chirurgie</s0><s5>14</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Surgery</s0><s5>14</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Cirugía</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Appareil circulatoire</s0><s5>15</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Circulatory system</s0><s5>15</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Aparato circulatorio</s0><s5>15</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Cardiologie</s0><s5>16</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Cardiology</s0><s5>16</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Cardiología</s0><s5>16</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Pneumologie</s0><s5>17</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Pneumology</s0><s5>17</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Neumología</s0><s5>17</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Traitement</s0><s5>78</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Treatment</s0><s5>78</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Tratamiento</s0><s5>78</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie des bronches</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Bronchus disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Bronquio patología</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pathologie des poumons</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Lung disease</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Pulmón patología</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Tumeur maligne</s0><s2>NM</s2><s5>40</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Malignant tumor</s0><s2>NM</s2><s5>40</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Tumor maligno</s0><s2>NM</s2><s5>40</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Annual Meeting of the European Association Cardio-Thoracic Surgery</s1><s2>22</s2><s3>Lisbon PRT</s3><s4>2008-09-14</s4></fA30></pR></standard><server><NO>PASCAL 09-0358790 INIST</NO><ET>Fast-track rehabilitation for lung cancer lobectomy: a five-year experience</ET><AU>DAS-NEVES-PEREIRA (Joa-Carlos); BAGAN (Patrick); COIMBRA-ISRAEL (Ana-Paula); GRIMAILLOF-JUNIOR (Antonio); CESAR-LOPEZ (Gillian); MILANEZ-DE-CAMPOS (Joséribas); RIQUET (Marc); BISCEGLI-JATENE (Fabio)</AU><AF>Thoracic Surgery Service of Brazilian Institute for Cancer Control (IBCC)/Sao Paulo/Brésil (3 aut., 4 aut., 5 aut.); Thoracic Surgery Department of Hôpital Européen Georges Pompidou/Paris/France (1 aut., 2 aut., 7 aut.); Thoracic Surgery Department of Sao Paulo University Medical School General Hospital/Sao Paulo/Brésil (1 aut., 6 aut., 8 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>European journal of cardio-thoracic surgery; ISSN 1010-7940; Coden EJCSE7; Pays-Bas; Da. 2009; Vol. 36; No. 2; Pp. 383-392; Bibl. 19 ref.</SO><LA>Anglais</LA><EA>Objective: Fast-track rehabilitation is a group of simple measures that reduces morbidity, postoperative complication and accelerates postoperative rehabilitation reducing hospital stay. It can be applied to lung cancer lobectomy. Fast-track rehabilitation cornerstones are: minimally invasive surgical techniques using video-assisted and muscle sparring incisions, normovolemia, normothermia, good oxygenation, euglicemia, no unnecessary antibiotics, epidural patient-controlled analgesia, systemic opiods-free analgesia, early ambulation and oral feeding. Our objective is to describe a five-year experience with fast-track rehabilitation for lung cancer lobectomy. Patients and methods: A retrospective non-controlled study including 109 consecutive patients submitted to fast-track rehabilitation in the postoperative care of lung cancer lobectomy was performed. Only collaborative patients who could receive double-lumen intubation, epidural catheters with patient-controlled analgesia, who had Karnofsky index of 100, previous normal feeding and ambulation, absence of morbid obesity, diabetes or asthma, were eligible. Postoperative oral feeding and aggressive ambulation started as soon as possible. Results: Immediate postoperative extubation even in the operation room was possible in 107 patients and oral feeding and ambulation were possible before the first hour in 101 patients. Six patients could not receive early oral feeding or ambulate due to hypnosis secondary to preoperative long effect benzodiazepines. Two patients could not ambulate immediately due to epidural catheter misplacement with important postoperative pain. Ninety-nine discharges occurred at the second postoperative day, four of them with a chest tube connected to a Heimlich valve due to air leak. No complication of early feeding and ambulation was observed. Postoperative hypnosis due to long duration benzodiazepines or pain does not allow early oral feeding or ambulation. Avoiding long duration preoperative benzodiazepines, immediate postoperative extubation, regional thoracic PCA and early oral feeding and ambulation were related to a lesser frequency of complication and a shorter hospital stay. Conclusion: Fast-track rehabilitation for lung cancer lobectomies can be safely performed in a selected group of patients if a motivated multidisciplinary group of professionals is available and seems to reduce postoperative complication and hospital stay.</EA><CC>002B11A; 002B12; 002B25E</CC><FD>Cancer du poumon; Réhabilitation; Réadaptation; Lobectomie; Expérience; Récupération; Chirurgie; Appareil circulatoire; Cardiologie; Pneumologie; Traitement</FD><FG>Pathologie de l'appareil respiratoire; Pathologie des bronches; Pathologie des poumons; Tumeur maligne; Cancer</FG><ED>Lung cancer; Rehabilitation; Rehabilitation(human); Lobectomy; Experience; Recovery; Surgery; Circulatory system; Cardiology; Pneumology; Treatment</ED><EG>Respiratory disease; Bronchus disease; Lung disease; Malignant tumor; Cancer</EG><SD>Cáncer del pulmón; Rehabilitación; Readaptación; Lobectomía; Experiencia; Recuperación; Cirugía; Aparato circulatorio; Cardiología; Neumología; Tratamiento</SD><LO>INIST-21307.354000187543340260</LO><ID>09-0358790</ID></server></inist></record>
000D36	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">TLR2-dependent mast cell activation contributes to the control of Mycobacterium tuberculosis infection</title><author><name sortKey="Carlos, Daniela" uniqKey="Carlos D">Daniela Carlos</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de Sào Paulo, Av. do Café, s/n</s1><s2>Ribeirào Preto, SP 14.040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Frantz, Fabiani G" uniqKey="Frantz F">Fabiani G. Frantz</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de Sào Paulo, Av. do Café, s/n</s1><s2>Ribeirào Preto, SP 14.040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Souza Junior, Devandir A" uniqKey="Souza Junior D">Devandir A. Souza-Junior</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Biologia Celular e Molecular e Bioagentes Patogênicos, Faculdade de Medicina de Ribeirão Preto, Universidade de Sào Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jamur, Maria C" uniqKey="Jamur M">Maria C. Jamur</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Biologia Celular e Molecular e Bioagentes Patogênicos, Faculdade de Medicina de Ribeirão Preto, Universidade de Sào Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Oliver, Constance" uniqKey="Oliver C">Constance Oliver</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Biologia Celular e Molecular e Bioagentes Patogênicos, Faculdade de Medicina de Ribeirão Preto, Universidade de Sào Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ramos, Simone G" uniqKey="Ramos S">Simone G. Ramos</name><affiliation><inist:fA14 i1="03"><s1>Departamento de Patologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Quesniaux, Valerie F" uniqKey="Quesniaux V">Valerie F. Quesniaux</name><affiliation><inist:fA14 i1="04"><s1>Molecular Immunology and Embryology, Centre National de la Recherche Scientifique</s1><s2>Orléans</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ryffel, Bernhard" uniqKey="Ryffel B">Bernhard Ryffel</name><affiliation><inist:fA14 i1="04"><s1>Molecular Immunology and Embryology, Centre National de la Recherche Scientifique</s1><s2>Orléans</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Silva, Celio L" uniqKey="Silva C">Célio L. Silva</name><affiliation><inist:fA14 i1="05"><s1>Departamento de Bioquímica e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bozza, Marcelo T" uniqKey="Bozza M">Marcelo T. Bozza</name><affiliation><inist:fA14 i1="06"><s1>Departamento de Imunologia, Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro</s1><s2>RJ</s2><s3>BRA</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Faccioli, L Cia H" uniqKey="Faccioli L">L Cia H. Faccioli</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de Sào Paulo, Av. do Café, s/n</s1><s2>Ribeirào Preto, SP 14.040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0359283</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0359283 INIST</idno><idno type="RBID">Pascal:09-0359283</idno><idno type="wicri:Area/Main/Corpus">001C45</idno></publicationStmt><seriesStmt><idno type="ISSN">1286-4579</idno><title level="j" type="abbreviated">Microbes infect.</title><title level="j" type="main">Microbes and infection</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cytokine</term><term>Inflammation</term><term>Mast cell</term><term>Mycobacterial infection</term><term>Mycobacterium tuberculosis</term><term>T-Lymphocyte</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Mycobacterium tuberculosis</term><term>Mastocyte</term><term>Cytokine</term><term>Inflammation</term><term>Lymphocyte T</term><term>Mycobactériose</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Mast Cells (MCs) express toll-like receptor 2 (TLR2), a receptor known to be triggered by several major mycobacterial ligands and involved in resistance against Mycobacterium tuberculosis (MTB) infection. This study investigated whether adoptive transfer of TLR2 positive MCs (TLR2<sup>+/+</sup>) corrects the increased susceptibility of TLR2<sup>-/-</sup> mice to MTB infection. TLR2<sup>-/-</sup> mice displayed increased mycobacterial burden, diminished myeloid cell recruitment and proinflammatory cytokine production accompanied by defective granuloma formation. The reconstitution of these mice with TLR2<sup>+/+</sup> MCs, but not TLR2<sup>-/-</sup>, confers better control of the infection, promotes the normalization of myeloid cell recruitment associated with reestablishment of the granuloma formation. In addition, adoptive transfer of TLR2<sup>+/+</sup> MC to TLR2<sup>-/-</sup> mice resulted in regulation of the pulmonary levels of IL-β, IL-6, TNF-α, enhanced Th1 response and activated CD8<sup>+</sup> T cell homing to the lungs. Our results suggest that activation of MCs via TLR2 is required to compensate the defect in protective immunity and inability of TLR2<sup>-/-</sup> mice to control MTB infection.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1286-4579</s0></fA01><fA03 i2="1"><s0>Microbes infect.</s0></fA03><fA05><s2>11</s2></fA05><fA06><s2>8-9</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>TLR2-dependent mast cell activation contributes to the control of Mycobacterium tuberculosis infection</s1></fA08><fA11 i1="01" i2="1"><s1>CARLOS (Daniela)</s1></fA11><fA11 i1="02" i2="1"><s1>FRANTZ (Fabiani G.)</s1></fA11><fA11 i1="03" i2="1"><s1>SOUZA-JUNIOR (Devandir A.)</s1></fA11><fA11 i1="04" i2="1"><s1>JAMUR (Maria C.)</s1></fA11><fA11 i1="05" i2="1"><s1>OLIVER (Constance)</s1></fA11><fA11 i1="06" i2="1"><s1>RAMOS (Simone G.)</s1></fA11><fA11 i1="07" i2="1"><s1>QUESNIAUX (Valerie F.)</s1></fA11><fA11 i1="08" i2="1"><s1>RYFFEL (Bernhard)</s1></fA11><fA11 i1="09" i2="1"><s1>SILVA (Célio L.)</s1></fA11><fA11 i1="10" i2="1"><s1>BOZZA (Marcelo T.)</s1></fA11><fA11 i1="11" i2="1"><s1>FACCIOLI (Lúcia H.)</s1></fA11><fA14 i1="01"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de Sào Paulo, Av. do Café, s/n</s1><s2>Ribeirào Preto, SP 14.040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Biologia Celular e Molecular e Bioagentes Patogênicos, Faculdade de Medicina de Ribeirão Preto, Universidade de Sào Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="03"><s1>Departamento de Patologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="04"><s1>Molecular Immunology and Embryology, Centre National de la Recherche Scientifique</s1><s2>Orléans</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="05"><s1>Departamento de Bioquímica e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo</s1><s2>Ribeirão Preto, SP</s2><s3>BRA</s3><sZ>9 aut.</sZ></fA14><fA14 i1="06"><s1>Departamento de Imunologia, Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro</s1><s2>RJ</s2><s3>BRA</s3><sZ>10 aut.</sZ></fA14><fA20><s1>770-778</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26816</s2><s5>354000170905320070</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>30 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0359283</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Microbes and infection</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Mast Cells (MCs) express toll-like receptor 2 (TLR2), a receptor known to be triggered by several major mycobacterial ligands and involved in resistance against Mycobacterium tuberculosis (MTB) infection. This study investigated whether adoptive transfer of TLR2 positive MCs (TLR2<sup>+/+</sup>) corrects the increased susceptibility of TLR2<sup>-/-</sup> mice to MTB infection. TLR2<sup>-/-</sup> mice displayed increased mycobacterial burden, diminished myeloid cell recruitment and proinflammatory cytokine production accompanied by defective granuloma formation. The reconstitution of these mice with TLR2<sup>+/+</sup> MCs, but not TLR2<sup>-/-</sup>, confers better control of the infection, promotes the normalization of myeloid cell recruitment associated with reestablishment of the granuloma formation. In addition, adoptive transfer of TLR2<sup>+/+</sup> MC to TLR2<sup>-/-</sup> mice resulted in regulation of the pulmonary levels of IL-β, IL-6, TNF-α, enhanced Th1 response and activated CD8<sup>+</sup> T cell homing to the lungs. Our results suggest that activation of MCs via TLR2 is required to compensate the defect in protective immunity and inability of TLR2<sup>-/-</sup> mice to control MTB infection.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05B15</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Mastocyte</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Mast cell</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Mastocito</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Cytokine</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Cytokine</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Citoquina</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Inflammation</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Inflammation</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Inflamación</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Lymphocyte T</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>T-Lymphocyte</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Linfocito T</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Mycobactériose</s0><s5>14</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Mycobacterial infection</s0><s5>14</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Micobacteriosis</s0><s5>14</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Infección</s0></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0359283 INIST</NO><ET>TLR2-dependent mast cell activation contributes to the control of Mycobacterium tuberculosis infection</ET><AU>CARLOS (Daniela); FRANTZ (Fabiani G.); SOUZA-JUNIOR (Devandir A.); JAMUR (Maria C.); OLIVER (Constance); RAMOS (Simone G.); QUESNIAUX (Valerie F.); RYFFEL (Bernhard); SILVA (Célio L.); BOZZA (Marcelo T.); FACCIOLI (Lúcia H.)</AU><AF>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de Sào Paulo, Av. do Café, s/n/Ribeirào Preto, SP 14.040-903/Brésil (1 aut., 2 aut., 11 aut.); Departamento de Biologia Celular e Molecular e Bioagentes Patogênicos, Faculdade de Medicina de Ribeirão Preto, Universidade de Sào Paulo/Ribeirão Preto, SP/Brésil (3 aut., 4 aut., 5 aut.); Departamento de Patologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo/Ribeirão Preto, SP/Brésil (6 aut.); Molecular Immunology and Embryology, Centre National de la Recherche Scientifique/Orléans/France (7 aut., 8 aut.); Departamento de Bioquímica e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo/Ribeirão Preto, SP/Brésil (9 aut.); Departamento de Imunologia, Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro/RJ/Brésil (10 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Microbes and infection; ISSN 1286-4579; France; Da. 2009; Vol. 11; No. 8-9; Pp. 770-778; Bibl. 30 ref.</SO><LA>Anglais</LA><EA>Mast Cells (MCs) express toll-like receptor 2 (TLR2), a receptor known to be triggered by several major mycobacterial ligands and involved in resistance against Mycobacterium tuberculosis (MTB) infection. This study investigated whether adoptive transfer of TLR2 positive MCs (TLR2<sup>+/+</sup>) corrects the increased susceptibility of TLR2<sup>-/-</sup> mice to MTB infection. TLR2<sup>-/-</sup> mice displayed increased mycobacterial burden, diminished myeloid cell recruitment and proinflammatory cytokine production accompanied by defective granuloma formation. The reconstitution of these mice with TLR2<sup>+/+</sup> MCs, but not TLR2<sup>-/-</sup>, confers better control of the infection, promotes the normalization of myeloid cell recruitment associated with reestablishment of the granuloma formation. In addition, adoptive transfer of TLR2<sup>+/+</sup> MC to TLR2<sup>-/-</sup> mice resulted in regulation of the pulmonary levels of IL-β, IL-6, TNF-α, enhanced Th1 response and activated CD8<sup>+</sup> T cell homing to the lungs. Our results suggest that activation of MCs via TLR2 is required to compensate the defect in protective immunity and inability of TLR2<sup>-/-</sup> mice to control MTB infection.</EA><CC>002A05B15</CC><FD>Mycobacterium tuberculosis; Mastocyte; Cytokine; Inflammation; Lymphocyte T; Mycobactériose</FD><FG>Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bactérie; Bactériose; Infection</FG><ED>Mycobacterium tuberculosis; Mast cell; Cytokine; Inflammation; T-Lymphocyte; Mycobacterial infection</ED><EG>Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bacteria; Bacteriosis; Infection</EG><SD>Mycobacterium tuberculosis; Mastocito; Citoquina; Inflamación; Linfocito T; Micobacteriosis</SD><LO>INIST-26816.354000170905320070</LO><ID>09-0359283</ID></server></inist></record>
000D37	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Updated Clinical Classification of Pulmonary Hypertension</title><author><name sortKey="Simonneau, Gerald" uniqKey="Simonneau G">Gérald Simonneau</name><affiliation><inist:fA14 i1="01"><s1>Centre National de Référence des Maladies Vasculaires Pulmonaires, Université Paris-Sud Hôpital Antoine Béclère</s1><s2>Clamart</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Robbins, Ivan M" uniqKey="Robbins I">Ivan M. Robbins</name><affiliation><inist:fA14 i1="02"><s1>Department of Medicine, Vanderbilt University Medical Center</s1><s2>Nashville, Tennessee</s2><s3>USA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Beghetti, Maurice" uniqKey="Beghetti M">Maurice Beghetti</name><affiliation><inist:fA14 i1="03"><s1>Pediatric Cardiology Unit, Hôpital des Enfants, University Hospital of Geneva</s1><s2>Geneva</s2><s3>CHE</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Channick, Richard N" uniqKey="Channick R">Richard N. Channick</name><affiliation><inist:fA14 i1="04"><s1>Division of Pulmonary and Critical Care Medicine, UCSD Medical Center</s1><s2>La Jolla, California</s2><s3>USA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Delcroix, Marion" uniqKey="Delcroix M">Marion Delcroix</name><affiliation><inist:fA14 i1="05"><s1>Center for Pulmonary Vascular Disease, Department of Pneumology, Gasthuisberg University Hospital</s1><s2>Leuven</s2><s3>BEL</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Denton, Christopher P" uniqKey="Denton C">Christopher P. Denton</name><affiliation><inist:fA14 i1="06"><s1>Centre for Rheumatology, Royal Free Hospital</s1><s2>London</s2><s3>GBR</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Elliott, C Gregory" uniqKey="Elliott C">C. Gregory Elliott</name><affiliation><inist:fA14 i1="07"><s1>Department of Medicine, Intermountain Medical Center, University of Utah</s1><s2>Salt Lake City, Utah</s2><s3>USA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gaine, Sean P" uniqKey="Gaine S">Sean P. Gaine</name><affiliation><inist:fA14 i1="08"><s1>Department of Respiratory Medicine, Mater Misericordiae University Hospital, University College Dublin</s1><s2>Dublin</s2><s3>IRL</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gladwin, Mark T" uniqKey="Gladwin M">Mark T. Gladwin</name><affiliation><inist:fA14 i1="09"><s1>Pulmonary, Allergy, and Critical Care Medicine, Hemostasis and Vascular Biology Research Institute, University of Pittsburgh</s1><s2>Pittsburgh, Pennsylvania</s2><s3>USA</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jing, Zhi Cheng" uniqKey="Jing Z">Zhi-Cheng Jing</name><affiliation><inist:fA14 i1="10"><s1>Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University</s1><s2>Shanghai</s2><s3>CHN</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Krowka, Michael J" uniqKey="Krowka M">Michael J. Krowka</name><affiliation><inist:fA14 i1="11"><s1>Department of Pulmonary and Critical Care Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Langleben, David" uniqKey="Langleben D">David Langleben</name><affiliation><inist:fA14 i1="12"><s1>Center for Pulmonary Vascular Disease, Sir Mortimer B. Davis Jewish General Hospital</s1><s2>Montréal, Québec</s2><s3>CAN</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nakanishi, Norifumi" uniqKey="Nakanishi N">Norifumi Nakanishi</name><affiliation><inist:fA14 i1="13"><s1>Divsion of Cardiology and Pulmonary Circulation, Department of Internal Medicine National Cardiovascular Center</s1><s2>Osaka</s2><s3>JPN</s3><sZ>13 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Souza, Rogerio" uniqKey="Souza R">Rogério Souza</name><affiliation><inist:fA14 i1="14"><s1>Pulmonary Department, Heart Institute, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>14 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0360357</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0360357 INIST</idno><idno type="RBID">Pascal:09-0360357</idno><idno type="wicri:Area/Main/Corpus">001C44</idno></publicationStmt><seriesStmt><idno type="ISSN">0735-1097</idno><title level="j" type="abbreviated">J. Am. Coll. Cardiol.</title><title level="j" type="main">Journal of the American College of Cardiology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cardiology</term><term>Circulatory system</term><term>Classification</term><term>Pulmonary hypertension</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Hypertension artérielle pulmonaire</term><term>Classification</term><term>Appareil circulatoire</term><term>Cardiologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in pathophysiologic mechanisms, clinical presentation, and therapeutic approaches. In 2003, during the 3rd World Symposium on Pulmonary Hypertension, the clinical classification of PH initially adopted in 1998 during the 2nd World Symposium was slightly modified. During the 4th World Symposium held in 2008, it was decided to maintain the general architecture and philosophy of the previous clinical classifications. The modifications adopted during this meeting principally concern Group 1, pulmonary arterial hypertension (PAH). This subgroup includes patients with PAH with a family history or patients with idiopathic PAH with germline mutations (e.g., bone morphogenetic protein receptor-2, activin receptor-like kinase type 1, and endoglin). In the new classification, schistosomiasis and chronic hemolytic anemia appear as separate entities in the subgroup of PAH associated with identified diseases. Finally, it was decided to place pulmonary venoocclusive disease and pulmonary capillary hemangiomatosis in a separate group, distinct from but very close to Group 1 (now called Group 1'). Thus, Group 1 of PAH is now more homogeneous.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0735-1097</s0></fA01><fA02 i1="01"><s0>JACCDI</s0></fA02><fA03 i2="1"><s0>J. Am. Coll. Cardiol.</s0></fA03><fA05><s2>54</s2></fA05><fA06><s2>1</s2><s3>SUP</s3></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Updated Clinical Classification of Pulmonary Hypertension</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Proceedings of the 4th World Symposium on Pulmonary Hypertension</s1></fA09><fA11 i1="01" i2="1"><s1>SIMONNEAU (Gérald)</s1></fA11><fA11 i1="02" i2="1"><s1>ROBBINS (Ivan M.)</s1></fA11><fA11 i1="03" i2="1"><s1>BEGHETTI (Maurice)</s1></fA11><fA11 i1="04" i2="1"><s1>CHANNICK (Richard N.)</s1></fA11><fA11 i1="05" i2="1"><s1>DELCROIX (Marion)</s1></fA11><fA11 i1="06" i2="1"><s1>DENTON (Christopher P.)</s1></fA11><fA11 i1="07" i2="1"><s1>ELLIOTT (C. Gregory)</s1></fA11><fA11 i1="08" i2="1"><s1>GAINE (Sean P.)</s1></fA11><fA11 i1="09" i2="1"><s1>GLADWIN (Mark T.)</s1></fA11><fA11 i1="10" i2="1"><s1>JING (Zhi-Cheng)</s1></fA11><fA11 i1="11" i2="1"><s1>KROWKA (Michael J.)</s1></fA11><fA11 i1="12" i2="1"><s1>LANGLEBEN (David)</s1></fA11><fA11 i1="13" i2="1"><s1>NAKANISHI (Norifumi)</s1></fA11><fA11 i1="14" i2="1"><s1>SOUZA (Rogério)</s1></fA11><fA12 i1="01" i2="1"><s1>HUMBERT (Marc)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>MCLAUGHLIN (Vallerie V.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Centre National de Référence des Maladies Vasculaires Pulmonaires, Université Paris-Sud Hôpital Antoine Béclère</s1><s2>Clamart</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Medicine, Vanderbilt University Medical Center</s1><s2>Nashville, Tennessee</s2><s3>USA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Pediatric Cardiology Unit, Hôpital des Enfants, University Hospital of Geneva</s1><s2>Geneva</s2><s3>CHE</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Division of Pulmonary and Critical Care Medicine, UCSD Medical Center</s1><s2>La Jolla, California</s2><s3>USA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Center for Pulmonary Vascular Disease, Department of Pneumology, Gasthuisberg University Hospital</s1><s2>Leuven</s2><s3>BEL</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Centre for Rheumatology, Royal Free Hospital</s1><s2>London</s2><s3>GBR</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Department of Medicine, Intermountain Medical Center, University of Utah</s1><s2>Salt Lake City, Utah</s2><s3>USA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="08"><s1>Department of Respiratory Medicine, Mater Misericordiae University Hospital, University College Dublin</s1><s2>Dublin</s2><s3>IRL</s3><sZ>8 aut.</sZ></fA14><fA14 i1="09"><s1>Pulmonary, Allergy, and Critical Care Medicine, Hemostasis and Vascular Biology Research Institute, University of Pittsburgh</s1><s2>Pittsburgh, Pennsylvania</s2><s3>USA</s3><sZ>9 aut.</sZ></fA14><fA14 i1="10"><s1>Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University</s1><s2>Shanghai</s2><s3>CHN</s3><sZ>10 aut.</sZ></fA14><fA14 i1="11"><s1>Department of Pulmonary and Critical Care Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="12"><s1>Center for Pulmonary Vascular Disease, Sir Mortimer B. Davis Jewish General Hospital</s1><s2>Montréal, Québec</s2><s3>CAN</s3><sZ>12 aut.</sZ></fA14><fA14 i1="13"><s1>Divsion of Cardiology and Pulmonary Circulation, Department of Internal Medicine National Cardiovascular Center</s1><s2>Osaka</s2><s3>JPN</s3><sZ>13 aut.</sZ></fA14><fA14 i1="14"><s1>Pulmonary Department, Heart Institute, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>14 aut.</sZ></fA14><fA15 i1="01"><s1>Université Paris-Sud, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine Béclère</s1><s2>Clamart</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Department of Internal Medicine, University of Michigan Health System</s1><s2>Ann Arbor, Michigan</s2><s3>USA</s3><sZ>2 aut.</sZ></fA15><fA20><s2>S43-S54</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20098</s2><s5>354000187238590050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>142 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0360357</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of the American College of Cardiology</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in pathophysiologic mechanisms, clinical presentation, and therapeutic approaches. In 2003, during the 3rd World Symposium on Pulmonary Hypertension, the clinical classification of PH initially adopted in 1998 during the 2nd World Symposium was slightly modified. During the 4th World Symposium held in 2008, it was decided to maintain the general architecture and philosophy of the previous clinical classifications. The modifications adopted during this meeting principally concern Group 1, pulmonary arterial hypertension (PAH). This subgroup includes patients with PAH with a family history or patients with idiopathic PAH with germline mutations (e.g., bone morphogenetic protein receptor-2, activin receptor-like kinase type 1, and endoglin). In the new classification, schistosomiasis and chronic hemolytic anemia appear as separate entities in the subgroup of PAH associated with identified diseases. Finally, it was decided to place pulmonary venoocclusive disease and pulmonary capillary hemangiomatosis in a separate group, distinct from but very close to Group 1 (now called Group 1'). Thus, Group 1 of PAH is now more homogeneous.</s0></fC01><fC02 i1="01" i2="X"><s0>002B12</s0></fC02><fC02 i1="02" i2="X"><s0>002B11C</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Hypertension artérielle pulmonaire</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Pulmonary hypertension</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Hipertensión arterial pulmonar</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Classification</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Classification</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Clasificación</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Appareil circulatoire</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Circulatory system</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Aparato circulatorio</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Cardiologie</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Cardiology</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Cardiología</s0><s5>11</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil circulatoire</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Cardiovascular disease</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>38</s5></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0360357 INIST</NO><ET>Updated Clinical Classification of Pulmonary Hypertension</ET><AU>SIMONNEAU (Gérald); ROBBINS (Ivan M.); BEGHETTI (Maurice); CHANNICK (Richard N.); DELCROIX (Marion); DENTON (Christopher P.); ELLIOTT (C. Gregory); GAINE (Sean P.); GLADWIN (Mark T.); JING (Zhi-Cheng); KROWKA (Michael J.); LANGLEBEN (David); NAKANISHI (Norifumi); SOUZA (Rogério); HUMBERT (Marc); MCLAUGHLIN (Vallerie V.)</AU><AF>Centre National de Référence des Maladies Vasculaires Pulmonaires, Université Paris-Sud Hôpital Antoine Béclère/Clamart/France (1 aut.); Department of Medicine, Vanderbilt University Medical Center/Nashville, Tennessee/Etats-Unis (2 aut.); Pediatric Cardiology Unit, Hôpital des Enfants, University Hospital of Geneva/Geneva/Suisse (3 aut.); Division of Pulmonary and Critical Care Medicine, UCSD Medical Center/La Jolla, California/Etats-Unis (4 aut.); Center for Pulmonary Vascular Disease, Department of Pneumology, Gasthuisberg University Hospital/Leuven/Belgique (5 aut.); Centre for Rheumatology, Royal Free Hospital/London/Royaume-Uni (6 aut.); Department of Medicine, Intermountain Medical Center, University of Utah/Salt Lake City, Utah/Etats-Unis (7 aut.); Department of Respiratory Medicine, Mater Misericordiae University Hospital, University College Dublin/Dublin/Irlande (8 aut.); Pulmonary, Allergy, and Critical Care Medicine, Hemostasis and Vascular Biology Research Institute, University of Pittsburgh/Pittsburgh, Pennsylvania/Etats-Unis (9 aut.); Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University/Shanghai/Chine (10 aut.); Department of Pulmonary and Critical Care Medicine, Division of Gastroenterology and Hepatology, Mayo Clinic/Rochester, Minnesota/Etats-Unis (11 aut.); Center for Pulmonary Vascular Disease, Sir Mortimer B. Davis Jewish General Hospital/Montréal, Québec/Canada (12 aut.); Divsion of Cardiology and Pulmonary Circulation, Department of Internal Medicine National Cardiovascular Center/Osaka/Japon (13 aut.); Pulmonary Department, Heart Institute, University of São Paulo Medical School/São Paulo/Brésil (14 aut.); Université Paris-Sud, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine Béclère/Clamart/France (1 aut.); Department of Internal Medicine, University of Michigan Health System/Ann Arbor, Michigan/Etats-Unis (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of the American College of Cardiology; ISSN 0735-1097; Coden JACCDI; Etats-Unis; Da. 2009; Vol. 54; No. 1 SUP; S43-S54; Bibl. 142 ref.</SO><LA>Anglais</LA><EA>The aim of a clinical classification of pulmonary hypertension (PH) is to group together different manifestations of disease sharing similarities in pathophysiologic mechanisms, clinical presentation, and therapeutic approaches. In 2003, during the 3rd World Symposium on Pulmonary Hypertension, the clinical classification of PH initially adopted in 1998 during the 2nd World Symposium was slightly modified. During the 4th World Symposium held in 2008, it was decided to maintain the general architecture and philosophy of the previous clinical classifications. The modifications adopted during this meeting principally concern Group 1, pulmonary arterial hypertension (PAH). This subgroup includes patients with PAH with a family history or patients with idiopathic PAH with germline mutations (e.g., bone morphogenetic protein receptor-2, activin receptor-like kinase type 1, and endoglin). In the new classification, schistosomiasis and chronic hemolytic anemia appear as separate entities in the subgroup of PAH associated with identified diseases. Finally, it was decided to place pulmonary venoocclusive disease and pulmonary capillary hemangiomatosis in a separate group, distinct from but very close to Group 1 (now called Group 1'). Thus, Group 1 of PAH is now more homogeneous.</EA><CC>002B12; 002B11C</CC><FD>Hypertension artérielle pulmonaire; Classification; Appareil circulatoire; Cardiologie</FD><FG>Pathologie de l'appareil circulatoire; Pathologie de l'appareil respiratoire</FG><ED>Pulmonary hypertension; Classification; Circulatory system; Cardiology</ED><EG>Cardiovascular disease; Respiratory disease</EG><SD>Hipertensión arterial pulmonar; Clasificación; Aparato circulatorio; Cardiología</SD><LO>INIST-20098.354000187238590050</LO><ID>09-0360357</ID></server></inist></record>
000D38	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Diagnosis, Assessment, and Treatment of Non-Pulmonary Arterial Hypertension Pulmonary Hypertension</title><author><name sortKey="Hoeper, Marius M" uniqKey="Hoeper M">Marius M. Hoeper</name><affiliation><inist:fA14 i1="01"><s1>Department of Respiratory Medicine, University of Hannover Medical School</s1><s2>Hannover</s2><s3>DEU</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Barbera, Joan Albert" uniqKey="Barbera J">Joan Albert Barbera</name><affiliation><inist:fA14 i1="02"><s1>Department of Respiratory Medicine, Hospital Clinic, CIBERES, University of Barcelona</s1><s2>Barcelona</s2><s3>ESP</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Channick, Richard N" uniqKey="Channick R">Richard N. Channick</name><affiliation><inist:fA14 i1="03"><s1>Division of Pulmonary and Critical Care Medicine, University of California, San Diego</s1><s2>La Jolla, California</s2><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hassoun, Paul M" uniqKey="Hassoun P">Paul M. Hassoun</name><affiliation><inist:fA14 i1="04"><s1>Department of Medicine, Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine</s1><s2>Baltimore, Maryland</s2><s3>USA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lang, Irene M" uniqKey="Lang I">Irene M. Lang</name><affiliation><inist:fA14 i1="05"><s1>Division of Cardiology, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Manes, Alessandra" uniqKey="Manes A">Alessandra Manes</name><affiliation><inist:fA14 i1="06"><s1>Institute of Cardiology, University of Bologna</s1><s2>Bologna</s2><s3>ITA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Martinez, Fernando J" uniqKey="Martinez F">Fernando J. Martinez</name><affiliation><inist:fA14 i1="07"><s1>Division of Pulmonary and Critical Care Medicine; University of Michigan Health System</s1><s2>Ann Arbor, Michigan</s2><s3>USA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Naeije, Robert" uniqKey="Naeije R">Robert Naeije</name><affiliation><inist:fA14 i1="08"><s1>Department of Pathophysiology, Free University of Brussels</s1><s2>Brussels</s2><s3>BEL</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Olschewski, Horst" uniqKey="Olschewski H">Horst Olschewski</name><affiliation><inist:fA14 i1="09"><s1>Department of Pulmonology, Medical University of Graz</s1><s2>Graz</s2><s3>AUT</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pepke Zaba, Joanna" uniqKey="Pepke Zaba J">Joanna Pepke-Zaba</name><affiliation><inist:fA14 i1="10"><s1>Pulmonary Vascular Disease Unit, Papworth Hospital</s1><s2>Cambridge</s2><s3>GBR</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Redfield, Margaret M" uniqKey="Redfield M">Margaret M. Redfield</name><affiliation><inist:fA14 i1="11"><s1>Department of Cardiology, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Robbins, Ivan M" uniqKey="Robbins I">Ivan M. Robbins</name><affiliation><inist:fA14 i1="12"><s1>Department of Allergy, Pulmonary and Critical Care Medicine; Vanderbilt University Medical Center</s1><s2>Nashville, Tennessee</s2><s3>USA</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Souza, Rogerio" uniqKey="Souza R">Rogério Souza</name><affiliation><inist:fA14 i1="13"><s1>Pulmonary Department, Heart Institute, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>13 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Torbicki, Adam" uniqKey="Torbicki A">Adam Torbicki</name><affiliation><inist:fA14 i1="14"><s1>Department of Chest Medicine, Institute of Tuberculosis and Lung Diseases, Medical University of Warsaw</s1><s2>Warsaw</s2><s3>POL</s3><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mcgoon, Michael" uniqKey="Mcgoon M">Michael Mcgoon</name><affiliation><inist:fA14 i1="15"><s1>Department of Cardiovascular Medicine, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>15 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0360367</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0360367 INIST</idno><idno type="RBID">Pascal:09-0360367</idno><idno type="wicri:Area/Main/Corpus">001C43</idno></publicationStmt><seriesStmt><idno type="ISSN">0735-1097</idno><title level="j" type="abbreviated">J. Am. Coll. Cardiol.</title><title level="j" type="main">Journal of the American College of Cardiology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Artery</term><term>Cardiology</term><term>Circulatory system</term><term>Diagnosis</term><term>Pulmonary hypertension</term><term>Treatment</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Hypertension artérielle pulmonaire</term><term>Diagnostic</term><term>Traitement</term><term>Artère</term><term>Appareil circulatoire</term><term>Cardiologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The 4th World Symposium on Pulmonary Hypertension was the first international meeting to focus not only on pulmonary arterial hypertension (PAH) but also on the so-called non-PAH forms of pulmonary hypertension (PH). The term &#34;non-PAH PH&#34; summarizes those forms of PH that are found in groups 2 to 5 of the current classification of PH, that is, those forms associated with left heart disease, chronic lung disease, recurrent venous throm-boembolism, and other diseases. Many of these forms of PH are much more common than PAH, but all of them have been less well studied, especially in terms of medical therapy. The working group on non-PAH PH focused mainly on 4 conditions: chronic obstructive lung disease, interstitial lung disease, chronic thromboembolic PH, and left heart disease. The medical literature regarding the role of PH in these diseases was reviewed, and recommendations regarding diagnosis and treatment of PH in these conditions are provided. Given the lack of robust clinical trials addressing PH in any of these conditions, it is important to conduct further studies to establish the role of medical therapy in non-PAH PH.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0735-1097</s0></fA01><fA02 i1="01"><s0>JACCDI</s0></fA02><fA03 i2="1"><s0>J. Am. Coll. Cardiol.</s0></fA03><fA05><s2>54</s2></fA05><fA06><s2>1</s2><s3>SUP</s3></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Diagnosis, Assessment, and Treatment of Non-Pulmonary Arterial Hypertension Pulmonary Hypertension</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Proceedings of the 4th World Symposium on Pulmonary Hypertension</s1></fA09><fA11 i1="01" i2="1"><s1>HOEPER (Marius M.)</s1></fA11><fA11 i1="02" i2="1"><s1>BARBERA (Joan Albert)</s1></fA11><fA11 i1="03" i2="1"><s1>CHANNICK (Richard N.)</s1></fA11><fA11 i1="04" i2="1"><s1>HASSOUN (Paul M.)</s1></fA11><fA11 i1="05" i2="1"><s1>LANG (Irene M.)</s1></fA11><fA11 i1="06" i2="1"><s1>MANES (Alessandra)</s1></fA11><fA11 i1="07" i2="1"><s1>MARTINEZ (Fernando J.)</s1></fA11><fA11 i1="08" i2="1"><s1>NAEIJE (Robert)</s1></fA11><fA11 i1="09" i2="1"><s1>OLSCHEWSKI (Horst)</s1></fA11><fA11 i1="10" i2="1"><s1>PEPKE-ZABA (Joanna)</s1></fA11><fA11 i1="11" i2="1"><s1>REDFIELD (Margaret M.)</s1></fA11><fA11 i1="12" i2="1"><s1>ROBBINS (Ivan M.)</s1></fA11><fA11 i1="13" i2="1"><s1>SOUZA (Rogério)</s1></fA11><fA11 i1="14" i2="1"><s1>TORBICKI (Adam)</s1></fA11><fA11 i1="15" i2="1"><s1>MCGOON (Michael)</s1></fA11><fA12 i1="01" i2="1"><s1>HUMBERT (Marc)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>MCLAUGHLIN (Vallerie V.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Department of Respiratory Medicine, University of Hannover Medical School</s1><s2>Hannover</s2><s3>DEU</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Respiratory Medicine, Hospital Clinic, CIBERES, University of Barcelona</s1><s2>Barcelona</s2><s3>ESP</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Division of Pulmonary and Critical Care Medicine, University of California, San Diego</s1><s2>La Jolla, California</s2><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Department of Medicine, Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine</s1><s2>Baltimore, Maryland</s2><s3>USA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Division of Cardiology, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Institute of Cardiology, University of Bologna</s1><s2>Bologna</s2><s3>ITA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Division of Pulmonary and Critical Care Medicine; University of Michigan Health System</s1><s2>Ann Arbor, Michigan</s2><s3>USA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="08"><s1>Department of Pathophysiology, Free University of Brussels</s1><s2>Brussels</s2><s3>BEL</s3><sZ>8 aut.</sZ></fA14><fA14 i1="09"><s1>Department of Pulmonology, Medical University of Graz</s1><s2>Graz</s2><s3>AUT</s3><sZ>9 aut.</sZ></fA14><fA14 i1="10"><s1>Pulmonary Vascular Disease Unit, Papworth Hospital</s1><s2>Cambridge</s2><s3>GBR</s3><sZ>10 aut.</sZ></fA14><fA14 i1="11"><s1>Department of Cardiology, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="12"><s1>Department of Allergy, Pulmonary and Critical Care Medicine; Vanderbilt University Medical Center</s1><s2>Nashville, Tennessee</s2><s3>USA</s3><sZ>12 aut.</sZ></fA14><fA14 i1="13"><s1>Pulmonary Department, Heart Institute, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>13 aut.</sZ></fA14><fA14 i1="14"><s1>Department of Chest Medicine, Institute of Tuberculosis and Lung Diseases, Medical University of Warsaw</s1><s2>Warsaw</s2><s3>POL</s3><sZ>14 aut.</sZ></fA14><fA14 i1="15"><s1>Department of Cardiovascular Medicine, Mayo Clinic</s1><s2>Rochester, Minnesota</s2><s3>USA</s3><sZ>15 aut.</sZ></fA14><fA15 i1="01"><s1>Université Paris-Sud, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine Béclère</s1><s2>Clamart</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Department of Internal Medicine, University of Michigan Health System</s1><s2>Ann Arbor, Michigan</s2><s3>USA</s3><sZ>2 aut.</sZ></fA15><fA20><s2>S85-S96</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20098</s2><s5>354000187238590090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>100 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0360367</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of the American College of Cardiology</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>The 4th World Symposium on Pulmonary Hypertension was the first international meeting to focus not only on pulmonary arterial hypertension (PAH) but also on the so-called non-PAH forms of pulmonary hypertension (PH). The term &#34;non-PAH PH&#34; summarizes those forms of PH that are found in groups 2 to 5 of the current classification of PH, that is, those forms associated with left heart disease, chronic lung disease, recurrent venous throm-boembolism, and other diseases. Many of these forms of PH are much more common than PAH, but all of them have been less well studied, especially in terms of medical therapy. The working group on non-PAH PH focused mainly on 4 conditions: chronic obstructive lung disease, interstitial lung disease, chronic thromboembolic PH, and left heart disease. The medical literature regarding the role of PH in these diseases was reviewed, and recommendations regarding diagnosis and treatment of PH in these conditions are provided. Given the lack of robust clinical trials addressing PH in any of these conditions, it is important to conduct further studies to establish the role of medical therapy in non-PAH PH.</s0></fC01><fC02 i1="01" i2="X"><s0>002B12</s0></fC02><fC02 i1="02" i2="X"><s0>002B11C</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Hypertension artérielle pulmonaire</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Pulmonary hypertension</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Hipertensión arterial pulmonar</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Diagnostic</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Diagnosis</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Diagnóstico</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Traitement</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Treatment</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Tratamiento</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Artère</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Artery</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Arteria</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Appareil circulatoire</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Circulatory system</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Aparato circulatorio</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Cardiologie</s0><s5>13</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Cardiology</s0><s5>13</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Cardiología</s0><s5>13</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil circulatoire</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Cardiovascular disease</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>38</s5></fC07><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0360367 INIST</NO><ET>Diagnosis, Assessment, and Treatment of Non-Pulmonary Arterial Hypertension Pulmonary Hypertension</ET><AU>HOEPER (Marius M.); BARBERA (Joan Albert); CHANNICK (Richard N.); HASSOUN (Paul M.); LANG (Irene M.); MANES (Alessandra); MARTINEZ (Fernando J.); NAEIJE (Robert); OLSCHEWSKI (Horst); PEPKE-ZABA (Joanna); REDFIELD (Margaret M.); ROBBINS (Ivan M.); SOUZA (Rogério); TORBICKI (Adam); MCGOON (Michael); HUMBERT (Marc); MCLAUGHLIN (Vallerie V.)</AU><AF>Department of Respiratory Medicine, University of Hannover Medical School/Hannover/Allemagne (1 aut.); Department of Respiratory Medicine, Hospital Clinic, CIBERES, University of Barcelona/Barcelona/Espagne (2 aut.); Division of Pulmonary and Critical Care Medicine, University of California, San Diego/La Jolla, California/Etats-Unis (3 aut.); Department of Medicine, Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine/Baltimore, Maryland/Etats-Unis (4 aut.); Division of Cardiology, Medical University of Vienna/Vienna/Autriche (5 aut.); Institute of Cardiology, University of Bologna/Bologna/Italie (6 aut.); Division of Pulmonary and Critical Care Medicine; University of Michigan Health System/Ann Arbor, Michigan/Etats-Unis (7 aut.); Department of Pathophysiology, Free University of Brussels/Brussels/Belgique (8 aut.); Department of Pulmonology, Medical University of Graz/Graz/Autriche (9 aut.); Pulmonary Vascular Disease Unit, Papworth Hospital/Cambridge/Royaume-Uni (10 aut.); Department of Cardiology, Mayo Clinic/Rochester, Minnesota/Etats-Unis (11 aut.); Department of Allergy, Pulmonary and Critical Care Medicine; Vanderbilt University Medical Center/Nashville, Tennessee/Etats-Unis (12 aut.); Pulmonary Department, Heart Institute, University of São Paulo Medical School/São Paulo/Brésil (13 aut.); Department of Chest Medicine, Institute of Tuberculosis and Lung Diseases, Medical University of Warsaw/Warsaw/Pologne (14 aut.); Department of Cardiovascular Medicine, Mayo Clinic/Rochester, Minnesota/Etats-Unis (15 aut.); Université Paris-Sud, Service de Pneumologie et Réanimation Respiratoire, Hôpital Antoine Béclère/Clamart/France (1 aut.); Department of Internal Medicine, University of Michigan Health System/Ann Arbor, Michigan/Etats-Unis (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of the American College of Cardiology; ISSN 0735-1097; Coden JACCDI; Etats-Unis; Da. 2009; Vol. 54; No. 1 SUP; S85-S96; Bibl. 100 ref.</SO><LA>Anglais</LA><EA>The 4th World Symposium on Pulmonary Hypertension was the first international meeting to focus not only on pulmonary arterial hypertension (PAH) but also on the so-called non-PAH forms of pulmonary hypertension (PH). The term &#34;non-PAH PH&#34; summarizes those forms of PH that are found in groups 2 to 5 of the current classification of PH, that is, those forms associated with left heart disease, chronic lung disease, recurrent venous throm-boembolism, and other diseases. Many of these forms of PH are much more common than PAH, but all of them have been less well studied, especially in terms of medical therapy. The working group on non-PAH PH focused mainly on 4 conditions: chronic obstructive lung disease, interstitial lung disease, chronic thromboembolic PH, and left heart disease. The medical literature regarding the role of PH in these diseases was reviewed, and recommendations regarding diagnosis and treatment of PH in these conditions are provided. Given the lack of robust clinical trials addressing PH in any of these conditions, it is important to conduct further studies to establish the role of medical therapy in non-PAH PH.</EA><CC>002B12; 002B11C</CC><FD>Hypertension artérielle pulmonaire; Diagnostic; Traitement; Artère; Appareil circulatoire; Cardiologie</FD><FG>Pathologie de l'appareil circulatoire; Pathologie de l'appareil respiratoire</FG><ED>Pulmonary hypertension; Diagnosis; Treatment; Artery; Circulatory system; Cardiology</ED><EG>Cardiovascular disease; Respiratory disease</EG><SD>Hipertensión arterial pulmonar; Diagnóstico; Tratamiento; Arteria; Aparato circulatorio; Cardiología</SD><LO>INIST-20098.354000187238590090</LO><ID>09-0360367</ID></server></inist></record>
000D39	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Determining the Dynamics of Entanglement</title><author><name sortKey="Jimenez Farias, O" uniqKey="Jimenez Farias O">O. Jimenez Farias</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Instituto de Ciencias Nucleares, Universidad National Autónoma de México (UNAM), Apdo. Postal 70-543</s1><s2>México 04510 D.F</s2><s3>MEX</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lombard Latune, C" uniqKey="Lombard Latune C">C. Lombard Latune</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>École Normale Supérieure, 24 rue Lhomond</s1><s2>75005 Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Walborn, S P" uniqKey="Walborn S">S. P. Walborn</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Davidovich, L" uniqKey="Davidovich L">L. Davidovich</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Souto Ribeiro, P H" uniqKey="Souto Ribeiro P">P. H. Souto Ribeiro</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0360593</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0360593 INIST</idno><idno type="RBID">Pascal:09-0360593</idno><idno type="wicri:Area/Main/Corpus">001C42</idno></publicationStmt><seriesStmt><idno type="ISSN">0036-8075</idno><title level="j" type="abbreviated">Science : (Wash. D.C.)</title><title level="j" type="main">Science : (Washington, D.C.)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dynamics</term><term>Mixed state</term><term>Quantum entanglement</term><term>Quantum information</term><term>Tomography</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dynamique</term><term>Intrication quantique</term><term>Information quantique</term><term>Tomographie</term><term>Etat mixte</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The estimation of the entanglement of multipartite systems undergoing decoherence is important for assessing the robustness of quantum information processes. It usually requires access to the final state and its full reconstruction through quantum tomography. General dynamical laws may simplify this task. We found that when one of the parties of an initially entangled two-qubit system is subject to a noisy channel, a single universal curve describes the dynamics of entanglement for both pure and mixed states, including those for which entanglement suddenly disappears. Our result, which is experimentally demonstrated using a linear optics setup, leads to a direct and efficient determination of entanglement through the knowledge of the initial state and single-party process tomography alone, foregoing the need to reconstruct the final state.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0036-8075</s0></fA01><fA02 i1="01"><s0>SCIEAS</s0></fA02><fA03 i2="1"><s0>Science : (Wash. D.C.)</s0></fA03><fA05><s2>324</s2></fA05><fA06><s2>5933</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Determining the Dynamics of Entanglement</s1></fA08><fA11 i1="01" i2="1"><s1>JIMENEZ FARIAS (O.)</s1></fA11><fA11 i1="02" i2="1"><s1>LOMBARD LATUNE (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>WALBORN (S. P.)</s1></fA11><fA11 i1="04" i2="1"><s1>DAVIDOVICH (L.)</s1></fA11><fA11 i1="05" i2="1"><s1>SOUTO RIBEIRO (P. H.)</s1></fA11><fA14 i1="01"><s1>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528</s1><s2>Rio de Janeiro R] 21941-972</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Instituto de Ciencias Nucleares, Universidad National Autónoma de México (UNAM), Apdo. Postal 70-543</s1><s2>México 04510 D.F</s2><s3>MEX</s3><sZ>1 aut.</sZ></fA14><fA14 i1="03"><s1>École Normale Supérieure, 24 rue Lhomond</s1><s2>75005 Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>1414-1417</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>6040</s2><s5>354000187118470150</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0360593</s0></fA47><fA60><s1>P</s1><s3>C</s3></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Science : (Washington, D.C.)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>The estimation of the entanglement of multipartite systems undergoing decoherence is important for assessing the robustness of quantum information processes. It usually requires access to the final state and its full reconstruction through quantum tomography. General dynamical laws may simplify this task. We found that when one of the parties of an initially entangled two-qubit system is subject to a noisy channel, a single universal curve describes the dynamics of entanglement for both pure and mixed states, including those for which entanglement suddenly disappears. Our result, which is experimentally demonstrated using a linear optics setup, leads to a direct and efficient determination of entanglement through the knowledge of the initial state and single-party process tomography alone, foregoing the need to reconstruct the final state.</s0></fC01><fC02 i1="01" i2="3"><s0>001B00C67</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Dynamique</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Dynamics</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Intrication quantique</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Quantum entanglement</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Information quantique</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Quantum information</s0><s5>28</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Tomographie</s0><s5>29</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Tomography</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Etat mixte</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Mixed state</s0><s5>30</s5></fC03><fN21><s1>257</s1></fN21></pA></standard><server><NO>PASCAL 09-0360593 INIST</NO><ET>Determining the Dynamics of Entanglement</ET><AU>JIMENEZ FARIAS (O.); LOMBARD LATUNE (C.); WALBORN (S. P.); DAVIDOVICH (L.); SOUTO RIBEIRO (P. H.)</AU><AF>Instituto de Fisica, Universidade Federal do Rio de Janeiro, Caixa Postal 68528/Rio de Janeiro R] 21941-972/Brésil (1 aut., 2 aut., 3 aut., 4 aut., 5 aut.); Instituto de Ciencias Nucleares, Universidad National Autónoma de México (UNAM), Apdo. Postal 70-543/México 04510 D.F/Mexique (1 aut.); École Normale Supérieure, 24 rue Lhomond/75005 Paris/France (2 aut.)</AF><DT>Publication en série; Compte-rendu; Niveau analytique</DT><SO>Science : (Washington, D.C.); ISSN 0036-8075; Coden SCIEAS; Etats-Unis; Da. 2009; Vol. 324; No. 5933; Pp. 1414-1417; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>The estimation of the entanglement of multipartite systems undergoing decoherence is important for assessing the robustness of quantum information processes. It usually requires access to the final state and its full reconstruction through quantum tomography. General dynamical laws may simplify this task. We found that when one of the parties of an initially entangled two-qubit system is subject to a noisy channel, a single universal curve describes the dynamics of entanglement for both pure and mixed states, including those for which entanglement suddenly disappears. Our result, which is experimentally demonstrated using a linear optics setup, leads to a direct and efficient determination of entanglement through the knowledge of the initial state and single-party process tomography alone, foregoing the need to reconstruct the final state.</EA><CC>001B00C67</CC><FD>Dynamique; Intrication quantique; Information quantique; Tomographie; Etat mixte</FD><ED>Dynamics; Quantum entanglement; Quantum information; Tomography; Mixed state</ED><LO>INIST-6040.354000187118470150</LO><ID>09-0360593</ID></server></inist></record>
000D40	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Evolution equation for short surface waves on water of finite depth</title><author><name sortKey="Artiles, W" uniqKey="Artiles W">W. Artiles</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Física Teórica, Universidade Estadual Paulista - UNESP, R Dr. Bento Teobaldo Ferraz 271, Bloco 11</s1><s2>01140-070 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kraenkel, R A" uniqKey="Kraenkel R">R. A. Kraenkel</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Física Teórica, Universidade Estadual Paulista - UNESP, R Dr. Bento Teobaldo Ferraz 271, Bloco 11</s1><s2>01140-070 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Manna, M A" uniqKey="Manna M">M. A. Manna</name><affiliation><inist:fA14 i1="02"><s1>Physique Théorique et Astroporticules, CNRS-UMR5207, Université Montpellier II, Place Eugène Bataillon</s1><s2>34095 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0360625</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0360625 INIST</idno><idno type="RBID">Pascal:09-0360625</idno><idno type="wicri:Area/Main/Corpus">001C41</idno></publicationStmt><seriesStmt><idno type="ISSN">0167-2789</idno><title level="j" type="abbreviated">Physica, D</title><title level="j" type="main">Physica. D</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Asymptotic expansion</term><term>Conformal mapping</term><term>Conformal transformation</term><term>Disturbances</term><term>Evolution equation</term><term>Integro-differential equations</term><term>Non linear phenomenon</term><term>Nonlinearity</term><term>Operator</term><term>Stokes equation</term><term>Stokes wave</term><term>Surface waves</term><term>Wave packets</term><term>Wave propagation</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Equation évolution</term><term>Onde surface</term><term>Propagation onde</term><term>Perturbation</term><term>Paquet onde</term><term>Transformation conforme</term><term>Opérateur</term><term>Développement asymptotique</term><term>Non linéarité</term><term>Equation intégrodifférentielle</term><term>Equation Stokes</term><term>Onde Stokes</term><term>Application conforme</term><term>Phénomène non linéaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We address the question of determining the evolution equation for surface waves propagating in water whose depth is much larger than the typical wavelength of the surface disturbance. We avoid making the usual approximation of supposing the evolution to be given in the form of a modulated wave-packet. We treat the problem by means of a conformal transformation allowing to explicitly find the Dirichletto-Neumann operator for the problem together with asymptotic expansions in parameters measuring the nonlinearity and depth. This allows us to obtain an equation in physical variables valid in the weakly nonlinear, deep-water regime. The equation is an integro-differential equation, which reduces to known cases for infinite depth. We discuss solutions in a perturbative setting and show that the evolution equation describes Stokes-like waves.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0167-2789</s0></fA01><fA02 i1="01"><s0>PDNPDT</s0></fA02><fA03 i2="1"><s0>Physica, D</s0></fA03><fA05><s2>238</s2></fA05><fA06><s2>17</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Evolution equation for short surface waves on water of finite depth</s1></fA08><fA11 i1="01" i2="1"><s1>ARTILES (W.)</s1></fA11><fA11 i1="02" i2="1"><s1>KRAENKEL (R. A.)</s1></fA11><fA11 i1="03" i2="1"><s1>MANNA (M. A.)</s1></fA11><fA14 i1="01"><s1>Instituto de Física Teórica, Universidade Estadual Paulista - UNESP, R Dr. Bento Teobaldo Ferraz 271, Bloco 11</s1><s2>01140-070 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Physique Théorique et Astroporticules, CNRS-UMR5207, Université Montpellier II, Place Eugène Bataillon</s1><s2>34095 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>1821-1825</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>145D</s2><s5>354000187575430080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0360625</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Physica. D</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>We address the question of determining the evolution equation for surface waves propagating in water whose depth is much larger than the typical wavelength of the surface disturbance. We avoid making the usual approximation of supposing the evolution to be given in the form of a modulated wave-packet. We treat the problem by means of a conformal transformation allowing to explicitly find the Dirichletto-Neumann operator for the problem together with asymptotic expansions in parameters measuring the nonlinearity and depth. This allows us to obtain an equation in physical variables valid in the weakly nonlinear, deep-water regime. The equation is an integro-differential equation, which reduces to known cases for infinite depth. We discuss solutions in a perturbative setting and show that the evolution equation describes Stokes-like waves.</s0></fC01><fC02 i1="01" i2="3"><s0>001B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Equation évolution</s0><s5>26</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Evolution equation</s0><s5>26</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Ecuación evolución</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Onde surface</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Surface waves</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Propagation onde</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Wave propagation</s0><s5>28</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Perturbation</s0><s5>29</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Disturbances</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Paquet onde</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Wave packets</s0><s5>30</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Transformation conforme</s0><s5>31</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Conformal transformation</s0><s5>31</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Transformación conforme</s0><s5>31</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Opérateur</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Operator</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Operador</s0><s5>32</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Développement asymptotique</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Asymptotic expansion</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Desarrollo asintótico</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Non linéarité</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Nonlinearity</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>No linealidad</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Equation intégrodifférentielle</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Integro-differential equations</s0><s5>35</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Equation Stokes</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Stokes equation</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Ecuación Stokes</s0><s5>36</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Onde Stokes</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Stokes wave</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Onda Stokes</s0><s5>37</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Application conforme</s0><s5>38</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Conformal mapping</s0><s5>38</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Phénomène non linéaire</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Non linear phenomenon</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Fenómeno no lineal</s0><s5>39</s5></fC03><fN21><s1>257</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0360625 INIST</NO><ET>Evolution equation for short surface waves on water of finite depth</ET><AU>ARTILES (W.); KRAENKEL (R. A.); MANNA (M. A.)</AU><AF>Instituto de Física Teórica, Universidade Estadual Paulista - UNESP, R Dr. Bento Teobaldo Ferraz 271, Bloco 11/01140-070 São Paulo/Brésil (1 aut., 2 aut.); Physique Théorique et Astroporticules, CNRS-UMR5207, Université Montpellier II, Place Eugène Bataillon/34095 Montpellier/France (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Physica. D; ISSN 0167-2789; Coden PDNPDT; Pays-Bas; Da. 2009; Vol. 238; No. 17; Pp. 1821-1825; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>We address the question of determining the evolution equation for surface waves propagating in water whose depth is much larger than the typical wavelength of the surface disturbance. We avoid making the usual approximation of supposing the evolution to be given in the form of a modulated wave-packet. We treat the problem by means of a conformal transformation allowing to explicitly find the Dirichletto-Neumann operator for the problem together with asymptotic expansions in parameters measuring the nonlinearity and depth. This allows us to obtain an equation in physical variables valid in the weakly nonlinear, deep-water regime. The equation is an integro-differential equation, which reduces to known cases for infinite depth. We discuss solutions in a perturbative setting and show that the evolution equation describes Stokes-like waves.</EA><CC>001B</CC><FD>Equation évolution; Onde surface; Propagation onde; Perturbation; Paquet onde; Transformation conforme; Opérateur; Développement asymptotique; Non linéarité; Equation intégrodifférentielle; Equation Stokes; Onde Stokes; Application conforme; Phénomène non linéaire</FD><ED>Evolution equation; Surface waves; Wave propagation; Disturbances; Wave packets; Conformal transformation; Operator; Asymptotic expansion; Nonlinearity; Integro-differential equations; Stokes equation; Stokes wave; Conformal mapping; Non linear phenomenon</ED><SD>Ecuación evolución; Transformación conforme; Operador; Desarrollo asintótico; No linealidad; Ecuación Stokes; Onda Stokes; Fenómeno no lineal</SD><LO>INIST-145D.354000187575430080</LO><ID>09-0360625</ID></server></inist></record>
000D41	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">Dette symbolique, autorité et justice : Questions de théorie</title><author><name sortKey="Birman, Joel" uniqKey="Birman J">Joel Birman</name><affiliation><inist:fA14 i1="01"><s1>Université Paris-VII</s1><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Rua Marquês de São Vicente, 250 Gávea</s1><s2>22451-040 Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0364846</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0364846 INIST</idno><idno type="RBID">Pascal:09-0364846</idno><idno type="wicri:Area/Main/Corpus">001C40</idno><idno type="stanalyst">FRANCIS 09-0364846 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">0014-3855</idno><title level="j" type="abbreviated">Evol. psychiatr.</title><title level="j" type="main">Evolution psychiatrique</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anthropology</term><term>Authority</term><term>Criminality</term><term>Debt</term><term>Father</term><term>Genealogy</term><term>Human</term><term>Justice</term><term>Psychoanalysis</term><term>Sociocultural environment</term><term>Violence</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Autorité</term><term>Justice</term><term>Père</term><term>Dette</term><term>Criminalité</term><term>Violence</term><term>Généalogie</term><term>Anthropologie</term><term>Psychanalyse</term><term>Environnement socioculturel</term><term>Homme</term><term>Symbolique</term><term>Théorie Sigmund Freud</term><term>Théorie Jacques Lacan</term><term>Théorie Claude Lévi-Strauss</term><term>Société contemporaine</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Le propos de cet article est celui de bien circonscrire le concept de dette symbolique en psychanalyse, en soulignant sa constitution historique et épistémologique, de Freud à Lacan. Ainsi, on souligne le rôle de la tradition anthropologique, de Mauss à Lévi-Strauss, pour l'émergence de ce concept-là chez Lacan. En outre, on esquisse les impasses dans la contemporanéité en ce qui concerne la dette symbolique, en soulignant la montée de la violence et de la criminalité.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0014-3855</s0></fA01><fA02 i1="01"><s0>EVPSAG</s0></fA02><fA03 i2="1"><s0>Evol. psychiatr.</s0></fA03><fA05><s2>74</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="FRE"><s1>Dette symbolique, autorité et justice : Questions de théorie</s1></fA08><fA11 i1="01" i2="1"><s1>BIRMAN (Joel)</s1></fA11><fA14 i1="01"><s1>Université Paris-VII</s1><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Rua Marquês de São Vicente, 250 Gávea</s1><s2>22451-040 Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA20><s1>175-187</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>5236</s2><s5>354000186268050010</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>23 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0364846</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Evolution psychiatrique</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA68 i1="01" i2="1" l="ENG"><s1>Symbolical debt, authority and justice</s1></fA68><fC01 i1="01" l="FRE"><s0>Le propos de cet article est celui de bien circonscrire le concept de dette symbolique en psychanalyse, en soulignant sa constitution historique et épistémologique, de Freud à Lacan. Ainsi, on souligne le rôle de la tradition anthropologique, de Mauss à Lévi-Strauss, pour l'émergence de ce concept-là chez Lacan. En outre, on esquisse les impasses dans la contemporanéité en ce qui concerne la dette symbolique, en soulignant la montée de la violence et de la criminalité.</s0></fC01><fC02 i1="01" i2="X"><s0>002A27B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Autorité</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Authority</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Autoridad</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Justice</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Justice</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Justicia</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Père</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Father</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Padre</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Dette</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Debt</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Criminalité</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Criminality</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Criminalidad</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Violence</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Violence</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Violencia</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Généalogie</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Genealogy</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Genealogía</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Anthropologie</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Anthropology</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Antropología</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Psychanalyse</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Psychoanalysis</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Psicoanálisis</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Environnement socioculturel</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Sociocultural environment</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Contexto sociocultural</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Homme</s0><s5>18</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Human</s0><s5>18</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Hombre</s0><s5>18</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Symbolique</s0><s4>INC</s4><s5>86</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Théorie Sigmund Freud</s0><s4>INC</s4><s5>87</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Théorie Jacques Lacan</s0><s4>INC</s4><s5>88</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Théorie Claude Lévi-Strauss</s0><s4>INC</s4><s5>89</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Société contemporaine</s0><s4>INC</s4><s5>90</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Environnement social</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Social environment</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Contexto social</s0><s5>37</s5></fC07><fN21><s1>264</s1></fN21></pA></standard><server><NO>PASCAL 09-0364846 INIST</NO><FT>Dette symbolique, autorité et justice : Questions de théorie</FT><ET>(Symbolical debt, authority and justice)</ET><AU>BIRMAN (Joel)</AU><AF>Université Paris-VII/France (1 aut.); Rua Marquês de São Vicente, 250 Gávea/22451-040 Rio de Janeiro/Brésil (1 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Evolution psychiatrique; ISSN 0014-3855; Coden EVPSAG; France; Da. 2009; Vol. 74; No. 2; Pp. 175-187; Abs. anglais; Bibl. 23 ref.</SO><LA>Français</LA><FA>Le propos de cet article est celui de bien circonscrire le concept de dette symbolique en psychanalyse, en soulignant sa constitution historique et épistémologique, de Freud à Lacan. Ainsi, on souligne le rôle de la tradition anthropologique, de Mauss à Lévi-Strauss, pour l'émergence de ce concept-là chez Lacan. En outre, on esquisse les impasses dans la contemporanéité en ce qui concerne la dette symbolique, en soulignant la montée de la violence et de la criminalité.</FA><CC>002A27B</CC><FD>Autorité; Justice; Père; Dette; Criminalité; Violence; Généalogie; Anthropologie; Psychanalyse; Environnement socioculturel; Homme; Symbolique; Théorie Sigmund Freud; Théorie Jacques Lacan; Théorie Claude Lévi-Strauss; Société contemporaine</FD><FG>Environnement social</FG><ED>Authority; Justice; Father; Debt; Criminality; Violence; Genealogy; Anthropology; Psychoanalysis; Sociocultural environment; Human</ED><EG>Social environment</EG><SD>Autoridad; Justicia; Padre; Criminalidad; Violencia; Genealogía; Antropología; Psicoanálisis; Contexto sociocultural; Hombre</SD><LO>INIST-5236.354000186268050010</LO><ID>09-0364846</ID></server></inist></record>
000D42	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Blind identification of multiuser nonlinear channels using tensor decomposition and precoding</title><author><name sortKey="Fernandes, Carlos Alexandre" uniqKey="Fernandes C">Carlos Alexandre Fernandes</name><affiliation><inist:fA14 i1="01"><s1>13S Laboratory, University of Nice-Sophia Antipolis/CNRS, Les Algorithmes/Euclide B-2000, route des Lucioles, BP 121</s1><s2>06903 Sophio-Antipolis</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Engenharia de Teleinformática, Federal University of Ceará, Campus do Pici, 60.755-640</s1><s2>6007 Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Favier, Gerard" uniqKey="Favier G">Gérard Favier</name><affiliation><inist:fA14 i1="01"><s1>13S Laboratory, University of Nice-Sophia Antipolis/CNRS, Les Algorithmes/Euclide B-2000, route des Lucioles, BP 121</s1><s2>06903 Sophio-Antipolis</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mota, Joao Cesar M" uniqKey="Mota J">Joao Cesar M. Mota</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Engenharia de Teleinformática, Federal University of Ceará, Campus do Pici, 60.755-640</s1><s2>6007 Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0366340</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0366340 INIST</idno><idno type="RBID">Pascal:09-0366340</idno><idno type="wicri:Area/Main/Corpus">001C39</idno></publicationStmt><seriesStmt><idno type="ISSN">0165-1684</idno><title level="j" type="abbreviated">Signal process.</title><title level="j" type="main">Signal processing</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Algorithm</term><term>Blind identification</term><term>Channel estimation</term><term>Coding</term><term>Computer simulation</term><term>Covariance</term><term>Markov chain</term><term>Memoryless channel</term><term>Multiple access</term><term>Multiuser channels</term><term>Non linear channel</term><term>Parameter estimation</term><term>Phase shift keying</term><term>Statistical method</term><term>System identification</term><term>Telecommunication system</term><term>Time correlation</term><term>Transition probability</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Identification système</term><term>Identification aveugle</term><term>Canal multiutilisateur</term><term>Canal non linéaire</term><term>Codage</term><term>Canal sans mémoire</term><term>Accès multiple</term><term>Système télécommunication</term><term>Covariance</term><term>Modulation déplacement phase</term><term>Chaîne Markov</term><term>Probabilité transition</term><term>Corrélation temporelle</term><term>Méthode statistique</term><term>Estimation canal</term><term>Algorithme</term><term>Simulation ordinateur</term><term>Estimation paramètre</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This paper presents two blind identification methods for nonlinear memoryless channels in multiuser communication systems. These methods are based on the parallel factor (PARAFAC) decomposition of a tensor composed of channel output covariances. Such a decomposition is possible owing to a new precoding scheme developed for phase-shift keying (PSK) signals modeled as Markov chains. Some conditions on the transition probability matrices (TPM) of the Markov chains are established to introduce temporal correlation and satisfy statistical correlation constraints inducing the PARAFAC decomposition of the considered tensor. The proposed blind channel estimation algorithms are evaluated by means of computer simulations.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0165-1684</s0></fA01><fA02 i1="01"><s0>SPRODR</s0></fA02><fA03 i2="1"><s0>Signal process.</s0></fA03><fA05><s2>89</s2></fA05><fA06><s2>12</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Blind identification of multiuser nonlinear channels using tensor decomposition and precoding</s1></fA08><fA11 i1="01" i2="1"><s1>FERNANDES (Carlos Alexandre)</s1></fA11><fA11 i1="02" i2="1"><s1>FAVIER (Gérard)</s1></fA11><fA11 i1="03" i2="1"><s1>MOTA (Joao Cesar M.)</s1></fA11><fA14 i1="01"><s1>13S Laboratory, University of Nice-Sophia Antipolis/CNRS, Les Algorithmes/Euclide B-2000, route des Lucioles, BP 121</s1><s2>06903 Sophio-Antipolis</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Engenharia de Teleinformática, Federal University of Ceará, Campus do Pici, 60.755-640</s1><s2>6007 Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA20><s1>2644-2656</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>18015</s2><s5>354000172591370270</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>36 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0366340</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Signal processing</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>This paper presents two blind identification methods for nonlinear memoryless channels in multiuser communication systems. These methods are based on the parallel factor (PARAFAC) decomposition of a tensor composed of channel output covariances. Such a decomposition is possible owing to a new precoding scheme developed for phase-shift keying (PSK) signals modeled as Markov chains. Some conditions on the transition probability matrices (TPM) of the Markov chains are established to introduce temporal correlation and satisfy statistical correlation constraints inducing the PARAFAC decomposition of the considered tensor. The proposed blind channel estimation algorithms are evaluated by means of computer simulations.</s0></fC01><fC02 i1="01" i2="X"><s0>001D04A04A2</s0></fC02><fC02 i1="02" i2="X"><s0>001D04A04B</s0></fC02><fC02 i1="03" i2="X"><s0>001D04A04F</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Identification système</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>System identification</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Identificación sistema</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Identification aveugle</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Blind identification</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Identificación ciega</s0><s5>02</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Canal multiutilisateur</s0><s5>03</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Multiuser channels</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Canal non linéaire</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Non linear channel</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Canal no lineal</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Codage</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Coding</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Codificación</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Canal sans mémoire</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Memoryless channel</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Canal sin memoria</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Accès multiple</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Multiple access</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Acceso múltiple</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Système télécommunication</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Telecommunication system</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Sistema telecomunicación</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Covariance</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Covariance</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Covariancia</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Modulation déplacement phase</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Phase shift keying</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Modulación desplazamiento fase</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Chaîne Markov</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Markov chain</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Cadena Markov</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Probabilité transition</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Transition probability</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Probabilidad transición</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Corrélation temporelle</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Time correlation</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Correlación temporal</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Méthode statistique</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Statistical method</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Método estadístico</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Estimation canal</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Channel estimation</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Estimación canal</s0><s5>15</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Algorithme</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Algorithm</s0><s5>16</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Algoritmo</s0><s5>16</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Simulation ordinateur</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Computer simulation</s0><s5>17</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Simulación computadora</s0><s5>17</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Estimation paramètre</s0><s5>31</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Parameter estimation</s0><s5>31</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Estimación parámetro</s0><s5>31</s5></fC03><fN21><s1>264</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0366340 INIST</NO><ET>Blind identification of multiuser nonlinear channels using tensor decomposition and precoding</ET><AU>FERNANDES (Carlos Alexandre); FAVIER (Gérard); MOTA (Joao Cesar M.)</AU><AF>13S Laboratory, University of Nice-Sophia Antipolis/CNRS, Les Algorithmes/Euclide B-2000, route des Lucioles, BP 121/06903 Sophio-Antipolis/France (1 aut., 2 aut.); Departamento de Engenharia de Teleinformática, Federal University of Ceará, Campus do Pici, 60.755-640/6007 Fortaleza/Brésil (1 aut., 3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Signal processing; ISSN 0165-1684; Coden SPRODR; Pays-Bas; Da. 2009; Vol. 89; No. 12; Pp. 2644-2656; Bibl. 36 ref.</SO><LA>Anglais</LA><EA>This paper presents two blind identification methods for nonlinear memoryless channels in multiuser communication systems. These methods are based on the parallel factor (PARAFAC) decomposition of a tensor composed of channel output covariances. Such a decomposition is possible owing to a new precoding scheme developed for phase-shift keying (PSK) signals modeled as Markov chains. Some conditions on the transition probability matrices (TPM) of the Markov chains are established to introduce temporal correlation and satisfy statistical correlation constraints inducing the PARAFAC decomposition of the considered tensor. The proposed blind channel estimation algorithms are evaluated by means of computer simulations.</EA><CC>001D04A04A2; 001D04A04B; 001D04A04F</CC><FD>Identification système; Identification aveugle; Canal multiutilisateur; Canal non linéaire; Codage; Canal sans mémoire; Accès multiple; Système télécommunication; Covariance; Modulation déplacement phase; Chaîne Markov; Probabilité transition; Corrélation temporelle; Méthode statistique; Estimation canal; Algorithme; Simulation ordinateur; Estimation paramètre</FD><ED>System identification; Blind identification; Multiuser channels; Non linear channel; Coding; Memoryless channel; Multiple access; Telecommunication system; Covariance; Phase shift keying; Markov chain; Transition probability; Time correlation; Statistical method; Channel estimation; Algorithm; Computer simulation; Parameter estimation</ED><SD>Identificación sistema; Identificación ciega; Canal no lineal; Codificación; Canal sin memoria; Acceso múltiple; Sistema telecomunicación; Covariancia; Modulación desplazamiento fase; Cadena Markov; Probabilidad transición; Correlación temporal; Método estadístico; Estimación canal; Algoritmo; Simulación computadora; Estimación parámetro</SD><LO>INIST-18015.354000172591370270</LO><ID>09-0366340</ID></server></inist></record>
000D43	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Nonequilibrium fluctuations for a tagged particle in mean-zero one-dimensional zero-range processes</title><author><name sortKey="Jara, M D" uniqKey="Jara M">M. D. Jara</name><affiliation><inist:fA14 i1="01"><s1>IMPA, Estrada Dona Castorina 110</s1><s2>Rio de Janeiro, CEP 22460</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Landim, C" uniqKey="Landim C">C. Landim</name><affiliation><inist:fA14 i1="02"><s1>CNRS UMR 6085, Avenue de l'Université, Technopôle du Madrillet, BP 1276801</s1><s2>Saint-Étienne-du-Rouvray</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sethuraman, S" uniqKey="Sethuraman S">S. Sethuraman</name><affiliation><inist:fA14 i1="03"><s1>Department of Mathematics, Iowa State University, 396 Carver Hall</s1><s2>Ames, IA 50011</s2><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0368310</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0368310 INIST</idno><idno type="RBID">Pascal:09-0368310</idno><idno type="wicri:Area/Main/Corpus">001C38</idno></publicationStmt><seriesStmt><idno type="ISSN">0178-8051</idno><title level="j" type="abbreviated">Probab. theory relat. fields</title><title level="j" type="main">Probability theory and related fields</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Asymptotic behavior</term><term>Central limit theorem</term><term>Fluctuations</term><term>Hydrodynamics</term><term>Mean estimation</term><term>Probability theory</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Fluctuation</term><term>Estimation moyenne</term><term>Théorème central limite</term><term>Comportement asymptotique</term><term>Hydrodynamique</term><term>Théorie probabilité</term><term>60F20</term><term>60F17</term><term>60F05</term><term>60H10</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We prove a non-equilibrium functional central limit theorem for the position of a tagged particle in mean-zero one-dimensional zero-range process. The asymptotic behavior of the tagged particle is described by a stochastic differential equation governed by the solution of the hydrodynamic equation.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0178-8051</s0></fA01><fA02 i1="01"><s0>PTRFEU</s0></fA02><fA03 i2="1"><s0>Probab. theory relat. fields</s0></fA03><fA05><s2>145</s2></fA05><fA06><s2>3-4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Nonequilibrium fluctuations for a tagged particle in mean-zero one-dimensional zero-range processes</s1></fA08><fA11 i1="01" i2="1"><s1>JARA (M. D.)</s1></fA11><fA11 i1="02" i2="1"><s1>LANDIM (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>SETHURAMAN (S.)</s1></fA11><fA14 i1="01"><s1>IMPA, Estrada Dona Castorina 110</s1><s2>Rio de Janeiro, CEP 22460</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>CNRS UMR 6085, Avenue de l'Université, Technopôle du Madrillet, BP 1276801</s1><s2>Saint-Étienne-du-Rouvray</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Department of Mathematics, Iowa State University, 396 Carver Hall</s1><s2>Ames, IA 50011</s2><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>565-590</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>9653</s2><s5>354000187591840080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>24 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0368310</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Probability theory and related fields</s0></fA64><fA66 i1="01"><s0>DEU</s0></fA66><fC01 i1="01" l="ENG"><s0>We prove a non-equilibrium functional central limit theorem for the position of a tagged particle in mean-zero one-dimensional zero-range process. The asymptotic behavior of the tagged particle is described by a stochastic differential equation governed by the solution of the hydrodynamic equation.</s0></fC01><fC02 i1="01" i2="X"><s0>001A02H01A</s0></fC02><fC02 i1="02" i2="X"><s0>001A02H01G</s0></fC02><fC02 i1="03" i2="X"><s0>001A02H01I</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Fluctuation</s0><s5>17</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Fluctuations</s0><s5>17</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Fluctuación</s0><s5>17</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Estimation moyenne</s0><s5>18</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Mean estimation</s0><s5>18</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Estimación promedio</s0><s5>18</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Théorème central limite</s0><s5>19</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Central limit theorem</s0><s5>19</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Teorema central límite</s0><s5>19</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Comportement asymptotique</s0><s5>20</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Asymptotic behavior</s0><s5>20</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Comportamiento asintótico</s0><s5>20</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Hydrodynamique</s0><s5>21</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Hydrodynamics</s0><s5>21</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Hidrodinámica</s0><s5>21</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Théorie probabilité</s0><s5>22</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Probability theory</s0><s5>22</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Teoría probabilidad</s0><s5>22</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>60F20</s0><s4>INC</s4><s5>70</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>60F17</s0><s4>INC</s4><s5>71</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>60F05</s0><s4>INC</s4><s5>72</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>60H10</s0><s4>INC</s4><s5>73</s5></fC03><fN21><s1>264</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0368310 INIST</NO><ET>Nonequilibrium fluctuations for a tagged particle in mean-zero one-dimensional zero-range processes</ET><AU>JARA (M. D.); LANDIM (C.); SETHURAMAN (S.)</AU><AF>IMPA, Estrada Dona Castorina 110/Rio de Janeiro, CEP 22460/Brésil (1 aut.); CNRS UMR 6085, Avenue de l'Université, Technopôle du Madrillet, BP 1276801/Saint-Étienne-du-Rouvray/France (2 aut.); Department of Mathematics, Iowa State University, 396 Carver Hall/Ames, IA 50011/Etats-Unis (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Probability theory and related fields; ISSN 0178-8051; Coden PTRFEU; Allemagne; Da. 2009; Vol. 145; No. 3-4; Pp. 565-590; Bibl. 24 ref.</SO><LA>Anglais</LA><EA>We prove a non-equilibrium functional central limit theorem for the position of a tagged particle in mean-zero one-dimensional zero-range process. The asymptotic behavior of the tagged particle is described by a stochastic differential equation governed by the solution of the hydrodynamic equation.</EA><CC>001A02H01A; 001A02H01G; 001A02H01I</CC><FD>Fluctuation; Estimation moyenne; Théorème central limite; Comportement asymptotique; Hydrodynamique; Théorie probabilité; 60F20; 60F17; 60F05; 60H10</FD><ED>Fluctuations; Mean estimation; Central limit theorem; Asymptotic behavior; Hydrodynamics; Probability theory</ED><SD>Fluctuación; Estimación promedio; Teorema central límite; Comportamiento asintótico; Hidrodinámica; Teoría probabilidad</SD><LO>INIST-9653.354000187591840080</LO><ID>09-0368310</ID></server></inist></record>
000D44	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Heavy ion irradiation of condensed CO<sub>2</sub>: sputtering and molecule formation</title><author><name sortKey="Seperuelo Duarte, E" uniqKey="Seperuelo Duarte E">E. Seperuelo Duarte</name><affiliation><inist:fA14 i1="01"><s1>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133</s1><s2>14070 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Physics Department, Pontifícia Universidade Católica, Rua Marquês de S. Vicente 225</s1><s2>22453-900 Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Grupo de Fisica e Astronomia - CEFET/Química de Nilópolis, Rua Lúcio Tavares 1045, Centro</s1><s2>26530-060 Nilópolis</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Boduch, P" uniqKey="Boduch P">P. Boduch</name><affiliation><inist:fA14 i1="01"><s1>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133</s1><s2>14070 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rothard, H" uniqKey="Rothard H">H. Rothard</name><affiliation><inist:fA14 i1="01"><s1>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133</s1><s2>14070 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Been, T" uniqKey="Been T">T. Been</name><affiliation><inist:fA14 i1="01"><s1>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133</s1><s2>14070 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dartois, E" uniqKey="Dartois E">E. Dartois</name><affiliation><inist:fA14 i1="04"><s1>Institut d' Astrophysique Spatiale, Astrochimie Expérimentale, UMR-8617 Université Paris-Sud, bâtiment 121</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Farenzena, L S" uniqKey="Farenzena L">L. S. Farenzena</name><affiliation><inist:fA14 i1="05"><s1>Physics Department, Universidade Federal de Santa Catarina</s1><s2>Florianópolis, SC</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Silveira, E F" uniqKey="Da Silveira E">E. F. Da Silveira</name><affiliation><inist:fA14 i1="02"><s1>Physics Department, Pontifícia Universidade Católica, Rua Marquês de S. Vicente 225</s1><s2>22453-900 Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0371287</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0371287 INIST</idno><idno type="RBID">Pascal:09-0371287</idno><idno type="wicri:Area/Main/Corpus">001C37</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cosmic irradiation</term><term>Cosmic radiation</term><term>Cross sections</term><term>Energy losses</term><term>GeV range</term><term>Heavy ions</term><term>Ice</term><term>Infrared spectroscopy</term><term>Ion irradiation</term><term>Molecular process</term><term>Protons</term><term>Solar wind</term><term>Stopping power</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Ion lourd</term><term>Irradiation ion</term><term>Glace</term><term>Irradiation cosmique</term><term>Domaine énergie GeV</term><term>Perte énergie</term><term>Proton</term><term>Spectrométrie IR</term><term>Section efficace</term><term>Vent solaire</term><term>Rayonnement cosmique</term><term>Pouvoir arrêt</term><term>Processus moléculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Context. Ices present in different astrophysical environments are exposed to ion irradiation from cosmic rays (H to heavier than Fe) in the keV to GeV energy range. Aims. The objective of this work is to study the effects produced in astrophysical ices by heavy ions at relatively high energies (MeV) in the electronic energy loss regime and compare them with those produced by protons. Methods. C<sup>18</sup>O<sub>2</sub> was condensed on a CsI substrate at 13 K and it was irradiated by 46 MeV <sup>58</sup>Ni<sup>11+</sup> up to a final fluence of 1.5 × 10<sup>13</sup> cm<sup>-2</sup> at a flux of 2 × 10<sup>9</sup> cm<sup>-2</sup> s<sup>-1</sup>. The ice was analyzed in situ by infrared spectroscopy (FTIR) in the 5000-600 cm<sup>-1</sup> range. Results. The CO<sub>2</sub> destruction was observed, as well as the formation of other species such as CO, CO<sub>3</sub>, O<sub>3</sub>, and C<sub>3</sub>. The destruction cross section of CO<sub>2</sub> is found to be 1.7 × 10<sup>-13</sup> cm<sup>2</sup>, while those for the formation of CO, CO<sub>3</sub>, and O<sub>3</sub> molecules are 1.6 × 10-<sup>13</sup> cm<sup>2</sup>, 4.5 × 10<sup>-14</sup> cm<sup>2</sup>, and 1.5 × 10<sup>-14</sup> cm<sup>2</sup> , respectively. The sputtering yield of the CO<sub>2</sub> ice is 4.0 × 10<sup>4</sup> molecules/impact, four orders of magnitude higher than for H projectiles at the same velocity. This allows us to estimate the contribution of the sputtering by heavy ions as compared to protons in the solar winds and in cosmic rays. Conclusions. The present results show that heavy ions play an important role in the sputtering of astrophysical ices. Furthermore, this work confirms the quadratic stopping power dependence of sputtering yields.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>502</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Heavy ion irradiation of condensed CO<sub>2</sub>: sputtering and molecule formation</s1></fA08><fA11 i1="01" i2="1"><s1>SEPERUELO DUARTE (E.)</s1></fA11><fA11 i1="02" i2="1"><s1>BODUCH (P.)</s1></fA11><fA11 i1="03" i2="1"><s1>ROTHARD (H.)</s1></fA11><fA11 i1="04" i2="1"><s1>BEEN (T.)</s1></fA11><fA11 i1="05" i2="1"><s1>DARTOIS (E.)</s1></fA11><fA11 i1="06" i2="1"><s1>FARENZENA (L. S.)</s1></fA11><fA11 i1="07" i2="1"><s1>DA SILVEIRA (E. F.)</s1></fA11><fA14 i1="01"><s1>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133</s1><s2>14070 Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Physics Department, Pontifícia Universidade Católica, Rua Marquês de S. Vicente 225</s1><s2>22453-900 Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Grupo de Fisica e Astronomia - CEFET/Química de Nilópolis, Rua Lúcio Tavares 1045, Centro</s1><s2>26530-060 Nilópolis</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="04"><s1>Institut d' Astrophysique Spatiale, Astrochimie Expérimentale, UMR-8617 Université Paris-Sud, bâtiment 121</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Physics Department, Universidade Federal de Santa Catarina</s1><s2>Florianópolis, SC</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>599-603</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000171820570220</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0371287</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Context. Ices present in different astrophysical environments are exposed to ion irradiation from cosmic rays (H to heavier than Fe) in the keV to GeV energy range. Aims. The objective of this work is to study the effects produced in astrophysical ices by heavy ions at relatively high energies (MeV) in the electronic energy loss regime and compare them with those produced by protons. Methods. C<sup>18</sup>O<sub>2</sub> was condensed on a CsI substrate at 13 K and it was irradiated by 46 MeV <sup>58</sup>Ni<sup>11+</sup> up to a final fluence of 1.5 × 10<sup>13</sup> cm<sup>-2</sup> at a flux of 2 × 10<sup>9</sup> cm<sup>-2</sup> s<sup>-1</sup>. The ice was analyzed in situ by infrared spectroscopy (FTIR) in the 5000-600 cm<sup>-1</sup> range. Results. The CO<sub>2</sub> destruction was observed, as well as the formation of other species such as CO, CO<sub>3</sub>, O<sub>3</sub>, and C<sub>3</sub>. The destruction cross section of CO<sub>2</sub> is found to be 1.7 × 10<sup>-13</sup> cm<sup>2</sup>, while those for the formation of CO, CO<sub>3</sub>, and O<sub>3</sub> molecules are 1.6 × 10-<sup>13</sup> cm<sup>2</sup>, 4.5 × 10<sup>-14</sup> cm<sup>2</sup>, and 1.5 × 10<sup>-14</sup> cm<sup>2</sup> , respectively. The sputtering yield of the CO<sub>2</sub> ice is 4.0 × 10<sup>4</sup> molecules/impact, four orders of magnitude higher than for H projectiles at the same velocity. This allows us to estimate the contribution of the sputtering by heavy ions as compared to protons in the solar winds and in cosmic rays. Conclusions. The present results show that heavy ions play an important role in the sputtering of astrophysical ices. Furthermore, this work confirms the quadratic stopping power dependence of sputtering yields.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Ion lourd</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Heavy ions</s0><s5>26</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Irradiation ion</s0><s5>27</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Ion irradiation</s0><s5>27</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Irradiación ión</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Glace</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Ice</s0><s5>28</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Irradiation cosmique</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Cosmic irradiation</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Irradiación cósmica</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Domaine énergie GeV</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>GeV range</s0><s5>30</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Perte énergie</s0><s5>31</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Energy losses</s0><s5>31</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Proton</s0><s5>32</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Protons</s0><s5>32</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Spectrométrie IR</s0><s5>33</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Infrared spectroscopy</s0><s5>33</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Section efficace</s0><s5>34</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Cross sections</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Vent solaire</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Solar wind</s0><s5>35</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Rayonnement cosmique</s0><s5>36</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Cosmic radiation</s0><s5>36</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Pouvoir arrêt</s0><s5>37</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Stopping power</s0><s5>37</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Processus moléculaire</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Molecular process</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Proceso molecular</s0><s5>38</s5></fC03><fN21><s1>264</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0371287 INIST</NO><ET>Heavy ion irradiation of condensed CO<sub>2</sub>: sputtering and molecule formation</ET><AU>SEPERUELO DUARTE (E.); BODUCH (P.); ROTHARD (H.); BEEN (T.); DARTOIS (E.); FARENZENA (L. S.); DA SILVEIRA (E. F.)</AU><AF>Centre de Recherche sur les Ions, les Matériaux et la Photonique (CEA /CNRS /ENSICAEN /Université de Caen-Basse Normandie), CIMAP - CIRIL - Ganil, Boulevard Henri Becquerel, BP 5133/14070 Caen/France (1 aut., 2 aut., 3 aut., 4 aut.); Physics Department, Pontifícia Universidade Católica, Rua Marquês de S. Vicente 225/22453-900 Rio de Janeiro/Brésil (1 aut., 7 aut.); Grupo de Fisica e Astronomia - CEFET/Química de Nilópolis, Rua Lúcio Tavares 1045, Centro/26530-060 Nilópolis/Brésil (1 aut.); Institut d' Astrophysique Spatiale, Astrochimie Expérimentale, UMR-8617 Université Paris-Sud, bâtiment 121/91405 Orsay/France (5 aut.); Physics Department, Universidade Federal de Santa Catarina/Florianópolis, SC/Brésil (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 502; No. 2; Pp. 599-603; Bibl. 1/2 p.</SO><LA>Anglais</LA><EA>Context. Ices present in different astrophysical environments are exposed to ion irradiation from cosmic rays (H to heavier than Fe) in the keV to GeV energy range. Aims. The objective of this work is to study the effects produced in astrophysical ices by heavy ions at relatively high energies (MeV) in the electronic energy loss regime and compare them with those produced by protons. Methods. C<sup>18</sup>O<sub>2</sub> was condensed on a CsI substrate at 13 K and it was irradiated by 46 MeV <sup>58</sup>Ni<sup>11+</sup> up to a final fluence of 1.5 × 10<sup>13</sup> cm<sup>-2</sup> at a flux of 2 × 10<sup>9</sup> cm<sup>-2</sup> s<sup>-1</sup>. The ice was analyzed in situ by infrared spectroscopy (FTIR) in the 5000-600 cm<sup>-1</sup> range. Results. The CO<sub>2</sub> destruction was observed, as well as the formation of other species such as CO, CO<sub>3</sub>, O<sub>3</sub>, and C<sub>3</sub>. The destruction cross section of CO<sub>2</sub> is found to be 1.7 × 10<sup>-13</sup> cm<sup>2</sup>, while those for the formation of CO, CO<sub>3</sub>, and O<sub>3</sub> molecules are 1.6 × 10-<sup>13</sup> cm<sup>2</sup>, 4.5 × 10<sup>-14</sup> cm<sup>2</sup>, and 1.5 × 10<sup>-14</sup> cm<sup>2</sup> , respectively. The sputtering yield of the CO<sub>2</sub> ice is 4.0 × 10<sup>4</sup> molecules/impact, four orders of magnitude higher than for H projectiles at the same velocity. This allows us to estimate the contribution of the sputtering by heavy ions as compared to protons in the solar winds and in cosmic rays. Conclusions. The present results show that heavy ions play an important role in the sputtering of astrophysical ices. Furthermore, this work confirms the quadratic stopping power dependence of sputtering yields.</EA><CC>001E03</CC><FD>Ion lourd; Irradiation ion; Glace; Irradiation cosmique; Domaine énergie GeV; Perte énergie; Proton; Spectrométrie IR; Section efficace; Vent solaire; Rayonnement cosmique; Pouvoir arrêt; Processus moléculaire</FD><ED>Heavy ions; Ion irradiation; Ice; Cosmic irradiation; GeV range; Energy losses; Protons; Infrared spectroscopy; Cross sections; Solar wind; Cosmic radiation; Stopping power; Molecular process</ED><SD>Irradiación ión; Irradiación cósmica; Proceso molecular</SD><LO>INIST-14176.354000171820570220</LO><ID>09-0371287</ID></server></inist></record>
000D45	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Kinematic analysis and membership status of TWA22 AB</title><author><name sortKey="Teixeira, R" uniqKey="Teixeira R">R. Teixeira</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciências Atmosféricas, Universidade de Sao Paulo, Rua do Matão, 1226 Cidade Universitária</s1><s2>05508-900 São Paulo - SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Observatoire Aquitaine des Sciences de l'Univers, CNRS-UMR 5804, BP 89</s1><s2>33270 Floirac</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ducourant, C" uniqKey="Ducourant C">C. Ducourant</name><affiliation><inist:fA14 i1="02"><s1>Observatoire Aquitaine des Sciences de l'Univers, CNRS-UMR 5804, BP 89</s1><s2>33270 Floirac</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chauvin, G" uniqKey="Chauvin G">G. Chauvin</name><affiliation><inist:fA14 i1="03"><s1>Laboratoire d'Astrophysique, Observatoire de Grenoble, 414 rue de la piscine</s1><s2>38400 Saint-Martin d'Hères</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Krone Martins, A" uniqKey="Krone Martins A">A. Krone-Martins</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciências Atmosféricas, Universidade de Sao Paulo, Rua do Matão, 1226 Cidade Universitária</s1><s2>05508-900 São Paulo - SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Observatoire Aquitaine des Sciences de l'Univers, CNRS-UMR 5804, BP 89</s1><s2>33270 Floirac</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bonnefoy, M" uniqKey="Bonnefoy M">M. Bonnefoy</name><affiliation><inist:fA14 i1="03"><s1>Laboratoire d'Astrophysique, Observatoire de Grenoble, 414 rue de la piscine</s1><s2>38400 Saint-Martin d'Hères</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Song, I" uniqKey="Song I">I. Song</name><affiliation><inist:fA14 i1="04"><s1>Department of Physics &#38; Astronomy, the University of Georgia</s1><s2>Athens, GA 30605</s2><s3>USA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0374655</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0374655 INIST</idno><idno type="RBID">Pascal:09-0374655</idno><idno type="wicri:Area/Main/Corpus">001C36</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Astrometry</term><term>Close binary stars</term><term>Galaxies</term><term>Galaxy clusters</term><term>Kinematics</term><term>Models</term><term>Open clusters</term><term>Positions</term><term>Probability</term><term>Proper motion</term><term>Radial motion</term><term>Radial velocity</term><term>Solar neighborhood</term><term>Star clusters</term><term>Uncertainty</term><term>Velocity dispersion</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cinématique</term><term>Modèle</term><term>Mouvement propre</term><term>Mouvement radial</term><term>Vitesse radiale</term><term>Position</term><term>Probabilité</term><term>Incertitude</term><term>Dispersion vitesse</term><term>Astrométrie</term><term>Binaire serrée</term><term>Amas galaxies</term><term>Amas ouvert</term><term>Galaxies</term><term>Voisinage solaire</term><term>Amas stellaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Context. TWA22 was initially regarded as a member of the TW Hydrae association (TWA). In addition to being one of the youngest (≃8 Myr) and nearest (≃20 pc) stars to Earth, TWA22 has proven to be very interesting after being resolved as a tight, very lowmass binary. This binary can serve as a very useful dynamical calibrator for pre-main sequence evolutionary models. However, its membership in the TWA has been recently questioned despite due to the lack of accurate kinematic measurements. Aims. Based on proper motion, radial velocity, and trigonometric parallax measurements, we aim here to re-analyze the membership of TWA22 to young, nearby associations. Methods. Using the ESO NTT/SUSI2 telescope, we observed TWA22 AB during 5 different observing runs over 1.2 years to measure its trigonometric parallax and proper motion. This is a part of a larger project measuring trigonometric parallaxes and proper motions of most known TWA members at a sub-milliarcsec level. HARPS at the ESO 3.6 m telescope was also used to measure the system's radial velocity over 2 years. Results. We report an absolute trigonometric parallax of TWA22 AB, π = 57.0 ± 0.7 mas, corresponding to a distance 17.5 ± 0.2 pc from Earth. Measured proper motions of TWA 22AB are μ<sub>α</sub> cos(δ)= -175.8 ± 0.8 mas/yr and μ<sub>δ</sub> = -21.3 ±0.8 mas/yr. Finally, from HARPS measurements, we obtain a radial velocity V<sub>rad</sub> = 14.8 ±2.1 km s<sup>-1</sup>. Conclusions. A kinematic analysis of TWA22 AB space motion and position implies that a membership of TWA22 AB to known young, nearby associations can be excluded except for the β Pictoris and TW Hydrae associations. Membership probabilities based on the system's Galactic space motion and/or the trace-back technique support a higher chance of being a member to the β Pictoris association. Membership of TWA22 in the TWA cannot be fully excluded because of large uncertainties in parallax measurements and radial velocities and to the uncertain internal velocity dispersion of its members.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>503</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Kinematic analysis and membership status of TWA22 AB</s1></fA08><fA11 i1="01" i2="1"><s1>TEIXEIRA (R.)</s1></fA11><fA11 i1="02" i2="1"><s1>DUCOURANT (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>CHAUVIN (G.)</s1></fA11><fA11 i1="04" i2="1"><s1>KRONE-MARTINS (A.)</s1></fA11><fA11 i1="05" i2="1"><s1>BONNEFOY (M.)</s1></fA11><fA11 i1="06" i2="1"><s1>SONG (I.)</s1></fA11><fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciências Atmosféricas, Universidade de Sao Paulo, Rua do Matão, 1226 Cidade Universitária</s1><s2>05508-900 São Paulo - SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Observatoire Aquitaine des Sciences de l'Univers, CNRS-UMR 5804, BP 89</s1><s2>33270 Floirac</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratoire d'Astrophysique, Observatoire de Grenoble, 414 rue de la piscine</s1><s2>38400 Saint-Martin d'Hères</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Department of Physics &#38; Astronomy, the University of Georgia</s1><s2>Athens, GA 30605</s2><s3>USA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>281-285</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000171830550310</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0374655</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Context. TWA22 was initially regarded as a member of the TW Hydrae association (TWA). In addition to being one of the youngest (≃8 Myr) and nearest (≃20 pc) stars to Earth, TWA22 has proven to be very interesting after being resolved as a tight, very lowmass binary. This binary can serve as a very useful dynamical calibrator for pre-main sequence evolutionary models. However, its membership in the TWA has been recently questioned despite due to the lack of accurate kinematic measurements. Aims. Based on proper motion, radial velocity, and trigonometric parallax measurements, we aim here to re-analyze the membership of TWA22 to young, nearby associations. Methods. Using the ESO NTT/SUSI2 telescope, we observed TWA22 AB during 5 different observing runs over 1.2 years to measure its trigonometric parallax and proper motion. This is a part of a larger project measuring trigonometric parallaxes and proper motions of most known TWA members at a sub-milliarcsec level. HARPS at the ESO 3.6 m telescope was also used to measure the system's radial velocity over 2 years. Results. We report an absolute trigonometric parallax of TWA22 AB, π = 57.0 ± 0.7 mas, corresponding to a distance 17.5 ± 0.2 pc from Earth. Measured proper motions of TWA 22AB are μ<sub>α</sub> cos(δ)= -175.8 ± 0.8 mas/yr and μ<sub>δ</sub> = -21.3 ±0.8 mas/yr. Finally, from HARPS measurements, we obtain a radial velocity V<sub>rad</sub> = 14.8 ±2.1 km s<sup>-1</sup>. Conclusions. A kinematic analysis of TWA22 AB space motion and position implies that a membership of TWA22 AB to known young, nearby associations can be excluded except for the β Pictoris and TW Hydrae associations. Membership probabilities based on the system's Galactic space motion and/or the trace-back technique support a higher chance of being a member to the β Pictoris association. Membership of TWA22 in the TWA cannot be fully excluded because of large uncertainties in parallax measurements and radial velocities and to the uncertain internal velocity dispersion of its members.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Cinématique</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Kinematics</s0><s5>26</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Modèle</s0><s5>27</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Models</s0><s5>27</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Modelo</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Mouvement propre</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Proper motion</s0><s5>28</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Mouvement radial</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Radial motion</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Movimiento radial</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Vitesse radiale</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Radial velocity</s0><s5>30</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Position</s0><s5>31</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Positions</s0><s5>31</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Probabilité</s0><s5>32</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Probability</s0><s5>32</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Incertitude</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Uncertainty</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Incertidumbre</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Dispersion vitesse</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Velocity dispersion</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Dispersión velocidad</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Astrométrie</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Astrometry</s0><s5>35</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Binaire serrée</s0><s5>36</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Close binary stars</s0><s5>36</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Amas galaxies</s0><s5>37</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Galaxy clusters</s0><s5>37</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Amas ouvert</s0><s5>38</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Open clusters</s0><s5>38</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Galaxies</s0><s5>39</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Galaxies</s0><s5>39</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Voisinage solaire</s0><s5>40</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Solar neighborhood</s0><s5>40</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Vecindad solar</s0><s5>40</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Amas stellaire</s0><s5>41</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Star clusters</s0><s5>41</s5></fC03><fN21><s1>271</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0374655 INIST</NO><ET>Kinematic analysis and membership status of TWA22 AB</ET><AU>TEIXEIRA (R.); DUCOURANT (C.); CHAUVIN (G.); KRONE-MARTINS (A.); BONNEFOY (M.); SONG (I.)</AU><AF>Instituto de Astronomia, Geofisica e Ciências Atmosféricas, Universidade de Sao Paulo, Rua do Matão, 1226 Cidade Universitária/05508-900 São Paulo - SP/Brésil (1 aut., 4 aut.); Observatoire Aquitaine des Sciences de l'Univers, CNRS-UMR 5804, BP 89/33270 Floirac/France (1 aut., 2 aut., 4 aut.); Laboratoire d'Astrophysique, Observatoire de Grenoble, 414 rue de la piscine/38400 Saint-Martin d'Hères/France (3 aut., 5 aut.); Department of Physics &#38; Astronomy, the University of Georgia/Athens, GA 30605/Etats-Unis (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 503; No. 1; Pp. 281-285; Bibl. 1/4 p.</SO><LA>Anglais</LA><EA>Context. TWA22 was initially regarded as a member of the TW Hydrae association (TWA). In addition to being one of the youngest (≃8 Myr) and nearest (≃20 pc) stars to Earth, TWA22 has proven to be very interesting after being resolved as a tight, very lowmass binary. This binary can serve as a very useful dynamical calibrator for pre-main sequence evolutionary models. However, its membership in the TWA has been recently questioned despite due to the lack of accurate kinematic measurements. Aims. Based on proper motion, radial velocity, and trigonometric parallax measurements, we aim here to re-analyze the membership of TWA22 to young, nearby associations. Methods. Using the ESO NTT/SUSI2 telescope, we observed TWA22 AB during 5 different observing runs over 1.2 years to measure its trigonometric parallax and proper motion. This is a part of a larger project measuring trigonometric parallaxes and proper motions of most known TWA members at a sub-milliarcsec level. HARPS at the ESO 3.6 m telescope was also used to measure the system's radial velocity over 2 years. Results. We report an absolute trigonometric parallax of TWA22 AB, π = 57.0 ± 0.7 mas, corresponding to a distance 17.5 ± 0.2 pc from Earth. Measured proper motions of TWA 22AB are μ<sub>α</sub> cos(δ)= -175.8 ± 0.8 mas/yr and μ<sub>δ</sub> = -21.3 ±0.8 mas/yr. Finally, from HARPS measurements, we obtain a radial velocity V<sub>rad</sub> = 14.8 ±2.1 km s<sup>-1</sup>. Conclusions. A kinematic analysis of TWA22 AB space motion and position implies that a membership of TWA22 AB to known young, nearby associations can be excluded except for the β Pictoris and TW Hydrae associations. Membership probabilities based on the system's Galactic space motion and/or the trace-back technique support a higher chance of being a member to the β Pictoris association. Membership of TWA22 in the TWA cannot be fully excluded because of large uncertainties in parallax measurements and radial velocities and to the uncertain internal velocity dispersion of its members.</EA><CC>001E03</CC><FD>Cinématique; Modèle; Mouvement propre; Mouvement radial; Vitesse radiale; Position; Probabilité; Incertitude; Dispersion vitesse; Astrométrie; Binaire serrée; Amas galaxies; Amas ouvert; Galaxies; Voisinage solaire; Amas stellaire</FD><ED>Kinematics; Models; Proper motion; Radial motion; Radial velocity; Positions; Probability; Uncertainty; Velocity dispersion; Astrometry; Close binary stars; Galaxy clusters; Open clusters; Galaxies; Solar neighborhood; Star clusters</ED><SD>Modelo; Movimiento radial; Incertidumbre; Dispersión velocidad; Vecindad solar</SD><LO>INIST-14176.354000171830550310</LO><ID>09-0374655</ID></server></inist></record>
000D46	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Tree-shaped vascular wall designs for localized intense cooling</title><author><name sortKey="Rocha, L A O" uniqKey="Rocha L">L. A. O. Rocha</name><affiliation><inist:fA14 i1="01"><s1>Federal University of Rio Grande, School of Engineering, Av. Itália km 8, Cx. P. 474</s1><s2>Rio Grande, RS 96.201-900</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lorente, S" uniqKey="Lorente S">S. Lorente</name><affiliation><inist:fA14 i1="02"><s1>Université de Toulouse, INSA, Laboratoire Matériaux et Durabilité des Constructions, 135, Avenue de Rangueil</s1><s2>31077 Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bejan, A" uniqKey="Bejan A">A. Bejan</name><affiliation><inist:fA14 i1="03"><s1>Duke University, Department of Mechanical Engineering and Materials Science, Box 90300</s1><s2>Durham, NC 27708-0300</s2><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0376387</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0376387 INIST</idno><idno type="RBID">Pascal:09-0376387</idno><idno type="wicri:Area/Main/Corpus">001C35</idno></publicationStmt><seriesStmt><idno type="ISSN">0017-9310</idno><title level="j" type="abbreviated">Int. j. heat mass transfer</title><title level="j" type="main">International journal of heat and mass transfer</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Avionics</term><term>Constructive theory</term><term>Cooling system</term><term>Dendritic structure</term><term>Design</term><term>Electronic component</term><term>Fuel cell</term><term>Heat transfer</term><term>Smart materials</term><term>Tree structure</term><term>Vascularization</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Composant électronique</term><term>Avionique</term><term>Transfert chaleur</term><term>Système refroidissement</term><term>Pile combustible</term><term>Structure arborescente</term><term>Matériau intelligent</term><term>Vascularisation</term><term>Théorie constructive</term><term>Conception</term><term>Structure dendritique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This paper is a proposal to embed tree-shaped vasculatures in a wall designed such that the wall withstands without excessive hot spots the intense heating that impinges on it. The vasculature is a quilt of square-shaped panels, each panel having a tree vasculature that connects the center with the perimeter. The coolant may flow in either direction, center-perimeter, or perimeter-center, although here only the center-perimeter flow direction is illustrated. Numerical simulations of conjugate heat and fluid flow in three directions show that it is possible to determine all the optimal geometric features of vasculatures with up to three levels of bifurcation (n <sub>=</sub> 3). The global performance is evaluated in terms of the overall thermal resistance, pressure difference, flow resistance and pumping power. The improvements in global performance diminish as the number of bifurcation levels increases. No flow architecture is universally superior. The dendritic designs are superior at the low and high ends of the pressure difference range. The radial designs are superior at intermediate pressure difference numbers.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0017-9310</s0></fA01><fA02 i1="01"><s0>IJHMAK</s0></fA02><fA03 i2="1"><s0>Int. j. heat mass transfer</s0></fA03><fA05><s2>52</s2></fA05><fA06><s2>19-20</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Tree-shaped vascular wall designs for localized intense cooling</s1></fA08><fA11 i1="01" i2="1"><s1>ROCHA (L. A. O.)</s1></fA11><fA11 i1="02" i2="1"><s1>LORENTE (S.)</s1></fA11><fA11 i1="03" i2="1"><s1>BEJAN (A.)</s1></fA11><fA14 i1="01"><s1>Federal University of Rio Grande, School of Engineering, Av. Itália km 8, Cx. P. 474</s1><s2>Rio Grande, RS 96.201-900</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Université de Toulouse, INSA, Laboratoire Matériaux et Durabilité des Constructions, 135, Avenue de Rangueil</s1><s2>31077 Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Duke University, Department of Mechanical Engineering and Materials Science, Box 90300</s1><s2>Durham, NC 27708-0300</s2><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>4535-4544</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>9415</s2><s5>354000172511260420</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0376387</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of heat and mass transfer</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>This paper is a proposal to embed tree-shaped vasculatures in a wall designed such that the wall withstands without excessive hot spots the intense heating that impinges on it. The vasculature is a quilt of square-shaped panels, each panel having a tree vasculature that connects the center with the perimeter. The coolant may flow in either direction, center-perimeter, or perimeter-center, although here only the center-perimeter flow direction is illustrated. Numerical simulations of conjugate heat and fluid flow in three directions show that it is possible to determine all the optimal geometric features of vasculatures with up to three levels of bifurcation (n <sub>=</sub> 3). The global performance is evaluated in terms of the overall thermal resistance, pressure difference, flow resistance and pumping power. The improvements in global performance diminish as the number of bifurcation levels increases. No flow architecture is universally superior. The dendritic designs are superior at the low and high ends of the pressure difference range. The radial designs are superior at intermediate pressure difference numbers.</s0></fC01><fC02 i1="01" i2="X"><s0>001D03F06A</s0></fC02><fC02 i1="02" i2="X"><s0>001D06D03E</s0></fC02><fC02 i1="03" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Composant électronique</s0><s5>08</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Electronic component</s0><s5>08</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Componente electrónico</s0><s5>08</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Avionique</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Avionics</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Aviónica</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Transfert chaleur</s0><s5>23</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Heat transfer</s0><s5>23</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Transferencia térmica</s0><s5>23</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Système refroidissement</s0><s5>24</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Cooling system</s0><s5>24</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Sistema enfriamiento</s0><s5>24</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Pile combustible</s0><s5>29</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Fuel cell</s0><s5>29</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Pila combustión</s0><s5>29</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Structure arborescente</s0><s5>30</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Tree structure</s0><s5>30</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Estructura arborescente</s0><s5>30</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Matériau intelligent</s0><s5>31</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Smart materials</s0><s5>31</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Vascularisation</s0><s5>32</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Vascularization</s0><s5>32</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Vascularización</s0><s5>32</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Théorie constructive</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Constructive theory</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Teoría constructiva</s0><s5>33</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Conception</s0><s5>34</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Design</s0><s5>34</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Diseño</s0><s5>34</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Structure dendritique</s0><s5>35</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Dendritic structure</s0><s5>35</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Estructura dendrítica</s0><s5>35</s5></fC03><fN21><s1>271</s1></fN21></pA></standard><server><NO>PASCAL 09-0376387 INIST</NO><ET>Tree-shaped vascular wall designs for localized intense cooling</ET><AU>ROCHA (L. A. O.); LORENTE (S.); BEJAN (A.)</AU><AF>Federal University of Rio Grande, School of Engineering, Av. Itália km 8, Cx. P. 474/Rio Grande, RS 96.201-900/Brésil (1 aut.); Université de Toulouse, INSA, Laboratoire Matériaux et Durabilité des Constructions, 135, Avenue de Rangueil/31077 Toulouse/France (2 aut.); Duke University, Department of Mechanical Engineering and Materials Science, Box 90300/Durham, NC 27708-0300/Etats-Unis (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of heat and mass transfer; ISSN 0017-9310; Coden IJHMAK; Royaume-Uni; Da. 2009; Vol. 52; No. 19-20; Pp. 4535-4544; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>This paper is a proposal to embed tree-shaped vasculatures in a wall designed such that the wall withstands without excessive hot spots the intense heating that impinges on it. The vasculature is a quilt of square-shaped panels, each panel having a tree vasculature that connects the center with the perimeter. The coolant may flow in either direction, center-perimeter, or perimeter-center, although here only the center-perimeter flow direction is illustrated. Numerical simulations of conjugate heat and fluid flow in three directions show that it is possible to determine all the optimal geometric features of vasculatures with up to three levels of bifurcation (n <sub>=</sub> 3). The global performance is evaluated in terms of the overall thermal resistance, pressure difference, flow resistance and pumping power. The improvements in global performance diminish as the number of bifurcation levels increases. No flow architecture is universally superior. The dendritic designs are superior at the low and high ends of the pressure difference range. The radial designs are superior at intermediate pressure difference numbers.</EA><CC>001D03F06A; 001D06D03E; 230</CC><FD>Composant électronique; Avionique; Transfert chaleur; Système refroidissement; Pile combustible; Structure arborescente; Matériau intelligent; Vascularisation; Théorie constructive; Conception; Structure dendritique</FD><ED>Electronic component; Avionics; Heat transfer; Cooling system; Fuel cell; Tree structure; Smart materials; Vascularization; Constructive theory; Design; Dendritic structure</ED><SD>Componente electrónico; Aviónica; Transferencia térmica; Sistema enfriamiento; Pila combustión; Estructura arborescente; Vascularización; Teoría constructiva; Diseño; Estructura dendrítica</SD><LO>INIST-9415.354000172511260420</LO><ID>09-0376387</ID></server></inist></record>
000D47	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Cluster and cluster galaxy evolution history from IR to X-ray observations of the young cluster RX J1257.2+4738 at z = 0.866</title><author><name sortKey="Ulmer, M P" uniqKey="Ulmer M">M. P. Ulmer</name><affiliation><inist:fA14 i1="01"><s1>LAM, Pôle de l'Etoile Site ChAteau-Gombert, 38 rue Frédéric Juliot-Curie</s1><s2>13388 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Department of Physics and Astronomy, Northwestern University, 2131 Sheridan Road</s1><s2>Evanston IL 60208-2900</s2><s3>USA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Adami, C" uniqKey="Adami C">C. Adami</name><affiliation><inist:fA14 i1="01"><s1>LAM, Pôle de l'Etoile Site ChAteau-Gombert, 38 rue Frédéric Juliot-Curie</s1><s2>13388 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lima, G B Neto" uniqKey="Lima G">G. B. Neto Lima</name><affiliation><inist:fA14 i1="03"><s1>Instituto de Astronomia, Geofísica e C. Atmosf./USP, R. do Matão 1226</s1><s2>05508-090 São Paulo/SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Durret, F" uniqKey="Durret F">F. Durret</name><affiliation><inist:fA14 i1="04"><s1>Institut d'Astrophysique de Paris, CNRS, UMR 7095, Université Pierre et Marie Curie, 98bis Bd Arago</s1><s2>75014 Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Covone, G" uniqKey="Covone G">G. Covone</name><affiliation><inist:fA14 i1="05"><s1>Università di Napolia &#34;Federico II&#34;, Dipartimento di Sciennze Fisiche and INAF - Observatorio Astronomico di Capodimonte, v. Moiariello 16</s1><s2>80131 Napoli</s2><s3>ITA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ilbert, O" uniqKey="Ilbert O">O. Ilbert</name><affiliation><inist:fA14 i1="01"><s1>LAM, Pôle de l'Etoile Site ChAteau-Gombert, 38 rue Frédéric Juliot-Curie</s1><s2>13388 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="06"><s1>Institute for Astronomy, 2680 Woodlawn Dr., University of Hawaii</s1><s2>Honolulu, Hawaii 96822</s2><s3>USA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cypriano, E S" uniqKey="Cypriano E">E. S. Cypriano</name><affiliation><inist:fA14 i1="03"><s1>Instituto de Astronomia, Geofísica e C. Atmosf./USP, R. do Matão 1226</s1><s2>05508-090 São Paulo/SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>Department of Physics and Astronomy, University College London, Gower Street</s1><s2>London WC1E 6BT</s2><s3>GBR</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Allam, S S" uniqKey="Allam S">S. S. Allam</name><affiliation><inist:fA14 i1="08"><s1>Fermi National Accelerator Laboratory, MS 127, PO Box 500</s1><s2>Batavia, IL 60510</s2><s3>USA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kron, R G" uniqKey="Kron R">R. G. Kron</name><affiliation><inist:fA14 i1="09"><s1>University of Chicago, Department of Astronomy and Astrophysics, 5640 South Ellis Avenue</s1><s2>Chicago, IL 60637</s2><s3>USA</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mahoney, W A" uniqKey="Mahoney W">W. A. Mahoney</name><affiliation><inist:fA14 i1="10"><s1>California Institute of Technology, Spitzer Science Center, MS 314-6, 1200 East California Blvd</s1><s2>Pasadena, CA 91125</s2><s3>USA</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gavazzi, R" uniqKey="Gavazzi R">R. Gavazzi</name><affiliation><inist:fA14 i1="04"><s1>Institut d'Astrophysique de Paris, CNRS, UMR 7095, Université Pierre et Marie Curie, 98bis Bd Arago</s1><s2>75014 Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0378710</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0378710 INIST</idno><idno type="RBID">Pascal:09-0378710</idno><idno type="wicri:Area/Main/Corpus">001C34</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cluster evolution</term><term>Galaxies</term><term>Galaxy clusters</term><term>Galaxy evolution</term><term>High temperature</term><term>Intracluster matter</term><term>Luminosity</term><term>Red shift</term><term>Spectroscopy</term><term>Star clusters</term><term>Star formation</term><term>X ray observation</term><term>Young cluster</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Evolution amas</term><term>Amas galaxies</term><term>Evolution galaxies</term><term>Observation RX</term><term>Amas jeune</term><term>Déplacement vers le rouge</term><term>Galaxies</term><term>Spectrométrie</term><term>Haute température</term><term>Luminosité</term><term>Matière intraamas</term><term>Formation stellaire</term><term>Amas stellaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Context. The cosmic time around the z ˜ 1 redshift range appears crucial in the cluster and galaxy evolution, since it is probably the epoch of the first mature galaxy clusters. Our knowledge of the properties of the galaxy populations in these clusters is limited because only a handful of z ˜ 1 clusters are presently known. Aims. In this framework, we report the discovery of a z ˜ 0.87 cluster and study its properties at various wavelengths. Methods. We gathered X-ray and optical data (imaging and spectroscopy), and near and far infrared data (imaging) in order to confirm the cluster nature of our candidate, to determine its dynamical state, and to give insight on its galaxy population evolution. Results. Our candidate structure appears to be a massive z ˜ 0.87 dynamically young cluster with an atypically high X-ray temperature as compared to its X-ray luminosity. It exhibits a significant percentage (˜90%) of galaxies that are also detected in the 24 μm band. Conclusions. The cluster RXJ1257.2+4738 appears to be still in the process of collapsing. Its relatively high temperature is probably the consequence of significant energy input into the intracluster medium besides the regular gravitational infall contribution. A significant part of its galaxies are red objects that are probably dusty with on-going star formation.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>503</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Cluster and cluster galaxy evolution history from IR to X-ray observations of the young cluster RX J1257.2+4738 at z = 0.866</s1></fA08><fA11 i1="01" i2="1"><s1>ULMER (M. P.)</s1></fA11><fA11 i1="02" i2="1"><s1>ADAMI (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>LIMA (G. B. NETO)</s1></fA11><fA11 i1="04" i2="1"><s1>DURRET (F.)</s1></fA11><fA11 i1="05" i2="1"><s1>COVONE (G.)</s1></fA11><fA11 i1="06" i2="1"><s1>ILBERT (O.)</s1></fA11><fA11 i1="07" i2="1"><s1>CYPRIANO (E. S.)</s1></fA11><fA11 i1="08" i2="1"><s1>ALLAM (S. S.)</s1></fA11><fA11 i1="09" i2="1"><s1>KRON (R. G.)</s1></fA11><fA11 i1="10" i2="1"><s1>MAHONEY (W. A.)</s1></fA11><fA11 i1="11" i2="1"><s1>GAVAZZI (R.)</s1></fA11><fA14 i1="01"><s1>LAM, Pôle de l'Etoile Site ChAteau-Gombert, 38 rue Frédéric Juliot-Curie</s1><s2>13388 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Physics and Astronomy, Northwestern University, 2131 Sheridan Road</s1><s2>Evanston IL 60208-2900</s2><s3>USA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="03"><s1>Instituto de Astronomia, Geofísica e C. Atmosf./USP, R. do Matão 1226</s1><s2>05508-090 São Paulo/SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="04"><s1>Institut d'Astrophysique de Paris, CNRS, UMR 7095, Université Pierre et Marie Curie, 98bis Bd Arago</s1><s2>75014 Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="05"><s1>Università di Napolia &#34;Federico II&#34;, Dipartimento di Sciennze Fisiche and INAF - Observatorio Astronomico di Capodimonte, v. Moiariello 16</s1><s2>80131 Napoli</s2><s3>ITA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Institute for Astronomy, 2680 Woodlawn Dr., University of Hawaii</s1><s2>Honolulu, Hawaii 96822</s2><s3>USA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Department of Physics and Astronomy, University College London, Gower Street</s1><s2>London WC1E 6BT</s2><s3>GBR</s3><sZ>7 aut.</sZ></fA14><fA14 i1="08"><s1>Fermi National Accelerator Laboratory, MS 127, PO Box 500</s1><s2>Batavia, IL 60510</s2><s3>USA</s3><sZ>8 aut.</sZ></fA14><fA14 i1="09"><s1>University of Chicago, Department of Astronomy and Astrophysics, 5640 South Ellis Avenue</s1><s2>Chicago, IL 60637</s2><s3>USA</s3><sZ>9 aut.</sZ></fA14><fA14 i1="10"><s1>California Institute of Technology, Spitzer Science Center, MS 314-6, 1200 East California Blvd</s1><s2>Pasadena, CA 91125</s2><s3>USA</s3><sZ>10 aut.</sZ></fA14><fA20><s1>399-408</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000187638140090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0378710</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Context. The cosmic time around the z ˜ 1 redshift range appears crucial in the cluster and galaxy evolution, since it is probably the epoch of the first mature galaxy clusters. Our knowledge of the properties of the galaxy populations in these clusters is limited because only a handful of z ˜ 1 clusters are presently known. Aims. In this framework, we report the discovery of a z ˜ 0.87 cluster and study its properties at various wavelengths. Methods. We gathered X-ray and optical data (imaging and spectroscopy), and near and far infrared data (imaging) in order to confirm the cluster nature of our candidate, to determine its dynamical state, and to give insight on its galaxy population evolution. Results. Our candidate structure appears to be a massive z ˜ 0.87 dynamically young cluster with an atypically high X-ray temperature as compared to its X-ray luminosity. It exhibits a significant percentage (˜90%) of galaxies that are also detected in the 24 μm band. Conclusions. The cluster RXJ1257.2+4738 appears to be still in the process of collapsing. Its relatively high temperature is probably the consequence of significant energy input into the intracluster medium besides the regular gravitational infall contribution. A significant part of its galaxies are red objects that are probably dusty with on-going star formation.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Evolution amas</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Cluster evolution</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Amas galaxies</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Galaxy clusters</s0><s5>27</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Evolution galaxies</s0><s5>28</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Galaxy evolution</s0><s5>28</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Evolución galaxias</s0><s5>28</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Observation RX</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>X ray observation</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Observación RX</s0><s5>29</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Amas jeune</s0><s5>30</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Young cluster</s0><s5>30</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Cúmulo joven</s0><s5>30</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Déplacement vers le rouge</s0><s5>31</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Red shift</s0><s5>31</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Galaxies</s0><s5>32</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Galaxies</s0><s5>32</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Spectrométrie</s0><s5>33</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Spectroscopy</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Haute température</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>High temperature</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Alta temperatura</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Luminosité</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Luminosity</s0><s5>35</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Matière intraamas</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Intracluster matter</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Materia intracúmulo</s0><s5>36</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Formation stellaire</s0><s5>37</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Star formation</s0><s5>37</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Amas stellaire</s0><s5>38</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Star clusters</s0><s5>38</s5></fC03><fN21><s1>271</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0378710 INIST</NO><ET>Cluster and cluster galaxy evolution history from IR to X-ray observations of the young cluster RX J1257.2+4738 at z = 0.866</ET><AU>ULMER (M. P.); ADAMI (C.); LIMA (G. B. NETO); DURRET (F.); COVONE (G.); ILBERT (O.); CYPRIANO (E. S.); ALLAM (S. S.); KRON (R. G.); MAHONEY (W. A.); GAVAZZI (R.)</AU><AF>LAM, Pôle de l'Etoile Site ChAteau-Gombert, 38 rue Frédéric Juliot-Curie/13388 Marseille/France (1 aut., 2 aut., 6 aut.); Department of Physics and Astronomy, Northwestern University, 2131 Sheridan Road/Evanston IL 60208-2900/Etats-Unis (1 aut.); Instituto de Astronomia, Geofísica e C. Atmosf./USP, R. do Matão 1226/05508-090 São Paulo/SP/Brésil (3 aut., 7 aut.); Institut d'Astrophysique de Paris, CNRS, UMR 7095, Université Pierre et Marie Curie, 98bis Bd Arago/75014 Paris/France (4 aut., 11 aut.); Università di Napolia &#34;Federico II&#34;, Dipartimento di Sciennze Fisiche and INAF - Observatorio Astronomico di Capodimonte, v. Moiariello 16/80131 Napoli/Italie (5 aut.); Institute for Astronomy, 2680 Woodlawn Dr., University of Hawaii/Honolulu, Hawaii 96822/Etats-Unis (6 aut.); Department of Physics and Astronomy, University College London, Gower Street/London WC1E 6BT/Royaume-Uni (7 aut.); Fermi National Accelerator Laboratory, MS 127, PO Box 500/Batavia, IL 60510/Etats-Unis (8 aut.); University of Chicago, Department of Astronomy and Astrophysics, 5640 South Ellis Avenue/Chicago, IL 60637/Etats-Unis (9 aut.); California Institute of Technology, Spitzer Science Center, MS 314-6, 1200 East California Blvd/Pasadena, CA 91125/Etats-Unis (10 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 503; No. 2; Pp. 399-408; Bibl. 1/2 p.</SO><LA>Anglais</LA><EA>Context. The cosmic time around the z ˜ 1 redshift range appears crucial in the cluster and galaxy evolution, since it is probably the epoch of the first mature galaxy clusters. Our knowledge of the properties of the galaxy populations in these clusters is limited because only a handful of z ˜ 1 clusters are presently known. Aims. In this framework, we report the discovery of a z ˜ 0.87 cluster and study its properties at various wavelengths. Methods. We gathered X-ray and optical data (imaging and spectroscopy), and near and far infrared data (imaging) in order to confirm the cluster nature of our candidate, to determine its dynamical state, and to give insight on its galaxy population evolution. Results. Our candidate structure appears to be a massive z ˜ 0.87 dynamically young cluster with an atypically high X-ray temperature as compared to its X-ray luminosity. It exhibits a significant percentage (˜90%) of galaxies that are also detected in the 24 μm band. Conclusions. The cluster RXJ1257.2+4738 appears to be still in the process of collapsing. Its relatively high temperature is probably the consequence of significant energy input into the intracluster medium besides the regular gravitational infall contribution. A significant part of its galaxies are red objects that are probably dusty with on-going star formation.</EA><CC>001E03</CC><FD>Evolution amas; Amas galaxies; Evolution galaxies; Observation RX; Amas jeune; Déplacement vers le rouge; Galaxies; Spectrométrie; Haute température; Luminosité; Matière intraamas; Formation stellaire; Amas stellaire</FD><ED>Cluster evolution; Galaxy clusters; Galaxy evolution; X ray observation; Young cluster; Red shift; Galaxies; Spectroscopy; High temperature; Luminosity; Intracluster matter; Star formation; Star clusters</ED><SD>Evolución galaxias; Observación RX; Cúmulo joven; Alta temperatura; Materia intracúmulo</SD><LO>INIST-14176.354000187638140090</LO><ID>09-0378710</ID></server></inist></record>
000D48	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Molecular characterization of invasive serogroup Y Neisseria meningitidis strains isolated in the Latin America region</title><author><name sortKey="Abad, Raquel" uniqKey="Abad R">Raquel Abad</name><affiliation><inist:fA14 i1="01"><s1>Reference Laboratory for Meningococci, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo, Km2</s1><s2>28220 Majadahonda, Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>13 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Agudelo, Clara I" uniqKey="Agudelo C">Clara I. Agudelo</name><affiliation><inist:fA14 i1="06"><s1>Microbiología, Instituto Nacional de Salud (INS)</s1><s2>Bogotá</s2><s3>COL</s3><sZ>2 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brandileone, M Cristina" uniqKey="Brandileone M">M. Cristina Brandileone</name><affiliation><inist:fA14 i1="02"><s1>Bacteriology Branch, Adolfo Lutz Institute</s1><s2>Sdo Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chanto, Grettel" uniqKey="Chanto G">Grettel Chanto</name><affiliation><inist:fA14 i1="03"><s1>Centro Nacional de Referencia en Bacteriología (INCIENSA)</s1><s2>San José</s2><s3>CRI</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gabastou, Jean Marc" uniqKey="Gabastou J">Jean Marc Gabastou</name><affiliation><inist:fA14 i1="04"><s1>Unidad de Medicamentos Esenciales, Vacunas y Tecnologías de Salud, Pan American Health Organization (PAHO)/World Health Organization (WHO)</s1><s2>Quito</s2><s3>ECU</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hormazabal, Juan Carlos" uniqKey="Hormazabal J">Juan Carlos Hormazabal</name><affiliation><inist:fA14 i1="05"><s1>Bacteriología, Instituto de Salud Pública (ISP)</s1><s2>Santiago de Chile</s2><s3>CHL</s3><sZ>6 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="O Gorla, M Cecilia" uniqKey="O Gorla M">M. Cecilia O Gorla</name><affiliation><inist:fA14 i1="02"><s1>Bacteriology Branch, Adolfo Lutz Institute</s1><s2>Sdo Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Maldonado, Aurora" uniqKey="Maldonado A">Aurora Maldonado</name><affiliation><inist:fA14 i1="05"><s1>Bacteriología, Instituto de Salud Pública (ISP)</s1><s2>Santiago de Chile</s2><s3>CHL</s3><sZ>6 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Moreno, Jaime" uniqKey="Moreno J">Jaime Moreno</name><affiliation><inist:fA14 i1="06"><s1>Microbiología, Instituto Nacional de Salud (INS)</s1><s2>Bogotá</s2><s3>COL</s3><sZ>2 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Muros Le Rouzic, Erwan" uniqKey="Muros Le Rouzic E">Erwan Muros-Le Rouzic</name><affiliation><inist:fA14 i1="07"><s1>Global Scientific and Medical Affairs, Sanofi-Pasteur</s1><s2>Lyon</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lersch, Robert" uniqKey="Lersch R">Robert Lersch</name><affiliation><inist:fA14 i1="07"><s1>Global Scientific and Medical Affairs, Sanofi-Pasteur</s1><s2>Lyon</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Regueira, Mabel" uniqKey="Regueira M">Mabel Regueira</name><affiliation><inist:fA14 i1="08"><s1>Bacteriología, Instituto Nacional de Enfermedades Infecciosas (INEI-ANLIS), Dr CG Malbrán</s1><s2>Buenos Aires</s2><s3>ARG</s3><sZ>12 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Salcedo, Celia" uniqKey="Salcedo C">Celia Salcedo</name><affiliation><inist:fA14 i1="01"><s1>Reference Laboratory for Meningococci, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo, Km2</s1><s2>28220 Majadahonda, Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>13 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sorhouet, Cecilia" uniqKey="Sorhouet C">Cecilia Sorhouet</name><affiliation><inist:fA14 i1="08"><s1>Bacteriología, Instituto Nacional de Enfermedades Infecciosas (INEI-ANLIS), Dr CG Malbrán</s1><s2>Buenos Aires</s2><s3>ARG</s3><sZ>12 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vazquez, Julio A" uniqKey="Vazquez J">Julio A. Vazquez</name><affiliation><inist:fA14 i1="01"><s1>Reference Laboratory for Meningococci, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo, Km2</s1><s2>28220 Majadahonda, Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>13 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0379686</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0379686 INIST</idno><idno type="RBID">Pascal:09-0379686</idno><idno type="wicri:Area/Main/Corpus">001C33</idno></publicationStmt><seriesStmt><idno type="ISSN">0163-4453</idno><title level="j" type="abbreviated">J. infect.</title><title level="j" type="main">The Journal of infection</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Latin America</term><term>Meningococcal disease</term><term>Neisseria meningitidis</term><term>Serogroup</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Méningococcie</term><term>Sérogroupe</term><term>Amérique Latine</term><term>Neisseria meningitidis</term><term>Forme invasive</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Objectives: To improve the understanding of serogroup Y invasive meningococcal disease (IMD) in Latin America, particularly IMD molecular epidemiology; 166 Y serogroup isolates received at the National Reference Laboratories of Argentina, Brazil, Chile, Colombia, and Costa Rica during 2000-2006 were characterized by their molecular markers. Methods: This analysis included serological assays to determine serogroup/serotype/serosubtype, DNA sequencing and genotyping of the porB and/or porA genes, multilocus sequence typing (MLST) and fetA allele determination. Results: Sixteen different antigenic combinations were observed. Sixty-two (37.3%) isolates were NT:P1.5 and 36 (21.7%) isolates were 14:NST. Thirty-two different STs appeared, but 3 STs (ST-1624, ST-23, and ST-5770) accounted for 69.9% (116) of the strains. Most of the IMD isolates belonged to the ST-23, ST-167 clonal complexes or the group composed by ST-5770 and related STs. Conclusions: Isolates obtained in Colombia and Costa Rica were similar to that of the United States, in that most sequence types belonged to the ST-23 clonal complex. IMD isolates found in Argentina appear to be the result of an independent event and did not spread from nearby countries, being the sequence type ST-1624 (ST-167 clonal complex) the most frequently found. We were unable to correlate an antigenic shift of outer membrane proteins with an increase of serogroup Y meningococcal cases in our collection of isolates.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0163-4453</s0></fA01><fA02 i1="01"><s0>JINFD2</s0></fA02><fA03 i2="1"><s0>J. infect.</s0></fA03><fA05><s2>59</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Molecular characterization of invasive serogroup Y Neisseria meningitidis strains isolated in the Latin America region</s1></fA08><fA11 i1="01" i2="1"><s1>ABAD (Raquel)</s1></fA11><fA11 i1="02" i2="1"><s1>AGUDELO (Clara I.)</s1></fA11><fA11 i1="03" i2="1"><s1>BRANDILEONE (M. Cristina)</s1></fA11><fA11 i1="04" i2="1"><s1>CHANTO (Grettel)</s1></fA11><fA11 i1="05" i2="1"><s1>GABASTOU (Jean Marc)</s1></fA11><fA11 i1="06" i2="1"><s1>HORMAZABAL (Juan Carlos)</s1></fA11><fA11 i1="07" i2="1"><s1>O GORLA (M. Cecilia)</s1></fA11><fA11 i1="08" i2="1"><s1>MALDONADO (Aurora)</s1></fA11><fA11 i1="09" i2="1"><s1>MORENO (Jaime)</s1></fA11><fA11 i1="10" i2="1"><s1>MUROS-LE ROUZIC (Erwan)</s1></fA11><fA11 i1="11" i2="1"><s1>LERSCH (Robert)</s1></fA11><fA11 i1="12" i2="1"><s1>REGUEIRA (Mabel)</s1></fA11><fA11 i1="13" i2="1"><s1>SALCEDO (Celia)</s1></fA11><fA11 i1="14" i2="1"><s1>SORHOUET (Cecilia)</s1></fA11><fA11 i1="15" i2="1"><s1>VAZQUEZ (Julio A.)</s1></fA11><fA14 i1="01"><s1>Reference Laboratory for Meningococci, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo, Km2</s1><s2>28220 Majadahonda, Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>13 aut.</sZ><sZ>15 aut.</sZ></fA14><fA14 i1="02"><s1>Bacteriology Branch, Adolfo Lutz Institute</s1><s2>Sdo Paulo</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Centro Nacional de Referencia en Bacteriología (INCIENSA)</s1><s2>San José</s2><s3>CRI</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Unidad de Medicamentos Esenciales, Vacunas y Tecnologías de Salud, Pan American Health Organization (PAHO)/World Health Organization (WHO)</s1><s2>Quito</s2><s3>ECU</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Bacteriología, Instituto de Salud Pública (ISP)</s1><s2>Santiago de Chile</s2><s3>CHL</s3><sZ>6 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="06"><s1>Microbiología, Instituto Nacional de Salud (INS)</s1><s2>Bogotá</s2><s3>COL</s3><sZ>2 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="07"><s1>Global Scientific and Medical Affairs, Sanofi-Pasteur</s1><s2>Lyon</s2><s3>FRA</s3><sZ>10 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="08"><s1>Bacteriología, Instituto Nacional de Enfermedades Infecciosas (INEI-ANLIS), Dr CG Malbrán</s1><s2>Buenos Aires</s2><s3>ARG</s3><sZ>12 aut.</sZ><sZ>14 aut.</sZ></fA14><fA20><s1>104-114</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>18250</s2><s5>354000171825370050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>17 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0379686</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>The Journal of infection</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Objectives: To improve the understanding of serogroup Y invasive meningococcal disease (IMD) in Latin America, particularly IMD molecular epidemiology; 166 Y serogroup isolates received at the National Reference Laboratories of Argentina, Brazil, Chile, Colombia, and Costa Rica during 2000-2006 were characterized by their molecular markers. Methods: This analysis included serological assays to determine serogroup/serotype/serosubtype, DNA sequencing and genotyping of the porB and/or porA genes, multilocus sequence typing (MLST) and fetA allele determination. Results: Sixteen different antigenic combinations were observed. Sixty-two (37.3%) isolates were NT:P1.5 and 36 (21.7%) isolates were 14:NST. Thirty-two different STs appeared, but 3 STs (ST-1624, ST-23, and ST-5770) accounted for 69.9% (116) of the strains. Most of the IMD isolates belonged to the ST-23, ST-167 clonal complexes or the group composed by ST-5770 and related STs. Conclusions: Isolates obtained in Colombia and Costa Rica were similar to that of the United States, in that most sequence types belonged to the ST-23 clonal complex. IMD isolates found in Argentina appear to be the result of an independent event and did not spread from nearby countries, being the sequence type ST-1624 (ST-167 clonal complex) the most frequently found. We were unable to correlate an antigenic shift of outer membrane proteins with an increase of serogroup Y meningococcal cases in our collection of isolates.</s0></fC01><fC02 i1="01" i2="X"><s0>002B01</s0></fC02><fC02 i1="02" i2="X"><s0>002B05B02I</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Méningococcie</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Meningococcal disease</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Meningococia</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Sérogroupe</s0><s5>07</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Serogroup</s0><s5>07</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Serogrupo</s0><s5>07</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Amérique Latine</s0><s2>NG</s2><s5>08</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Latin America</s0><s2>NG</s2><s5>08</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>America latina</s0><s2>NG</s2><s5>08</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Neisseria meningitidis</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Forme invasive</s0><s4>INC</s4><s5>86</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Neisseriaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Micrococcales</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fN21><s1>271</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0379686 INIST</NO><ET>Molecular characterization of invasive serogroup Y Neisseria meningitidis strains isolated in the Latin America region</ET><AU>ABAD (Raquel); AGUDELO (Clara I.); BRANDILEONE (M. Cristina); CHANTO (Grettel); GABASTOU (Jean Marc); HORMAZABAL (Juan Carlos); O GORLA (M. Cecilia); MALDONADO (Aurora); MORENO (Jaime); MUROS-LE ROUZIC (Erwan); LERSCH (Robert); REGUEIRA (Mabel); SALCEDO (Celia); SORHOUET (Cecilia); VAZQUEZ (Julio A.)</AU><AF>Reference Laboratory for Meningococci, Centro Nacional de Microbiologia, Instituto de Salud Carlos III, Ctra Majadahonda-Pozuelo, Km2/28220 Majadahonda, Madrid/Espagne (1 aut., 13 aut., 15 aut.); Bacteriology Branch, Adolfo Lutz Institute/Sdo Paulo/Brésil (3 aut., 7 aut.); Centro Nacional de Referencia en Bacteriología (INCIENSA)/San José/Costa Rica (4 aut.); Unidad de Medicamentos Esenciales, Vacunas y Tecnologías de Salud, Pan American Health Organization (PAHO)/World Health Organization (WHO)/Quito/Equateur (5 aut.); Bacteriología, Instituto de Salud Pública (ISP)/Santiago de Chile/Chili (6 aut., 8 aut.); Microbiología, Instituto Nacional de Salud (INS)/Bogotá/Colombie (2 aut., 9 aut.); Global Scientific and Medical Affairs, Sanofi-Pasteur/Lyon/France (10 aut., 11 aut.); Bacteriología, Instituto Nacional de Enfermedades Infecciosas (INEI-ANLIS), Dr CG Malbrán/Buenos Aires/Argentine (12 aut., 14 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>The Journal of infection; ISSN 0163-4453; Coden JINFD2; Royaume-Uni; Da. 2009; Vol. 59; No. 2; Pp. 104-114; Bibl. 17 ref.</SO><LA>Anglais</LA><EA>Objectives: To improve the understanding of serogroup Y invasive meningococcal disease (IMD) in Latin America, particularly IMD molecular epidemiology; 166 Y serogroup isolates received at the National Reference Laboratories of Argentina, Brazil, Chile, Colombia, and Costa Rica during 2000-2006 were characterized by their molecular markers. Methods: This analysis included serological assays to determine serogroup/serotype/serosubtype, DNA sequencing and genotyping of the porB and/or porA genes, multilocus sequence typing (MLST) and fetA allele determination. Results: Sixteen different antigenic combinations were observed. Sixty-two (37.3%) isolates were NT:P1.5 and 36 (21.7%) isolates were 14:NST. Thirty-two different STs appeared, but 3 STs (ST-1624, ST-23, and ST-5770) accounted for 69.9% (116) of the strains. Most of the IMD isolates belonged to the ST-23, ST-167 clonal complexes or the group composed by ST-5770 and related STs. Conclusions: Isolates obtained in Colombia and Costa Rica were similar to that of the United States, in that most sequence types belonged to the ST-23 clonal complex. IMD isolates found in Argentina appear to be the result of an independent event and did not spread from nearby countries, being the sequence type ST-1624 (ST-167 clonal complex) the most frequently found. We were unable to correlate an antigenic shift of outer membrane proteins with an increase of serogroup Y meningococcal cases in our collection of isolates.</EA><CC>002B01; 002B05B02I</CC><FD>Méningococcie; Sérogroupe; Amérique Latine; Neisseria meningitidis; Forme invasive</FD><FG>Bactériose; Infection; Amérique; Neisseriaceae; Micrococcales; Bactérie</FG><ED>Meningococcal disease; Serogroup; Latin America; Neisseria meningitidis</ED><EG>Bacteriosis; Infection; America; Neisseriaceae; Micrococcales; Bacteria</EG><SD>Meningococia; Serogrupo; America latina; Neisseria meningitidis</SD><LO>INIST-18250.354000171825370050</LO><ID>09-0379686</ID></server></inist></record>
000D49	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Diversity of β-Lactamases Produced by Ceftazidime-Resistant Pseudomonas aeruginosa Isolates Causing Bloodstream Infections in Brazil</title><author><name sortKey="Picao, Renata C" uniqKey="Picao R">Renata C. Picao</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Laboratório ALERTA, Universidade Federal de São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Poirel, Laurent" uniqKey="Poirel L">Laurent Poirel</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gales, Ana C" uniqKey="Gales A">Ana C. Gales</name><affiliation><inist:fA14 i1="02"><s1>Laboratório ALERTA, Universidade Federal de São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nordmann, Patrice" uniqKey="Nordmann P">Patrice Nordmann</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0379761</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0379761 INIST</idno><idno type="RBID">Pascal:09-0379761</idno><idno type="wicri:Area/Main/Corpus">001C32</idno></publicationStmt><seriesStmt><idno type="ISSN">0066-4804</idno><title level="j" type="abbreviated">Antimicrob. agents chemother.</title><title level="j" type="main">Antimicrobial agents and chemotherapy</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacteremia</term><term>Brazil</term><term>Diversity</term><term>Isolate</term><term>Pseudomonas aeruginosa</term><term>β-Lactamase</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Diversité</term><term>β-Lactamase</term><term>Pseudomonas aeruginosa</term><term>Isolat</term><term>Bactériémie</term><term>Brésil</term><term>Souche résistante ceftazidime</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A retrospective survey was conducted to characterize β-lactamases in a collection of 43 ceftazidime-resistant Pseudomonas aeruginosa isolates recovered from patients with bloodstream infections hospitalized at a Brazilian teaching hospital between January and December 2005. Resistance rates for carbapenems, aminoglycosides, and quinolones were over 80%, with only colistin remaining active against all isolates. Pulsed-field gel electrophoresis analysis identified seven different genotypes. AmpC overproduction was found to be the sole β-lactamase-mediated mechanism responsible for ceftazidime resistance in four isolates (9.3%). Nine isolates (20.9%) produced an extended-spectrum β-lactamase (ESBL), either GES-1 (n = 7, 16.3%) or CTX-M-2 (n = 2, 4.6%). Carbapenemase activity was detected in 30 (70%) additional isolates. Among those isolates, two isolates (4.6%) produced the ESBL GES-5, possessing the ability to hydrolyze imipenem; a single isolate (2.3%) produced the metallo-β-lactamase (MBL) IMP-1; and 27 isolates produced the MBL SPM-1 (62.8%). None of the isolates coproduced both ESBL and MBL. Insertion sequence elements ISCR4 and ISCR1 were associated with bla<sub>SPM-1</sub> and Mo<sub>CTX-M-2</sub> genes, respectively, whereas the bla<sub>GES-1</sub> and bla<sub>GES-5</sub> genes were part of class 1 integron structures. This study underlines the spread of MBL- and ESBL-producing P. aeruginosa isolates as an important source of ceftazidime resistance in Brazil.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0066-4804</s0></fA01><fA02 i1="01"><s0>AACHAX</s0></fA02><fA03 i2="1"><s0>Antimicrob. agents chemother.</s0></fA03><fA05><s2>53</s2></fA05><fA06><s2>9</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Diversity of β-Lactamases Produced by Ceftazidime-Resistant Pseudomonas aeruginosa Isolates Causing Bloodstream Infections in Brazil</s1></fA08><fA11 i1="01" i2="1"><s1>PICAO (Renata C.)</s1></fA11><fA11 i1="02" i2="1"><s1>POIREL (Laurent)</s1></fA11><fA11 i1="03" i2="1"><s1>GALES (Ana C.)</s1></fA11><fA11 i1="04" i2="1"><s1>NORDMANN (Patrice)</s1></fA11><fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Laboratório ALERTA, Universidade Federal de São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA20><s1>3908-3913</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>13334</s2><s5>354000171827920390</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>42 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0379761</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Antimicrobial agents and chemotherapy</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>A retrospective survey was conducted to characterize β-lactamases in a collection of 43 ceftazidime-resistant Pseudomonas aeruginosa isolates recovered from patients with bloodstream infections hospitalized at a Brazilian teaching hospital between January and December 2005. Resistance rates for carbapenems, aminoglycosides, and quinolones were over 80%, with only colistin remaining active against all isolates. Pulsed-field gel electrophoresis analysis identified seven different genotypes. AmpC overproduction was found to be the sole β-lactamase-mediated mechanism responsible for ceftazidime resistance in four isolates (9.3%). Nine isolates (20.9%) produced an extended-spectrum β-lactamase (ESBL), either GES-1 (n = 7, 16.3%) or CTX-M-2 (n = 2, 4.6%). Carbapenemase activity was detected in 30 (70%) additional isolates. Among those isolates, two isolates (4.6%) produced the ESBL GES-5, possessing the ability to hydrolyze imipenem; a single isolate (2.3%) produced the metallo-β-lactamase (MBL) IMP-1; and 27 isolates produced the MBL SPM-1 (62.8%). None of the isolates coproduced both ESBL and MBL. Insertion sequence elements ISCR4 and ISCR1 were associated with bla<sub>SPM-1</sub> and Mo<sub>CTX-M-2</sub> genes, respectively, whereas the bla<sub>GES-1</sub> and bla<sub>GES-5</sub> genes were part of class 1 integron structures. This study underlines the spread of MBL- and ESBL-producing P. aeruginosa isolates as an important source of ceftazidime resistance in Brazil.</s0></fC01><fC02 i1="01" i2="X"><s0>002B02S</s0></fC02><fC02 i1="02" i2="X"><s0>002B05B02M</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Diversité</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Diversity</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Diversidad</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>β-Lactamase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>β-Lactamase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>β-Lactamase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Pseudomonas aeruginosa</s0><s2>NS</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Pseudomonas aeruginosa</s0><s2>NS</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Pseudomonas aeruginosa</s0><s2>NS</s2><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Isolat</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Isolate</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Aislado</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Bactériémie</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Bacteremia</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Bacteriemia</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Souche résistante ceftazidime</s0><s4>INC</s4><s5>86</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pseudomonadaceae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Pseudomonadaceae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Pseudomonadaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Pseudomonadales</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Pseudomonadales</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Pseudomonadales</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="08" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="08" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="09" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="09" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="09" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>271</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0379761 INIST</NO><ET>Diversity of β-Lactamases Produced by Ceftazidime-Resistant Pseudomonas aeruginosa Isolates Causing Bloodstream Infections in Brazil</ET><AU>PICAO (Renata C.); POIREL (Laurent); GALES (Ana C.); NORDMANN (Patrice)</AU><AF>Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine Paris Sud/K.-Bicêtre/France (1 aut., 2 aut., 4 aut.); Laboratório ALERTA, Universidade Federal de São Paulo/São Paulo/Brésil (1 aut., 3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Antimicrobial agents and chemotherapy; ISSN 0066-4804; Coden AACHAX; Etats-Unis; Da. 2009; Vol. 53; No. 9; Pp. 3908-3913; Bibl. 42 ref.</SO><LA>Anglais</LA><EA>A retrospective survey was conducted to characterize β-lactamases in a collection of 43 ceftazidime-resistant Pseudomonas aeruginosa isolates recovered from patients with bloodstream infections hospitalized at a Brazilian teaching hospital between January and December 2005. Resistance rates for carbapenems, aminoglycosides, and quinolones were over 80%, with only colistin remaining active against all isolates. Pulsed-field gel electrophoresis analysis identified seven different genotypes. AmpC overproduction was found to be the sole β-lactamase-mediated mechanism responsible for ceftazidime resistance in four isolates (9.3%). Nine isolates (20.9%) produced an extended-spectrum β-lactamase (ESBL), either GES-1 (n = 7, 16.3%) or CTX-M-2 (n = 2, 4.6%). Carbapenemase activity was detected in 30 (70%) additional isolates. Among those isolates, two isolates (4.6%) produced the ESBL GES-5, possessing the ability to hydrolyze imipenem; a single isolate (2.3%) produced the metallo-β-lactamase (MBL) IMP-1; and 27 isolates produced the MBL SPM-1 (62.8%). None of the isolates coproduced both ESBL and MBL. Insertion sequence elements ISCR4 and ISCR1 were associated with bla<sub>SPM-1</sub> and Mo<sub>CTX-M-2</sub> genes, respectively, whereas the bla<sub>GES-1</sub> and bla<sub>GES-5</sub> genes were part of class 1 integron structures. This study underlines the spread of MBL- and ESBL-producing P. aeruginosa isolates as an important source of ceftazidime resistance in Brazil.</EA><CC>002B02S; 002B05B02M</CC><FD>Diversité; β-Lactamase; Pseudomonas aeruginosa; Isolat; Bactériémie; Brésil; Souche résistante ceftazidime</FD><FG>Hydrolases; Enzyme; Pseudomonadaceae; Pseudomonadales; Bactérie; Bactériose; Infection; Amérique du Sud; Amérique</FG><ED>Diversity; β-Lactamase; Pseudomonas aeruginosa; Isolate; Bacteremia; Brazil</ED><EG>Hydrolases; Enzyme; Pseudomonadaceae; Pseudomonadales; Bacteria; Bacteriosis; Infection; South America; America</EG><SD>Diversidad; β-Lactamase; Pseudomonas aeruginosa; Aislado; Bacteriemia; Brasil</SD><LO>INIST-13334.354000171827920390</LO><ID>09-0379761</ID></server></inist></record>
000D50	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">NAVÁS' TYPE AND NON-TYPE SPECIMENS OF CHRYSOPIDAE IN THE MNHN, PARIS [NEUROPTERA]</title><author><name sortKey="Legrand, Jean" uniqKey="Legrand J">Jean Legrand</name><affiliation><inist:fA14 i1="01"><s1>Muséum national d'Histoire naturelle, Département Systématique et Évolution, UMR 7205 MNHN-CNRS, Entomologie, CP 50, 45 rue Buffon</s1><s2>75231 Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Tauber, Catherine A" uniqKey="Tauber C">Catherine A. Tauber</name><affiliation><inist:fA14 i1="02"><s1>Department of Entomology, Comstock Hall, Cornell University</s1><s2>Ithaca, NY 14853</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Albuquerque, Gilberto S" uniqKey="Albuquerque G">Gilberto S. Albuquerque</name><affiliation><inist:fA14 i1="03"><s1>Laboratório de Entomologia e Fitopatologia, CCTA, Universidade Estadual do Norte Fluminense, Campos dos Goytacazes</s1><s2>Rio de Janeiro, 28013-602</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Tauber, Maurice J" uniqKey="Tauber M">Maurice J. Tauber</name><affiliation><inist:fA14 i1="02"><s1>Department of Entomology, Comstock Hall, Cornell University</s1><s2>Ithaca, NY 14853</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0380167</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0380167 INIST</idno><idno type="RBID">Pascal:09-0380167</idno><idno type="wicri:Area/Main/Corpus">001C31</idno></publicationStmt><seriesStmt><idno type="ISSN">0181-0863</idno><title level="j" type="abbreviated">Rev. fr. entomol. : (1979)</title><title level="j" type="main">Revue française d'entomologie : (1979)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chrysopidae</term><term>Collection</term><term>Faunal survey</term><term>Museum</term><term>Paris</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Inventaire faunistique</term><term>Collection</term><term>Musée</term><term>Paris</term><term>Chrysopidae</term><term>Muséum national d'histoire naturelle</term><term>Longinos Navás</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Longinos Navás a décrit approximativement 680 espèces de Chrysopidae. Les spécimens type porte-nom conservés au Muséum national d'Histoire naturelle à Paris (MNHN) représentent environ le quart de ces espèces (soit 174). Ci-après, nous fournissons les données concernant les spécimens types, ainsi que l'historique des changements de nom pour chacune des espèces décrites par Navás et conservées dans les collections entomologiques du MNHN. En plus des 5 holotypes et 58 lectotypes précédemment identifiés de ces collections, 13 holotypes sont nouvellement reconnus, 88 lectotypes sont désignés, et des syntypes sont identifiés pour 10 espèces. Les nouvelles synonymies suivantes sont proposées: Chrysopa aroguesina Navàs, 1929 est un synonyme junior de Ungla laufferi (Navás 1922); Chrysopa camposana Navás, 1935 est un synonyme junior de Ceraeochrysa valida (Banks, 1895); Ceraeochrysa (= Chrysopa) caligata (Banks, 1946) est un synonyme junior de Ceraeochrysa cornuta (Navás, 1925); Chrysopa dampfina Navás 1928 est un synonyme junior de Chrysopodes (Chrysopodes) figuralis (Banks, 1915); Nodita morenoi Navás, 1934 est un synonyme junior de Leucochrysa (Nodita) camposi (Navàs, 1933); Chrysopa rochina Navás, 1915 est un synonyme junior de Ceraeochrysa cincta (Schneider, 1851); Dichochrysa sjostedti [= Chrysopa sjoestedti] (van der Weele, 1910) est un synonyme junior de Dichochrysa nubilata (Navás, 1910). Les nouvelles combinaisons sont établies pour les cinq espèces suivantes: Chrysopodes (Chrysopodes) apurinus (Navás, 1935), Plesiochrysa climacia (Navás, 1935), Ungla favrei (Navás, 1935), Chrysopodes (Chrysopodes) geayi (Navás, 1910), et Ungla laufferi (Navás, 1922). Nous donnons la liste des six types de Navás réputés pour être au Muséum qui n'ont pas été retrouvés. Huit noms d'espèces devront être considéres comme des nomina dubia: jusqu'à ce que les types soient trouvés ou que des néotypes soient désignés, ce sont: Ancylopteryx alluaudi Navás, 1910; A. elgonica Navás, 1936; Chrysopa aegyptiaca Navás, 1915; C. nymphulina Navás, 1915; C. ricciana Navás, 1910; C. rothschildi Navás, 1915; C. silvana Navás, 1913; Nothochrysa sordidata Navás, 1908. Approximativement 50 espèces de Navás, représentées dans les collections du Musée par des spécimens examinés par Navás (comprenant des paralectotypes), sont listées. Enfin nous donnons la liste de plusieurs spécimens que Navás avait considérés comme des espèces nouvelles mais qu'il n'a jamais décrites.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0181-0863</s0></fA01><fA02 i1="01"><s0>RFENDE</s0></fA02><fA03 i2="1"><s0>Rev. fr. entomol. : (1979)</s0></fA03><fA05><s2>30</s2></fA05><fA06><s2>2-4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>NAVÁS' TYPE AND NON-TYPE SPECIMENS OF CHRYSOPIDAE IN THE MNHN, PARIS [NEUROPTERA]</s1></fA08><fA11 i1="01" i2="1"><s1>LEGRAND (Jean)</s1></fA11><fA11 i1="02" i2="1"><s1>TAUBER (Catherine A.)</s1></fA11><fA11 i1="03" i2="1"><s1>ALBUQUERQUE (Gilberto S.)</s1></fA11><fA11 i1="04" i2="1"><s1>TAUBER (Maurice J.)</s1></fA11><fA14 i1="01"><s1>Muséum national d'Histoire naturelle, Département Systématique et Évolution, UMR 7205 MNHN-CNRS, Entomologie, CP 50, 45 rue Buffon</s1><s2>75231 Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Entomology, Comstock Hall, Cornell University</s1><s2>Ithaca, NY 14853</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratório de Entomologia e Fitopatologia, CCTA, Universidade Estadual do Norte Fluminense, Campos dos Goytacazes</s1><s2>Rio de Janeiro, 28013-602</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>103-183</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>871</s2><s5>354000188483670070</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>5 p.3/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0380167</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Revue française d'entomologie : (1979)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>Longinos Navás a décrit approximativement 680 espèces de Chrysopidae. Les spécimens type porte-nom conservés au Muséum national d'Histoire naturelle à Paris (MNHN) représentent environ le quart de ces espèces (soit 174). Ci-après, nous fournissons les données concernant les spécimens types, ainsi que l'historique des changements de nom pour chacune des espèces décrites par Navás et conservées dans les collections entomologiques du MNHN. En plus des 5 holotypes et 58 lectotypes précédemment identifiés de ces collections, 13 holotypes sont nouvellement reconnus, 88 lectotypes sont désignés, et des syntypes sont identifiés pour 10 espèces. Les nouvelles synonymies suivantes sont proposées: Chrysopa aroguesina Navàs, 1929 est un synonyme junior de Ungla laufferi (Navás 1922); Chrysopa camposana Navás, 1935 est un synonyme junior de Ceraeochrysa valida (Banks, 1895); Ceraeochrysa (= Chrysopa) caligata (Banks, 1946) est un synonyme junior de Ceraeochrysa cornuta (Navás, 1925); Chrysopa dampfina Navás 1928 est un synonyme junior de Chrysopodes (Chrysopodes) figuralis (Banks, 1915); Nodita morenoi Navás, 1934 est un synonyme junior de Leucochrysa (Nodita) camposi (Navàs, 1933); Chrysopa rochina Navás, 1915 est un synonyme junior de Ceraeochrysa cincta (Schneider, 1851); Dichochrysa sjostedti [= Chrysopa sjoestedti] (van der Weele, 1910) est un synonyme junior de Dichochrysa nubilata (Navás, 1910). Les nouvelles combinaisons sont établies pour les cinq espèces suivantes: Chrysopodes (Chrysopodes) apurinus (Navás, 1935), Plesiochrysa climacia (Navás, 1935), Ungla favrei (Navás, 1935), Chrysopodes (Chrysopodes) geayi (Navás, 1910), et Ungla laufferi (Navás, 1922). Nous donnons la liste des six types de Navás réputés pour être au Muséum qui n'ont pas été retrouvés. Huit noms d'espèces devront être considéres comme des nomina dubia: jusqu'à ce que les types soient trouvés ou que des néotypes soient désignés, ce sont: Ancylopteryx alluaudi Navás, 1910; A. elgonica Navás, 1936; Chrysopa aegyptiaca Navás, 1915; C. nymphulina Navás, 1915; C. ricciana Navás, 1910; C. rothschildi Navás, 1915; C. silvana Navás, 1913; Nothochrysa sordidata Navás, 1908. Approximativement 50 espèces de Navás, représentées dans les collections du Musée par des spécimens examinés par Navás (comprenant des paralectotypes), sont listées. Enfin nous donnons la liste de plusieurs spécimens que Navás avait considérés comme des espèces nouvelles mais qu'il n'a jamais décrites.</s0></fC01><fC02 i1="01" i2="X"><s0>002A12J01</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Inventaire faunistique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Faunal survey</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Inventario fauna</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Collection</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Collection</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Colección</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Musée</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Museum</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Museo</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Paris</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Paris</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>París</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Chrysopidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Chrysopidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Chrysopidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Muséum national d'histoire naturelle</s0><s4>INC</s4><s5>87</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Longinos Navás</s0><s4>INC</s4><s5>88</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Ile de France</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Ile-de-France</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Ile de France</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>France</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>France</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Francia</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Europe</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Europe</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Europa</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Neuroptera</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Neuroptera</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Neuroptera</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Invertebrata</s0><s2>NS</s2></fC07><fN21><s1>271</s1></fN21></pA></standard><server><NO>PASCAL 09-0380167 INIST</NO><ET>NAVÁS' TYPE AND NON-TYPE SPECIMENS OF CHRYSOPIDAE IN THE MNHN, PARIS [NEUROPTERA]</ET><AU>LEGRAND (Jean); TAUBER (Catherine A.); ALBUQUERQUE (Gilberto S.); TAUBER (Maurice J.)</AU><AF>Muséum national d'Histoire naturelle, Département Systématique et Évolution, UMR 7205 MNHN-CNRS, Entomologie, CP 50, 45 rue Buffon/75231 Paris/France (1 aut.); Department of Entomology, Comstock Hall, Cornell University/Ithaca, NY 14853/Etats-Unis (2 aut., 4 aut.); Laboratório de Entomologia e Fitopatologia, CCTA, Universidade Estadual do Norte Fluminense, Campos dos Goytacazes/Rio de Janeiro, 28013-602/Brésil (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Revue française d'entomologie : (1979); ISSN 0181-0863; Coden RFENDE; France; Da. 2008; Vol. 30; No. 2-4; Pp. 103-183; Abs. français; Bibl. 5 p.3/4</SO><LA>Anglais</LA><FA>Longinos Navás a décrit approximativement 680 espèces de Chrysopidae. Les spécimens type porte-nom conservés au Muséum national d'Histoire naturelle à Paris (MNHN) représentent environ le quart de ces espèces (soit 174). Ci-après, nous fournissons les données concernant les spécimens types, ainsi que l'historique des changements de nom pour chacune des espèces décrites par Navás et conservées dans les collections entomologiques du MNHN. En plus des 5 holotypes et 58 lectotypes précédemment identifiés de ces collections, 13 holotypes sont nouvellement reconnus, 88 lectotypes sont désignés, et des syntypes sont identifiés pour 10 espèces. Les nouvelles synonymies suivantes sont proposées: Chrysopa aroguesina Navàs, 1929 est un synonyme junior de Ungla laufferi (Navás 1922); Chrysopa camposana Navás, 1935 est un synonyme junior de Ceraeochrysa valida (Banks, 1895); Ceraeochrysa (= Chrysopa) caligata (Banks, 1946) est un synonyme junior de Ceraeochrysa cornuta (Navás, 1925); Chrysopa dampfina Navás 1928 est un synonyme junior de Chrysopodes (Chrysopodes) figuralis (Banks, 1915); Nodita morenoi Navás, 1934 est un synonyme junior de Leucochrysa (Nodita) camposi (Navàs, 1933); Chrysopa rochina Navás, 1915 est un synonyme junior de Ceraeochrysa cincta (Schneider, 1851); Dichochrysa sjostedti [= Chrysopa sjoestedti] (van der Weele, 1910) est un synonyme junior de Dichochrysa nubilata (Navás, 1910). Les nouvelles combinaisons sont établies pour les cinq espèces suivantes: Chrysopodes (Chrysopodes) apurinus (Navás, 1935), Plesiochrysa climacia (Navás, 1935), Ungla favrei (Navás, 1935), Chrysopodes (Chrysopodes) geayi (Navás, 1910), et Ungla laufferi (Navás, 1922). Nous donnons la liste des six types de Navás réputés pour être au Muséum qui n'ont pas été retrouvés. Huit noms d'espèces devront être considéres comme des nomina dubia: jusqu'à ce que les types soient trouvés ou que des néotypes soient désignés, ce sont: Ancylopteryx alluaudi Navás, 1910; A. elgonica Navás, 1936; Chrysopa aegyptiaca Navás, 1915; C. nymphulina Navás, 1915; C. ricciana Navás, 1910; C. rothschildi Navás, 1915; C. silvana Navás, 1913; Nothochrysa sordidata Navás, 1908. Approximativement 50 espèces de Navás, représentées dans les collections du Musée par des spécimens examinés par Navás (comprenant des paralectotypes), sont listées. Enfin nous donnons la liste de plusieurs spécimens que Navás avait considérés comme des espèces nouvelles mais qu'il n'a jamais décrites.</FA><CC>002A12J01</CC><FD>Inventaire faunistique; Collection; Musée; Paris; Chrysopidae; Muséum national d'histoire naturelle; Longinos Navás</FD><FG>Ile de France; France; Europe; Neuroptera; Insecta; Arthropoda; Invertebrata</FG><ED>Faunal survey; Collection; Museum; Paris; Chrysopidae</ED><EG>Ile-de-France; France; Europe; Neuroptera; Insecta; Arthropoda; Invertebrata</EG><SD>Inventario fauna; Colección; Museo; París; Chrysopidae</SD><LO>INIST-871.354000188483670070</LO><ID>09-0380167</ID></server></inist></record>
000D51	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Delay in the Diagnosis of Cerebral Vein and Dural Sinus Thrombosis: Influence on Outcome</title><author><name sortKey="Ferro, Jose M" uniqKey="Ferro J">José M. Ferro</name><affiliation><inist:fA14 i1="01"><s1>Department of Neurology Hospital Santa Maria, University of Lisboa</s1><s2>Lisboa</s2><s3>PRT</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Canhao, Patricia" uniqKey="Canhao P">Patricia Canhao</name><affiliation><inist:fA14 i1="01"><s1>Department of Neurology Hospital Santa Maria, University of Lisboa</s1><s2>Lisboa</s2><s3>PRT</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Stam, Jan" uniqKey="Stam J">Jan Stam</name><affiliation><inist:fA14 i1="02"><s1>Academic Medical Centre</s1><s2>Amsterdam</s2><s3>NLD</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bousser, Marie Germaine" uniqKey="Bousser M">Marie-Germaine Bousser</name><affiliation><inist:fA14 i1="03"><s1>Hôpital Lariboisière</s1><s2>Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Barinagarrementeria, Fernando" uniqKey="Barinagarrementeria F">Fernando Barinagarrementeria</name><affiliation><inist:fA14 i1="04"><s1>Instituto Nacional de Neurologia y Neurocirurgia</s1><s2>México City</s2><s3>MEX</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Massaro, Ayrton" uniqKey="Massaro A">Ayrton Massaro</name><affiliation><inist:fA14 i1="05"><s1>Hospital das Clinicas Universidade de São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ducrocq, Xavier" uniqKey="Ducrocq X">Xavier Ducrocq</name><affiliation><inist:fA14 i1="06"><s1>Hôpital Central</s1><s2>Nancy</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kasner, Scott E" uniqKey="Kasner S">Scott E. Kasner</name><affiliation><inist:fA14 i1="07"><s1>University of Pennsylvania Medical Center</s1><s2>Philadelphia, Pa</s2><s3>USA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0380787</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0380787 INIST</idno><idno type="RBID">Pascal:09-0380787</idno><idno type="wicri:Area/Main/Corpus">001C30</idno></publicationStmt><seriesStmt><idno type="ISSN">0039-2499</idno><title level="j" type="abbreviated">Stroke : (1970)</title><title level="j" type="main">Stroke : (1970)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cerebral vein</term><term>Cerebrovascular disease</term><term>Diagnosis</term><term>Nervous system diseases</term><term>Prognosis</term><term>Stroke</term><term>Venous thrombosis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Thrombose veineuse</term><term>Pathologie du   système nerveux</term><term>Pathologie cérébrovasculaire</term><term>Accident cérébrovasculaire</term><term>Diagnostic</term><term>Veine cérébrale</term><term>Pronostic</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background and Purpose-Diagnostic delay of cerebral vein and dural sinus thrombosis may have an impact on outcome. Methods-In the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT) cohort (624 patients with cerebral vein and dural sinus thrombosis), we analyzed the predictors and the impact on outcome of diagnostic delay. Primary outcome was a modified Rankin Scale score &#62;2 at the end of follow-up. Secondary outcomes were modified Rankin Scale score 0 to 1 at the end of follow-up, death, and visual deficits (visual acuity or visual field). Results-Median delay was 7 days (interquartile range, 3 to 16). Patients with disturbance of consciousness (P&#60;0.001) and of mental status (P=0.042), seizure (&#60;0.001), and with parenchymal lesions on admission CT/MR (P&#60;0.001) were diagnosed earlier, whereas men (P=0.01) and those with isolated intracranial hypertension syndrome (P=0.04) were diagnosed later. Between patients diagnosed earlier and later than the median delay, no statistically significant differences were found in the primary (P=0.33) and in secondary outcomes: modified Rankin Scale score 0 to 1 (P=0.86) or deaths (P=0.53). Persistent visual deficits were more frequent in patients diagnosed later (P=0.05). In patients with isolated intracranial hypertension syndrome, modified Rankin Scale score &#62;2 at the end of follow-up was more frequent in patients diagnosed later (P=0.02). Conclusions-Diagnostic delay was considerable in this cohort and was associated with an increased risk of visual deficit. In patients with isolated intracranial hypertension syndrome, diagnostic delay was also associated with death or dependency.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0039-2499</s0></fA01><fA02 i1="01"><s0>SJCCA7</s0></fA02><fA03 i2="1"><s0>Stroke : (1970)</s0></fA03><fA05><s2>40</s2></fA05><fA06><s2>9</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Delay in the Diagnosis of Cerebral Vein and Dural Sinus Thrombosis: Influence on Outcome</s1></fA08><fA11 i1="01" i2="1"><s1>FERRO (José M.)</s1></fA11><fA11 i1="02" i2="1"><s1>CANHAO (Patricia)</s1></fA11><fA11 i1="03" i2="1"><s1>STAM (Jan)</s1></fA11><fA11 i1="04" i2="1"><s1>BOUSSER (Marie-Germaine)</s1></fA11><fA11 i1="05" i2="1"><s1>BARINAGARREMENTERIA (Fernando)</s1></fA11><fA11 i1="06" i2="1"><s1>MASSARO (Ayrton)</s1></fA11><fA11 i1="07" i2="1"><s1>DUCROCQ (Xavier)</s1></fA11><fA11 i1="08" i2="1"><s1>KASNER (Scott E.)</s1></fA11><fA14 i1="01"><s1>Department of Neurology Hospital Santa Maria, University of Lisboa</s1><s2>Lisboa</s2><s3>PRT</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Academic Medical Centre</s1><s2>Amsterdam</s2><s3>NLD</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Hôpital Lariboisière</s1><s2>Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Instituto Nacional de Neurologia y Neurocirurgia</s1><s2>México City</s2><s3>MEX</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Hospital das Clinicas Universidade de São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="06"><s1>Hôpital Central</s1><s2>Nancy</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>University of Pennsylvania Medical Center</s1><s2>Philadelphia, Pa</s2><s3>USA</s3><sZ>8 aut.</sZ></fA14><fA17 i1="01" i2="1"><s1>ISCVT Investigators</s1><s3>INC</s3></fA17><fA20><s1>3133-3138</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>4004</s2><s5>354000187651240330</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>4 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0380787</s0></fA47><fA60><s1>P</s1><s3>CR</s3></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Stroke : (1970)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Background and Purpose-Diagnostic delay of cerebral vein and dural sinus thrombosis may have an impact on outcome. Methods-In the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT) cohort (624 patients with cerebral vein and dural sinus thrombosis), we analyzed the predictors and the impact on outcome of diagnostic delay. Primary outcome was a modified Rankin Scale score &#62;2 at the end of follow-up. Secondary outcomes were modified Rankin Scale score 0 to 1 at the end of follow-up, death, and visual deficits (visual acuity or visual field). Results-Median delay was 7 days (interquartile range, 3 to 16). Patients with disturbance of consciousness (P&#60;0.001) and of mental status (P=0.042), seizure (&#60;0.001), and with parenchymal lesions on admission CT/MR (P&#60;0.001) were diagnosed earlier, whereas men (P=0.01) and those with isolated intracranial hypertension syndrome (P=0.04) were diagnosed later. Between patients diagnosed earlier and later than the median delay, no statistically significant differences were found in the primary (P=0.33) and in secondary outcomes: modified Rankin Scale score 0 to 1 (P=0.86) or deaths (P=0.53). Persistent visual deficits were more frequent in patients diagnosed later (P=0.05). In patients with isolated intracranial hypertension syndrome, modified Rankin Scale score &#62;2 at the end of follow-up was more frequent in patients diagnosed later (P=0.02). Conclusions-Diagnostic delay was considerable in this cohort and was associated with an increased risk of visual deficit. In patients with isolated intracranial hypertension syndrome, diagnostic delay was also associated with death or dependency.</s0></fC01><fC02 i1="01" i2="X"><s0>002B17C</s0></fC02><fC02 i1="02" i2="X"><s0>002B17A03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Thrombose veineuse</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Venous thrombosis</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Trombosis venosa</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Pathologie du   système nerveux</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Nervous system diseases</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Sistema nervioso patología</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Pathologie cérébrovasculaire</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Cerebrovascular disease</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Vaso sanguíneo encéfalo patología</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Accident cérébrovasculaire</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Stroke</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Accidente cerebrovascular</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Diagnostic</s0><s5>09</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Diagnosis</s0><s5>09</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Diagnóstico</s0><s5>09</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Veine cérébrale</s0><s5>10</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Cerebral vein</s0><s5>10</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Vena cerebral</s0><s5>10</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Pronostic</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Prognosis</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Pronóstico</s0><s5>11</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'encéphale</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Cerebral disorder</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Encéfalo patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie du   système nerveux central</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Central nervous system disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pathologie de l'appareil circulatoire</s0><s5>40</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Cardiovascular disease</s0><s5>40</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0><s5>40</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Pathologie des vaisseaux sanguins</s0><s5>41</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Vascular disease</s0><s5>41</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Vaso sanguíneo patología</s0><s5>41</s5></fC07><fN21><s1>271</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0380787 INIST</NO><ET>Delay in the Diagnosis of Cerebral Vein and Dural Sinus Thrombosis: Influence on Outcome</ET><AU>FERRO (José M.); CANHAO (Patricia); STAM (Jan); BOUSSER (Marie-Germaine); BARINAGARREMENTERIA (Fernando); MASSARO (Ayrton); DUCROCQ (Xavier); KASNER (Scott E.)</AU><AF>Department of Neurology Hospital Santa Maria, University of Lisboa/Lisboa/Portugal (1 aut., 2 aut.); Academic Medical Centre/Amsterdam/Pays-Bas (3 aut.); Hôpital Lariboisière/Paris/France (4 aut.); Instituto Nacional de Neurologia y Neurocirurgia/México City/Mexique (5 aut.); Hospital das Clinicas Universidade de São Paulo/São Paulo/Brésil (6 aut.); Hôpital Central/Nancy/France (7 aut.); University of Pennsylvania Medical Center/Philadelphia, Pa/Etats-Unis (8 aut.)</AF><DT>Publication en série; Correspondance, lettre; Niveau analytique</DT><SO>Stroke : (1970); ISSN 0039-2499; Coden SJCCA7; Etats-Unis; Da. 2009; Vol. 40; No. 9; Pp. 3133-3138; Bibl. 4 ref.</SO><LA>Anglais</LA><EA>Background and Purpose-Diagnostic delay of cerebral vein and dural sinus thrombosis may have an impact on outcome. Methods-In the International Study on Cerebral Vein and Dural Sinus Thrombosis (ISCVT) cohort (624 patients with cerebral vein and dural sinus thrombosis), we analyzed the predictors and the impact on outcome of diagnostic delay. Primary outcome was a modified Rankin Scale score &#62;2 at the end of follow-up. Secondary outcomes were modified Rankin Scale score 0 to 1 at the end of follow-up, death, and visual deficits (visual acuity or visual field). Results-Median delay was 7 days (interquartile range, 3 to 16). Patients with disturbance of consciousness (P&#60;0.001) and of mental status (P=0.042), seizure (&#60;0.001), and with parenchymal lesions on admission CT/MR (P&#60;0.001) were diagnosed earlier, whereas men (P=0.01) and those with isolated intracranial hypertension syndrome (P=0.04) were diagnosed later. Between patients diagnosed earlier and later than the median delay, no statistically significant differences were found in the primary (P=0.33) and in secondary outcomes: modified Rankin Scale score 0 to 1 (P=0.86) or deaths (P=0.53). Persistent visual deficits were more frequent in patients diagnosed later (P=0.05). In patients with isolated intracranial hypertension syndrome, modified Rankin Scale score &#62;2 at the end of follow-up was more frequent in patients diagnosed later (P=0.02). Conclusions-Diagnostic delay was considerable in this cohort and was associated with an increased risk of visual deficit. In patients with isolated intracranial hypertension syndrome, diagnostic delay was also associated with death or dependency.</EA><CC>002B17C; 002B17A03</CC><FD>Thrombose veineuse; Pathologie du   système nerveux; Pathologie cérébrovasculaire; Accident cérébrovasculaire; Diagnostic; Veine cérébrale; Pronostic</FD><FG>Pathologie de l'encéphale; Pathologie du   système nerveux central; Pathologie de l'appareil circulatoire; Pathologie des vaisseaux sanguins</FG><ED>Venous thrombosis; Nervous system diseases; Cerebrovascular disease; Stroke; Diagnosis; Cerebral vein; Prognosis</ED><EG>Cerebral disorder; Central nervous system disease; Cardiovascular disease; Vascular disease</EG><SD>Trombosis venosa; Sistema nervioso patología; Vaso sanguíneo encéfalo patología; Accidente cerebrovascular; Diagnóstico; Vena cerebral; Pronóstico</SD><LO>INIST-4004.354000187651240330</LO><ID>09-0380787</ID></server></inist></record>
000D52	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Cyclohexane and toluene oxidation catalyzed by 1,10-phenantroline Cu(II) complexes</title><author><name sortKey="Detoni, Chaline" uniqKey="Detoni C">Chaline Detoni</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco A-641</s1><s2>Rio de Janeiro 21945-970, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Escola de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco E</s1><s2>Rio de Janeiro 21941-909, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Carvalho, Nakedia M F" uniqKey="Carvalho N">Nakédia M. F. Carvalho</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco A-641</s1><s2>Rio de Janeiro 21945-970, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Aranda, Donato A G" uniqKey="Aranda D">Donato A. G. Aranda</name><affiliation><inist:fA14 i1="02"><s1>Escola de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco E</s1><s2>Rio de Janeiro 21941-909, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Louis, B" uniqKey="Louis B">B. Louis</name><affiliation><inist:fA14 i1="03"><s1>Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515 du CNRS, Part of European Laboratory for Catalysis and Surface Science, Université de Strasbourg, 25 rue Becquerel</s1><s2>67087 Strasbourg</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Antunes, O A C" uniqKey="Antunes O">O. A. C. Antunes</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco A-641</s1><s2>Rio de Janeiro 21945-970, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0381274</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0381274 INIST</idno><idno type="RBID">Pascal:09-0381274</idno><idno type="wicri:Area/Main/Corpus">001C29</idno></publicationStmt><seriesStmt><idno type="ISSN">0926-860X</idno><title level="j" type="abbreviated">Appl. catal., A Gen.</title><title level="j" type="main">Applied catalysis. A, General</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acetonitrile</term><term>Adipic acid</term><term>Catalytic reaction</term><term>Complexes</term><term>Conversion</term><term>Cyclic voltammetry</term><term>Cyclohexane</term><term>Cyclohexanol</term><term>Cyclohexanone</term><term>Hydrogen peroxide</term><term>Nitrile</term><term>Oxidant</term><term>Oxidation</term><term>Peroxides</term><term>Room temperature</term><term>Toluene</term><term>Water</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Cyclohexane</term><term>Toluène</term><term>Oxydation</term><term>Réaction catalytique</term><term>Complexe</term><term>Peroxyde</term><term>Voltammétrie cyclique</term><term>Peroxyde d'hydrogène</term><term>Oxydant</term><term>Nitrile</term><term>Acétonitrile</term><term>Eau</term><term>Cyclohexanol</term><term>Cyclohexanone</term><term>Acide adipique</term><term>Conversion</term><term>Température ambiante</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In this work, we present the cyclohexane oxidation catalyzed by the mononuclear 1,10-phenantroline Cu(II) complexes: [Cu(phen)<sub>3</sub>]Cl<sub>2</sub>.7H<sub>2</sub>O (1), [Cu(phen)<sub>2</sub>Cl]Cl.5H<sub>2</sub>O (2), [Cu(phen)Cl<sub>2</sub>](3). using hydrogen peroxide as oxidant, in acetonitrile:water (3.5:1) solution. The reactions were carried out at temperatures ranging from 25 °C to 70 °C. All complexes were able to oxidize cyclohexane into cyclohexanol and cyclohexanone with low to moderate yields. Adipic acid was also formed in the reaction. The highest conversion was obtained with the system [Cu(phen)<sub>2</sub>Cl]Cl/H<sub>2</sub>O<sub>2</sub>/70 °C. with 67% total yield. Furthermore, these complexes were also able to oxidize toluene at room temperature.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0926-860X</s0></fA01><fA03 i2="1"><s0>Appl. catal., A Gen.</s0></fA03><fA05><s2>365</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Cyclohexane and toluene oxidation catalyzed by 1,10-phenantroline Cu(II) complexes</s1></fA08><fA11 i1="01" i2="1"><s1>DETONI (Chaline)</s1></fA11><fA11 i1="02" i2="1"><s1>CARVALHO (Nakédia M. F.)</s1></fA11><fA11 i1="03" i2="1"><s1>ARANDA (Donato A. G.)</s1></fA11><fA11 i1="04" i2="1"><s1>LOUIS (B.)</s1></fA11><fA11 i1="05" i2="1"><s1>ANTUNES (O. A. C.)</s1></fA11><fA14 i1="01"><s1>Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco A-641</s1><s2>Rio de Janeiro 21945-970, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Escola de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco E</s1><s2>Rio de Janeiro 21941-909, RJ</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515 du CNRS, Part of European Laboratory for Catalysis and Surface Science, Université de Strasbourg, 25 rue Becquerel</s1><s2>67087 Strasbourg</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA20><s1>281-286</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>18840A</s2><s5>354000187588890200</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0381274</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied catalysis. A, General</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>In this work, we present the cyclohexane oxidation catalyzed by the mononuclear 1,10-phenantroline Cu(II) complexes: [Cu(phen)<sub>3</sub>]Cl<sub>2</sub>.7H<sub>2</sub>O (1), [Cu(phen)<sub>2</sub>Cl]Cl.5H<sub>2</sub>O (2), [Cu(phen)Cl<sub>2</sub>](3). using hydrogen peroxide as oxidant, in acetonitrile:water (3.5:1) solution. The reactions were carried out at temperatures ranging from 25 °C to 70 °C. All complexes were able to oxidize cyclohexane into cyclohexanol and cyclohexanone with low to moderate yields. Adipic acid was also formed in the reaction. The highest conversion was obtained with the system [Cu(phen)<sub>2</sub>Cl]Cl/H<sub>2</sub>O<sub>2</sub>/70 °C. with 67% total yield. Furthermore, these complexes were also able to oxidize toluene at room temperature.</s0></fC01><fC02 i1="01" i2="X"><s0>001C01A03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Cyclohexane</s0><s2>NK</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Cyclohexane</s0><s2>NK</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Ciclohexano</s0><s2>NK</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Toluène</s0><s2>NK</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Toluene</s0><s2>NK</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Tolueno</s0><s2>NK</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Oxydation</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Oxidation</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Oxidación</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Réaction catalytique</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Catalytic reaction</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Reacción catalítica</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Complexe</s0><s2>NA</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Complexes</s0><s2>NA</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Complejo</s0><s2>NA</s2><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Peroxyde</s0><s2>NA</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Peroxides</s0><s2>NA</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Peróxido</s0><s2>NA</s2><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Voltammétrie cyclique</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Cyclic voltammetry</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Voltametría cíclica</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Peroxyde d'hydrogène</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Hydrogen peroxide</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Peróxido de hydrogeno</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Oxydant</s0><s5>12</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Oxidant</s0><s5>12</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Oxidante</s0><s5>12</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Nitrile</s0><s5>13</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Nitrile</s0><s5>13</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Nitrilo</s0><s5>13</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Acétonitrile</s0><s2>NK</s2><s5>14</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Acetonitrile</s0><s2>NK</s2><s5>14</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Acetonitrilo</s0><s2>NK</s2><s5>14</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Eau</s0><s5>15</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Water</s0><s5>15</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Agua</s0><s5>15</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Cyclohexanol</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Cyclohexanol</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Ciclohexanol</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Cyclohexanone</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Cyclohexanone</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Ciclohexanona</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Acide adipique</s0><s2>NK</s2><s5>18</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Adipic acid</s0><s2>NK</s2><s5>18</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Adípico ácido</s0><s2>NK</s2><s5>18</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Conversion</s0><s5>19</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Conversion</s0><s5>19</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Conversión</s0><s5>19</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Température ambiante</s0><s5>20</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Room temperature</s0><s5>20</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Temperatura ambiente</s0><s5>20</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Hydrocarbure</s0><s2>FX</s2><s5>09</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Hydrocarbon</s0><s2>FX</s2><s5>09</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Hidrocarburo</s0><s2>FX</s2><s5>09</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Composé benzénique</s0><s5>10</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Benzenic compound</s0><s5>10</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Compuesto bencénico</s0><s5>10</s5></fC07><fN21><s1>278</s1></fN21></pA></standard><server><NO>PASCAL 09-0381274 INIST</NO><ET>Cyclohexane and toluene oxidation catalyzed by 1,10-phenantroline Cu(II) complexes</ET><AU>DETONI (Chaline); CARVALHO (Nakédia M. F.); ARANDA (Donato A. G.); LOUIS (B.); ANTUNES (O. A. C.)</AU><AF>Instituto de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco A-641/Rio de Janeiro 21945-970, RJ/Brésil (1 aut., 2 aut., 5 aut.); Escola de Química, Universidade Federal do Rio de Janeiro, Cidade Universitária CT Bloco E/Rio de Janeiro 21941-909, RJ/Brésil (1 aut., 3 aut.); Laboratoire des Matériaux, Surfaces et Procédés pour la Catalyse (LMSPC), UMR 7515 du CNRS, Part of European Laboratory for Catalysis and Surface Science, Université de Strasbourg, 25 rue Becquerel/67087 Strasbourg/France (4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Applied catalysis. A, General; ISSN 0926-860X; Pays-Bas; Da. 2009; Vol. 365; No. 2; Pp. 281-286; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>In this work, we present the cyclohexane oxidation catalyzed by the mononuclear 1,10-phenantroline Cu(II) complexes: [Cu(phen)<sub>3</sub>]Cl<sub>2</sub>.7H<sub>2</sub>O (1), [Cu(phen)<sub>2</sub>Cl]Cl.5H<sub>2</sub>O (2), [Cu(phen)Cl<sub>2</sub>](3). using hydrogen peroxide as oxidant, in acetonitrile:water (3.5:1) solution. The reactions were carried out at temperatures ranging from 25 °C to 70 °C. All complexes were able to oxidize cyclohexane into cyclohexanol and cyclohexanone with low to moderate yields. Adipic acid was also formed in the reaction. The highest conversion was obtained with the system [Cu(phen)<sub>2</sub>Cl]Cl/H<sub>2</sub>O<sub>2</sub>/70 °C. with 67% total yield. Furthermore, these complexes were also able to oxidize toluene at room temperature.</EA><CC>001C01A03</CC><FD>Cyclohexane; Toluène; Oxydation; Réaction catalytique; Complexe; Peroxyde; Voltammétrie cyclique; Peroxyde d'hydrogène; Oxydant; Nitrile; Acétonitrile; Eau; Cyclohexanol; Cyclohexanone; Acide adipique; Conversion; Température ambiante</FD><FG>Hydrocarbure; Composé benzénique</FG><ED>Cyclohexane; Toluene; Oxidation; Catalytic reaction; Complexes; Peroxides; Cyclic voltammetry; Hydrogen peroxide; Oxidant; Nitrile; Acetonitrile; Water; Cyclohexanol; Cyclohexanone; Adipic acid; Conversion; Room temperature</ED><EG>Hydrocarbon; Benzenic compound</EG><SD>Ciclohexano; Tolueno; Oxidación; Reacción catalítica; Complejo; Peróxido; Voltametría cíclica; Peróxido de hydrogeno; Oxidante; Nitrilo; Acetonitrilo; Agua; Ciclohexanol; Ciclohexanona; Adípico ácido; Conversión; Temperatura ambiente</SD><LO>INIST-18840A.354000187588890200</LO><ID>09-0381274</ID></server></inist></record>
000D53	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Heparin-binding hemagglutinin (HBHA) of Mycobacterium leprae is expressed during infection and enhances bacterial adherence to epithelial cells</title><author><name sortKey="Soares De Lima, Cristiana" uniqKey="Soares De Lima C">Cristiana Soares De Lima</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Marques, Maria A M" uniqKey="Marques M">Maria A. M. Marques</name><affiliation><inist:fA14 i1="02"><s1>Department of Microbiology, Immunology and Pathology, Colorado State University</s1><s2>Fort Collins, CO</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Debrie, Anne Sophie" uniqKey="Debrie A">Anne-Sophie Debrie</name><affiliation><inist:fA14 i1="03"><s1>INSERM U629</s1><s2>Lille</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Almeida, Elza C C" uniqKey="Almeida E">Elza C. C. Almeida</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Silva, Carlos A M" uniqKey="Silva C">Carlos A. M. Silva</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brennan, Patrick J" uniqKey="Brennan P">Patrick J. Brennan</name><affiliation><inist:fA14 i1="02"><s1>Department of Microbiology, Immunology and Pathology, Colorado State University</s1><s2>Fort Collins, CO</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sarno, Euzenir N" uniqKey="Sarno E">Euzenir N. Sarno</name><affiliation><inist:fA14 i1="04"><s1>Leprosy Laboratory, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Menozzi, Franco D" uniqKey="Menozzi F">Franco D. Menozzi</name><affiliation><inist:fA14 i1="03"><s1>INSERM U629</s1><s2>Lille</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>Institut Pasteur de Lille</s1><s2>Lille</s2><s3>FRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="06"><s1>IFR142</s1><s2>Lille</s2><s3>FRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pessolani, Maria C V" uniqKey="Pessolani M">Maria C. V. Pessolani</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0383671</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0383671 LGMI</idno><idno type="RBID">Pascal:09-0383671</idno><idno type="wicri:Area/Main/Corpus">001C28</idno></publicationStmt><seriesStmt><idno type="ISSN">0378-1097</idno><title level="j" type="abbreviated">FEMS microbiol. lett.</title><title level="j" type="main">FEMS microbiology letters</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adhesin</term><term>Epithelial cell</term><term>Hemagglutinin</term><term>Heparin</term><term>Mycobacterium leprae</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Mycobacterium leprae</term><term>Adhésine</term><term>Héparine</term><term>Hémagglutinine</term><term>Cellule épithéliale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A heparin-binding hemagglutinin (HBHA) expressed on the surface of Mycobacterium tuberculosis is an antigenic protein that has been implicated in bacterial adherence to epithelial cells and systemic dissemination. In this study, the potential role of the Mycobacterium leprae HBHA (ML-HBHA) homologue in leprosy was investigated. Initially, the in vivo expression of HBHA and its association with the M. leprae cell envelope was confirmed by immunoblotting and proteomic analysis. Mycobacterium leprae recombinant HBHA (rML-HBHA) bound to a heparin-Sepharose column, and its capacity to act as an adhesin was demonstrated in experiments showing that the exogenous addition of the protein to latex beads or to M. leprae cells promotes a dramatic increase in association with epithelial cells. Finally, serum anti-HBHA immunoglobulin G levels were investigated in individuals infected with M. leprae. Altogether, our data indicate that HBHA is recognized during the course of bacterial infection in humans and may play a role in leprosy pathogenesis.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0378-1097</s0></fA01><fA02 i1="01"><s0>FMLED7</s0></fA02><fA03 i2="1"><s0>FEMS microbiol. lett.</s0></fA03><fA05><s2>292</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Heparin-binding hemagglutinin (HBHA) of Mycobacterium leprae is expressed during infection and enhances bacterial adherence to epithelial cells</s1></fA08><fA11 i1="01" i2="1"><s1>SOARES DE LIMA (Cristiana)</s1></fA11><fA11 i1="02" i2="1"><s1>MARQUES (Maria A. M.)</s1></fA11><fA11 i1="03" i2="1"><s1>DEBRIE (Anne-Sophie)</s1></fA11><fA11 i1="04" i2="1"><s1>ALMEIDA (Elza C. C.)</s1></fA11><fA11 i1="05" i2="1"><s1>SILVA (Carlos A. M.)</s1></fA11><fA11 i1="06" i2="1"><s1>BRENNAN (Patrick J.)</s1></fA11><fA11 i1="07" i2="1"><s1>SARNO (Euzenir N.)</s1></fA11><fA11 i1="08" i2="1"><s1>MENOZZI (Franco D.)</s1></fA11><fA11 i1="09" i2="1"><s1>PESSOLANI (Maria C. V.)</s1></fA11><fA14 i1="01"><s1>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Microbiology, Immunology and Pathology, Colorado State University</s1><s2>Fort Collins, CO</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="03"><s1>INSERM U629</s1><s2>Lille</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="04"><s1>Leprosy Laboratory, Instituto Oswaldo Cruz</s1><s2>Fiocruz, Rio de Janerio</s2><s3>BRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="05"><s1>Institut Pasteur de Lille</s1><s2>Lille</s2><s3>FRA</s3><sZ>8 aut.</sZ></fA14><fA14 i1="06"><s1>IFR142</s1><s2>Lille</s2><s3>FRA</s3><sZ>8 aut.</sZ></fA14><fA20><s1>162-169</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>17567A</s2><s5>354000185457730020</s5></fA43><fA44><s0>A700</s0></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0383671</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>FEMS microbiology letters</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>A heparin-binding hemagglutinin (HBHA) expressed on the surface of Mycobacterium tuberculosis is an antigenic protein that has been implicated in bacterial adherence to epithelial cells and systemic dissemination. In this study, the potential role of the Mycobacterium leprae HBHA (ML-HBHA) homologue in leprosy was investigated. Initially, the in vivo expression of HBHA and its association with the M. leprae cell envelope was confirmed by immunoblotting and proteomic analysis. Mycobacterium leprae recombinant HBHA (rML-HBHA) bound to a heparin-Sepharose column, and its capacity to act as an adhesin was demonstrated in experiments showing that the exogenous addition of the protein to latex beads or to M. leprae cells promotes a dramatic increase in association with epithelial cells. Finally, serum anti-HBHA immunoglobulin G levels were investigated in individuals infected with M. leprae. Altogether, our data indicate that HBHA is recognized during the course of bacterial infection in humans and may play a role in leprosy pathogenesis.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05B08</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Mycobacterium leprae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Mycobacterium leprae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Mycobacterium leprae</s0><s2>NS</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Adhésine</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Adhesin</s0><s5>05</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Adesina</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Héparine</s0><s2>FR</s2><s5>06</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Heparin</s0><s2>FR</s2><s5>06</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Heparina</s0><s2>FR</s2><s5>06</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Hémagglutinine</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Hemagglutinin</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Hemoaglutinina</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Cellule épithéliale</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Epithelial cell</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Célula epitelial</s0><s5>08</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fN21><s1>278</s1></fN21><fN44 i1="01"><s1>PSI</s1></fN44><fN82><s1>PSI</s1></fN82></pA></standard><server><NO>PASCAL 09-0383671 LGMI</NO><ET>Heparin-binding hemagglutinin (HBHA) of Mycobacterium leprae is expressed during infection and enhances bacterial adherence to epithelial cells</ET><AU>SOARES DE LIMA (Cristiana); MARQUES (Maria A. M.); DEBRIE (Anne-Sophie); ALMEIDA (Elza C. C.); SILVA (Carlos A. M.); BRENNAN (Patrick J.); SARNO (Euzenir N.); MENOZZI (Franco D.); PESSOLANI (Maria C. V.)</AU><AF>Laboratory of Cellular Microbiology, Instituto Oswaldo Cruz/Fiocruz, Rio de Janerio/Brésil (1 aut., 4 aut., 5 aut., 9 aut.); Department of Microbiology, Immunology and Pathology, Colorado State University/Fort Collins, CO/Etats-Unis (2 aut., 6 aut.); INSERM U629/Lille/France (3 aut., 8 aut.); Leprosy Laboratory, Instituto Oswaldo Cruz/Fiocruz, Rio de Janerio/Brésil (7 aut.); Institut Pasteur de Lille/Lille/France (8 aut.); IFR142/Lille/France (8 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>FEMS microbiology letters; ISSN 0378-1097; Coden FMLED7; Royaume-Uni; Da. 2009; Vol. 292; No. 2; Pp. 162-169; Bibl. 1 p.1/4</SO><LA>Anglais</LA><EA>A heparin-binding hemagglutinin (HBHA) expressed on the surface of Mycobacterium tuberculosis is an antigenic protein that has been implicated in bacterial adherence to epithelial cells and systemic dissemination. In this study, the potential role of the Mycobacterium leprae HBHA (ML-HBHA) homologue in leprosy was investigated. Initially, the in vivo expression of HBHA and its association with the M. leprae cell envelope was confirmed by immunoblotting and proteomic analysis. Mycobacterium leprae recombinant HBHA (rML-HBHA) bound to a heparin-Sepharose column, and its capacity to act as an adhesin was demonstrated in experiments showing that the exogenous addition of the protein to latex beads or to M. leprae cells promotes a dramatic increase in association with epithelial cells. Finally, serum anti-HBHA immunoglobulin G levels were investigated in individuals infected with M. leprae. Altogether, our data indicate that HBHA is recognized during the course of bacterial infection in humans and may play a role in leprosy pathogenesis.</EA><CC>002A05B08</CC><FD>Mycobacterium leprae; Adhésine; Héparine; Hémagglutinine; Cellule épithéliale</FD><FG>Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bactérie</FG><ED>Mycobacterium leprae; Adhesin; Heparin; Hemagglutinin; Epithelial cell</ED><EG>Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bacteria</EG><SD>Mycobacterium leprae; Adesina; Heparina; Hemoaglutinina; Célula epitelial</SD><LO>INIST-17567A.354000185457730020</LO><ID>09-0383671</ID></server></inist></record>
000D54	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Mutual influence of forests and pastures on the seedbanks in the Eastern Amazon</title><author><name sortKey="Miranda, I S" uniqKey="Miranda I">I. S. Miranda</name><affiliation><inist:fA14 i1="01"><s1>Universidade Federal Rural da Amazônia, Programa de Pós-Graduação em Ciências Florestais</s1><s2>Belém, Pará</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mitja, D" uniqKey="Mitja D">D. Mitja</name><affiliation><inist:fA14 i1="02"><s1>IRD, Maison de la télédétection - MTD IRD/Unité ESPACE- U 140</s1><s2>34093 Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Silva, T S" uniqKey="Silva T">T. S. Silva</name><affiliation><inist:fA14 i1="01"><s1>Universidade Federal Rural da Amazônia, Programa de Pós-Graduação em Ciências Florestais</s1><s2>Belém, Pará</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0385469</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0385469 INIST</idno><idno type="RBID">Pascal:09-0385469</idno><idno type="wicri:Area/Main/Corpus">001C27</idno></publicationStmt><seriesStmt><idno type="ISSN">0043-1737</idno><title level="j" type="abbreviated">Weed res. : (Print)</title><title level="j" type="main">Weed research : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Density</term><term>Pasture</term><term>Regeneration</term><term>Seed bank</term><term>Small farms</term><term>Small scale</term><term>Species</term><term>Species diversity</term><term>Tropical zone</term><term>Weed science</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Pâture</term><term>Potentiel semencier</term><term>Petite exploitation agricole</term><term>Zone tropicale</term><term>Diversité espèces</term><term>Densité</term><term>Espèce</term><term>Régénération</term><term>Malherbologie</term><term>Echelle petite</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The objective of this study was to compare the floristic composition and species diversity existing in the seedbanks of forests and pastures. The seedbanks were sampled in three forest and three pastures areas in a community of smallholder farmers, in Pará state, Brazil. Seedling emergence in a glasshouse was used to quantify and identify the seeds. The total densities and diversity of the seedbanks were not significantly different among the pastures and forests, but the floristic composition was different. The herbaceous species predominated in both the pastures and the forests, but in the forest the abundance of shrub and tree was higher than herb. The seed density of several pioneer woody species was higher in the forests and the density of several herbaceous species was greater in the pastures. The influence of the forest species on the pastures and of the pastures species on the forests is a result of the initial process of human occupation and illustrates a dynamic that can lead to both the conservation of forest species and the spread of weed species. Actions should be carried out to avoid disturbance in the forests and improve biodiversity preservation in rural areas.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0043-1737</s0></fA01><fA02 i1="01"><s0>WEREAT</s0></fA02><fA03 i2="1"><s0>Weed res. : (Print)</s0></fA03><fA05><s2>49</s2></fA05><fA06><s2>5</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Mutual influence of forests and pastures on the seedbanks in the Eastern Amazon</s1></fA08><fA11 i1="01" i2="1"><s1>MIRANDA (I. S.)</s1></fA11><fA11 i1="02" i2="1"><s1>MITJA (D.)</s1></fA11><fA11 i1="03" i2="1"><s1>SILVA (T. S.)</s1></fA11><fA14 i1="01"><s1>Universidade Federal Rural da Amazônia, Programa de Pós-Graduação em Ciências Florestais</s1><s2>Belém, Pará</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>IRD, Maison de la télédétection - MTD IRD/Unité ESPACE- U 140</s1><s2>34093 Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>499-505</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>12168</s2><s5>354000187618590060</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0385469</s0></fA47><fA60><s1>P</s1><s3>PR</s3></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Weed research : (Print)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The objective of this study was to compare the floristic composition and species diversity existing in the seedbanks of forests and pastures. The seedbanks were sampled in three forest and three pastures areas in a community of smallholder farmers, in Pará state, Brazil. Seedling emergence in a glasshouse was used to quantify and identify the seeds. The total densities and diversity of the seedbanks were not significantly different among the pastures and forests, but the floristic composition was different. The herbaceous species predominated in both the pastures and the forests, but in the forest the abundance of shrub and tree was higher than herb. The seed density of several pioneer woody species was higher in the forests and the density of several herbaceous species was greater in the pastures. The influence of the forest species on the pastures and of the pastures species on the forests is a result of the initial process of human occupation and illustrates a dynamic that can lead to both the conservation of forest species and the spread of weed species. Actions should be carried out to avoid disturbance in the forests and improve biodiversity preservation in rural areas.</s0></fC01><fC02 i1="01" i2="X"><s0>002A34H</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Pâture</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Pasture</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Pastizal</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Potentiel semencier</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Seed bank</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Banco de semillas</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Petite exploitation agricole</s0><s2>563</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Small farms</s0><s2>563</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Explotación en pequeña escala</s0><s2>563</s2><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Zone tropicale</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Tropical zone</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Zona tropical</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Diversité espèces</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Species diversity</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Diversidad especies</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Densité</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Density</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Densidad</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Espèce</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Species</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Especie</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Régénération</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Regeneration</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Regeneración</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Malherbologie</s0><s5>28</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Weed science</s0><s5>28</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Ciencia malas hierbas</s0><s5>28</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Echelle petite</s0><s5>29</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Small scale</s0><s5>29</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Escala pequeña</s0><s5>29</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Exploitation agricole</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Farming</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Explotación agrícola</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Diversité biologique</s0><s5>33</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Biodiversity</s0><s5>33</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Diversidad biológica</s0><s5>33</s5></fC07><fN21><s1>278</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0385469 INIST</NO><ET>Mutual influence of forests and pastures on the seedbanks in the Eastern Amazon</ET><AU>MIRANDA (I. S.); MITJA (D.); SILVA (T. S.)</AU><AF>Universidade Federal Rural da Amazônia, Programa de Pós-Graduação em Ciências Florestais/Belém, Pará/Brésil (1 aut., 3 aut.); IRD, Maison de la télédétection - MTD IRD/Unité ESPACE- U 140/34093 Montpellier/France (2 aut.)</AF><DT>Publication en série; Papier de recherche; Niveau analytique</DT><SO>Weed research : (Print); ISSN 0043-1737; Coden WEREAT; Royaume-Uni; Da. 2009; Vol. 49; No. 5; Pp. 499-505; Bibl. 1 p.1/4</SO><LA>Anglais</LA><EA>The objective of this study was to compare the floristic composition and species diversity existing in the seedbanks of forests and pastures. The seedbanks were sampled in three forest and three pastures areas in a community of smallholder farmers, in Pará state, Brazil. Seedling emergence in a glasshouse was used to quantify and identify the seeds. The total densities and diversity of the seedbanks were not significantly different among the pastures and forests, but the floristic composition was different. The herbaceous species predominated in both the pastures and the forests, but in the forest the abundance of shrub and tree was higher than herb. The seed density of several pioneer woody species was higher in the forests and the density of several herbaceous species was greater in the pastures. The influence of the forest species on the pastures and of the pastures species on the forests is a result of the initial process of human occupation and illustrates a dynamic that can lead to both the conservation of forest species and the spread of weed species. Actions should be carried out to avoid disturbance in the forests and improve biodiversity preservation in rural areas.</EA><CC>002A34H</CC><FD>Pâture; Potentiel semencier; Petite exploitation agricole; Zone tropicale; Diversité espèces; Densité; Espèce; Régénération; Malherbologie; Echelle petite</FD><FG>Exploitation agricole; Diversité biologique</FG><ED>Pasture; Seed bank; Small farms; Tropical zone; Species diversity; Density; Species; Regeneration; Weed science; Small scale</ED><EG>Farming; Biodiversity</EG><SD>Pastizal; Banco de semillas; Explotación en pequeña escala; Zona tropical; Diversidad especies; Densidad; Especie; Regeneración; Ciencia malas hierbas; Escala pequeña</SD><LO>INIST-12168.354000187618590060</LO><ID>09-0385469</ID></server></inist></record>
000D55	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">The triple system HIP 96515: a low-mass eclipsing binary with a DB white dwarf companion</title><author><name sortKey="Huelamo, N" uniqKey="Huelamo N">N. Huelamo</name><affiliation><inist:fA14 i1="01"><s1>LAEX-CAB (INTA-CSIC); Postal address: LAEFF, PO Box 78, 28691 Villanueva de la Cañada</s1><s2>Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vaz, L P R" uniqKey="Vaz L">L. P. R. Vaz</name><affiliation><inist:fA14 i1="02"><s1>Depto. de Fisica, Universidade Federal de Minas Gerais, C.P.702</s1><s2>30161-970 - Belo Horizonte, MG</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Torres, C A O" uniqKey="Torres C">C. A. O. Torres</name><affiliation><inist:fA14 i1="03"><s1>Laboratório Nacional de Astrofísica/MCT, Rua Estados Unidos 154</s1><s2>37504-364 Itajubá</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bergeron, P" uniqKey="Bergeron P">P. Bergeron</name><affiliation><inist:fA14 i1="04"><s1>Département de Physique, Université de Montréal, C.P. 6128, Succ. Centre-Ville</s1><s2>Montréal, Québec H3C 3J7</s2><s3>CAN</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Melo, C H F" uniqKey="Melo C">C. H. F. Melo</name><affiliation><inist:fA14 i1="05"><s1>European Southern Observatory, Karl-Schwarzschild-Strasse 2</s1><s2>85748 Garching bei Muenchen</s2><s3>DEU</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Quast, G R" uniqKey="Quast G">G. R. Quast</name><affiliation><inist:fA14 i1="03"><s1>Laboratório Nacional de Astrofísica/MCT, Rua Estados Unidos 154</s1><s2>37504-364 Itajubá</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Barrado Y Navascues, D" uniqKey="Barrado Y Navascues D">D. Barrado Y Navascues</name><affiliation><inist:fA14 i1="01"><s1>LAEX-CAB (INTA-CSIC); Postal address: LAEFF, PO Box 78, 28691 Villanueva de la Cañada</s1><s2>Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sterzik, M F" uniqKey="Sterzik M">M. F. Sterzik</name><affiliation><inist:fA14 i1="06"><s1>European Southern Observatory, Alonso de Cordova 3107, Casilla 19</s1><s2>Santiago</s2><s3>CHL</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chauvin, G" uniqKey="Chauvin G">G. Chauvin</name><affiliation><inist:fA14 i1="07"><s1>Laboratoire d'Astrophysique, Observatoire de Grenoble, BP 53</s1><s2>38041 Grenoble</s2><s3>FRA</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bouy, H" uniqKey="Bouy H">H. Bouy</name><affiliation><inist:fA14 i1="08"><s1>Instituto de Astrofísica de Canarias, C Via Láctea, s/n, E38205 - La Laguna (Tenerife)</s1><s3>ESP</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Landin, N R" uniqKey="Landin N">N. R. Landin</name><affiliation><inist:fA14 i1="02"><s1>Depto. de Fisica, Universidade Federal de Minas Gerais, C.P.702</s1><s2>30161-970 - Belo Horizonte, MG</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0386273</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0386273 INIST</idno><idno type="RBID">Pascal:09-0386273</idno><idno type="wicri:Area/Main/Corpus">001C26</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Age</term><term>Astrometry</term><term>Astronomical catalogues</term><term>Color</term><term>Dwarf stars</term><term>Eclipsing binary stars</term><term>Infrared observation</term><term>Light curves</term><term>Mass ratio</term><term>Models</term><term>Optical spectrum</term><term>Periodic variations</term><term>Photometric observation</term><term>Proper motion</term><term>Spectroscopic binary stars</term><term>Spectroscopical observation</term><term>White dwarf stars</term><term>Young stars</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Binaire éclipse</term><term>Naine blanche</term><term>Binaire spectroscopique</term><term>Catalogue astronomique</term><term>Etoile jeune</term><term>Couleur</term><term>Observation spectroscopique</term><term>Observation photométrique</term><term>Mouvement propre</term><term>Astrométrie</term><term>Observation IR</term><term>Spectre optique</term><term>Rapport masse</term><term>Courbe lumière</term><term>Variation périodique</term><term>Modèle</term><term>Age</term><term>Etoile naine</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Context. HIP 96515 A is a double-lined spectroscopic binary included in the SACY catalog as a potential young star. It has a visual companion (CCDM 19371-5134 B, HIP 96515 B) at 8&#34;.6. If bound to the primary, the optical and infrared colors of this wide companion are consistent with those of a white dwarf. Aims. We attempt to characterize the system HIP 96515 A&#38;B by studying each of its components. Methods. We analyzed spectroscopic and photometric observations of HIP 96515 A and its visual companion, HIP 96515 B. To confirm the system as a common proper-motion pair, we analyzed the astrometry of the components using high-angular resolution infrared observations obtained within a time span of two years, and archival astrometry. Results. The high-resolution optical spectrum of HIP 96515 A was used to derive a mass ratio, M<sub>2/</sub>M<sub>1</sub>, close to 0.9. The optical lightcurve of HIP 96515 A shows periodic variations with P<sub>orbital</sub> = 2.3456 days, revealing that HIP 96515 A is an eclipsing binary with preliminary orbital parameters of i = 89°.0 ± 0°.2, and M<sub>1</sub> = 0.59 ± 0.03 M<sub>◦.</sub> and M<sub>2</sub> = 0.54 ± 0.03 M<sub>◦.</sub>, for the primary and secondary, respectively, at an estimated distance of 42 ± 3 pc. This is a new eclipsing binary with component masses below 0.6 M<sub>◦.</sub>. Multi-epoch observations of HIP 96515 A&#38;B show that the system is a common proper-motion pair. The optical spectrum of HIP 96515 B is consistent with a pure helium atmosphere (DB) white dwarf. The comparison with evolutionary cooling sequence models provides T<sub>eff,wD</sub> = 19 126 ± 195 K, log g<sub>wD</sub> = 8.08, M<sub>WD/</sub>M<sub>◦.</sub> = 0.6, and a distance of ˜46 pc. The estimated WD cooling age its ˜ 100 Myr and the total age of the object (including the main-sequence phase) is ˜400 Myr. Finally, if HIP 96515 A&#38;B are coeval, and assuming a common age of ˜400 Myr, the comparison of the masses of the eclipsing binary members with evolutionary tracks shows that they are underestimated by ˜15% and 10%, for the primary and secondary, respectively.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>503</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>The triple system HIP 96515: a low-mass eclipsing binary with a DB white dwarf companion</s1></fA08><fA11 i1="01" i2="1"><s1>HUELAMO (N.)</s1></fA11><fA11 i1="02" i2="1"><s1>VAZ (L. P. R.)</s1></fA11><fA11 i1="03" i2="1"><s1>TORRES (C. A. O.)</s1></fA11><fA11 i1="04" i2="1"><s1>BERGERON (P.)</s1></fA11><fA11 i1="05" i2="1"><s1>MELO (C. H. F.)</s1></fA11><fA11 i1="06" i2="1"><s1>QUAST (G. R.)</s1></fA11><fA11 i1="07" i2="1"><s1>BARRADO Y NAVASCUES (D.)</s1></fA11><fA11 i1="08" i2="1"><s1>STERZIK (M. F.)</s1></fA11><fA11 i1="09" i2="1"><s1>CHAUVIN (G.)</s1></fA11><fA11 i1="10" i2="1"><s1>BOUY (H.)</s1></fA11><fA11 i1="11" i2="1"><s1>LANDIN (N. R.)</s1></fA11><fA14 i1="01"><s1>LAEX-CAB (INTA-CSIC); Postal address: LAEFF, PO Box 78, 28691 Villanueva de la Cañada</s1><s2>Madrid</s2><s3>ESP</s3><sZ>1 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Depto. de Fisica, Universidade Federal de Minas Gerais, C.P.702</s1><s2>30161-970 - Belo Horizonte, MG</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratório Nacional de Astrofísica/MCT, Rua Estados Unidos 154</s1><s2>37504-364 Itajubá</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="04"><s1>Département de Physique, Université de Montréal, C.P. 6128, Succ. Centre-Ville</s1><s2>Montréal, Québec H3C 3J7</s2><s3>CAN</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>European Southern Observatory, Karl-Schwarzschild-Strasse 2</s1><s2>85748 Garching bei Muenchen</s2><s3>DEU</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>European Southern Observatory, Alonso de Cordova 3107, Casilla 19</s1><s2>Santiago</s2><s3>CHL</s3><sZ>8 aut.</sZ></fA14><fA14 i1="07"><s1>Laboratoire d'Astrophysique, Observatoire de Grenoble, BP 53</s1><s2>38041 Grenoble</s2><s3>FRA</s3><sZ>9 aut.</sZ></fA14><fA14 i1="08"><s1>Instituto de Astrofísica de Canarias, C Via Láctea, s/n, E38205 - La Laguna (Tenerife)</s1><s3>ESP</s3><sZ>10 aut.</sZ></fA14><fA20><s1>873-881</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000171032020240</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0386273</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>Context. HIP 96515 A is a double-lined spectroscopic binary included in the SACY catalog as a potential young star. It has a visual companion (CCDM 19371-5134 B, HIP 96515 B) at 8&#34;.6. If bound to the primary, the optical and infrared colors of this wide companion are consistent with those of a white dwarf. Aims. We attempt to characterize the system HIP 96515 A&#38;B by studying each of its components. Methods. We analyzed spectroscopic and photometric observations of HIP 96515 A and its visual companion, HIP 96515 B. To confirm the system as a common proper-motion pair, we analyzed the astrometry of the components using high-angular resolution infrared observations obtained within a time span of two years, and archival astrometry. Results. The high-resolution optical spectrum of HIP 96515 A was used to derive a mass ratio, M<sub>2/</sub>M<sub>1</sub>, close to 0.9. The optical lightcurve of HIP 96515 A shows periodic variations with P<sub>orbital</sub> = 2.3456 days, revealing that HIP 96515 A is an eclipsing binary with preliminary orbital parameters of i = 89°.0 ± 0°.2, and M<sub>1</sub> = 0.59 ± 0.03 M<sub>◦.</sub> and M<sub>2</sub> = 0.54 ± 0.03 M<sub>◦.</sub>, for the primary and secondary, respectively, at an estimated distance of 42 ± 3 pc. This is a new eclipsing binary with component masses below 0.6 M<sub>◦.</sub>. Multi-epoch observations of HIP 96515 A&#38;B show that the system is a common proper-motion pair. The optical spectrum of HIP 96515 B is consistent with a pure helium atmosphere (DB) white dwarf. The comparison with evolutionary cooling sequence models provides T<sub>eff,wD</sub> = 19 126 ± 195 K, log g<sub>wD</sub> = 8.08, M<sub>WD/</sub>M<sub>◦.</sub> = 0.6, and a distance of ˜46 pc. The estimated WD cooling age its ˜ 100 Myr and the total age of the object (including the main-sequence phase) is ˜400 Myr. Finally, if HIP 96515 A&#38;B are coeval, and assuming a common age of ˜400 Myr, the comparison of the masses of the eclipsing binary members with evolutionary tracks shows that they are underestimated by ˜15% and 10%, for the primary and secondary, respectively.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Binaire éclipse</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Eclipsing binary stars</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Naine blanche</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>White dwarf stars</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Binaire spectroscopique</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Spectroscopic binary stars</s0><s5>28</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Catalogue astronomique</s0><s5>29</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Astronomical catalogues</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Etoile jeune</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Young stars</s0><s5>30</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Couleur</s0><s5>31</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Color</s0><s5>31</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Observation spectroscopique</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Spectroscopical observation</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Observación espectroscópica</s0><s5>32</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Observation photométrique</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Photometric observation</s0><s5>33</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Observación fotométrica</s0><s5>33</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Mouvement propre</s0><s5>34</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Proper motion</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Astrométrie</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Astrometry</s0><s5>35</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Observation IR</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Infrared observation</s0><s5>36</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Observación IR</s0><s5>36</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Spectre optique</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Optical spectrum</s0><s5>37</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Espectro óptico</s0><s5>37</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Rapport masse</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Mass ratio</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Relación masa</s0><s5>38</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Courbe lumière</s0><s5>39</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Light curves</s0><s5>39</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>Variation périodique</s0><s5>40</s5></fC03><fC03 i1="15" i2="3" l="ENG"><s0>Periodic variations</s0><s5>40</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Modèle</s0><s5>41</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Models</s0><s5>41</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Modelo</s0><s5>41</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Age</s0><s5>42</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Age</s0><s5>42</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Edad</s0><s5>42</s5></fC03><fC03 i1="18" i2="3" l="FRE"><s0>Etoile naine</s0><s5>43</s5></fC03><fC03 i1="18" i2="3" l="ENG"><s0>Dwarf stars</s0><s5>43</s5></fC03><fN21><s1>278</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0386273 INIST</NO><ET>The triple system HIP 96515: a low-mass eclipsing binary with a DB white dwarf companion</ET><AU>HUELAMO (N.); VAZ (L. P. R.); TORRES (C. A. O.); BERGERON (P.); MELO (C. H. F.); QUAST (G. R.); BARRADO Y NAVASCUES (D.); STERZIK (M. F.); CHAUVIN (G.); BOUY (H.); LANDIN (N. R.)</AU><AF>LAEX-CAB (INTA-CSIC); Postal address: LAEFF, PO Box 78, 28691 Villanueva de la Cañada/Madrid/Espagne (1 aut., 7 aut.); Depto. de Fisica, Universidade Federal de Minas Gerais, C.P.702/30161-970 - Belo Horizonte, MG/Brésil (2 aut., 11 aut.); Laboratório Nacional de Astrofísica/MCT, Rua Estados Unidos 154/37504-364 Itajubá/Brésil (3 aut., 6 aut.); Département de Physique, Université de Montréal, C.P. 6128, Succ. Centre-Ville/Montréal, Québec H3C 3J7/Canada (4 aut.); European Southern Observatory, Karl-Schwarzschild-Strasse 2/85748 Garching bei Muenchen/Allemagne (5 aut.); European Southern Observatory, Alonso de Cordova 3107, Casilla 19/Santiago/Chili (8 aut.); Laboratoire d'Astrophysique, Observatoire de Grenoble, BP 53/38041 Grenoble/France (9 aut.); Instituto de Astrofísica de Canarias, C Via Láctea, s/n, E38205 - La Laguna (Tenerife)/Espagne (10 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 503; No. 3; Pp. 873-881; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Context. HIP 96515 A is a double-lined spectroscopic binary included in the SACY catalog as a potential young star. It has a visual companion (CCDM 19371-5134 B, HIP 96515 B) at 8&#34;.6. If bound to the primary, the optical and infrared colors of this wide companion are consistent with those of a white dwarf. Aims. We attempt to characterize the system HIP 96515 A&#38;B by studying each of its components. Methods. We analyzed spectroscopic and photometric observations of HIP 96515 A and its visual companion, HIP 96515 B. To confirm the system as a common proper-motion pair, we analyzed the astrometry of the components using high-angular resolution infrared observations obtained within a time span of two years, and archival astrometry. Results. The high-resolution optical spectrum of HIP 96515 A was used to derive a mass ratio, M<sub>2/</sub>M<sub>1</sub>, close to 0.9. The optical lightcurve of HIP 96515 A shows periodic variations with P<sub>orbital</sub> = 2.3456 days, revealing that HIP 96515 A is an eclipsing binary with preliminary orbital parameters of i = 89°.0 ± 0°.2, and M<sub>1</sub> = 0.59 ± 0.03 M<sub>◦.</sub> and M<sub>2</sub> = 0.54 ± 0.03 M<sub>◦.</sub>, for the primary and secondary, respectively, at an estimated distance of 42 ± 3 pc. This is a new eclipsing binary with component masses below 0.6 M<sub>◦.</sub>. Multi-epoch observations of HIP 96515 A&#38;B show that the system is a common proper-motion pair. The optical spectrum of HIP 96515 B is consistent with a pure helium atmosphere (DB) white dwarf. The comparison with evolutionary cooling sequence models provides T<sub>eff,wD</sub> = 19 126 ± 195 K, log g<sub>wD</sub> = 8.08, M<sub>WD/</sub>M<sub>◦.</sub> = 0.6, and a distance of ˜46 pc. The estimated WD cooling age its ˜ 100 Myr and the total age of the object (including the main-sequence phase) is ˜400 Myr. Finally, if HIP 96515 A&#38;B are coeval, and assuming a common age of ˜400 Myr, the comparison of the masses of the eclipsing binary members with evolutionary tracks shows that they are underestimated by ˜15% and 10%, for the primary and secondary, respectively.</EA><CC>001E03</CC><FD>Binaire éclipse; Naine blanche; Binaire spectroscopique; Catalogue astronomique; Etoile jeune; Couleur; Observation spectroscopique; Observation photométrique; Mouvement propre; Astrométrie; Observation IR; Spectre optique; Rapport masse; Courbe lumière; Variation périodique; Modèle; Age; Etoile naine</FD><ED>Eclipsing binary stars; White dwarf stars; Spectroscopic binary stars; Astronomical catalogues; Young stars; Color; Spectroscopical observation; Photometric observation; Proper motion; Astrometry; Infrared observation; Optical spectrum; Mass ratio; Light curves; Periodic variations; Models; Age; Dwarf stars</ED><SD>Observación espectroscópica; Observación fotométrica; Observación IR; Espectro óptico; Relación masa; Modelo; Edad</SD><LO>INIST-14176.354000171032020240</LO><ID>09-0386273</ID></server></inist></record>
000D56	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Smooth Karhunen-Loève decomposition to analyze randomly vibrating systems</title><author><name sortKey="Bellizzi, S" uniqKey="Bellizzi S">S. Bellizzi</name><affiliation><inist:fA14 i1="01"><s1>Laboratoire de Mécanique et d'Acoustique, CNRS, 31 chemin Joseph Aiguier</s1><s2>13402 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sampaio, R" uniqKey="Sampaio R">R. Sampaio</name><affiliation><inist:fA14 i1="02"><s1>Department of Mechanical Engineering, PUC-Rio. Rua Marquês de São Vicente 225</s1><s2>Rio de Janeiro, RJ 22453-900</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0386491</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0386491 INIST</idno><idno type="RBID">Pascal:09-0386491</idno><idno type="wicri:Area/Main/Corpus">001C25</idno></publicationStmt><seriesStmt><idno type="ISSN">0022-460X</idno><title level="j" type="abbreviated">J. sound vib.</title><title level="j" type="main">Journal of sound and vibration</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Covariance matrix</term><term>Eigenmode</term><term>Karhunen Loeve transformation</term><term>Modal analysis</term><term>Probabilistic approach</term><term>Random excitation</term><term>Random matrix</term><term>Random vibration</term><term>White noise</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Excitation aléatoire</term><term>Vibration aléatoire</term><term>Mode propre</term><term>Transformation Karhunen Loeve</term><term>Approche probabiliste</term><term>Matrice covariance</term><term>Matrice aléatoire</term><term>Analyse modale</term><term>Bruit blanc</term><term>.</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">This paper deals with the application of smooth Karhunen-Loève decomposition (SKLD) procedure applied to random fields. The SKLD is obtained by solving a generalized eigenproblem defined by combining the covariance matrix of the random field with that of the associated time-derivative random field. The main properties of the SKLD procedure thus obtained are described and compared with the classical Karhunen--Loève decomposition. The SKLD is then applied to the responses of randomly excited vibrating systems in order to perform modal analysis. The resulting SKLD characteristics are discussed, in the case of linear vibrating systems subjected to white noise excitation, in terms of normal modes.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0022-460X</s0></fA01><fA02 i1="01"><s0>JSVIAG</s0></fA02><fA03 i2="1"><s0>J. sound vib.</s0></fA03><fA05><s2>325</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Smooth Karhunen-Loève decomposition to analyze randomly vibrating systems</s1></fA08><fA11 i1="01" i2="1"><s1>BELLIZZI (S.)</s1></fA11><fA11 i1="02" i2="1"><s1>SAMPAIO (R.)</s1></fA11><fA14 i1="01"><s1>Laboratoire de Mécanique et d'Acoustique, CNRS, 31 chemin Joseph Aiguier</s1><s2>13402 Marseille</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Mechanical Engineering, PUC-Rio. Rua Marquês de São Vicente 225</s1><s2>Rio de Janeiro, RJ 22453-900</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>491-498</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>11530</s2><s5>354000187255400010</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>20 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0386491</s0></fA47><fA60><s1>P</s1><s3>CC</s3></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of sound and vibration</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>This paper deals with the application of smooth Karhunen-Loève decomposition (SKLD) procedure applied to random fields. The SKLD is obtained by solving a generalized eigenproblem defined by combining the covariance matrix of the random field with that of the associated time-derivative random field. The main properties of the SKLD procedure thus obtained are described and compared with the classical Karhunen--Loève decomposition. The SKLD is then applied to the responses of randomly excited vibrating systems in order to perform modal analysis. The resulting SKLD characteristics are discussed, in the case of linear vibrating systems subjected to white noise excitation, in terms of normal modes.</s0></fC01><fC02 i1="01" i2="X"><s0>001B40F30M</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Excitation aléatoire</s0><s5>06</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Random excitation</s0><s5>06</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Excitación aleatoria</s0><s5>06</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Vibration aléatoire</s0><s5>07</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Random vibration</s0><s5>07</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Vibración aleatoria</s0><s5>07</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Mode propre</s0><s5>08</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Eigenmode</s0><s5>08</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Modo propio</s0><s5>08</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Transformation Karhunen Loeve</s0><s5>23</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Karhunen Loeve transformation</s0><s5>23</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Transformación Karhunen Loeve</s0><s5>23</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Approche probabiliste</s0><s5>24</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Probabilistic approach</s0><s5>24</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Enfoque probabilista</s0><s5>24</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Matrice covariance</s0><s5>25</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Covariance matrix</s0><s5>25</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Matriz covariancia</s0><s5>25</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Matrice aléatoire</s0><s5>26</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Random matrix</s0><s5>26</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Matriz aleatoria</s0><s5>26</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Analyse modale</s0><s5>27</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Modal analysis</s0><s5>27</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Análisis modal</s0><s5>27</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Bruit blanc</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>White noise</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Ruido blanco</s0><s5>33</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>.</s0><s4>INC</s4><s5>82</s5></fC03><fN21><s1>278</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0386491 INIST</NO><ET>Smooth Karhunen-Loève decomposition to analyze randomly vibrating systems</ET><AU>BELLIZZI (S.); SAMPAIO (R.)</AU><AF>Laboratoire de Mécanique et d'Acoustique, CNRS, 31 chemin Joseph Aiguier/13402 Marseille/France (1 aut.); Department of Mechanical Engineering, PUC-Rio. Rua Marquês de São Vicente 225/Rio de Janeiro, RJ 22453-900/Brésil (2 aut.)</AF><DT>Publication en série; Courte communication, note brève; Niveau analytique</DT><SO>Journal of sound and vibration; ISSN 0022-460X; Coden JSVIAG; Royaume-Uni; Da. 2009; Vol. 325; No. 3; Pp. 491-498; Bibl. 20 ref.</SO><LA>Anglais</LA><EA>This paper deals with the application of smooth Karhunen-Loève decomposition (SKLD) procedure applied to random fields. The SKLD is obtained by solving a generalized eigenproblem defined by combining the covariance matrix of the random field with that of the associated time-derivative random field. The main properties of the SKLD procedure thus obtained are described and compared with the classical Karhunen--Loève decomposition. The SKLD is then applied to the responses of randomly excited vibrating systems in order to perform modal analysis. The resulting SKLD characteristics are discussed, in the case of linear vibrating systems subjected to white noise excitation, in terms of normal modes.</EA><CC>001B40F30M</CC><FD>Excitation aléatoire; Vibration aléatoire; Mode propre; Transformation Karhunen Loeve; Approche probabiliste; Matrice covariance; Matrice aléatoire; Analyse modale; Bruit blanc; .</FD><ED>Random excitation; Random vibration; Eigenmode; Karhunen Loeve transformation; Probabilistic approach; Covariance matrix; Random matrix; Modal analysis; White noise</ED><SD>Excitación aleatoria; Vibración aleatoria; Modo propio; Transformación Karhunen Loeve; Enfoque probabilista; Matriz covariancia; Matriz aleatoria; Análisis modal; Ruido blanco</SD><LO>INIST-11530.354000187255400010</LO><ID>09-0386491</ID></server></inist></record>
000D57	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">In vitro and in vivo studies of 6,8-(diaryl)imidazo[1,2-a]pyrazin-3(7H)-ones as new antioxidants</title><author><name sortKey="De Wael, Frederic" uniqKey="De Wael F">Frederic De Wael</name><affiliation><inist:fA14 i1="01"><s1>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jeanjot, Paul" uniqKey="Jeanjot P">Paul Jeanjot</name><affiliation><inist:fA14 i1="01"><s1>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Moens, Cedric" uniqKey="Moens C">Cédric Moens</name><affiliation><inist:fA14 i1="01"><s1>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Institut des Sciences de la vie, Université catholique de Louvain, Bâtiment Camoy, Place Croix du Sud 5</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Verbeuren, Tony" uniqKey="Verbeuren T">Tony Verbeuren</name><affiliation><inist:fA14 i1="03"><s1>Institut de Recherches Servier, Rue des Moulineaux 11</s1><s2>92150 Suresnes</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cordi, Alex" uniqKey="Cordi A">Alex Cordi</name><affiliation><inist:fA14 i1="03"><s1>Institut de Recherches Servier, Rue des Moulineaux 11</s1><s2>92150 Suresnes</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bouskela, Eliete" uniqKey="Bouskela E">Eliete Bouskela</name><affiliation><inist:fA14 i1="04"><s1>Laboratorio de Pesquisas em Microcirculaçao, Universidade do estado do Rio de Janeiro, Rua Sao Francisco Xavier 524</s1><s2>20550-013 Rio de Janeiro</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rees, Jean Francois" uniqKey="Rees J">Jean-François Rees</name><affiliation><inist:fA14 i1="02"><s1>Institut des Sciences de la vie, Université catholique de Louvain, Bâtiment Camoy, Place Croix du Sud 5</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Marchand Brynaert, Jacqueline" uniqKey="Marchand Brynaert J">Jacqueline Marchand-Brynaert</name><affiliation><inist:fA14 i1="01"><s1>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0387591</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0387591 INIST</idno><idno type="RBID">Pascal:09-0387591</idno><idno type="wicri:Area/Main/Corpus">001C24</idno></publicationStmt><seriesStmt><idno type="ISSN">0968-0896</idno><title level="j" type="abbreviated">Bioorg. med. chem.</title><title level="j" type="main">Bioorganic &#38; medicinal chemistry</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animal</term><term>Antioxidant</term><term>Biological activity</term><term>Chemical synthesis</term><term>Hamster</term><term>In vitro</term><term>In vivo</term><term>Ischemia reperfusion</term><term>Oxidation</term><term>Pyrazine derivatives</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>In vitro</term><term>In vivo</term><term>Antioxydant</term><term>Dérivé de la pyrazine</term><term>Ischémie reperfusion</term><term>Synthèse chimique</term><term>Oxydation</term><term>Activité biologique</term><term>Hamster</term><term>Animal</term><term>Imidazo[1,2-a]pyrazine dérivé</term><term>Imidazo[1,2-a]pyrazin-3-one dérivé</term><term>Imidazopyrazine</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A series of 5-aryl and 3,5-diaryl-2-amino-1,4-pyrazines and the derived imidazopyrazinones has been synthesized to study the chemical oxidative degradation of the bicyclic systems in vitro. Imidazopyrazinones mainly degraded following two independent pathways producing their precursors, namely aminopyrazines, and the corresponding amidopyrazines, respectively. Despite the fact that there is no influence of the substituent of the 3-aryl group on the ratio of the products aminopyrazine/amidopyrazine, diarylimidazopyrazinones and diarylaminopyrazines are good antioxidants in vivo. They protected against microvascular damages in ischemia/reperfusion with similar efficiencies.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0968-0896</s0></fA01><fA03 i2="1"><s0>Bioorg. med. chem.</s0></fA03><fA05><s2>17</s2></fA05><fA06><s2>13</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>In vitro and in vivo studies of 6,8-(diaryl)imidazo[1,2-a]pyrazin-3(7H)-ones as new antioxidants</s1></fA08><fA11 i1="01" i2="1"><s1>DE WAEL (Frederic)</s1></fA11><fA11 i1="02" i2="1"><s1>JEANJOT (Paul)</s1></fA11><fA11 i1="03" i2="1"><s1>MOENS (Cédric)</s1></fA11><fA11 i1="04" i2="1"><s1>VERBEUREN (Tony)</s1></fA11><fA11 i1="05" i2="1"><s1>CORDI (Alex)</s1></fA11><fA11 i1="06" i2="1"><s1>BOUSKELA (Eliete)</s1></fA11><fA11 i1="07" i2="1"><s1>REES (Jean-François)</s1></fA11><fA11 i1="08" i2="1"><s1>MARCHAND-BRYNAERT (Jacqueline)</s1></fA11><fA14 i1="01"><s1>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="02"><s1>Institut des Sciences de la vie, Université catholique de Louvain, Bâtiment Camoy, Place Croix du Sud 5</s1><s2>1348 Louvain-la-Neuve</s2><s3>BEL</s3><sZ>3 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Institut de Recherches Servier, Rue des Moulineaux 11</s1><s2>92150 Suresnes</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Laboratorio de Pesquisas em Microcirculaçao, Universidade do estado do Rio de Janeiro, Rua Sao Francisco Xavier 524</s1><s2>20550-013 Rio de Janeiro</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>4336-4344</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26564</s2><s5>354000188356040100</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA47 i1="01" i2="1"><s0>09-0387591</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Bioorganic &#38; medicinal chemistry</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fA99><s0>1/2 p. ref. et notes</s0></fA99><fC01 i1="01" l="ENG"><s0>A series of 5-aryl and 3,5-diaryl-2-amino-1,4-pyrazines and the derived imidazopyrazinones has been synthesized to study the chemical oxidative degradation of the bicyclic systems in vitro. Imidazopyrazinones mainly degraded following two independent pathways producing their precursors, namely aminopyrazines, and the corresponding amidopyrazines, respectively. Despite the fact that there is no influence of the substituent of the 3-aryl group on the ratio of the products aminopyrazine/amidopyrazine, diarylimidazopyrazinones and diarylaminopyrazines are good antioxidants in vivo. They protected against microvascular damages in ischemia/reperfusion with similar efficiencies.</s0></fC01><fC02 i1="01" i2="X"><s0>002B02N</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>In vitro</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>In vitro</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>In vitro</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>In vivo</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>In vivo</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>In vivo</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Antioxydant</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Antioxidant</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Antioxidante</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Dérivé de la pyrazine</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Pyrazine derivatives</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Pirazina derivado</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Ischémie reperfusion</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Ischemia reperfusion</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Isquemia reperfusión</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Synthèse chimique</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Chemical synthesis</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Síntesis química</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Oxydation</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Oxidation</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Oxidación</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Activité biologique</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Biological activity</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Actividad biológica</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Hamster</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Hamster</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Hamster</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Animal</s0><s5>33</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Animal</s0><s5>33</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Animal</s0><s5>33</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Imidazo[1,2-a]pyrazine dérivé</s0><s4>INC</s4><s5>76</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Imidazo[1,2-a]pyrazin-3-one dérivé</s0><s4>INC</s4><s5>77</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Imidazopyrazine</s0><s4>INC</s4><s5>91</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Rodentia</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Rodentia</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Rodentia</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Mammalia</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Mammalia</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Mammalia</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Vertebrata</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Vertebrata</s0><s2>NS</s2></fC07><fN21><s1>278</s1></fN21></pA></standard><server><NO>PASCAL 09-0387591 INIST</NO><ET>In vitro and in vivo studies of 6,8-(diaryl)imidazo[1,2-a]pyr azin-3(7H)-ones as new antioxidants</ET><AU>DE WAEL (Frederic); JEANJOT (Paul); MOENS (Cédric); VERBEUREN (Tony); CORDI (Alex); BOUSKELA (Eliete); REES (Jean-François); MARCHAND-BRYNAERT (Jacqueline)</AU><AF>Unité de Chimie Organique et Médicinale, Université catholique de Louvain, Bâtiment Lavoisier, Place Louis Pasteur 1/1348 Louvain-la-Neuve/Belgique (1 aut., 2 aut., 3 aut., 8 aut.); Institut des Sciences de la vie, Université catholique de Louvain, Bâtiment Camoy, Place Croix du Sud 5/1348 Louvain-la-Neuve/Belgique (3 aut., 7 aut.); Institut de Recherches Servier, Rue des Moulineaux 11/92150 Suresnes/France (4 aut., 5 aut.); Laboratorio de Pesquisas em Microcirculaçao, Universidade do estado do Rio de Janeiro, Rua Sao Francisco Xavier 524/20550-013 Rio de Janeiro/Brésil (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Bioorganic &#38; medicinal chemistry; ISSN 0968-0896; Royaume-Uni; Da. 2009; Vol. 17; No. 13; Pp. 4336-4344</SO><LA>Anglais</LA><EA>A series of 5-aryl and 3,5-diaryl-2-amino-1,4-pyrazines and the derived imidazopyrazinones has been synthesized to study the chemical oxidative degradation of the bicyclic systems in vitro. Imidazopyrazinones mainly degraded following two independent pathways producing their precursors, namely aminopyrazines, and the corresponding amidopyrazines, respectively. Despite the fact that there is no influence of the substituent of the 3-aryl group on the ratio of the products aminopyrazine/amidopyrazine, diarylimidazopyrazinones and diarylaminopyrazines are good antioxidants in vivo. They protected against microvascular damages in ischemia/reperfusion with similar efficiencies.</EA><CC>002B02N</CC><FD>In vitro; In vivo; Antioxydant; Dérivé de la pyrazine; Ischémie reperfusion; Synthèse chimique; Oxydation; Activité biologique; Hamster; Animal; Imidazo[1,2-a]pyrazine dérivé; Imidazo[1,2-a]pyrazin-3-one dérivé; Imidazopyrazine</FD><FG>Rodentia; Mammalia; Vertebrata</FG><ED>In vitro; In vivo; Antioxidant; Pyrazine derivatives; Ischemia reperfusion; Chemical synthesis; Oxidation; Biological activity; Hamster; Animal</ED><EG>Rodentia; Mammalia; Vertebrata</EG><SD>In vitro; In vivo; Antioxidante; Pirazina derivado; Isquemia reperfusión; Síntesis química; Oxidación; Actividad biológica; Hamster; Animal</SD><LO>INIST-26564.354000188356040100</LO><ID>09-0387591</ID></server></inist></record>
000D58	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">A COMPARATIVE ANALYSIS BETWEEN BRAZIL ANDTHE USA IN ETHANOL LOGISTICS</title><author><name sortKey="Taioli, Flavio" uniqKey="Taioli F">Flavio Taioli</name><affiliation><inist:fA14 i1="01"><s1>Universidade Ibirapuera</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Moutinho Dos Santos, Edmilson" uniqKey="Moutinho Dos Santos E">Edmilson Moutinho Dos Santos</name><affiliation><inist:fA14 i1="02"><s1>Universidade de Sao Paulo -IEE</s1><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Colin, Jacques" uniqKey="Colin J">Jacques Colin</name><affiliation><inist:fA14 i1="03"><s1>Université Aix-Marseille II -CRET-LOG</s1><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0387602</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0387602 INIST</idno><idno type="RBID">Pascal:09-0387602</idno><idno type="wicri:Area/Main/Corpus">001C23</idno></publicationStmt><seriesStmt><idno type="ISSN">0303-240X</idno><title level="j" type="abbreviated">Rev. énerg.</title><title level="j" type="main">Revue de l'énergie</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Biofuel</term><term>Brazil</term><term>Comparative study</term><term>Competitiveness</term><term>Economic impact</term><term>Economic importance</term><term>Ethanol</term><term>Industrial development</term><term>Logistics</term><term>Market penetration</term><term>Performance</term><term>Production</term><term>Technicoeconomic study</term><term>Transport</term><term>United States</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Biocarburant</term><term>Ethanol</term><term>Logistique</term><term>Transport</term><term>Performance</term><term>Etude technicoéconomique</term><term>Compétitivité</term><term>Etude comparative</term><term>Brésil</term><term>Etats-Unis</term><term>Impact économique</term><term>Production</term><term>Développement industriel</term><term>Pénétration marché</term><term>Importance économique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Après avoir souligné l'importance de la logistique dans le développement d'une nouvelle industrie, les auteurs présentent une analyse comparative concernant l'éthanol entre le Brésil et les états-Unis. La logistique américaine est la plus développée et la moins coûteuse du monde. L'utilisation de modes de transport diversifiés est un facteur essentiel pour réduire les coûts totaux en Amérique du Nord. À l'opposé, au Brésil, ces coûts sont très élevés parce que le pays dépend principalement du transport routier. De tels contextes logistiques ont des effets majeurs sur la croissance rapide de l'industrie de l'éthanol dans les deux États. Les barrières logistiques représentent les principaux obstacles pour l'expansion continue de la production d'éthanol. L'article décrit les caractéristiques importantes des logistiques américaine et brésilienne, montrant que celles qui visent aussi bien les marchés domestiques que les importations et exportations, ne sont pas susceptibles de soutenir la croissance industrielle à long terme. Les auteurs concluent en soulignant l'importance de la logistique à la fois pour développer l'industrie de l'éthanol au niveau mondial, et aussi pour réussir à transformer l'éthanol en une véritable ressource énergétique.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0303-240X</s0></fA01><fA02 i1="01"><s0>REEND7</s0></fA02><fA03 i2="1"><s0>Rev. énerg.</s0></fA03><fA06><s2>586</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>A COMPARATIVE ANALYSIS BETWEEN BRAZIL ANDTHE USA IN ETHANOL LOGISTICS</s1></fA08><fA11 i1="01" i2="1"><s1>TAIOLI (Flavio)</s1></fA11><fA11 i1="02" i2="1"><s1>MOUTINHO DOS SANTOS (Edmilson)</s1></fA11><fA11 i1="03" i2="1"><s1>COLIN (Jacques)</s1></fA11><fA14 i1="01"><s1>Universidade Ibirapuera</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Universidade de Sao Paulo -IEE</s1><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Université Aix-Marseille II -CRET-LOG</s1><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA20><s2>352, 371-382 [13 p.]</s2></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>7701</s2><s5>354000184135190030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0387602</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Revue de l'énergie</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>Après avoir souligné l'importance de la logistique dans le développement d'une nouvelle industrie, les auteurs présentent une analyse comparative concernant l'éthanol entre le Brésil et les états-Unis. La logistique américaine est la plus développée et la moins coûteuse du monde. L'utilisation de modes de transport diversifiés est un facteur essentiel pour réduire les coûts totaux en Amérique du Nord. À l'opposé, au Brésil, ces coûts sont très élevés parce que le pays dépend principalement du transport routier. De tels contextes logistiques ont des effets majeurs sur la croissance rapide de l'industrie de l'éthanol dans les deux États. Les barrières logistiques représentent les principaux obstacles pour l'expansion continue de la production d'éthanol. L'article décrit les caractéristiques importantes des logistiques américaine et brésilienne, montrant que celles qui visent aussi bien les marchés domestiques que les importations et exportations, ne sont pas susceptibles de soutenir la croissance industrielle à long terme. Les auteurs concluent en soulignant l'importance de la logistique à la fois pour développer l'industrie de l'éthanol au niveau mondial, et aussi pour réussir à transformer l'éthanol en une véritable ressource énergétique.</s0></fC01><fC02 i1="01" i2="X"><s0>001D06A01C5</s0></fC02><fC02 i1="02" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Biocarburant</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Biofuel</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Biocarburante</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Ethanol</s0><s2>NK</s2><s2>FR</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Ethanol</s0><s2>NK</s2><s2>FR</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Etanol</s0><s2>NK</s2><s2>FR</s2><s2>FX</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Logistique</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Logistics</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Logística</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Transport</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Transport</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Transporte</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Performance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Performance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Rendimiento</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Etude technicoéconomique</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Technicoeconomic study</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Estudio técnicoeconómico</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Compétitivité</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Competitiveness</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Competitividad</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Etude comparative</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Comparative study</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Estudio comparativo</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Etats-Unis</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>United States</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estados Unidos</s0><s2>NG</s2><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Impact économique</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Economic impact</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Impacto económico</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Production</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Production</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Producción</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Développement industriel</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Industrial development</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Desarrollo industrial</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Pénétration marché</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Market penetration</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Penetración mercado</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Importance économique</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Economic importance</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Importancia económica</s0><s5>15</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Amérique du Nord</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>North America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>America del norte</s0><s2>NG</s2></fC07><fN21><s1>278</s1></fN21></pA></standard><server><NO>PASCAL 09-0387602 INIST</NO><ET>A COMPARATIVE ANALYSIS BETWEEN BRAZIL ANDTHE USA IN ETHANOL LOGISTICS</ET><AU>TAIOLI (Flavio); MOUTINHO DOS SANTOS (Edmilson); COLIN (Jacques)</AU><AF>Universidade Ibirapuera/Brésil (1 aut.); Universidade de Sao Paulo -IEE/Brésil (2 aut.); Université Aix-Marseille II -CRET-LOG/France (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Revue de l'énergie; ISSN 0303-240X; Coden REEND7; France; Da. 2008; No. 586; 352, 371-382 [13 p.]; Abs. français; Bibl. 1 p.</SO><LA>Anglais</LA><FA>Après avoir souligné l'importance de la logistique dans le développement d'une nouvelle industrie, les auteurs présentent une analyse comparative concernant l'éthanol entre le Brésil et les états-Unis. La logistique américaine est la plus développée et la moins coûteuse du monde. L'utilisation de modes de transport diversifiés est un facteur essentiel pour réduire les coûts totaux en Amérique du Nord. À l'opposé, au Brésil, ces coûts sont très élevés parce que le pays dépend principalement du transport routier. De tels contextes logistiques ont des effets majeurs sur la croissance rapide de l'industrie de l'éthanol dans les deux États. Les barrières logistiques représentent les principaux obstacles pour l'expansion continue de la production d'éthanol. L'article décrit les caractéristiques importantes des logistiques américaine et brésilienne, montrant que celles qui visent aussi bien les marchés domestiques que les importations et exportations, ne sont pas susceptibles de soutenir la croissance industrielle à long terme. Les auteurs concluent en soulignant l'importance de la logistique à la fois pour développer l'industrie de l'éthanol au niveau mondial, et aussi pour réussir à transformer l'éthanol en une véritable ressource énergétique.</FA><CC>001D06A01C5; 230</CC><FD>Biocarburant; Ethanol; Logistique; Transport; Performance; Etude technicoéconomique; Compétitivité; Etude comparative; Brésil; Etats-Unis; Impact économique; Production; Développement industriel; Pénétration marché; Importance économique</FD><FG>Amérique du Sud; Amérique; Amérique du Nord</FG><ED>Biofuel; Ethanol; Logistics; Transport; Performance; Technicoeconomic study; Competitiveness; Comparative study; Brazil; United States; Economic impact; Production; Industrial development; Market penetration; Economic importance</ED><EG>South America; America; North America</EG><SD>Biocarburante; Etanol; Logística; Transporte; Rendimiento; Estudio técnicoeconómico; Competitividad; Estudio comparativo; Brasil; Estados Unidos; Impacto económico; Producción; Desarrollo industrial; Penetración mercado; Importancia económica</SD><LO>INIST-7701.354000184135190030</LO><ID>09-0387602</ID></server></inist></record>
000D59	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Functional Phosphodiesterase 11 A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors</title><author><name sortKey="Horvath, Anelia" uniqKey="Horvath A">Anelia Horvath</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Korde, Larissa" uniqKey="Korde L">Larissa Korde</name><affiliation><inist:fA14 i1="02"><s1>Clinical Genetics Branch, National Cancer Institute</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Greene, Mark H" uniqKey="Greene M">Mark H. Greene</name><affiliation><inist:fA14 i1="02"><s1>Clinical Genetics Branch, National Cancer Institute</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Libe, Rossella" uniqKey="Libe R">Rossella Libe</name><affiliation><inist:fA14 i1="05"><s1>Institut National de la Sante et de la Recherche Medicale U567, and Institut Cochin, Centre National de laRecherche Scientifique UMR8104, Hôpital Cochin, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Osorio, Paulo" uniqKey="Osorio P">Paulo Osorio</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>Laboratory of Molecular Genetics, Pontificia Universidade Catolica do Parana</s1><s2>Curitiba</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rueda Faucez, Fabio" uniqKey="Rueda Faucez F">Fabio Rueda Faucez</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>Laboratory of Molecular Genetics, Pontificia Universidade Catolica do Parana</s1><s2>Curitiba</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Raffin Sanson, Marie Laure" uniqKey="Raffin Sanson M">Marie Laure Raffin-Sanson</name><affiliation><inist:fA14 i1="06"><s1>Institut National de la Sante et de la Recherche Medicale U567, Departement Endocrinologie, Metabolisme and Cancer, Institut Cochin, and Centre National de la Recherche Scientifique UMR8104</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="08"><s1>Hôpital Ambroise Paré, Department of Endocrinology</s1><s2>Boulogne sur Seine</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="09"><s1>Université de Versailles</s1><s2>St. Quentin en Yvelines</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name>KIT MAN TSANG</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Drori Herishanu, Limor" uniqKey="Drori Herishanu L">Limor Drori-Herishanu</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Patronas, Yianna" uniqKey="Patronas Y">Yianna Patronas</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Reamers, Elaine F" uniqKey="Reamers E">Elaine F. Reamers</name><affiliation><inist:fA14 i1="04"><s1>Genetics and Genomics Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Eleni Nikita, Maria" uniqKey="Eleni Nikita M">Maria Eleni Nikita</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Moran, Jason" uniqKey="Moran J">Jason Moran</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Greene, Joseph" uniqKey="Greene J">Joseph Greene</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nesterova, Maria" uniqKey="Nesterova M">Maria Nesterova</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Merino, Maria" uniqKey="Merino M">Maria Merino</name><affiliation><inist:fA14 i1="03"><s1>Laboratory of Pathology, National Cancer Institute</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>16 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bertherat, Jerome" uniqKey="Bertherat J">Jerome Bertherat</name><affiliation><inist:fA14 i1="05"><s1>Institut National de la Sante et de la Recherche Medicale U567, and Institut Cochin, Centre National de laRecherche Scientifique UMR8104, Hôpital Cochin, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Stratakis, Constantine A" uniqKey="Stratakis C">Constantine A. Stratakis</name><affiliation><inist:fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0389452</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0389452 INIST</idno><idno type="RBID">Pascal:09-0389452</idno><idno type="wicri:Area/Main/Corpus">001C22</idno></publicationStmt><seriesStmt><idno type="ISSN">0008-5472</idno><title level="j" type="abbreviated">Cancer res. : (Baltimore)</title><title level="j" type="main">Cancer research : (Baltimore)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bilateral</term><term>Genetics</term><term>Mutation</term><term>Risk factor</term><term>Testicle cancer</term><term>Testicular germ cell tumor</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Mutation</term><term>Génétique</term><term>Facteur risque</term><term>Bilatéral</term><term>Cancer du testicule</term><term>Tumeur germinale du testicule</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Inactivating germline mutations in phosphodiesterase 11A (PDE11A) have been implicated in adrenal tumor susceptibility. PDE11A is highly expressed in endocrine steroidogenic tissues, especially the testis, and mice with inactivated Pde11α exhibit male infertility, a known testicular germ cell tumor (TGCT) risk factor. We sequenced the PDE11A gene-coding region in 95 patients with TGCT from 64 unrelated kindreds. We identified 8 nonsynonymous substitutions in 20 patients from 15 families: four (R52T, F258Y, G291R, and V820M) were newly recognized, three (R804H, R867G, and M878V) were functional variants previously implicated in adrenal tumor predisposition, and one (Y727C) was a known polymorphism. We compared the frequency of these variants in our patients to unrelated controls that had been screened and found negative for any endocrine diseases: only the two previously reported variants, R804H and R867G, known to be frequent in general population, were detected in these controls. The frequency of all PDE11A-gene variants (combined) was significantly higher among patients with TGCT (P = 0.0002), present in 19% of the families of our cohort. Most variants were detected in the general population, but functional studies showed that all these mutations reduced PDE activity, and that PDE11A protein expression was decreased (or absent) in TGCT samples from carriers. This is the first demonstration of the involvement of a PDE gene in TGCT, although the cyclic AMP signaling pathway has been investigated extensively in reproductive organ function and their diseases. In conclusion, we report that PDE11A-inactivating sequence variants may modify the risk of familial and bilateral TGCT.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0008-5472</s0></fA01><fA02 i1="01"><s0>CNREA8</s0></fA02><fA03 i2="1"><s0>Cancer res. : (Baltimore)</s0></fA03><fA05><s2>69</s2></fA05><fA06><s2>13</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Functional Phosphodiesterase 11 A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors</s1></fA08><fA11 i1="01" i2="1"><s1>HORVATH (Anelia)</s1></fA11><fA11 i1="02" i2="1"><s1>KORDE (Larissa)</s1></fA11><fA11 i1="03" i2="1"><s1>GREENE (Mark H.)</s1></fA11><fA11 i1="04" i2="1"><s1>LIBE (Rossella)</s1></fA11><fA11 i1="05" i2="1"><s1>OSORIO (Paulo)</s1></fA11><fA11 i1="06" i2="1"><s1>RUEDA FAUCEZ (Fabio)</s1></fA11><fA11 i1="07" i2="1"><s1>RAFFIN-SANSON (Marie Laure)</s1></fA11><fA11 i1="08" i2="1"><s1>KIT MAN TSANG</s1></fA11><fA11 i1="09" i2="1"><s1>DRORI-HERISHANU (Limor)</s1></fA11><fA11 i1="10" i2="1"><s1>PATRONAS (Yianna)</s1></fA11><fA11 i1="11" i2="1"><s1>REAMERS (Elaine F.)</s1></fA11><fA11 i1="12" i2="1"><s1>ELENI NIKITA (Maria)</s1></fA11><fA11 i1="13" i2="1"><s1>MORAN (Jason)</s1></fA11><fA11 i1="14" i2="1"><s1>GREENE (Joseph)</s1></fA11><fA11 i1="15" i2="1"><s1>NESTEROVA (Maria)</s1></fA11><fA11 i1="16" i2="1"><s1>MERINO (Maria)</s1></fA11><fA11 i1="17" i2="1"><s1>BERTHERAT (Jerome)</s1></fA11><fA11 i1="18" i2="1"><s1>STRATAKIS (Constantine A.)</s1></fA11><fA14 i1="01"><s1>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>18 aut.</sZ></fA14><fA14 i1="02"><s1>Clinical Genetics Branch, National Cancer Institute</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratory of Pathology, National Cancer Institute</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>16 aut.</sZ></fA14><fA14 i1="04"><s1>Genetics and Genomics Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH</s1><s2>Bethesda, Maryland</s2><s3>USA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="05"><s1>Institut National de la Sante et de la Recherche Medicale U567, and Institut Cochin, Centre National de laRecherche Scientifique UMR8104, Hôpital Cochin, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>17 aut.</sZ></fA14><fA14 i1="06"><s1>Institut National de la Sante et de la Recherche Medicale U567, Departement Endocrinologie, Metabolisme and Cancer, Institut Cochin, and Centre National de la Recherche Scientifique UMR8104</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>Laboratory of Molecular Genetics, Pontificia Universidade Catolica do Parana</s1><s2>Curitiba</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="08"><s1>Hôpital Ambroise Paré, Department of Endocrinology</s1><s2>Boulogne sur Seine</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="09"><s1>Université de Versailles</s1><s2>St. Quentin en Yvelines</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA20><s1>5301-5306</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>5088</s2><s5>354000187642910060</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>20 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0389452</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Cancer research : (Baltimore)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Inactivating germline mutations in phosphodiesterase 11A (PDE11A) have been implicated in adrenal tumor susceptibility. PDE11A is highly expressed in endocrine steroidogenic tissues, especially the testis, and mice with inactivated Pde11α exhibit male infertility, a known testicular germ cell tumor (TGCT) risk factor. We sequenced the PDE11A gene-coding region in 95 patients with TGCT from 64 unrelated kindreds. We identified 8 nonsynonymous substitutions in 20 patients from 15 families: four (R52T, F258Y, G291R, and V820M) were newly recognized, three (R804H, R867G, and M878V) were functional variants previously implicated in adrenal tumor predisposition, and one (Y727C) was a known polymorphism. We compared the frequency of these variants in our patients to unrelated controls that had been screened and found negative for any endocrine diseases: only the two previously reported variants, R804H and R867G, known to be frequent in general population, were detected in these controls. The frequency of all PDE11A-gene variants (combined) was significantly higher among patients with TGCT (P = 0.0002), present in 19% of the families of our cohort. Most variants were detected in the general population, but functional studies showed that all these mutations reduced PDE activity, and that PDE11A protein expression was decreased (or absent) in TGCT samples from carriers. This is the first demonstration of the involvement of a PDE gene in TGCT, although the cyclic AMP signaling pathway has been investigated extensively in reproductive organ function and their diseases. In conclusion, we report that PDE11A-inactivating sequence variants may modify the risk of familial and bilateral TGCT.</s0></fC01><fC02 i1="01" i2="X"><s0>002B02R</s0></fC02><fC02 i1="02" i2="X"><s0>002B04</s0></fC02><fC02 i1="03" i2="X"><s0>002B20B02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Mutation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Mutation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Mutación</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Génétique</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Genetics</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Genética</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Facteur risque</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Risk factor</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Factor riesgo</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Bilatéral</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Bilateral</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Bilateral</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Cancer du testicule</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Testicle cancer</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Cáncer del testículo</s0><s2>NM</s2><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Tumeur germinale du testicule</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Testicular germ cell tumor</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Tumor germinal de testículo</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil génital mâle</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Male genital diseases</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Aparato genital macho patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie du testicule</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Testicular diseases</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Testículo patología</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Tumeur maligne</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Malignant tumor</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Tumor maligno</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fN21><s1>278</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0389452 INIST</NO><ET>Functional Phosphodiesterase 11 A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors</ET><AU>HORVATH (Anelia); KORDE (Larissa); GREENE (Mark H.); LIBE (Rossella); OSORIO (Paulo); RUEDA FAUCEZ (Fabio); RAFFIN-SANSON (Marie Laure); KIT MAN TSANG; DRORI-HERISHANU (Limor); PATRONAS (Yianna); REAMERS (Elaine F.); ELENI NIKITA (Maria); MORAN (Jason); GREENE (Joseph); NESTEROVA (Maria); MERINO (Maria); BERTHERAT (Jerome); STRATAKIS (Constantine A.)</AU><AF>Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development/Bethesda, Maryland/Etats-Unis (1 aut., 5 aut., 6 aut., 8 aut., 9 aut., 10 aut., 12 aut., 13 aut., 14 aut., 15 aut., 18 aut.); Clinical Genetics Branch, National Cancer Institute/Bethesda, Maryland/Etats-Unis (2 aut., 3 aut.); Laboratory of Pathology, National Cancer Institute/Bethesda, Maryland/Etats-Unis (16 aut.); Genetics and Genomics Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH/Bethesda, Maryland/Etats-Unis (11 aut.); Institut National de la Sante et de la Recherche Medicale U567, and Institut Cochin, Centre National de laRecherche Scientifique UMR8104, Hôpital Cochin, Université Paris Descartes/Paris/France (4 aut., 17 aut.); Institut National de la Sante et de la Recherche Medicale U567, Departement Endocrinologie, Metabolisme and Cancer, Institut Cochin, and Centre National de la Recherche Scientifique UMR8104/Paris/France (7 aut.); Laboratory of Molecular Genetics, Pontificia Universidade Catolica do Parana/Curitiba/Brésil (5 aut., 6 aut.); Hôpital Ambroise Paré, Department of Endocrinology/Boulogne sur Seine/France (7 aut.); Université de Versailles/St. Quentin en Yvelines/France (7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Cancer research : (Baltimore); ISSN 0008-5472; Coden CNREA8; Etats-Unis; Da. 2009; Vol. 69; No. 13; Pp. 5301-5306; Bibl. 20 ref.</SO><LA>Anglais</LA><EA>Inactivating germline mutations in phosphodiesterase 11A (PDE11A) have been implicated in adrenal tumor susceptibility. PDE11A is highly expressed in endocrine steroidogenic tissues, especially the testis, and mice with inactivated Pde11α exhibit male infertility, a known testicular germ cell tumor (TGCT) risk factor. We sequenced the PDE11A gene-coding region in 95 patients with TGCT from 64 unrelated kindreds. We identified 8 nonsynonymous substitutions in 20 patients from 15 families: four (R52T, F258Y, G291R, and V820M) were newly recognized, three (R804H, R867G, and M878V) were functional variants previously implicated in adrenal tumor predisposition, and one (Y727C) was a known polymorphism. We compared the frequency of these variants in our patients to unrelated controls that had been screened and found negative for any endocrine diseases: only the two previously reported variants, R804H and R867G, known to be frequent in general population, were detected in these controls. The frequency of all PDE11A-gene variants (combined) was significantly higher among patients with TGCT (P = 0.0002), present in 19% of the families of our cohort. Most variants were detected in the general population, but functional studies showed that all these mutations reduced PDE activity, and that PDE11A protein expression was decreased (or absent) in TGCT samples from carriers. This is the first demonstration of the involvement of a PDE gene in TGCT, although the cyclic AMP signaling pathway has been investigated extensively in reproductive organ function and their diseases. In conclusion, we report that PDE11A-inactivating sequence variants may modify the risk of familial and bilateral TGCT.</EA><CC>002B02R; 002B04; 002B20B02</CC><FD>Mutation; Génétique; Facteur risque; Bilatéral; Cancer du testicule; Tumeur germinale du testicule</FD><FG>Pathologie de l'appareil génital mâle; Pathologie du testicule; Tumeur maligne; Cancer</FG><ED>Mutation; Genetics; Risk factor; Bilateral; Testicle cancer; Testicular germ cell tumor</ED><EG>Male genital diseases; Testicular diseases; Malignant tumor; Cancer</EG><SD>Mutación; Genética; Factor riesgo; Bilateral; Cáncer del testículo; Tumor germinal de testículo</SD><LO>INIST-5088.354000187642910060</LO><ID>09-0389452</ID></server></inist></record>
000D60	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">New insights to the MLL recombinome of acute leukemias</title><author><name sortKey="Meyer, C" uniqKey="Meyer C">C. Meyer</name><affiliation><inist:fA14 i1="01"><s1>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt</s1><s2>Frankfurt/Main</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>52 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kowarz, E" uniqKey="Kowarz E">E. Kowarz</name><affiliation><inist:fA14 i1="01"><s1>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt</s1><s2>Frankfurt/Main</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>52 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hofmann, J" uniqKey="Hofmann J">J. Hofmann</name><affiliation><inist:fA14 i1="01"><s1>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt</s1><s2>Frankfurt/Main</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>52 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Renneville, A" uniqKey="Renneville A">A. Renneville</name><affiliation><inist:fA14 i1="02"><s1>Department of Hematology, Biology and Pathology Center, CHU of Lille</s1><s2>Lille</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>INSERM, U-837, Team 3</s1><s2>Lille</s2><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Zuna, J" uniqKey="Zuna J">J. Zuna</name><affiliation><inist:fA14 i1="04"><s1>CLIP, Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University Prague</s1><s2>Prague</s2><s3>CZE</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Trka, J" uniqKey="Trka J">J. Trka</name><affiliation><inist:fA14 i1="04"><s1>CLIP, Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University Prague</s1><s2>Prague</s2><s3>CZE</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ben Abdelaii, R" uniqKey="Ben Abdelaii R">R. Ben Abdelaii</name><affiliation><inist:fA14 i1="05"><s1>Biological Hematology, AP-HP Necker, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Macintyre, E" uniqKey="Macintyre E">E. Macintyre</name><affiliation><inist:fA14 i1="05"><s1>Biological Hematology, AP-HP Necker, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Braekeleer, E" uniqKey="De Braekeleer E">E. De Braekeleer</name><affiliation><inist:fA14 i1="06"><s1>Faculté de Médecine et des Sciences de la Santé, Laboratoire d'Histologie, Embryologie et Cytogénétique, Université de Bretagne Occidentale</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>INSERM-U613</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Braekeleer, M" uniqKey="De Braekeleer M">M. De Braekeleer</name><affiliation><inist:fA14 i1="06"><s1>Faculté de Médecine et des Sciences de la Santé, Laboratoire d'Histologie, Embryologie et Cytogénétique, Université de Bretagne Occidentale</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>INSERM-U613</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Delabesse, E" uniqKey="Delabesse E">E. Delabesse</name><affiliation><inist:fA14 i1="08"><s1>CHU Purpan, Laboratoire d'Hématologie</s1><s2>Toulouse</s2><s3>FRA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Oliveira, M P" uniqKey="De Oliveira M">M. P. De Oliveira</name><affiliation><inist:fA14 i1="09"><s1>Pediatric HematologyOncology Program, Research Center, Instituto Nacional de Cancer Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>12 aut.</sZ><sZ>50 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cave, H" uniqKey="Cave H">H. Cave</name><affiliation><inist:fA14 i1="10"><s1>Déparfemenf de Génétique, Hopital Robert Debré</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Clappier, E" uniqKey="Clappier E">E. Clappier</name><affiliation><inist:fA14 i1="10"><s1>Déparfemenf de Génétique, Hopital Robert Debré</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Van Dongen, Jjm" uniqKey="Van Dongen J">Jjm Van Dongen</name><affiliation><inist:fA14 i1="11"><s1>Department of Immunology, Erasmus MC, Sophia Children's Hospital</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Balgobind, B V" uniqKey="Balgobind B">B. V. Balgobind</name><affiliation><inist:fA14 i1="12"><s1>Department of Pediatric Oncology/Hematology, Erasmus MC, Sophia Children's Hospital</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Van Den Heuvel Eibrink, M M" uniqKey="Van Den Heuvel Eibrink M">M. M. Van Den Heuvel-Eibrink</name><affiliation><inist:fA14 i1="12"><s1>Department of Pediatric Oncology/Hematology, Erasmus MC, Sophia Children's Hospital</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Beverloo, H B" uniqKey="Beverloo H">H. B. Beverloo</name><affiliation><inist:fA14 i1="13"><s1>Department of Clinical Genetics, Erasmus MC</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Panzer Gr Mayer, R" uniqKey="Panzer Gr Mayer R">R. Panzer-Gr Mayer</name></author><author><name sortKey="Teigler Schlegel, A" uniqKey="Teigler Schlegel A">A. Teigler-Schlegel</name></author><author><name sortKey="Harbott, J" uniqKey="Harbott J">J. Harbott</name></author><author><name sortKey="Kjeldsen, E" uniqKey="Kjeldsen E">E. Kjeldsen</name></author><author><name sortKey="Schnittger, S" uniqKey="Schnittger S">S. Schnittger</name></author><author><name sortKey="Koehl, U" uniqKey="Koehl U">U. Koehl</name></author><author><name sortKey="Gruhn, B" uniqKey="Gruhn B">B. Gruhn</name></author><author><name sortKey="Heidenreich, O" uniqKey="Heidenreich O">O. Heidenreich</name></author><author><name sortKey="Chan, L C" uniqKey="Chan L">L. C. Chan</name></author><author><name sortKey="Yip, S F" uniqKey="Yip S">S. F. Yip</name></author><author><name sortKey="Krzywinski, M" uniqKey="Krzywinski M">M. Krzywinski</name></author><author><name sortKey="Eckert, C" uniqKey="Eckert C">C. Eckert</name></author><author><name sortKey="Moricke, A" uniqKey="Moricke A">A. Möricke</name></author><author><name sortKey="Schrappe, M" uniqKey="Schrappe M">M. Schrappe</name></author><author><name sortKey="Alonso, C N" uniqKey="Alonso C">C. N. Alonso</name></author><author><name sortKey="Sch Fer, B W" uniqKey="Sch Fer B">B. W. Sch Fer</name></author><author><name sortKey="Krauter, J" uniqKey="Krauter J">J. Krauter</name></author><author><name sortKey="Lee, D A" uniqKey="Lee D">D. A. Lee</name></author><author><name sortKey="Zur Stadt, U" uniqKey="Zur Stadt U">U. Zur Stadt</name></author><author><name sortKey="Te Kronnie, G" uniqKey="Te Kronnie G">G. Te Kronnie</name></author><author><name sortKey="Sutton, R" uniqKey="Sutton R">R. Sutton</name></author><author><name sortKey="Izraeli, S" uniqKey="Izraeli S">S. Izraeli</name></author><author><name sortKey="Trakhtenbrot, L" uniqKey="Trakhtenbrot L">L. Trakhtenbrot</name></author><author><name sortKey="Lo Nigro, L" uniqKey="Lo Nigro L">L. Lo Nigro</name></author><author><name sortKey="Tsaur, G" uniqKey="Tsaur G">G. Tsaur</name></author><author><name sortKey="Fechina, L" uniqKey="Fechina L">L. Fechina</name></author><author><name sortKey="Szczepanski, T" uniqKey="Szczepanski T">T. Szczepanski</name></author><author><name sortKey="Strehl, S" uniqKey="Strehl S">S. Strehl</name></author><author><name sortKey="Ilencikova, D" uniqKey="Ilencikova D">D. Ilencikova</name></author><author><name sortKey="Molkentin, M" uniqKey="Molkentin M">M. Molkentin</name></author><author><name sortKey="Burmeister, T" uniqKey="Burmeister T">T. Burmeister</name></author><author><name sortKey="Dingermann, T" uniqKey="Dingermann T">T. Dingermann</name><affiliation><inist:fA14 i1="09"><s1>Pediatric HematologyOncology Program, Research Center, Instituto Nacional de Cancer Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>12 aut.</sZ><sZ>50 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Klingebiel, T" uniqKey="Klingebiel T">T. Klingebiel</name></author><author><name sortKey="Marschalek, R" uniqKey="Marschalek R">R. Marschalek</name><affiliation><inist:fA14 i1="01"><s1>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt</s1><s2>Frankfurt/Main</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>52 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0389923</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0389923 INIST</idno><idno type="RBID">Pascal:09-0389923</idno><idno type="wicri:Area/Main/Corpus">001C21</idno></publicationStmt><seriesStmt><idno type="ISSN">0887-6924</idno><title level="j" type="abbreviated">Leukemia</title><title level="j" type="main">Leukemia</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acute leukemia</term><term>Acute lymphocytic leukemia</term><term>Acute myelogenous leukemia</term><term>C-Onc gene</term><term>Chromosome translocation</term><term>Gene rearrangement</term><term>Hematology</term><term>Human</term><term>Protooncogene</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Leucémie aiguë</term><term>Protooncogène</term><term>Gène onc cellulaire</term><term>Translocation chromosomique</term><term>Leucémie aiguë myéloblastique</term><term>Hématologie</term><term>Leucémie aiguë lymphoblastique</term><term>Réarrangement génique</term><term>Homme</term><term>Gène MLL</term><term>Gène partenaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Chromosomal rearrangements of the human MLL gene are associated with high-risk pediatric, adult and therapy-associated acute leukemias. These patients need to be identified, treated appropriately and minimal residual disease was monitored by quantitative PCR techniques. Genomic DNA was isolated from individual acute leukemia patients to identify and characterize chromosomal rearrangements involving the human MLL gene. A total of 760 MLL-rearranged biopsy samples obtained from 384 pediatric and 376 adult leukemia patients were characterized at the molecular level. The distribution of MLL breakpoints for clinical subtypes (acute lymphoblastic leukemia, acute myeloid leukemia, pediatric and adult) and fused translocation partner genes (TPGs) will be presented, including novel MLL fusion genes. Combined data of our study and recently published data revealed 104 different MLL rearrangements of which 64 TPGs are now characterized on the molecular level. Nine TPGs seem to be predominantly involved in genetic recombinations of MLL: AFF1/AF4, MLLT3/ AF9, MLLT1/ENL, MLLT10/AF10, MLLT4/AF6, ELL, EPS15/AF1P, MLLT6/AF17 and SEPT6, respectively. Moreover, we describe for the first time the genetic network of reciprocal MLL gene fusions deriving from complex rearrangements.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0887-6924</s0></fA01><fA02 i1="01"><s0>LEUKED</s0></fA02><fA03 i2="1"><s0>Leukemia</s0></fA03><fA05><s2>23</s2></fA05><fA06><s2>8</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>New insights to the MLL recombinome of acute leukemias</s1></fA08><fA11 i1="01" i2="1"><s1>MEYER (C.)</s1></fA11><fA11 i1="02" i2="1"><s1>KOWARZ (E.)</s1></fA11><fA11 i1="03" i2="1"><s1>HOFMANN (J.)</s1></fA11><fA11 i1="04" i2="1"><s1>RENNEVILLE (A.)</s1></fA11><fA11 i1="05" i2="1"><s1>ZUNA (J.)</s1></fA11><fA11 i1="06" i2="1"><s1>TRKA (J.)</s1></fA11><fA11 i1="07" i2="1"><s1>BEN ABDELAII (R.)</s1></fA11><fA11 i1="08" i2="1"><s1>MACINTYRE (E.)</s1></fA11><fA11 i1="09" i2="1"><s1>DE BRAEKELEER (E.)</s1></fA11><fA11 i1="10" i2="1"><s1>DE BRAEKELEER (M.)</s1></fA11><fA11 i1="11" i2="1"><s1>DELABESSE (E.)</s1></fA11><fA11 i1="12" i2="1"><s1>DE OLIVEIRA (M. P.)</s1></fA11><fA11 i1="13" i2="1"><s1>CAVE (H.)</s1></fA11><fA11 i1="14" i2="1"><s1>CLAPPIER (E.)</s1></fA11><fA11 i1="15" i2="1"><s1>VAN DONGEN (Jjm)</s1></fA11><fA11 i1="16" i2="1"><s1>BALGOBIND (B. V.)</s1></fA11><fA11 i1="17" i2="1"><s1>VAN DEN HEUVEL-EIBRINK (M. M.)</s1></fA11><fA11 i1="18" i2="1"><s1>BEVERLOO (H. B.)</s1></fA11><fA11 i1="19" i2="1"><s1>PANZER-GRÜMAYER (R.)</s1></fA11><fA11 i1="20" i2="1"><s1>TEIGLER-SCHLEGEL (A.)</s1></fA11><fA11 i1="21" i2="1"><s1>HARBOTT (J.)</s1></fA11><fA11 i1="22" i2="1"><s1>KJELDSEN (E.)</s1></fA11><fA11 i1="23" i2="1"><s1>SCHNITTGER (S.)</s1></fA11><fA11 i1="24" i2="1"><s1>KOEHL (U.)</s1></fA11><fA11 i1="25" i2="1"><s1>GRUHN (B.)</s1></fA11><fA11 i1="26" i2="1"><s1>HEIDENREICH (O.)</s1></fA11><fA11 i1="27" i2="1"><s1>CHAN (L. C.)</s1></fA11><fA11 i1="28" i2="1"><s1>YIP (S. F.)</s1></fA11><fA11 i1="29" i2="1"><s1>KRZYWINSKI (M.)</s1></fA11><fA11 i1="30" i2="1"><s1>ECKERT (C.)</s1></fA11><fA11 i1="31" i2="1"><s1>MÖRICKE (A.)</s1></fA11><fA11 i1="32" i2="1"><s1>SCHRAPPE (M.)</s1></fA11><fA11 i1="33" i2="1"><s1>ALONSO (C. N.)</s1></fA11><fA11 i1="34" i2="1"><s1>SCHÄFER (B. W.)</s1></fA11><fA11 i1="35" i2="1"><s1>KRAUTER (J.)</s1></fA11><fA11 i1="36" i2="1"><s1>LEE (D. A.)</s1></fA11><fA11 i1="37" i2="1"><s1>ZUR STADT (U.)</s1></fA11><fA11 i1="38" i2="1"><s1>TE KRONNIE (G.)</s1></fA11><fA11 i1="39" i2="1"><s1>SUTTON (R.)</s1></fA11><fA11 i1="40" i2="1"><s1>IZRAELI (S.)</s1></fA11><fA11 i1="41" i2="1"><s1>TRAKHTENBROT (L.)</s1></fA11><fA11 i1="42" i2="1"><s1>LO NIGRO (L.)</s1></fA11><fA11 i1="43" i2="1"><s1>TSAUR (G.)</s1></fA11><fA11 i1="44" i2="1"><s1>FECHINA (L.)</s1></fA11><fA11 i1="45" i2="1"><s1>SZCZEPANSKI (T.)</s1></fA11><fA11 i1="46" i2="1"><s1>STREHL (S.)</s1></fA11><fA11 i1="47" i2="1"><s1>ILENCIKOVA (D.)</s1></fA11><fA11 i1="48" i2="1"><s1>MOLKENTIN (M.)</s1></fA11><fA11 i1="49" i2="1"><s1>BURMEISTER (T.)</s1></fA11><fA11 i1="50" i2="1"><s1>DINGERMANN (T.)</s1></fA11><fA11 i1="51" i2="1"><s1>KLINGEBIEL (T.)</s1></fA11><fA11 i1="52" i2="1"><s1>MARSCHALEK (R.)</s1></fA11><fA14 i1="01"><s1>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt</s1><s2>Frankfurt/Main</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>52 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Hematology, Biology and Pathology Center, CHU of Lille</s1><s2>Lille</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="03"><s1>INSERM, U-837, Team 3</s1><s2>Lille</s2><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>CLIP, Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University Prague</s1><s2>Prague</s2><s3>CZE</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="05"><s1>Biological Hematology, AP-HP Necker, Université Paris Descartes</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="06"><s1>Faculté de Médecine et des Sciences de la Santé, Laboratoire d'Histologie, Embryologie et Cytogénétique, Université de Bretagne Occidentale</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="07"><s1>INSERM-U613</s1><s2>Brest</s2><s3>FRA</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="08"><s1>CHU Purpan, Laboratoire d'Hématologie</s1><s2>Toulouse</s2><s3>FRA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="09"><s1>Pediatric HematologyOncology Program, Research Center, Instituto Nacional de Cancer Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>12 aut.</sZ><sZ>50 aut.</sZ></fA14><fA14 i1="10"><s1>Déparfemenf de Génétique, Hopital Robert Debré</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ><sZ>14 aut.</sZ></fA14><fA14 i1="11"><s1>Department of Immunology, Erasmus MC, Sophia Children's Hospital</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>15 aut.</sZ></fA14><fA14 i1="12"><s1>Department of Pediatric Oncology/Hematology, Erasmus MC, Sophia Children's Hospital</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>16 aut.</sZ><sZ>17 aut.</sZ></fA14><fA14 i1="13"><s1>Department of Clinical Genetics, Erasmus MC</s1><s2>Rotterdam</s2><s3>NLD</s3><sZ>18 aut.</sZ></fA14><fA20><s1>1490-1499</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>21129</s2><s5>354000125102110170</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>42 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0389923</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Leukemia</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Chromosomal rearrangements of the human MLL gene are associated with high-risk pediatric, adult and therapy-associated acute leukemias. These patients need to be identified, treated appropriately and minimal residual disease was monitored by quantitative PCR techniques. Genomic DNA was isolated from individual acute leukemia patients to identify and characterize chromosomal rearrangements involving the human MLL gene. A total of 760 MLL-rearranged biopsy samples obtained from 384 pediatric and 376 adult leukemia patients were characterized at the molecular level. The distribution of MLL breakpoints for clinical subtypes (acute lymphoblastic leukemia, acute myeloid leukemia, pediatric and adult) and fused translocation partner genes (TPGs) will be presented, including novel MLL fusion genes. Combined data of our study and recently published data revealed 104 different MLL rearrangements of which 64 TPGs are now characterized on the molecular level. Nine TPGs seem to be predominantly involved in genetic recombinations of MLL: AFF1/AF4, MLLT3/ AF9, MLLT1/ENL, MLLT10/AF10, MLLT4/AF6, ELL, EPS15/AF1P, MLLT6/AF17 and SEPT6, respectively. Moreover, we describe for the first time the genetic network of reciprocal MLL gene fusions deriving from complex rearrangements.</s0></fC01><fC02 i1="01" i2="X"><s0>002B19B</s0></fC02><fC02 i1="02" i2="X"><s0>002B23B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Leucémie aiguë</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Acute leukemia</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Leucemia aguda</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Protooncogène</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Protooncogene</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Protooncogen</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Gène onc cellulaire</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>C-Onc gene</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Gen onc celular</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Translocation chromosomique</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Chromosome translocation</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Translocación cromosómica</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Leucémie aiguë myéloblastique</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Acute myelogenous leukemia</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Leucemia aguda mieloblástica</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Hématologie</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Hematology</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Hematología</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Leucémie aiguë lymphoblastique</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Acute lymphocytic leukemia</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Leucemia aguda linfoblástica</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Réarrangement génique</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Gene rearrangement</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Redisposición génica</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Homme</s0><s5>12</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Human</s0><s5>12</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Hombre</s0><s5>12</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Gène MLL</s0><s4>INC</s4><s5>86</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Gène partenaire</s0><s4>INC</s4><s5>87</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Chromosome anormal</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Abnormal chromosome</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Cromosoma anormal</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Aberration chromosomique</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Chromosomal aberration</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Aberración cromosómica</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Hémopathie maligne</s0><s2>NM</s2><s5>37</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Malignant hemopathy</s0><s2>NM</s2><s5>37</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Hemopatía maligna</s0><s2>NM</s2><s5>37</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Syndrome lymphoprolifératif</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Lymphoproliferative syndrome</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Linfoproliferativo síndrome</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Génétique</s0><s5>40</s5></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Genetics</s0><s5>40</s5></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Genética</s0><s5>40</s5></fC07><fN21><s1>278</s1></fN21></pA></standard><server><NO>PASCAL 09-0389923 INIST</NO><ET>New insights to the MLL recombinome of acute leukemias</ET><AU>MEYER (C.); KOWARZ (E.); HOFMANN (J.); RENNEVILLE (A.); ZUNA (J.); TRKA (J.); BEN ABDELAII (R.); MACINTYRE (E.); DE BRAEKELEER (E.); DE BRAEKELEER (M.); DELABESSE (E.); DE OLIVEIRA (M. P.); CAVE (H.); CLAPPIER (E.); VAN DONGEN (Jjm); BALGOBIND (B. V.); VAN DEN HEUVEL-EIBRINK (M. M.); BEVERLOO (H. B.); PANZER-GRÜMAYER (R.); TEIGLER-SCHLEGEL (A.); HARBOTT (J.); KJELDSEN (E.); SCHNITTGER (S.); KOEHL (U.); GRUHN (B.); HEIDENREICH (O.); CHAN (L. C.); YIP (S. F.); KRZYWINSKI (M.); ECKERT (C.); MÖRICKE (A.); SCHRAPPE (M.); ALONSO (C. N.); SCHÄFER (B. W.); KRAUTER (J.); LEE (D. A.); ZUR STADT (U.); TE KRONNIE (G.); SUTTON (R.); IZRAELI (S.); TRAKHTENBROT (L.); LO NIGRO (L.); TSAUR (G.); FECHINA (L.); SZCZEPANSKI (T.); STREHL (S.); ILENCIKOVA (D.); MOLKENTIN (M.); BURMEISTER (T.); DINGERMANN (T.); KLINGEBIEL (T.); MARSCHALEK (R.)</AU><AF>Diagnostic Center of Acute Leukemia, Institute of Pharmaceutical Biology, ZAFES, University of Frankfurt/Frankfurt/Main/Allemagne (1 aut., 2 aut., 3 aut., 52 aut.); Department of Hematology, Biology and Pathology Center, CHU of Lille/Lille/France (4 aut.); INSERM, U-837, Team 3/Lille/France (4 aut.); CLIP, Department of Paediatric Haematology/Oncology, Second Faculty of Medicine, Charles University Prague/Prague/Tchèque, République (5 aut., 6 aut.); Biological Hematology, AP-HP Necker, Université Paris Descartes/Paris/France (7 aut., 8 aut.); Faculté de Médecine et des Sciences de la Santé, Laboratoire d'Histologie, Embryologie et Cytogénétique, Université de Bretagne Occidentale/Brest/France (9 aut., 10 aut.); INSERM-U613/Brest/France (9 aut., 10 aut.); CHU Purpan, Laboratoire d'Hématologie/Toulouse/France (11 aut.); Pediatric HematologyOncology Program, Research Center, Instituto Nacional de Cancer Rio de Janeiro/Rio de Janeiro/Brésil (12 aut., 50 aut.); Déparfemenf de Génétique, Hopital Robert Debré/Paris/France (13 aut., 14 aut.); Department of Immunology, Erasmus MC, Sophia Children's Hospital/Rotterdam/Pays-Bas (15 aut.); Department of Pediatric Oncology/Hematology, Erasmus MC, Sophia Children's Hospital/Rotterdam/Pays-Bas (16 aut., 17 aut.); Department of Clinical Genetics, Erasmus MC/Rotterdam/Pays-Bas (18 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Leukemia; ISSN 0887-6924; Coden LEUKED; Royaume-Uni; Da. 2009; Vol. 23; No. 8; Pp. 1490-1499; Bibl. 42 ref.</SO><LA>Anglais</LA><EA>Chromosomal rearrangements of the human MLL gene are associated with high-risk pediatric, adult and therapy-associated acute leukemias. These patients need to be identified, treated appropriately and minimal residual disease was monitored by quantitative PCR techniques. Genomic DNA was isolated from individual acute leukemia patients to identify and characterize chromosomal rearrangements involving the human MLL gene. A total of 760 MLL-rearranged biopsy samples obtained from 384 pediatric and 376 adult leukemia patients were characterized at the molecular level. The distribution of MLL breakpoints for clinical subtypes (acute lymphoblastic leukemia, acute myeloid leukemia, pediatric and adult) and fused translocation partner genes (TPGs) will be presented, including novel MLL fusion genes. Combined data of our study and recently published data revealed 104 different MLL rearrangements of which 64 TPGs are now characterized on the molecular level. Nine TPGs seem to be predominantly involved in genetic recombinations of MLL: AFF1/AF4, MLLT3/ AF9, MLLT1/ENL, MLLT10/AF10, MLLT4/AF6, ELL, EPS15/AF1P, MLLT6/AF17 and SEPT6, respectively. Moreover, we describe for the first time the genetic network of reciprocal MLL gene fusions deriving from complex rearrangements.</EA><CC>002B19B; 002B23B</CC><FD>Leucémie aiguë; Protooncogène; Gène onc cellulaire; Translocation chromosomique; Leucémie aiguë myéloblastique; Hématologie; Leucémie aiguë lymphoblastique; Réarrangement génique; Homme; Gène MLL; Gène partenaire</FD><FG>Chromosome anormal; Aberration chromosomique; Hémopathie maligne; Cancer; Syndrome lymphoprolifératif; Génétique</FG><ED>Acute leukemia; Protooncogene; C-Onc gene; Chromosome translocation; Acute myelogenous leukemia; Hematology; Acute lymphocytic leukemia; Gene rearrangement; Human</ED><EG>Abnormal chromosome; Chromosomal aberration; Malignant hemopathy; Cancer; Lymphoproliferative syndrome; Genetics</EG><SD>Leucemia aguda; Protooncogen; Gen onc celular; Translocación cromosómica; Leucemia aguda mieloblástica; Hematología; Leucemia aguda linfoblástica; Redisposición génica; Hombre</SD><LO>INIST-21129.354000125102110170</LO><ID>09-0389923</ID></server></inist></record>
000D61	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Spin density wave dislocation in chromium probed by coherent X-ray diffraction</title><author><name sortKey="Jacques, V L R" uniqKey="Jacques V">V. L. R. Jacques</name><affiliation><inist:fA14 i1="01"><s1>Laboratoire de Physique des Solides, Univ. Paris-Sud, CNRS, UMR 8502</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Synchrotron SOLEIL, L'Orme des merisiers, Saint-Aubin BP 48</s1><s2>91192 Gif-sur-Yvette</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Le Bolloc H, D" uniqKey="Le Bolloc H D">D. Le Bolloc H</name><affiliation><inist:fA14 i1="01"><s1>Laboratoire de Physique des Solides, Univ. Paris-Sud, CNRS, UMR 8502</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ravy, S" uniqKey="Ravy S">S. Ravy</name><affiliation><inist:fA14 i1="02"><s1>Synchrotron SOLEIL, L'Orme des merisiers, Saint-Aubin BP 48</s1><s2>91192 Gif-sur-Yvette</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Giles, C" uniqKey="Giles C">C. Giles</name><affiliation><inist:fA14 i1="03"><s1>Instituto de Fisica &#34;Gleb Wataghin&#34;, UNICAMP</s1><s2>Campinas-SP, C.P. 6165, 13083-970</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Livet, F" uniqKey="Livet F">F. Livet</name><affiliation><inist:fA14 i1="04"><s1>LTPCM (CNRS-UMR 5614), ENSEEG-Domaine Universitaire, BP 75</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wilkins, S B" uniqKey="Wilkins S">S. B. Wilkins</name><affiliation><inist:fA14 i1="05"><s1>Brookhaven National Lab</s1><s2>Upton NY 11973</s2><s3>USA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0391565</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0391565 INIST</idno><idno type="RBID">Pascal:09-0391565</idno><idno type="wicri:Area/Main/Corpus">001C20</idno></publicationStmt><seriesStmt><idno type="ISSN">1434-6028</idno><title level="j" type="abbreviated">Eur. phys. j., B Cond. matter phys.</title><title level="j" type="main">The European physical journal. B, Condensed matter physics</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Charge density waves</term><term>Chromium</term><term>Coherence length</term><term>Dislocations</term><term>Force constants</term><term>Incommensurate phases</term><term>Magnetic ordering</term><term>Spin density waves</term><term>XRD</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Onde densité spin</term><term>Dislocation</term><term>Diffraction RX</term><term>Phase incommensurable</term><term>Ordre magnétique</term><term>Onde densité charge</term><term>Longueur cohérence</term><term>Constante force</term><term>Chrome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report on the study of a magnetic dislocation in pure chromium. Coherent X-ray diffraction profiles obtained on the incommensurate Spin Density Wave (SDW) reflection are consistent with the presence of a dislocation of the magnetic order, embedded at a few micrometers from the surface of the sample. Beyond the specific case of magnetic dislocations in chromium, this work may open up a new method for the study of magnetic defects embedded in the bulk.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1434-6028</s0></fA01><fA03 i2="1"><s0>Eur. phys. j., B Cond. matter phys.</s0></fA03><fA05><s2>70</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Spin density wave dislocation in chromium probed by coherent X-ray diffraction</s1></fA08><fA11 i1="01" i2="1"><s1>JACQUES (V. L. R.)</s1></fA11><fA11 i1="02" i2="1"><s1>LE BOLLOC'H (D.)</s1></fA11><fA11 i1="03" i2="1"><s1>RAVY (S.)</s1></fA11><fA11 i1="04" i2="1"><s1>GILES (C.)</s1></fA11><fA11 i1="05" i2="1"><s1>LIVET (F.)</s1></fA11><fA11 i1="06" i2="1"><s1>WILKINS (S. B.)</s1></fA11><fA14 i1="01"><s1>Laboratoire de Physique des Solides, Univ. Paris-Sud, CNRS, UMR 8502</s1><s2>91405 Orsay</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Synchrotron SOLEIL, L'Orme des merisiers, Saint-Aubin BP 48</s1><s2>91192 Gif-sur-Yvette</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Instituto de Fisica &#34;Gleb Wataghin&#34;, UNICAMP</s1><s2>Campinas-SP, C.P. 6165, 13083-970</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>LTPCM (CNRS-UMR 5614), ENSEEG-Domaine Universitaire, BP 75</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Brookhaven National Lab</s1><s2>Upton NY 11973</s2><s3>USA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>317-325</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26688</s2><s5>354000187602810030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>43 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0391565</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>The European physical journal. B, Condensed matter physics</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>We report on the study of a magnetic dislocation in pure chromium. Coherent X-ray diffraction profiles obtained on the incommensurate Spin Density Wave (SDW) reflection are consistent with the presence of a dislocation of the magnetic order, embedded at a few micrometers from the surface of the sample. Beyond the specific case of magnetic dislocations in chromium, this work may open up a new method for the study of magnetic defects embedded in the bulk.</s0></fC01><fC02 i1="01" i2="3"><s0>001B70E25</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Onde densité spin</s0><s5>02</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Spin density waves</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Dislocation</s0><s5>03</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Dislocations</s0><s5>03</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Diffraction RX</s0><s5>04</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>XRD</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Phase incommensurable</s0><s5>05</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Incommensurate phases</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Ordre magnétique</s0><s5>06</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Magnetic ordering</s0><s5>06</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Onde densité charge</s0><s5>07</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Charge density waves</s0><s5>07</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Longueur cohérence</s0><s5>08</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Coherence length</s0><s5>08</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Constante force</s0><s5>09</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Force constants</s0><s5>09</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Chrome</s0><s2>NC</s2><s5>15</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Chromium</s0><s2>NC</s2><s5>15</s5></fC03><fN21><s1>285</s1></fN21></pA></standard><server><NO>PASCAL 09-0391565 INIST</NO><ET>Spin density wave dislocation in chromium probed by coherent X-ray diffraction</ET><AU>JACQUES (V. L. R.); LE BOLLOC'H (D.); RAVY (S.); GILES (C.); LIVET (F.); WILKINS (S. B.)</AU><AF>Laboratoire de Physique des Solides, Univ. Paris-Sud, CNRS, UMR 8502/91405 Orsay/France (1 aut., 2 aut.); Synchrotron SOLEIL, L'Orme des merisiers, Saint-Aubin BP 48/91192 Gif-sur-Yvette/France (1 aut., 3 aut.); Instituto de Fisica &#34;Gleb Wataghin&#34;, UNICAMP/Campinas-SP, C.P. 6165, 13083-970/Brésil (4 aut.); LTPCM (CNRS-UMR 5614), ENSEEG-Domaine Universitaire, BP 75/38402 Saint Martin d'Hères/France (5 aut.); Brookhaven National Lab/Upton NY 11973/Etats-Unis (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>The European physical journal. B, Condensed matter physics; ISSN 1434-6028; France; Da. 2009; Vol. 70; No. 3; Pp. 317-325; Bibl. 43 ref.</SO><LA>Anglais</LA><EA>We report on the study of a magnetic dislocation in pure chromium. Coherent X-ray diffraction profiles obtained on the incommensurate Spin Density Wave (SDW) reflection are consistent with the presence of a dislocation of the magnetic order, embedded at a few micrometers from the surface of the sample. Beyond the specific case of magnetic dislocations in chromium, this work may open up a new method for the study of magnetic defects embedded in the bulk.</EA><CC>001B70E25</CC><FD>Onde densité spin; Dislocation; Diffraction RX; Phase incommensurable; Ordre magnétique; Onde densité charge; Longueur cohérence; Constante force; Chrome</FD><ED>Spin density waves; Dislocations; XRD; Incommensurate phases; Magnetic ordering; Charge density waves; Coherence length; Force constants; Chromium</ED><LO>INIST-26688.354000187602810030</LO><ID>09-0391565</ID></server></inist></record>
000D62	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Multiplexing technique for direction of departure and direction of arrival estimation</title><author><name sortKey="Martinez, S" uniqKey="Martinez S">S. Martinez</name><affiliation><inist:fA14 i1="01"><s1>Institut Telecom, TELECOM ParisTech, LTCI CNRS, UMR 5141, 46 Rue Barrault</s1><s2>Paris 75013</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Braga, A J" uniqKey="Braga A">A. J. Braga</name><affiliation><inist:fA14 i1="02"><s1>PPGEE, ITEC, Federal University of Para, P.O. Box 8619</s1><s2>Belem 66075 110</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Huyart, B" uniqKey="Huyart B">B. Huyart</name><affiliation><inist:fA14 i1="01"><s1>Institut Telecom, TELECOM ParisTech, LTCI CNRS, UMR 5141, 46 Rue Barrault</s1><s2>Paris 75013</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cousin, J C" uniqKey="Cousin J">J. C. Cousin</name><affiliation><inist:fA14 i1="01"><s1>Institut Telecom, TELECOM ParisTech, LTCI CNRS, UMR 5141, 46 Rue Barrault</s1><s2>Paris 75013</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0391961</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0391961 INIST</idno><idno type="RBID">Pascal:09-0391961</idno><idno type="wicri:Area/Main/Corpus">001C19</idno></publicationStmt><seriesStmt><idno type="ISSN">1751-8725</idno><title level="j" type="main">IET microwaves, antennas &#38; propagation : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Algorithm</term><term>Anechoic room</term><term>Antenna array</term><term>Continuous time</term><term>Delay time</term><term>Direction-of-arrival estimation</term><term>High resolution</term><term>Parameter estimation</term><term>Receiver</term><term>Selector switch</term><term>Signal estimation</term><term>Simulation</term><term>Time division multiplexing</term><term>Time domain method</term><term>Time variable channel</term><term>Transmission channel</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Multiplexage temps</term><term>Estimation direction arrivée</term><term>Antenne réseau</term><term>Commutateur</term><term>Canal variant dans temps</term><term>Temps retard</term><term>Canal transmission</term><term>Méthode domaine temps</term><term>Temps continu</term><term>Récepteur</term><term>Haute résolution</term><term>Algorithme</term><term>Simulation</term><term>Chambre anéchoïque</term><term>Estimation signal</term><term>Estimation paramètre</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">A novel multiplexing technique for angular estimation that avoids the use of switches and multiple RF chains is presented. The principle of operation is as simple as connecting cables of different electrical lengths to the antennas. The advantages are simplicity and fast measurements, which enables the study of time-variant channels. If the duration of the excitation signal is less than a certain limit (which depends on the delays introduced by cables and on the delay spread of the propagation channel), the technique performs a time-domain multiplexing. However, the technique is especially interesting in the case that the excitation signal duration exceeds this limit. In that case, it requires the frequency of the signal to increase or to decrease linearly in time, regardless if the variation is discrete or continuous in time. The post-processing of the receiver output used to separate the signals corresponding to each antenna is detailed in this study. Once separated, the signals can be processed with a high-resolution algorithm to estimate the direction of departure and the direction of arrival. To validate the capability of this method, simulation results and measurements in an anechoic chamber are presented.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1751-8725</s0></fA01><fA05><s2>3</s2></fA05><fA06><s2>6</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Multiplexing technique for direction of departure and direction of arrival estimation</s1></fA08><fA11 i1="01" i2="1"><s1>MARTINEZ (S.)</s1></fA11><fA11 i1="02" i2="1"><s1>BRAGA (A. J.)</s1></fA11><fA11 i1="03" i2="1"><s1>HUYART (B.)</s1></fA11><fA11 i1="04" i2="1"><s1>COUSIN (J. C.)</s1></fA11><fA14 i1="01"><s1>Institut Telecom, TELECOM ParisTech, LTCI CNRS, UMR 5141, 46 Rue Barrault</s1><s2>Paris 75013</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>PPGEE, ITEC, Federal University of Para, P.O. Box 8619</s1><s2>Belem 66075 110</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA20><s1>1011-1017</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>7573H</s2><s5>354000196200960140</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>14 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0391961</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>IET microwaves, antennas &#38; propagation : (Print)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>A novel multiplexing technique for angular estimation that avoids the use of switches and multiple RF chains is presented. The principle of operation is as simple as connecting cables of different electrical lengths to the antennas. The advantages are simplicity and fast measurements, which enables the study of time-variant channels. If the duration of the excitation signal is less than a certain limit (which depends on the delays introduced by cables and on the delay spread of the propagation channel), the technique performs a time-domain multiplexing. However, the technique is especially interesting in the case that the excitation signal duration exceeds this limit. In that case, it requires the frequency of the signal to increase or to decrease linearly in time, regardless if the variation is discrete or continuous in time. The post-processing of the receiver output used to separate the signals corresponding to each antenna is detailed in this study. Once separated, the signals can be processed with a high-resolution algorithm to estimate the direction of departure and the direction of arrival. To validate the capability of this method, simulation results and measurements in an anechoic chamber are presented.</s0></fC01><fC02 i1="01" i2="X"><s0>001D04B04D</s0></fC02><fC02 i1="02" i2="X"><s0>001D03G02A7</s0></fC02><fC02 i1="03" i2="X"><s0>001D04B04E</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Multiplexage temps</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Time division multiplexing</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Multiplaje tiempo</s0><s5>01</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Estimation direction arrivée</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Direction-of-arrival estimation</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Antenne réseau</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Antenna array</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Antena red</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Commutateur</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Selector switch</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Conmutador</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Canal variant dans temps</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Time variable channel</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Canal variable con el tiempo</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Temps retard</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Delay time</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Tiempo retardo</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Canal transmission</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Transmission channel</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Canal transmisión</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Méthode domaine temps</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Time domain method</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Método dominio tiempo</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Temps continu</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Continuous time</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Tiempo continuo</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Récepteur</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Receiver</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Receptor</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Haute résolution</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>High resolution</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Alta resolucion</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Algorithme</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Algorithm</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Algoritmo</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Simulation</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Simulation</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Simulación</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Chambre anéchoïque</s0><s5>14</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Anechoic room</s0><s5>14</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Estimation signal</s0><s5>31</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Signal estimation</s0><s5>31</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Estimación señal</s0><s5>31</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Estimation paramètre</s0><s5>32</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Parameter estimation</s0><s5>32</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Estimación parámetro</s0><s5>32</s5></fC03><fN21><s1>285</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0391961 INIST</NO><ET>Multiplexing technique for direction of departure and direction of arrival estimation</ET><AU>MARTINEZ (S.); BRAGA (A. J.); HUYART (B.); COUSIN (J. C.)</AU><AF>Institut Telecom, TELECOM ParisTech, LTCI CNRS, UMR 5141, 46 Rue Barrault/Paris 75013/France (1 aut., 3 aut., 4 aut.); PPGEE, ITEC, Federal University of Para, P.O. Box 8619/Belem 66075 110/Brésil (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>IET microwaves, antennas &#38; propagation : (Print); ISSN 1751-8725; Royaume-Uni; Da. 2009; Vol. 3; No. 6; Pp. 1011-1017; Bibl. 14 ref.</SO><LA>Anglais</LA><EA>A novel multiplexing technique for angular estimation that avoids the use of switches and multiple RF chains is presented. The principle of operation is as simple as connecting cables of different electrical lengths to the antennas. The advantages are simplicity and fast measurements, which enables the study of time-variant channels. If the duration of the excitation signal is less than a certain limit (which depends on the delays introduced by cables and on the delay spread of the propagation channel), the technique performs a time-domain multiplexing. However, the technique is especially interesting in the case that the excitation signal duration exceeds this limit. In that case, it requires the frequency of the signal to increase or to decrease linearly in time, regardless if the variation is discrete or continuous in time. The post-processing of the receiver output used to separate the signals corresponding to each antenna is detailed in this study. Once separated, the signals can be processed with a high-resolution algorithm to estimate the direction of departure and the direction of arrival. To validate the capability of this method, simulation results and measurements in an anechoic chamber are presented.</EA><CC>001D04B04D; 001D03G02A7; 001D04B04E</CC><FD>Multiplexage temps; Estimation direction arrivée; Antenne réseau; Commutateur; Canal variant dans temps; Temps retard; Canal transmission; Méthode domaine temps; Temps continu; Récepteur; Haute résolution; Algorithme; Simulation; Chambre anéchoïque; Estimation signal; Estimation paramètre</FD><ED>Time division multiplexing; Direction-of-arrival estimation; Antenna array; Selector switch; Time variable channel; Delay time; Transmission channel; Time domain method; Continuous time; Receiver; High resolution; Algorithm; Simulation; Anechoic room; Signal estimation; Parameter estimation</ED><SD>Multiplaje tiempo; Antena red; Conmutador; Canal variable con el tiempo; Tiempo retardo; Canal transmisión; Método dominio tiempo; Tiempo continuo; Receptor; Alta resolucion; Algoritmo; Simulación; Estimación señal; Estimación parámetro</SD><LO>INIST-7573H.354000196200960140</LO><ID>09-0391961</ID></server></inist></record>
000D63	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Immunohistochemistry and polymerase chain reaction on paraffin-embedded material improve the diagnosis of cutaneous leishmaniasis in the Amazon region</title><author><name sortKey="Sabbaga Amato, Valdir" uniqKey="Sabbaga Amato V">Valdir Sabbaga Amato</name><affiliation><inist:fA14 i1="01"><s1>Infectious and Parasitic Diseases Clinic and Laboratory of Medical Investigation, Parasitology (LIM 46), Hospital das Clinicas</s1><s2>São Paulo</s2><s3>BRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Department of Infectious Diseases, Laboratory of Protozoology, Institute of Tropical Medicine of Sao Paulo</s1><s2>São Paulo</s2><s3>BRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Laboratory of the Discipline of Pathology of Transmissible Diseases, and NUMETROP, Núcleo de Extensão em Medicina Tropical, Department of Infectious Diseases, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>FRA</s3></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Laboratory of Trypanosomatids, Physiology Department, Biosciences Institute and Seroepidemiology Laboratory, Instituto de Medicina Tropical de São Paulo, University of São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3></inist:fA14></affiliation></author><author><name sortKey="Francisco Tuon, Felipe" uniqKey="Francisco Tuon F">Felipe Francisco Tuon</name></author><author><name sortKey="Franco De Andrade, Heitor Jr" uniqKey="Franco De Andrade H">Heitor Jr Franco De Andrade</name></author><author><name sortKey="Bacha, Helio" uniqKey="Bacha H">Helio Bacha</name></author><author><name sortKey="Pagliari, Carla" uniqKey="Pagliari C">Carla Pagliari</name></author><author><name sortKey="Raniero Fernandes, Elaine" uniqKey="Raniero Fernandes E">Elaine Raniero Fernandes</name></author><author><name sortKey="Seixas Duarte, Maria Irma" uniqKey="Seixas Duarte M">Maria Irma Seixas Duarte</name></author><author><name sortKey="Amato Neto, Vicente" uniqKey="Amato Neto V">Vicente Amato Neto</name></author><author><name sortKey="Andrade Zampieri, Ricardo" uniqKey="Andrade Zampieri R">Ricardo Andrade Zampieri</name></author><author><name sortKey="Floeter Winter, Lucile Maria" uniqKey="Floeter Winter L">Lucile Maria Floeter-Winter</name></author><author><name sortKey="Celeste, Beatriz J" uniqKey="Celeste B">Beatriz J. Celeste</name></author><author><name sortKey="Oliveira, Juliane" uniqKey="Oliveira J">Juliane Oliveira</name></author><author><name sortKey="Martinez Quiroga, Mariana" uniqKey="Martinez Quiroga M">Mariana Martinez Quiroga</name></author><author><name sortKey="Mascheretti, Melissa" uniqKey="Mascheretti M">Melissa Mascheretti</name></author><author><name sortKey="Boulos, Marcos" uniqKey="Boulos M">Marcos Boulos</name></author></titleStmt><publicationStmt><idno type="inist">09-0393065</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0393065 INIST</idno><idno type="RBID">Pascal:09-0393065</idno><idno type="wicri:Area/Main/Corpus">001C18</idno></publicationStmt><seriesStmt><idno type="ISSN">0011-9059</idno><title level="j" type="abbreviated">Int. j. dermatol.</title><title level="j" type="main">International journal of dermatology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cutaneous leishmaniasis</term><term>Dermatology</term><term>Diagnosis</term><term>Immunohistochemistry</term><term>Polymerase chain reaction</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Leishmaniose cutanée</term><term>Immunohistochimie</term><term>Réaction chaîne polymérase</term><term>Diagnostic</term><term>Dermatologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background Recently, there has been an increase in the incidence of cutaneous leishmaniasis (CL), which represents an important health problem. This increase may be related to the epidemiologic expansion of the infective agent and the increase in tourism in tropical areas. The difficulty in clinical diagnosis, mainly in areas in which CL is not the first consideration of local physicians, has intensified efforts to describe diagnostic tests, which should be specific, sensitive, and practical. Amongst the new tests described are those including nucleic acid amplification (polymerase chain reaction, PCR) and immunohistochemistry (IHC). Methods In this study, we evaluated the sensitivity of a PCR based on small subunit (SSU) ribosomal DNA, in comparison with IHC using Leishmania spp. antibodies, in biopsies embedded in paraffin. Result The results indicated a total sensitivity of 96% (90.9% with PCR and 68.8% with IHC), showing the possibility of using paraffin-embedded biopsies to diagnose CL. Conclusion We propose the use of the two tests together as a routine protocol for diagnosis. This would require the provision of local medical services to perform molecular biology techniques and adequate Leishmania antibodies.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0011-9059</s0></fA01><fA02 i1="01"><s0>IJDEBB</s0></fA02><fA03 i2="1"><s0>Int. j. dermatol.</s0></fA03><fA05><s2>48</s2></fA05><fA06><s2>10</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Immunohistochemistry and polymerase chain reaction on paraffin-embedded material improve the diagnosis of cutaneous leishmaniasis in the Amazon region</s1></fA08><fA11 i1="01" i2="1"><s1>SABBAGA AMATO (Valdir)</s1></fA11><fA11 i1="02" i2="1"><s1>FRANCISCO TUON (Felipe)</s1></fA11><fA11 i1="03" i2="1"><s1>FRANCO DE ANDRADE (Heitor JR)</s1></fA11><fA11 i1="04" i2="1"><s1>BACHA (Helio)</s1></fA11><fA11 i1="05" i2="1"><s1>PAGLIARI (Carla)</s1></fA11><fA11 i1="06" i2="1"><s1>RANIERO FERNANDES (Elaine)</s1></fA11><fA11 i1="07" i2="1"><s1>SEIXAS DUARTE (Maria Irma)</s1></fA11><fA11 i1="08" i2="1"><s1>AMATO NETO (Vicente)</s1></fA11><fA11 i1="09" i2="1"><s1>ANDRADE ZAMPIERI (Ricardo)</s1></fA11><fA11 i1="10" i2="1"><s1>FLOETER-WINTER (Lucile Maria)</s1></fA11><fA11 i1="11" i2="1"><s1>CELESTE (Beatriz J.)</s1></fA11><fA11 i1="12" i2="1"><s1>OLIVEIRA (Juliane)</s1></fA11><fA11 i1="13" i2="1"><s1>MARTINEZ QUIROGA (Mariana)</s1></fA11><fA11 i1="14" i2="1"><s1>MASCHERETTI (Melissa)</s1></fA11><fA11 i1="15" i2="1"><s1>BOULOS (Marcos)</s1></fA11><fA14 i1="01"><s1>Infectious and Parasitic Diseases Clinic and Laboratory of Medical Investigation, Parasitology (LIM 46), Hospital das Clinicas</s1><s2>São Paulo</s2><s3>BRA</s3></fA14><fA14 i1="02"><s1>Department of Infectious Diseases, Laboratory of Protozoology, Institute of Tropical Medicine of Sao Paulo</s1><s2>São Paulo</s2><s3>BRA</s3></fA14><fA14 i1="03"><s1>Laboratory of the Discipline of Pathology of Transmissible Diseases, and NUMETROP, Núcleo de Extensão em Medicina Tropical, Department of Infectious Diseases, University of São Paulo Medical School</s1><s2>São Paulo</s2><s3>FRA</s3></fA14><fA14 i1="04"><s1>Laboratory of Trypanosomatids, Physiology Department, Biosciences Institute and Seroepidemiology Laboratory, Instituto de Medicina Tropical de São Paulo, University of São Paulo</s1><s2>São Paulo</s2><s3>BRA</s3></fA14><fA20><s1>1091-1095</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>11580</s2><s5>354000170200750110</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>22 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0393065</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of dermatology</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Background Recently, there has been an increase in the incidence of cutaneous leishmaniasis (CL), which represents an important health problem. This increase may be related to the epidemiologic expansion of the infective agent and the increase in tourism in tropical areas. The difficulty in clinical diagnosis, mainly in areas in which CL is not the first consideration of local physicians, has intensified efforts to describe diagnostic tests, which should be specific, sensitive, and practical. Amongst the new tests described are those including nucleic acid amplification (polymerase chain reaction, PCR) and immunohistochemistry (IHC). Methods In this study, we evaluated the sensitivity of a PCR based on small subunit (SSU) ribosomal DNA, in comparison with IHC using Leishmania spp. antibodies, in biopsies embedded in paraffin. Result The results indicated a total sensitivity of 96% (90.9% with PCR and 68.8% with IHC), showing the possibility of using paraffin-embedded biopsies to diagnose CL. Conclusion We propose the use of the two tests together as a routine protocol for diagnosis. This would require the provision of local medical services to perform molecular biology techniques and adequate Leishmania antibodies.</s0></fC01><fC02 i1="01" i2="X"><s0>002B08</s0></fC02><fC02 i1="02" i2="X"><s0>002B05E02B3</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Leishmaniose cutanée</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Cutaneous leishmaniasis</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Leishmaniasis  cutánea</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Immunohistochimie</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Immunohistochemistry</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Inmunohistoquímica</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Réaction chaîne polymérase</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Polymerase chain reaction</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Reacción cadena polimerasa</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Diagnostic</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Diagnosis</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Diagnóstico</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Dermatologie</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Dermatology</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Dermatología</s0><s5>08</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Anatomopathologie</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Anatomic pathology</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Anatomía patológica</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Biologie moléculaire</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Molecular biology</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Biología molecular</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pathologie de la peau</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Skin disease</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Piel patología</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Protozoose</s0><s5>40</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Protozoal disease</s0><s5>40</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Protozoosis</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Parasitose</s0></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Parasitosis</s0></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Parasitosis</s0></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Infección</s0></fC07><fN21><s1>285</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0393065 INIST</NO><ET>Immunohistochemistry and polymerase chain reaction on paraffin-embedded material improve the diagnosis of cutaneous leishmaniasis in the Amazon region</ET><AU>SABBAGA AMATO (Valdir); FRANCISCO TUON (Felipe); FRANCO DE ANDRADE (Heitor JR); BACHA (Helio); PAGLIARI (Carla); RANIERO FERNANDES (Elaine); SEIXAS DUARTE (Maria Irma); AMATO NETO (Vicente); ANDRADE ZAMPIERI (Ricardo); FLOETER-WINTER (Lucile Maria); CELESTE (Beatriz J.); OLIVEIRA (Juliane); MARTINEZ QUIROGA (Mariana); MASCHERETTI (Melissa); BOULOS (Marcos)</AU><AF>Infectious and Parasitic Diseases Clinic and Laboratory of Medical Investigation, Parasitology (LIM 46), Hospital das Clinicas/São Paulo/Brésil; Department of Infectious Diseases, Laboratory of Protozoology, Institute of Tropical Medicine of Sao Paulo/São Paulo/Brésil; Laboratory of the Discipline of Pathology of Transmissible Diseases, and NUMETROP, Núcleo de Extensão em Medicina Tropical, Department of Infectious Diseases, University of São Paulo Medical School/São Paulo/France; Laboratory of Trypanosomatids, Physiology Department, Biosciences Institute and Seroepidemiology Laboratory, Instituto de Medicina Tropical de São Paulo, University of São Paulo/São Paulo/Brésil</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of dermatology; ISSN 0011-9059; Coden IJDEBB; Royaume-Uni; Da. 2009; Vol. 48; No. 10; Pp. 1091-1095; Bibl. 22 ref.</SO><LA>Anglais</LA><EA>Background Recently, there has been an increase in the incidence of cutaneous leishmaniasis (CL), which represents an important health problem. This increase may be related to the epidemiologic expansion of the infective agent and the increase in tourism in tropical areas. The difficulty in clinical diagnosis, mainly in areas in which CL is not the first consideration of local physicians, has intensified efforts to describe diagnostic tests, which should be specific, sensitive, and practical. Amongst the new tests described are those including nucleic acid amplification (polymerase chain reaction, PCR) and immunohistochemistry (IHC). Methods In this study, we evaluated the sensitivity of a PCR based on small subunit (SSU) ribosomal DNA, in comparison with IHC using Leishmania spp. antibodies, in biopsies embedded in paraffin. Result The results indicated a total sensitivity of 96% (90.9% with PCR and 68.8% with IHC), showing the possibility of using paraffin-embedded biopsies to diagnose CL. Conclusion We propose the use of the two tests together as a routine protocol for diagnosis. This would require the provision of local medical services to perform molecular biology techniques and adequate Leishmania antibodies.</EA><CC>002B08; 002B05E02B3</CC><FD>Leishmaniose cutanée; Immunohistochimie; Réaction chaîne polymérase; Diagnostic; Dermatologie</FD><FG>Anatomopathologie; Biologie moléculaire; Pathologie de la peau; Protozoose; Parasitose; Infection</FG><ED>Cutaneous leishmaniasis; Immunohistochemistry; Polymerase chain reaction; Diagnosis; Dermatology</ED><EG>Anatomic pathology; Molecular biology; Skin disease; Protozoal disease; Parasitosis; Infection</EG><SD>Leishmaniasis  cutánea; Inmunohistoquímica; Reacción cadena polimerasa; Diagnóstico; Dermatología</SD><LO>INIST-11580.354000170200750110</LO><ID>09-0393065</ID></server></inist></record>
000D64	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">A search for thermally emitting isolated neutron stars in the 2XMMp catalogue</title><author><name sortKey="Pires, A M" uniqKey="Pires A">A. M. Pires</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciencias Atmosf6ricas, Universidade de São Paulo, R. do Matão 1226</s1><s2>05508-090 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>CNRS, Université de Strasbourg, Observatoire Astronomique, 11 rue de l'Université</s1><s2>67000 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Motch, C" uniqKey="Motch C">C. Motch</name><affiliation><inist:fA14 i1="02"><s1>CNRS, Université de Strasbourg, Observatoire Astronomique, 11 rue de l'Université</s1><s2>67000 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Janot Pacheco, E" uniqKey="Janot Pacheco E">E. Janot-Pacheco</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciencias Atmosf6ricas, Universidade de São Paulo, R. do Matão 1226</s1><s2>05508-090 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0393102</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0393102 INIST</idno><idno type="RBID">Pascal:09-0393102</idno><idno type="wicri:Area/Main/Corpus">001C17</idno></publicationStmt><seriesStmt><idno type="ISSN">0004-6361</idno><title level="j" type="abbreviated">Astron. astrophys. : (Berl., Print)</title><title level="j" type="main">Astronomy and astrophysics : (Berlin. Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Active galaxies</term><term>Active galaxy nuclei</term><term>Anomaly</term><term>Astronomical catalogues</term><term>Cataclysmic variable stars</term><term>Color</term><term>Galaxy nuclei</term><term>High density</term><term>Interstellar absorption</term><term>Neutron stars</term><term>Optical counterpart</term><term>Screening</term><term>Sky surveys</term><term>Soft X radiation</term><term>Solar neighborhood</term><term>X-ray spectra</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Etoile neutron</term><term>Catalogue astronomique</term><term>Etude ciel</term><term>Voisinage solaire</term><term>Rayon X mou</term><term>Spectre RX</term><term>Absorption interstellaire</term><term>Effet écran</term><term>Contrepartie optique</term><term>Etoile variable cataclysmique</term><term>Noyau galactique actif</term><term>Couleur</term><term>Densité élevée</term><term>Anomalie</term><term>Galaxies actives</term><term>Noyau galaxies</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The relatively large number of nearby radio-quiet and thermally emitting isolated neutron stars (INSs) discovered in the ROSAT All-Sky Survey, dubbed the &#34;Magnificent Seven&#34;, suggests that they belong to a formerly neglected major component of the overall INS population. So far, attempts to discover similar INSs beyond the solar vicinity failed to confirm any reliable candidate. The good positional accuracy and soft X-ray sensitivity of the EPIC cameras onboard the XMM-Newton satellite allow us to efficiently search for new thermally emitting INSs. We used the 2XMMp catalogue to select sources with no catalogued candidate counterparts and with X-ray spectra similar to those of the Magnificent Seven, but seen at greater distances and thus undergoing higher interstellar absorptions. Identifications in more than 170 astronomical catalogues and visual screening allowed us to select fewer than 30 good INS candidates. In order to rule out alternative identifications, we obtained deep ESO-VLT and SOAR optical imaging for the X-ray brightest candidates. We report here on the optical follow-up results of our search and discuss the possible nature of 8 of our candidates. A high X-ray-to-optical flux ratio together with a stable flux and soft X-ray spectrum make the brightest source of our sample, 2XMM J104608.7-594306, a newly discovered thermally emitting INS. The X-ray source 2XMM J010642.3+005032 has no evident optical counterpart and should be further investigated. The remaining X-ray sources are most probably identified with cataclysmic variables and active galactic nuclei, as inferred from the colours and flux ratios of their likely optical counterparts. Beyond the finding of new thermally emitting INSs, our study aims at constraining the space density of this Galactic population at great distances and at determining whether their apparently high density is a local anomaly or not.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0004-6361</s0></fA01><fA02 i1="01"><s0>AAEJAF</s0></fA02><fA03 i2="1"><s0>Astron. astrophys. : (Berl., Print)</s0></fA03><fA05><s2>504</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>A search for thermally emitting isolated neutron stars in the 2XMMp catalogue</s1></fA08><fA11 i1="01" i2="1"><s1>PIRES (A. M.)</s1></fA11><fA11 i1="02" i2="1"><s1>MOTCH (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>JANOT-PACHECO (E.)</s1></fA11><fA14 i1="01"><s1>Instituto de Astronomia, Geofisica e Ciencias Atmosf6ricas, Universidade de São Paulo, R. do Matão 1226</s1><s2>05508-090 São Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>CNRS, Université de Strasbourg, Observatoire Astronomique, 11 rue de l'Université</s1><s2>67000 Strasbourg</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA20><s1>185-197</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>14176</s2><s5>354000171067670200</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0393102</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Astronomy and astrophysics : (Berlin. Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>The relatively large number of nearby radio-quiet and thermally emitting isolated neutron stars (INSs) discovered in the ROSAT All-Sky Survey, dubbed the &#34;Magnificent Seven&#34;, suggests that they belong to a formerly neglected major component of the overall INS population. So far, attempts to discover similar INSs beyond the solar vicinity failed to confirm any reliable candidate. The good positional accuracy and soft X-ray sensitivity of the EPIC cameras onboard the XMM-Newton satellite allow us to efficiently search for new thermally emitting INSs. We used the 2XMMp catalogue to select sources with no catalogued candidate counterparts and with X-ray spectra similar to those of the Magnificent Seven, but seen at greater distances and thus undergoing higher interstellar absorptions. Identifications in more than 170 astronomical catalogues and visual screening allowed us to select fewer than 30 good INS candidates. In order to rule out alternative identifications, we obtained deep ESO-VLT and SOAR optical imaging for the X-ray brightest candidates. We report here on the optical follow-up results of our search and discuss the possible nature of 8 of our candidates. A high X-ray-to-optical flux ratio together with a stable flux and soft X-ray spectrum make the brightest source of our sample, 2XMM J104608.7-594306, a newly discovered thermally emitting INS. The X-ray source 2XMM J010642.3+005032 has no evident optical counterpart and should be further investigated. The remaining X-ray sources are most probably identified with cataclysmic variables and active galactic nuclei, as inferred from the colours and flux ratios of their likely optical counterparts. Beyond the finding of new thermally emitting INSs, our study aims at constraining the space density of this Galactic population at great distances and at determining whether their apparently high density is a local anomaly or not.</s0></fC01><fC02 i1="01" i2="3"><s0>001E03</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Etoile neutron</s0><s5>26</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Neutron stars</s0><s5>26</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Catalogue astronomique</s0><s5>27</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Astronomical catalogues</s0><s5>27</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Etude ciel</s0><s5>28</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Sky surveys</s0><s5>28</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Voisinage solaire</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Solar neighborhood</s0><s5>29</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Vecindad solar</s0><s5>29</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Rayon X mou</s0><s5>30</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Soft X radiation</s0><s5>30</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Spectre RX</s0><s5>31</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>X-ray spectra</s0><s5>31</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Absorption interstellaire</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Interstellar absorption</s0><s5>32</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Absorción interestelar</s0><s5>32</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Effet écran</s0><s5>33</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Screening</s0><s5>33</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Contrepartie optique</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Optical counterpart</s0><s5>34</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Contrapartida óptica</s0><s5>34</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Etoile variable cataclysmique</s0><s5>35</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Cataclysmic variable stars</s0><s5>35</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Noyau galactique actif</s0><s5>36</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Active galaxy nuclei</s0><s5>36</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Couleur</s0><s5>37</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Color</s0><s5>37</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Densité élevée</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>High density</s0><s5>38</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Densidad elevada</s0><s5>38</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Anomalie</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Anomaly</s0><s5>39</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Anomalía</s0><s5>39</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>Galaxies actives</s0><s5>40</s5></fC03><fC03 i1="15" i2="3" l="ENG"><s0>Active galaxies</s0><s5>40</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Noyau galaxies</s0><s5>41</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Galaxy nuclei</s0><s5>41</s5></fC03><fN21><s1>285</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0393102 INIST</NO><ET>A search for thermally emitting isolated neutron stars in the 2XMMp catalogue</ET><AU>PIRES (A. M.); MOTCH (C.); JANOT-PACHECO (E.)</AU><AF>Instituto de Astronomia, Geofisica e Ciencias Atmosf6ricas, Universidade de São Paulo, R. do Matão 1226/05508-090 São Paulo/Brésil (1 aut., 3 aut.); CNRS, Université de Strasbourg, Observatoire Astronomique, 11 rue de l'Université/67000 Strasbourg/France (1 aut., 2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Astronomy and astrophysics : (Berlin. Print); ISSN 0004-6361; Coden AAEJAF; France; Da. 2009; Vol. 504; No. 1; Pp. 185-197; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>The relatively large number of nearby radio-quiet and thermally emitting isolated neutron stars (INSs) discovered in the ROSAT All-Sky Survey, dubbed the &#34;Magnificent Seven&#34;, suggests that they belong to a formerly neglected major component of the overall INS population. So far, attempts to discover similar INSs beyond the solar vicinity failed to confirm any reliable candidate. The good positional accuracy and soft X-ray sensitivity of the EPIC cameras onboard the XMM-Newton satellite allow us to efficiently search for new thermally emitting INSs. We used the 2XMMp catalogue to select sources with no catalogued candidate counterparts and with X-ray spectra similar to those of the Magnificent Seven, but seen at greater distances and thus undergoing higher interstellar absorptions. Identifications in more than 170 astronomical catalogues and visual screening allowed us to select fewer than 30 good INS candidates. In order to rule out alternative identifications, we obtained deep ESO-VLT and SOAR optical imaging for the X-ray brightest candidates. We report here on the optical follow-up results of our search and discuss the possible nature of 8 of our candidates. A high X-ray-to-optical flux ratio together with a stable flux and soft X-ray spectrum make the brightest source of our sample, 2XMM J104608.7-594306, a newly discovered thermally emitting INS. The X-ray source 2XMM J010642.3+005032 has no evident optical counterpart and should be further investigated. The remaining X-ray sources are most probably identified with cataclysmic variables and active galactic nuclei, as inferred from the colours and flux ratios of their likely optical counterparts. Beyond the finding of new thermally emitting INSs, our study aims at constraining the space density of this Galactic population at great distances and at determining whether their apparently high density is a local anomaly or not.</EA><CC>001E03</CC><FD>Etoile neutron; Catalogue astronomique; Etude ciel; Voisinage solaire; Rayon X mou; Spectre RX; Absorption interstellaire; Effet écran; Contrepartie optique; Etoile variable cataclysmique; Noyau galactique actif; Couleur; Densité élevée; Anomalie; Galaxies actives; Noyau galaxies</FD><ED>Neutron stars; Astronomical catalogues; Sky surveys; Solar neighborhood; Soft X radiation; X-ray spectra; Interstellar absorption; Screening; Optical counterpart; Cataclysmic variable stars; Active galaxy nuclei; Color; High density; Anomaly; Active galaxies; Galaxy nuclei</ED><SD>Vecindad solar; Absorción interestelar; Contrapartida óptica; Densidad elevada; Anomalía</SD><LO>INIST-14176.354000171067670200</LO><ID>09-0393102</ID></server></inist></record>
000D65	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Accuracy of WHO CD4 cell count criteria for virological failure of antiretroviral therapy</title><author><name sortKey="Keiser, Olivia" uniqKey="Keiser O">Olivia Keiser</name><affiliation><inist:fA14 i1="01"><s1>Institute of Social and Preventive Medicine (ISPM), University of Bern</s1><s2>Bern</s2><s3>CHE</s3><sZ>1 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Macphail, Patrick" uniqKey="Macphail P">Patrick Macphail</name><affiliation><inist:fA14 i1="02"><s1>Clinical HIV Research Unit, Department of Medicine, Faculty of Health Sciences, University of Witwatersrand</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Boulle, Andrew" uniqKey="Boulle A">Andrew Boulle</name><affiliation><inist:fA14 i1="03"><s1>School of Public Health and Family Medicine, University of Cape Town</s1><s2>Cape Town</s2><s3>ZAF</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wood, Robin" uniqKey="Wood R">Robin Wood</name><affiliation><inist:fA14 i1="04"><s1>The Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town</s1><s2>Cape Town</s2><s3>ZAF</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Schechter, Mauro" uniqKey="Schechter M">Mauro Schechter</name><affiliation><inist:fA14 i1="05"><s1>Hospital Universitario Clementino Fraga Filho, Universidade Federal do Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dabis, Francois" uniqKey="Dabis F">François Dabis</name><affiliation><inist:fA14 i1="06"><s1>INSERM U.593, ISPED, Université Victor Segalen</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sprinz, Eduardo" uniqKey="Sprinz E">Eduardo Sprinz</name><affiliation><inist:fA14 i1="07"><s1>Hospital de Clinicas, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Egger, Matthias" uniqKey="Egger M">Matthias Egger</name><affiliation><inist:fA14 i1="01"><s1>Institute of Social and Preventive Medicine (ISPM), University of Bern</s1><s2>Bern</s2><s3>CHE</s3><sZ>1 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0393611</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0393611 INIST</idno><idno type="RBID">Pascal:09-0393611</idno><idno type="wicri:Area/Main/Corpus">001C16</idno></publicationStmt><seriesStmt><idno type="ISSN">1360-2276</idno><title level="j" type="abbreviated">TM IH, Trop. med. int. health</title><title level="j" type="main">TM &#38; IH. Tropical medicine &#38; international health</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>AIDS</term><term>Accuracy</term><term>Africa</term><term>Antiretroviral agent</term><term>Antiviral</term><term>Chemotherapy</term><term>Diagnosis</term><term>Failure</term><term>Immunological investigation</term><term>Numeration</term><term>T-Lymphocyte</term><term>Technique</term><term>Treatment</term><term>Tropical medicine</term><term>Viral load</term><term>WHO</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>SIDA</term><term>Exploration immunologique</term><term>Numération</term><term>Antiviral</term><term>Précision</term><term>OMS</term><term>Lymphocyte T</term><term>Echec</term><term>Traitement</term><term>Antirétroviral</term><term>Chimiothérapie</term><term>Charge virale</term><term>Diagnostic</term><term>Technique</term><term>Afrique</term><term>Médecine tropicale</term><term>Antigène CD4</term><term>Protocole HAART</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">OBJECTIVES To examine the accuracy of the World Health Organization immunological criteria for virological failure of antiretroviral treatment. METHODS Analysis of 10 treatment programmes in Africa and South America that monitor both CD4 cell counts and HIV-1 viral load. Adult patients with at least two CD4 counts and viral load measurements between month 6 and 18 after starting a non-nucleoside reverse transcriptase inhibitor-based regimen were included. WHO immunological criteria include CD4 counts persistently &#60;100 cells/μl, a fall below the baseline CD4 count, or a fall of &#62;50% from the peak value. Virological failure was defined as two measurements &#62;10 0000 copies/ml (higher threshold) or ≥500 copies/ml (lower threshold). Measures of accuracy with exact binomial 95% confidence intervals (CI) were calculated. RESULTS A total of 2009 patients were included. During 1856 person-years of follow up 63 patients met the immunological criteria and 35 patients (higher threshold) and 95 patients (lower threshold) met the virological criteria. Sensitivity [95% confidence interval (CI)] was 17.1% (6.6-33.6%) for the higher and 12.6% (6.7-21.0%) for the lower threshold. Corresponding results for specificity were 97.1% (96.3-97.8%) and 97.3% (96.5-98.0%), for positive predictive value 9.5% (3.6-19.6%) and 19.0% (10.2-30.9%) and for negative predictive value 98.5% (97.9-99.0%) and 95.7% (94.7-96.6%). CONCLUSIONS The positive predictive value of the WHO immunological criteria for virological failure of antiretroviral treatment in resource-limited settings is poor, but the negative predictive value is high. Immunological criteria are more appropriate for ruling out than for ruling in virological failure in resource-limited settings.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1360-2276</s0></fA01><fA03 i2="1"><s0>TM IH, Trop. med. int. health</s0></fA03><fA05><s2>14</s2></fA05><fA06><s2>10</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Accuracy of WHO CD4 cell count criteria for virological failure of antiretroviral therapy</s1></fA08><fA11 i1="01" i2="1"><s1>KEISER (Olivia)</s1></fA11><fA11 i1="02" i2="1"><s1>MACPHAIL (Patrick)</s1></fA11><fA11 i1="03" i2="1"><s1>BOULLE (Andrew)</s1></fA11><fA11 i1="04" i2="1"><s1>WOOD (Robin)</s1></fA11><fA11 i1="05" i2="1"><s1>SCHECHTER (Mauro)</s1></fA11><fA11 i1="06" i2="1"><s1>DABIS (François)</s1></fA11><fA11 i1="07" i2="1"><s1>SPRINZ (Eduardo)</s1></fA11><fA11 i1="08" i2="1"><s1>EGGER (Matthias)</s1></fA11><fA14 i1="01"><s1>Institute of Social and Preventive Medicine (ISPM), University of Bern</s1><s2>Bern</s2><s3>CHE</s3><sZ>1 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="02"><s1>Clinical HIV Research Unit, Department of Medicine, Faculty of Health Sciences, University of Witwatersrand</s1><s2>Johannesburg</s2><s3>ZAF</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>School of Public Health and Family Medicine, University of Cape Town</s1><s2>Cape Town</s2><s3>ZAF</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>The Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town</s1><s2>Cape Town</s2><s3>ZAF</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Hospital Universitario Clementino Fraga Filho, Universidade Federal do Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>INSERM U.593, ISPED, Université Victor Segalen</s1><s2>Bordeaux</s2><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Hospital de Clinicas, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>7 aut.</sZ></fA14><fA17 i1="01" i2="1"><s1>ART-LINC Collaboration of the International Databases to Evaluate AIDS (leDEA)</s1><s3>INC</s3></fA17><fA20><s1>1220-1225</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>26295</s2><s5>354000196205180080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0393611</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>TM &#38; IH. Tropical medicine &#38; international health</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>OBJECTIVES To examine the accuracy of the World Health Organization immunological criteria for virological failure of antiretroviral treatment. METHODS Analysis of 10 treatment programmes in Africa and South America that monitor both CD4 cell counts and HIV-1 viral load. Adult patients with at least two CD4 counts and viral load measurements between month 6 and 18 after starting a non-nucleoside reverse transcriptase inhibitor-based regimen were included. WHO immunological criteria include CD4 counts persistently &#60;100 cells/μl, a fall below the baseline CD4 count, or a fall of &#62;50% from the peak value. Virological failure was defined as two measurements &#62;10 0000 copies/ml (higher threshold) or ≥500 copies/ml (lower threshold). Measures of accuracy with exact binomial 95% confidence intervals (CI) were calculated. RESULTS A total of 2009 patients were included. During 1856 person-years of follow up 63 patients met the immunological criteria and 35 patients (higher threshold) and 95 patients (lower threshold) met the virological criteria. Sensitivity [95% confidence interval (CI)] was 17.1% (6.6-33.6%) for the higher and 12.6% (6.7-21.0%) for the lower threshold. Corresponding results for specificity were 97.1% (96.3-97.8%) and 97.3% (96.5-98.0%), for positive predictive value 9.5% (3.6-19.6%) and 19.0% (10.2-30.9%) and for negative predictive value 98.5% (97.9-99.0%) and 95.7% (94.7-96.6%). CONCLUSIONS The positive predictive value of the WHO immunological criteria for virological failure of antiretroviral treatment in resource-limited settings is poor, but the negative predictive value is high. Immunological criteria are more appropriate for ruling out than for ruling in virological failure in resource-limited settings.</s0></fC01><fC02 i1="01" i2="X"><s0>002B01</s0></fC02><fC02 i1="02" i2="X"><s0>002B05C02D</s0></fC02><fC02 i1="03" i2="X"><s0>002B02S05</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>SIDA</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>AIDS</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>SIDA</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Exploration immunologique</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Immunological investigation</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Análisis inmunológico</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Numération</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Numeration</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Numeración</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Antiviral</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Antiviral</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Antiviral</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Précision</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Accuracy</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Precisión</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>OMS</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>WHO</s0><s5>08</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>OMS</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Lymphocyte T</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>T-Lymphocyte</s0><s5>09</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Linfocito T</s0><s5>09</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Echec</s0><s5>13</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Failure</s0><s5>13</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Fracaso</s0><s5>13</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Traitement</s0><s5>14</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Treatment</s0><s5>14</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Tratamiento</s0><s5>14</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Antirétroviral</s0><s5>15</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Antiretroviral agent</s0><s5>15</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Antiretroviral</s0><s5>15</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Chimiothérapie</s0><s5>16</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Chemotherapy</s0><s5>16</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Quimioterapia</s0><s5>16</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Charge virale</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Viral load</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Carga vírica</s0><s5>17</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Diagnostic</s0><s5>18</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Diagnosis</s0><s5>18</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Diagnóstico</s0><s5>18</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Technique</s0><s5>19</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Technique</s0><s5>19</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Técnica</s0><s5>19</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Afrique</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Africa</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Africa</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Médecine tropicale</s0><s5>21</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Tropical medicine</s0><s5>21</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Medicina tropical</s0><s5>21</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Antigène CD4</s0><s4>INC</s4><s5>86</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Protocole HAART</s0><s4>INC</s4><s5>87</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Virose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Viral disease</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Virosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Immunodéficit</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Immune deficiency</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Inmunodeficiencia</s0><s5>37</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Immunopathologie</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Immunopathology</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Inmunopatología</s0><s5>39</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Exploration microbiologique</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Microbiological investigation</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Análisis microbiológico</s0><s5>40</s5></fC07><fN21><s1>285</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0393611 INIST</NO><ET>Accuracy of WHO CD4 cell count criteria for virological failure of antiretroviral therapy</ET><AU>KEISER (Olivia); MACPHAIL (Patrick); BOULLE (Andrew); WOOD (Robin); SCHECHTER (Mauro); DABIS (François); SPRINZ (Eduardo); EGGER (Matthias)</AU><AF>Institute of Social and Preventive Medicine (ISPM), University of Bern/Bern/Suisse (1 aut., 8 aut.); Clinical HIV Research Unit, Department of Medicine, Faculty of Health Sciences, University of Witwatersrand/Johannesburg/Afrique du Sud (2 aut.); School of Public Health and Family Medicine, University of Cape Town/Cape Town/Afrique du Sud (3 aut.); The Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town/Cape Town/Afrique du Sud (4 aut.); Hospital Universitario Clementino Fraga Filho, Universidade Federal do Rio de Janeiro/Rio de Janeiro/Brésil (5 aut.); INSERM U.593, ISPED, Université Victor Segalen/Bordeaux/France (6 aut.); Hospital de Clinicas, Universidade Federal do Rio Grande do Sul/Porto Alegre/Brésil (7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>TM &#38; IH. Tropical medicine &#38; international health; ISSN 1360-2276; Royaume-Uni; Da. 2009; Vol. 14; No. 10; Pp. 1220-1225; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>OBJECTIVES To examine the accuracy of the World Health Organization immunological criteria for virological failure of antiretroviral treatment. METHODS Analysis of 10 treatment programmes in Africa and South America that monitor both CD4 cell counts and HIV-1 viral load. Adult patients with at least two CD4 counts and viral load measurements between month 6 and 18 after starting a non-nucleoside reverse transcriptase inhibitor-based regimen were included. WHO immunological criteria include CD4 counts persistently &#60;100 cells/μl, a fall below the baseline CD4 count, or a fall of &#62;50% from the peak value. Virological failure was defined as two measurements &#62;10 0000 copies/ml (higher threshold) or ≥500 copies/ml (lower threshold). Measures of accuracy with exact binomial 95% confidence intervals (CI) were calculated. RESULTS A total of 2009 patients were included. During 1856 person-years of follow up 63 patients met the immunological criteria and 35 patients (higher threshold) and 95 patients (lower threshold) met the virological criteria. Sensitivity [95% confidence interval (CI)] was 17.1% (6.6-33.6%) for the higher and 12.6% (6.7-21.0%) for the lower threshold. Corresponding results for specificity were 97.1% (96.3-97.8%) and 97.3% (96.5-98.0%), for positive predictive value 9.5% (3.6-19.6%) and 19.0% (10.2-30.9%) and for negative predictive value 98.5% (97.9-99.0%) and 95.7% (94.7-96.6%). CONCLUSIONS The positive predictive value of the WHO immunological criteria for virological failure of antiretroviral treatment in resource-limited settings is poor, but the negative predictive value is high. Immunological criteria are more appropriate for ruling out than for ruling in virological failure in resource-limited settings.</EA><CC>002B01; 002B05C02D; 002B02S05</CC><FD>SIDA; Exploration immunologique; Numération; Antiviral; Précision; OMS; Lymphocyte T; Echec; Traitement; Antirétroviral; Chimiothérapie; Charge virale; Diagnostic; Technique; Afrique; Médecine tropicale; Antigène CD4; Protocole HAART</FD><FG>Virose; Infection; Immunodéficit; Immunopathologie; Exploration microbiologique</FG><ED>AIDS; Immunological investigation; Numeration; Antiviral; Accuracy; WHO; T-Lymphocyte; Failure; Treatment; Antiretroviral agent; Chemotherapy; Viral load; Diagnosis; Technique; Africa; Tropical medicine</ED><EG>Viral disease; Infection; Immune deficiency; Immunopathology; Microbiological investigation</EG><SD>SIDA; Análisis inmunológico; Numeración; Antiviral; Precisión; OMS; Linfocito T; Fracaso; Tratamiento; Antiretroviral; Quimioterapia; Carga vírica; Diagnóstico; Técnica; Africa; Medicina tropical</SD><LO>INIST-26295.354000196205180080</LO><ID>09-0393611</ID></server></inist></record>
000D66	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Thin film growth of multiferroic BiMn<sub>2</sub>O<sub>5</sub> using pulsed laser ablation and its characterization</title><author><name sortKey="Shukla, D K" uniqKey="Shukla D">D. K. Shukla</name><affiliation><inist:fA14 i1="01"><s1>Department of Physics, Aligarh Muslim University</s1><s2>Aligarh 202002</s2><s3>IND</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kumar, Ravi" uniqKey="Kumar R">Ravi Kumar</name><affiliation><inist:fA14 i1="02"><s1>Inter University Accelerator Centre, Aruna Asaf ali Marg</s1><s2>New Delhi 110067</s2><s3>IND</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sharma, S K" uniqKey="Sharma S">S. K. Sharma</name><affiliation><inist:fA14 i1="03"><s1>Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP) Campinas</s1><s2>13.083-970, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Thakur, P" uniqKey="Thakur P">P. Thakur</name><affiliation><inist:fA14 i1="04"><s1>European Synchrotron Radiation Facility, BP220</s1><s2>38043 Grenoble</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Choudhary, R J" uniqKey="Choudhary R">R. J. Choudhary</name><affiliation><inist:fA14 i1="05"><s1>UGC-DAE Consortium for Scientific Research</s1><s2>Indore 452001</s2><s3>IND</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mollah, S" uniqKey="Mollah S">S. Mollah</name><affiliation><inist:fA14 i1="01"><s1>Department of Physics, Aligarh Muslim University</s1><s2>Aligarh 202002</s2><s3>IND</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brookes, N B" uniqKey="Brookes N">N. B. Brookes</name><affiliation><inist:fA14 i1="04"><s1>European Synchrotron Radiation Facility, BP220</s1><s2>38043 Grenoble</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Knobel, M" uniqKey="Knobel M">M. Knobel</name><affiliation><inist:fA14 i1="03"><s1>Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP) Campinas</s1><s2>13.083-970, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Chae, K H" uniqKey="Chae K">K. H. Chae</name><affiliation><inist:fA14 i1="06"><s1>Materials Science and Technology Research Division, KIST</s1><s2>Seoul 136-791</s2><s3>KOR</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Choi, W K" uniqKey="Choi W">W. K. Choi</name><affiliation><inist:fA14 i1="06"><s1>Materials Science and Technology Research Division, KIST</s1><s2>Seoul 136-791</s2><s3>KOR</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0393942</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0393942 INIST</idno><idno type="RBID">Pascal:09-0393942</idno><idno type="wicri:Area/Main/Corpus">001C15</idno></publicationStmt><seriesStmt><idno type="ISSN">0022-3727</idno><title level="j" type="abbreviated">J. phys., D. Appl. phys. : (Print)</title><title level="j" type="main">Journal of physics. D, Applied physics : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antiferromagnetism</term><term>Atomic force microscopy</term><term>Bismuth Manganese Oxides Mixed</term><term>Ferroic material</term><term>Magnetic hysteresis</term><term>Magnetic susceptibility</term><term>Magnetization</term><term>Orthorhombic lattices</term><term>Polycrystals</term><term>Pulsed laser deposition</term><term>Raman spectra</term><term>Spin glasses</term><term>Surface morphology</term><term>Thin films</term><term>Valence</term><term>XANES</term><term>XRD</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dépôt laser pulsé</term><term>Diffraction RX</term><term>Spectre Raman</term><term>XANES</term><term>Hystérésis magnétique</term><term>Valence</term><term>Aimantation</term><term>Verre spin</term><term>Antiferromagnétisme</term><term>Bismuth Manganèse Oxyde Mixte</term><term>Susceptibilité magnétique</term><term>Microscopie force atomique</term><term>Morphologie surface</term><term>Couche mince</term><term>Matériau multiferroïque</term><term>Polycristal</term><term>Réseau orthorhombique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Single phase polycrystalline thin films of multiferroic BiMn<sub>2</sub>O<sub>5</sub> have been prepared on an LaAl0<sub>3</sub> (LAO) substrate using the pulsed laser deposition technique. X-ray diffraction and Raman scattering data show that the films are highly strained and have a single phase orthorhombic structure. Near edge x-ray absorption fine structure data of the O K-edge and the Mn L<sub>3,2</sub>-edge show no change in the electronic structure and the valence state of the BiMn<sub>2</sub>O<sub>5</sub> thin films from that of the bulk. However, magnetic measurements performed over a wide range of temperature (2-300 K) and field (0-2 T) demonstrate a spectacular change in the magnetic behaviour of the BiMn<sub>2</sub>O<sub>5</sub> thin films compared with the bulk. The zero field cooled magnetization confirms the antiferromagnetic transition, similar to the bulk sample, whereas field cooled magnetization data, surprisingly, show spin glass (SG) behaviour. The antiferromagnetic ordering at low temperature (5 K) is confirmed from M-H hysteresis measurements. Atomic force microscopy (AFM) measurement used to study the surface morphology shows unevenly spaced patterns of size ∼ 1-2 μm, separated by ridges of peak-to-valley height ∼40 nm. The observed magnetic behaviour is explained in the context of the highly strained structure of the films as observed by XRD, Raman scattering and AFM data.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0022-3727</s0></fA01><fA02 i1="01"><s0>JPAPBE</s0></fA02><fA03 i2="1"><s0>J. phys., D. Appl. phys. : (Print)</s0></fA03><fA05><s2>42</s2></fA05><fA06><s2>12</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Thin film growth of multiferroic BiMn<sub>2</sub>O<sub>5</sub> using pulsed laser ablation and its characterization</s1></fA08><fA11 i1="01" i2="1"><s1>SHUKLA (D. K.)</s1></fA11><fA11 i1="02" i2="1"><s1>KUMAR (Ravi)</s1></fA11><fA11 i1="03" i2="1"><s1>SHARMA (S. K.)</s1></fA11><fA11 i1="04" i2="1"><s1>THAKUR (P.)</s1></fA11><fA11 i1="05" i2="1"><s1>CHOUDHARY (R. J.)</s1></fA11><fA11 i1="06" i2="1"><s1>MOLLAH (S.)</s1></fA11><fA11 i1="07" i2="1"><s1>BROOKES (N. B.)</s1></fA11><fA11 i1="08" i2="1"><s1>KNOBEL (M.)</s1></fA11><fA11 i1="09" i2="1"><s1>CHAE (K. H.)</s1></fA11><fA11 i1="10" i2="1"><s1>CHOI (W. K.)</s1></fA11><fA14 i1="01"><s1>Department of Physics, Aligarh Muslim University</s1><s2>Aligarh 202002</s2><s3>IND</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Inter University Accelerator Centre, Aruna Asaf ali Marg</s1><s2>New Delhi 110067</s2><s3>IND</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP) Campinas</s1><s2>13.083-970, SP</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="04"><s1>European Synchrotron Radiation Facility, BP220</s1><s2>38043 Grenoble</s2><s3>FRA</s3><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="05"><s1>UGC-DAE Consortium for Scientific Research</s1><s2>Indore 452001</s2><s3>IND</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Materials Science and Technology Research Division, KIST</s1><s2>Seoul 136-791</s2><s3>KOR</s3><sZ>9 aut.</sZ><sZ>10 aut.</sZ></fA14><fA20><s2>125304.1-125304.6</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>5841</s2><s5>354000188337240350</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>29 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0393942</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of physics. D, Applied physics : (Print)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Single phase polycrystalline thin films of multiferroic BiMn<sub>2</sub>O<sub>5</sub> have been prepared on an LaAl0<sub>3</sub> (LAO) substrate using the pulsed laser deposition technique. X-ray diffraction and Raman scattering data show that the films are highly strained and have a single phase orthorhombic structure. Near edge x-ray absorption fine structure data of the O K-edge and the Mn L<sub>3,2</sub>-edge show no change in the electronic structure and the valence state of the BiMn<sub>2</sub>O<sub>5</sub> thin films from that of the bulk. However, magnetic measurements performed over a wide range of temperature (2-300 K) and field (0-2 T) demonstrate a spectacular change in the magnetic behaviour of the BiMn<sub>2</sub>O<sub>5</sub> thin films compared with the bulk. The zero field cooled magnetization confirms the antiferromagnetic transition, similar to the bulk sample, whereas field cooled magnetization data, surprisingly, show spin glass (SG) behaviour. The antiferromagnetic ordering at low temperature (5 K) is confirmed from M-H hysteresis measurements. Atomic force microscopy (AFM) measurement used to study the surface morphology shows unevenly spaced patterns of size ∼ 1-2 μm, separated by ridges of peak-to-valley height ∼40 nm. The observed magnetic behaviour is explained in the context of the highly strained structure of the films as observed by XRD, Raman scattering and AFM data.</s0></fC01><fC02 i1="01" i2="3"><s0>001B70E70A</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Dépôt laser pulsé</s0><s5>02</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Pulsed laser deposition</s0><s5>02</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Diffraction RX</s0><s5>03</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>XRD</s0><s5>03</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Spectre Raman</s0><s5>04</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>Raman spectra</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>XANES</s0><s5>05</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>XANES</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Hystérésis magnétique</s0><s5>06</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Magnetic hysteresis</s0><s5>06</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Valence</s0><s5>07</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Valence</s0><s5>07</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Aimantation</s0><s5>08</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Magnetization</s0><s5>08</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Verre spin</s0><s5>09</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Spin glasses</s0><s5>09</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Antiferromagnétisme</s0><s5>10</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Antiferromagnetism</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Bismuth Manganèse Oxyde Mixte</s0><s2>NC</s2><s2>NA</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Bismuth Manganese Oxides Mixed</s0><s2>NC</s2><s2>NA</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Mixto</s0><s2>NC</s2><s2>NA</s2><s5>11</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Susceptibilité magnétique</s0><s5>12</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Magnetic susceptibility</s0><s5>12</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Microscopie force atomique</s0><s5>13</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Atomic force microscopy</s0><s5>13</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Morphologie surface</s0><s5>14</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Surface morphology</s0><s5>14</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Couche mince</s0><s5>15</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Thin films</s0><s5>15</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Matériau multiferroïque</s0><s5>16</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Ferroic material</s0><s5>16</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Material ferroico</s0><s5>16</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Polycristal</s0><s5>17</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Polycrystals</s0><s5>17</s5></fC03><fC03 i1="17" i2="3" l="FRE"><s0>Réseau orthorhombique</s0><s5>18</s5></fC03><fC03 i1="17" i2="3" l="ENG"><s0>Orthorhombic lattices</s0><s5>18</s5></fC03><fN21><s1>285</s1></fN21></pA></standard><server><NO>PASCAL 09-0393942 INIST</NO><ET>Thin film growth of multiferroic BiMn<sub>2</sub>O<sub>5</sub> using pulsed laser ablation and its characterization</ET><AU>SHUKLA (D. K.); KUMAR (Ravi); SHARMA (S. K.); THAKUR (P.); CHOUDHARY (R. J.); MOLLAH (S.); BROOKES (N. B.); KNOBEL (M.); CHAE (K. H.); CHOI (W. K.)</AU><AF>Department of Physics, Aligarh Muslim University/Aligarh 202002/Inde (1 aut., 6 aut.); Inter University Accelerator Centre, Aruna Asaf ali Marg/New Delhi 110067/Inde (2 aut.); Instituto de Fisica Gleb Wataghin, Universidade Estadual de Campinas (UNICAMP) Campinas/13.083-970, SP/Brésil (3 aut., 8 aut.); European Synchrotron Radiation Facility, BP220/38043 Grenoble/France (4 aut., 7 aut.); UGC-DAE Consortium for Scientific Research/Indore 452001/Inde (5 aut.); Materials Science and Technology Research Division, KIST/Seoul 136-791/Corée, République de (9 aut., 10 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of physics. D, Applied physics : (Print); ISSN 0022-3727; Coden JPAPBE; Royaume-Uni; Da. 2009; Vol. 42; No. 12; 125304.1-125304.6; Bibl. 29 ref.</SO><LA>Anglais</LA><EA>Single phase polycrystalline thin films of multiferroic BiMn<sub>2</sub>O<sub>5</sub> have been prepared on an LaAl0<sub>3</sub> (LAO) substrate using the pulsed laser deposition technique. X-ray diffraction and Raman scattering data show that the films are highly strained and have a single phase orthorhombic structure. Near edge x-ray absorption fine structure data of the O K-edge and the Mn L<sub>3,2</sub>-edge show no change in the electronic structure and the valence state of the BiMn<sub>2</sub>O<sub>5</sub> thin films from that of the bulk. However, magnetic measurements performed over a wide range of temperature (2-300 K) and field (0-2 T) demonstrate a spectacular change in the magnetic behaviour of the BiMn<sub>2</sub>O<sub>5</sub> thin films compared with the bulk. The zero field cooled magnetization confirms the antiferromagnetic transition, similar to the bulk sample, whereas field cooled magnetization data, surprisingly, show spin glass (SG) behaviour. The antiferromagnetic ordering at low temperature (5 K) is confirmed from M-H hysteresis measurements. Atomic force microscopy (AFM) measurement used to study the surface morphology shows unevenly spaced patterns of size ∼ 1-2 μm, separated by ridges of peak-to-valley height ∼40 nm. The observed magnetic behaviour is explained in the context of the highly strained structure of the films as observed by XRD, Raman scattering and AFM data.</EA><CC>001B70E70A</CC><FD>Dépôt laser pulsé; Diffraction RX; Spectre Raman; XANES; Hystérésis magnétique; Valence; Aimantation; Verre spin; Antiferromagnétisme; Bismuth Manganèse Oxyde Mixte; Susceptibilité magnétique; Microscopie force atomique; Morphologie surface; Couche mince; Matériau multiferroïque; Polycristal; Réseau orthorhombique</FD><ED>Pulsed laser deposition; XRD; Raman spectra; XANES; Magnetic hysteresis; Valence; Magnetization; Spin glasses; Antiferromagnetism; Bismuth Manganese Oxides Mixed; Magnetic susceptibility; Atomic force microscopy; Surface morphology; Thin films; Ferroic material; Polycrystals; Orthorhombic lattices</ED><SD>Mixto; Material ferroico</SD><LO>INIST-5841.354000188337240350</LO><ID>09-0393942</ID></server></inist></record>
000D67	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Assessing land availability to produce biomass for energy : The case of Brazilian charcoal for steel making</title><author><name sortKey="Piketty, Marie Gabrielle" uniqKey="Piketty M">Marie-Gabrielle Piketty</name><affiliation><inist:fA14 i1="01"><s1>CIRAD and Sao Paulo University (Economic Department and Environmental Science Program)</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Universidade de Sao Paulo -FEA -Avenida Prof. Luciano Gualberto, 908</s1><s2>CEP: 05 508-900, Sao Paulo, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wichert, Marcos" uniqKey="Wichert M">Marcos Wichert</name><affiliation><inist:fA14 i1="03"><s1>São Paulo University, ESALQ, Forestry Science, Avenida Pádua Dias, 11 CP 9 Piracicaba</s1><s2>SP, CEP 13418-900</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fallot, Abigail" uniqKey="Fallot A">Abigail Fallot</name><affiliation><inist:fA14 i1="04"><s1>CIRAD, 73 rue Jean-François Breton, TA B-42/16 (Bât. 16, Bur. 26)</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Aimola, Luis" uniqKey="Aimola L">Luis Aimola</name><affiliation><inist:fA14 i1="05"><s1>São Paulo University, Environmental Science Program, Brazil, PROCAM-USP Rua do Anfiteatro, 181 Colméia, Favo 15</s1><s2>CEP 05508-900, Cidade Universitdria, SP</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0394359</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0394359 INIST</idno><idno type="RBID">Pascal:09-0394359</idno><idno type="wicri:Area/Main/Corpus">001C14</idno></publicationStmt><seriesStmt><idno type="ISSN">0961-9534</idno><title level="j" type="abbreviated">Biomass bioenergy</title><title level="j" type="main">Biomass &#38; bioenergy</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Biomass</term><term>Brazil</term><term>Charcoal</term><term>Land use</term><term>Multicriteria analysis</term><term>Production capacity</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Biomasse</term><term>Brésil</term><term>Occupation sol</term><term>Capacité production</term><term>Charbon bois</term><term>Analyse multicritère</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The paper discusses the availability of biomass in Brazil to supply charcoal to the steel industry on the bases of an initial global assessment of land potentially available for plantations and of Brazilian data that allows refining the assessment and specifying the issue of practical availability. Technical potentials are first assessed through a series of simple rules against direct competition with agriculture, forests and protected areas, and of quantitative criteria, whether geo-climatic (rainfall), demographic (population density) or legal (reserves). Institutional, social and economic factors are then identified and discussed so as to account for the practical availability of Brazilian biomass through six criteria. The ranking of nine Brazilian States according to these criteria brings out the necessary trade-offs in the selection of land for plantations that would efficiently supply charcoal to the steel industry.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0961-9534</s0></fA01><fA03 i2="1"><s0>Biomass bioenergy</s0></fA03><fA05><s2>33</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Assessing land availability to produce biomass for energy : The case of Brazilian charcoal for steel making</s1></fA08><fA11 i1="01" i2="1"><s1>PIKETTY (Marie-Gabrielle)</s1></fA11><fA11 i1="02" i2="1"><s1>WICHERT (Marcos)</s1></fA11><fA11 i1="03" i2="1"><s1>FALLOT (Abigail)</s1></fA11><fA11 i1="04" i2="1"><s1>AIMOLA (Luis)</s1></fA11><fA14 i1="01"><s1>CIRAD and Sao Paulo University (Economic Department and Environmental Science Program)</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Universidade de Sao Paulo -FEA -Avenida Prof. Luciano Gualberto, 908</s1><s2>CEP: 05 508-900, Sao Paulo, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="03"><s1>São Paulo University, ESALQ, Forestry Science, Avenida Pádua Dias, 11 CP 9 Piracicaba</s1><s2>SP, CEP 13418-900</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="04"><s1>CIRAD, 73 rue Jean-François Breton, TA B-42/16 (Bât. 16, Bur. 26)</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="05"><s1>São Paulo University, Environmental Science Program, Brazil, PROCAM-USP Rua do Anfiteatro, 181 Colméia, Favo 15</s1><s2>CEP 05508-900, Cidade Universitdria, SP</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA20><s1>180-190</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27204</s2><s5>354000185439270030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>34 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0394359</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Biomass &#38; bioenergy</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The paper discusses the availability of biomass in Brazil to supply charcoal to the steel industry on the bases of an initial global assessment of land potentially available for plantations and of Brazilian data that allows refining the assessment and specifying the issue of practical availability. Technical potentials are first assessed through a series of simple rules against direct competition with agriculture, forests and protected areas, and of quantitative criteria, whether geo-climatic (rainfall), demographic (population density) or legal (reserves). Institutional, social and economic factors are then identified and discussed so as to account for the practical availability of Brazilian biomass through six criteria. The ranking of nine Brazilian States according to these criteria brings out the necessary trade-offs in the selection of land for plantations that would efficiently supply charcoal to the steel industry.</s0></fC01><fC02 i1="01" i2="X"><s0>001D06C06</s0></fC02><fC02 i1="02" i2="X"><s0>001D06A01C5</s0></fC02><fC02 i1="03" i2="X"><s0>001D06A01A</s0></fC02><fC02 i1="04" i2="X"><s0>230</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Biomasse</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Biomass</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Biomasa</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Occupation sol</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Land use</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Ocupación terreno</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Capacité production</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Production capacity</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Capacidad producción</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Charbon bois</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Charcoal</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Carbón madera</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Analyse multicritère</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Multicriteria analysis</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Análisis multicriterio</s0><s5>06</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>285</s1></fN21></pA></standard><server><NO>PASCAL 09-0394359 INIST</NO><ET>Assessing land availability to produce biomass for energy : The case of Brazilian charcoal for steel making</ET><AU>PIKETTY (Marie-Gabrielle); WICHERT (Marcos); FALLOT (Abigail); AIMOLA (Luis)</AU><AF>CIRAD and Sao Paulo University (Economic Department and Environmental Science Program)/Brésil (1 aut.); Universidade de Sao Paulo -FEA -Avenida Prof. Luciano Gualberto, 908/CEP: 05 508-900, Sao Paulo, SP/Brésil (1 aut.); São Paulo University, ESALQ, Forestry Science, Avenida Pádua Dias, 11 CP 9 Piracicaba/SP, CEP 13418-900/Brésil (2 aut.); CIRAD, 73 rue Jean-François Breton, TA B-42/16 (Bât. 16, Bur. 26)/34398 Montpellier/France (3 aut.); São Paulo University, Environmental Science Program, Brazil, PROCAM-USP Rua do Anfiteatro, 181 Colméia, Favo 15/CEP 05508-900, Cidade Universitdria, SP/Brésil (4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Biomass &#38; bioenergy; ISSN 0961-9534; Royaume-Uni; Da. 2009; Vol. 33; No. 2; Pp. 180-190; Bibl. 34 ref.</SO><LA>Anglais</LA><EA>The paper discusses the availability of biomass in Brazil to supply charcoal to the steel industry on the bases of an initial global assessment of land potentially available for plantations and of Brazilian data that allows refining the assessment and specifying the issue of practical availability. Technical potentials are first assessed through a series of simple rules against direct competition with agriculture, forests and protected areas, and of quantitative criteria, whether geo-climatic (rainfall), demographic (population density) or legal (reserves). Institutional, social and economic factors are then identified and discussed so as to account for the practical availability of Brazilian biomass through six criteria. The ranking of nine Brazilian States according to these criteria brings out the necessary trade-offs in the selection of land for plantations that would efficiently supply charcoal to the steel industry.</EA><CC>001D06C06; 001D06A01C5; 001D06A01A; 230</CC><FD>Biomasse; Brésil; Occupation sol; Capacité production; Charbon bois; Analyse multicritère</FD><FG>Amérique du Sud; Amérique</FG><ED>Biomass; Brazil; Land use; Production capacity; Charcoal; Multicriteria analysis</ED><EG>South America; America</EG><SD>Biomasa; Brasil; Ocupación terreno; Capacidad producción; Carbón madera; Análisis multicriterio</SD><LO>INIST-27204.354000185439270030</LO><ID>09-0394359</ID></server></inist></record>
000D68	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">GRADIENT DESCENT AND FAST ARTIFICIAL TIME INTEGRATION</title><author><name sortKey="Ascher, Uri M" uniqKey="Ascher U">Uri M. Ascher</name><affiliation><inist:fA14 i1="01"><s1>Department of Computer Science, University of British Columbia</s1><s2>Vancouver</s2><s3>CAN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Van Den Doel, Kees" uniqKey="Van Den Doel K">Kees Van Den Doel</name><affiliation><inist:fA14 i1="01"><s1>Department of Computer Science, University of British Columbia</s1><s2>Vancouver</s2><s3>CAN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name>HUI HUANG</name><affiliation><inist:fA14 i1="02"><s1>Department of Mathematics, University of British Columbia</s1><s2>Vancouver</s2><s3>CAN</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Svaiter, Benar F" uniqKey="Svaiter B">Benar F. Svaiter</name><affiliation><inist:fA14 i1="03"><s1>Institute of Pure and Applied Mathematics (IMPA)</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0395888</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0395888 INIST</idno><idno type="RBID">Pascal:09-0395888</idno><idno type="wicri:Area/Main/Corpus">001C13</idno></publicationStmt><seriesStmt><idno type="ISSN">0764-583X</idno><title level="j" type="abbreviated">Modél. math. anal. numér. : (Print)</title><title level="j" type="main">Modélisation mathématique et analyse numérique : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Descent method</term><term>Differential equation</term><term>Euler scheme</term><term>Greedy algorithm</term><term>Ill posed problem</term><term>Integration</term><term>Inverse problem</term><term>Mathematical model</term><term>Numerical analysis</term><term>Numerical linear algebra</term><term>Numerical stability</term><term>Partial differential equation</term><term>Regularization</term><term>Regularization method</term><term>Smoothing</term><term>Smoothing methods</term><term>Steady state</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Algèbre linéaire numérique</term><term>Problème mal posé</term><term>Intégration</term><term>Régime permanent</term><term>Equation différentielle</term><term>Equation dérivée partielle</term><term>Schéma Euler</term><term>Algorithme glouton</term><term>Méthode descente</term><term>Lissage</term><term>Méthode lissage</term><term>Problème inverse</term><term>Régularisation</term><term>Méthode régularisation</term><term>Stabilité numérique</term><term>Analyse numérique</term><term>Modèle mathématique</term><term>28XX</term><term>34XX</term><term>65Lxx</term><term>35XX</term><term>Méthode Euler</term><term>40G05</term><term>41A60</term><term>65F22</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The integration to steady state of many initial value ODEs and PDEs using the forward Euler method can alternatively be considered as gradient descent for an associated minimization problem. Greedy algorithms such as steepest descent for determining the step size are as slow to reach steady state as is forward Euler integration with the best uniform step size. But other, much faster methods using bolder step size selection exist. Various alternatives are investigated from both theoretical and practical points of view. The steepest descent method is also known for the regularizing or smoothing effect that the first few steps have for certain inverse problems, amounting to a finite time regularization. We further investigate the retention of this property using the faster gradient descent variants in the context of two applications. When the combination of regularization and accuracy demands more than a dozen or so steepest descent steps, the alternatives offer an advantage, even though (indeed because) the absolute stability limit of forward Euler is carefully yet severely violated.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0764-583X</s0></fA01><fA02 i1="01"><s0>RMMAEV</s0></fA02><fA03 i2="1"><s0>Modél. math. anal. numér. : (Print)</s0></fA03><fA05><s2>43</s2></fA05><fA06><s2>4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>GRADIENT DESCENT AND FAST ARTIFICIAL TIME INTEGRATION</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Special Issue on Numerical ODEs today</s1></fA09><fA11 i1="01" i2="1"><s1>ASCHER (Uri M.)</s1></fA11><fA11 i1="02" i2="1"><s1>VAN DEN DOEL (Kees)</s1></fA11><fA11 i1="03" i2="1"><s1>HUI HUANG</s1></fA11><fA11 i1="04" i2="1"><s1>SVAITER (Benar F.)</s1></fA11><fA12 i1="01" i2="1"><s1>CHARTIER (Philippe)</s1><s9>limin.</s9></fA12><fA12 i1="02" i2="1"><s1>PETZOLD (Linda)</s1><s9>limin.</s9></fA12><fA14 i1="01"><s1>Department of Computer Science, University of British Columbia</s1><s2>Vancouver</s2><s3>CAN</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>Department of Mathematics, University of British Columbia</s1><s2>Vancouver</s2><s3>CAN</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Institute of Pure and Applied Mathematics (IMPA)</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA15 i1="01"><s1>INRIA Rennes and Ecole Normale Supérieure de Cachan, Antenne de Bretagne, Avenue Robert Schumann</s1><s2>35170 Bruz</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Dept. of Mechanical Engineering, University of California Santa Barbara</s1><s2>Santa Barbara, CA 93106</s2><s3>USA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>689-708</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>9323B1</s2><s5>354000172402280060</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>36 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0395888</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Modélisation mathématique et analyse numérique : (Print)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="ENG"><s0>The integration to steady state of many initial value ODEs and PDEs using the forward Euler method can alternatively be considered as gradient descent for an associated minimization problem. Greedy algorithms such as steepest descent for determining the step size are as slow to reach steady state as is forward Euler integration with the best uniform step size. But other, much faster methods using bolder step size selection exist. Various alternatives are investigated from both theoretical and practical points of view. The steepest descent method is also known for the regularizing or smoothing effect that the first few steps have for certain inverse problems, amounting to a finite time regularization. We further investigate the retention of this property using the faster gradient descent variants in the context of two applications. When the combination of regularization and accuracy demands more than a dozen or so steepest descent steps, the alternatives offer an advantage, even though (indeed because) the absolute stability limit of forward Euler is carefully yet severely violated.</s0></fC01><fC02 i1="01" i2="X"><s0>001A02E02</s0></fC02><fC02 i1="02" i2="X"><s0>001A02E07</s0></fC02><fC02 i1="03" i2="X"><s0>001A02I01I</s0></fC02><fC02 i1="04" i2="X"><s0>001A02E08</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Algèbre linéaire numérique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Numerical linear algebra</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Algebra lineal numérica</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Problème mal posé</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Ill posed problem</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Problema mal planteado</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Intégration</s0><s5>17</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Integration</s0><s5>17</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Integración</s0><s5>17</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Régime permanent</s0><s5>18</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Steady state</s0><s5>18</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Régimen permanente</s0><s5>18</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Equation différentielle</s0><s5>19</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Differential equation</s0><s5>19</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Ecuación diferencial</s0><s5>19</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Equation dérivée partielle</s0><s5>20</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Partial differential equation</s0><s5>20</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Ecuación derivada parcial</s0><s5>20</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Schéma Euler</s0><s5>21</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Euler scheme</s0><s5>21</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Esquema Euler</s0><s5>21</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Algorithme glouton</s0><s5>22</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Greedy algorithm</s0><s5>22</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Algoritmo glotón</s0><s5>22</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Méthode descente</s0><s5>23</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Descent method</s0><s5>23</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Método descenso</s0><s5>23</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Lissage</s0><s5>24</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Smoothing</s0><s5>24</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Alisamiento</s0><s5>24</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Méthode lissage</s0><s5>25</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Smoothing methods</s0><s5>25</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Problème inverse</s0><s5>26</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Inverse problem</s0><s5>26</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Problema inverso</s0><s5>26</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Régularisation</s0><s5>27</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Regularization</s0><s5>27</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Regularización</s0><s5>27</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Méthode régularisation</s0><s5>28</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Regularization method</s0><s5>28</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Método regularización</s0><s5>28</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Stabilité numérique</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Numerical stability</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Estabilidad numérica</s0><s5>29</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Analyse numérique</s0><s5>30</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Numerical analysis</s0><s5>30</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Análisis numérico</s0><s5>30</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Modèle mathématique</s0><s5>31</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Mathematical model</s0><s5>31</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Modelo matemático</s0><s5>31</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>28XX</s0><s4>INC</s4><s5>70</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>34XX</s0><s4>INC</s4><s5>71</s5></fC03><fC03 i1="20" i2="X" l="FRE"><s0>65Lxx</s0><s4>INC</s4><s5>72</s5></fC03><fC03 i1="21" i2="X" l="FRE"><s0>35XX</s0><s4>INC</s4><s5>73</s5></fC03><fC03 i1="22" i2="X" l="FRE"><s0>Méthode Euler</s0><s4>INC</s4><s5>74</s5></fC03><fC03 i1="23" i2="X" l="FRE"><s0>40G05</s0><s4>INC</s4><s5>75</s5></fC03><fC03 i1="24" i2="X" l="FRE"><s0>41A60</s0><s4>INC</s4><s5>76</s5></fC03><fC03 i1="25" i2="X" l="FRE"><s0>65F22</s0><s4>INC</s4><s5>77</s5></fC03><fN21><s1>285</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0395888 INIST</NO><ET>GRADIENT DESCENT AND FAST ARTIFICIAL TIME INTEGRATION</ET><AU>ASCHER (Uri M.); VAN DEN DOEL (Kees); HUI HUANG; SVAITER (Benar F.); CHARTIER (Philippe); PETZOLD (Linda)</AU><AF>Department of Computer Science, University of British Columbia/Vancouver/Canada (1 aut., 2 aut.); Department of Mathematics, University of British Columbia/Vancouver/Canada (3 aut.); Institute of Pure and Applied Mathematics (IMPA)/Rio de Janeiro/Brésil (4 aut.); INRIA Rennes and Ecole Normale Supérieure de Cachan, Antenne de Bretagne, Avenue Robert Schumann/35170 Bruz/France (1 aut.); Dept. of Mechanical Engineering, University of California Santa Barbara/Santa Barbara, CA 93106/Etats-Unis (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Modélisation mathématique et analyse numérique : (Print); ISSN 0764-583X; Coden RMMAEV; France; Da. 2009; Vol. 43; No. 4; Pp. 689-708; Bibl. 36 ref.</SO><LA>Anglais</LA><EA>The integration to steady state of many initial value ODEs and PDEs using the forward Euler method can alternatively be considered as gradient descent for an associated minimization problem. Greedy algorithms such as steepest descent for determining the step size are as slow to reach steady state as is forward Euler integration with the best uniform step size. But other, much faster methods using bolder step size selection exist. Various alternatives are investigated from both theoretical and practical points of view. The steepest descent method is also known for the regularizing or smoothing effect that the first few steps have for certain inverse problems, amounting to a finite time regularization. We further investigate the retention of this property using the faster gradient descent variants in the context of two applications. When the combination of regularization and accuracy demands more than a dozen or so steepest descent steps, the alternatives offer an advantage, even though (indeed because) the absolute stability limit of forward Euler is carefully yet severely violated.</EA><CC>001A02E02; 001A02E07; 001A02I01I; 001A02E08</CC><FD>Algèbre linéaire numérique; Problème mal posé; Intégration; Régime permanent; Equation différentielle; Equation dérivée partielle; Schéma Euler; Algorithme glouton; Méthode descente; Lissage; Méthode lissage; Problème inverse; Régularisation; Méthode régularisation; Stabilité numérique; Analyse numérique; Modèle mathématique; 28XX; 34XX; 65Lxx; 35XX; Méthode Euler; 40G05; 41A60; 65F22</FD><ED>Numerical linear algebra; Ill posed problem; Integration; Steady state; Differential equation; Partial differential equation; Euler scheme; Greedy algorithm; Descent method; Smoothing; Smoothing methods; Inverse problem; Regularization; Regularization method; Numerical stability; Numerical analysis; Mathematical model</ED><SD>Algebra lineal numérica; Problema mal planteado; Integración; Régimen permanente; Ecuación diferencial; Ecuación derivada parcial; Esquema Euler; Algoritmo glotón; Método descenso; Alisamiento; Problema inverso; Regularización; Método regularización; Estabilidad numérica; Análisis numérico; Modelo matemático</SD><LO>INIST-9323B1.354000172402280060</LO><ID>09-0395888</ID></server></inist></record>
000D69	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Immobilization of anionic iron(III) porphyrins into ordered macroporous layered double hydroxides and investigation of catalytic activity in oxidation reactions</title><author><name sortKey="Halma, Matilte" uniqKey="Halma M">Matilte Halma</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081</s1><s2>Zip Code 81531-980, Curitiba, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dias De Freitas Castro, Kelly Aparecida" uniqKey="Dias De Freitas Castro K">Kelly Aparecida Dias De Freitas Castro</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081</s1><s2>Zip Code 81531-980, Curitiba, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Prevot, Vanessa" uniqKey="Prevot V">Vanessa Prevot</name><affiliation><inist:fA14 i1="02"><s1>Laboratoire des Matériaux Inorganiques, UMR CNRS 6002, Université Blaise Pascal</s1><s2>63177 Aubière</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Forano, Claude" uniqKey="Forano C">Claude Forano</name><affiliation><inist:fA14 i1="02"><s1>Laboratoire des Matériaux Inorganiques, UMR CNRS 6002, Université Blaise Pascal</s1><s2>63177 Aubière</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wypych, Fernando" uniqKey="Wypych F">Fernando Wypych</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081</s1><s2>Zip Code 81531-980, Curitiba, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nakagaki, Shirley" uniqKey="Nakagaki S">Shirley Nakagaki</name><affiliation><inist:fA14 i1="01"><s1>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081</s1><s2>Zip Code 81531-980, Curitiba, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0400039</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0400039 INIST</idno><idno type="RBID">Pascal:09-0400039</idno><idno type="wicri:Area/Main/Corpus">001C12</idno></publicationStmt><seriesStmt><idno type="ISSN">1381-1169</idno><title level="j" type="abbreviated">J. mol. catal., A Chem.</title><title level="j" type="main">Journal of molecular catalysis. A, Chemical</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Catalysis</term><term>Catalytic reaction</term><term>Cytochrome</term><term>Immobilization</term><term>Iron III</term><term>Layered double hydroxide</term><term>Macroporosity</term><term>Models</term><term>Oxidation</term><term>Porous material</term><term>Porphyrin</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Immobilisation</term><term>Fer III</term><term>Porphyrine</term><term>Matériau poreux</term><term>Macroporosité</term><term>Hydroxyde double lamellaire</term><term>Réaction catalytique</term><term>Oxydation</term><term>Cytochrome</term><term>Modèle</term><term>Catalyse</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The first generation anionic iron(III) porphyrin [Fe(TSPP)] and the second generation anionic complexes [Fe(TDFSPP)], [Fe(TCFSPP)], and [Fe(TDCSPP)] were immobilized into three-dimensionally macroporous layered double hydroxide (3DM-LDH), using the direct reconstruction of 3DM-LDH from macroporous mixed oxides MOX or the anionic exchange on DDS intercalated 3DM-LDH. The macroporous layered double hydroxides were obtained at the surface of nanometric polystyrene spheres, which were synthesized by an inverse opal method. Polystyrene was removed after calcination in oxidizing atmosphere, nanostructured mixed oxides (3DM-MOX)were obtained,which after reconstruction give origin to macroporous layered double hydroxide (3DM-LDH). Following metalloporphyrin immobilization, the resulting materials were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), UV-vis (glycerin mull) spectroscopy, attenuated total reflectance Fourier transform infrared spectroscopy (ATR/FTIR), and electron paramagnetic resonance (EPR). Results revealed that the complexes are either immobilized at the surface of the macroporous layered double hydroxide or intercalated between the layers, displacing some dodecylsufate anions. The obtained materials were investigated as catalysts for oxidation reactions, to find out whether they function as cytochrome P-450 models.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1381-1169</s0></fA01><fA03 i2="1"><s0>J. mol. catal., A Chem.</s0></fA03><fA05><s2>310</s2></fA05><fA06><s2>1-2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Immobilization of anionic iron(III) porphyrins into ordered macroporous layered double hydroxides and investigation of catalytic activity in oxidation reactions</s1></fA08><fA11 i1="01" i2="1"><s1>HALMA (Matilte)</s1></fA11><fA11 i1="02" i2="1"><s1>DIAS DE FREITAS CASTRO (Kelly Aparecida)</s1></fA11><fA11 i1="03" i2="1"><s1>PREVOT (Vanessa)</s1></fA11><fA11 i1="04" i2="1"><s1>FORANO (Claude)</s1></fA11><fA11 i1="05" i2="1"><s1>WYPYCH (Fernando)</s1></fA11><fA11 i1="06" i2="1"><s1>NAKAGAKI (Shirley)</s1></fA11><fA14 i1="01"><s1>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081</s1><s2>Zip Code 81531-980, Curitiba, PR</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Laboratoire des Matériaux Inorganiques, UMR CNRS 6002, Université Blaise Pascal</s1><s2>63177 Aubière</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA20><s1>42-50</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>17107A</s2><s5>354000187615520060</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>86 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0400039</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of molecular catalysis. A, Chemical</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>The first generation anionic iron(III) porphyrin [Fe(TSPP)] and the second generation anionic complexes [Fe(TDFSPP)], [Fe(TCFSPP)], and [Fe(TDCSPP)] were immobilized into three-dimensionally macroporous layered double hydroxide (3DM-LDH), using the direct reconstruction of 3DM-LDH from macroporous mixed oxides MOX or the anionic exchange on DDS intercalated 3DM-LDH. The macroporous layered double hydroxides were obtained at the surface of nanometric polystyrene spheres, which were synthesized by an inverse opal method. Polystyrene was removed after calcination in oxidizing atmosphere, nanostructured mixed oxides (3DM-MOX)were obtained,which after reconstruction give origin to macroporous layered double hydroxide (3DM-LDH). Following metalloporphyrin immobilization, the resulting materials were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), UV-vis (glycerin mull) spectroscopy, attenuated total reflectance Fourier transform infrared spectroscopy (ATR/FTIR), and electron paramagnetic resonance (EPR). Results revealed that the complexes are either immobilized at the surface of the macroporous layered double hydroxide or intercalated between the layers, displacing some dodecylsufate anions. The obtained materials were investigated as catalysts for oxidation reactions, to find out whether they function as cytochrome P-450 models.</s0></fC01><fC02 i1="01" i2="X"><s0>001C01A03</s0></fC02><fC02 i1="02" i2="X"><s0>001C01J08</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Immobilisation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Immobilization</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Inmovilización</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Fer III</s0><s2>NC</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Iron III</s0><s2>NC</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Hierro III</s0><s2>NC</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Porphyrine</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Porphyrin</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Porfirina</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Matériau poreux</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Porous material</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Material poroso</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Macroporosité</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Macroporosity</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Macroporosidad</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Hydroxyde double lamellaire</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Layered double hydroxide</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Hidróxido doble laminar</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Réaction catalytique</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Catalytic reaction</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Reacción catalítica</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Oxydation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Oxidation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Oxidación</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Cytochrome</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Cytochrome</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Citocromo</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Modèle</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Models</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Modelo</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Catalyse</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Catalysis</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Catálisis</s0><s5>11</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Hétérocycle azote</s0><s5>12</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Nitrogen heterocycle</s0><s5>12</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Heterociclo nitrógeno</s0><s5>12</s5></fC07><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0400039 INIST</NO><ET>Immobilization of anionic iron(III) porphyrins into ordered macroporous layered double hydroxides and investigation of catalytic activity in oxidation reactions</ET><AU>HALMA (Matilte); DIAS DE FREITAS CASTRO (Kelly Aparecida); PREVOT (Vanessa); FORANO (Claude); WYPYCH (Fernando); NAKAGAKI (Shirley)</AU><AF>Laboratory of Bioinorganic Chemistry and Catalysis, Department of Chemistry, Federal University of Paraná, P.O. Box 19081/Zip Code 81531-980, Curitiba, PR/Brésil (1 aut., 2 aut., 5 aut., 6 aut.); Laboratoire des Matériaux Inorganiques, UMR CNRS 6002, Université Blaise Pascal/63177 Aubière/France (3 aut., 4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of molecular catalysis. A, Chemical; ISSN 1381-1169; Pays-Bas; Da. 2009; Vol. 310; No. 1-2; Pp. 42-50; Bibl. 86 ref.</SO><LA>Anglais</LA><EA>The first generation anionic iron(III) porphyrin [Fe(TSPP)] and the second generation anionic complexes [Fe(TDFSPP)], [Fe(TCFSPP)], and [Fe(TDCSPP)] were immobilized into three-dimensionally macroporous layered double hydroxide (3DM-LDH), using the direct reconstruction of 3DM-LDH from macroporous mixed oxides MOX or the anionic exchange on DDS intercalated 3DM-LDH. The macroporous layered double hydroxides were obtained at the surface of nanometric polystyrene spheres, which were synthesized by an inverse opal method. Polystyrene was removed after calcination in oxidizing atmosphere, nanostructured mixed oxides (3DM-MOX)were obtained,which after reconstruction give origin to macroporous layered double hydroxide (3DM-LDH). Following metalloporphyrin immobilization, the resulting materials were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), UV-vis (glycerin mull) spectroscopy, attenuated total reflectance Fourier transform infrared spectroscopy (ATR/FTIR), and electron paramagnetic resonance (EPR). Results revealed that the complexes are either immobilized at the surface of the macroporous layered double hydroxide or intercalated between the layers, displacing some dodecylsufate anions. The obtained materials were investigated as catalysts for oxidation reactions, to find out whether they function as cytochrome P-450 models.</EA><CC>001C01A03; 001C01J08</CC><FD>Immobilisation; Fer III; Porphyrine; Matériau poreux; Macroporosité; Hydroxyde double lamellaire; Réaction catalytique; Oxydation; Cytochrome; Modèle; Catalyse</FD><FG>Hétérocycle azote</FG><ED>Immobilization; Iron III; Porphyrin; Porous material; Macroporosity; Layered double hydroxide; Catalytic reaction; Oxidation; Cytochrome; Models; Catalysis</ED><EG>Nitrogen heterocycle</EG><SD>Inmovilización; Hierro III; Porfirina; Material poroso; Macroporosidad; Hidróxido doble laminar; Reacción catalítica; Oxidación; Citocromo; Modelo; Catálisis</SD><LO>INIST-17107A.354000187615520060</LO><ID>09-0400039</ID></server></inist></record>
000D70	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Cassava bagasse cellulose nanofibrils reinforced thermoplastic cassava starch</title><author><name sortKey="Teixeira, Eliangela De M" uniqKey="Teixeira E">Eliangela De M. Teixeira</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química de Sâo Carlos, Universidade de São Paulo, C.P. 780</s1><s2>13560-970 São Carlos, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pasquini, Daniel" uniqKey="Pasquini D">Daniel Pasquini</name><affiliation><inist:fA14 i1="02"><s1>CICECO e Departamento de Química, Universidade de Aveiro</s1><s2>3810-193 Aveiro</s2><s3>PRT</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Curvelo, Antonio A S" uniqKey="Curvelo A">Antônio A. S. Curvelo</name><affiliation><inist:fA14 i1="01"><s1>Instituto de Química de Sâo Carlos, Universidade de São Paulo, C.P. 780</s1><s2>13560-970 São Carlos, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Corradini, Elisangela" uniqKey="Corradini E">Elisangela Corradini</name><affiliation><inist:fA14 i1="03"><s1>Departamento de Engenharia de Materiais, Universidade Federal de São Carlos, C.P. 676</s1><s2>13560-095 São Carlos, SP</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Belgacem, Mohamed N" uniqKey="Belgacem M">Mohamed N. Belgacem</name><affiliation><inist:fA14 i1="04"><s1>Grenohle Institute of Technology, The International School of Paper, Print Media and Biomaterials (Grenoble INP - Pagora), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dufresne, Alain" uniqKey="Dufresne A">Alain Dufresne</name><affiliation><inist:fA14 i1="04"><s1>Grenohle Institute of Technology, The International School of Paper, Print Media and Biomaterials (Grenoble INP - Pagora), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0400587</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0400587 INIST</idno><idno type="RBID">Pascal:09-0400587</idno><idno type="wicri:Area/Main/Corpus">001C11</idno></publicationStmt><seriesStmt><idno type="ISSN">0144-8617</idno><title level="j" type="abbreviated">Carbohydr. polym.</title><title level="j" type="main">Carbohydrate polymers</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bagasse</term><term>Cassava</term><term>Cellulose</term><term>Crystallinity</term><term>Dynamic mechanical properties</term><term>Experimental study</term><term>Mechanical properties</term><term>Moisture regain</term><term>Morphology</term><term>Nanocomposite</term><term>Nanofiber</term><term>Natural fiber</term><term>Solvent extraction</term><term>Starch</term><term>Strengthening</term><term>Thermal stability</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Bagasse</term><term>Manioc</term><term>Extraction solvant</term><term>Nanofibre</term><term>Fibre naturelle</term><term>Cellulose</term><term>Morphologie</term><term>Renforcement mécanique</term><term>Amidon</term><term>Nanocomposite</term><term>Cristallinité</term><term>Reprise humidité</term><term>Propriété dynamomécanique</term><term>Propriété mécanique</term><term>Stabilité thermique</term><term>Etude expérimentale</term><term>Amidon manioc</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Cellulose cassava bagasse nanofibrils (CBN) were directly extracted from a by-product of the cassava starch (CS) industry, viz. the cassava bagasse (CB). The morphological structure of the ensuing nanoparticles was investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), presence of other components such as sugars by high performance liquid chromatography (HPLC), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) experiments. The resulting nanofibrils display a relatively low crystallinity and were found to be around 2-11 nm thick and 360-1700 nm long. These nanofibrils were used as reinforcing nanoparticles in a thermoplastic cassava starch matrix plasticized using either glycerol or a mixture of glycerol/sorbitol (1:1 ) as plasticizer. Nano-composite films were prepared by a melting process. The reinforcing effect of the filler evaluated by dynamical mechanical tests (DMA) and tensile tests was found to depend on the nature of the plasticizer employed. Thus, for the glycerol-plasticized matrix-based composites, it was limited especially due to additional plasticization by sugars originating from starch hydrolysis during the acid extraction. This effect was evidenced by the reduction of glass vitreous temperature of starch after the incorporation of nanofibrils in TPSG and by the increase of elongation at break in tensile test. On the other hand, for glycerol/sorbitol plasticized nanocomposites the transcrystallization of amylopectin in nanofibrils surface hindered good performances of CBN as reinforcing agent for thermoplastic cassava starch. The incorporation of cassava bagasse cellulose nanofibrils in the thermoplastic starch matrices has resulted in a decrease of its hydrophilic character especially for glycerol plasticized sample.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0144-8617</s0></fA01><fA02 i1="01"><s0>CAPOD8</s0></fA02><fA03 i2="1"><s0>Carbohydr. polym.</s0></fA03><fA05><s2>78</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Cassava bagasse cellulose nanofibrils reinforced thermoplastic cassava starch</s1></fA08><fA11 i1="01" i2="1"><s1>TEIXEIRA (Eliangela De M.)</s1></fA11><fA11 i1="02" i2="1"><s1>PASQUINI (Daniel)</s1></fA11><fA11 i1="03" i2="1"><s1>CURVELO (Antônio A. S.)</s1></fA11><fA11 i1="04" i2="1"><s1>CORRADINI (Elisangela)</s1></fA11><fA11 i1="05" i2="1"><s1>BELGACEM (Mohamed N.)</s1></fA11><fA11 i1="06" i2="1"><s1>DUFRESNE (Alain)</s1></fA11><fA14 i1="01"><s1>Instituto de Química de Sâo Carlos, Universidade de São Paulo, C.P. 780</s1><s2>13560-970 São Carlos, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>CICECO e Departamento de Química, Universidade de Aveiro</s1><s2>3810-193 Aveiro</s2><s3>PRT</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Departamento de Engenharia de Materiais, Universidade Federal de São Carlos, C.P. 676</s1><s2>13560-095 São Carlos, SP</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>Grenohle Institute of Technology, The International School of Paper, Print Media and Biomaterials (Grenoble INP - Pagora), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA20><s1>422-431</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>19272</s2><s5>354000170203560080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0400587</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Carbohydrate polymers</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Cellulose cassava bagasse nanofibrils (CBN) were directly extracted from a by-product of the cassava starch (CS) industry, viz. the cassava bagasse (CB). The morphological structure of the ensuing nanoparticles was investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), presence of other components such as sugars by high performance liquid chromatography (HPLC), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) experiments. The resulting nanofibrils display a relatively low crystallinity and were found to be around 2-11 nm thick and 360-1700 nm long. These nanofibrils were used as reinforcing nanoparticles in a thermoplastic cassava starch matrix plasticized using either glycerol or a mixture of glycerol/sorbitol (1:1 ) as plasticizer. Nano-composite films were prepared by a melting process. The reinforcing effect of the filler evaluated by dynamical mechanical tests (DMA) and tensile tests was found to depend on the nature of the plasticizer employed. Thus, for the glycerol-plasticized matrix-based composites, it was limited especially due to additional plasticization by sugars originating from starch hydrolysis during the acid extraction. This effect was evidenced by the reduction of glass vitreous temperature of starch after the incorporation of nanofibrils in TPSG and by the increase of elongation at break in tensile test. On the other hand, for glycerol/sorbitol plasticized nanocomposites the transcrystallization of amylopectin in nanofibrils surface hindered good performances of CBN as reinforcing agent for thermoplastic cassava starch. The incorporation of cassava bagasse cellulose nanofibrils in the thermoplastic starch matrices has resulted in a decrease of its hydrophilic character especially for glycerol plasticized sample.</s0></fC01><fC02 i1="01" i2="X"><s0>001D10A06H</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Bagasse</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Bagasse</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Bagazo</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Manioc</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Cassava</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Mandioca</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Extraction solvant</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Solvent extraction</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Extracción solvente</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Nanofibre</s0><s1>SEC</s1><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Nanofiber</s0><s1>SEC</s1><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Nanofibra</s0><s1>SEC</s1><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Fibre naturelle</s0><s1>SEC</s1><s5>07</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Natural fiber</s0><s1>SEC</s1><s5>07</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Fibra natural</s0><s1>SEC</s1><s5>07</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Cellulose</s0><s1>SEC</s1><s2>NK</s2><s5>08</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Cellulose</s0><s1>SEC</s1><s2>NK</s2><s5>08</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Celulosa</s0><s1>SEC</s1><s2>NK</s2><s5>08</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Morphologie</s0><s5>10</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Morphology</s0><s5>10</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Morfología</s0><s5>10</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Renforcement mécanique</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Strengthening</s0><s5>11</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Refuerzo mecánico</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Amidon</s0><s5>13</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Starch</s0><s5>13</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Almidón</s0><s5>13</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Nanocomposite</s0><s5>14</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Nanocomposite</s0><s5>14</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Nanocompuesto</s0><s5>14</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Cristallinité</s0><s5>15</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Crystallinity</s0><s5>15</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Cristalinidad</s0><s5>15</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Reprise humidité</s0><s5>16</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Moisture regain</s0><s5>16</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Reactivación humedad</s0><s5>16</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Propriété dynamomécanique</s0><s5>17</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Dynamic mechanical properties</s0><s5>17</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Propiedad dinamomecánica</s0><s5>17</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Propriété mécanique</s0><s5>18</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Mechanical properties</s0><s5>18</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Propiedad mecánica</s0><s5>18</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Stabilité thermique</s0><s5>19</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Thermal stability</s0><s5>19</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Estabilidad térmica</s0><s5>19</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Etude expérimentale</s0><s5>20</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Experimental study</s0><s5>20</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Estudio experimental</s0><s5>20</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Amidon manioc</s0><s2>NK</s2><s4>INC</s4><s5>32</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Oside polymère</s0><s2>NK</s2><s5>12</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Oside polymer</s0><s2>NK</s2><s5>12</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Osido polímero</s0><s2>NK</s2><s5>12</s5></fC07><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>PSI</s1></fN44><fN82><s1>PSI</s1></fN82></pA></standard><server><NO>PASCAL 09-0400587 INIST</NO><ET>Cassava bagasse cellulose nanofibrils reinforced thermoplastic cassava starch</ET><AU>TEIXEIRA (Eliangela De M.); PASQUINI (Daniel); CURVELO (Antônio A. S.); CORRADINI (Elisangela); BELGACEM (Mohamed N.); DUFRESNE (Alain)</AU><AF>Instituto de Química de Sâo Carlos, Universidade de São Paulo, C.P. 780/13560-970 São Carlos, SP/Brésil (1 aut., 3 aut.); CICECO e Departamento de Química, Universidade de Aveiro/3810-193 Aveiro/Portugal (2 aut.); Departamento de Engenharia de Materiais, Universidade Federal de São Carlos, C.P. 676/13560-095 São Carlos, SP/Brésil (4 aut.); Grenohle Institute of Technology, The International School of Paper, Print Media and Biomaterials (Grenoble INP - Pagora), BP65/38402 Saint Martin d'Hères/France (5 aut., 6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Carbohydrate polymers; ISSN 0144-8617; Coden CAPOD8; Royaume-Uni; Da. 2009; Vol. 78; No. 3; Pp. 422-431; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Cellulose cassava bagasse nanofibrils (CBN) were directly extracted from a by-product of the cassava starch (CS) industry, viz. the cassava bagasse (CB). The morphological structure of the ensuing nanoparticles was investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), presence of other components such as sugars by high performance liquid chromatography (HPLC), thermogravimetric analysis (TGA), and X-ray diffraction (XRD) experiments. The resulting nanofibrils display a relatively low crystallinity and were found to be around 2-11 nm thick and 360-1700 nm long. These nanofibrils were used as reinforcing nanoparticles in a thermoplastic cassava starch matrix plasticized using either glycerol or a mixture of glycerol/sorbitol (1:1 ) as plasticizer. Nano-composite films were prepared by a melting process. The reinforcing effect of the filler evaluated by dynamical mechanical tests (DMA) and tensile tests was found to depend on the nature of the plasticizer employed. Thus, for the glycerol-plasticized matrix-based composites, it was limited especially due to additional plasticization by sugars originating from starch hydrolysis during the acid extraction. This effect was evidenced by the reduction of glass vitreous temperature of starch after the incorporation of nanofibrils in TPSG and by the increase of elongation at break in tensile test. On the other hand, for glycerol/sorbitol plasticized nanocomposites the transcrystallization of amylopectin in nanofibrils surface hindered good performances of CBN as reinforcing agent for thermoplastic cassava starch. The incorporation of cassava bagasse cellulose nanofibrils in the thermoplastic starch matrices has resulted in a decrease of its hydrophilic character especially for glycerol plasticized sample.</EA><CC>001D10A06H</CC><FD>Bagasse; Manioc; Extraction solvant; Nanofibre; Fibre naturelle; Cellulose; Morphologie; Renforcement mécanique; Amidon; Nanocomposite; Cristallinité; Reprise humidité; Propriété dynamomécanique; Propriété mécanique; Stabilité thermique; Etude expérimentale; Amidon manioc</FD><FG>Oside polymère</FG><ED>Bagasse; Cassava; Solvent extraction; Nanofiber; Natural fiber; Cellulose; Morphology; Strengthening; Starch; Nanocomposite; Crystallinity; Moisture regain; Dynamic mechanical properties; Mechanical properties; Thermal stability; Experimental study</ED><EG>Oside polymer</EG><SD>Bagazo; Mandioca; Extracción solvente; Nanofibra; Fibra natural; Celulosa; Morfología; Refuerzo mecánico; Almidón; Nanocompuesto; Cristalinidad; Reactivación humedad; Propiedad dinamomecánica; Propiedad mecánica; Estabilidad térmica; Estudio experimental</SD><LO>INIST-19272.354000170203560080</LO><ID>09-0400587</ID></server></inist></record>
000D71	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Ants as biological indicators of Wayana Amerindian land use in French Guiana</title><author><name sortKey="Delabie, Jacques H C" uniqKey="Delabie J">Jacques H. C. Delabie</name><affiliation><inist:fA14 i1="01"><s1>U.P.A. Laboratório de Mirmecologia, Convênio UESC/CEPLAC, Centro de Pesquisa do Cacau, C.P. 7</s1><s2>45600-000 Itabuna, Bahia</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cereghino, Regis" uniqKey="Cereghino R">Régis Cereghino</name><affiliation><inist:fA14 i1="02"><s1>Ecolab, Laboratoire d'écologie fonctionnelle (UMR CNRS-UPS-INP 5245), Université Toulouse III, 118, route de Narbonne</s1><s2>31062 Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Groc, Sarah" uniqKey="Groc S">Sarah Groc</name><affiliation><inist:fA14 i1="03"><s1>Écologie des forêts de Guyane (UMR-CNRS 8772), campus agronomique</s1><s2>97379 Kourou</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dejean, Andrea" uniqKey="Dejean A">Andrea Dejean</name><affiliation><inist:fA14 i1="03"><s1>Écologie des forêts de Guyane (UMR-CNRS 8772), campus agronomique</s1><s2>97379 Kourou</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gibernau, Marc" uniqKey="Gibernau M">Marc Gibernau</name><affiliation><inist:fA14 i1="04"><s1>Laboratoire d'évolution et diversité biologique, Université Toulouse III, 118, route de Narbonne</s1><s2>31062 Toulouse</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Corbara, Bruno" uniqKey="Corbara B">Bruno Corbara</name><affiliation><inist:fA14 i1="05"><s1>Laboratoire microorganismes: génome &#38; environnement (UMR-CNRS 6023), Université Clermont II</s1><s2>63177 Aubière</s2><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dejean, Alain" uniqKey="Dejean A">Alain Dejean</name><affiliation><inist:fA14 i1="03"><s1>Écologie des forêts de Guyane (UMR-CNRS 8772), campus agronomique</s1><s2>97379 Kourou</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0402288</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0402288 INIST</idno><idno type="RBID">Pascal:09-0402288</idno><idno type="wicri:Area/Main/Corpus">001C10</idno></publicationStmt><seriesStmt><idno type="ISSN">1631-0691</idno><title level="j" type="abbreviated">C. r., biol.</title><title level="j" type="main">Comptes rendus. Biologies</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amerindian</term><term>Animal community</term><term>Biological indicator</term><term>Faunal survey</term><term>Formicidae</term><term>French Guiana</term><term>Habitat</term><term>Land use</term><term>Landscape ecology</term><term>Social insect</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Communauté animale</term><term>Insecte social</term><term>Indicateur biologique</term><term>Occupation sol</term><term>Amérindien</term><term>Habitat</term><term>Inventaire faunistique</term><term>Guyane Française</term><term>Formicidae</term><term>Ecologie paysage</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Nous avons examiné l'impact de l'utilisation traditionnelle de la terre par les Amérindiens Wayanas de Guyane Française en utilisant les fourmis comme bio-indicateurs. Ces fourmis ont été capturées grâce à une méthode d'échantillonnage rapide et les résultats analysés au moyen de cartes auto-organisatrices de Kohonen (SOM). Nous avons échantillonné: (1) le village Wayana; (2) une plantation de manioc; (3) une plantation abandonnée depuis 6 ans; (4) un fragment de forêt près du village; (5) une ripisylve ; et (6) une forêt primaire. La diversité des fourmis décroît en fonction du degré de perturbation de l'habitat. Le SOM permet de suivre la succession écologique entre les six habitats. Le protocole utilisé est robuste car les mêmes conclusions sont atteintes après contrôle utilisant une information fragmentaire.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1631-0691</s0></fA01><fA03 i2="1"><s0>C. r., biol.</s0></fA03><fA05><s2>332</s2></fA05><fA06><s2>7</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Ants as biological indicators of Wayana Amerindian land use in French Guiana</s1></fA08><fA11 i1="01" i2="1"><s1>DELABIE (Jacques H. C.)</s1></fA11><fA11 i1="02" i2="1"><s1>CEREGHINO (Régis)</s1></fA11><fA11 i1="03" i2="1"><s1>GROC (Sarah)</s1></fA11><fA11 i1="04" i2="1"><s1>DEJEAN (Andrea)</s1></fA11><fA11 i1="05" i2="1"><s1>GIBERNAU (Marc)</s1></fA11><fA11 i1="06" i2="1"><s1>CORBARA (Bruno)</s1></fA11><fA11 i1="07" i2="1"><s1>DEJEAN (Alain)</s1></fA11><fA14 i1="01"><s1>U.P.A. Laboratório de Mirmecologia, Convênio UESC/CEPLAC, Centro de Pesquisa do Cacau, C.P. 7</s1><s2>45600-000 Itabuna, Bahia</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Ecolab, Laboratoire d'écologie fonctionnelle (UMR CNRS-UPS-INP 5245), Université Toulouse III, 118, route de Narbonne</s1><s2>31062 Toulouse</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Écologie des forêts de Guyane (UMR-CNRS 8772), campus agronomique</s1><s2>97379 Kourou</s2><s3>FRA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="04"><s1>Laboratoire d'évolution et diversité biologique, Université Toulouse III, 118, route de Narbonne</s1><s2>31062 Toulouse</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Laboratoire microorganismes: génome &#38; environnement (UMR-CNRS 6023), Université Clermont II</s1><s2>63177 Aubière</s2><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>673-684</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>116D</s2><s5>354000188325360090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>39 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0402288</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Comptes rendus. Biologies</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>Nous avons examiné l'impact de l'utilisation traditionnelle de la terre par les Amérindiens Wayanas de Guyane Française en utilisant les fourmis comme bio-indicateurs. Ces fourmis ont été capturées grâce à une méthode d'échantillonnage rapide et les résultats analysés au moyen de cartes auto-organisatrices de Kohonen (SOM). Nous avons échantillonné: (1) le village Wayana; (2) une plantation de manioc; (3) une plantation abandonnée depuis 6 ans; (4) un fragment de forêt près du village; (5) une ripisylve ; et (6) une forêt primaire. La diversité des fourmis décroît en fonction du degré de perturbation de l'habitat. Le SOM permet de suivre la succession écologique entre les six habitats. Le protocole utilisé est robuste car les mêmes conclusions sont atteintes après contrôle utilisant une information fragmentaire.</s0></fC01><fC02 i1="01" i2="X"><s0>002A14B04B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Communauté animale</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Animal community</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Comunidad animal</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Insecte social</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Social insect</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Insecto social</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Indicateur biologique</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Biological indicator</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Indicador biológico</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Occupation sol</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Land use</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Ocupación terreno</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Amérindien</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Amerindian</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Amerindio</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Habitat</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Habitat</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Habitat</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Inventaire faunistique</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Faunal survey</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Inventario fauna</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Guyane Française</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>French Guiana</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Guayana francesa</s0><s2>NG</s2><s5>19</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Formicidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Formicidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Formicidae</s0><s2>NS</s2><s5>55</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Ecologie paysage</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Landscape ecology</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Ecología del paisaje</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Formicoidea</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Formicoidea</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Formicoidea</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Aculeata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Aculeata</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Aculeata</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Hymenoptera</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Hymenoptera</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Hymenoptera</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Insecta</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Arthropoda</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Invertebrata</s0><s2>NS</s2></fC07><fN21><s1>292</s1></fN21></pA></standard><server><NO>PASCAL 09-0402288 INIST</NO><ET>Ants as biological indicators of Wayana Amerindian land use in French Guiana</ET><AU>DELABIE (Jacques H. C.); CEREGHINO (Régis); GROC (Sarah); DEJEAN (Andrea); GIBERNAU (Marc); CORBARA (Bruno); DEJEAN (Alain)</AU><AF>U.P.A. Laboratório de Mirmecologia, Convênio UESC/CEPLAC, Centro de Pesquisa do Cacau, C.P. 7/45600-000 Itabuna, Bahia/Brésil (1 aut.); Ecolab, Laboratoire d'écologie fonctionnelle (UMR CNRS-UPS-INP 5245), Université Toulouse III, 118, route de Narbonne/31062 Toulouse/France (2 aut.); Écologie des forêts de Guyane (UMR-CNRS 8772), campus agronomique/97379 Kourou/France (3 aut., 4 aut., 7 aut.); Laboratoire d'évolution et diversité biologique, Université Toulouse III, 118, route de Narbonne/31062 Toulouse/France (5 aut.); Laboratoire microorganismes: génome &#38; environnement (UMR-CNRS 6023), Université Clermont II/63177 Aubière/France (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Comptes rendus. Biologies; ISSN 1631-0691; France; Da. 2009; Vol. 332; No. 7; Pp. 673-684; Abs. français; Bibl. 39 ref.</SO><LA>Anglais</LA><FA>Nous avons examiné l'impact de l'utilisation traditionnelle de la terre par les Amérindiens Wayanas de Guyane Française en utilisant les fourmis comme bio-indicateurs. Ces fourmis ont été capturées grâce à une méthode d'échantillonnage rapide et les résultats analysés au moyen de cartes auto-organisatrices de Kohonen (SOM). Nous avons échantillonné: (1) le village Wayana; (2) une plantation de manioc; (3) une plantation abandonnée depuis 6 ans; (4) un fragment de forêt près du village; (5) une ripisylve ; et (6) une forêt primaire. La diversité des fourmis décroît en fonction du degré de perturbation de l'habitat. Le SOM permet de suivre la succession écologique entre les six habitats. Le protocole utilisé est robuste car les mêmes conclusions sont atteintes après contrôle utilisant une information fragmentaire.</FA><CC>002A14B04B</CC><FD>Communauté animale; Insecte social; Indicateur biologique; Occupation sol; Amérindien; Habitat; Inventaire faunistique; Guyane Française; Formicidae; Ecologie paysage</FD><FG>Amérique du Sud; Amérique; Formicoidea; Aculeata; Hymenoptera; Insecta; Arthropoda; Invertebrata</FG><ED>Animal community; Social insect; Biological indicator; Land use; Amerindian; Habitat; Faunal survey; French Guiana; Formicidae; Landscape ecology</ED><EG>South America; America; Formicoidea; Aculeata; Hymenoptera; Insecta; Arthropoda; Invertebrata</EG><SD>Comunidad animal; Insecto social; Indicador biológico; Ocupación terreno; Amerindio; Habitat; Inventario fauna; Guayana francesa; Formicidae; Ecología del paisaje</SD><LO>INIST-116D.354000188325360090</LO><ID>09-0402288</ID></server></inist></record>
000D72	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Dasatinib or High-Dose Imatinib for Chronic-Phase Chronic Myeloid Leukemia Resistant to Imatinib at a Dose of 400 to 600 Milligrams Daily: Two-Year Follow-Up of a Randomized Phase 2 Study (START-R)</title><author><name sortKey="Kantarjian, Hagop" uniqKey="Kantarjian H">Hagop Kantarjian</name><affiliation><inist:fA14 i1="01"><s1>Department of Leukemia, The University of Texas M. D. Anderson Cancer Center</s1><s2>Houston, Texas</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pasquini, Ricardo" uniqKey="Pasquini R">Ricardo Pasquini</name><affiliation><inist:fA14 i1="02"><s1>Hospital De Clinicas De Curitiba</s1><s2>Parana</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Levy, Vincent" uniqKey="Levy V">Vincent Levy</name><affiliation><inist:fA14 i1="03"><s1>Clinical Investigation Center, AP-HP, INSERM U9504, Hôpital Saint-Louis</s1><s2>Paris</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jootar, Saengsuree" uniqKey="Jootar S">Saengsuree Jootar</name><affiliation><inist:fA14 i1="04"><s1>Ramathibodi Hospital, Mahidol University</s1><s2>Bangkok</s2><s3>THA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Holowiecki, Jerzy" uniqKey="Holowiecki J">Jerzy Holowiecki</name><affiliation><inist:fA14 i1="05"><s1>University Hospital-SPSKM</s1><s2>Katowice</s2><s3>POL</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hamerschlak, Nelson" uniqKey="Hamerschlak N">Nelson Hamerschlak</name><affiliation><inist:fA14 i1="06"><s1>Hospital Israelita Albert Einstein</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hughes, Timothy" uniqKey="Hughes T">Timothy Hughes</name><affiliation><inist:fA14 i1="07"><s1>Division of Hematology, Institute of Medical and Veterinary Science</s1><s2>Adelaide, South Australia</s2><s3>AUS</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bleickardt, Eric" uniqKey="Bleickardt E">Eric Bleickardt</name><affiliation><inist:fA14 i1="08"><s1>Bristol-Myers Squibb</s1><s2>Wallingford, Connecticut</s2><s3>USA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dejardin, David" uniqKey="Dejardin D">David Dejardin</name><affiliation><inist:fA14 i1="08"><s1>Bristol-Myers Squibb</s1><s2>Wallingford, Connecticut</s2><s3>USA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cortes, Jorge" uniqKey="Cortes J">Jorge Cortes</name><affiliation><inist:fA14 i1="01"><s1>Department of Leukemia, The University of Texas M. D. Anderson Cancer Center</s1><s2>Houston, Texas</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Shah, Neil P" uniqKey="Shah N">Neil P. Shah</name><affiliation><inist:fA14 i1="09"><s1>Division of Hematology and Oncology, University of California at San Francisco School of Medicine</s1><s2>San Francisco, California</s2><s3>USA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0402349</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0402349 INIST</idno><idno type="RBID">Pascal:09-0402349</idno><idno type="wicri:Area/Main/Corpus">001C09</idno></publicationStmt><seriesStmt><idno type="ISSN">0008-543X</idno><title level="j" type="abbreviated">Cancer</title><title level="j" type="main">Cancer</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Antineoplastic agent</term><term>Cancerology</term><term>Chronic myelogenous leukemia</term><term>Dasatinib</term><term>Enzyme inhibitor</term><term>Follow up study</term><term>High dose</term><term>Imatinib</term><term>Phase II trial</term><term>Protein-tyrosine kinase</term><term>Randomization</term><term>Treatment resistance</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Dasatinib</term><term>Anticancéreux</term><term>Dose forte</term><term>Imatinib</term><term>Protein-tyrosine kinase</term><term>Inhibiteur enzyme</term><term>Essai clinique phase II</term><term>Leucémie myéloïde chronique</term><term>Résistance traitement</term><term>Etude longitudinale</term><term>Randomisation</term><term>Cancérologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">BACKGROUND: In patients with chronic-phase chronic myeloid leukemia (CP-CML), imatinib resistance is of increasing importance. Imatinib dose escalation was the main treatment option before dasatinib, which has 325-fold more potent inhibition than imatinib against unmutated Bcr-Abl in vitro. Data with a minimum of 2 years of follow-up were available for the current study of dasatinib and high-dose imatinib in CP-CML resistant to imatinib at daily doses from 400 mg to 600 mg. METHODS: A phase 2, open-label study was initiated of 150 patients with imatinib-resistant CP-CML who were randomized (2:1) to receive either dasatinib 70 mg twice daily (n = 101) or high-dose imatinib 800 mg (400 mg twice daily; n = 49). RESULTS: At a minimum follow-up of 2 years, dasatinib demonstrated higher rates of complete hematologic response (93% vs 82%; P = .034), major cytogenetic response (MCyR) (53% vs 33%; P=.017), and complete cytogenetic response (44% vs 18%; P =.0025). At 18 months, the MCyR was maintained in 90% of patients on the dasatinib arm and in 74% of patients on the high-dose imatinib arm. Major molecular response rates also were more frequent with dasatinib than with high-dose imatinib (29% vs 12%; P = .028). The estimated progression-free survival also favored dasatinib (unstratified log-rank test; P =.0012). CONCLUSIONS: After 2 years of follow-up, dasatinib demonstrated durable responses and improved response and progression-free survival rates relative to high-dose imatinib.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0008-543X</s0></fA01><fA02 i1="01"><s0>CANCAR</s0></fA02><fA03 i2="1"><s0>Cancer</s0></fA03><fA05><s2>115</s2></fA05><fA06><s2>18</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Dasatinib or High-Dose Imatinib for Chronic-Phase Chronic Myeloid Leukemia Resistant to Imatinib at a Dose of 400 to 600 Milligrams Daily: Two-Year Follow-Up of a Randomized Phase 2 Study (START-R)</s1></fA08><fA11 i1="01" i2="1"><s1>KANTARJIAN (Hagop)</s1></fA11><fA11 i1="02" i2="1"><s1>PASQUINI (Ricardo)</s1></fA11><fA11 i1="03" i2="1"><s1>LEVY (Vincent)</s1></fA11><fA11 i1="04" i2="1"><s1>JOOTAR (Saengsuree)</s1></fA11><fA11 i1="05" i2="1"><s1>HOLOWIECKI (Jerzy)</s1></fA11><fA11 i1="06" i2="1"><s1>HAMERSCHLAK (Nelson)</s1></fA11><fA11 i1="07" i2="1"><s1>HUGHES (Timothy)</s1></fA11><fA11 i1="08" i2="1"><s1>BLEICKARDT (Eric)</s1></fA11><fA11 i1="09" i2="1"><s1>DEJARDIN (David)</s1></fA11><fA11 i1="10" i2="1"><s1>CORTES (Jorge)</s1></fA11><fA11 i1="11" i2="1"><s1>SHAH (Neil P.)</s1></fA11><fA14 i1="01"><s1>Department of Leukemia, The University of Texas M. D. Anderson Cancer Center</s1><s2>Houston, Texas</s2><s3>USA</s3><sZ>1 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="02"><s1>Hospital De Clinicas De Curitiba</s1><s2>Parana</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Clinical Investigation Center, AP-HP, INSERM U9504, Hôpital Saint-Louis</s1><s2>Paris</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Ramathibodi Hospital, Mahidol University</s1><s2>Bangkok</s2><s3>THA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>University Hospital-SPSKM</s1><s2>Katowice</s2><s3>POL</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Hospital Israelita Albert Einstein</s1><s2>Sao Paulo</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Division of Hematology, Institute of Medical and Veterinary Science</s1><s2>Adelaide, South Australia</s2><s3>AUS</s3><sZ>7 aut.</sZ></fA14><fA14 i1="08"><s1>Bristol-Myers Squibb</s1><s2>Wallingford, Connecticut</s2><s3>USA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="09"><s1>Division of Hematology and Oncology, University of California at San Francisco School of Medicine</s1><s2>San Francisco, California</s2><s3>USA</s3><sZ>11 aut.</sZ></fA14><fA20><s1>4136-4147</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2701</s2><s5>354000171090270120</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>28 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0402349</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Cancer</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>BACKGROUND: In patients with chronic-phase chronic myeloid leukemia (CP-CML), imatinib resistance is of increasing importance. Imatinib dose escalation was the main treatment option before dasatinib, which has 325-fold more potent inhibition than imatinib against unmutated Bcr-Abl in vitro. Data with a minimum of 2 years of follow-up were available for the current study of dasatinib and high-dose imatinib in CP-CML resistant to imatinib at daily doses from 400 mg to 600 mg. METHODS: A phase 2, open-label study was initiated of 150 patients with imatinib-resistant CP-CML who were randomized (2:1) to receive either dasatinib 70 mg twice daily (n = 101) or high-dose imatinib 800 mg (400 mg twice daily; n = 49). RESULTS: At a minimum follow-up of 2 years, dasatinib demonstrated higher rates of complete hematologic response (93% vs 82%; P = .034), major cytogenetic response (MCyR) (53% vs 33%; P=.017), and complete cytogenetic response (44% vs 18%; P =.0025). At 18 months, the MCyR was maintained in 90% of patients on the dasatinib arm and in 74% of patients on the high-dose imatinib arm. Major molecular response rates also were more frequent with dasatinib than with high-dose imatinib (29% vs 12%; P = .028). The estimated progression-free survival also favored dasatinib (unstratified log-rank test; P =.0012). CONCLUSIONS: After 2 years of follow-up, dasatinib demonstrated durable responses and improved response and progression-free survival rates relative to high-dose imatinib.</s0></fC01><fC02 i1="01" i2="X"><s0>002B04</s0></fC02><fC02 i1="02" i2="X"><s0>002B19B</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Dasatinib</s0><s2>FR</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Anticancéreux</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Antineoplastic agent</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Anticanceroso</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Dose forte</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>High dose</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Dosis fuerte</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Imatinib</s0><s2>FR</s2><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Protein-tyrosine kinase</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Inhibiteur enzyme</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Enzyme inhibitor</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Inhibidor enzima</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Essai clinique phase II</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Phase II trial</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Ensayo clínico fase II</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Leucémie myéloïde chronique</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Chronic myelogenous leukemia</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Leucemia mieloidea crónica</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Résistance traitement</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Treatment resistance</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Resistencia tratamiento</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Etude longitudinale</s0><s5>11</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Follow up study</s0><s5>11</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Estudio longitudinal</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Randomisation</s0><s5>12</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Randomization</s0><s5>12</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Aleatorización</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Cancérologie</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Cancerology</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Cancerología</s0><s5>17</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Transferases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Inhibiteur de la tyrosine kinase</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Tyrosine kinase inhibitor</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Inhibidor tyrosine kinase</s0><s5>37</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Inhibiteur multikinase</s0><s5>38</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Multikinase inhibitor</s0><s5>38</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>inhibidor multicinasa</s0><s5>38</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Hémopathie maligne</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Malignant hemopathy</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Hemopatía maligna</s0><s2>NM</s2><s5>39</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Syndrome myéloprolifératif</s0><s5>40</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Myeloproliferative syndrome</s0><s5>40</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Mieloproliferativo síndrome</s0><s5>40</s5></fC07><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0402349 INIST</NO><ET>Dasatinib or High-Dose Imatinib for Chronic-Phase Chronic Myeloid Leukemia Resistant to Imatinib at a Dose of 400 to 600 Milligrams Daily: Two-Year Follow-Up of a Randomized Phase 2 Study (START-R)</ET><AU>KANTARJIAN (Hagop); PASQUINI (Ricardo); LEVY (Vincent); JOOTAR (Saengsuree); HOLOWIECKI (Jerzy); HAMERSCHLAK (Nelson); HUGHES (Timothy); BLEICKARDT (Eric); DEJARDIN (David); CORTES (Jorge); SHAH (Neil P.)</AU><AF>Department of Leukemia, The University of Texas M. D. Anderson Cancer Center/Houston, Texas/Etats-Unis (1 aut., 10 aut.); Hospital De Clinicas De Curitiba/Parana/Brésil (2 aut.); Clinical Investigation Center, AP-HP, INSERM U9504, Hôpital Saint-Louis/Paris/France (3 aut.); Ramathibodi Hospital, Mahidol University/Bangkok/Thaïlande (4 aut.); University Hospital-SPSKM/Katowice/Pologne (5 aut.); Hospital Israelita Albert Einstein/Sao Paulo/Brésil (6 aut.); Division of Hematology, Institute of Medical and Veterinary Science/Adelaide, South Australia/Australie (7 aut.); Bristol-Myers Squibb/Wallingford, Connecticut/Etats-Unis (8 aut., 9 aut.); Division of Hematology and Oncology, University of California at San Francisco School of Medicine/San Francisco, California/Etats-Unis (11 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Cancer; ISSN 0008-543X; Coden CANCAR; Etats-Unis; Da. 2009; Vol. 115; No. 18; Pp. 4136-4147; Bibl. 28 ref.</SO><LA>Anglais</LA><EA>BACKGROUND: In patients with chronic-phase chronic myeloid leukemia (CP-CML), imatinib resistance is of increasing importance. Imatinib dose escalation was the main treatment option before dasatinib, which has 325-fold more potent inhibition than imatinib against unmutated Bcr-Abl in vitro. Data with a minimum of 2 years of follow-up were available for the current study of dasatinib and high-dose imatinib in CP-CML resistant to imatinib at daily doses from 400 mg to 600 mg. METHODS: A phase 2, open-label study was initiated of 150 patients with imatinib-resistant CP-CML who were randomized (2:1) to receive either dasatinib 70 mg twice daily (n = 101) or high-dose imatinib 800 mg (400 mg twice daily; n = 49). RESULTS: At a minimum follow-up of 2 years, dasatinib demonstrated higher rates of complete hematologic response (93% vs 82%; P = .034), major cytogenetic response (MCyR) (53% vs 33%; P=.017), and complete cytogenetic response (44% vs 18%; P =.0025). At 18 months, the MCyR was maintained in 90% of patients on the dasatinib arm and in 74% of patients on the high-dose imatinib arm. Major molecular response rates also were more frequent with dasatinib than with high-dose imatinib (29% vs 12%; P = .028). The estimated progression-free survival also favored dasatinib (unstratified log-rank test; P =.0012). CONCLUSIONS: After 2 years of follow-up, dasatinib demonstrated durable responses and improved response and progression-free survival rates relative to high-dose imatinib.</EA><CC>002B04; 002B19B</CC><FD>Dasatinib; Anticancéreux; Dose forte; Imatinib; Protein-tyrosine kinase; Inhibiteur enzyme; Essai clinique phase II; Leucémie myéloïde chronique; Résistance traitement; Etude longitudinale; Randomisation; Cancérologie</FD><FG>Transferases; Enzyme; Inhibiteur de la tyrosine kinase; Inhibiteur multikinase; Hémopathie maligne; Cancer; Syndrome myéloprolifératif</FG><ED>Dasatinib; Antineoplastic agent; High dose; Imatinib; Protein-tyrosine kinase; Enzyme inhibitor; Phase II trial; Chronic myelogenous leukemia; Treatment resistance; Follow up study; Randomization; Cancerology</ED><EG>Transferases; Enzyme; Tyrosine kinase inhibitor; Multikinase inhibitor; Malignant hemopathy; Cancer; Myeloproliferative syndrome</EG><SD>Dasatinib; Anticanceroso; Dosis fuerte; Imatinib; Protein-tyrosine kinase; Inhibidor enzima; Ensayo clínico fase II; Leucemia mieloidea crónica; Resistencia tratamiento; Estudio longitudinal; Aleatorización; Cancerología</SD><LO>INIST-2701.354000171090270120</LO><ID>09-0402349</ID></server></inist></record>
000D73	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">Les défis de l'enseignement du journalisme au Brésil</title><author><name sortKey="Cardoso Dalla Costa, Rosa Maria" uniqKey="Cardoso Dalla Costa R">Rosa Maria Cardoso Dalla Costa</name><affiliation><inist:fA14 i1="01"><s1>université fédérale du Paranà</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0403398</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0403398 INIST</idno><idno type="RBID">Pascal:09-0403398</idno><idno type="wicri:Area/Main/Corpus">001C08</idno><idno type="stanalyst">FRANCIS 09-0403398 INIST</idno></publicationStmt><seriesStmt><idno type="ISSN">1626-1429</idno><title level="j" type="abbreviated">MédiaMorphoses : (Bry-sur-Marne)</title><title level="j" type="main">MédiaMorphoses : (Bry-sur-Marne)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Journalism</term><term>Mass media</term><term>Occupational education</term><term>Occupational training</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Brésil</term><term>Mass media</term><term>Journalisme</term><term>Formation professionnelle</term><term>Enseignement professionnel</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1626-1429</s0></fA01><fA03 i2="1"><s0>MédiaMorphoses : (Bry-sur-Marne)</s0></fA03><fA06><s2>24</s2></fA06><fA08 i1="01" i2="1" l="FRE"><s1>Les défis de l'enseignement du journalisme au Brésil</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>Faut-il encore former les journalistes ?</s1></fA09><fA11 i1="01" i2="1"><s1>CARDOSO DALLA COSTA (Rosa Maria)</s1></fA11><fA12 i1="01" i2="1"><s1>LAMBERT (Frédéric)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>LAVILLE (Camille)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>université fédérale du Paranà</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA15 i1="01"><s1>Institut français de presse, Université de Paris 2</s1><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Université de Nice Sophia-Antipolis</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>127-132</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27925</s2><s5>354000185847070150</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0403398</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>MédiaMorphoses : (Bry-sur-Marne)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA99><s0>7 notes</s0></fA99><fC02 i1="01" i2="X"><s0>001A01I10</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Mass media</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Mass media</s0><s5>04</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Medios comunicación de masas</s0><s5>04</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Journalisme</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Journalism</s0><s5>05</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Periodismo</s0><s5>05</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Formation professionnelle</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Occupational training</s0><s5>06</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Formación profesional</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Enseignement professionnel</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Occupational education</s0><s5>07</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Enseñanza profesional</s0><s5>07</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>292</s1></fN21></pA></standard><server><NO>PASCAL 09-0403398 INIST</NO><FT>Les défis de l'enseignement du journalisme au Brésil</FT><AU>CARDOSO DALLA COSTA (Rosa Maria); LAMBERT (Frédéric); LAVILLE (Camille)</AU><AF>université fédérale du Paranà/Brésil (1 aut.); Institut français de presse, Université de Paris 2/France (1 aut.); Université de Nice Sophia-Antipolis/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>MédiaMorphoses : (Bry-sur-Marne); ISSN 1626-1429; France; Da. 2008; No. 24; Pp. 127-132; Bibl. 1/2 p.</SO><LA>Français</LA><CC>001A01I10</CC><FD>Brésil; Mass media; Journalisme; Formation professionnelle; Enseignement professionnel</FD><FG>Amérique du Sud; Amérique</FG><ED>Brazil; Mass media; Journalism; Occupational training; Occupational education</ED><EG>South America; America</EG><SD>Brasil; Medios comunicación de masas; Periodismo; Formación profesional; Enseñanza profesional</SD><LO>INIST-27925.354000185847070150</LO><ID>09-0403398</ID></server></inist></record>
000D74	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Cover Crop and Nitrogen Effects on Maize Productivity in No-Tillage Systems of the Brazilian Cerrados</title><author><name sortKey="Maltas, A" uniqKey="Maltas A">A. Maltas</name><affiliation><inist:fA14 i1="01"><s1>CIRAD-SupAgro, UMR SYSTEM, Bâtiment 27,2 place Viala</s1><s2>Montpellier, 34060</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Corbeels, M" uniqKey="Corbeels M">M. Corbeels</name><affiliation><inist:fA14 i1="02"><s1>CIRAD, UR 102 SCA, TA B 102/02 Avenue Agropolis</s1><s2>Montpellier, 34398</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Scopel, E" uniqKey="Scopel E">E. Scopel</name><affiliation><inist:fA14 i1="02"><s1>CIRAD, UR 102 SCA, TA B 102/02 Avenue Agropolis</s1><s2>Montpellier, 34398</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wery, J" uniqKey="Wery J">J. Wery</name><affiliation><inist:fA14 i1="01"><s1>CIRAD-SupAgro, UMR SYSTEM, Bâtiment 27,2 place Viala</s1><s2>Montpellier, 34060</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Macena Da Silva, F A" uniqKey="Macena Da Silva F">F. A. Macena Da Silva</name><affiliation><inist:fA14 i1="03"><s1>Empraba, Cerrados, P.O. Box 8223</s1><s2>Planaltina, DF, 73301-970</s2><s3>BRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0404598</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0404598 INIST</idno><idno type="RBID">Pascal:09-0404598</idno><idno type="wicri:Area/Main/Corpus">001C07</idno></publicationStmt><seriesStmt><idno type="ISSN">0002-1962</idno><title level="j" type="abbreviated">Agron. j. : (Print)</title><title level="j" type="main">Agronomy journal : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Agronomy</term><term>Brazil</term><term>Cerrado</term><term>Cover crop</term><term>Nitrogen</term><term>Productivity</term><term>Savannah</term><term>System</term><term>Tropical zone</term><term>Zea mays</term><term>Zero tillage</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Plante de couverture</term><term>Productivité</term><term>Non travail sol</term><term>Système</term><term>Cerrado</term><term>Savane</term><term>Zone tropicale</term><term>Agronomie</term><term>Zea mays</term><term>Azote</term><term>Brésil</term><term>Plante en C4</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Cover crops in direct seeding mulch-based cropping (DMC) systems can be an effective tool to optimize N management for crop production in the Brazilian cerrados. The objective of this study was to determine the effect of four cover crops on maize (Zea mays L.) grain yields in two fields that had been under DMC for 3 and 14 yr. We hypothesized that cover crops would optimize N supply to the maize crop, thereby leading to increased yields. Cover crop treatments were: bare fallow (BF), pigeon pea (PP) [Cajanus cajan (L.) Huth], pearl millet [Pennisetum glaucum (L.) R. Br.]-Congo signal grass (PM-CS) (Brachiaria ruziziensis Germain &#38; Evrard), pigeon pea-finger millet (PP-FM) [Eleusine coracana (L.) Gaertn.], and sorghum (S) [Sorghum bicolor (L.) Moench]. Experiments were conducted during the 2003-2004 and 2004-2005 growing seasons. In 2003-2004 on the DMC-14 field, cover crops increased N uptake of zero-N fertilized maize with 25 to 66 kg N ha<sup>-1</sup> compared to BF, which resulted in an increase in grain yield of 0.4 to 2.4 Mg ha<sup>-1</sup>. Effects on fertilized maize were much less. The highest yield benefits were obtained with pigeon pea and sorghum as sole cover crop. No significant cover crop effects were recorded in 2004-2005. Nitrogen losses under maize estimated on the basis of a simple soil mineral nitrogen balance ranged from 40 to 90 kg N ha<sup>-1</sup> in 2003-2004, while they were smaller in 2004-2005 (10-25 kg N ha<sup>-1</sup>), presumably due to the lower rainfall. Cover crops can have an immediate positive effect on maize productivity under DMC in the cerrados, provided that they are sown immediately after harvest of the main crop.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0002-1962</s0></fA01><fA02 i1="01"><s0>AGJOAT</s0></fA02><fA03 i2="1"><s0>Agron. j. : (Print)</s0></fA03><fA05><s2>101</s2></fA05><fA06><s2>5</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Cover Crop and Nitrogen Effects on Maize Productivity in No-Tillage Systems of the Brazilian Cerrados</s1></fA08><fA11 i1="01" i2="1"><s1>MALTAS (A.)</s1></fA11><fA11 i1="02" i2="1"><s1>CORBEELS (M.)</s1></fA11><fA11 i1="03" i2="1"><s1>SCOPEL (E.)</s1></fA11><fA11 i1="04" i2="1"><s1>WERY (J.)</s1></fA11><fA11 i1="05" i2="1"><s1>MACENA DA SILVA (F. A.)</s1></fA11><fA14 i1="01"><s1>CIRAD-SupAgro, UMR SYSTEM, Bâtiment 27,2 place Viala</s1><s2>Montpellier, 34060</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>CIRAD, UR 102 SCA, TA B 102/02 Avenue Agropolis</s1><s2>Montpellier, 34398</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Empraba, Cerrados, P.O. Box 8223</s1><s2>Planaltina, DF, 73301-970</s2><s3>BRA</s3><sZ>5 aut.</sZ></fA14><fA20><s1>1036-1046</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>553</s2><s5>354000171078980030</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0404598</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Agronomy journal : (Print)</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Cover crops in direct seeding mulch-based cropping (DMC) systems can be an effective tool to optimize N management for crop production in the Brazilian cerrados. The objective of this study was to determine the effect of four cover crops on maize (Zea mays L.) grain yields in two fields that had been under DMC for 3 and 14 yr. We hypothesized that cover crops would optimize N supply to the maize crop, thereby leading to increased yields. Cover crop treatments were: bare fallow (BF), pigeon pea (PP) [Cajanus cajan (L.) Huth], pearl millet [Pennisetum glaucum (L.) R. Br.]-Congo signal grass (PM-CS) (Brachiaria ruziziensis Germain &#38; Evrard), pigeon pea-finger millet (PP-FM) [Eleusine coracana (L.) Gaertn.], and sorghum (S) [Sorghum bicolor (L.) Moench]. Experiments were conducted during the 2003-2004 and 2004-2005 growing seasons. In 2003-2004 on the DMC-14 field, cover crops increased N uptake of zero-N fertilized maize with 25 to 66 kg N ha<sup>-1</sup> compared to BF, which resulted in an increase in grain yield of 0.4 to 2.4 Mg ha<sup>-1</sup>. Effects on fertilized maize were much less. The highest yield benefits were obtained with pigeon pea and sorghum as sole cover crop. No significant cover crop effects were recorded in 2004-2005. Nitrogen losses under maize estimated on the basis of a simple soil mineral nitrogen balance ranged from 40 to 90 kg N ha<sup>-1</sup> in 2003-2004, while they were smaller in 2004-2005 (10-25 kg N ha<sup>-1</sup>), presumably due to the lower rainfall. Cover crops can have an immediate positive effect on maize productivity under DMC in the cerrados, provided that they are sown immediately after harvest of the main crop.</s0></fC01><fC02 i1="01" i2="X"><s0>002A32</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Plante de couverture</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Cover crop</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Planta de cobertura</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Productivité</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Productivity</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Productividad</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Non travail sol</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Zero tillage</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Cero labranza</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Système</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>System</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" 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i2="X" l="SPA"><s0>Acondicionamiento suelo</s0><s5>35</s5></fC07><fC07 i1="13" i2="X" l="FRE"><s0>Formation végétale</s0><s5>36</s5></fC07><fC07 i1="13" i2="X" l="ENG"><s0>Vegetation type</s0><s5>36</s5></fC07><fC07 i1="13" i2="X" l="SPA"><s0>Formación vegetal</s0><s5>36</s5></fC07><fC07 i1="14" i2="X" l="FRE"><s0>Végétation</s0><s5>37</s5></fC07><fC07 i1="14" i2="X" l="ENG"><s0>Vegetation</s0><s5>37</s5></fC07><fC07 i1="14" i2="X" l="SPA"><s0>Vegetación</s0><s5>37</s5></fC07><fC07 i1="15" i2="X" l="FRE"><s0>Végétal</s0><s5>39</s5></fC07><fC07 i1="15" i2="X" l="ENG"><s0>Vegetals</s0><s5>39</s5></fC07><fC07 i1="15" i2="X" l="SPA"><s0>Vegetal</s0><s5>39</s5></fC07><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0404598 INIST</NO><ET>Cover Crop and Nitrogen Effects on Maize Productivity in No-Tillage Systems of the Brazilian Cerrados</ET><AU>MALTAS (A.); CORBEELS (M.); SCOPEL (E.); WERY (J.); MACENA DA SILVA (F. A.)</AU><AF>CIRAD-SupAgro, UMR SYSTEM, Bâtiment 27,2 place Viala/Montpellier, 34060/France (1 aut., 4 aut.); CIRAD, UR 102 SCA, TA B 102/02 Avenue Agropolis/Montpellier, 34398/France (2 aut., 3 aut.); Empraba, Cerrados, P.O. Box 8223/Planaltina, DF, 73301-970/Brésil (5 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Agronomy journal : (Print); ISSN 0002-1962; Coden AGJOAT; Etats-Unis; Da. 2009; Vol. 101; No. 5; Pp. 1036-1046; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Cover crops in direct seeding mulch-based cropping (DMC) systems can be an effective tool to optimize N management for crop production in the Brazilian cerrados. The objective of this study was to determine the effect of four cover crops on maize (Zea mays L.) grain yields in two fields that had been under DMC for 3 and 14 yr. We hypothesized that cover crops would optimize N supply to the maize crop, thereby leading to increased yields. Cover crop treatments were: bare fallow (BF), pigeon pea (PP) [Cajanus cajan (L.) Huth], pearl millet [Pennisetum glaucum (L.) R. Br.]-Congo signal grass (PM-CS) (Brachiaria ruziziensis Germain &#38; Evrard), pigeon pea-finger millet (PP-FM) [Eleusine coracana (L.) Gaertn.], and sorghum (S) [Sorghum bicolor (L.) Moench]. Experiments were conducted during the 2003-2004 and 2004-2005 growing seasons. In 2003-2004 on the DMC-14 field, cover crops increased N uptake of zero-N fertilized maize with 25 to 66 kg N ha<sup>-1</sup> compared to BF, which resulted in an increase in grain yield of 0.4 to 2.4 Mg ha<sup>-1</sup>. Effects on fertilized maize were much less. The highest yield benefits were obtained with pigeon pea and sorghum as sole cover crop. No significant cover crop effects were recorded in 2004-2005. Nitrogen losses under maize estimated on the basis of a simple soil mineral nitrogen balance ranged from 40 to 90 kg N ha<sup>-1</sup> in 2003-2004, while they were smaller in 2004-2005 (10-25 kg N ha<sup>-1</sup>), presumably due to the lower rainfall. Cover crops can have an immediate positive effect on maize productivity under DMC in the cerrados, provided that they are sown immediately after harvest of the main crop.</EA><CC>002A32</CC><FD>Plante de couverture; Productivité; Non travail sol; Système; Cerrado; Savane; Zone tropicale; Agronomie; Zea mays; Azote; Brésil; Plante en C4</FD><FG>Biome; Gramineae; Monocotyledones; Angiospermae; Spermatophyta; Amérique du Sud; Amérique; Type C4; Plante céréalière; Non métal; Elément groupe VA; Aménagement sol; Formation végétale; Végétation; Végétal</FG><ED>Cover crop; Productivity; Zero tillage; System; Cerrado; Savannah; Tropical zone; Agronomy; Zea mays; Nitrogen; Brazil</ED><EG>Biome; Gramineae; Monocotyledones; Angiospermae; Spermatophyta; South America; America; C4-Type; Cereal crop; Non metal; Group VA element; Soil management; Vegetation type; Vegetation; Vegetals</EG><SD>Planta de cobertura; Productividad; Cero labranza; Sistema; Cerrado; Sabana; Zona tropical; Agronomía; Zea mays; Nitrógeno; Brasil</SD><LO>INIST-553.354000171078980030</LO><ID>09-0404598</ID></server></inist></record>
000D75	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Extrusion and characterization of functionalized cellulose whiskers reinforced polyethylene nanocomposites</title><author><name sortKey="Junior De Menezes, Aparecido" uniqKey="Junior De Menezes A">Aparecido Junior De Menezes</name><affiliation><inist:fA14 i1="01"><s1>Grenoble Institute of Technology, The International School of Paper, Print Media and Biomaterials (PAGORA), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Siqueira, Gilberto" uniqKey="Siqueira G">Gilberto Siqueira</name><affiliation><inist:fA14 i1="01"><s1>Grenoble Institute of Technology, The International School of Paper, Print Media and Biomaterials (PAGORA), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Curvelo, Antonio A S" uniqKey="Curvelo A">Antonio A. S. Curvelo</name><affiliation><inist:fA14 i1="02"><s1>Instltuto de Química de São Carlos (IQSC), Universidade de São Paulo (USP), C.P. 780</s1><s2>13560-970 São Carlos</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dufresne, Alain" uniqKey="Dufresne A">Alain Dufresne</name><affiliation><inist:fA14 i1="01"><s1>Grenoble Institute of Technology, The International School of Paper, Print Media and Biomaterials (PAGORA), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0405803</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0405803 INIST</idno><idno type="RBID">Pascal:09-0405803</idno><idno type="wicri:Area/Main/Corpus">001C06</idno></publicationStmt><seriesStmt><idno type="ISSN">0032-3861</idno><title level="j" type="abbreviated">Polymer : (Guildf.)</title><title level="j" type="main">Polymer : (Guildford)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cellulose</term><term>Cellulose organic ester</term><term>Chemical degradation</term><term>Chemical modification</term><term>Concentration effect</term><term>Crystallinity</term><term>Esterification</term><term>Experimental study</term><term>Filler</term><term>Growth from melt</term><term>Hydrolysis</term><term>Low density ethylene polymer</term><term>Mechanical properties</term><term>Mixing</term><term>Morphology</term><term>Nanocomposite</term><term>Nanocrystal</term><term>Preparation</term><term>Surface reaction</term><term>Thermal stability</term><term>Whisker</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Matière charge</term><term>Cellulose ester organique</term><term>Trichite</term><term>Nanocristal</term><term>Préparation</term><term>Dégradation chimique</term><term>Hydrolyse</term><term>Cellulose</term><term>Modification chimique</term><term>Estérification</term><term>Réaction surface</term><term>Mélangeage</term><term>Méthode phase fondue</term><term>Nanocomposite</term><term>Ethylène basse densité polymère</term><term>Morphologie</term><term>Cristallinité</term><term>Propriété mécanique</term><term>Stabilité thermique</term><term>Effet concentration</term><term>Etude expérimentale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The surface of ramie cellulose whiskers has been chemically modified by grafting organic acid chlorides presenting different lengths of the aliphatic chain by an esterification reaction. The occurrence of the chemical modification was evaluated by FTIR and X-ray photoelectron spectroscopies, elemental analysis and contact angle measurements. The crystallinity of the particles was not altered by the chain grafting, but it was shown that covalently grafted chains were able to crystallize at the cellulose surface when using C18. Both unmodified and functionalized nanoparticles were extruded with low density polyethylene to prepare nanocomposite materials. The homogeneity of the ensuing nanocomposites was found to increase with the length of the grafted chains. The thermomechanical properties of processed nanocomposites were studied by differential scanning calorimetry (DSC), dynamical mechanical analysis (DMA) and tensile tests. A significant improvement in terms of elongation at break was observed when sufficiently long chains were grafted on the surface of the nanoparticles. It was ascribed to improved dispersion of the nanoparticles within the LDPE matrix.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0032-3861</s0></fA01><fA02 i1="01"><s0>POLMAG</s0></fA02><fA03 i2="1"><s0>Polymer : (Guildf.)</s0></fA03><fA05><s2>50</s2></fA05><fA06><s2>19</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Extrusion and characterization of functionalized cellulose whiskers reinforced polyethylene nanocomposites</s1></fA08><fA11 i1="01" i2="1"><s1>JUNIOR DE MENEZES (Aparecido)</s1></fA11><fA11 i1="02" i2="1"><s1>SIQUEIRA (Gilberto)</s1></fA11><fA11 i1="03" i2="1"><s1>CURVELO (Antonio A. S.)</s1></fA11><fA11 i1="04" i2="1"><s1>DUFRESNE (Alain)</s1></fA11><fA14 i1="01"><s1>Grenoble Institute of Technology, The International School of Paper, Print Media and Biomaterials (PAGORA), BP65</s1><s2>38402 Saint Martin d'Hères</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>Instltuto de Química de São Carlos (IQSC), Universidade de São Paulo (USP), C.P. 780</s1><s2>13560-970 São Carlos</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>4552-4563</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>11463</s2><s5>354000171964460190</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0405803</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Polymer : (Guildford)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The surface of ramie cellulose whiskers has been chemically modified by grafting organic acid chlorides presenting different lengths of the aliphatic chain by an esterification reaction. The occurrence of the chemical modification was evaluated by FTIR and X-ray photoelectron spectroscopies, elemental analysis and contact angle measurements. The crystallinity of the particles was not altered by the chain grafting, but it was shown that covalently grafted chains were able to crystallize at the cellulose surface when using C18. Both unmodified and functionalized nanoparticles were extruded with low density polyethylene to prepare nanocomposite materials. The homogeneity of the ensuing nanocomposites was found to increase with the length of the grafted chains. The thermomechanical properties of processed nanocomposites were studied by differential scanning calorimetry (DSC), dynamical mechanical analysis (DMA) and tensile tests. A significant improvement in terms of elongation at break was observed when sufficiently long chains were grafted on the surface of the nanoparticles. It was ascribed to improved dispersion of the nanoparticles within the LDPE matrix.</s0></fC01><fC02 i1="01" i2="X"><s0>001D09C01</s0></fC02><fC02 i1="02" i2="X"><s0>001D10A06H</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Matière charge</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Filler</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Materia carga</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Cellulose ester organique</s0><s1>FIN</s1><s1>SEC</s1><s2>NK</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Cellulose organic ester</s0><s1>FIN</s1><s1>SEC</s1><s2>NK</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Celulosa ester orgánico</s0><s1>FIN</s1><s1>SEC</s1><s2>NK</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Trichite</s0><s1>SEC</s1><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Whisker</s0><s1>SEC</s1><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Triquito</s0><s1>SEC</s1><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Nanocristal</s0><s1>SEC</s1><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Nanocrystal</s0><s1>SEC</s1><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Nanocristal</s0><s1>SEC</s1><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Préparation</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Preparation</s0><s5>06</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Preparación</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Dégradation chimique</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Chemical degradation</s0><s5>07</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Degradación química</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Hydrolyse</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Hydrolysis</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Hidrólisis</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Cellulose</s0><s1>ENT</s1><s2>NK</s2><s5>09</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Cellulose</s0><s1>ENT</s1><s2>NK</s2><s5>09</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Celulosa</s0><s1>ENT</s1><s2>NK</s2><s5>09</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Modification chimique</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Chemical modification</s0><s5>11</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Modificación química</s0><s5>11</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Estérification</s0><s5>12</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Esterification</s0><s5>12</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Esterificación</s0><s5>12</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Réaction surface</s0><s5>13</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Surface reaction</s0><s5>13</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Reacción superficie</s0><s5>13</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Mélangeage</s0><s5>14</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Mixing</s0><s5>14</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Mezclado</s0><s5>14</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Méthode phase fondue</s0><s5>15</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Growth from melt</s0><s5>15</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Método fase fundida</s0><s5>15</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Nanocomposite</s0><s5>16</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Nanocomposite</s0><s5>16</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Nanocompuesto</s0><s5>16</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Ethylène basse densité polymère</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Low density ethylene polymer</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Etileno baja densidad polímero</s0><s2>NK</s2><s5>17</s5></fC03><fC03 i1="16" i2="X" l="FRE"><s0>Morphologie</s0><s5>18</s5></fC03><fC03 i1="16" i2="X" l="ENG"><s0>Morphology</s0><s5>18</s5></fC03><fC03 i1="16" i2="X" l="SPA"><s0>Morfología</s0><s5>18</s5></fC03><fC03 i1="17" i2="X" l="FRE"><s0>Cristallinité</s0><s5>19</s5></fC03><fC03 i1="17" i2="X" l="ENG"><s0>Crystallinity</s0><s5>19</s5></fC03><fC03 i1="17" i2="X" l="SPA"><s0>Cristalinidad</s0><s5>19</s5></fC03><fC03 i1="18" i2="X" l="FRE"><s0>Propriété mécanique</s0><s5>20</s5></fC03><fC03 i1="18" i2="X" l="ENG"><s0>Mechanical properties</s0><s5>20</s5></fC03><fC03 i1="18" i2="X" l="SPA"><s0>Propiedad mecánica</s0><s5>20</s5></fC03><fC03 i1="19" i2="X" l="FRE"><s0>Stabilité thermique</s0><s5>21</s5></fC03><fC03 i1="19" i2="X" l="ENG"><s0>Thermal stability</s0><s5>21</s5></fC03><fC03 i1="19" i2="X" l="SPA"><s0>Estabilidad térmica</s0><s5>21</s5></fC03><fC03 i1="20" i2="X" l="FRE"><s0>Effet concentration</s0><s5>22</s5></fC03><fC03 i1="20" i2="X" l="ENG"><s0>Concentration effect</s0><s5>22</s5></fC03><fC03 i1="20" i2="X" l="SPA"><s0>Efecto concentración</s0><s5>22</s5></fC03><fC03 i1="21" i2="X" l="FRE"><s0>Etude expérimentale</s0><s5>23</s5></fC03><fC03 i1="21" i2="X" l="ENG"><s0>Experimental study</s0><s5>23</s5></fC03><fC03 i1="21" i2="X" l="SPA"><s0>Estudio experimental</s0><s5>23</s5></fC03><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>PSI</s1></fN44><fN82><s1>PSI</s1></fN82></pA></standard><server><NO>PASCAL 09-0405803 INIST</NO><ET>Extrusion and characterization of functionalized cellulose whiskers reinforced polyethylene nanocomposites</ET><AU>JUNIOR DE MENEZES (Aparecido); SIQUEIRA (Gilberto); CURVELO (Antonio A. S.); DUFRESNE (Alain)</AU><AF>Grenoble Institute of Technology, The International School of Paper, Print Media and Biomaterials (PAGORA), BP65/38402 Saint Martin d'Hères/France (1 aut., 2 aut., 4 aut.); Instltuto de Química de São Carlos (IQSC), Universidade de São Paulo (USP), C.P. 780/13560-970 São Carlos/Brésil (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Polymer : (Guildford); ISSN 0032-3861; Coden POLMAG; Royaume-Uni; Da. 2009; Vol. 50; No. 19; Pp. 4552-4563; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>The surface of ramie cellulose whiskers has been chemically modified by grafting organic acid chlorides presenting different lengths of the aliphatic chain by an esterification reaction. The occurrence of the chemical modification was evaluated by FTIR and X-ray photoelectron spectroscopies, elemental analysis and contact angle measurements. The crystallinity of the particles was not altered by the chain grafting, but it was shown that covalently grafted chains were able to crystallize at the cellulose surface when using C18. Both unmodified and functionalized nanoparticles were extruded with low density polyethylene to prepare nanocomposite materials. The homogeneity of the ensuing nanocomposites was found to increase with the length of the grafted chains. The thermomechanical properties of processed nanocomposites were studied by differential scanning calorimetry (DSC), dynamical mechanical analysis (DMA) and tensile tests. A significant improvement in terms of elongation at break was observed when sufficiently long chains were grafted on the surface of the nanoparticles. It was ascribed to improved dispersion of the nanoparticles within the LDPE matrix.</EA><CC>001D09C01; 001D10A06H</CC><FD>Matière charge; Cellulose ester organique; Trichite; Nanocristal; Préparation; Dégradation chimique; Hydrolyse; Cellulose; Modification chimique; Estérification; Réaction surface; Mélangeage; Méthode phase fondue; Nanocomposite; Ethylène basse densité polymère; Morphologie; Cristallinité; Propriété mécanique; Stabilité thermique; Effet concentration; Etude expérimentale</FD><ED>Filler; Cellulose organic ester; Whisker; Nanocrystal; Preparation; Chemical degradation; Hydrolysis; Cellulose; Chemical modification; Esterification; Surface reaction; Mixing; Growth from melt; Nanocomposite; Low density ethylene polymer; Morphology; Crystallinity; Mechanical properties; Thermal stability; Concentration effect; Experimental study</ED><SD>Materia carga; Celulosa ester orgánico; Triquito; Nanocristal; Preparación; Degradación química; Hidrólisis; Celulosa; Modificación química; Esterificación; Reacción superficie; Mezclado; Método fase fundida; Nanocompuesto; Etileno baja densidad polímero; Morfología; Cristalinidad; Propiedad mecánica; Estabilidad térmica; Efecto concentración; Estudio experimental</SD><LO>INIST-11463.354000171964460190</LO><ID>09-0405803</ID></server></inist></record>
000D76	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">What connection is there between the learning process and territorial governance? The 'SAC' example on Reunion Island</title><author><name sortKey="Chia, Eduardo" uniqKey="Chia E">Eduardo Chia</name><affiliation><inist:fA14 i1="01"><s1>Centre International de Recherche Agronomique pour le Développement (CIRAD)/ Institut National de Recherche Agronomique (INRA), Avenue Agropolis 34398</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dulcire, Michel" uniqKey="Dulcire M">Michel Dulcire</name><affiliation><inist:fA14 i1="01"><s1>Centre International de Recherche Agronomique pour le Développement (CIRAD)/ Institut National de Recherche Agronomique (INRA), Avenue Agropolis 34398</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Piraux, Marc" uniqKey="Piraux M">Marc Piraux</name><affiliation><inist:fA14 i1="02"><s1>UMR Tetis (Territoires, Environnement, Télédétection et Information Spatiale), CIRAD, CEMAGREF, ENGREF, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD)</s1><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Visiting Professor at the University Federal of Campina Grande</s1><s2>Paraiba</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0406136</idno><date when="2008">2008</date><idno type="stanalyst">PASCAL 09-0406136 INIST</idno><idno type="RBID">Pascal:09-0406136</idno><idno type="wicri:Area/Main/Corpus">001C05</idno></publicationStmt><seriesStmt><idno type="ISSN">0960-1406</idno><title level="j" type="abbreviated">Int. j. sustain. dev</title><title level="j" type="main">International journal of sustainable development</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Agriculture</term><term>Governance</term><term>Learning</term><term>Models</term><term>Reunion island</term><term>Rural environment</term><term>Sustainable development</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Apprentissage</term><term>Gouvernance</term><term>Ile Réunion</term><term>Modèle</term><term>Milieu rural</term><term>Agriculture</term><term>Développement durable</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Territorial governance has become a major issue for public authorities. Studying the information generated by implementing sustainable agricultural contracts (SAC) on Reunion Island (Île de la Réunion) has contributed to the development of new types of territorial governance projects. The surveys conducted with rural development actors have revealed that learning was significant both at the individual and collective levels. This mainly involves organisational learning processes. The SAC toot has been used for developing a new type of governance, by coordinating actors with different interests and logics. This process has developed the practical and organisational practices of actors. But it has not modified their values (common project) or the development model. Thus, we believe that in order to promote 'dual loop' learning, implementing a local project is essential as it gives a meaning to the actions being carried out. As a result, the governance process would be reinforced.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0960-1406</s0></fA01><fA03 i2="1"><s0>Int. j. sustain. dev</s0></fA03><fA05><s2>11</s2></fA05><fA06><s2>2-4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>What connection is there between the learning process and territorial governance? The 'SAC' example on Reunion Island</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Governance: Institutional and Learning Plans Facilitating the Appropriation of Sustainable Development</s1></fA09><fA11 i1="01" i2="1"><s1>CHIA (Eduardo)</s1></fA11><fA11 i1="02" i2="1"><s1>DULCIRE (Michel)</s1></fA11><fA11 i1="03" i2="1"><s1>PIRAUX (Marc)</s1></fA11><fA12 i1="01" i2="1"><s1>REY-VALETTE (Hélène)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>LARDON (Sylvie)</s1><s9>ed.</s9></fA12><fA12 i1="03" i2="1"><s1>CHIA (Eduardo)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Centre International de Recherche Agronomique pour le Développement (CIRAD)/ Institut National de Recherche Agronomique (INRA), Avenue Agropolis 34398</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>UMR Tetis (Territoires, Environnement, Télédétection et Information Spatiale), CIRAD, CEMAGREF, ENGREF, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD)</s1><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Visiting Professor at the University Federal of Campina Grande</s1><s2>Paraiba</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>LAMETA Laboratoire Montpelliérain d'Economique Théorique et Appliquée, Faculté de Sciences Economiques, CS 79606</s1><s2>34960 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>INRA &#38; AgroParisTech-ENGREF, Domaine des Cézeaux, BP 90 054, 24, Avenue des Landais</s1><s2>63171 Aubière</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA15 i1="03"><s1>Centre International de Recherche Agronomique pour le Développement (CIRAD)/Institut National de Recherche Agronomique (INRA), Avenue Agropolis</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA15><fA20><s1>171-186</s1></fA20><fA21><s1>2008</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>27521</s2><s5>354000187990320040</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0406136</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of sustainable development</s0></fA64><fA66 i1="01"><s0>CHE</s0></fA66><fA99><s0>10 notes</s0></fA99><fC01 i1="01" l="ENG"><s0>Territorial governance has become a major issue for public authorities. Studying the information generated by implementing sustainable agricultural contracts (SAC) on Reunion Island (Île de la Réunion) has contributed to the development of new types of territorial governance projects. The surveys conducted with rural development actors have revealed that learning was significant both at the individual and collective levels. This mainly involves organisational learning processes. The SAC toot has been used for developing a new type of governance, by coordinating actors with different interests and logics. This process has developed the practical and organisational practices of actors. But it has not modified their values (common project) or the development model. Thus, we believe that in order to promote 'dual loop' learning, implementing a local project is essential as it gives a meaning to the actions being carried out. As a result, the governance process would be reinforced.</s0></fC01><fC02 i1="01" i2="X"><s0>002A14D06</s0></fC02><fC02 i1="02" i2="X"><s0>002A32C01B1</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Apprentissage</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Learning</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Aprendizaje</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Gouvernance</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Governance</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Gobernanza</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Ile Réunion</s0><s2>NG</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Reunion island</s0><s2>NG</s2><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Isla Reunión</s0><s2>NG</s2><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Modèle</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Models</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Modelo</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Milieu rural</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Rural environment</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Medio rural</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Agriculture</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Agriculture</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Agricultura</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Développement durable</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Sustainable development</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Desarrollo sostenible</s0><s5>07</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Iles Océan Indien</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Indian Ocean Islands</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Islas Océano Indico</s0><s2>NG</s2></fC07><fN21><s1>292</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0406136 INIST</NO><ET>What connection is there between the learning process and territorial governance? The 'SAC' example on Reunion Island</ET><AU>CHIA (Eduardo); DULCIRE (Michel); PIRAUX (Marc); REY-VALETTE (Hélène); LARDON (Sylvie); CHIA (Eduardo)</AU><AF>Centre International de Recherche Agronomique pour le Développement (CIRAD)/ Institut National de Recherche Agronomique (INRA), Avenue Agropolis 34398/Montpellier/France (1 aut., 2 aut.); UMR Tetis (Territoires, Environnement, Télédétection et Information Spatiale), CIRAD, CEMAGREF, ENGREF, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD)/France (3 aut.); Visiting Professor at the University Federal of Campina Grande/Paraiba/Brésil (3 aut.); LAMETA Laboratoire Montpelliérain d'Economique Théorique et Appliquée, Faculté de Sciences Economiques, CS 79606/34960 Montpellier/France (1 aut.); INRA &#38; AgroParisTech-ENGREF, Domaine des Cézeaux, BP 90 054, 24, Avenue des Landais/63171 Aubière/France (2 aut.); Centre International de Recherche Agronomique pour le Développement (CIRAD)/Institut National de Recherche Agronomique (INRA), Avenue Agropolis/34398 Montpellier/France (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of sustainable development; ISSN 0960-1406; Suisse; Da. 2008; Vol. 11; No. 2-4; Pp. 171-186; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Territorial governance has become a major issue for public authorities. Studying the information generated by implementing sustainable agricultural contracts (SAC) on Reunion Island (Île de la Réunion) has contributed to the development of new types of territorial governance projects. The surveys conducted with rural development actors have revealed that learning was significant both at the individual and collective levels. This mainly involves organisational learning processes. The SAC toot has been used for developing a new type of governance, by coordinating actors with different interests and logics. This process has developed the practical and organisational practices of actors. But it has not modified their values (common project) or the development model. Thus, we believe that in order to promote 'dual loop' learning, implementing a local project is essential as it gives a meaning to the actions being carried out. As a result, the governance process would be reinforced.</EA><CC>002A14D06; 002A32C01B1</CC><FD>Apprentissage; Gouvernance; Ile Réunion; Modèle; Milieu rural; Agriculture; Développement durable</FD><FG>Iles Océan Indien</FG><ED>Learning; Governance; Reunion island; Models; Rural environment; Agriculture; Sustainable development</ED><EG>Indian Ocean Islands</EG><SD>Aprendizaje; Gobernanza; Isla Reunión; Modelo; Medio rural; Agricultura; Desarrollo sostenible</SD><LO>INIST-27521.354000187990320040</LO><ID>09-0406136</ID></server></inist></record>
000D77	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Differentially expressed genes in cotton plant genotypes infected with Meloidogyne incognita</title><author><name sortKey="De Deus Barbosa, Aulus Estevao Anjos" uniqKey="De Deus Barbosa A">Aulus Estevao Anjos De Deus Barbosa</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Doutorado em Ciências Genômicas e Bioternologia. UCB</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Da Rocha Fragoso, Rodrigo" uniqKey="Da Rocha Fragoso R">Rodrigo Da Rocha Fragoso</name><affiliation><inist:fA14 i1="04"><s1>Embrapa Cerrados</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Lima E Souza, Djair Dos Santos" uniqKey="De Lima E Souza D">Djair Dos Santos De Lima E Souza</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Biologia Celular, UnB</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Freire, Erika" uniqKey="Freire E">Erika Freire</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brilhante De Oliveira, Osmundo Neto" uniqKey="Brilhante De Oliveira O">Osmundo Neto Brilhante De Oliveira</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Viana, Antbnio Americo Barbosa" uniqKey="Viana A">Antbnio Américo Barbosa Viana</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Coiti Togawa, Roberto" uniqKey="Coiti Togawa R">Roberto Coiti Togawa</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mourao Guimaraes, Luciane" uniqKey="Mourao Guimaraes L">Luciane Mourao Guimaraes</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Florencio Martins, Natalia" uniqKey="Florencio Martins N">Natalia Florencio Martins</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cia, Edivaldo" uniqKey="Cia E">Edivaldo Cia</name><affiliation><inist:fA14 i1="05"><s1>IAC</s1><s2>Campinas-SP</s2><s3>BRA</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fernandez, Diana" uniqKey="Fernandez D">Diana Fernandez</name><affiliation><inist:fA14 i1="06"><s1>IRD</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Lima, Liziane Maria" uniqKey="De Lima L">Liziane Maria De Lima</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mattar Silva, Maria Cristina" uniqKey="Mattar Silva M">Maria Cristina Mattar Silva</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rocha, Thales Lima" uniqKey="Rocha T">Thales Lima Rocha</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Grossi De Sa, Maria Fatima" uniqKey="Grossi De Sa M">Maria Fatima Grossi-De-Sa</name><affiliation><inist:fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Doutorado em Ciências Genômicas e Bioternologia. UCB</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>15 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0407882</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0407882 INIST</idno><idno type="RBID">Pascal:09-0407882</idno><idno type="wicri:Area/Main/Corpus">001C04</idno></publicationStmt><seriesStmt><idno type="ISSN">0168-9452</idno><title level="j" type="abbreviated">Plant sci. : (Limerick)</title><title level="j" type="main">Plant science : (Limerick)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Gene expression</term><term>Genetic determinism</term><term>Genotype</term><term>Gossypium hirsutum</term><term>Infection</term><term>Meloidogyne incognita</term><term>Pest</term><term>Plant biology</term><term>Resistance</term><term>Resistance gene</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Expression génique</term><term>Génotype</term><term>Infection</term><term>Déprédateur</term><term>Résistance</term><term>Déterminisme génétique</term><term>Biologie végétale</term><term>Gossypium hirsutum</term><term>Meloidogyne incognita</term><term>Gène de résistance</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Meloidogyne incognita is a nematode responsible for huge losses of economically important crops. The control of this pathogen is heavily centered on chemical nematicides, which are toxic to humans and environment, besides being very expensive. Alternatively, resistant varieties of cotton generated from conventional breeding programs represent an attractive strategy for the control of M. incognita. In this context, the goal of the work reported here was to analyze the gene expression profile of one resistant and one susceptible cotton genotype infected with M. incognita aiming to understand the mechanisms involved in resistance. EST libraries of cotton in both resistant and susceptible to infection by M. incognita were constructed and sequenced, generating 2261 sequences that were assembled into 233 contigs and 1593 singlets. Genes differentially expressed were observed in both resistant and susceptible cotton. Twenty genes were found to be expressed exclusively in the resistant cotton genotype, with functions related to pathogen recognition, signal transduction, defense mechanisms and protein synthesis transport and activation. The coordinated action of these genes suggests the existence of a complex defense pathway towards nematode attack in cotton. Our data indicate some candidate genes for validation and use through transformation in other agronomically important plants.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0168-9452</s0></fA01><fA02 i1="01"><s0>PLSCE4</s0></fA02><fA03 i2="1"><s0>Plant sci. : (Limerick)</s0></fA03><fA05><s2>177</s2></fA05><fA06><s2>5</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Differentially expressed genes in cotton plant genotypes infected with Meloidogyne incognita</s1></fA08><fA11 i1="01" i2="1"><s1>DE DEUS BARBOSA (Aulus Estevao Anjos)</s1></fA11><fA11 i1="02" i2="1"><s1>DA ROCHA FRAGOSO (Rodrigo)</s1></fA11><fA11 i1="03" i2="1"><s1>DE LIMA E SOUZA (Djair Dos Santos)</s1></fA11><fA11 i1="04" i2="1"><s1>FREIRE (Erika)</s1></fA11><fA11 i1="05" i2="1"><s1>BRILHANTE DE OLIVEIRA (Osmundo NETO)</s1></fA11><fA11 i1="06" i2="1"><s1>VIANA (Antbnio Américo Barbosa)</s1></fA11><fA11 i1="07" i2="1"><s1>COITI TOGAWA (Roberto)</s1></fA11><fA11 i1="08" i2="1"><s1>MOURAO GUIMARAES (Luciane)</s1></fA11><fA11 i1="09" i2="1"><s1>FLORENCIO MARTINS (Natalia)</s1></fA11><fA11 i1="10" i2="1"><s1>CIA (Edivaldo)</s1></fA11><fA11 i1="11" i2="1"><s1>FERNANDEZ (Diana)</s1></fA11><fA11 i1="12" i2="1"><s1>DE LIMA (Liziane Maria)</s1></fA11><fA11 i1="13" i2="1"><s1>MATTAR SILVA (Maria Cristina)</s1></fA11><fA11 i1="14" i2="1"><s1>ROCHA (Thales Lima)</s1></fA11><fA11 i1="15" i2="1"><s1>GROSSI-DE-SA (Maria Fatima)</s1></fA11><fA14 i1="01"><s1>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final</s1><s2>Brasília-DF 70770-900</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>12 aut.</sZ><sZ>13 aut.</sZ><sZ>14 aut.</sZ><sZ>15 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Biologia Celular, UnB</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>Doutorado em Ciências Genômicas e Bioternologia. UCB</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>15 aut.</sZ></fA14><fA14 i1="04"><s1>Embrapa Cerrados</s1><s2>Brasília-DF</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="05"><s1>IAC</s1><s2>Campinas-SP</s2><s3>BRA</s3><sZ>10 aut.</sZ></fA14><fA14 i1="06"><s1>IRD</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>11 aut.</sZ></fA14><fA20><s1>492-497</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>15982</s2><s5>354000171929080130</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>51 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0407882</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Plant science : (Limerick)</s0></fA64><fA66 i1="01"><s0>IRL</s0></fA66><fC01 i1="01" l="ENG"><s0>Meloidogyne incognita is a nematode responsible for huge losses of economically important crops. The control of this pathogen is heavily centered on chemical nematicides, which are toxic to humans and environment, besides being very expensive. Alternatively, resistant varieties of cotton generated from conventional breeding programs represent an attractive strategy for the control of M. incognita. In this context, the goal of the work reported here was to analyze the gene expression profile of one resistant and one susceptible cotton genotype infected with M. incognita aiming to understand the mechanisms involved in resistance. EST libraries of cotton in both resistant and susceptible to infection by M. incognita were constructed and sequenced, generating 2261 sequences that were assembled into 233 contigs and 1593 singlets. Genes differentially expressed were observed in both resistant and susceptible cotton. Twenty genes were found to be expressed exclusively in the resistant cotton genotype, with functions related to pathogen recognition, signal transduction, defense mechanisms and protein synthesis transport and activation. The coordinated action of these genes suggests the existence of a complex defense pathway towards nematode attack in cotton. Our data indicate some candidate genes for validation and use through transformation in other agronomically important plants.</s0></fC01><fC02 i1="01" i2="X"><s0>002A</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Expression génique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Gene expression</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Expresión genética</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Génotype</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Genotype</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Genotipo</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Infection</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Infection</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Infección</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Déprédateur</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Pest</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Plaga</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Résistance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Resistance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Resistencia</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Déterminisme génétique</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Genetic determinism</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Determinismo genético</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Biologie végétale</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Plant biology</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Biología vegetal</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Gossypium hirsutum</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Gossypium hirsutum</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Gossypium hirsutum</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Meloidogyne incognita</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Meloidogyne incognita</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Meloidogyne incognita</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Gène de résistance</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Resistance gene</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Gen de resistencia</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Malvaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Malvaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Malvaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Nematoda</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Nematoda</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Nematoda</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Nemathelminthia</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Nemathelminthia</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Nemathelminthia</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Helmintha</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Helmintha</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Helmintha</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Invertebrata</s0><s2>NS</s2></fC07><fC07 i1="09" i2="X" l="FRE"><s0>Plante à fibres</s0><s5>31</s5></fC07><fC07 i1="09" i2="X" l="ENG"><s0>Fiber crop</s0><s5>31</s5></fC07><fC07 i1="09" i2="X" l="SPA"><s0>Planta de fibras</s0><s5>31</s5></fC07><fC07 i1="10" i2="X" l="FRE"><s0>Meloidogynidae</s0><s2>NS</s2><s5>32</s5></fC07><fC07 i1="10" i2="X" l="ENG"><s0>Meloidogynidae</s0><s2>NS</s2><s5>32</s5></fC07><fC07 i1="10" i2="X" l="SPA"><s0>Meloidogynidae</s0><s2>NS</s2><s5>32</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0407882 INIST</NO><ET>Differentially expressed genes in cotton plant genotypes infected with Meloidogyne incognita</ET><AU>DE DEUS BARBOSA (Aulus Estevao Anjos); DA ROCHA FRAGOSO (Rodrigo); DE LIMA E SOUZA (Djair Dos Santos); FREIRE (Erika); BRILHANTE DE OLIVEIRA (Osmundo NETO); VIANA (Antbnio Américo Barbosa); COITI TOGAWA (Roberto); MOURAO GUIMARAES (Luciane); FLORENCIO MARTINS (Natalia); CIA (Edivaldo); FERNANDEZ (Diana); DE LIMA (Liziane Maria); MATTAR SILVA (Maria Cristina); ROCHA (Thales Lima); GROSSI-DE-SA (Maria Fatima)</AU><AF>Embrapa Recursos Genéticos e Biotecnologia, PqEB - Parque Estaçáo Biológica, W5 Norte Final/Brasília-DF 70770-900/Brésil (1 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 8 aut., 9 aut., 12 aut., 13 aut., 14 aut., 15 aut.); Departamento de Biologia Celular, UnB/Brasília-DF/Brésil (3 aut.); Doutorado em Ciências Genômicas e Bioternologia. UCB/Brasília-DF/Brésil (1 aut., 15 aut.); Embrapa Cerrados/Brasília-DF/Brésil (2 aut.); IAC/Campinas-SP/Brésil (10 aut.); IRD/Montpellier/France (11 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Plant science : (Limerick); ISSN 0168-9452; Coden PLSCE4; Irlande; Da. 2009; Vol. 177; No. 5; Pp. 492-497; Bibl. 51 ref.</SO><LA>Anglais</LA><EA>Meloidogyne incognita is a nematode responsible for huge losses of economically important crops. The control of this pathogen is heavily centered on chemical nematicides, which are toxic to humans and environment, besides being very expensive. Alternatively, resistant varieties of cotton generated from conventional breeding programs represent an attractive strategy for the control of M. incognita. In this context, the goal of the work reported here was to analyze the gene expression profile of one resistant and one susceptible cotton genotype infected with M. incognita aiming to understand the mechanisms involved in resistance. EST libraries of cotton in both resistant and susceptible to infection by M. incognita were constructed and sequenced, generating 2261 sequences that were assembled into 233 contigs and 1593 singlets. Genes differentially expressed were observed in both resistant and susceptible cotton. Twenty genes were found to be expressed exclusively in the resistant cotton genotype, with functions related to pathogen recognition, signal transduction, defense mechanisms and protein synthesis transport and activation. The coordinated action of these genes suggests the existence of a complex defense pathway towards nematode attack in cotton. Our data indicate some candidate genes for validation and use through transformation in other agronomically important plants.</EA><CC>002A</CC><FD>Expression génique; Génotype; Infection; Déprédateur; Résistance; Déterminisme génétique; Biologie végétale; Gossypium hirsutum; Meloidogyne incognita; Gène de résistance</FD><FG>Malvaceae; Dicotyledones; Angiospermae; Spermatophyta; Nematoda; Nemathelminthia; Helmintha; Invertebrata; Plante à fibres; Meloidogynidae</FG><ED>Gene expression; Genotype; Infection; Pest; Resistance; Genetic determinism; Plant biology; Gossypium hirsutum; Meloidogyne incognita; Resistance gene</ED><EG>Malvaceae; Dicotyledones; Angiospermae; Spermatophyta; Nematoda; Nemathelminthia; Helmintha; Invertebrata; Fiber crop; Meloidogynidae</EG><SD>Expresión genética; Genotipo; Infección; Plaga; Resistencia; Determinismo genético; Biología vegetal; Gossypium hirsutum; Meloidogyne incognita; Gen de resistencia</SD><LO>INIST-15982.354000171929080130</LO><ID>09-0407882</ID></server></inist></record>
000D78	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">RENAISSANCE PYRRHONISM : A RELATIVE PHENOMENON</title><author><name sortKey="Naya, Emmanuel" uniqKey="Naya E">Emmanuel Naya</name><affiliation><inist:fA14 i1="01"><s1>Université LumièreLyon2</s1><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0408053</idno><date when="2009">2009</date><idno type="stanalyst">FRANCIS 09-0408053 INIST</idno><idno type="RBID">Francis:09-0408053</idno><idno type="wicri:Area/Main/Corpus">001F90</idno></publicationStmt><seriesStmt><idno type="ISSN">0066-6610</idno><title level="j" type="abbreviated">Arch. int. hist. idées</title><title level="j" type="main">Archives internationales d'histoire des idées</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Pyrrhonism</term><term>Renaissance</term><term>Scepticism</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Renaissance</term><term>Scepticisme</term><term>Pyrrhonisme</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0066-6610</s0></fA01><fA03 i2="1"><s0>Arch. int. hist. idées</s0></fA03><fA05><s2>199</s2></fA05><fA08 i1="01" i2="1" l="ENG"><s1>RENAISSANCE PYRRHONISM : A RELATIVE PHENOMENON</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Renaissance Scepticisms</s1></fA09><fA11 i1="01" i2="1"><s1>NAYA (Emmanuel)</s1></fA11><fA12 i1="01" i2="1"><s1>PAGANINI (Gianni)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>MAIA (José R. Neto)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Université LumièreLyon2</s1><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA15 i1="01"><s1>Università degli Studi del Piemonte Orientale</s1><s2>Vercelli</s2><s3>ITA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Universidade Federal de Minas Gerais</s1><s2>Belo Horizonte</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>15-32</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>25123</s2><s5>354000184518160010</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA47 i1="01" i2="1"><s0>09-0408053</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Archives internationales d'histoire des idées</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fA68 i1="01" i2="1" l="FRE"><s1>Le pyrrhonisme de la renaissance : un phénomène relatif</s1></fA68><fA69 i1="01" i2="1" l="FRE"><s1>Les scepticismes de la Renaissance</s1></fA69><fA99><s0>ref. et notes dissem.</s0></fA99><fC02 i1="01" i2="T"><s0>52241</s0><s1>I</s1></fC02><fC02 i1="02" i2="T"><s0>522</s0></fC02><fC03 i1="01" i2="T" l="FRE"><s0>Renaissance</s0><s5>01</s5></fC03><fC03 i1="01" i2="T" l="ENG"><s0>Renaissance</s0><s5>01</s5></fC03><fC03 i1="01" i2="T" l="SPA"><s0>Renacimiento</s0><s5>01</s5></fC03><fC03 i1="02" i2="T" l="FRE"><s0>Scepticisme</s0><s5>02</s5></fC03><fC03 i1="02" i2="T" l="ENG"><s0>Scepticism</s0><s5>02</s5></fC03><fC03 i1="02" i2="T" l="SPA"><s0>Escepticismo</s0><s5>02</s5></fC03><fC03 i1="03" i2="P" l="FRE"><s0>Pyrrhonisme</s0><s5>03</s5></fC03><fC03 i1="03" i2="P" l="ENG"><s0>Pyrrhonism</s0><s5>03</s5></fC03><fN21><s1>299</s1></fN21></pA></standard><server><NO>FRANCIS 09-0408053 INIST</NO><FT>(Le pyrrhonisme de la renaissance : un phénomène relatif)</FT><ET>RENAISSANCE PYRRHONISM : A RELATIVE PHENOMENON</ET><AU>NAYA (Emmanuel); PAGANINI (Gianni); MAIA (José R. Neto)</AU><AF>Université LumièreLyon2/France (1 aut.); Università degli Studi del Piemonte Orientale/Vercelli/Italie (1 aut.); Universidade Federal de Minas Gerais/Belo Horizonte/Brésil (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Archives internationales d'histoire des idées; ISSN 0066-6610; Pays-Bas; Da. 2009; Vol. 199; Pp. 15-32</SO><LA>Anglais</LA><CC>52241; 522</CC><FD>Renaissance; Scepticisme; Pyrrhonisme</FD><ED>Renaissance; Scepticism; Pyrrhonism</ED><SD>Renacimiento; Escepticismo</SD><LO>INIST-25123.354000184518160010</LO><ID>09-0408053</ID></server></inist></record>
000D79	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Simulations of multipurpose water availability in a semi-arid catchment under different management strategies</title><author><name sortKey="Burte, Julien" uniqKey="Burte J">Julien Burte</name><affiliation><inist:fA14 i1="01"><s1>IRD, Great Ice (UR IRD 032), CC 57, University of Montpellier 2</s1><s2>34095 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>CIRAD, UMR G-EAU</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>UFC, Department of Hydraulic and Environmental Engineering, Federal University of Ceará</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>FUNCEME, Department of Hydrology</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jamin, Jean Yves" uniqKey="Jamin J">Jean-Yves Jamin</name><affiliation><inist:fA14 i1="02"><s1>CIRAD, UMR G-EAU</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Coudrain, Anne" uniqKey="Coudrain A">Anne Coudrain</name><affiliation><inist:fA14 i1="01"><s1>IRD, Great Ice (UR IRD 032), CC 57, University of Montpellier 2</s1><s2>34095 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Frischkorn, Horst" uniqKey="Frischkorn H">Horst Frischkorn</name><affiliation><inist:fA14 i1="03"><s1>UFC, Department of Hydraulic and Environmental Engineering, Federal University of Ceará</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Savio Martins, Eduardo" uniqKey="Savio Martins E">Eduardo Savio Martins</name><affiliation><inist:fA14 i1="04"><s1>FUNCEME, Department of Hydrology</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0408103</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0408103 INIST</idno><idno type="RBID">Pascal:09-0408103</idno><idno type="wicri:Area/Main/Corpus">001C03</idno></publicationStmt><seriesStmt><idno type="ISSN">0378-3774</idno><title level="j" type="abbreviated">Agric. water manage.</title><title level="j" type="main">Agricultural water management</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aquifers</term><term>Environmental engineering</term><term>Modeling</term><term>Multifunctionality</term><term>Scenario (modeling)</term><term>Semi arid zone</term><term>Simulation</term><term>Strategy</term><term>Use</term><term>Water availability</term><term>Water engineering</term><term>Water management</term><term>Water resource management</term><term>Water supply</term><term>Watershed</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Simulation</term><term>Multifonctionnalité</term><term>Approvisionnement eau</term><term>Bassin versant</term><term>Stratégie</term><term>Gestion eau</term><term>Gestion ressource eau</term><term>Nappe eau</term><term>Modélisation</term><term>Zone semi aride</term><term>Utilisation</term><term>Aménagement hydraulique</term><term>Ingénierie environnement</term><term>Eau disponible</term><term>Scénario (modélisation)</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In the semi-arid Brazilian Northeast, the exploitation of alluvial aquifers for irrigation and domestic supply to rural communities over the last 10 years has upset the traditional mechanisms of water resources management. In the Forquilha watershed (221 km<sup>2</sup> ; 5°17&#34;S, 39°30&#34;W), the two main water resources are reservoirs (with a capacity exceeding 0.9-6.7 x 10<sup>6</sup> m<sup>3</sup>), used for domestic water supply only, and an alluvial aquifer (2.3 x 10<sup>6</sup> m<sup>3</sup>), used for irrigation and domestic water supply. From 1998 to 2006, the irrigated area with alluvial groundwater increased from 0 to 75 ha, and the fraction of population supplied through domestic water networks, using reservoirs and the aquifer, increased from 1% to 70%. Based on physical and socioeconomic issues, three main water territories have been defined (&#34;Aquifer&#34;, &#34;Reservoirs&#34;, and &#34;Disperse Habitat&#34;). Considering the next 30 years with a realistic population growth, three hypotheses regarding irrigated area (i.e., 0, 75, or 150 ha), and several possible water-management scenarios, hydrological balance models were built and used to simulate the different impacts on water resource availability and salinity. Simulation results showed that, in all cases, releases from the upstream main reservoir are necessary to keep reservoir salinity below 0.7 g L<sup>-1</sup> and for guaranteeing domestic needs in the whole watershed. As a consequence, a management approach that takes into account the interrelations among the three territories is necessary. Moreover, the simulations showed that the area of irrigated fields cannot exceed the current extent (75 ha), or serious restrictions on water availability and salinity will take place. Moreover, important socioeconomic problems are expected, including a high cost of palliative water supply with tank trucks from external sources.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0378-3774</s0></fA01><fA02 i1="01"><s0>AWMADF</s0></fA02><fA03 i2="1"><s0>Agric. water manage.</s0></fA03><fA05><s2>96</s2></fA05><fA06><s2>8</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Simulations of multipurpose water availability in a semi-arid catchment under different management strategies</s1></fA08><fA11 i1="01" i2="1"><s1>BURTE (Julien)</s1></fA11><fA11 i1="02" i2="1"><s1>JAMIN (Jean-Yves)</s1></fA11><fA11 i1="03" i2="1"><s1>COUDRAIN (Anne)</s1></fA11><fA11 i1="04" i2="1"><s1>FRISCHKORN (Horst)</s1></fA11><fA11 i1="05" i2="1"><s1>SAVIO MARTINS (Eduardo)</s1></fA11><fA14 i1="01"><s1>IRD, Great Ice (UR IRD 032), CC 57, University of Montpellier 2</s1><s2>34095 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="02"><s1>CIRAD, UMR G-EAU</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>UFC, Department of Hydraulic and Environmental Engineering, Federal University of Ceará</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>FUNCEME, Department of Hydrology</s1><s2>Fortaleza</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></fA14><fA20><s1>1181-1190</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>15970</s2><s5>354000188590180010</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1/2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0408103</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Agricultural water management</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>In the semi-arid Brazilian Northeast, the exploitation of alluvial aquifers for irrigation and domestic supply to rural communities over the last 10 years has upset the traditional mechanisms of water resources management. In the Forquilha watershed (221 km<sup>2</sup> ; 5°17&#34;S, 39°30&#34;W), the two main water resources are reservoirs (with a capacity exceeding 0.9-6.7 x 10<sup>6</sup> m<sup>3</sup>), used for domestic water supply only, and an alluvial aquifer (2.3 x 10<sup>6</sup> m<sup>3</sup>), used for irrigation and domestic water supply. From 1998 to 2006, the irrigated area with alluvial groundwater increased from 0 to 75 ha, and the fraction of population supplied through domestic water networks, using reservoirs and the aquifer, increased from 1% to 70%. Based on physical and socioeconomic issues, three main water territories have been defined (&#34;Aquifer&#34;, &#34;Reservoirs&#34;, and &#34;Disperse Habitat&#34;). Considering the next 30 years with a realistic population growth, three hypotheses regarding irrigated area (i.e., 0, 75, or 150 ha), and several possible water-management scenarios, hydrological balance models were built and used to simulate the different impacts on water resource availability and salinity. Simulation results showed that, in all cases, releases from the upstream main reservoir are necessary to keep reservoir salinity below 0.7 g L<sup>-1</sup> and for guaranteeing domestic needs in the whole watershed. As a consequence, a management approach that takes into account the interrelations among the three territories is necessary. Moreover, the simulations showed that the area of irrigated fields cannot exceed the current extent (75 ha), or serious restrictions on water availability and salinity will take place. Moreover, important socioeconomic problems are expected, including a high cost of palliative water supply with tank trucks from external sources.</s0></fC01><fC02 i1="01" i2="X"><s0>002A32C03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Simulation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Simulation</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Simulación</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Multifonctionnalité</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Multifunctionality</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Multifuncionalidad</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Approvisionnement eau</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Water supply</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Alimentación agua</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Bassin versant</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Watershed</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Cuenca</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Stratégie</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Strategy</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Estrategia</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Gestion eau</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Water management</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Gestión del agua</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Gestion ressource eau</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Water resource management</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Gestión recurso agua</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Nappe eau</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Aquifers</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Capa agua</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Modélisation</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Modeling</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Modelización</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Zone semi aride</s0><s5>20</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Semi arid zone</s0><s5>20</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Zona semiárida</s0><s5>20</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Utilisation</s0><s5>28</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Use</s0><s5>28</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Uso</s0><s5>28</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Aménagement hydraulique</s0><s5>29</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Water engineering</s0><s5>29</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Aprovechamiento hidráulico</s0><s5>29</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Ingénierie environnement</s0><s5>30</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Environmental engineering</s0><s5>30</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Ingeniería ambiental</s0><s5>30</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Eau disponible</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Water availability</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Disponibilidad del agua</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Scénario (modélisation)</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Scenario (modeling)</s0><s4>CD</s4><s5>97</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Scenario (modelización)</s0><s4>CD</s4><s5>97</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Zone climatique</s0><s5>33</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Climatic zone</s0><s5>33</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Zona climática</s0><s5>33</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Milieu aride</s0><s5>34</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Arid environment</s0><s5>34</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Medio árido</s0><s5>34</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0408103 INIST</NO><ET>Simulations of multipurpose water availability in a semi-arid catchment under different management strategies</ET><AU>BURTE (Julien); JAMIN (Jean-Yves); COUDRAIN (Anne); FRISCHKORN (Horst); SAVIO MARTINS (Eduardo)</AU><AF>IRD, Great Ice (UR IRD 032), CC 57, University of Montpellier 2/34095 Montpellier/France (1 aut., 3 aut.); CIRAD, UMR G-EAU/34398 Montpellier/France (1 aut., 2 aut.); UFC, Department of Hydraulic and Environmental Engineering, Federal University of Ceará/Fortaleza/Brésil (1 aut., 4 aut.); FUNCEME, Department of Hydrology/Fortaleza/Brésil (1 aut., 5 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Agricultural water management; ISSN 0378-3774; Coden AWMADF; Pays-Bas; Da. 2009; Vol. 96; No. 8; Pp. 1181-1190; Bibl. 1/2 p.</SO><LA>Anglais</LA><EA>In the semi-arid Brazilian Northeast, the exploitation of alluvial aquifers for irrigation and domestic supply to rural communities over the last 10 years has upset the traditional mechanisms of water resources management. In the Forquilha watershed (221 km<sup>2</sup> ; 5°17&#34;S, 39°30&#34;W), the two main water resources are reservoirs (with a capacity exceeding 0.9-6.7 x 10<sup>6</sup> m<sup>3</sup>), used for domestic water supply only, and an alluvial aquifer (2.3 x 10<sup>6</sup> m<sup>3</sup>), used for irrigation and domestic water supply. From 1998 to 2006, the irrigated area with alluvial groundwater increased from 0 to 75 ha, and the fraction of population supplied through domestic water networks, using reservoirs and the aquifer, increased from 1% to 70%. Based on physical and socioeconomic issues, three main water territories have been defined (&#34;Aquifer&#34;, &#34;Reservoirs&#34;, and &#34;Disperse Habitat&#34;). Considering the next 30 years with a realistic population growth, three hypotheses regarding irrigated area (i.e., 0, 75, or 150 ha), and several possible water-management scenarios, hydrological balance models were built and used to simulate the different impacts on water resource availability and salinity. Simulation results showed that, in all cases, releases from the upstream main reservoir are necessary to keep reservoir salinity below 0.7 g L<sup>-1</sup> and for guaranteeing domestic needs in the whole watershed. As a consequence, a management approach that takes into account the interrelations among the three territories is necessary. Moreover, the simulations showed that the area of irrigated fields cannot exceed the current extent (75 ha), or serious restrictions on water availability and salinity will take place. Moreover, important socioeconomic problems are expected, including a high cost of palliative water supply with tank trucks from external sources.</EA><CC>002A32C03</CC><FD>Simulation; Multifonctionnalité; Approvisionnement eau; Bassin versant; Stratégie; Gestion eau; Gestion ressource eau; Nappe eau; Modélisation; Zone semi aride; Utilisation; Aménagement hydraulique; Ingénierie environnement; Eau disponible; Scénario (modélisation)</FD><FG>Zone climatique; Milieu aride</FG><ED>Simulation; Multifunctionality; Water supply; Watershed; Strategy; Water management; Water resource management; Aquifers; Modeling; Semi arid zone; Use; Water engineering; Environmental engineering; Water availability; Scenario (modeling)</ED><EG>Climatic zone; Arid environment</EG><SD>Simulación; Multifuncionalidad; Alimentación agua; Cuenca; Estrategia; Gestión del agua; Gestión recurso agua; Capa agua; Modelización; Zona semiárida; Uso; Aprovechamiento hidráulico; Ingeniería ambiental; Disponibilidad del agua; Scenario (modelización)</SD><LO>INIST-15970.354000188590180010</LO><ID>09-0408103</ID></server></inist></record>
000D80	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Biphasic haustorial differentiation of coffee rust (Nemileia vastatrix race 11) associated with defence responses in resistant and susceptible coffee cultivars</title><author><name sortKey="Ramiro, D A" uniqKey="Ramiro D">D. A. Ramiro</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Escoute, J" uniqKey="Escoute J">J. Escoute</name><affiliation><inist:fA14 i1="02"><s1>Cirad, UMR1096 DAP, Montpellier RIO Imaging</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Petitot, A S" uniqKey="Petitot A">A.-S. Petitot</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nicole, M" uniqKey="Nicole M">M. Nicole</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Maluf, M P" uniqKey="Maluf M">M. P. Maluf</name><affiliation><inist:fA14 i1="03"><s1>Embrapa Café, Instituto Agronômico de Campinas, Centro de Café 'Alcides Carvalho', CP 28</s1><s2>13.001-970 Campinas</s2><s3>BRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fernandez, D" uniqKey="Fernandez D">D. Fernandez</name><affiliation><inist:fA14 i1="01"><s1>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0408293</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0408293 INIST</idno><idno type="RBID">Pascal:09-0408293</idno><idno type="wicri:Area/Main/Corpus">001C02</idno></publicationStmt><seriesStmt><idno type="ISSN">0032-0862</idno><title level="j" type="abbreviated">Plant pathol.</title><title level="j" type="main">Plant pathology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Coffea arabica</term><term>Cultivar</term><term>Defensive response</term><term>Differentiation</term><term>Gene</term><term>Haustorium</term><term>Molecular biology</term><term>Pathogenesis</term><term>Plant pathology</term><term>Polymerase chain reaction</term><term>Race</term><term>Reactive oxygen species</term><term>Real time</term><term>Sensitivity resistance</term><term>Tropical crop</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Haustorium</term><term>Différenciation</term><term>Race</term><term>Réponse défensive</term><term>Sensibilité résistance</term><term>Pathogénie</term><term>Gène</term><term>Temps réel</term><term>Réaction chaîne polymérase</term><term>Cultivar</term><term>Coffea arabica</term><term>Espèces réactives de l'oxygène</term><term>Phytopathologie</term><term>Culture tropicale</term><term>Biologie moléculaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible high-yielding Brazilian coffee cultivars showed that the fungus produced 'pioneer' haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed 'secondary haustoria' which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H<sub>2</sub>O<sub>2</sub> generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secreted into, the subsidiary and adjacent cells of the stomata. Additionally, the present study provides new insights into the colonization process of the coffee rust fungus.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0032-0862</s0></fA01><fA02 i1="01"><s0>PLPAAD</s0></fA02><fA03 i2="1"><s0>Plant pathol.</s0></fA03><fA05><s2>58</s2></fA05><fA06><s2>5</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Biphasic haustorial differentiation of coffee rust (Nemileia vastatrix race 11) associated with defence responses in resistant and susceptible coffee cultivars</s1></fA08><fA11 i1="01" i2="1"><s1>RAMIRO (D. A.)</s1></fA11><fA11 i1="02" i2="1"><s1>ESCOUTE (J.)</s1></fA11><fA11 i1="03" i2="1"><s1>PETITOT (A.-S.)</s1></fA11><fA11 i1="04" i2="1"><s1>NICOLE (M.)</s1></fA11><fA11 i1="05" i2="1"><s1>MALUF (M. P.)</s1></fA11><fA11 i1="06" i2="1"><s1>FERNANDEZ (D.)</s1></fA11><fA14 i1="01"><s1>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501</s1><s2>34394 Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Cirad, UMR1096 DAP, Montpellier RIO Imaging</s1><s2>34398 Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Embrapa Café, Instituto Agronômico de Campinas, Centro de Café 'Alcides Carvalho', CP 28</s1><s2>13.001-970 Campinas</s2><s3>BRA</s3><sZ>5 aut.</sZ></fA14><fA20><s1>944-955</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>7414</s2><s5>354000171933020150</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0408293</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Plant pathology</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>The objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible high-yielding Brazilian coffee cultivars showed that the fungus produced 'pioneer' haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed 'secondary haustoria' which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H<sub>2</sub>O<sub>2</sub> generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secreted into, the subsidiary and adjacent cells of the stomata. Additionally, the present study provides new insights into the colonization process of the coffee rust fungus.</s0></fC01><fC02 i1="01" i2="X"><s0>002A34</s0></fC02><fC02 i1="02" i2="X"><s0>002A32D</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Haustorium</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Haustorium</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Différenciation</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Differentiation</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Diferenciación</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Race</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Race</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Raza</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Réponse défensive</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Defensive response</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Respuesta defensiva</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Sensibilité résistance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Sensitivity resistance</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Sensibilidad resistencia</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Pathogénie</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Pathogenesis</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Patogenia</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Gène</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Gene</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Gen</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Temps réel</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Real time</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Tiempo real</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Réaction chaîne polymérase</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Polymerase chain reaction</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Reacción cadena polimerasa</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Cultivar</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Cultivar</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Cultivar</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Coffea arabica</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Coffea arabica</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Coffea arabica</s0><s2>NS</s2><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Espèces réactives de l'oxygène</s0><s2>NK</s2><s5>15</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Reactive oxygen species</s0><s2>NK</s2><s5>15</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Especies reactivas del oxígeno</s0><s2>NK</s2><s5>15</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Phytopathologie</s0><s5>28</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Plant pathology</s0><s5>28</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Fitopatología</s0><s5>28</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Culture tropicale</s0><s5>29</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Tropical crop</s0><s5>29</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Cultivo tropical</s0><s5>29</s5></fC03><fC03 i1="15" i2="X" l="FRE"><s0>Biologie moléculaire</s0><s5>30</s5></fC03><fC03 i1="15" i2="X" l="ENG"><s0>Molecular biology</s0><s5>30</s5></fC03><fC03 i1="15" i2="X" l="SPA"><s0>Biología molecular</s0><s5>30</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Rubiaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Rubiaceae</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Rubiaceae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Plante stimulante</s0><s5>31</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Stimulant plant</s0><s5>31</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Planta estimulante</s0><s5>31</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Plante pérenne</s0><s5>32</s5></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Perennial plant</s0><s5>32</s5></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Planta perenne</s0><s5>32</s5></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Oxydant</s0><s5>50</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Oxidant</s0><s5>50</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Oxidante</s0><s5>50</s5></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Méthode moléculaire</s0><s4>INC</s4><s5>68</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0408293 INIST</NO><ET>Biphasic haustorial differentiation of coffee rust (Nemileia vastatrix race 11) associated with defence responses in resistant and susceptible coffee cultivars</ET><AU>RAMIRO (D. A.); ESCOUTE (J.); PETITOT (A.-S.); NICOLE (M.); MALUF (M. P.); FERNANDEZ (D.)</AU><AF>Institut de Recherche pour le Développement, UMR186 IRD/CIRAD/Univ. Montpellier2, Résistance des Plantes aux Bioagresseurs (RPB), BP64501/34394 Montpellier/France (1 aut., 3 aut., 4 aut., 6 aut.); Cirad, UMR1096 DAP, Montpellier RIO Imaging/34398 Montpellier/France (2 aut.); Embrapa Café, Instituto Agronômico de Campinas, Centro de Café 'Alcides Carvalho', CP 28/13.001-970 Campinas/Brésil (5 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Plant pathology; ISSN 0032-0862; Coden PLPAAD; Royaume-Uni; Da. 2009; Vol. 58; No. 5; Pp. 944-955; Bibl. 1 p.1/4</SO><LA>Anglais</LA><EA>The objective of this study was to assess whether defence responses in coffee (Coffea arabica) were linked to a specific developmental stage of the rust fungus Hemileia vastatrix. Histological observations in compatible and incompatible high-yielding Brazilian coffee cultivars showed that the fungus produced 'pioneer' haustoria in adjacent and subsidiary stomatal cells soon after entering the stomata, followed by later developed 'secondary haustoria' which invade mesophyll cells. In the incompatible interaction between Race II and cv. Tupi, a strong and transient H<sub>2</sub>O<sub>2</sub> generation at infection sites was detected at 39 h post inoculation (hpi) during secondary haustoria formation. In addition, clear-cut differences in defence gene expression between compatible and incompatible interactions were only observed during the secondary haustoria formation. Transcripts of the pathogenesis-related (PR) genes CaPR1b and CaPR10 accumulated to maximal levels at 39 hpi (38- and 86-fold, respectively) in the incompatible interaction, but stayed at low levels in the compatible interaction. In contrast, the CaWRKY1 gene and the CaRLK gene were only induced in the susceptible cultivar. These results indicated that the specific resistance of cv. Tupi was expressed after differentiation of the H. vastatrix secondary haustoria. Analysis showed no evidence of specific recognition of coffee rust at the pioneer haustoria stage, suggesting that haustoria components are not recognized by, or not secreted into, the subsidiary and adjacent cells of the stomata. Additionally, the present study provides new insights into the colonization process of the coffee rust fungus.</EA><CC>002A34; 002A32D</CC><FD>Haustorium; Différenciation; Race; Réponse défensive; Sensibilité résistance; Pathogénie; Gène; Temps réel; Réaction chaîne polymérase; Cultivar; Coffea arabica; Espèces réactives de l'oxygène; Phytopathologie; Culture tropicale; Biologie moléculaire</FD><FG>Rubiaceae; Dicotyledones; Angiospermae; Spermatophyta; Plante stimulante; Plante pérenne; Oxydant; Méthode moléculaire</FG><ED>Haustorium; Differentiation; Race; Defensive response; Sensitivity resistance; Pathogenesis; Gene; Real time; Polymerase chain reaction; Cultivar; Coffea arabica; Reactive oxygen species; Plant pathology; Tropical crop; Molecular biology</ED><EG>Rubiaceae; Dicotyledones; Angiospermae; Spermatophyta; Stimulant plant; Perennial plant; Oxidant</EG><SD>Diferenciación; Raza; Respuesta defensiva; Sensibilidad resistencia; Patogenia; Gen; Tiempo real; Reacción cadena polimerasa; Cultivar; Coffea arabica; Especies reactivas del oxígeno; Fitopatología; Cultivo tropical; Biología molecular</SD><LO>INIST-7414.354000171933020150</LO><ID>09-0408293</ID></server></inist></record>
000D81	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Unmet needs in severe chronic upper airway disease (SCUAD)</title><author><name sortKey="Bousquet, Jean" uniqKey="Bousquet J">Jean Bousquet</name><affiliation><inist:fA14 i1="01"><s1>University Hospital</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bachert, Claus" uniqKey="Bachert C">Claus Bachert</name><affiliation><inist:fA14 i1="02"><s1>UZG, University Hospital Ghent</s1><s3>DEU</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Canonica, Giorgio W" uniqKey="Canonica G">Giorgio W. Canonica</name><affiliation><inist:fA14 i1="03"><s1>Allergy and Respiratory Diseases Clinic, University of Genova</s1><s3>DEU</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Casale, Thomas B" uniqKey="Casale T">Thomas B. Casale</name><affiliation><inist:fA14 i1="04"><s1>Creighton University</s1><s2>Omaha</s2><s3>USA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cruz, Alvaro A" uniqKey="Cruz A">Alvaro A. Cruz</name><affiliation><inist:fA14 i1="05"><s1>ProAR-FMB, Federal University of Bahia</s1><s2>Salvador</s2><s3>BRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lockey, Richard J" uniqKey="Lockey R">Richard J. Lockey</name><affiliation><inist:fA14 i1="06"><s1>Joy McCann Culver-house, University of South Florida College of Medicine</s1><s2>Tampa</s2><s3>USA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Zuberbier, Torsten" uniqKey="Zuberbier T">Torsten Zuberbier</name><affiliation><inist:fA14 i1="07"><s1>Allergy Centre Charité, Charite-Universitatsmedizin Berlin</s1><s3>DEU</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0408595</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0408595 INIST</idno><idno type="RBID">Pascal:09-0408595</idno><idno type="wicri:Area/Main/Corpus">001C01</idno></publicationStmt><seriesStmt><idno type="ISSN">0091-6749</idno><title level="j" type="abbreviated">J. allergy clin. immunol.</title><title level="j" type="main">Journal of allergy and clinical immunology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Chronic disease</term><term>Immunology</term><term>Immunopathology</term><term>Need</term><term>Rhinitis</term><term>Sinusitis</term><term>Upper respiratory tract</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Maladie chronique</term><term>Rhinite</term><term>Sinusite</term><term>Besoin</term><term>Voie respiratoire supérieure</term><term>Immunologie</term><term>Immunopathologie</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Although the majority of patients with chronic upper airway diseases have controlled symptoms during treatment, many patients have severe chronic upper airway diseases (SCUADs). SCUAD defines those patients whose symptoms are inadequately controlled despite adequate (ie, effective, safe, and acceptable) pharmacologic treatment based on guidelines. These patients have impaired quality of life, social functioning, sleep, and school/work performance. Severe uncontrolled allergic rhinitis, nonallergic rhinitis, chronic rhinosinusitis, aspirin-exacerbated respiratory diseases, or occupational airway diseases are defined as SCUADs. Pediatric SCUADs are still unclear. In developing countries SCUADs exist, but risk factors can differ from those seen in developed countries. Comorbidities are common in patients with SCUADs and might increase their severity. The present document is the position of a group of experts considering that SCUADs should be considered differently from mild chronic upper airway diseases. It reviews the state of the art, highlighting gaps in our knowledge, and proposes several areas for a better understanding, prevention, and management of SCUADs. This document can also serve to optimize the pharmacoeconomic evaluation of SCUADs by means of comparison with mild chronic upper airway diseases.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0091-6749</s0></fA01><fA02 i1="01"><s0>JACIBY</s0></fA02><fA03 i2="1"><s0>J. allergy clin. immunol.</s0></fA03><fA05><s2>124</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Unmet needs in severe chronic upper airway disease (SCUAD)</s1></fA08><fA11 i1="01" i2="1"><s1>BOUSQUET (Jean)</s1></fA11><fA11 i1="02" i2="1"><s1>BACHERT (Claus)</s1></fA11><fA11 i1="03" i2="1"><s1>CANONICA (Giorgio W.)</s1></fA11><fA11 i1="04" i2="1"><s1>CASALE (Thomas B.)</s1></fA11><fA11 i1="05" i2="1"><s1>CRUZ (Alvaro A.)</s1></fA11><fA11 i1="06" i2="1"><s1>LOCKEY (Richard J.)</s1></fA11><fA11 i1="07" i2="1"><s1>ZUBERBIER (Torsten)</s1></fA11><fA14 i1="01"><s1>University Hospital</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>UZG, University Hospital Ghent</s1><s3>DEU</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Allergy and Respiratory Diseases Clinic, University of Genova</s1><s3>DEU</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Creighton University</s1><s2>Omaha</s2><s3>USA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>ProAR-FMB, Federal University of Bahia</s1><s2>Salvador</s2><s3>BRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Joy McCann Culver-house, University of South Florida College of Medicine</s1><s2>Tampa</s2><s3>USA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="07"><s1>Allergy Centre Charité, Charite-Universitatsmedizin Berlin</s1><s3>DEU</s3><sZ>7 aut.</sZ></fA14><fA17 i1="01" i2="1"><s1>Extended Global Allergy and Asthma European Network, World Allergy Organization and Allergic Rhinitis and its Impact on Asthma</s1><s3>EUR</s3></fA17><fA20><s1>428-433</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2059</s2><s5>354000171936580050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>27 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0408595</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Journal of allergy and clinical immunology</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Although the majority of patients with chronic upper airway diseases have controlled symptoms during treatment, many patients have severe chronic upper airway diseases (SCUADs). SCUAD defines those patients whose symptoms are inadequately controlled despite adequate (ie, effective, safe, and acceptable) pharmacologic treatment based on guidelines. These patients have impaired quality of life, social functioning, sleep, and school/work performance. Severe uncontrolled allergic rhinitis, nonallergic rhinitis, chronic rhinosinusitis, aspirin-exacerbated respiratory diseases, or occupational airway diseases are defined as SCUADs. Pediatric SCUADs are still unclear. In developing countries SCUADs exist, but risk factors can differ from those seen in developed countries. Comorbidities are common in patients with SCUADs and might increase their severity. The present document is the position of a group of experts considering that SCUADs should be considered differently from mild chronic upper airway diseases. It reviews the state of the art, highlighting gaps in our knowledge, and proposes several areas for a better understanding, prevention, and management of SCUADs. This document can also serve to optimize the pharmacoeconomic evaluation of SCUADs by means of comparison with mild chronic upper airway diseases.</s0></fC01><fC02 i1="01" i2="X"><s0>002A06</s0></fC02><fC02 i1="02" i2="X"><s0>002B07</s0></fC02><fC02 i1="03" i2="X"><s0>002B06</s0></fC02><fC02 i1="04" i2="X"><s0>002B10B02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Maladie chronique</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Chronic disease</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Enfermedad crónica</s0><s2>NM</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Rhinite</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Rhinitis</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Rinitis</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Sinusite</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Sinusitis</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Sinusitis</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Besoin</s0><s5>09</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Need</s0><s5>09</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Necesidad</s0><s5>09</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Voie respiratoire supérieure</s0><s5>10</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Upper respiratory tract</s0><s5>10</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Vía respiratoria superior</s0><s5>10</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Immunologie</s0><s5>11</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Immunology</s0><s5>11</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Inmunología</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Immunopathologie</s0><s5>12</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Immunopathology</s0><s5>12</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Inmunopatología</s0><s5>12</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie ORL</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>ENT disease</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>ORL patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie du nez</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Nose disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Nariz patología</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pathologie des sinus de la face</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Paranasal sinus disease</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Seno paranasal patología</s0><s5>39</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0408595 INIST</NO><ET>Unmet needs in severe chronic upper airway disease (SCUAD)</ET><AU>BOUSQUET (Jean); BACHERT (Claus); CANONICA (Giorgio W.); CASALE (Thomas B.); CRUZ (Alvaro A.); LOCKEY (Richard J.); ZUBERBIER (Torsten)</AU><AF>University Hospital/Montpellier/France (1 aut.); UZG, University Hospital Ghent/Allemagne (2 aut.); Allergy and Respiratory Diseases Clinic, University of Genova/Allemagne (3 aut.); Creighton University/Omaha/Etats-Unis (4 aut.); ProAR-FMB, Federal University of Bahia/Salvador/Brésil (5 aut.); Joy McCann Culver-house, University of South Florida College of Medicine/Tampa/Etats-Unis (6 aut.); Allergy Centre Charité, Charite-Universitatsmedizin Berlin/Allemagne (7 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Journal of allergy and clinical immunology; ISSN 0091-6749; Coden JACIBY; Etats-Unis; Da. 2009; Vol. 124; No. 3; Pp. 428-433; Bibl. 27 ref.</SO><LA>Anglais</LA><EA>Although the majority of patients with chronic upper airway diseases have controlled symptoms during treatment, many patients have severe chronic upper airway diseases (SCUADs). SCUAD defines those patients whose symptoms are inadequately controlled despite adequate (ie, effective, safe, and acceptable) pharmacologic treatment based on guidelines. These patients have impaired quality of life, social functioning, sleep, and school/work performance. Severe uncontrolled allergic rhinitis, nonallergic rhinitis, chronic rhinosinusitis, aspirin-exacerbated respiratory diseases, or occupational airway diseases are defined as SCUADs. Pediatric SCUADs are still unclear. In developing countries SCUADs exist, but risk factors can differ from those seen in developed countries. Comorbidities are common in patients with SCUADs and might increase their severity. The present document is the position of a group of experts considering that SCUADs should be considered differently from mild chronic upper airway diseases. It reviews the state of the art, highlighting gaps in our knowledge, and proposes several areas for a better understanding, prevention, and management of SCUADs. This document can also serve to optimize the pharmacoeconomic evaluation of SCUADs by means of comparison with mild chronic upper airway diseases.</EA><CC>002A06; 002B07; 002B06; 002B10B02</CC><FD>Maladie chronique; Rhinite; Sinusite; Besoin; Voie respiratoire supérieure; Immunologie; Immunopathologie</FD><FG>Pathologie ORL; Pathologie du nez; Pathologie des sinus de la face</FG><ED>Chronic disease; Rhinitis; Sinusitis; Need; Upper respiratory tract; Immunology; Immunopathology</ED><EG>ENT disease; Nose disease; Paranasal sinus disease</EG><SD>Enfermedad crónica; Rinitis; Sinusitis; Necesidad; Vía respiratoria superior; Inmunología; Inmunopatología</SD><LO>INIST-2059.354000171936580050</LO><ID>09-0408595</ID></server></inist></record>
000D82	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Application of abrupt cut-off models in the analysis of the capacitance spectra of conjugated polymer devices</title><author><name sortKey="Reis, F T" uniqKey="Reis F">F. T. Reis</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Física, Universidade Federal de Santa Catarina</s1><s2>88040-900, Florianópolis, SC</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Santos, L F" uniqKey="Santos L">L. F. Santos</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Física, IBILCE/UNESP</s1><s2>15054-000 São José do Rio Preto, SP</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bianchi, R F" uniqKey="Bianchi R">R. F. Bianchi</name><affiliation><inist:fA14 i1="03"><s1>Departamento de Física, Universidade Federal de Ouro Preto</s1><s2>35400-000 Ouro Preto, MG</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cunha, H N" uniqKey="Cunha H">H. N. Cunha</name><affiliation><inist:fA14 i1="04"><s1>Departamento de Física, Universidade Federal do Piauí</s1><s2>64049-550 Teresina, PI</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mencaraglia, D" uniqKey="Mencaraglia D">D. Mencaraglia</name><affiliation><inist:fA14 i1="05"><s1>Laboratoire de Génie Électrique de Paris (CNRS, UMR 8507), École Supérieure d'Électricité, Universités Paris VI et Paris XI, Plateau de Moulon</s1><s2>91192 Gif-sur-Yvette</s2><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Faria, R M" uniqKey="Faria R">R. M. Faria</name><affiliation><inist:fA14 i1="06"><s1>Instituto de Física de São Carlos, Universidade de São Paulo</s1><s2>13560-970 São Carlos, SP</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0408740</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0408740 INIST</idno><idno type="RBID">Pascal:09-0408740</idno><idno type="wicri:Area/Main/Corpus">001C00</idno></publicationStmt><seriesStmt><idno type="ISSN">0947-8396</idno><title level="j" type="abbreviated">Appl. phys., A Mater. sci. process. : (Print)</title><title level="j" type="main">Applied physics. A, Materials science &#38; processing : (Print)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aluminium</term><term>Capacitance</term><term>Conducting polymers</term><term>Conjugated polymer</term><term>Cut-off</term><term>Debye length</term><term>Doping</term><term>Energy gap</term><term>Fermi level</term><term>Gold</term><term>IV characteristic</term><term>Metal-semiconductor contacts</term><term>Organic semiconductors</term><term>Polyanilines</term><term>Space charge</term><term>Transition elements</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Capacité électrique</term><term>Dopage</term><term>Caractéristique courant tension</term><term>Bande interdite</term><term>Longueur Debye</term><term>Niveau Fermi</term><term>Charge espace</term><term>Aluminium</term><term>Cut-off</term><term>Polymère conjugué</term><term>Aniline polymère</term><term>Semiconducteur organique</term><term>Polymère conducteur</term><term>Contact métal semiconducteur</term><term>Or</term><term>Métal transition</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">In this paper, a detailed study of the capacitance spectra obtained from Au/doped-polyaniline/Al structures in the frequency domain (0.05 Hz-10 MHz), and at different temperatures (150-340 K) is carried out. The capacitance spectra behavior in semiconductors can be appropriately described by using abrupt cut-off models, since they assume that the electronic gap states that can follow the ac modulation have response times varying rapidly with a certain abscissa, which is dependent on both temperature and frequency. Two models based on the abrupt cutoff concept, formerly developed to describe inorganic semiconductor devices, have been used to analyze the capacitance spectra of devices based on doped polyaniline (PANI), which is a well-known polymeric semiconductor with in-numerous potential technological applications. The application of these models allowed the determination of significant parameters, such as Debye length (≃20 nm), position of bulk Fermi level (≃320 meV) and associated density of states (≃2 x 10<sup>18</sup> eV<sup>-1</sup> cm<sup>-3</sup>), width of the space charge region (≃70 nm), built-in potential (≃780 meV), and the gap states' distribution.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0947-8396</s0></fA01><fA03 i2="1"><s0>Appl. phys., A Mater. sci. process. : (Print)</s0></fA03><fA05><s2>96</s2></fA05><fA06><s2>4</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Application of abrupt cut-off models in the analysis of the capacitance spectra of conjugated polymer devices</s1></fA08><fA11 i1="01" i2="1"><s1>REIS (F. T.)</s1></fA11><fA11 i1="02" i2="1"><s1>SANTOS (L. F.)</s1></fA11><fA11 i1="03" i2="1"><s1>BIANCHI (R. F.)</s1></fA11><fA11 i1="04" i2="1"><s1>CUNHA (H. N.)</s1></fA11><fA11 i1="05" i2="1"><s1>MENCARAGLIA (D.)</s1></fA11><fA11 i1="06" i2="1"><s1>FARIA (R. M.)</s1></fA11><fA14 i1="01"><s1>Departamento de Física, Universidade Federal de Santa Catarina</s1><s2>88040-900, Florianópolis, SC</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Física, IBILCE/UNESP</s1><s2>15054-000 São José do Rio Preto, SP</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Departamento de Física, Universidade Federal de Ouro Preto</s1><s2>35400-000 Ouro Preto, MG</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Departamento de Física, Universidade Federal do Piauí</s1><s2>64049-550 Teresina, PI</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Laboratoire de Génie Électrique de Paris (CNRS, UMR 8507), École Supérieure d'Électricité, Universités Paris VI et Paris XI, Plateau de Moulon</s1><s2>91192 Gif-sur-Yvette</s2><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Instituto de Física de São Carlos, Universidade de São Paulo</s1><s2>13560-970 São Carlos, SP</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>909-914</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>16194A</s2><s5>354000170843030160</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>26 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0408740</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied physics. A, Materials science &#38; processing : (Print)</s0></fA64><fA66 i1="01"><s0>DEU</s0></fA66><fC01 i1="01" l="ENG"><s0>In this paper, a detailed study of the capacitance spectra obtained from Au/doped-polyaniline/Al structures in the frequency domain (0.05 Hz-10 MHz), and at different temperatures (150-340 K) is carried out. The capacitance spectra behavior in semiconductors can be appropriately described by using abrupt cut-off models, since they assume that the electronic gap states that can follow the ac modulation have response times varying rapidly with a certain abscissa, which is dependent on both temperature and frequency. Two models based on the abrupt cutoff concept, formerly developed to describe inorganic semiconductor devices, have been used to analyze the capacitance spectra of devices based on doped polyaniline (PANI), which is a well-known polymeric semiconductor with in-numerous potential technological applications. The application of these models allowed the determination of significant parameters, such as Debye length (≃20 nm), position of bulk Fermi level (≃320 meV) and associated density of states (≃2 x 10<sup>18</sup> eV<sup>-1</sup> cm<sup>-3</sup>), width of the space charge region (≃70 nm), built-in potential (≃780 meV), and the gap states' distribution.</s0></fC01><fC02 i1="01" i2="3"><s0>001B70G22J</s0></fC02><fC02 i1="02" i2="3"><s0>001B70C40S</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Capacité électrique</s0><s5>02</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Capacitance</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Dopage</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Doping</s0><s5>03</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Doping</s0><s5>03</s5></fC03><fC03 i1="03" i2="3" l="FRE"><s0>Caractéristique courant tension</s0><s5>04</s5></fC03><fC03 i1="03" i2="3" l="ENG"><s0>IV characteristic</s0><s5>04</s5></fC03><fC03 i1="04" i2="3" l="FRE"><s0>Bande interdite</s0><s5>05</s5></fC03><fC03 i1="04" i2="3" l="ENG"><s0>Energy gap</s0><s5>05</s5></fC03><fC03 i1="05" i2="3" l="FRE"><s0>Longueur Debye</s0><s5>10</s5></fC03><fC03 i1="05" i2="3" l="ENG"><s0>Debye length</s0><s5>10</s5></fC03><fC03 i1="06" i2="3" l="FRE"><s0>Niveau Fermi</s0><s5>11</s5></fC03><fC03 i1="06" i2="3" l="ENG"><s0>Fermi level</s0><s5>11</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Charge espace</s0><s5>12</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Space charge</s0><s5>12</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Aluminium</s0><s2>NC</s2><s5>13</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Aluminium</s0><s2>NC</s2><s5>13</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Cut-off</s0><s5>14</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Cut-off</s0><s5>14</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Polymère conjugué</s0><s5>15</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Conjugated polymer</s0><s5>15</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Polímero conjugado</s0><s5>15</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Aniline polymère</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Polyanilines</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="12" i2="3" l="FRE"><s0>Semiconducteur organique</s0><s5>18</s5></fC03><fC03 i1="12" i2="3" l="ENG"><s0>Organic semiconductors</s0><s5>18</s5></fC03><fC03 i1="13" i2="3" l="FRE"><s0>Polymère conducteur</s0><s5>19</s5></fC03><fC03 i1="13" i2="3" l="ENG"><s0>Conducting polymers</s0><s5>19</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>Contact métal semiconducteur</s0><s5>20</s5></fC03><fC03 i1="14" i2="3" l="ENG"><s0>Metal-semiconductor contacts</s0><s5>20</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>Or</s0><s2>NC</s2><s5>21</s5></fC03><fC03 i1="15" i2="3" l="ENG"><s0>Gold</s0><s2>NC</s2><s5>21</s5></fC03><fC03 i1="16" i2="3" l="FRE"><s0>Métal transition</s0><s5>48</s5></fC03><fC03 i1="16" i2="3" l="ENG"><s0>Transition elements</s0><s5>48</s5></fC03><fN21><s1>299</s1></fN21></pA></standard><server><NO>PASCAL 09-0408740 INIST</NO><ET>Application of abrupt cut-off models in the analysis of the capacitance spectra of conjugated polymer devices</ET><AU>REIS (F. T.); SANTOS (L. F.); BIANCHI (R. F.); CUNHA (H. N.); MENCARAGLIA (D.); FARIA (R. M.)</AU><AF>Departamento de Física, Universidade Federal de Santa Catarina/88040-900, Florianópolis, SC/Brésil (1 aut.); Departamento de Física, IBILCE/UNESP/15054-000 São José do Rio Preto, SP/Brésil (2 aut.); Departamento de Física, Universidade Federal de Ouro Preto/35400-000 Ouro Preto, MG/Brésil (3 aut.); Departamento de Física, Universidade Federal do Piauí/64049-550 Teresina, PI/Brésil (4 aut.); Laboratoire de Génie Électrique de Paris (CNRS, UMR 8507), École Supérieure d'Électricité, Universités Paris VI et Paris XI, Plateau de Moulon/91192 Gif-sur-Yvette/France (5 aut.); Instituto de Física de São Carlos, Universidade de São Paulo/13560-970 São Carlos, SP/Brésil (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Applied physics. A, Materials science &#38; processing : (Print); ISSN 0947-8396; Allemagne; Da. 2009; Vol. 96; No. 4; Pp. 909-914; Bibl. 26 ref.</SO><LA>Anglais</LA><EA>In this paper, a detailed study of the capacitance spectra obtained from Au/doped-polyaniline/Al structures in the frequency domain (0.05 Hz-10 MHz), and at different temperatures (150-340 K) is carried out. The capacitance spectra behavior in semiconductors can be appropriately described by using abrupt cut-off models, since they assume that the electronic gap states that can follow the ac modulation have response times varying rapidly with a certain abscissa, which is dependent on both temperature and frequency. Two models based on the abrupt cutoff concept, formerly developed to describe inorganic semiconductor devices, have been used to analyze the capacitance spectra of devices based on doped polyaniline (PANI), which is a well-known polymeric semiconductor with in-numerous potential technological applications. The application of these models allowed the determination of significant parameters, such as Debye length (≃20 nm), position of bulk Fermi level (≃320 meV) and associated density of states (≃2 x 10<sup>18</sup> eV<sup>-1</sup> cm<sup>-3</sup>), width of the space charge region (≃70 nm), built-in potential (≃780 meV), and the gap states' distribution.</EA><CC>001B70G22J; 001B70C40S</CC><FD>Capacité électrique; Dopage; Caractéristique courant tension; Bande interdite; Longueur Debye; Niveau Fermi; Charge espace; Aluminium; Cut-off; Polymère conjugué; Aniline polymère; Semiconducteur organique; Polymère conducteur; Contact métal semiconducteur; Or; Métal transition</FD><ED>Capacitance; Doping; IV characteristic; Energy gap; Debye length; Fermi level; Space charge; Aluminium; Cut-off; Conjugated polymer; Polyanilines; Organic semiconductors; Conducting polymers; Metal-semiconductor contacts; Gold; Transition elements</ED><SD>Doping; Polímero conjugado</SD><LO>INIST-16194A.354000170843030160</LO><ID>09-0408740</ID></server></inist></record>
000D83	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Prognostic factors and outcomes for osteosarcoma: An international collaboration</title><author><name sortKey="Pakos, Emilios E" uniqKey="Pakos E">Emilios E. Pakos</name><affiliation><inist:fA14 i1="01"><s1>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine</s1><s2>Ioannina 45110</s2><s3>GRC</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>31 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nearchou, Andreas D" uniqKey="Nearchou A">Andreas D. Nearchou</name><affiliation><inist:fA14 i1="01"><s1>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine</s1><s2>Ioannina 45110</s2><s3>GRC</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>31 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Grimer, Robert J" uniqKey="Grimer R">Robert J. Grimer</name><affiliation><inist:fA14 i1="02"><s1>The Royal Orthopaedic Hospital, Bristol Road South</s1><s2>Northfield, Birmingham</s2><s3>GBR</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Koumoullis, Haris D" uniqKey="Koumoullis H">Haris D. Koumoullis</name><affiliation><inist:fA14 i1="01"><s1>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine</s1><s2>Ioannina 45110</s2><s3>GRC</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>31 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Abudu, Adesegun" uniqKey="Abudu A">Adesegun Abudu</name><affiliation><inist:fA14 i1="02"><s1>The Royal Orthopaedic Hospital, Bristol Road South</s1><s2>Northfield, Birmingham</s2><s3>GBR</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bramer, Jos A M" uniqKey="Bramer J">Jos A. M. Bramer</name><affiliation><inist:fA14 i1="02"><s1>The Royal Orthopaedic Hospital, Bristol Road South</s1><s2>Northfield, Birmingham</s2><s3>GBR</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jeys, Lee M" uniqKey="Jeys L">Lee M. Jeys</name><affiliation><inist:fA14 i1="02"><s1>The Royal Orthopaedic Hospital, Bristol Road South</s1><s2>Northfield, Birmingham</s2><s3>GBR</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Franchi, Alessandro" uniqKey="Franchi A">Alessandro Franchi</name><affiliation><inist:fA14 i1="03"><s1>Department of Human Pathology and Oncology, University of Florence</s1><s2>Florence</s2><s3>ITA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Scoccianti, Guido" uniqKey="Scoccianti G">Guido Scoccianti</name><affiliation><inist:fA14 i1="03"><s1>Department of Human Pathology and Oncology, University of Florence</s1><s2>Florence</s2><s3>ITA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Campanacci, Domenico" uniqKey="Campanacci D">Domenico Campanacci</name><affiliation><inist:fA14 i1="03"><s1>Department of Human Pathology and Oncology, University of Florence</s1><s2>Florence</s2><s3>ITA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Capanna, Rodolfo" uniqKey="Capanna R">Rodolfo Capanna</name><affiliation><inist:fA14 i1="03"><s1>Department of Human Pathology and Oncology, University of Florence</s1><s2>Florence</s2><s3>ITA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Aparicio, Jorge" uniqKey="Aparicio J">Jorge Aparicio</name><affiliation><inist:fA14 i1="04"><s1>Department of Medical Oncology, Hospital Universitario La Fe</s1><s2>Valencia</s2><s3>ESP</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Tabone, Marie Dominique" uniqKey="Tabone M">Marie-Dominique Tabone</name><affiliation><inist:fA14 i1="05"><s1>Seruice d' Hemato-Oncologie Pediatrique, Hopital d'enfants Armand Trousseau</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Holzer, Gerold" uniqKey="Holzer G">Gerold Holzer</name><affiliation><inist:fA14 i1="06"><s1>Department of Orthopaedics, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Abdolvahab, Fashid" uniqKey="Abdolvahab F">Fashid Abdolvahab</name><affiliation><inist:fA14 i1="06"><s1>Department of Orthopaedics, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Funovics, Philipp" uniqKey="Funovics P">Philipp Funovics</name><affiliation><inist:fA14 i1="06"><s1>Department of Orthopaedics, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dominkus, Martin" uniqKey="Dominkus M">Martin Dominkus</name><affiliation><inist:fA14 i1="06"><s1>Department of Orthopaedics, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>16 aut.</sZ><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ilhan, Inci" uniqKey="Ilhan I">Inci Ilhan</name><affiliation><inist:fA14 i1="07"><s1>Department of Pediatric Oncology, Ankara Oncology Hospital, Demetevler</s1><s2>Ankara</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="08"><s1>Department of Pediatric Hematology-Oncology, Marmara University Medical Center, Altunizade</s1><s2>Istanbul</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Berrak, Su G" uniqKey="Berrak S">Su G. Berrak</name><affiliation><inist:fA14 i1="07"><s1>Department of Pediatric Oncology, Ankara Oncology Hospital, Demetevler</s1><s2>Ankara</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="08"><s1>Department of Pediatric Hematology-Oncology, Marmara University Medical Center, Altunizade</s1><s2>Istanbul</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Patino Garcia, Ana" uniqKey="Patino Garcia A">Ana Patino-Garcia</name><affiliation><inist:fA14 i1="09"><s1>Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra</s1><s2>Pamplona</s2><s3>ESP</s3><sZ>20 aut.</sZ><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sierrasesumaga, Luis" uniqKey="Sierrasesumaga L">Luis Sierrasesumaga</name><affiliation><inist:fA14 i1="09"><s1>Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra</s1><s2>Pamplona</s2><s3>ESP</s3><sZ>20 aut.</sZ><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="San Julian, Mikel" uniqKey="San Julian M">Mikel San-Julian</name><affiliation><inist:fA14 i1="09"><s1>Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra</s1><s2>Pamplona</s2><s3>ESP</s3><sZ>20 aut.</sZ><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Garraus, Moira" uniqKey="Garraus M">Moira Garraus</name><affiliation><inist:fA14 i1="09"><s1>Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra</s1><s2>Pamplona</s2><s3>ESP</s3><sZ>20 aut.</sZ><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Sergio Petrilli, Antonio" uniqKey="Sergio Petrilli A">Antonio Sergio Petrilli</name><affiliation><inist:fA14 i1="10"><s1>Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP</s1><s2>Sao Paolo</s2><s3>BRA</s3><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Garcia, Reynaldo Jesus Filho" uniqKey="Garcia R">Reynaldo Jesus Filho Garcia</name><affiliation><inist:fA14 i1="10"><s1>Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP</s1><s2>Sao Paolo</s2><s3>BRA</s3><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Donato Macedo, Carla Renata Pacheco" uniqKey="Donato Macedo C">Carla Renata Pacheco Donato Macedo</name><affiliation><inist:fA14 i1="10"><s1>Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP</s1><s2>Sao Paolo</s2><s3>BRA</s3><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="De Seixas Alves, Maria Teresa" uniqKey="De Seixas Alves M">Maria Teresa De Seixas Alves</name><affiliation><inist:fA14 i1="10"><s1>Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP</s1><s2>Sao Paolo</s2><s3>BRA</s3><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Seiwerth, Sven" uniqKey="Seiwerth S">Sven Seiwerth</name><affiliation><inist:fA14 i1="11"><s1>Institute of Pathology Medical Faculty Zagreb</s1><s2>Zagreb</s2><s3>HRV</s3><sZ>28 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nagarajan, Rajaram" uniqKey="Nagarajan R">Rajaram Nagarajan</name><affiliation><inist:fA14 i1="12"><s1>Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center</s1><s2>Cincinnati, OH</s2><s3>USA</s3><sZ>29 aut.</sZ><sZ>30 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cripe, Timothy P" uniqKey="Cripe T">Timothy P. Cripe</name><affiliation><inist:fA14 i1="12"><s1>Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center</s1><s2>Cincinnati, OH</s2><s3>USA</s3><sZ>29 aut.</sZ><sZ>30 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Ioannidis, John P A" uniqKey="Ioannidis J">John P. A. Ioannidis</name><affiliation><inist:fA14 i1="01"><s1>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine</s1><s2>Ioannina 45110</s2><s3>GRC</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>31 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="13"><s1>Institute for Clinical Research and Health Policy Studies, Department of Medicine, Tufts Medical Center, Tufts University School of Medicine</s1><s2>Boston, MA</s2><s3>USA</s3><sZ>31 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0409008</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0409008 INIST</idno><idno type="RBID">Pascal:09-0409008</idno><idno type="wicri:Area/Main/Corpus">001B99</idno></publicationStmt><seriesStmt><idno type="ISSN">0959-8049</idno><title level="j" type="abbreviated">Eur. j. cancer : (1990)</title><title level="j" type="main">European journal of cancer : (1990)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bone</term><term>Cancerology</term><term>International</term><term>Metastasis</term><term>Osteosarcoma</term><term>Predictive factor</term><term>Prognosis</term><term>Sarcoma</term><term>Survival</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Ostéosarcome</term><term>Pronostic</term><term>International</term><term>Métastase</term><term>Facteur prédictif</term><term>Survie</term><term>Cancérologie</term><term>Os</term><term>Sarcome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We aimed to evaluate the prognostic significance of traditional clinical predictors in osteosarcoma through an international collaboration of 10 teams of investigators (2680 patients) who participated. In multivariate models the mortality risk increased with older age, presence of metastatic disease at diagnosis, development of local recurrence when the patient was first seen, use of amputation instead of limb salvage/wide resection, employment of unusual treatments, use of chemotherapeutic regimens other than anthracycline and platinum and use of methotrexate. It was also influenced by the site of the tumour. The risk of metastasis increased when metastatic disease was present at the time the patient was first seen and also increased with use of amputation or unusual treatment combinations or chemotherapy regimens not including anthracycline and platinum. Local recurrence risk was higher in older patients, in those who had local recurrence when first seen and when no anthracycline and platinum were used in chemotherapy. Results were similar when limited to patients seen after 1990 and treated with surgery plus combination chemotherapy. This large-scale international collaboration identifies strong predictors of major clinical outcomes in osteosarcoma.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0959-8049</s0></fA01><fA03 i2="1"><s0>Eur. j. cancer : (1990)</s0></fA03><fA05><s2>45</s2></fA05><fA06><s2>13</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Prognostic factors and outcomes for osteosarcoma: An international collaboration</s1></fA08><fA11 i1="01" i2="1"><s1>PAKOS (Emilios E.)</s1></fA11><fA11 i1="02" i2="1"><s1>NEARCHOU (Andreas D.)</s1></fA11><fA11 i1="03" i2="1"><s1>GRIMER (Robert J.)</s1></fA11><fA11 i1="04" i2="1"><s1>KOUMOULLIS (Haris D.)</s1></fA11><fA11 i1="05" i2="1"><s1>ABUDU (Adesegun)</s1></fA11><fA11 i1="06" i2="1"><s1>BRAMER (Jos A. M.)</s1></fA11><fA11 i1="07" i2="1"><s1>JEYS (Lee M.)</s1></fA11><fA11 i1="08" i2="1"><s1>FRANCHI (Alessandro)</s1></fA11><fA11 i1="09" i2="1"><s1>SCOCCIANTI (Guido)</s1></fA11><fA11 i1="10" i2="1"><s1>CAMPANACCI (Domenico)</s1></fA11><fA11 i1="11" i2="1"><s1>CAPANNA (Rodolfo)</s1></fA11><fA11 i1="12" i2="1"><s1>APARICIO (Jorge)</s1></fA11><fA11 i1="13" i2="1"><s1>TABONE (Marie-Dominique)</s1></fA11><fA11 i1="14" i2="1"><s1>HOLZER (Gerold)</s1></fA11><fA11 i1="15" i2="1"><s1>ABDOLVAHAB (Fashid)</s1></fA11><fA11 i1="16" i2="1"><s1>FUNOVICS (Philipp)</s1></fA11><fA11 i1="17" i2="1"><s1>DOMINKUS (Martin)</s1></fA11><fA11 i1="18" i2="1"><s1>ILHAN (Inci)</s1></fA11><fA11 i1="19" i2="1"><s1>BERRAK (Su G.)</s1></fA11><fA11 i1="20" i2="1"><s1>PATINO-GARCIA (Ana)</s1></fA11><fA11 i1="21" i2="1"><s1>SIERRASESUMAGA (Luis)</s1></fA11><fA11 i1="22" i2="1"><s1>SAN-JULIAN (Mikel)</s1></fA11><fA11 i1="23" i2="1"><s1>GARRAUS (Moira)</s1></fA11><fA11 i1="24" i2="1"><s1>SERGIO PETRILLI (Antonio)</s1></fA11><fA11 i1="25" i2="1"><s1>GARCIA (Reynaldo Jesus FILHO)</s1></fA11><fA11 i1="26" i2="1"><s1>DONATO MACEDO (Carla Renata Pacheco)</s1></fA11><fA11 i1="27" i2="1"><s1>DE SEIXAS ALVES (Maria Teresa)</s1></fA11><fA11 i1="28" i2="1"><s1>SEIWERTH (Sven)</s1></fA11><fA11 i1="29" i2="1"><s1>NAGARAJAN (Rajaram)</s1></fA11><fA11 i1="30" i2="1"><s1>CRIPE (Timothy P.)</s1></fA11><fA11 i1="31" i2="1"><s1>IOANNIDIS (John P. A.)</s1></fA11><fA14 i1="01"><s1>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine</s1><s2>Ioannina 45110</s2><s3>GRC</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>31 aut.</sZ></fA14><fA14 i1="02"><s1>The Royal Orthopaedic Hospital, Bristol Road South</s1><s2>Northfield, Birmingham</s2><s3>GBR</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="03"><s1>Department of Human Pathology and Oncology, University of Florence</s1><s2>Florence</s2><s3>ITA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>10 aut.</sZ><sZ>11 aut.</sZ></fA14><fA14 i1="04"><s1>Department of Medical Oncology, Hospital Universitario La Fe</s1><s2>Valencia</s2><s3>ESP</s3><sZ>12 aut.</sZ></fA14><fA14 i1="05"><s1>Seruice d' Hemato-Oncologie Pediatrique, Hopital d'enfants Armand Trousseau</s1><s2>Paris</s2><s3>FRA</s3><sZ>13 aut.</sZ></fA14><fA14 i1="06"><s1>Department of Orthopaedics, Medical University of Vienna</s1><s2>Vienna</s2><s3>AUT</s3><sZ>14 aut.</sZ><sZ>15 aut.</sZ><sZ>16 aut.</sZ><sZ>17 aut.</sZ></fA14><fA14 i1="07"><s1>Department of Pediatric Oncology, Ankara Oncology Hospital, Demetevler</s1><s2>Ankara</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></fA14><fA14 i1="08"><s1>Department of Pediatric Hematology-Oncology, Marmara University Medical Center, Altunizade</s1><s2>Istanbul</s2><s3>TUR</s3><sZ>18 aut.</sZ><sZ>19 aut.</sZ></fA14><fA14 i1="09"><s1>Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra</s1><s2>Pamplona</s2><s3>ESP</s3><sZ>20 aut.</sZ><sZ>21 aut.</sZ><sZ>22 aut.</sZ><sZ>23 aut.</sZ></fA14><fA14 i1="10"><s1>Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP</s1><s2>Sao Paolo</s2><s3>BRA</s3><sZ>24 aut.</sZ><sZ>25 aut.</sZ><sZ>26 aut.</sZ><sZ>27 aut.</sZ></fA14><fA14 i1="11"><s1>Institute of Pathology Medical Faculty Zagreb</s1><s2>Zagreb</s2><s3>HRV</s3><sZ>28 aut.</sZ></fA14><fA14 i1="12"><s1>Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center</s1><s2>Cincinnati, OH</s2><s3>USA</s3><sZ>29 aut.</sZ><sZ>30 aut.</sZ></fA14><fA14 i1="13"><s1>Institute for Clinical Research and Health Policy Studies, Department of Medicine, Tufts Medical Center, Tufts University School of Medicine</s1><s2>Boston, MA</s2><s3>USA</s3><sZ>31 aut.</sZ></fA14><fA20><s1>2367-2375</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>12648</s2><s5>354000188110430190</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>30 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0409008</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European journal of cancer : (1990)</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>We aimed to evaluate the prognostic significance of traditional clinical predictors in osteosarcoma through an international collaboration of 10 teams of investigators (2680 patients) who participated. In multivariate models the mortality risk increased with older age, presence of metastatic disease at diagnosis, development of local recurrence when the patient was first seen, use of amputation instead of limb salvage/wide resection, employment of unusual treatments, use of chemotherapeutic regimens other than anthracycline and platinum and use of methotrexate. It was also influenced by the site of the tumour. The risk of metastasis increased when metastatic disease was present at the time the patient was first seen and also increased with use of amputation or unusual treatment combinations or chemotherapy regimens not including anthracycline and platinum. Local recurrence risk was higher in older patients, in those who had local recurrence when first seen and when no anthracycline and platinum were used in chemotherapy. Results were similar when limited to patients seen after 1990 and treated with surgery plus combination chemotherapy. This large-scale international collaboration identifies strong predictors of major clinical outcomes in osteosarcoma.</s0></fC01><fC02 i1="01" i2="X"><s0>002B02</s0></fC02><fC02 i1="02" i2="X"><s0>002B04</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Ostéosarcome</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Osteosarcoma</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Osteosarcoma</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Pronostic</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Prognosis</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Pronóstico</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>International</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>International</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Internacional</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Métastase</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Metastasis</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Metástasis</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Facteur prédictif</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Predictive factor</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Factor predictivo</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Survie</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Survival</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Sobrevivencia</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Cancérologie</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Cancerology</s0><s5>08</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Cancerología</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Os</s0><s5>25</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Bone</s0><s5>25</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Hueso</s0><s5>25</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Sarcome</s0><s5>26</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Sarcoma</s0><s5>26</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Sarcoma</s0><s5>26</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie du système ostéoarticulaire</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Diseases of the osteoarticular system</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Sistema osteoarticular patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Tumeur maligne</s0><s2>NM</s2><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Malignant tumor</s0><s2>NM</s2><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Tumor maligno</s0><s2>NM</s2><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Système ostéoarticulaire</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Osteoarticular system</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Sistema osteoarticular</s0><s5>39</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0409008 INIST</NO><ET>Prognostic factors and outcomes for osteosarcoma: An international collaboration</ET><AU>PAKOS (Emilios E.); NEARCHOU (Andreas D.); GRIMER (Robert J.); KOUMOULLIS (Haris D.); ABUDU (Adesegun); BRAMER (Jos A. M.); JEYS (Lee M.); FRANCHI (Alessandro); SCOCCIANTI (Guido); CAMPANACCI (Domenico); CAPANNA (Rodolfo); APARICIO (Jorge); TABONE (Marie-Dominique); HOLZER (Gerold); ABDOLVAHAB (Fashid); FUNOVICS (Philipp); DOMINKUS (Martin); ILHAN (Inci); BERRAK (Su G.); PATINO-GARCIA (Ana); SIERRASESUMAGA (Luis); SAN-JULIAN (Mikel); GARRAUS (Moira); SERGIO PETRILLI (Antonio); GARCIA (Reynaldo Jesus FILHO); DONATO MACEDO (Carla Renata Pacheco); DE SEIXAS ALVES (Maria Teresa); SEIWERTH (Sven); NAGARAJAN (Rajaram); CRIPE (Timothy P.); IOANNIDIS (John P. A.)</AU><AF>Clinical and Molecular Epidemiology Unit, Department of Hygiene and Epidemiology, University of Ioannina School of Medicine/Ioannina 45110/Grèce (1 aut., 2 aut., 4 aut., 31 aut.); The Royal Orthopaedic Hospital, Bristol Road South/Northfield, Birmingham/Royaume-Uni (3 aut., 5 aut., 6 aut., 7 aut.); Department of Human Pathology and Oncology, University of Florence/Florence/Italie (8 aut., 9 aut., 10 aut., 11 aut.); Department of Medical Oncology, Hospital Universitario La Fe/Valencia/Espagne (12 aut.); Seruice d' Hemato-Oncologie Pediatrique, Hopital d'enfants Armand Trousseau/Paris/France (13 aut.); Department of Orthopaedics, Medical University of Vienna/Vienna/Autriche (14 aut., 15 aut., 16 aut., 17 aut.); Department of Pediatric Oncology, Ankara Oncology Hospital, Demetevler/Ankara/Turquie (18 aut., 19 aut.); Department of Pediatric Hematology-Oncology, Marmara University Medical Center, Altunizade/Istanbul/Turquie (18 aut., 19 aut.); Departments of Pediatrics and Orthopedics, University of Navarra and University Clinic of Navarra/Pamplona/Espagne (20 aut., 21 aut., 22 aut., 23 aut.); Pediatric Oncology Section, Instituto de Oncologia Pediαtrica, GRAACC/UNIFESP/Sao Paolo/Brésil (24 aut., 25 aut., 26 aut., 27 aut.); Institute of Pathology Medical Faculty Zagreb/Zagreb/Croatie (28 aut.); Pediatric Hematology/Oncology, Cincinnati Children's Hospital Medical Center/Cincinnati, OH/Etats-Unis (29 aut., 30 aut.); Institute for Clinical Research and Health Policy Studies, Department of Medicine, Tufts Medical Center, Tufts University School of Medicine/Boston, MA/Etats-Unis (31 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>European journal of cancer : (1990); ISSN 0959-8049; Royaume-Uni; Da. 2009; Vol. 45; No. 13; Pp. 2367-2375; Bibl. 30 ref.</SO><LA>Anglais</LA><EA>We aimed to evaluate the prognostic significance of traditional clinical predictors in osteosarcoma through an international collaboration of 10 teams of investigators (2680 patients) who participated. In multivariate models the mortality risk increased with older age, presence of metastatic disease at diagnosis, development of local recurrence when the patient was first seen, use of amputation instead of limb salvage/wide resection, employment of unusual treatments, use of chemotherapeutic regimens other than anthracycline and platinum and use of methotrexate. It was also influenced by the site of the tumour. The risk of metastasis increased when metastatic disease was present at the time the patient was first seen and also increased with use of amputation or unusual treatment combinations or chemotherapy regimens not including anthracycline and platinum. Local recurrence risk was higher in older patients, in those who had local recurrence when first seen and when no anthracycline and platinum were used in chemotherapy. Results were similar when limited to patients seen after 1990 and treated with surgery plus combination chemotherapy. This large-scale international collaboration identifies strong predictors of major clinical outcomes in osteosarcoma.</EA><CC>002B02; 002B04</CC><FD>Ostéosarcome; Pronostic; International; Métastase; Facteur prédictif; Survie; Cancérologie; Os; Sarcome</FD><FG>Pathologie du système ostéoarticulaire; Tumeur maligne; Cancer; Système ostéoarticulaire</FG><ED>Osteosarcoma; Prognosis; International; Metastasis; Predictive factor; Survival; Cancerology; Bone; Sarcoma</ED><EG>Diseases of the osteoarticular system; Malignant tumor; Cancer; Osteoarticular system</EG><SD>Osteosarcoma; Pronóstico; Internacional; Metástasis; Factor predictivo; Sobrevivencia; Cancerología; Hueso; Sarcoma</SD><LO>INIST-12648.354000188110430190</LO><ID>09-0409008</ID></server></inist></record>
000D84	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">GIORDANO BRUNO ON SCEPTICISM</title><author><name sortKey="Dagron, Tristan" uniqKey="Dagron T">Tristan Dagron</name><affiliation><inist:fA14 i1="01"><s1>CNRS/CERPHI, Ecole Normale Supérieure Lettres et Sciences Humaines</s1><s2>Lyon</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0411975</idno><date when="2009">2009</date><idno type="stanalyst">FRANCIS 09-0411975 INIST</idno><idno type="RBID">Francis:09-0411975</idno><idno type="wicri:Area/Main/Corpus">001F89</idno></publicationStmt><seriesStmt><idno type="ISSN">0066-6610</idno><title level="j" type="abbreviated">Arch. int. hist. idées</title><title level="j" type="main">Archives internationales d'histoire des idées</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bruno (G.)</term><term>Renaissance</term><term>Scepticism</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Scepticisme</term><term>Bruno (G.)</term><term>Renaissance</term></keywords></textClass></profileDesc></teiHeader></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0066-6610</s0></fA01><fA03 i2="1"><s0>Arch. int. hist. idées</s0></fA03><fA05><s2>199</s2></fA05><fA08 i1="01" i2="1" l="ENG"><s1>GIORDANO BRUNO ON SCEPTICISM</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Renaissance Scepticisms</s1></fA09><fA11 i1="01" i2="1"><s1>DAGRON (Tristan)</s1></fA11><fA12 i1="01" i2="1"><s1>PAGANINI (Gianni)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>MAIA (José R. Neto)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>CNRS/CERPHI, Ecole Normale Supérieure Lettres et Sciences Humaines</s1><s2>Lyon</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA15 i1="01"><s1>Università degli Studi del Piemonte Orientale</s1><s2>Vercelli</s2><s3>ITA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Universidade Federal de Minas Gerais</s1><s2>Belo Horizonte</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>231-248</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>25123</s2><s5>354000184518160100</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA47 i1="01" i2="1"><s0>09-0411975</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Archives internationales d'histoire des idées</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fA68 i1="01" i2="1" l="FRE"><s1>Le scepticisme selon Giordano Bruno</s1></fA68><fA69 i1="01" i2="1" l="FRE"><s1>Les scepticismes de la Renaissance</s1></fA69><fA99><s0>ref. et notes dissem.</s0></fA99><fC02 i1="01" i2="T"><s0>52241</s0><s1>I</s1></fC02><fC02 i1="02" i2="T"><s0>522</s0></fC02><fC03 i1="01" i2="T" l="FRE"><s0>Scepticisme</s0><s5>01</s5></fC03><fC03 i1="01" i2="T" l="ENG"><s0>Scepticism</s0><s5>01</s5></fC03><fC03 i1="01" i2="T" l="SPA"><s0>Escepticismo</s0><s5>01</s5></fC03><fC03 i1="02" i2="T" l="FRE"><s0>Bruno (G.)</s0><s2>NF</s2><s5>02</s5></fC03><fC03 i1="02" i2="T" l="ENG"><s0>Bruno (G.)</s0><s2>NF</s2><s5>02</s5></fC03><fC03 i1="02" i2="T" l="SPA"><s0>Bruno (G.)</s0><s2>NF</s2><s5>02</s5></fC03><fC03 i1="03" i2="T" l="FRE"><s0>Renaissance</s0><s5>03</s5></fC03><fC03 i1="03" i2="T" l="ENG"><s0>Renaissance</s0><s5>03</s5></fC03><fC03 i1="03" i2="T" l="SPA"><s0>Renacimiento</s0><s5>03</s5></fC03><fN21><s1>299</s1></fN21></pA></standard><server><NO>FRANCIS 09-0411975 INIST</NO><FT>(Le scepticisme selon Giordano Bruno)</FT><ET>GIORDANO BRUNO ON SCEPTICISM</ET><AU>DAGRON (Tristan); PAGANINI (Gianni); MAIA (José R. Neto)</AU><AF>CNRS/CERPHI, Ecole Normale Supérieure Lettres et Sciences Humaines/Lyon/France (1 aut.); Università degli Studi del Piemonte Orientale/Vercelli/Italie (1 aut.); Universidade Federal de Minas Gerais/Belo Horizonte/Brésil (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Archives internationales d'histoire des idées; ISSN 0066-6610; Pays-Bas; Da. 2009; Vol. 199; Pp. 231-248</SO><LA>Anglais</LA><CC>52241; 522</CC><FD>Scepticisme; Bruno (G.); Renaissance</FD><ED>Scepticism; Bruno (G.); Renaissance</ED><SD>Escepticismo; Bruno (G.); Renacimiento</SD><LO>INIST-25123.354000184518160100</LO><ID>09-0411975</ID></server></inist></record>
000D85	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Spirometry Centile Charts for Young Caucasian Children The Asthma UK Collaborative Initiative</title><author><name sortKey="Stanojevic, Sanja" uniqKey="Stanojevic S">Sanja Stanojevic</name><affiliation><inist:fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Medical Research Council, Center of Epidemiology for Child Health, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Wade, Angie" uniqKey="Wade A">Angie Wade</name><affiliation><inist:fA14 i1="02"><s1>Medical Research Council, Center of Epidemiology for Child Health, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cole, Tim J" uniqKey="Cole T">Tim J. Cole</name><affiliation><inist:fA14 i1="02"><s1>Medical Research Council, Center of Epidemiology for Child Health, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lum, Sooky" uniqKey="Lum S">Sooky Lum</name><affiliation><inist:fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Custovic, Adnan" uniqKey="Custovic A">Adnan Custovic</name><affiliation><inist:fA14 i1="03"><s1>University of Manchester and National Institute of Health Research Translational Research Facility in Respiratory Medicine, University Hospital of South Manchester</s1><s2>Manchester</s2><s3>GBR</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Silverman, Mike" uniqKey="Silverman M">Mike Silverman</name><affiliation><inist:fA14 i1="04"><s1>Child Health, Institute for Lung Health, University of Leicester</s1><s2>Leicester</s2><s3>GBR</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hall, Graham L" uniqKey="Hall G">Graham L. Hall</name><affiliation><inist:fA14 i1="05"><s1>Respiratory Medicine, Princess Margaret Hospital and School of Paediatric and Child Health, University of Western Australia</s1><s2>Perth</s2><s3>AUS</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Welsh, Liam" uniqKey="Welsh L">Liam Welsh</name><affiliation><inist:fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Kirkby, Jane" uniqKey="Kirkby J">Jane Kirkby</name><affiliation><inist:fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nystad, Wenche" uniqKey="Nystad W">Wenche Nystad</name><affiliation><inist:fA14 i1="06"><s1>Division of Epidemiology, Norwegian Institute of Public Health</s1><s2>Oslo</s2><s3>NOR</s3><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Badier, Monique" uniqKey="Badier M">Monique Badier</name><affiliation><inist:fA14 i1="07"><s1>Lung Function Laboratory, Hôpital Sainte Marguerite</s1><s2>Marseille</s2><s3>FRA</s3><sZ>11 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Davis, Stephanie" uniqKey="Davis S">Stephanie Davis</name><affiliation><inist:fA14 i1="08"><s1>Department of Pediatrics, North Carolina Children's Hospital, University of North Carolina at Chapel Hill</s1><s2>Chapel Hill, North Carolina</s2><s3>USA</s3><sZ>12 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Turner, Steven" uniqKey="Turner S">Steven Turner</name><affiliation><inist:fA14 i1="09"><s1>Academic Child Health, University of Aberdeen</s1><s2>Aberdeen</s2><s3>GBR</s3><sZ>13 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Piccioni, Pavilio" uniqKey="Piccioni P">Pavilio Piccioni</name><affiliation><inist:fA14 i1="10"><s1>Pneumology, National Health Service</s1><s2>Turin</s2><s3>ITA</s3><sZ>14 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vilozni, Daphna" uniqKey="Vilozni D">Daphna Vilozni</name><affiliation><inist:fA14 i1="11"><s1>Edmond and Lili Safra Children's Hospital, Sheba Medical Center</s1><s2>Tel Aviv</s2><s3>ISR</s3><sZ>15 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Eigen, Howard" uniqKey="Eigen H">Howard Eigen</name><affiliation><inist:fA14 i1="12"><s1>Section of Pediatric Pulmonology, Riley Hospital for Children</s1><s2>Indianapolis, Indiana</s2><s3>USA</s3><sZ>16 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vlachos Mayer, Helen" uniqKey="Vlachos Mayer H">Helen Vlachos-Mayer</name><affiliation><inist:fA14 i1="13"><s1>Division of Respiratory Medicine, Department of Pediatrics, Center Hospitalier Universitaire de Sherbrooke-Hôpital Fleurimont, University of Sherbrooke</s1><s2>Sherbrooke</s2><s3>CAN</s3><sZ>17 aut.</sZ></inist:fA14></affiliation></author><author><name>JINPING ZHENG</name><affiliation><inist:fA14 i1="14"><s1>State Key Laboratory of Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University</s1><s2>Guangzhou</s2><s3>CHN</s3><sZ>18 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Tomalak, Waldemar" uniqKey="Tomalak W">Waldemar Tomalak</name><affiliation><inist:fA14 i1="15"><s1>Department of Physiopathology of the Respiratory System, Institute for Tuberculosis and Lung Diseases, Rabka Branch</s1><s2>Rabka</s2><s3>POL</s3><sZ>19 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Jones, Marcus" uniqKey="Jones M">Marcus Jones</name><affiliation><inist:fA14 i1="16"><s1>Division of Pediatric Pulmonary, Hospital São Lucas Pontifícia Universidade Católica do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>20 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hankinson, John L" uniqKey="Hankinson J">John L. Hankinson</name><affiliation><inist:fA14 i1="17"><s1>Hankinson Consulting, Inc.</s1><s2>Valdosta, Georgia</s2><s3>USA</s3><sZ>21 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Stocks, Janet" uniqKey="Stocks J">Janet Stocks</name><affiliation><inist:fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0412310</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0412310 INIST</idno><idno type="RBID">Pascal:09-0412310</idno><idno type="wicri:Area/Main/Corpus">001B98</idno></publicationStmt><seriesStmt><idno type="ISSN">1073-449X</idno><title level="j" type="abbreviated">Am. j. respir. crit. care med.</title><title level="j" type="main">American journal of respiratory and critical care medicine</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Asthma</term><term>Child</term><term>Intensive care</term><term>Resuscitation</term><term>Spirometry</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Asthme</term><term>Spirométrie</term><term>Enfant</term><term>Réanimation</term><term>Soin intensif</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Rationale: Advances in spirometry measurement techniques have made it possible to obtain measurements in children as young as 3 years of age; however, in practice, application remains limited by the lack of appropriate reference data for young children, which are often based on limited population-specific samples. Objectives: We aimed to build on previous models by collating existing reference data in young children (aged 3-7 yr), to produce updated prediction equations that span the preschool years and that are also linked to established reference equations for older children and adults. Methods: The Asthma UK Collaborative Initiative was established to collate lung function data from healthy young children aged 3 to 7 years. Collaborators included researchers with access to pulmonary function test data in healthy preschool children. Spirometry centiles were created using the LMS (λ, μ, σ) method and extend previously published equations down to 3 years of age. Measurements and Main Results The Asthma UK centile charts for spirometry are based on the largest sample of healthy young Caucasian children aged 3-7 years (n = 3,777) from 15 centers across 11 countries and provide a continuous reference with a smooth transition into adolescence and adulthood. These equations improve existing pediatric equations by considering the between-subject variability to define a more appropriate age-dependent lower limit of normal. The collated data set reflects a variety of equipment, measurement protocols, and population characteristics and may be generalizable across different populations. Conclusions: We present prediction equations for spirometry for preschool children and provide a foundation that will facilitate continued updating.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1073-449X</s0></fA01><fA03 i2="1"><s0>Am. j. respir. crit. care med.</s0></fA03><fA05><s2>180</s2></fA05><fA06><s2>6</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Spirometry Centile Charts for Young Caucasian Children The Asthma UK Collaborative Initiative</s1></fA08><fA11 i1="01" i2="1"><s1>STANOJEVIC (Sanja)</s1></fA11><fA11 i1="02" i2="1"><s1>WADE (Angie)</s1></fA11><fA11 i1="03" i2="1"><s1>COLE (Tim J.)</s1></fA11><fA11 i1="04" i2="1"><s1>LUM (Sooky)</s1></fA11><fA11 i1="05" i2="1"><s1>CUSTOVIC (Adnan)</s1></fA11><fA11 i1="06" i2="1"><s1>SILVERMAN (Mike)</s1></fA11><fA11 i1="07" i2="1"><s1>HALL (Graham L.)</s1></fA11><fA11 i1="08" i2="1"><s1>WELSH (Liam)</s1></fA11><fA11 i1="09" i2="1"><s1>KIRKBY (Jane)</s1></fA11><fA11 i1="10" i2="1"><s1>NYSTAD (Wenche)</s1></fA11><fA11 i1="11" i2="1"><s1>BADIER (Monique)</s1></fA11><fA11 i1="12" i2="1"><s1>DAVIS (Stephanie)</s1></fA11><fA11 i1="13" i2="1"><s1>TURNER (Steven)</s1></fA11><fA11 i1="14" i2="1"><s1>PICCIONI (Pavilio)</s1></fA11><fA11 i1="15" i2="1"><s1>VILOZNI (Daphna)</s1></fA11><fA11 i1="16" i2="1"><s1>EIGEN (Howard)</s1></fA11><fA11 i1="17" i2="1"><s1>VLACHOS-MAYER (Helen)</s1></fA11><fA11 i1="18" i2="1"><s1>JINPING ZHENG</s1></fA11><fA11 i1="19" i2="1"><s1>TOMALAK (Waldemar)</s1></fA11><fA11 i1="20" i2="1"><s1>JONES (Marcus)</s1></fA11><fA11 i1="21" i2="1"><s1>HANKINSON (John L.)</s1></fA11><fA11 i1="22" i2="1"><s1>STOCKS (Janet)</s1></fA11><fA14 i1="01"><s1>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>4 aut.</sZ><sZ>8 aut.</sZ><sZ>9 aut.</sZ><sZ>22 aut.</sZ></fA14><fA14 i1="02"><s1>Medical Research Council, Center of Epidemiology for Child Health, Institute of Child Health, University College London</s1><s2>London</s2><s3>GBR</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>University of Manchester and National Institute of Health Research Translational Research Facility in Respiratory Medicine, University Hospital of South Manchester</s1><s2>Manchester</s2><s3>GBR</s3><sZ>5 aut.</sZ></fA14><fA14 i1="04"><s1>Child Health, Institute for Lung Health, University of Leicester</s1><s2>Leicester</s2><s3>GBR</s3><sZ>6 aut.</sZ></fA14><fA14 i1="05"><s1>Respiratory Medicine, Princess Margaret Hospital and School of Paediatric and Child Health, University of Western Australia</s1><s2>Perth</s2><s3>AUS</s3><sZ>7 aut.</sZ></fA14><fA14 i1="06"><s1>Division of Epidemiology, Norwegian Institute of Public Health</s1><s2>Oslo</s2><s3>NOR</s3><sZ>10 aut.</sZ></fA14><fA14 i1="07"><s1>Lung Function Laboratory, Hôpital Sainte Marguerite</s1><s2>Marseille</s2><s3>FRA</s3><sZ>11 aut.</sZ></fA14><fA14 i1="08"><s1>Department of Pediatrics, North Carolina Children's Hospital, University of North Carolina at Chapel Hill</s1><s2>Chapel Hill, North Carolina</s2><s3>USA</s3><sZ>12 aut.</sZ></fA14><fA14 i1="09"><s1>Academic Child Health, University of Aberdeen</s1><s2>Aberdeen</s2><s3>GBR</s3><sZ>13 aut.</sZ></fA14><fA14 i1="10"><s1>Pneumology, National Health Service</s1><s2>Turin</s2><s3>ITA</s3><sZ>14 aut.</sZ></fA14><fA14 i1="11"><s1>Edmond and Lili Safra Children's Hospital, Sheba Medical Center</s1><s2>Tel Aviv</s2><s3>ISR</s3><sZ>15 aut.</sZ></fA14><fA14 i1="12"><s1>Section of Pediatric Pulmonology, Riley Hospital for Children</s1><s2>Indianapolis, Indiana</s2><s3>USA</s3><sZ>16 aut.</sZ></fA14><fA14 i1="13"><s1>Division of Respiratory Medicine, Department of Pediatrics, Center Hospitalier Universitaire de Sherbrooke-Hôpital Fleurimont, University of Sherbrooke</s1><s2>Sherbrooke</s2><s3>CAN</s3><sZ>17 aut.</sZ></fA14><fA14 i1="14"><s1>State Key Laboratory of Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University</s1><s2>Guangzhou</s2><s3>CHN</s3><sZ>18 aut.</sZ></fA14><fA14 i1="15"><s1>Department of Physiopathology of the Respiratory System, Institute for Tuberculosis and Lung Diseases, Rabka Branch</s1><s2>Rabka</s2><s3>POL</s3><sZ>19 aut.</sZ></fA14><fA14 i1="16"><s1>Division of Pediatric Pulmonary, Hospital São Lucas Pontifícia Universidade Católica do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>20 aut.</sZ></fA14><fA14 i1="17"><s1>Hankinson Consulting, Inc.</s1><s2>Valdosta, Georgia</s2><s3>USA</s3><sZ>21 aut.</sZ></fA14><fA17 i1="01" i2="1"><s1>Asthma UK Spirometry Collaborative Group</s1><s3>GBR</s3></fA17><fA20><s1>547-552</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2013</s2><s5>354000170224020100</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>21 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0412310</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>American journal of respiratory and critical care medicine</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Rationale: Advances in spirometry measurement techniques have made it possible to obtain measurements in children as young as 3 years of age; however, in practice, application remains limited by the lack of appropriate reference data for young children, which are often based on limited population-specific samples. Objectives: We aimed to build on previous models by collating existing reference data in young children (aged 3-7 yr), to produce updated prediction equations that span the preschool years and that are also linked to established reference equations for older children and adults. Methods: The Asthma UK Collaborative Initiative was established to collate lung function data from healthy young children aged 3 to 7 years. Collaborators included researchers with access to pulmonary function test data in healthy preschool children. Spirometry centiles were created using the LMS (λ, μ, σ) method and extend previously published equations down to 3 years of age. Measurements and Main Results The Asthma UK centile charts for spirometry are based on the largest sample of healthy young Caucasian children aged 3-7 years (n = 3,777) from 15 centers across 11 countries and provide a continuous reference with a smooth transition into adolescence and adulthood. These equations improve existing pediatric equations by considering the between-subject variability to define a more appropriate age-dependent lower limit of normal. The collated data set reflects a variety of equipment, measurement protocols, and population characteristics and may be generalizable across different populations. Conclusions: We present prediction equations for spirometry for preschool children and provide a foundation that will facilitate continued updating.</s0></fC01><fC02 i1="01" i2="X"><s0>002B27B</s0></fC02><fC02 i1="02" i2="X"><s0>002B24H</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Asthme</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Asthma</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Asma</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Spirométrie</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Spirometry</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Espirometría</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Enfant</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Child</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Niño</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Réanimation</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Resuscitation</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Reanimación</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Soin intensif</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Intensive care</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Cuidado intensivo</s0><s5>12</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Homme</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Human</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Hombre</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>37</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Bronchopneumopathie obstructive</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Obstructive pulmonary disease</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Enfermedad pulmonar obstructiva</s0><s5>38</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Pathologie des bronches</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Bronchus disease</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Bronquio patología</s0><s5>39</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Pathologie des poumons</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Lung disease</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Pulmón patología</s0><s5>40</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0412310 INIST</NO><ET>Spirometry Centile Charts for Young Caucasian Children The Asthma UK Collaborative Initiative</ET><AU>STANOJEVIC (Sanja); WADE (Angie); COLE (Tim J.); LUM (Sooky); CUSTOVIC (Adnan); SILVERMAN (Mike); HALL (Graham L.); WELSH (Liam); KIRKBY (Jane); NYSTAD (Wenche); BADIER (Monique); DAVIS (Stephanie); TURNER (Steven); PICCIONI (Pavilio); VILOZNI (Daphna); EIGEN (Howard); VLACHOS-MAYER (Helen); JINPING ZHENG; TOMALAK (Waldemar); JONES (Marcus); HANKINSON (John L.); STOCKS (Janet)</AU><AF>Portex Unit, Respiratory Physiology and Medicine, Institute of Child Health, University College London/London/Royaume-Uni (1 aut., 4 aut., 8 aut., 9 aut., 22 aut.); Medical Research Council, Center of Epidemiology for Child Health, Institute of Child Health, University College London/London/Royaume-Uni (1 aut., 2 aut., 3 aut.); University of Manchester and National Institute of Health Research Translational Research Facility in Respiratory Medicine, University Hospital of South Manchester/Manchester/Royaume-Uni (5 aut.); Child Health, Institute for Lung Health, University of Leicester/Leicester/Royaume-Uni (6 aut.); Respiratory Medicine, Princess Margaret Hospital and School of Paediatric and Child Health, University of Western Australia/Perth/Australie (7 aut.); Division of Epidemiology, Norwegian Institute of Public Health/Oslo/Norvège (10 aut.); Lung Function Laboratory, Hôpital Sainte Marguerite/Marseille/France (11 aut.); Department of Pediatrics, North Carolina Children's Hospital, University of North Carolina at Chapel Hill/Chapel Hill, North Carolina/Etats-Unis (12 aut.); Academic Child Health, University of Aberdeen/Aberdeen/Royaume-Uni (13 aut.); Pneumology, National Health Service/Turin/Italie (14 aut.); Edmond and Lili Safra Children's Hospital, Sheba Medical Center/Tel Aviv/Israël (15 aut.); Section of Pediatric Pulmonology, Riley Hospital for Children/Indianapolis, Indiana/Etats-Unis (16 aut.); Division of Respiratory Medicine, Department of Pediatrics, Center Hospitalier Universitaire de Sherbrooke-Hôpital Fleurimont, University of Sherbrooke/Sherbrooke/Canada (17 aut.); State Key Laboratory of Respiratory Disease, First Affiliated Hospital of Guangzhou Medical University/Guangzhou/Chine (18 aut.); Department of Physiopathology of the Respiratory System, Institute for Tuberculosis and Lung Diseases, Rabka Branch/Rabka/Pologne (19 aut.); Division of Pediatric Pulmonary, Hospital São Lucas Pontifícia Universidade Católica do Rio Grande do Sul/Porto Alegre/Brésil (20 aut.); Hankinson Consulting, Inc./Valdosta, Georgia/Etats-Unis (21 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>American journal of respiratory and critical care medicine; ISSN 1073-449X; Etats-Unis; Da. 2009; Vol. 180; No. 6; Pp. 547-552; Bibl. 21 ref.</SO><LA>Anglais</LA><EA>Rationale: Advances in spirometry measurement techniques have made it possible to obtain measurements in children as young as 3 years of age; however, in practice, application remains limited by the lack of appropriate reference data for young children, which are often based on limited population-specific samples. Objectives: We aimed to build on previous models by collating existing reference data in young children (aged 3-7 yr), to produce updated prediction equations that span the preschool years and that are also linked to established reference equations for older children and adults. Methods: The Asthma UK Collaborative Initiative was established to collate lung function data from healthy young children aged 3 to 7 years. Collaborators included researchers with access to pulmonary function test data in healthy preschool children. Spirometry centiles were created using the LMS (λ, μ, σ) method and extend previously published equations down to 3 years of age. Measurements and Main Results The Asthma UK centile charts for spirometry are based on the largest sample of healthy young Caucasian children aged 3-7 years (n = 3,777) from 15 centers across 11 countries and provide a continuous reference with a smooth transition into adolescence and adulthood. These equations improve existing pediatric equations by considering the between-subject variability to define a more appropriate age-dependent lower limit of normal. The collated data set reflects a variety of equipment, measurement protocols, and population characteristics and may be generalizable across different populations. Conclusions: We present prediction equations for spirometry for preschool children and provide a foundation that will facilitate continued updating.</EA><CC>002B27B; 002B24H</CC><FD>Asthme; Spirométrie; Enfant; Réanimation; Soin intensif</FD><FG>Homme; Pathologie de l'appareil respiratoire; Bronchopneumopathie obstructive; Pathologie des bronches; Pathologie des poumons</FG><ED>Asthma; Spirometry; Child; Resuscitation; Intensive care</ED><EG>Human; Respiratory disease; Obstructive pulmonary disease; Bronchus disease; Lung disease</EG><SD>Asma; Espirometría; Niño; Reanimación; Cuidado intensivo</SD><LO>INIST-2013.354000170224020100</LO><ID>09-0412310</ID></server></inist></record>
000D86	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Land use, tillage, texture and organic matter stock and composition in tropical and subtropical Brazilian soils</title><author><name sortKey="Dieckow, J" uniqKey="Dieckow J">J. Dieckow</name><affiliation><inist:fA14 i1="01"><s1>Departamento de Solos e Engenharia Agrícola, Universidade Federal do Paraná</s1><s2>Curitiba</s2><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bayer, C" uniqKey="Bayer C">C. Bayer</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Solos, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Conceicao, P C" uniqKey="Conceicao P">P. C. Conceicao</name><affiliation><inist:fA14 i1="03"><s1>Unidade Dois Vizinhos, Universidade Tecnológica Federal do Paraná</s1><s2>Dois Vizinhos</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Zanatta, J A" uniqKey="Zanatta J">J. A. Zanatta</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Solos, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Martin Neto, L" uniqKey="Martin Neto L">L. Martin-Neto</name><affiliation><inist:fA14 i1="04"><s1>Embrapa Instrumentação Agropecudria</s1><s2>Sdo Carlos</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Milori, D B M" uniqKey="Milori D">D. B. M. Milori</name><affiliation><inist:fA14 i1="04"><s1>Embrapa Instrumentação Agropecudria</s1><s2>Sdo Carlos</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Salton, J C" uniqKey="Salton J">J. C. Salton</name><affiliation><inist:fA14 i1="05"><s1>Embrapa Agropecuária Oeste</s1><s2>Dourados</s2><s3>BRA</s3><sZ>7 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Macedo, M M" uniqKey="Macedo M">M. M. Macedo</name><affiliation><inist:fA14 i1="06"><s1>Embrapa Gado de Corte</s1><s2>Campo Grande</s2><s3>BRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Mielniczuk, J" uniqKey="Mielniczuk J">J. Mielniczuk</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Solos, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hernani, L C" uniqKey="Hernani L">L. C. Hernani</name><affiliation><inist:fA14 i1="05"><s1>Embrapa Agropecuária Oeste</s1><s2>Dourados</s2><s3>BRA</s3><sZ>7 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0412656</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0412656 INIST</idno><idno type="RBID">Pascal:09-0412656</idno><idno type="wicri:Area/Main/Corpus">001B97</idno></publicationStmt><seriesStmt><idno type="ISSN">1351-0754</idno><title level="j" type="abbreviated">Eur. j. soil sci.</title><title level="j" type="main">European journal of soil science</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Agroecosystem</term><term>Brazil</term><term>Earth science</term><term>Organic matter cycle</term><term>Soil science</term><term>Soil tillage</term><term>Tropical soil</term><term>land cover</term><term>organic materials</term><term>subtropical zone</term><term>textures</term><term>tropical zone</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Occupation sol</term><term>Travail sol</term><term>Texture</term><term>Zone tropicale</term><term>Science terre</term><term>Science du sol</term><term>Cycle matière organique</term><term>Agroécosystème</term><term>Matière organique</term><term>Zone subtropicale</term><term>Brésil</term><term>Sol tropical</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We examined the influence of land use change, tillage system and soil texture on organic carbon (C) stocks and on organic matter composition of tropical and subtropical soils from Brazil at four long-term experiments (11-25 years) based on fine- and coarse-textured soils. Soil samples were collected from the 0-5, 5-10 and 10-20 cm layers of conventional tillage (CT) and no-till (NT) plots, and of the adjoining soil under native vegetation (NV) of Cerrado (tropical) or grassland (subtropical). Conversion of NV to CT resulted in losses of 7-29% of the original C stock of 0-20 cm; conversion to NT increased this C stock by 0-12% compared with CT. Organic matter composition of the 0-5 cm layer, assessed by solid state CPMAS-<sup>13</sup>C-NMR, ESR and laser induced fluorescence spectroscopies, was affected by land use and tillage systems. Conversion of NV to CT decreased O-alkyl and increased aromatic, carbonyl, aromatic/O-alkyl ratio, free radicals concentration and fluorescence signal. The opposite trend was observed when NT replaced CT. The relative losses and gains of C and qualitative changes resulting from land use and tillage were less evident in fine- than in coarse-textured soils, suggesting a greater resistance and a smaller resilience of fine- compared with coarse-textured soils. The direct relation between increase in C stock and increase in potentially labile moieties (e.g. O-alkyl) and the decrease in more recalcitrant moieties (e.g. aromatics) in NT soils suggests that spatial inaccessibility by aggregates is playing a major role, compared with selective preservation, in promoting C accumulation in NT soils.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1351-0754</s0></fA01><fA03 i2="1"><s0>Eur. j. soil sci.</s0></fA03><fA05><s2>60</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Land use, tillage, texture and organic matter stock and composition in tropical and subtropical Brazilian soils</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Organic Matter Dynamics in Agro-ecosystems</s1></fA09><fA11 i1="01" i2="1"><s1>DIECKOW (J.)</s1></fA11><fA11 i1="02" i2="1"><s1>BAYER (C.)</s1></fA11><fA11 i1="03" i2="1"><s1>CONCEICAO (P. C.)</s1></fA11><fA11 i1="04" i2="1"><s1>ZANATTA (J. A.)</s1></fA11><fA11 i1="05" i2="1"><s1>MARTIN-NETO (L.)</s1></fA11><fA11 i1="06" i2="1"><s1>MILORI (D. B. M.)</s1></fA11><fA11 i1="07" i2="1"><s1>SALTON (J. C.)</s1></fA11><fA11 i1="08" i2="1"><s1>MACEDO (M. M.)</s1></fA11><fA11 i1="09" i2="1"><s1>MIELNICZUK (J.)</s1></fA11><fA11 i1="10" i2="1"><s1>HERNANI (L. C.)</s1></fA11><fA12 i1="01" i2="1"><s1>CHABBI (A.)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>RUMPEL (C.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Departamento de Solos e Engenharia Agrícola, Universidade Federal do Paraná</s1><s2>Curitiba</s2><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Solos, Universidade Federal do Rio Grande do Sul</s1><s2>Porto Alegre</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>4 aut.</sZ><sZ>9 aut.</sZ></fA14><fA14 i1="03"><s1>Unidade Dois Vizinhos, Universidade Tecnológica Federal do Paraná</s1><s2>Dois Vizinhos</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Embrapa Instrumentação Agropecudria</s1><s2>Sdo Carlos</s2><s3>BRA</s3><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="05"><s1>Embrapa Agropecuária Oeste</s1><s2>Dourados</s2><s3>BRA</s3><sZ>7 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="06"><s1>Embrapa Gado de Corte</s1><s2>Campo Grande</s2><s3>BRA</s3><sZ>8 aut.</sZ></fA14><fA15 i1="01"><s1>UEFE, INRA Poitou-Charentes</s1><s2>86600 Lusignan</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>CNRS, Laboratoire de Biogéochimie des Milieux Continentaux (UMR CNRS, INRA, Université Paris VI, IRD), Campus ParisAgroTech</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>240-249</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2402</s2><s5>354000185560360090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0412656</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European journal of soil science</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>We examined the influence of land use change, tillage system and soil texture on organic carbon (C) stocks and on organic matter composition of tropical and subtropical soils from Brazil at four long-term experiments (11-25 years) based on fine- and coarse-textured soils. Soil samples were collected from the 0-5, 5-10 and 10-20 cm layers of conventional tillage (CT) and no-till (NT) plots, and of the adjoining soil under native vegetation (NV) of Cerrado (tropical) or grassland (subtropical). Conversion of NV to CT resulted in losses of 7-29% of the original C stock of 0-20 cm; conversion to NT increased this C stock by 0-12% compared with CT. Organic matter composition of the 0-5 cm layer, assessed by solid state CPMAS-<sup>13</sup>C-NMR, ESR and laser induced fluorescence spectroscopies, was affected by land use and tillage systems. Conversion of NV to CT decreased O-alkyl and increased aromatic, carbonyl, aromatic/O-alkyl ratio, free radicals concentration and fluorescence signal. The opposite trend was observed when NT replaced CT. The relative losses and gains of C and qualitative changes resulting from land use and tillage were less evident in fine- than in coarse-textured soils, suggesting a greater resistance and a smaller resilience of fine- compared with coarse-textured soils. The direct relation between increase in C stock and increase in potentially labile moieties (e.g. O-alkyl) and the decrease in more recalcitrant moieties (e.g. aromatics) in NT soils suggests that spatial inaccessibility by aggregates is playing a major role, compared with selective preservation, in promoting C accumulation in NT soils.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01P03</s0></fC02><fC02 i1="02" i2="X"><s0>002A32B03B3</s0></fC02><fC02 i1="03" i2="X"><s0>002A32C04B2</s0></fC02><fC02 i1="04" i2="2"><s0>226C03</s0></fC02><fC03 i1="01" i2="2" l="FRE"><s0>Occupation sol</s0><s5>01</s5></fC03><fC03 i1="01" i2="2" l="ENG"><s0>land cover</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Travail sol</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Soil tillage</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Labranza</s0><s5>02</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Texture</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>textures</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="SPA"><s0>Textura</s0><s5>03</s5></fC03><fC03 i1="04" i2="2" l="FRE"><s0>Zone tropicale</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="ENG"><s0>tropical zone</s0><s5>04</s5></fC03><fC03 i1="04" i2="2" l="SPA"><s0>Zona tropical</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Science terre</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Earth science</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Ciencia tierra</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Science du sol</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Soil science</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Ciencia del suelo</s0><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Cycle matière organique</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Organic matter cycle</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Ciclo materia orgánica</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Agroécosystème</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Agroecosystem</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Agroecosistema</s0><s5>08</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Matière organique</s0><s5>15</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>organic materials</s0><s5>15</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Materia orgánica</s0><s5>15</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Zone subtropicale</s0><s5>20</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>subtropical zone</s0><s5>20</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Zona subtropical</s0><s5>20</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>21</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Sol tropical</s0><s2>NT</s2><s5>24</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Tropical soil</s0><s2>NT</s2><s5>24</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Suelo tropical</s0><s2>NT</s2><s5>24</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="01" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fC07 i1="02" i2="2" l="FRE"><s0>Aménagement sol</s0><s5>33</s5></fC07><fC07 i1="02" i2="2" l="ENG"><s0>soil management</s0><s5>33</s5></fC07><fC07 i1="02" i2="2" l="SPA"><s0>Acondicionamiento suelo</s0><s5>33</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Technique culturale</s0><s5>34</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Cultural practice</s0><s5>34</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Técnica cultivo</s0><s5>34</s5></fC07><fC07 i1="04" i2="2" l="FRE"><s0>Propriété physique</s0><s5>35</s5></fC07><fC07 i1="04" i2="2" l="ENG"><s0>physical properties</s0><s5>35</s5></fC07><fC07 i1="04" i2="2" l="SPA"><s0>Propiedad física</s0><s5>35</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0412656 INIST</NO><ET>Land use, tillage, texture and organic matter stock and composition in tropical and subtropical Brazilian soils</ET><AU>DIECKOW (J.); BAYER (C.); CONCEICAO (P. C.); ZANATTA (J. A.); MARTIN-NETO (L.); MILORI (D. B. M.); SALTON (J. C.); MACEDO (M. M.); MIELNICZUK (J.); HERNANI (L. C.); CHABBI (A.); RUMPEL (C.)</AU><AF>Departamento de Solos e Engenharia Agrícola, Universidade Federal do Paraná/Curitiba/Brésil (1 aut.); Departamento de Solos, Universidade Federal do Rio Grande do Sul/Porto Alegre/Brésil (2 aut., 4 aut., 9 aut.); Unidade Dois Vizinhos, Universidade Tecnológica Federal do Paraná/Dois Vizinhos/Brésil (3 aut.); Embrapa Instrumentação Agropecudria/Sdo Carlos/Brésil (5 aut., 6 aut.); Embrapa Agropecuária Oeste/Dourados/Brésil (7 aut., 10 aut.); Embrapa Gado de Corte/Campo Grande/Brésil (8 aut.); UEFE, INRA Poitou-Charentes/86600 Lusignan/France (1 aut.); CNRS, Laboratoire de Biogéochimie des Milieux Continentaux (UMR CNRS, INRA, Université Paris VI, IRD), Campus ParisAgroTech/78850 Thiverval-Grignon/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>European journal of soil science; ISSN 1351-0754; Royaume-Uni; Da. 2009; Vol. 60; No. 2; Pp. 240-249; Bibl. 1 p.1/4</SO><LA>Anglais</LA><EA>We examined the influence of land use change, tillage system and soil texture on organic carbon (C) stocks and on organic matter composition of tropical and subtropical soils from Brazil at four long-term experiments (11-25 years) based on fine- and coarse-textured soils. Soil samples were collected from the 0-5, 5-10 and 10-20 cm layers of conventional tillage (CT) and no-till (NT) plots, and of the adjoining soil under native vegetation (NV) of Cerrado (tropical) or grassland (subtropical). Conversion of NV to CT resulted in losses of 7-29% of the original C stock of 0-20 cm; conversion to NT increased this C stock by 0-12% compared with CT. Organic matter composition of the 0-5 cm layer, assessed by solid state CPMAS-<sup>13</sup>C-NMR, ESR and laser induced fluorescence spectroscopies, was affected by land use and tillage systems. Conversion of NV to CT decreased O-alkyl and increased aromatic, carbonyl, aromatic/O-alkyl ratio, free radicals concentration and fluorescence signal. The opposite trend was observed when NT replaced CT. The relative losses and gains of C and qualitative changes resulting from land use and tillage were less evident in fine- than in coarse-textured soils, suggesting a greater resistance and a smaller resilience of fine- compared with coarse-textured soils. The direct relation between increase in C stock and increase in potentially labile moieties (e.g. O-alkyl) and the decrease in more recalcitrant moieties (e.g. aromatics) in NT soils suggests that spatial inaccessibility by aggregates is playing a major role, compared with selective preservation, in promoting C accumulation in NT soils.</EA><CC>001E01P03; 002A32B03B3; 002A32C04B2; 226C03</CC><FD>Occupation sol; Travail sol; Texture; Zone tropicale; Science terre; Science du sol; Cycle matière organique; Agroécosystème; Matière organique; Zone subtropicale; Brésil; Sol tropical</FD><FG>Amérique du Sud; Aménagement sol; Technique culturale; Propriété physique</FG><ED>land cover; Soil tillage; textures; tropical zone; Earth science; Soil science; Organic matter cycle; Agroecosystem; organic materials; subtropical zone; Brazil; Tropical soil</ED><EG>South America; soil management; Cultural practice; physical properties</EG><SD>Labranza; Textura; Zona tropical; Ciencia tierra; Ciencia del suelo; Ciclo materia orgánica; Agroecosistema; Materia orgánica; Zona subtropical; Brasil; Suelo tropical</SD><LO>INIST-2402.354000185560360090</LO><ID>09-0412656</ID></server></inist></record>
000D87	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Short-term temporal changes of bare soil CO<sub>2</sub> fluxes after tillage described by first-order decay models</title><author><name sortKey="Scala, N La Jr" uniqKey="Scala N">N. La Jr Scala</name><affiliation><inist:fA14 i1="01"><s1>FCAV-UNESP, Via de Acesso Prof. Paulo Donato Castellane s/n</s1><s2>14884-900, Jahoticabal, Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lofes, A" uniqKey="Lofes A">A. Lofes</name><affiliation><inist:fA14 i1="01"><s1>FCAV-UNESP, Via de Acesso Prof. Paulo Donato Castellane s/n</s1><s2>14884-900, Jahoticabal, Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Spokas, K" uniqKey="Spokas K">K. Spokas</name><affiliation><inist:fA14 i1="02"><s1>USDA-ARS, USDA-ARS Soil and Water Management Unit, 1991 Upper Buford Circle</s1><s2>St Paul, MN 55108</s2><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Archer, D W" uniqKey="Archer D">D. W. Archer</name><affiliation><inist:fA14 i1="03"><s1>USDA-ARS, Northern Great Plains Research Laboratory, PO Box 459, 1701 10th Avenue SW</s1><s2>Mandan, ND 58554</s2><s3>USA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Reicosky, D C" uniqKey="Reicosky D">D. C. Reicosky</name><affiliation><inist:fA14 i1="04"><s1>USDA-ARS, North Central Soil Conservation Research Laboratory, 803 Iowa Avenue</s1><s2>Morris, MN 56267</s2><s3>USA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0412668</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0412668 INIST</idno><idno type="RBID">Pascal:09-0412668</idno><idno type="wicri:Area/Main/Corpus">001B96</idno></publicationStmt><seriesStmt><idno type="ISSN">1351-0754</idno><title level="j" type="abbreviated">Eur. j. soil sci.</title><title level="j" type="main">European journal of soil science</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Carbon dioxide</term><term>Earth science</term><term>First order</term><term>Gas exchange</term><term>Gas flux</term><term>Material flow</term><term>Modeling</term><term>Organic matter cycle</term><term>Short term</term><term>Soil science</term><term>Soil tillage</term><term>bare soils</term><term>decomposition</term><term>models</term><term>time variations</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Court terme</term><term>Variation temporelle</term><term>Echange gazeux</term><term>Flux matière</term><term>Travail sol</term><term>Ordre 1</term><term>Décomposition</term><term>Modélisation</term><term>Science terre</term><term>Dioxyde de carbone</term><term>Sol nu</term><term>Science du sol</term><term>Modèle</term><term>Cycle matière organique</term><term>Flux de gaz</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">To further understand the impact of tillage on carbon dioxide (CO<sub>2</sub>) emission, we compare the performance of two conceptual models that describe CO<sub>2</sub> emission after tillage as a function of the non-tilled emission plus a correction resulting from the tillage disturbance. The models assume that C in the readily decomposable organic matter follows a first-order reaction kinetics equation as dC<sub>son</sub>(t)/dt = - kC<sub>soil</sub>(t) and that soil C-CO<sub>2</sub> emission is proportional to the C decay rate in soil, where C<sub>soil</sub>(t) is the available labile soil C (g m<sup>-2</sup>) at any time (t) and k is the decay constant (time<sup>-1</sup>). Two possible relationships are derived between non-tilled (F<sub>NT</sub>) and tilled (F<sub>T</sub>) soil fluxes: F<sub>T</sub> = F<sub>NT</sub> + a<sub>1</sub> e<sup>-a2t</sup>(model 1) and F<sub>T</sub> = a<sub>3</sub>F<sub>NT</sub> e<sup>-a4t</sup> (model 2), where t is time after tillage. The difference between these two models comes from an assumption related to the k factor of labile C in the tilled plot and its similarity to the k factor of labile C in the non-till plot. Statistical fit of experimental data to conceptual models showed good agreement between predicted and observed CO<sub>2</sub> fluxes based on the index of agreement (d-index) and with model efficiency as large as 0.97. Comparisons reveal that model 2, where all C pools are assigned the same k factor, produces a better statistical fit than model 1. The advantage of this modelling approach is that temporal variability of tillage-induced emissions can be described by a simple analytical function that includes the non-tilled emission plus an exponential term, which is dependent upon tillage and environmental conditions.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1351-0754</s0></fA01><fA03 i2="1"><s0>Eur. j. soil sci.</s0></fA03><fA05><s2>60</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Short-term temporal changes of bare soil CO<sub>2</sub> fluxes after tillage described by first-order decay models</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Organic Matter Dynamics in Agro-ecosystems</s1></fA09><fA11 i1="01" i2="1"><s1>SCALA (N. La JR)</s1></fA11><fA11 i1="02" i2="1"><s1>LOFES (A.)</s1></fA11><fA11 i1="03" i2="1"><s1>SPOKAS (K.)</s1></fA11><fA11 i1="04" i2="1"><s1>ARCHER (D. W.)</s1></fA11><fA11 i1="05" i2="1"><s1>REICOSKY (D. C.)</s1></fA11><fA12 i1="01" i2="1"><s1>CHABBI (A.)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>RUMPEL (C.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>FCAV-UNESP, Via de Acesso Prof. Paulo Donato Castellane s/n</s1><s2>14884-900, Jahoticabal, Sao Paulo</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ></fA14><fA14 i1="02"><s1>USDA-ARS, USDA-ARS Soil and Water Management Unit, 1991 Upper Buford Circle</s1><s2>St Paul, MN 55108</s2><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="03"><s1>USDA-ARS, Northern Great Plains Research Laboratory, PO Box 459, 1701 10th Avenue SW</s1><s2>Mandan, ND 58554</s2><s3>USA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="04"><s1>USDA-ARS, North Central Soil Conservation Research Laboratory, 803 Iowa Avenue</s1><s2>Morris, MN 56267</s2><s3>USA</s3><sZ>5 aut.</sZ></fA14><fA15 i1="01"><s1>UEFE, INRA Poitou-Charentes</s1><s2>86600 Lusignan</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>CNRS, Laboratoire de Biogéochimie des Milieux Continentaux (UMR CNRS, INRA, Université Paris VI, IRD), Campus ParisAgroTech</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s1>258-264</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2402</s2><s5>354000185560360110</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0412668</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European journal of soil science</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>To further understand the impact of tillage on carbon dioxide (CO<sub>2</sub>) emission, we compare the performance of two conceptual models that describe CO<sub>2</sub> emission after tillage as a function of the non-tilled emission plus a correction resulting from the tillage disturbance. The models assume that C in the readily decomposable organic matter follows a first-order reaction kinetics equation as dC<sub>son</sub>(t)/dt = - kC<sub>soil</sub>(t) and that soil C-CO<sub>2</sub> emission is proportional to the C decay rate in soil, where C<sub>soil</sub>(t) is the available labile soil C (g m<sup>-2</sup>) at any time (t) and k is the decay constant (time<sup>-1</sup>). Two possible relationships are derived between non-tilled (F<sub>NT</sub>) and tilled (F<sub>T</sub>) soil fluxes: F<sub>T</sub> = F<sub>NT</sub> + a<sub>1</sub> e<sup>-a2t</sup>(model 1) and F<sub>T</sub> = a<sub>3</sub>F<sub>NT</sub> e<sup>-a4t</sup> (model 2), where t is time after tillage. The difference between these two models comes from an assumption related to the k factor of labile C in the tilled plot and its similarity to the k factor of labile C in the non-till plot. Statistical fit of experimental data to conceptual models showed good agreement between predicted and observed CO<sub>2</sub> fluxes based on the index of agreement (d-index) and with model efficiency as large as 0.97. Comparisons reveal that model 2, where all C pools are assigned the same k factor, produces a better statistical fit than model 1. The advantage of this modelling approach is that temporal variability of tillage-induced emissions can be described by a simple analytical function that includes the non-tilled emission plus an exponential term, which is dependent upon tillage and environmental conditions.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01P03</s0></fC02><fC02 i1="02" i2="X"><s0>002A32B</s0></fC02><fC02 i1="03" i2="X"><s0>002A32C04B2</s0></fC02><fC02 i1="04" i2="2"><s0>226C03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Court terme</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Short term</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Corto plazo</s0><s5>01</s5></fC03><fC03 i1="02" i2="2" l="FRE"><s0>Variation temporelle</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="ENG"><s0>time variations</s0><s5>02</s5></fC03><fC03 i1="02" i2="2" l="SPA"><s0>Variación temporal</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Echange gazeux</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Gas exchange</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Intercambio gaseoso</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Flux matière</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Material flow</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Flujo materia</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Travail sol</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Soil tillage</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Labranza</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Ordre 1</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>First order</s0><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Orden 1</s0><s5>06</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Décomposition</s0><s5>07</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>decomposition</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Modélisation</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Modeling</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Modelización</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Science terre</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Earth science</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Ciencia tierra</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Dioxyde de carbone</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Carbon dioxide</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Carbono dióxido</s0><s2>NK</s2><s2>FX</s2><s5>15</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Sol nu</s0><s5>24</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>bare soils</s0><s5>24</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Science du sol</s0><s5>28</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Soil science</s0><s5>28</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Ciencia del suelo</s0><s5>28</s5></fC03><fC03 i1="13" i2="2" l="FRE"><s0>Modèle</s0><s5>29</s5></fC03><fC03 i1="13" i2="2" l="ENG"><s0>models</s0><s5>29</s5></fC03><fC03 i1="13" i2="2" l="SPA"><s0>Modelo</s0><s5>29</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Cycle matière organique</s0><s5>30</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Organic matter cycle</s0><s5>30</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Ciclo materia orgánica</s0><s5>30</s5></fC03><fC03 i1="15" i2="2" l="FRE"><s0>Flux de gaz</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="15" i2="2" l="ENG"><s0>Gas flux</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="15" i2="2" l="SPA"><s0>Flujo de gas</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="2" l="FRE"><s0>Aménagement sol</s0><s5>33</s5></fC07><fC07 i1="01" i2="2" l="ENG"><s0>soil management</s0><s5>33</s5></fC07><fC07 i1="01" i2="2" l="SPA"><s0>Acondicionamiento suelo</s0><s5>33</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Technique culturale</s0><s5>34</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Cultural practice</s0><s5>34</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Técnica cultivo</s0><s5>34</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0412668 INIST</NO><ET>Short-term temporal changes of bare soil CO<sub>2</sub> fluxes after tillage described by first-order decay models</ET><AU>SCALA (N. La JR); LOFES (A.); SPOKAS (K.); ARCHER (D. W.); REICOSKY (D. C.); CHABBI (A.); RUMPEL (C.)</AU><AF>FCAV-UNESP, Via de Acesso Prof. Paulo Donato Castellane s/n/14884-900, Jahoticabal, Sao Paulo/Brésil (1 aut., 2 aut.); USDA-ARS, USDA-ARS Soil and Water Management Unit, 1991 Upper Buford Circle/St Paul, MN 55108/Etats-Unis (3 aut.); USDA-ARS, Northern Great Plains Research Laboratory, PO Box 459, 1701 10th Avenue SW/Mandan, ND 58554/Etats-Unis (4 aut.); USDA-ARS, North Central Soil Conservation Research Laboratory, 803 Iowa Avenue/Morris, MN 56267/Etats-Unis (5 aut.); UEFE, INRA Poitou-Charentes/86600 Lusignan/France (1 aut.); CNRS, Laboratoire de Biogéochimie des Milieux Continentaux (UMR CNRS, INRA, Université Paris VI, IRD), Campus ParisAgroTech/78850 Thiverval-Grignon/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>European journal of soil science; ISSN 1351-0754; Royaume-Uni; Da. 2009; Vol. 60; No. 2; Pp. 258-264; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>To further understand the impact of tillage on carbon dioxide (CO<sub>2</sub>) emission, we compare the performance of two conceptual models that describe CO<sub>2</sub> emission after tillage as a function of the non-tilled emission plus a correction resulting from the tillage disturbance. The models assume that C in the readily decomposable organic matter follows a first-order reaction kinetics equation as dC<sub>son</sub>(t)/dt = - kC<sub>soil</sub>(t) and that soil C-CO<sub>2</sub> emission is proportional to the C decay rate in soil, where C<sub>soil</sub>(t) is the available labile soil C (g m<sup>-2</sup>) at any time (t) and k is the decay constant (time<sup>-1</sup>). Two possible relationships are derived between non-tilled (F<sub>NT</sub>) and tilled (F<sub>T</sub>) soil fluxes: F<sub>T</sub> = F<sub>NT</sub> + a<sub>1</sub> e<sup>-a2t</sup>(model 1) and F<sub>T</sub> = a<sub>3</sub>F<sub>NT</sub> e<sup>-a4t</sup> (model 2), where t is time after tillage. The difference between these two models comes from an assumption related to the k factor of labile C in the tilled plot and its similarity to the k factor of labile C in the non-till plot. Statistical fit of experimental data to conceptual models showed good agreement between predicted and observed CO<sub>2</sub> fluxes based on the index of agreement (d-index) and with model efficiency as large as 0.97. Comparisons reveal that model 2, where all C pools are assigned the same k factor, produces a better statistical fit than model 1. The advantage of this modelling approach is that temporal variability of tillage-induced emissions can be described by a simple analytical function that includes the non-tilled emission plus an exponential term, which is dependent upon tillage and environmental conditions.</EA><CC>001E01P03; 002A32B; 002A32C04B2; 226C03</CC><FD>Court terme; Variation temporelle; Echange gazeux; Flux matière; Travail sol; Ordre 1; Décomposition; Modélisation; Science terre; Dioxyde de carbone; Sol nu; Science du sol; Modèle; Cycle matière organique; Flux de gaz</FD><FG>Aménagement sol; Technique culturale</FG><ED>Short term; time variations; Gas exchange; Material flow; Soil tillage; First order; decomposition; Modeling; Earth science; Carbon dioxide; bare soils; Soil science; models; Organic matter cycle; Gas flux</ED><EG>soil management; Cultural practice</EG><SD>Corto plazo; Variación temporal; Intercambio gaseoso; Flujo materia; Labranza; Orden 1; Modelización; Ciencia tierra; Carbono dióxido; Ciencia del suelo; Modelo; Ciclo materia orgánica; Flujo de gas</SD><LO>INIST-2402.354000185560360110</LO><ID>09-0412668</ID></server></inist></record>
000D88	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">Natura et les vendeuses d'herbes de Belém: cosmétique éthique contre savoirs traditionnels</title><author><name sortKey="Arouca Belas, Carla" uniqKey="Arouca Belas C">Carla Arouca Belas</name><affiliation><inist:fA14 i1="01"><s1>Université fédérale rurale de Rio de Janeiro (CDPA/UFFRJ)</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Centre national de foklore et de culture populaire de l'Institut du patrimoine historique et artistique national (CNFCP/IPHAN). CPDA/UFFRJ, Universidade Federal Rural do Rio de Janeiro</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Buclet, Benjamin" uniqKey="Buclet B">Benjamin Buclet</name><affiliation><inist:fA14 i1="03"><s1>(EHESS)</s1><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="04"><s1>Institut de recherche pour le Développement (IRD)</s1><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="05"><s1>IRD, 44 Boulevard de Dunkerque, CS 90009</s1><s2>13572 Marseille</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Barbosa De Lima, Daniela Fortunato" uniqKey="Barbosa De Lima D">Daniela Fortunato Barbosa De Lima</name><affiliation><inist:fA14 i1="06"><s1>Institut de Recherches Scientifiques et Technologiques de l'Amapà (IEPA)</s1><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="07"><s1>Commission d'accès à la Biodiversité (CARB/ SEMA). Instituto de Pesquisas Cientificas e Tecnolôgicas do Amapâ -IEPA. Avenida Feliciano Coelho, n° 1509, Bairro Trem.</s1><s2>Macapà - Amapâ CEP 68900-260</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0413001</idno><date when="2009">2009</date><idno type="stanalyst">FRANCIS 09-0413001 INIST</idno><idno type="RBID">Francis:09-0413001</idno><idno type="wicri:Area/Main/Corpus">001F88</idno></publicationStmt><seriesStmt><idno type="ISSN">1278-3986</idno><title level="j" type="abbreviated">Autrepart : (La Tour d' Aigues)</title><title level="j" type="main">Autrepart : (La Tour d'Aigues)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Access to resources</term><term>Amazonia</term><term>Belem</term><term>Brazil</term><term>Business</term><term>Cosmetics</term><term>Fragrant plant</term><term>Genetics</term><term>Herb</term><term>Inheritance</term><term>Intellectual property</term><term>Knowledge</term><term>Law suit</term><term>Market</term><term>Patent</term><term>Redistribution</term><term>Regulation</term><term>Saler person</term><term>South America</term><term>Tradition</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Propriété intellectuelle</term><term>Patrimoine</term><term>Génétique</term><term>Savoir</term><term>Tradition</term><term>Amazonie</term><term>Brésil</term><term>Amérique du Sud</term><term>Cosmétique</term><term>Vendeur</term><term>Marché</term><term>Herbe</term><term>Belem</term><term>Accès aux ressources</term><term>Plante aromatique</term><term>Entreprise</term><term>Brevet</term><term>Redistribution</term><term>Règlementation</term><term>Procès</term><term>Accord</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Natura, entreprise brésilienne qui fait de la « cosmétique éthique », inaugurait le 22 avril 2005 à Paris son premier magasin en France. Au même moment, à Belém, se négociait l'utilisation d'une herbe aromatique appelée Priprioca, entre les prospecteurs de Natura et les vendeuses du marché « Ver-o-Peso ». Un an plus tard, celles-ci exigèrent une compensation financière pour l'utilisation de leur savoir-faire immémorial. L'affaire devint un cas emblématique de la protection des savoirs traditionnels. Un accord fut finalement signé et les vendeuses d'herbes apaisées. La description du conflit et l'analyse des arguments des parties permettent d'identifier les points de tensions entre les pratiques juridico-légales liées à la préservation de la socio biodiversité et les réalités socio-économiques dans le contexte brésilien. On souligne en particulier les conséquences de la transformation d'une pratique coutumière en enjeu économique sur les équilibres sociaux.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1278-3986</s0></fA01><fA03 i2="1"><s0>Autrepart : (La Tour d' Aigues)</s0></fA03><fA06><s2>50</s2></fA06><fA08 i1="01" i2="1" l="FRE"><s1>Natura et les vendeuses d'herbes de Belém: cosmétique éthique contre savoirs traditionnels</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>Les produits de terroir au service de la diversité biologique et culturelle ?</s1></fA09><fA11 i1="01" i2="1"><s1>AROUCA BELAS (Carla)</s1></fA11><fA11 i1="02" i2="1"><s1>BUCLET (Benjamin)</s1></fA11><fA11 i1="03" i2="1"><s1>BARBOSA DE LIMA (Daniela Fortunato)</s1></fA11><fA12 i1="01" i2="1"><s1>CORMIER-SALEM (Marie-Christine)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>ROUSSEL (Bernard)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Université fédérale rurale de Rio de Janeiro (CDPA/UFFRJ)</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Centre national de foklore et de culture populaire de l'Institut du patrimoine historique et artistique national (CNFCP/IPHAN). CPDA/UFFRJ, Universidade Federal Rural do Rio de Janeiro</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="03"><s1>(EHESS)</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="04"><s1>Institut de recherche pour le Développement (IRD)</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="05"><s1>IRD, 44 Boulevard de Dunkerque, CS 90009</s1><s2>13572 Marseille</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="06"><s1>Institut de Recherches Scientifiques et Technologiques de l'Amapà (IEPA)</s1><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="07"><s1>Commission d'accès à la Biodiversité (CARB/ SEMA). Instituto de Pesquisas Cientificas e Tecnolôgicas do Amapâ -IEPA. Avenida Feliciano Coelho, n° 1509, Bairro Trem.</s1><s2>Macapà - Amapâ CEP 68900-260</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA15 i1="01"><s1>Institut de recherche pour le développement (IRD), UMR 208 (IRD/MNHN)</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Muséum national d'histoire naturelle (MNHN), UMR 208 (IRD/MNHN)</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s2>33-50, 206, 210 [20 p.]</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>10882E</s2><s5>354000188228670020</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>2 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0413001</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Autrepart : (La Tour d'Aigues)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA68 i1="01" i2="1" l="ENG"><s1>Natura in Belém: ethical cosmetics confronts traditional knowledge</s1></fA68><fA69 i1="01" i2="1" l="ENG"><s1>The products of land in the service of biological and cultural diversity?</s1></fA69><fC01 i1="01" l="FRE"><s0>Natura, entreprise brésilienne qui fait de la « cosmétique éthique », inaugurait le 22 avril 2005 à Paris son premier magasin en France. Au même moment, à Belém, se négociait l'utilisation d'une herbe aromatique appelée Priprioca, entre les prospecteurs de Natura et les vendeuses du marché « Ver-o-Peso ». Un an plus tard, celles-ci exigèrent une compensation financière pour l'utilisation de leur savoir-faire immémorial. L'affaire devint un cas emblématique de la protection des savoirs traditionnels. Un accord fut finalement signé et les vendeuses d'herbes apaisées. La description du conflit et l'analyse des arguments des parties permettent d'identifier les points de tensions entre les pratiques juridico-légales liées à la préservation de la socio biodiversité et les réalités socio-économiques dans le contexte brésilien. On souligne en particulier les conséquences de la transformation d'une pratique coutumière en enjeu économique sur les équilibres sociaux.</s0></fC01><fC02 i1="01" i2="N"><s0>52941</s0><s1>III</s1></fC02><fC02 i1="02" i2="N"><s0>52942B</s0><s1>III</s1></fC02><fC02 i1="03" i2="N"><s0>529</s0></fC02><fC03 i1="01" i2="S" l="FRE"><s0>Propriété intellectuelle</s0><s5>01</s5></fC03><fC03 i1="01" i2="S" l="ENG"><s0>Intellectual property</s0><s5>01</s5></fC03><fC03 i1="02" i2="N" l="FRE"><s0>Patrimoine</s0><s5>02</s5></fC03><fC03 i1="02" i2="N" l="ENG"><s0>Inheritance</s0><s5>02</s5></fC03><fC03 i1="03" i2="N" l="FRE"><s0>Génétique</s0><s5>03</s5></fC03><fC03 i1="03" i2="N" l="ENG"><s0>Genetics</s0><s5>03</s5></fC03><fC03 i1="04" i2="S" l="FRE"><s0>Savoir</s0><s5>04</s5></fC03><fC03 i1="04" i2="S" l="ENG"><s0>Knowledge</s0><s5>04</s5></fC03><fC03 i1="05" i2="N" l="FRE"><s0>Tradition</s0><s5>05</s5></fC03><fC03 i1="05" i2="N" l="ENG"><s0>Tradition</s0><s5>05</s5></fC03><fC03 i1="06" i2="N" l="FRE"><s0>Amazonie</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="N" l="ENG"><s0>Amazonia</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="07" i2="N" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>07</s5></fC03><fC03 i1="07" i2="N" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>07</s5></fC03><fC03 i1="08" i2="N" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2><s5>08</s5></fC03><fC03 i1="08" i2="N" l="ENG"><s0>South America</s0><s2>NG</s2><s5>08</s5></fC03><fC03 i1="09" i2="N" l="FRE"><s0>Cosmétique</s0><s5>09</s5></fC03><fC03 i1="09" i2="N" l="ENG"><s0>Cosmetics</s0><s5>09</s5></fC03><fC03 i1="10" i2="S" l="FRE"><s0>Vendeur</s0><s5>10</s5></fC03><fC03 i1="10" i2="S" l="ENG"><s0>Saler person</s0><s5>10</s5></fC03><fC03 i1="11" i2="N" l="FRE"><s0>Marché</s0><s5>11</s5></fC03><fC03 i1="11" i2="N" l="ENG"><s0>Market</s0><s5>11</s5></fC03><fC03 i1="12" i2="N" l="FRE"><s0>Herbe</s0><s5>12</s5></fC03><fC03 i1="12" i2="N" l="ENG"><s0>Herb</s0><s5>12</s5></fC03><fC03 i1="13" i2="N" l="FRE"><s0>Belem</s0><s2>NG</s2><s5>13</s5></fC03><fC03 i1="13" i2="N" l="ENG"><s0>Belem</s0><s2>NG</s2><s5>13</s5></fC03><fC03 i1="14" i2="N" l="FRE"><s0>Accès aux ressources</s0><s5>14</s5></fC03><fC03 i1="14" i2="N" l="ENG"><s0>Access to resources</s0><s5>14</s5></fC03><fC03 i1="15" i2="N" l="FRE"><s0>Plante aromatique</s0><s5>15</s5></fC03><fC03 i1="15" i2="N" l="ENG"><s0>Fragrant plant</s0><s5>15</s5></fC03><fC03 i1="16" i2="N" l="FRE"><s0>Entreprise</s0><s5>16</s5></fC03><fC03 i1="16" i2="N" l="ENG"><s0>Business</s0><s5>16</s5></fC03><fC03 i1="17" i2="S" l="FRE"><s0>Brevet</s0><s5>17</s5></fC03><fC03 i1="17" i2="S" l="ENG"><s0>Patent</s0><s5>17</s5></fC03><fC03 i1="18" i2="N" l="FRE"><s0>Redistribution</s0><s5>18</s5></fC03><fC03 i1="18" i2="N" l="ENG"><s0>Redistribution</s0><s5>18</s5></fC03><fC03 i1="19" i2="N" l="FRE"><s0>Règlementation</s0><s5>19</s5></fC03><fC03 i1="19" i2="N" l="ENG"><s0>Regulation</s0><s5>19</s5></fC03><fC03 i1="20" i2="N" l="FRE"><s0>Procès</s0><s5>20</s5></fC03><fC03 i1="20" i2="N" l="ENG"><s0>Law suit</s0><s5>20</s5></fC03><fC03 i1="21" i2="N" l="FRE"><s0>Accord</s0><s4>INC</s4><s5>26</s5></fC03><fN21><s1>299</s1></fN21></pA></standard><server><NO>FRANCIS 09-0413001 INIST</NO><FT>Natura et les vendeuses d'herbes de Belém: cosmétique éthique contre savoirs traditionnels</FT><ET>(Natura in Belém: ethical cosmetics confronts traditional knowledge)</ET><AU>AROUCA BELAS (Carla); BUCLET (Benjamin); BARBOSA DE LIMA (Daniela Fortunato); CORMIER-SALEM (Marie-Christine); ROUSSEL (Bernard)</AU><AF>Université fédérale rurale de Rio de Janeiro (CDPA/UFFRJ)/Brésil (1 aut.); Centre national de foklore et de culture populaire de l'Institut du patrimoine historique et artistique national (CNFCP/IPHAN). CPDA/UFFRJ, Universidade Federal Rural do Rio de Janeiro/Brésil (1 aut.); (EHESS)/France (2 aut.); Institut de recherche pour le Développement (IRD)/France (2 aut.); IRD, 44 Boulevard de Dunkerque, CS 90009/13572 Marseille/France (2 aut.); Institut de Recherches Scientifiques et Technologiques de l'Amapà (IEPA)/Brésil (3 aut.); Commission d'accès à la Biodiversité (CARB/ SEMA). Instituto de Pesquisas Cientificas e Tecnolôgicas do Amapâ -IEPA. Avenida Feliciano Coelho, n° 1509, Bairro Trem./Macapà - Amapâ CEP 68900-260/Brésil (3 aut.); Institut de recherche pour le développement (IRD), UMR 208 (IRD/MNHN)/Paris/France (1 aut.); Muséum national d'histoire naturelle (MNHN), UMR 208 (IRD/MNHN)/Paris/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Autrepart : (La Tour d'Aigues); ISSN 1278-3986; France; Da. 2009; No. 50; 33-50, 206, 210 [20 p.]; Abs. anglais; Bibl. 2 p.</SO><LA>Français</LA><FA>Natura, entreprise brésilienne qui fait de la « cosmétique éthique », inaugurait le 22 avril 2005 à Paris son premier magasin en France. Au même moment, à Belém, se négociait l'utilisation d'une herbe aromatique appelée Priprioca, entre les prospecteurs de Natura et les vendeuses du marché « Ver-o-Peso ». Un an plus tard, celles-ci exigèrent une compensation financière pour l'utilisation de leur savoir-faire immémorial. L'affaire devint un cas emblématique de la protection des savoirs traditionnels. Un accord fut finalement signé et les vendeuses d'herbes apaisées. La description du conflit et l'analyse des arguments des parties permettent d'identifier les points de tensions entre les pratiques juridico-légales liées à la préservation de la socio biodiversité et les réalités socio-économiques dans le contexte brésilien. On souligne en particulier les conséquences de la transformation d'une pratique coutumière en enjeu économique sur les équilibres sociaux.</FA><CC>52941; 52942B; 529</CC><FD>Propriété intellectuelle; Patrimoine; Génétique; Savoir; Tradition; Amazonie; Brésil; Amérique du Sud; Cosmétique; Vendeur; Marché; Herbe; Belem; Accès aux ressources; Plante aromatique; Entreprise; Brevet; Redistribution; Règlementation; Procès; Accord</FD><ED>Intellectual property; Inheritance; Genetics; Knowledge; Tradition; Amazonia; Brazil; South America; Cosmetics; Saler person; Market; Herb; Belem; Access to resources; Fragrant plant; Business; Patent; Redistribution; Regulation; Law suit</ED><LO>INIST-10882E.354000188228670020</LO><ID>09-0413001</ID></server></inist></record>
000D89	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Predominance of CTX-M-type extended-spectrum β-lactamase genes among enterobacterial isolates from outpatients in Brazil</title><author><name sortKey="Minarini, Luciene A R" uniqKey="Minarini L">Luciene A. R. Minarini</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 &#34;Emerging Resistance to Antibiotics&#34;, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine et Université Paris-Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP</s1><s2>Ribeirão Preto, SP 14040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Poirel, Laurent" uniqKey="Poirel L">Laurent Poirel</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 &#34;Emerging Resistance to Antibiotics&#34;, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine et Université Paris-Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Trevisani, Nathalia A C" uniqKey="Trevisani N">Nathalia A. C. Trevisani</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP</s1><s2>Ribeirão Preto, SP 14040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Darini, Ana Lucia C" uniqKey="Darini A">Ana Lucia C. Darini</name><affiliation><inist:fA14 i1="02"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP</s1><s2>Ribeirão Preto, SP 14040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nordmann, Patrice" uniqKey="Nordmann P">Patrice Nordmann</name><affiliation><inist:fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 &#34;Emerging Resistance to Antibiotics&#34;, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine et Université Paris-Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0413055</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0413055 INIST</idno><idno type="RBID">Pascal:09-0413055</idno><idno type="wicri:Area/Main/Corpus">001B95</idno></publicationStmt><seriesStmt><idno type="ISSN">0732-8893</idno><title level="j" type="abbreviated">Diagn. microbiol. infect. dis.</title><title level="j" type="main">Diagnostic microbiology and infectious disease</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Ambulatory</term><term>Brazil</term><term>Extended-spectrum β-lactamase</term><term>Gene</term><term>Infection</term><term>Isolate</term><term>Microbiology</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>β-Lactamase à spectre étendu</term><term>Gène</term><term>Isolat</term><term>Ambulatoire</term><term>Brésil</term><term>Microbiologie</term><term>Infection</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Two hundred fifty-seven nalidixic acid-resistant enterobacterial isolates were collected in a Brazilian community from January 2000 to May 2005 to determine the prevalence of plasmid-encoded extended-spectrum β-lactamases. The bla<sub>CTX-M</sub> genetic environment was determined by polymerase chain reaction and sequencing. Eleven isolates (4.2%) harbored a bla<sub>CTX-M-2 </sub>gene, 3 isolates bla<sub>CTX-M-9</sub>, 2 isolates bla<sub>CTX-M-8</sub>, and 6 isolates bla<sub>SHV-5</sub>. Two novel bla<sub>CTX-M-2</sub> variants, namely, bla<sub>CTX-M-74</sub> and bla<sub>CTX-M</sub>-<sub>75</sub>, were identified.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0732-8893</s0></fA01><fA02 i1="01"><s0>DMIDDZ</s0></fA02><fA03 i2="1"><s0>Diagn. microbiol. infect. dis.</s0></fA03><fA05><s2>65</s2></fA05><fA06><s2>2</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Predominance of CTX-M-type extended-spectrum β-lactamase genes among enterobacterial isolates from outpatients in Brazil</s1></fA08><fA11 i1="01" i2="1"><s1>MINARINI (Luciene A. R.)</s1></fA11><fA11 i1="02" i2="1"><s1>POIREL (Laurent)</s1></fA11><fA11 i1="03" i2="1"><s1>TREVISANI (Nathalia A. C.)</s1></fA11><fA11 i1="04" i2="1"><s1>DARINI (Ana Lucia C.)</s1></fA11><fA11 i1="05" i2="1"><s1>NORDMANN (Patrice)</s1></fA11><fA14 i1="01"><s1>Service de Bactériologie-Virologie, INSERM U914 &#34;Emerging Resistance to Antibiotics&#34;, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine et Université Paris-Sud</s1><s2>K.-Bicêtre</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP</s1><s2>Ribeirão Preto, SP 14040-903</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA20><s1>202-206</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20217</s2><s5>354000170229800220</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0413055</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Diagnostic microbiology and infectious disease</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Two hundred fifty-seven nalidixic acid-resistant enterobacterial isolates were collected in a Brazilian community from January 2000 to May 2005 to determine the prevalence of plasmid-encoded extended-spectrum β-lactamases. The bla<sub>CTX-M</sub> genetic environment was determined by polymerase chain reaction and sequencing. Eleven isolates (4.2%) harbored a bla<sub>CTX-M-2 </sub>gene, 3 isolates bla<sub>CTX-M-9</sub>, 2 isolates bla<sub>CTX-M-8</sub>, and 6 isolates bla<sub>SHV-5</sub>. Two novel bla<sub>CTX-M-2</sub> variants, namely, bla<sub>CTX-M-74</sub> and bla<sub>CTX-M</sub>-<sub>75</sub>, were identified.</s0></fC01><fC02 i1="01" i2="X"><s0>002A05</s0></fC02><fC02 i1="02" i2="X"><s0>002B05</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>β-Lactamase à spectre étendu</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Extended-spectrum β-lactamase</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>β-lactamasa de espectro extendido</s0><s2>FE</s2><s5>05</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Gène</s0><s5>06</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Gene</s0><s5>06</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Gen</s0><s5>06</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Isolat</s0><s5>07</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Isolate</s0><s5>07</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Aislado</s0><s5>07</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Ambulatoire</s0><s5>08</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Ambulatory</s0><s5>08</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Ambulatorio</s0><s5>08</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>09</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Microbiologie</s0><s5>10</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Microbiology</s0><s5>10</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Microbiología</s0><s5>10</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Infection</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Infection</s0><s5>11</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Infección</s0><s5>11</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0413055 INIST</NO><ET>Predominance of CTX-M-type extended-spectrum β-lactamase genes among enterobacterial isolates from outpatients in Brazil</ET><AU>MINARINI (Luciene A. R.); POIREL (Laurent); TREVISANI (Nathalia A. C.); DARINI (Ana Lucia C.); NORDMANN (Patrice)</AU><AF>Service de Bactériologie-Virologie, INSERM U914 &#34;Emerging Resistance to Antibiotics&#34;, Hôpital de Bicêtre, Assistance Publique/Hôpitaux de Paris, Faculté de Médecine et Université Paris-Sud/K.-Bicêtre/France (1 aut., 2 aut., 5 aut.); Departamento de Análises Clinicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, USP/Ribeirão Preto, SP 14040-903/Brésil (1 aut., 3 aut., 4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Diagnostic microbiology and infectious disease; ISSN 0732-8893; Coden DMIDDZ; Etats-Unis; Da. 2009; Vol. 65; No. 2; Pp. 202-206; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Two hundred fifty-seven nalidixic acid-resistant enterobacterial isolates were collected in a Brazilian community from January 2000 to May 2005 to determine the prevalence of plasmid-encoded extended-spectrum β-lactamases. The bla<sub>CTX-M</sub> genetic environment was determined by polymerase chain reaction and sequencing. Eleven isolates (4.2%) harbored a bla<sub>CTX-M-2 </sub>gene, 3 isolates bla<sub>CTX-M-9</sub>, 2 isolates bla<sub>CTX-M-8</sub>, and 6 isolates bla<sub>SHV-5</sub>. Two novel bla<sub>CTX-M-2</sub> variants, namely, bla<sub>CTX-M-74</sub> and bla<sub>CTX-M</sub>-<sub>75</sub>, were identified.</EA><CC>002A05; 002B05</CC><FD>β-Lactamase à spectre étendu; Gène; Isolat; Ambulatoire; Brésil; Microbiologie; Infection</FD><FG>Amérique du Sud; Amérique</FG><ED>Extended-spectrum β-lactamase; Gene; Isolate; Ambulatory; Brazil; Microbiology; Infection</ED><EG>South America; America</EG><SD>β-lactamasa de espectro extendido; Gen; Aislado; Ambulatorio; Brasil; Microbiología; Infección</SD><LO>INIST-20217.354000170229800220</LO><ID>09-0413055</ID></server></inist></record>
000D90	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Unprotected left main revascularization in patients with acute coronary syndromes</title><author><name sortKey="Montalescot, Gilles" uniqKey="Montalescot G">Gilles Montalescot</name><affiliation><inist:fA14 i1="01"><s1>Institut de Cardiologie, Bureau 2-236, Centre Hospitalier Universitaire Pitié-Salpêtrière, 47 Blvd de l'Hôpital</s1><s2>75013 Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brieger, David" uniqKey="Brieger D">David Brieger</name><affiliation><inist:fA14 i1="02"><s1>Concord Hospital</s1><s2>Sydney, NSW</s2><s3>AUS</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Eagle, Kim A" uniqKey="Eagle K">Kim A. Eagle</name><affiliation><inist:fA14 i1="03"><s1>University of Michigan Cardiovascular Center</s1><s2>Ann Arbor, MI</s2><s3>USA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Anderson, Frederick A Jr" uniqKey="Anderson F">Frederick A. Jr Anderson</name><affiliation><inist:fA14 i1="04"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1><s2>Worcester, MA</s2><s3>USA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fitzgerald, Gordon" uniqKey="Fitzgerald G">Gordon Fitzgerald</name><affiliation><inist:fA14 i1="04"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1><s2>Worcester, MA</s2><s3>USA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lee, Michael S" uniqKey="Lee M">Michael S. Lee</name><affiliation><inist:fA14 i1="05"><s1>UCLA Medical Center, University of California, Los Angeles School of Medicine</s1><s2>Los Angeles, CA</s2><s3>USA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gabriel Steg, Ph" uniqKey="Gabriel Steg P">Ph. Gabriel Steg</name><affiliation><inist:fA14 i1="06"><s1>Department of Cardiology, INSERM U-698, Université Paris 7 and Assistance Publique - Hôpitaux de Paris</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Avezum, Alvaro" uniqKey="Avezum A">Alvaro Avezum</name><affiliation><inist:fA14 i1="07"><s1>Dante Pazzanese Institute of Cardiology</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Goodman, Shaun G" uniqKey="Goodman S">Shaun G. Goodman</name><affiliation><inist:fA14 i1="08"><s1>Canadian Heart Research Centre and Terrence Donnelly Heart Centre, Division of Cardiology, St. Michael's Hospital, University of Toronto</s1><s2>Toronto, ON</s2><s3>CAN</s3><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gore, Joel M" uniqKey="Gore J">Joel M. Gore</name></author></titleStmt><publicationStmt><idno type="inist">09-0414803</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0414803 INIST</idno><idno type="RBID">Pascal:09-0414803</idno><idno type="wicri:Area/Main/Corpus">001B94</idno></publicationStmt><seriesStmt><idno type="ISSN">0195-668X</idno><title level="j" type="abbreviated">Eur. heart j.</title><title level="j" type="main">European heart journal</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acute coronary syndrome</term><term>Cardiology</term><term>Circulatory system</term><term>Disease</term><term>Human</term><term>Left</term><term>Patient</term><term>Revascularization</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Gauche</term><term>Revascularisation</term><term>Homme</term><term>Malade</term><term>Maladie</term><term>Appareil circulatoire</term><term>Cardiologie</term><term>Syndrome coronaire aigu</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Aims In acute coronary syndromes (ACS), the optimal revascularization strategy for unprotected left main coronary disease (ULMCD) has been little studied. The objectives of the present study were to describe the practice of ULMCD revascularization in ACS patients and its evolution over an 8-year period, analyse the prognosis of this population and determine the effect of revascularization on outcome. Methods Of 43 018 patients enrolled in the Global Registry of Acute Coronary Events (GRACE) between 2000 and 2007, and results 1799 had significant ULMCD and underwent percutaneous coronary intervention (PCI) alone (n = 514), coronary artery bypass graft (CABG) alone (n = 612), or no revascularization (n = 673). Mortality was 7.7% in hospital and 14% at 6 months. Over the 8-year study, the GRACE risk score remained constant, but there was a steady shift to more PCI than CABG over time. Patients undergoing PCI presented more frequently with ST-segment elevation myocardial infarction (STEMI), after cardiac arrest, or in cardiogenic shock; 48% of PCI patients underwent revascularization on the day of admission vs. 5.1 % in the CABG group. After adjustment, revascularization was associated with an early hazard of hospital death vs. no revascularization, significant for PCI (hazard ratio (HR) 2.60, 95% confidence interval (CI) 1.62-4.18) but not for CABG (1.26, 0.72-2.22). From discharge to 6 months, both PCI (HR 0.45, 95% Cl 0.23-0.85) and CABG (0.11, 0.04-0.28) were significantly associated with improved survival in comparison with an initial strategy of no revascularization. Coronary artery bypass graft revascularization was associated with a five-fold increase in stroke compared with the other two groups. Conclusion Unprotected left main coronary disease in ACS is associated with high mortality, especially in patients with STEMI and/or haemodynamic or arrhythmic instability. Percutaneous coronary intervention is now the most common revascularization strategy and preferred in higher risk patients. Coronary artery bypass graft is often delayed and performed in lower risk patients, leading to good 6-month survival. The two approaches therefore appear complementary.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0195-668X</s0></fA01><fA03 i2="1"><s0>Eur. heart j.</s0></fA03><fA05><s2>30</s2></fA05><fA06><s2>19</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Unprotected left main revascularization in patients with acute coronary syndromes</s1></fA08><fA11 i1="01" i2="1"><s1>MONTALESCOT (Gilles)</s1></fA11><fA11 i1="02" i2="1"><s1>BRIEGER (David)</s1></fA11><fA11 i1="03" i2="1"><s1>EAGLE (Kim A.)</s1></fA11><fA11 i1="04" i2="1"><s1>ANDERSON (Frederick A. JR)</s1></fA11><fA11 i1="05" i2="1"><s1>FITZGERALD (Gordon)</s1></fA11><fA11 i1="06" i2="1"><s1>LEE (Michael S.)</s1></fA11><fA11 i1="07" i2="1"><s1>GABRIEL STEG (Ph.)</s1></fA11><fA11 i1="08" i2="1"><s1>AVEZUM (Alvaro)</s1></fA11><fA11 i1="09" i2="1"><s1>GOODMAN (Shaun G.)</s1></fA11><fA11 i1="10" i2="1"><s1>GORE (Joel M.)</s1></fA11><fA14 i1="01"><s1>Institut de Cardiologie, Bureau 2-236, Centre Hospitalier Universitaire Pitié-Salpêtrière, 47 Blvd de l'Hôpital</s1><s2>75013 Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Concord Hospital</s1><s2>Sydney, NSW</s2><s3>AUS</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>University of Michigan Cardiovascular Center</s1><s2>Ann Arbor, MI</s2><s3>USA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Center for Outcomes Research, University of Massachusetts Medical School</s1><s2>Worcester, MA</s2><s3>USA</s3><sZ>4 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>UCLA Medical Center, University of California, Los Angeles School of Medicine</s1><s2>Los Angeles, CA</s2><s3>USA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="06"><s1>Department of Cardiology, INSERM U-698, Université Paris 7 and Assistance Publique - Hôpitaux de Paris</s1><s2>Paris</s2><s3>FRA</s3><sZ>7 aut.</sZ></fA14><fA14 i1="07"><s1>Dante Pazzanese Institute of Cardiology</s1><s2>São Paulo</s2><s3>BRA</s3><sZ>8 aut.</sZ></fA14><fA14 i1="08"><s1>Canadian Heart Research Centre and Terrence Donnelly Heart Centre, Division of Cardiology, St. Michael's Hospital, University of Toronto</s1><s2>Toronto, ON</s2><s3>CAN</s3><sZ>9 aut.</sZ></fA14><fA20><s1>2308-2317</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>18785</s2><s5>354000170236160070</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>26 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0414803</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European heart journal</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Aims In acute coronary syndromes (ACS), the optimal revascularization strategy for unprotected left main coronary disease (ULMCD) has been little studied. The objectives of the present study were to describe the practice of ULMCD revascularization in ACS patients and its evolution over an 8-year period, analyse the prognosis of this population and determine the effect of revascularization on outcome. Methods Of 43 018 patients enrolled in the Global Registry of Acute Coronary Events (GRACE) between 2000 and 2007, and results 1799 had significant ULMCD and underwent percutaneous coronary intervention (PCI) alone (n = 514), coronary artery bypass graft (CABG) alone (n = 612), or no revascularization (n = 673). Mortality was 7.7% in hospital and 14% at 6 months. Over the 8-year study, the GRACE risk score remained constant, but there was a steady shift to more PCI than CABG over time. Patients undergoing PCI presented more frequently with ST-segment elevation myocardial infarction (STEMI), after cardiac arrest, or in cardiogenic shock; 48% of PCI patients underwent revascularization on the day of admission vs. 5.1 % in the CABG group. After adjustment, revascularization was associated with an early hazard of hospital death vs. no revascularization, significant for PCI (hazard ratio (HR) 2.60, 95% confidence interval (CI) 1.62-4.18) but not for CABG (1.26, 0.72-2.22). From discharge to 6 months, both PCI (HR 0.45, 95% Cl 0.23-0.85) and CABG (0.11, 0.04-0.28) were significantly associated with improved survival in comparison with an initial strategy of no revascularization. Coronary artery bypass graft revascularization was associated with a five-fold increase in stroke compared with the other two groups. Conclusion Unprotected left main coronary disease in ACS is associated with high mortality, especially in patients with STEMI and/or haemodynamic or arrhythmic instability. Percutaneous coronary intervention is now the most common revascularization strategy and preferred in higher risk patients. Coronary artery bypass graft is often delayed and performed in lower risk patients, leading to good 6-month survival. The two approaches therefore appear complementary.</s0></fC01><fC02 i1="01" i2="X"><s0>002B12A03</s0></fC02><fC02 i1="02" i2="X"><s0>002B12A05</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Gauche</s0><s5>09</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Left</s0><s5>09</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Izquierdo</s0><s5>09</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Revascularisation</s0><s5>10</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Revascularization</s0><s5>10</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Revascularización</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Homme</s0><s5>11</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Human</s0><s5>11</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Hombre</s0><s5>11</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Malade</s0><s5>12</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Patient</s0><s5>12</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Enfermo</s0><s5>12</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Maladie</s0><s5>13</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Disease</s0><s5>13</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Enfermedad</s0><s5>13</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Appareil circulatoire</s0><s5>14</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Circulatory system</s0><s5>14</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Aparato circulatorio</s0><s5>14</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Cardiologie</s0><s5>15</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Cardiology</s0><s5>15</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Cardiología</s0><s5>15</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Syndrome coronaire aigu</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Acute coronary syndrome</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Síndrome coronario agudo</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Pathologie de l'appareil circulatoire</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Cardiovascular disease</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Aparato circulatorio patología</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Cardiopathie coronaire</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Coronary heart disease</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Cardiopatía coronaria</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Pathologie du myocarde</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Myocardial disease</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Miocardio patología</s0><s5>39</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0414803 INIST</NO><ET>Unprotected left main revascularization in patients with acute coronary syndromes</ET><AU>MONTALESCOT (Gilles); BRIEGER (David); EAGLE (Kim A.); ANDERSON (Frederick A. JR); FITZGERALD (Gordon); LEE (Michael S.); GABRIEL STEG (Ph.); AVEZUM (Alvaro); GOODMAN (Shaun G.); GORE (Joel M.)</AU><AF>Institut de Cardiologie, Bureau 2-236, Centre Hospitalier Universitaire Pitié-Salpêtrière, 47 Blvd de l'Hôpital/75013 Paris/France (1 aut.); Concord Hospital/Sydney, NSW/Australie (2 aut.); University of Michigan Cardiovascular Center/Ann Arbor, MI/Etats-Unis (3 aut.); Center for Outcomes Research, University of Massachusetts Medical School/Worcester, MA/Etats-Unis (4 aut., 5 aut.); UCLA Medical Center, University of California, Los Angeles School of Medicine/Los Angeles, CA/Etats-Unis (6 aut.); Department of Cardiology, INSERM U-698, Université Paris 7 and Assistance Publique - Hôpitaux de Paris/Paris/France (7 aut.); Dante Pazzanese Institute of Cardiology/São Paulo/Brésil (8 aut.); Canadian Heart Research Centre and Terrence Donnelly Heart Centre, Division of Cardiology, St. Michael's Hospital, University of Toronto/Toronto, ON/Canada (9 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>European heart journal; ISSN 0195-668X; Royaume-Uni; Da. 2009; Vol. 30; No. 19; Pp. 2308-2317; Bibl. 26 ref.</SO><LA>Anglais</LA><EA>Aims In acute coronary syndromes (ACS), the optimal revascularization strategy for unprotected left main coronary disease (ULMCD) has been little studied. The objectives of the present study were to describe the practice of ULMCD revascularization in ACS patients and its evolution over an 8-year period, analyse the prognosis of this population and determine the effect of revascularization on outcome. Methods Of 43 018 patients enrolled in the Global Registry of Acute Coronary Events (GRACE) between 2000 and 2007, and results 1799 had significant ULMCD and underwent percutaneous coronary intervention (PCI) alone (n = 514), coronary artery bypass graft (CABG) alone (n = 612), or no revascularization (n = 673). Mortality was 7.7% in hospital and 14% at 6 months. Over the 8-year study, the GRACE risk score remained constant, but there was a steady shift to more PCI than CABG over time. Patients undergoing PCI presented more frequently with ST-segment elevation myocardial infarction (STEMI), after cardiac arrest, or in cardiogenic shock; 48% of PCI patients underwent revascularization on the day of admission vs. 5.1 % in the CABG group. After adjustment, revascularization was associated with an early hazard of hospital death vs. no revascularization, significant for PCI (hazard ratio (HR) 2.60, 95% confidence interval (CI) 1.62-4.18) but not for CABG (1.26, 0.72-2.22). From discharge to 6 months, both PCI (HR 0.45, 95% Cl 0.23-0.85) and CABG (0.11, 0.04-0.28) were significantly associated with improved survival in comparison with an initial strategy of no revascularization. Coronary artery bypass graft revascularization was associated with a five-fold increase in stroke compared with the other two groups. Conclusion Unprotected left main coronary disease in ACS is associated with high mortality, especially in patients with STEMI and/or haemodynamic or arrhythmic instability. Percutaneous coronary intervention is now the most common revascularization strategy and preferred in higher risk patients. Coronary artery bypass graft is often delayed and performed in lower risk patients, leading to good 6-month survival. The two approaches therefore appear complementary.</EA><CC>002B12A03; 002B12A05</CC><FD>Gauche; Revascularisation; Homme; Malade; Maladie; Appareil circulatoire; Cardiologie; Syndrome coronaire aigu</FD><FG>Pathologie de l'appareil circulatoire; Cardiopathie coronaire; Pathologie du myocarde</FG><ED>Left; Revascularization; Human; Patient; Disease; Circulatory system; Cardiology; Acute coronary syndrome</ED><EG>Cardiovascular disease; Coronary heart disease; Myocardial disease</EG><SD>Izquierdo; Revascularización; Hombre; Enfermo; Enfermedad; Aparato circulatorio; Cardiología; Síndrome coronario agudo</SD><LO>INIST-18785.354000170236160070</LO><ID>09-0414803</ID></server></inist></record>
000D91	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Depletion of soil organic carbon and nitrogen under Pinus taeda plantations in Southern Brazilian grasslands ( Campos)</title><author><name sortKey="Wiesmeier, M" uniqKey="Wiesmeier M">M. Wiesmeier</name><affiliation><inist:fA14 i1="01"><s1>Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München</s1><s2>85350 Freising-Weihenstephan</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dick, D P" uniqKey="Dick D">D. P. Dick</name><affiliation><inist:fA14 i1="02"><s1>Instituto de Quimica, UFRGS, Avenida Bento Gonçalves, 9500</s1><s2>CEP 91501-970, Porto Alegre, RS</s2><s3>BRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Rumpel, C" uniqKey="Rumpel C">C. Rumpel</name><affiliation><inist:fA14 i1="03"><s1>CNRS, Laboratoire de Biogeochimie des Milieux Continentaux, (UMR CNRS, INRA, Université Paris VI, IRD), Campus AgroParisTech, Batiment EGER</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dalmolin, R S D" uniqKey="Dalmolin R">R. S. D. Dalmolin</name><affiliation><inist:fA14 i1="04"><s1>Departamento de Solos, UFSM, Campus Universitário</s1><s2>Santa Maria, RS, CEP 97105-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hilscher, A" uniqKey="Hilscher A">A. Hilscher</name><affiliation><inist:fA14 i1="01"><s1>Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München</s1><s2>85350 Freising-Weihenstephan</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Knicker, H" uniqKey="Knicker H">H. Knicker</name><affiliation><inist:fA14 i1="01"><s1>Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München</s1><s2>85350 Freising-Weihenstephan</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0414862</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0414862 INIST</idno><idno type="RBID">Pascal:09-0414862</idno><idno type="wicri:Area/Main/Corpus">001B93</idno></publicationStmt><seriesStmt><idno type="ISSN">1351-0754</idno><title level="j" type="abbreviated">Eur. j. soil sci.</title><title level="j" type="main">European journal of soil science</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Decrease</term><term>Depletion</term><term>Earth science</term><term>Organic nitrogen</term><term>Pinus taeda</term><term>Plantations</term><term>Soil science</term><term>grasslands</term><term>organic carbon</term><term>soils</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Déplétion</term><term>Diminution</term><term>Prairie</term><term>Science terre</term><term>Science du sol</term><term>Pinus taeda</term><term>Carbone organique</term><term>Azote organique</term><term>Brésil</term><term>Sol</term><term>Plantations</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Establishment of pine (Pinus spp.) plantations on grasslands could increase carbon (C) sequestration to counteract increased atmospheric carbon dioxide concentrations. In the grasslands of the southern Brazilian highland (Campos), large areas have been converted to Pinus plantations over the last 30 years. In order to assess the impact of this land-use change on the amount and composition of soil organic matter (SOM), we investigated a grassland pasture site (G), and both an 8-year-old (P8) and a 30-year-old (P30) plantation with Pinus taeda. Soil samples down to 45 cm were analysed for texture, pH, soil organic carbon (SOC) and total nitrogen (N<sub>tot</sub>) concentrations. Chemical composition of SOM was determined by using cross-polarization magic angle spinning (CPMAS) <sup>13</sup>C NMR spectroscopy. We analysed for stable C isotope (δ<sup>13</sup>C) and assessed the lignin composition by CuO oxidation. Additionally, contents of pyrogenic organic material (PyOM) were determined because the Campos is regularly burnt. Both pine plantations revealed<sup> </sup>relatively small SOC concentrations in the mineral soil of 72.6 mg g<sup>-1</sup> (P8) and 56.8 mg g<sup>-1</sup> (P30) and N<sub>tot</sub> concentrations of 4.0 mg g<sup>-1</sup> (P8) and 2.9 mg g<sup>-1</sup> (P30) for the A horizon, while grassland showed significantly (P &#60; 0.01) larger contents of 100.2 mg g<sup>-1</sup> for SOC and 5.9 mg g<sup>-1</sup> for N<sub>tot</sub>. Accumulation of litter layers suggests decreased input of organic material into the mineral soil under pine, which was confirmed by the δ<sup>13</sup>C values and lignin composition. Smaller contents of vanillyl- (V), syringyl- (S), and cinnamyl (C)-phenols, smaller ratios of S/V and C/V, and smaller ratios of acidic to aldehydic forms of V and S phenols indicated a high degree of decomposition of residual grass-derived SOM in the upper part of the mineral soil (0-10 cm) under pine plantations. This was confirmed by CPMAS <sup>13</sup>C NMR spectroscopy, showing an increasing Alkyl C/O-Alkyl C ratio at the same depth. No significant changes in the contents of PyOM could be detected, but all sites tended to show the greatest concentrations at deeper soil depths &#62; 15 cm, indicating a vertical relocation of PyOM. The results suggest that decomposition of residual SOM originating from grassland species contributes to the decrease of SOC and N<sub>tot</sub> and to an acidification in the topsoil under pine plantations. We also suggest that slow litter decomposition and incorporation and the absence of fires at the plantations are additional reasons for the reduced amount of SOM. Depletion of SOM and the acidification of the topsoil may reduce the availability and supply of nutrients and diminish the C sequestration potential of the mineral soil.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1351-0754</s0></fA01><fA03 i2="1"><s0>Eur. j. soil sci.</s0></fA03><fA05><s2>60</s2></fA05><fA06><s2>3</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Depletion of soil organic carbon and nitrogen under Pinus taeda plantations in Southern Brazilian grasslands ( Campos)</s1></fA08><fA11 i1="01" i2="1"><s1>WIESMEIER (M.)</s1></fA11><fA11 i1="02" i2="1"><s1>DICK (D. P.)</s1></fA11><fA11 i1="03" i2="1"><s1>RUMPEL (C.)</s1></fA11><fA11 i1="04" i2="1"><s1>DALMOLIN (R. S. D.)</s1></fA11><fA11 i1="05" i2="1"><s1>HILSCHER (A.)</s1></fA11><fA11 i1="06" i2="1"><s1>KNICKER (H.)</s1></fA11><fA14 i1="01"><s1>Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München</s1><s2>85350 Freising-Weihenstephan</s2><s3>DEU</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>Instituto de Quimica, UFRGS, Avenida Bento Gonçalves, 9500</s1><s2>CEP 91501-970, Porto Alegre, RS</s2><s3>BRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>CNRS, Laboratoire de Biogeochimie des Milieux Continentaux, (UMR CNRS, INRA, Université Paris VI, IRD), Campus AgroParisTech, Batiment EGER</s1><s2>78850 Thiverval-Grignon</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Departamento de Solos, UFSM, Campus Universitário</s1><s2>Santa Maria, RS, CEP 97105-900</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA20><s1>347-359</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>2402</s2><s5>354000186114500050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/2</s0></fA45><fA47 i1="01" i2="1"><s0>09-0414862</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>European journal of soil science</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Establishment of pine (Pinus spp.) plantations on grasslands could increase carbon (C) sequestration to counteract increased atmospheric carbon dioxide concentrations. In the grasslands of the southern Brazilian highland (Campos), large areas have been converted to Pinus plantations over the last 30 years. In order to assess the impact of this land-use change on the amount and composition of soil organic matter (SOM), we investigated a grassland pasture site (G), and both an 8-year-old (P8) and a 30-year-old (P30) plantation with Pinus taeda. Soil samples down to 45 cm were analysed for texture, pH, soil organic carbon (SOC) and total nitrogen (N<sub>tot</sub>) concentrations. Chemical composition of SOM was determined by using cross-polarization magic angle spinning (CPMAS) <sup>13</sup>C NMR spectroscopy. We analysed for stable C isotope (δ<sup>13</sup>C) and assessed the lignin composition by CuO oxidation. Additionally, contents of pyrogenic organic material (PyOM) were determined because the Campos is regularly burnt. Both pine plantations revealed<sup> </sup>relatively small SOC concentrations in the mineral soil of 72.6 mg g<sup>-1</sup> (P8) and 56.8 mg g<sup>-1</sup> (P30) and N<sub>tot</sub> concentrations of 4.0 mg g<sup>-1</sup> (P8) and 2.9 mg g<sup>-1</sup> (P30) for the A horizon, while grassland showed significantly (P &#60; 0.01) larger contents of 100.2 mg g<sup>-1</sup> for SOC and 5.9 mg g<sup>-1</sup> for N<sub>tot</sub>. Accumulation of litter layers suggests decreased input of organic material into the mineral soil under pine, which was confirmed by the δ<sup>13</sup>C values and lignin composition. Smaller contents of vanillyl- (V), syringyl- (S), and cinnamyl (C)-phenols, smaller ratios of S/V and C/V, and smaller ratios of acidic to aldehydic forms of V and S phenols indicated a high degree of decomposition of residual grass-derived SOM in the upper part of the mineral soil (0-10 cm) under pine plantations. This was confirmed by CPMAS <sup>13</sup>C NMR spectroscopy, showing an increasing Alkyl C/O-Alkyl C ratio at the same depth. No significant changes in the contents of PyOM could be detected, but all sites tended to show the greatest concentrations at deeper soil depths &#62; 15 cm, indicating a vertical relocation of PyOM. The results suggest that decomposition of residual SOM originating from grassland species contributes to the decrease of SOC and N<sub>tot</sub> and to an acidification in the topsoil under pine plantations. We also suggest that slow litter decomposition and incorporation and the absence of fires at the plantations are additional reasons for the reduced amount of SOM. Depletion of SOM and the acidification of the topsoil may reduce the availability and supply of nutrients and diminish the C sequestration potential of the mineral soil.</s0></fC01><fC02 i1="01" i2="2"><s0>001E01P03</s0></fC02><fC02 i1="02" i2="X"><s0>002A32B03B3</s0></fC02><fC02 i1="03" i2="2"><s0>226C03</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Déplétion</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Depletion</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Depleción</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Diminution</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Decrease</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Disminución</s0><s5>02</s5></fC03><fC03 i1="03" i2="2" l="FRE"><s0>Prairie</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="ENG"><s0>grasslands</s0><s5>03</s5></fC03><fC03 i1="03" i2="2" l="SPA"><s0>Pradera</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Science terre</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Earth science</s0><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Ciencia tierra</s0><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Science du sol</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Soil science</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Ciencia del suelo</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Pinus taeda</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Pinus taeda</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Pinus taeda</s0><s2>NS</s2><s5>10</s5></fC03><fC03 i1="07" i2="2" l="FRE"><s0>Carbone organique</s0><s5>15</s5></fC03><fC03 i1="07" i2="2" l="ENG"><s0>organic carbon</s0><s5>15</s5></fC03><fC03 i1="07" i2="2" l="SPA"><s0>Carbono orgánico</s0><s5>15</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Azote organique</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Organic nitrogen</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Nitrógeno orgánico</s0><s2>NK</s2><s5>16</s5></fC03><fC03 i1="09" i2="2" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="09" i2="2" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="09" i2="2" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>20</s5></fC03><fC03 i1="10" i2="2" l="FRE"><s0>Sol</s0><s2>NT</s2><s5>24</s5></fC03><fC03 i1="10" i2="2" l="ENG"><s0>soils</s0><s2>NT</s2><s5>24</s5></fC03><fC03 i1="10" i2="2" l="SPA"><s0>Suelo</s0><s2>NT</s2><s5>24</s5></fC03><fC03 i1="11" i2="2" l="FRE"><s0>Plantations</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="2" l="ENG"><s0>Plantations</s0><s4>CD</s4><s5>96</s5></fC03><fC03 i1="11" i2="2" l="SPA"><s0>Plantationes</s0><s4>CD</s4><s5>96</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Coniferales</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Gymnospermae</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="04" i2="2" l="FRE"><s0>Amérique du Sud</s0><s2>564</s2></fC07><fC07 i1="04" i2="2" l="ENG"><s0>South America</s0><s2>564</s2></fC07><fC07 i1="04" i2="2" l="SPA"><s0>America del sur</s0><s2>564</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Arbre forestier résineux</s0><s5>31</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Softwood forest tree</s0><s5>31</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Arbol forestal resinoso</s0><s5>31</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Arbre forestier</s0><s5>32</s5></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Forest tree</s0><s5>32</s5></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Arbol forestal</s0><s5>32</s5></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Plante ligneuse</s0><s5>39</s5></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Woody plant</s0><s5>39</s5></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Planta leñosa</s0><s5>39</s5></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Végétal</s0><s5>40</s5></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Vegetals</s0><s5>40</s5></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Vegetal</s0><s5>40</s5></fC07><fC07 i1="09" i2="2" l="FRE"><s0>Matière organique</s0><s5>50</s5></fC07><fC07 i1="09" i2="2" l="ENG"><s0>organic materials</s0><s5>50</s5></fC07><fC07 i1="09" i2="2" l="SPA"><s0>Materia orgánica</s0><s5>50</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0414862 INIST</NO><ET>Depletion of soil organic carbon and nitrogen under Pinus taeda plantations in Southern Brazilian grasslands ( Campos)</ET><AU>WIESMEIER (M.); DICK (D. P.); RUMPEL (C.); DALMOLIN (R. S. D.); HILSCHER (A.); KNICKER (H.)</AU><AF>Lehrstuhl für Bodenkunde, Department für Ökologie und Ökosystemmanagement, Wissenschaftszentrum Weihenstephan für Ernährung, Landnutzung und Umwelt, Technische Universität München/85350 Freising-Weihenstephan/Allemagne (1 aut., 5 aut., 6 aut.); Instituto de Quimica, UFRGS, Avenida Bento Gonçalves, 9500/CEP 91501-970, Porto Alegre, RS/Brésil (2 aut.); CNRS, Laboratoire de Biogeochimie des Milieux Continentaux, (UMR CNRS, INRA, Université Paris VI, IRD), Campus AgroParisTech, Batiment EGER/78850 Thiverval-Grignon/France (3 aut.); Departamento de Solos, UFSM, Campus Universitário/Santa Maria, RS, CEP 97105-900/Brésil (4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>European journal of soil science; ISSN 1351-0754; Royaume-Uni; Da. 2009; Vol. 60; No. 3; Pp. 347-359; Bibl. 1 p.1/2</SO><LA>Anglais</LA><EA>Establishment of pine (Pinus spp.) plantations on grasslands could increase carbon (C) sequestration to counteract increased atmospheric carbon dioxide concentrations. In the grasslands of the southern Brazilian highland (Campos), large areas have been converted to Pinus plantations over the last 30 years. In order to assess the impact of this land-use change on the amount and composition of soil organic matter (SOM), we investigated a grassland pasture site (G), and both an 8-year-old (P8) and a 30-year-old (P30) plantation with Pinus taeda. Soil samples down to 45 cm were analysed for texture, pH, soil organic carbon (SOC) and total nitrogen (N<sub>tot</sub>) concentrations. Chemical composition of SOM was determined by using cross-polarization magic angle spinning (CPMAS) <sup>13</sup>C NMR spectroscopy. We analysed for stable C isotope (δ<sup>13</sup>C) and assessed the lignin composition by CuO oxidation. Additionally, contents of pyrogenic organic material (PyOM) were determined because the Campos is regularly burnt. Both pine plantations revealed<sup> </sup>relatively small SOC concentrations in the mineral soil of 72.6 mg g<sup>-1</sup> (P8) and 56.8 mg g<sup>-1</sup> (P30) and N<sub>tot</sub> concentrations of 4.0 mg g<sup>-1</sup> (P8) and 2.9 mg g<sup>-1</sup> (P30) for the A horizon, while grassland showed significantly (P &#60; 0.01) larger contents of 100.2 mg g<sup>-1</sup> for SOC and 5.9 mg g<sup>-1</sup> for N<sub>tot</sub>. Accumulation of litter layers suggests decreased input of organic material into the mineral soil under pine, which was confirmed by the δ<sup>13</sup>C values and lignin composition. Smaller contents of vanillyl- (V), syringyl- (S), and cinnamyl (C)-phenols, smaller ratios of S/V and C/V, and smaller ratios of acidic to aldehydic forms of V and S phenols indicated a high degree of decomposition of residual grass-derived SOM in the upper part of the mineral soil (0-10 cm) under pine plantations. This was confirmed by CPMAS <sup>13</sup>C NMR spectroscopy, showing an increasing Alkyl C/O-Alkyl C ratio at the same depth. No significant changes in the contents of PyOM could be detected, but all sites tended to show the greatest concentrations at deeper soil depths &#62; 15 cm, indicating a vertical relocation of PyOM. The results suggest that decomposition of residual SOM originating from grassland species contributes to the decrease of SOC and N<sub>tot</sub> and to an acidification in the topsoil under pine plantations. We also suggest that slow litter decomposition and incorporation and the absence of fires at the plantations are additional reasons for the reduced amount of SOM. Depletion of SOM and the acidification of the topsoil may reduce the availability and supply of nutrients and diminish the C sequestration potential of the mineral soil.</EA><CC>001E01P03; 002A32B03B3; 226C03</CC><FD>Déplétion; Diminution; Prairie; Science terre; Science du sol; Pinus taeda; Carbone organique; Azote organique; Brésil; Sol; Plantations</FD><FG>Coniferales; Gymnospermae; Spermatophyta; Amérique du Sud; Arbre forestier résineux; Arbre forestier; Plante ligneuse; Végétal; Matière organique</FG><ED>Depletion; Decrease; grasslands; Earth science; Soil science; Pinus taeda; organic carbon; Organic nitrogen; Brazil; soils; Plantations</ED><EG>Coniferales; Gymnospermae; Spermatophyta; South America; Softwood forest tree; Forest tree; Woody plant; Vegetals; organic materials</EG><SD>Depleción; Disminución; Pradera; Ciencia tierra; Ciencia del suelo; Pinus taeda; Carbono orgánico; Nitrógeno orgánico; Brasil; Suelo; Plantationes</SD><LO>INIST-2402.354000186114500050</LO><ID>09-0414862</ID></server></inist></record>
000D92	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">La diversité biologique et culturelle dans les démarches de qualité et de valorisation de l'origine au Sud Brésil</title><author><name sortKey="Cerdan, Claire" uniqKey="Cerdan C">Claire Cerdan</name><affiliation><inist:fA14 i1="01"><s1>Cirad UMR Innovation, Sup'Agro-Cirad-Inra UMR951 « Innovation », UFSC Floriano-polis</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Vitrolles, Delphine" uniqKey="Vitrolles D">Delphine Vitrolles</name><affiliation><inist:fA14 i1="02"><s1>Laboratoire d'Études Rurales, Université Lumière Lyon 2</s1><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Delfosse, Claire" uniqKey="Delfosse C">Claire Delfosse</name><affiliation><inist:fA14 i1="03"><s1>Laboratoire d'Études Rurales, Université Lumière Lyon 2</s1><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Quiumento Velloso, Carolina" uniqKey="Quiumento Velloso C">Carolina Quiumento Velloso</name><affiliation><inist:fA14 i1="04"><s1>Centre de Sciences Agraires de l'Université Fédérale de Santa Catarina (CCA / UFSC)</s1><s3>FRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Nabinger, Carlos" uniqKey="Nabinger C">Carlos Nabinger</name><affiliation><inist:fA14 i1="05"><s1>Université Fédérale de Rio Grande do Sul, Faculté d'Agronomie, Département de Plantes Fourragères et d'Agro-météorologie</s1><s3>FRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lima Da Silva, Aparecido" uniqKey="Lima Da Silva A">Aparecido Lima Da Silva</name><affiliation><inist:fA14 i1="06"><s1>Université Fédérale de Santa Catarina, Centre de Sciences Agraires, Département de Phytotechnie</s1><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0415205</idno><date when="2009">2009</date><idno type="stanalyst">FRANCIS 09-0415205 INIST</idno><idno type="RBID">Francis:09-0415205</idno><idno type="wicri:Area/Main/Corpus">001F87</idno></publicationStmt><seriesStmt><idno type="ISSN">1278-3986</idno><title level="j" type="abbreviated">Autrepart : (La Tour d' Aigues)</title><title level="j" type="main">Autrepart : (La Tour d'Aigues)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cultural diversity</term><term>Meat</term><term>Origin</term><term>Ox</term><term>Promotion (Occupational)</term><term>Protection of the patrimony</term><term>Quality</term><term>Self-actualization</term><term>South</term><term>South America</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Diversité culturelle</term><term>Qualité</term><term>Valorisation</term><term>Origine</term><term>Sud</term><term>Amérique du Sud</term><term>Promotion</term><term>Viande</term><term>Boeuf</term><term>Protection du patrimoine</term><term>Diversité biologique</term><term>Indication géographique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Notre article analyse comment les acteurs dans les États de Santa Catarina et Rio Grande do Sul au Brésil élaborent et mettent en oeuvre des dispositifs de valorisation des spécialités locales. Dans le cadre de ces dispositifs la prise en compte de la diversité biologique et culturelle s'impose, au moins de façon indirecte. L'article repose sur l'étude de deux expériences de promotion par l'origine, la viande de boeuf produite dans les prairies de la Pampa Brésilienne (protégée par une indication géographique ou IG depuis 2006) et le vin élaboré dans la région d'Urussanga (demande d'IG en cours). Celles-ci s'inscrivent, au niveau brésilien, dans des débats sur les IG et sur la protection du patrimoine national.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1278-3986</s0></fA01><fA03 i2="1"><s0>Autrepart : (La Tour d' Aigues)</s0></fA03><fA06><s2>50</s2></fA06><fA08 i1="01" i2="1" l="FRE"><s1>La diversité biologique et culturelle dans les démarches de qualité et de valorisation de l'origine au Sud Brésil</s1></fA08><fA09 i1="01" i2="1" l="FRE"><s1>Les produits de terroir au service de la diversité biologique et culturelle ?</s1></fA09><fA11 i1="01" i2="1"><s1>CERDAN (Claire)</s1></fA11><fA11 i1="02" i2="1"><s1>VITROLLES (Delphine)</s1></fA11><fA11 i1="03" i2="1"><s1>DELFOSSE (Claire)</s1></fA11><fA11 i1="04" i2="1"><s1>QUIUMENTO VELLOSO (Carolina)</s1></fA11><fA11 i1="05" i2="1"><s1>NABINGER (Carlos)</s1></fA11><fA11 i1="06" i2="1"><s1>LIMA DA SILVA (Aparecido)</s1></fA11><fA12 i1="01" i2="1"><s1>CORMIER-SALEM (Marie-Christine)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>ROUSSEL (Bernard)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Cirad UMR Innovation, Sup'Agro-Cirad-Inra UMR951 « Innovation », UFSC Floriano-polis</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Laboratoire d'Études Rurales, Université Lumière Lyon 2</s1><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Laboratoire d'Études Rurales, Université Lumière Lyon 2</s1><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Centre de Sciences Agraires de l'Université Fédérale de Santa Catarina (CCA / UFSC)</s1><s3>FRA</s3><sZ>4 aut.</sZ></fA14><fA14 i1="05"><s1>Université Fédérale de Rio Grande do Sul, Faculté d'Agronomie, Département de Plantes Fourragères et d'Agro-météorologie</s1><s3>FRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="06"><s1>Université Fédérale de Santa Catarina, Centre de Sciences Agraires, Département de Phytotechnie</s1><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA15 i1="01"><s1>Institut de recherche pour le développement (IRD), UMR 208 (IRD/MNHN)</s1><s2>Paris</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Muséum national d'histoire naturelle (MNHN), UMR 208 (IRD/MNHN)</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA15><fA20><s2>153-166, 208, 212 [16 p.]</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>10882E</s2><s5>354000188228670080</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/2</s0></fA45><fA47 i1="01" i2="1"><s0>09-0415205</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Autrepart : (La Tour d'Aigues)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA68 i1="01" i2="1" l="ENG"><s1>Biological and cultural diversity in the process designed to enhance the value of quality and origin in the South of Brazil</s1></fA68><fA69 i1="01" i2="1" l="ENG"><s1>The products of land in the service of biological and cultural diversity?</s1></fA69><fC01 i1="01" l="FRE"><s0>Notre article analyse comment les acteurs dans les États de Santa Catarina et Rio Grande do Sul au Brésil élaborent et mettent en oeuvre des dispositifs de valorisation des spécialités locales. Dans le cadre de ces dispositifs la prise en compte de la diversité biologique et culturelle s'impose, au moins de façon indirecte. L'article repose sur l'étude de deux expériences de promotion par l'origine, la viande de boeuf produite dans les prairies de la Pampa Brésilienne (protégée par une indication géographique ou IG depuis 2006) et le vin élaboré dans la région d'Urussanga (demande d'IG en cours). Celles-ci s'inscrivent, au niveau brésilien, dans des débats sur les IG et sur la protection du patrimoine national.</s0></fC01><fC02 i1="01" i2="N"><s0>52940B</s0><s1>III</s1></fC02><fC02 i1="02" i2="N"><s0>52942B</s0><s1>III</s1></fC02><fC02 i1="03" i2="N"><s0>529</s0></fC02><fC03 i1="01" i2="N" l="FRE"><s0>Diversité culturelle</s0><s2>NI</s2><s5>01</s5></fC03><fC03 i1="01" i2="N" l="ENG"><s0>Cultural diversity</s0><s2>NI</s2><s5>01</s5></fC03><fC03 i1="02" i2="S" l="FRE"><s0>Qualité</s0><s5>02</s5></fC03><fC03 i1="02" i2="S" l="ENG"><s0>Quality</s0><s5>02</s5></fC03><fC03 i1="03" i2="S" l="FRE"><s0>Valorisation</s0><s5>03</s5></fC03><fC03 i1="03" i2="S" l="ENG"><s0>Self-actualization</s0><s5>03</s5></fC03><fC03 i1="04" i2="N" l="FRE"><s0>Origine</s0><s5>04</s5></fC03><fC03 i1="04" i2="N" l="ENG"><s0>Origin</s0><s5>04</s5></fC03><fC03 i1="05" i2="N" l="FRE"><s0>Sud</s0><s5>05</s5></fC03><fC03 i1="05" i2="N" l="ENG"><s0>South</s0><s5>05</s5></fC03><fC03 i1="06" i2="N" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="06" i2="N" l="ENG"><s0>South America</s0><s2>NG</s2><s5>06</s5></fC03><fC03 i1="07" i2="S" l="FRE"><s0>Promotion</s0><s5>07</s5></fC03><fC03 i1="07" i2="S" l="ENG"><s0>Promotion (Occupational)</s0><s5>07</s5></fC03><fC03 i1="08" i2="N" l="FRE"><s0>Viande</s0><s5>08</s5></fC03><fC03 i1="08" i2="N" l="ENG"><s0>Meat</s0><s5>08</s5></fC03><fC03 i1="09" i2="N" l="FRE"><s0>Boeuf</s0><s5>09</s5></fC03><fC03 i1="09" i2="N" l="ENG"><s0>Ox</s0><s5>09</s5></fC03><fC03 i1="10" i2="N" l="FRE"><s0>Protection du patrimoine</s0><s5>10</s5></fC03><fC03 i1="10" i2="N" l="ENG"><s0>Protection of the patrimony</s0><s5>10</s5></fC03><fC03 i1="11" i2="N" l="FRE"><s0>Diversité biologique</s0><s4>INC</s4><s5>26</s5></fC03><fC03 i1="12" i2="N" l="FRE"><s0>Indication géographique</s0><s4>INC</s4><s5>27</s5></fC03><fN21><s1>299</s1></fN21></pA></standard><server><NO>FRANCIS 09-0415205 INIST</NO><FT>La diversité biologique et culturelle dans les démarches de qualité et de valorisation de l'origine au Sud Brésil</FT><ET>(Biological and cultural diversity in the process designed to enhance the value of quality and origin in the South of Brazil)</ET><AU>CERDAN (Claire); VITROLLES (Delphine); DELFOSSE (Claire); QUIUMENTO VELLOSO (Carolina); NABINGER (Carlos); LIMA DA SILVA (Aparecido); CORMIER-SALEM (Marie-Christine); ROUSSEL (Bernard)</AU><AF>Cirad UMR Innovation, Sup'Agro-Cirad-Inra UMR951 « Innovation », UFSC Floriano-polis/Brésil (1 aut.); Laboratoire d'Études Rurales, Université Lumière Lyon 2/France (2 aut.); Laboratoire d'Études Rurales, Université Lumière Lyon 2/France (3 aut.); Centre de Sciences Agraires de l'Université Fédérale de Santa Catarina (CCA / UFSC)/France (4 aut.); Université Fédérale de Rio Grande do Sul, Faculté d'Agronomie, Département de Plantes Fourragères et d'Agro-météorologie/France (5 aut.); Université Fédérale de Santa Catarina, Centre de Sciences Agraires, Département de Phytotechnie/France (6 aut.); Institut de recherche pour le développement (IRD), UMR 208 (IRD/MNHN)/Paris/France (1 aut.); Muséum national d'histoire naturelle (MNHN), UMR 208 (IRD/MNHN)/Paris/France (2 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Autrepart : (La Tour d'Aigues); ISSN 1278-3986; France; Da. 2009; No. 50; 153-166, 208, 212 [16 p.]; Abs. anglais; Bibl. 1 p.1/2</SO><LA>Français</LA><FA>Notre article analyse comment les acteurs dans les États de Santa Catarina et Rio Grande do Sul au Brésil élaborent et mettent en oeuvre des dispositifs de valorisation des spécialités locales. Dans le cadre de ces dispositifs la prise en compte de la diversité biologique et culturelle s'impose, au moins de façon indirecte. L'article repose sur l'étude de deux expériences de promotion par l'origine, la viande de boeuf produite dans les prairies de la Pampa Brésilienne (protégée par une indication géographique ou IG depuis 2006) et le vin élaboré dans la région d'Urussanga (demande d'IG en cours). Celles-ci s'inscrivent, au niveau brésilien, dans des débats sur les IG et sur la protection du patrimoine national.</FA><CC>52940B; 52942B; 529</CC><FD>Diversité culturelle; Qualité; Valorisation; Origine; Sud; Amérique du Sud; Promotion; Viande; Boeuf; Protection du patrimoine; Diversité biologique; Indication géographique</FD><ED>Cultural diversity; Quality; Self-actualization; Origin; South; South America; Promotion (Occupational); Meat; Ox; Protection of the patrimony</ED><LO>INIST-10882E.354000188228670080</LO><ID>09-0415205</ID></server></inist></record>
000D93	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Physicochemical and morphological characterisation of açai (Euterpe oleraceae Mart.) powder produced with different carrier agents</title><author><name sortKey="Tonon, Renata V" uniqKey="Tonon R">Renata V. Tonon</name><affiliation><inist:fA14 i1="01"><s1>Faculty of Food Engineering - State University of Campinas, PO Box 6121</s1><s2>13083-862, Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brabet, Catherine" uniqKey="Brabet C">Catherine Brabet</name><affiliation><inist:fA14 i1="02"><s1>Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Department PERSYST- UMR QualiSud</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pallet, Dominique" uniqKey="Pallet D">Dominique Pallet</name><affiliation><inist:fA14 i1="02"><s1>Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Department PERSYST- UMR QualiSud</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Brat, Pierre" uniqKey="Brat P">Pierre Brat</name><affiliation><inist:fA14 i1="02"><s1>Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Department PERSYST- UMR QualiSud</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hubinger, Miriam D" uniqKey="Hubinger M">Miriam D. Hubinger</name><affiliation><inist:fA14 i1="01"><s1>Faculty of Food Engineering - State University of Campinas, PO Box 6121</s1><s2>13083-862, Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0415430</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0415430 INIST</idno><idno type="RBID">Pascal:09-0415430</idno><idno type="wicri:Area/Main/Corpus">001B92</idno></publicationStmt><seriesStmt><idno type="ISSN">0950-5423</idno><title level="j" type="abbreviated">Int. j. food sci. technol.</title><title level="j" type="main">International journal of food science &#38; technology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Morphology</term><term>Physicochemical properties</term><term>Powder</term><term>Spray drying</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Morphologie</term><term>Poudre</term><term>Propriété physicochimique</term><term>Séchage pulvérisation</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Physicochemical and morphological properties of açai powder produced with different carrier agents were evaluated in this work. Powders were produced by spray drying, using maltodextrin 10DE, maltodextrin 20DE, gum arabic and tapioca starch as carrier agents. Powder characterisation included analysis of moisture content, water activity, solubility, hygroscopicity, particle size distribution, morphology, total polyphenolics and antioxidant activity. Results showed that the samples produced with maltodextrin 20DE and gum arabic presented the smallest size and highest hygroscopicity. The powder produced with tapioca starch exhibited the lowest hygroscopity and solubility, and the highest mean diameter. With regard to morphology, all particles exhibited spherical and shrivelled surfaces, except those produced with tapioca starch, which exhibited rounded and smooth surfaces. Powders produced with maltodextrins and gum arabic showed high polyphenolic retention and antioxidant activity preservation after storage at 40 °C for 15 days, while for the particles produced with tapioca starch, this protective effect was less pronounced.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0950-5423</s0></fA01><fA02 i1="01"><s0>IJFTEZ</s0></fA02><fA03 i2="1"><s0>Int. j. food sci. technol.</s0></fA03><fA05><s2>44</s2></fA05><fA06><s2>10</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Physicochemical and morphological characterisation of açai (Euterpe oleraceae Mart.) powder produced with different carrier agents</s1></fA08><fA11 i1="01" i2="1"><s1>TONON (Renata V.)</s1></fA11><fA11 i1="02" i2="1"><s1>BRABET (Catherine)</s1></fA11><fA11 i1="03" i2="1"><s1>PALLET (Dominique)</s1></fA11><fA11 i1="04" i2="1"><s1>BRAT (Pierre)</s1></fA11><fA11 i1="05" i2="1"><s1>HUBINGER (Miriam D.)</s1></fA11><fA14 i1="01"><s1>Faculty of Food Engineering - State University of Campinas, PO Box 6121</s1><s2>13083-862, Campinas, SP</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="02"><s1>Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Department PERSYST- UMR QualiSud</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA14><fA20><s1>1950-1958</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>13345</s2><s5>354000171965520110</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>3/4 p.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0415430</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of food science &#38; technology</s0></fA64><fA66 i1="01"><s0>GBR</s0></fA66><fC01 i1="01" l="ENG"><s0>Physicochemical and morphological properties of açai powder produced with different carrier agents were evaluated in this work. Powders were produced by spray drying, using maltodextrin 10DE, maltodextrin 20DE, gum arabic and tapioca starch as carrier agents. Powder characterisation included analysis of moisture content, water activity, solubility, hygroscopicity, particle size distribution, morphology, total polyphenolics and antioxidant activity. Results showed that the samples produced with maltodextrin 20DE and gum arabic presented the smallest size and highest hygroscopicity. The powder produced with tapioca starch exhibited the lowest hygroscopity and solubility, and the highest mean diameter. With regard to morphology, all particles exhibited spherical and shrivelled surfaces, except those produced with tapioca starch, which exhibited rounded and smooth surfaces. Powders produced with maltodextrins and gum arabic showed high polyphenolic retention and antioxidant activity preservation after storage at 40 °C for 15 days, while for the particles produced with tapioca starch, this protective effect was less pronounced.</s0></fC01><fC02 i1="01" i2="X"><s0>002A35</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Morphologie</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Morphology</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Morfología</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Poudre</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Powder</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Polvo</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Propriété physicochimique</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Physicochemical properties</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Propiedad fisicoquímica</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Séchage pulvérisation</s0><s5>19</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Spray drying</s0><s5>19</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Secado pulverización</s0><s5>19</s5></fC03><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0415430 INIST</NO><ET>Physicochemical and morphological characterisation of açai (Euterpe oleraceae Mart.) powder produced with different carrier agents</ET><AU>TONON (Renata V.); BRABET (Catherine); PALLET (Dominique); BRAT (Pierre); HUBINGER (Miriam D.)</AU><AF>Faculty of Food Engineering - State University of Campinas, PO Box 6121/13083-862, Campinas, SP/Brésil (1 aut., 5 aut.); Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Department PERSYST- UMR QualiSud/Montpellier/France (2 aut., 3 aut., 4 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of food science &#38; technology; ISSN 0950-5423; Coden IJFTEZ; Royaume-Uni; Da. 2009; Vol. 44; No. 10; Pp. 1950-1958; Bibl. 3/4 p.</SO><LA>Anglais</LA><EA>Physicochemical and morphological properties of açai powder produced with different carrier agents were evaluated in this work. Powders were produced by spray drying, using maltodextrin 10DE, maltodextrin 20DE, gum arabic and tapioca starch as carrier agents. Powder characterisation included analysis of moisture content, water activity, solubility, hygroscopicity, particle size distribution, morphology, total polyphenolics and antioxidant activity. Results showed that the samples produced with maltodextrin 20DE and gum arabic presented the smallest size and highest hygroscopicity. The powder produced with tapioca starch exhibited the lowest hygroscopity and solubility, and the highest mean diameter. With regard to morphology, all particles exhibited spherical and shrivelled surfaces, except those produced with tapioca starch, which exhibited rounded and smooth surfaces. Powders produced with maltodextrins and gum arabic showed high polyphenolic retention and antioxidant activity preservation after storage at 40 °C for 15 days, while for the particles produced with tapioca starch, this protective effect was less pronounced.</EA><CC>002A35</CC><FD>Morphologie; Poudre; Propriété physicochimique; Séchage pulvérisation</FD><ED>Morphology; Powder; Physicochemical properties; Spray drying</ED><SD>Morfología; Polvo; Propiedad fisicoquímica; Secado pulverización</SD><LO>INIST-13345.354000171965520110</LO><ID>09-0415430</ID></server></inist></record>
000D94	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Screening for tuberculosis on admission to highly endemic prisons? The case of Rio de Janeiro State prisons</title><author><name sortKey="Sanchez, A" uniqKey="Sanchez A">A. Sanchez</name><affiliation><inist:fA14 i1="01"><s1>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Larouze, B" uniqKey="Larouze B">B. Larouze</name><affiliation><inist:fA14 i1="02"><s1>Institut National de la Santé et de la Recherche Médicale U707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Université Pierre et Marie Curie-Sciences et Médecine, Paris 6, UMR-S 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Espinola, A B" uniqKey="Espinola A">A. B. Espinola</name><affiliation><inist:fA14 i1="01"><s1>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Pires, J" uniqKey="Pires J">J. Pires</name><affiliation><inist:fA14 i1="01"><s1>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Capone, D" uniqKey="Capone D">D. Capone</name><affiliation><inist:fA14 i1="04"><s1>Universidade do Estado e Universidade Federal</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Gerhardt, G" uniqKey="Gerhardt G">G. Gerhardt</name><affiliation><inist:fA14 i1="05"><s1>Fundação Athaulfo de Paiva</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Cesconi, V" uniqKey="Cesconi V">V. Cesconi</name><affiliation><inist:fA14 i1="01"><s1>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Procopio, M J" uniqKey="Procopio M">M. J. Procopio</name><affiliation><inist:fA14 i1="06"><s1>Centro de Referência Hélio Fraga, SVS/MS, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Hijjar, M" uniqKey="Hijjar M">M. Hijjar</name><affiliation><inist:fA14 i1="06"><s1>Centro de Referência Hélio Fraga, SVS/MS, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Massari, V" uniqKey="Massari V">V. Massari</name><affiliation><inist:fA14 i1="02"><s1>Institut National de la Santé et de la Recherche Médicale U707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="03"><s1>Université Pierre et Marie Curie-Sciences et Médecine, Paris 6, UMR-S 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0415579</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0415579 INIST</idno><idno type="RBID">Pascal:09-0415579</idno><idno type="wicri:Area/Main/Corpus">001B91</idno></publicationStmt><seriesStmt><idno type="ISSN">1027-3719</idno><title level="j" type="abbreviated">Int. j. tuberc. lung dis.</title><title level="j" type="main">International journal of tuberculosis and lung disease</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Brazil</term><term>Carceral environment</term><term>Case study</term><term>Control</term><term>Human</term><term>Medical screening</term><term>Pneumology</term><term>Respiratory disease</term><term>Tuberculosis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Tuberculose</term><term>Pathologie de l'appareil respiratoire</term><term>Dépistage</term><term>Milieu carcéral</term><term>Etude cas</term><term>Commande</term><term>Brésil</term><term>Pneumologie</term><term>Homme</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">CADRE: Prisons de l'état de Rio de Janeiro (RJ) de haute endémicité tuberculeuse. MÉTHODES: Un dépistage radiologique de la tuberculose (TB) a été réalisé chez 1696 détenus à leur entrée dans trois prisons de RJ. La radio de thorax a été suivie d'un examen bactériologique des crachats (frottis, culture) en cas d'anomalie radiologique pulmonaire, pleurale ou médiastinale. Le diagnostic de TB a reposé sur la bactériologie ou, en cas de négativité, sur la réponse au traitement antituberculeux. RÉSULTATS: La prévalence de la TB était de 2,7%, et 32/46 cas identifiés étaient bactériologiquement confirmés, dont 19 cas par une bacilloscopie positive. Les lésions radiologiques étaient fréquemment étendues. Etaient associés à la TB, en régression logistique, l'analphabétisme (OR ajusté 2,10 ; IC95 % 1,02-4,34), la toux ≥3 semaines (ORa 2,85 ; IC95% 1,54-5,27), un traitement antituberculeux antérieur (ORa 3,61 ; IC95% 1,76-7,39), et le fait de vivre dans la banlieue (ORa 4,54 ; IC95% 1,02-20,07) et dans la ville de Rio (ORa 5,48 ; IC95% 1,29-23,33). Un dépistage basé sur la toux ≥3 semaines suivi d'un examen du frottis de crachat n'aurait identifié que 10 des 46 cas. CONCLUSION: Ces résultats plaident pour la mise en œuvre d'un dépistage de la TB à l'entrée en prison et pour la nécessité urgente d'améliorer les conditions de détention et l'assistance médicale dans les commissariats.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1027-3719</s0></fA01><fA03 i2="1"><s0>Int. j. tuberc. lung dis.</s0></fA03><fA05><s2>13</s2></fA05><fA06><s2>10</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Screening for tuberculosis on admission to highly endemic prisons? The case of Rio de Janeiro State prisons</s1></fA08><fA11 i1="01" i2="1"><s1>SANCHEZ (A.)</s1></fA11><fA11 i1="02" i2="1"><s1>LAROUZE (B.)</s1></fA11><fA11 i1="03" i2="1"><s1>ESPINOLA (A. B.)</s1></fA11><fA11 i1="04" i2="1"><s1>PIRES (J.)</s1></fA11><fA11 i1="05" i2="1"><s1>CAPONE (D.)</s1></fA11><fA11 i1="06" i2="1"><s1>GERHARDT (G.)</s1></fA11><fA11 i1="07" i2="1"><s1>CESCONI (V.)</s1></fA11><fA11 i1="08" i2="1"><s1>PROCOPIO (M. J.)</s1></fA11><fA11 i1="09" i2="1"><s1>HIJJAR (M.)</s1></fA11><fA11 i1="10" i2="1"><s1>MASSARI (V.)</s1></fA11><fA14 i1="01"><s1>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>7 aut.</sZ></fA14><fA14 i1="02"><s1>Institut National de la Santé et de la Recherche Médicale U707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="03"><s1>Université Pierre et Marie Curie-Sciences et Médecine, Paris 6, UMR-S 707</s1><s2>Paris</s2><s3>FRA</s3><sZ>2 aut.</sZ><sZ>10 aut.</sZ></fA14><fA14 i1="04"><s1>Universidade do Estado e Universidade Federal</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>5 aut.</sZ></fA14><fA14 i1="05"><s1>Fundação Athaulfo de Paiva</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>6 aut.</sZ></fA14><fA14 i1="06"><s1>Centro de Referência Hélio Fraga, SVS/MS, Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>8 aut.</sZ><sZ>9 aut.</sZ></fA14><fA20><s1>1247-1252</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA24 i1="02"><s0>spa</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>26450</s2><s5>354000171106520110</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>28 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0415579</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of tuberculosis and lung disease</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>CADRE: Prisons de l'état de Rio de Janeiro (RJ) de haute endémicité tuberculeuse. MÉTHODES: Un dépistage radiologique de la tuberculose (TB) a été réalisé chez 1696 détenus à leur entrée dans trois prisons de RJ. La radio de thorax a été suivie d'un examen bactériologique des crachats (frottis, culture) en cas d'anomalie radiologique pulmonaire, pleurale ou médiastinale. Le diagnostic de TB a reposé sur la bactériologie ou, en cas de négativité, sur la réponse au traitement antituberculeux. RÉSULTATS: La prévalence de la TB était de 2,7%, et 32/46 cas identifiés étaient bactériologiquement confirmés, dont 19 cas par une bacilloscopie positive. Les lésions radiologiques étaient fréquemment étendues. Etaient associés à la TB, en régression logistique, l'analphabétisme (OR ajusté 2,10 ; IC95 % 1,02-4,34), la toux ≥3 semaines (ORa 2,85 ; IC95% 1,54-5,27), un traitement antituberculeux antérieur (ORa 3,61 ; IC95% 1,76-7,39), et le fait de vivre dans la banlieue (ORa 4,54 ; IC95% 1,02-20,07) et dans la ville de Rio (ORa 5,48 ; IC95% 1,29-23,33). Un dépistage basé sur la toux ≥3 semaines suivi d'un examen du frottis de crachat n'aurait identifié que 10 des 46 cas. CONCLUSION: Ces résultats plaident pour la mise en œuvre d'un dépistage de la TB à l'entrée en prison et pour la nécessité urgente d'améliorer les conditions de détention et l'assistance médicale dans les commissariats.</s0></fC01><fC02 i1="01" i2="X"><s0>002B11D</s0></fC02><fC02 i1="02" i2="X"><s0>002B05B02O</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Tuberculose</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Dépistage</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Medical screening</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Descubrimiento</s0><s5>09</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Milieu carcéral</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Carceral environment</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Medio carcelario</s0><s5>10</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Etude cas</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Case study</s0><s5>11</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Estudio caso</s0><s5>11</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Commande</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Control</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Control</s0><s5>12</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Brésil</s0><s2>NG</s2><s5>13</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Brazil</s0><s2>NG</s2><s5>13</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Brasil</s0><s2>NG</s2><s5>13</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Pneumologie</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Pneumology</s0><s5>14</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Neumología</s0><s5>14</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Homme</s0><s5>78</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Human</s0><s5>78</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Hombre</s0><s5>78</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Mycobactériose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Mycobacterial infection</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Micobacteriosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Amérique du Sud</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>South America</s0><s2>NG</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>America del sur</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Amérique</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>America</s0><s2>NG</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>America</s0><s2>NG</s2></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0415579 INIST</NO><ET>Screening for tuberculosis on admission to highly endemic prisons? The case of Rio de Janeiro State prisons</ET><AU>SANCHEZ (A.); LAROUZE (B.); ESPINOLA (A. B.); PIRES (J.); CAPONE (D.); GERHARDT (G.); CESCONI (V.); PROCOPIO (M. J.); HIJJAR (M.); MASSARI (V.)</AU><AF>Programa de Controle de Tuberculose, Coordenação de Gestão em Saude Penitenciária, Rio de Janeiro/Rio de Janeiro/Brésil (1 aut., 3 aut., 4 aut., 7 aut.); Institut National de la Santé et de la Recherche Médicale U707/Paris/France (2 aut., 10 aut.); Université Pierre et Marie Curie-Sciences et Médecine, Paris 6, UMR-S 707/Paris/France (2 aut., 10 aut.); Universidade do Estado e Universidade Federal/Rio de Janeiro/Brésil (5 aut.); Fundação Athaulfo de Paiva/Rio de Janeiro/Brésil (6 aut.); Centro de Referência Hélio Fraga, SVS/MS, Rio de Janeiro/Rio de Janeiro/Brésil (8 aut., 9 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of tuberculosis and lung disease; ISSN 1027-3719; France; Da. 2009; Vol. 13; No. 10; Pp. 1247-1252; Abs. français/espagnol; Bibl. 28 ref.</SO><LA>Anglais</LA><FA>CADRE: Prisons de l'état de Rio de Janeiro (RJ) de haute endémicité tuberculeuse. MÉTHODES: Un dépistage radiologique de la tuberculose (TB) a été réalisé chez 1696 détenus à leur entrée dans trois prisons de RJ. La radio de thorax a été suivie d'un examen bactériologique des crachats (frottis, culture) en cas d'anomalie radiologique pulmonaire, pleurale ou médiastinale. Le diagnostic de TB a reposé sur la bactériologie ou, en cas de négativité, sur la réponse au traitement antituberculeux. RÉSULTATS: La prévalence de la TB était de 2,7%, et 32/46 cas identifiés étaient bactériologiquement confirmés, dont 19 cas par une bacilloscopie positive. Les lésions radiologiques étaient fréquemment étendues. Etaient associés à la TB, en régression logistique, l'analphabétisme (OR ajusté 2,10 ; IC95 % 1,02-4,34), la toux ≥3 semaines (ORa 2,85 ; IC95% 1,54-5,27), un traitement antituberculeux antérieur (ORa 3,61 ; IC95% 1,76-7,39), et le fait de vivre dans la banlieue (ORa 4,54 ; IC95% 1,02-20,07) et dans la ville de Rio (ORa 5,48 ; IC95% 1,29-23,33). Un dépistage basé sur la toux ≥3 semaines suivi d'un examen du frottis de crachat n'aurait identifié que 10 des 46 cas. CONCLUSION: Ces résultats plaident pour la mise en œuvre d'un dépistage de la TB à l'entrée en prison et pour la nécessité urgente d'améliorer les conditions de détention et l'assistance médicale dans les commissariats.</FA><CC>002B11D; 002B05B02O</CC><FD>Tuberculose; Pathologie de l'appareil respiratoire; Dépistage; Milieu carcéral; Etude cas; Commande; Brésil; Pneumologie; Homme</FD><FG>Mycobactériose; Bactériose; Infection; Amérique du Sud; Amérique</FG><ED>Tuberculosis; Respiratory disease; Medical screening; Carceral environment; Case study; Control; Brazil; Pneumology; Human</ED><EG>Mycobacterial infection; Bacteriosis; Infection; South America; America</EG><SD>Tuberculosis; Aparato respiratorio patología; Descubrimiento; Medio carcelario; Estudio caso; Control; Brasil; Neumología; Hombre</SD><LO>INIST-26450.354000171106520110</LO><ID>09-0415579</ID></server></inist></record>
000D95	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Thin-layer agar for detection of resistance to rifampicin, ofloxacin and kanamycin in Mycobacterium tuberculosis isolates</title><author><name sortKey="Martin, A" uniqKey="Martin A">A. Martin</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Paasch, F" uniqKey="Paasch F">F. Paasch</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Von Groll, A" uniqKey="Von Groll A">A. Von Groll</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Laboratory of Mycobacteriology, Universidade Federal do Rio Grande</s1><s2>Rio Grande do Sul</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Fissette, K" uniqKey="Fissette K">K. Fissette</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Almeida, P" uniqKey="Almeida P">P. Almeida</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Laboratory of Mycobacteriology, Universidade Federal do Rio Grande</s1><s2>Rio Grande do Sul</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Varaine, F" uniqKey="Varaine F">F. Varaine</name><affiliation><inist:fA14 i1="03"><s1>Médecins Sans Frontières</s1><s2>Paris</s2><s3>FRA</s3><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Portaels, F" uniqKey="Portaels F">F. Portaels</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Palomino, J C" uniqKey="Palomino J">J.-C. Palomino</name><affiliation><inist:fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0415587</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0415587 INIST</idno><idno type="RBID">Pascal:09-0415587</idno><idno type="wicri:Area/Main/Corpus">001B90</idno></publicationStmt><seriesStmt><idno type="ISSN">1027-3719</idno><title level="j" type="abbreviated">Int. j. tuberc. lung dis.</title><title level="j" type="main">International journal of tuberculosis and lung disease</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Agar</term><term>Antibacterial agent</term><term>Antibiotic</term><term>Antituberculous agent</term><term>Detection</term><term>Isolate</term><term>Kanamycin</term><term>Mycobacterium tuberculosis</term><term>Ofloxacin</term><term>Pneumology</term><term>Respiratory disease</term><term>Rifampicin</term><term>Treatment resistance</term><term>Tuberculosis</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Tuberculose</term><term>Pathologie de l'appareil respiratoire</term><term>Gélose</term><term>Détection</term><term>Rifampicine</term><term>Antibactérien</term><term>Antibiotique</term><term>Ofloxacine</term><term>Kanamycine</term><term>Mycobacterium tuberculosis</term><term>Isolat</term><term>Résistance traitement</term><term>Pneumologie</term><term>Antituberculeux</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">CONTEXTE: Dans les pays à faibles revenus, des méthodes économiques de détermination de la sensibilité de Mycobacterium tuberculosis aux antibiotiques sont nécessaires. OBJECTIF: Evaluer la méthode thin layer agar (culture sur agar en couche mince ; TLA) pour la détection rapide de la résistance à la rifampicine (RMP), à l'ofloxacine (OFX) et à la kanamycine (KM) dans des isolats cliniques de M. tuberculosis et de déterminer, par rapport à la méthode de référence, la sensibilité, la spécificité et la durée avant positivité de la méthode TLA. MÉTHODES: On a étudié 147 isolats cliniques de M. tuberculosis. Pour la méthode TLA, on a utilisé une boite de Pétri divisée en quatre quartiers préparée avec de l'agar 7H11 contenant les médicaments correspondants RMP, OFX et KM. Les résultats ont été comparés à la méthode gold standard MGIT960 pour la RMP et à la méthode des proportions sur agar 7H11 pour OFX et KM. RÉSULTATS: La sensibilité et la spécificité pour RMP et OFX ont été de 100% et pour KM, la sensibilité a été de 100% et la spécificité de 98,7%. L'utilisation de la plaque TLA divisée en quatre quartiers permet la détection rapide de la résistance de M. tuberculosis à l'égard des trois médicaments antituberculeux RMP, OFX et KM après une durée médiane de 10 jours. CONCLUSION: La TLA s'est avéré une méthode précise pour la détection de la résistance aux trois médicaments étudiés. Cette méthode plus rapide, d'emploi aisé, fournit une méthode alternative lorsque des techniques plus sophistiquées ne sont pas disponibles dans des contextes à faibles revenus.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>1027-3719</s0></fA01><fA03 i2="1"><s0>Int. j. tuberc. lung dis.</s0></fA03><fA05><s2>13</s2></fA05><fA06><s2>10</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Thin-layer agar for detection of resistance to rifampicin, ofloxacin and kanamycin in Mycobacterium tuberculosis isolates</s1></fA08><fA11 i1="01" i2="1"><s1>MARTIN (A.)</s1></fA11><fA11 i1="02" i2="1"><s1>PAASCH (F.)</s1></fA11><fA11 i1="03" i2="1"><s1>VON GROLL (A.)</s1></fA11><fA11 i1="04" i2="1"><s1>FISSETTE (K.)</s1></fA11><fA11 i1="05" i2="1"><s1>ALMEIDA (P.)</s1></fA11><fA11 i1="06" i2="1"><s1>VARAINE (F.)</s1></fA11><fA11 i1="07" i2="1"><s1>PORTAELS (F.)</s1></fA11><fA11 i1="08" i2="1"><s1>PALOMINO (J.-C.)</s1></fA11><fA14 i1="01"><s1>Institute of Tropical Medicine, Mycobacteriology Unit</s1><s2>Antwerp</s2><s3>BEL</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>3 aut.</sZ><sZ>4 aut.</sZ><sZ>5 aut.</sZ><sZ>7 aut.</sZ><sZ>8 aut.</sZ></fA14><fA14 i1="02"><s1>Laboratory of Mycobacteriology, Universidade Federal do Rio Grande</s1><s2>Rio Grande do Sul</s2><s3>BRA</s3><sZ>3 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="03"><s1>Médecins Sans Frontières</s1><s2>Paris</s2><s3>FRA</s3><sZ>6 aut.</sZ></fA14><fA20><s1>1301-1304</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA24 i1="01"><s0>fre</s0></fA24><fA24 i1="02"><s0>spa</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>26450</s2><s5>354000171106520190</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>12 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0415587</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>International journal of tuberculosis and lung disease</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fC01 i1="01" l="FRE"><s0>CONTEXTE: Dans les pays à faibles revenus, des méthodes économiques de détermination de la sensibilité de Mycobacterium tuberculosis aux antibiotiques sont nécessaires. OBJECTIF: Evaluer la méthode thin layer agar (culture sur agar en couche mince ; TLA) pour la détection rapide de la résistance à la rifampicine (RMP), à l'ofloxacine (OFX) et à la kanamycine (KM) dans des isolats cliniques de M. tuberculosis et de déterminer, par rapport à la méthode de référence, la sensibilité, la spécificité et la durée avant positivité de la méthode TLA. MÉTHODES: On a étudié 147 isolats cliniques de M. tuberculosis. Pour la méthode TLA, on a utilisé une boite de Pétri divisée en quatre quartiers préparée avec de l'agar 7H11 contenant les médicaments correspondants RMP, OFX et KM. Les résultats ont été comparés à la méthode gold standard MGIT960 pour la RMP et à la méthode des proportions sur agar 7H11 pour OFX et KM. RÉSULTATS: La sensibilité et la spécificité pour RMP et OFX ont été de 100% et pour KM, la sensibilité a été de 100% et la spécificité de 98,7%. L'utilisation de la plaque TLA divisée en quatre quartiers permet la détection rapide de la résistance de M. tuberculosis à l'égard des trois médicaments antituberculeux RMP, OFX et KM après une durée médiane de 10 jours. CONCLUSION: La TLA s'est avéré une méthode précise pour la détection de la résistance aux trois médicaments étudiés. Cette méthode plus rapide, d'emploi aisé, fournit une méthode alternative lorsque des techniques plus sophistiquées ne sont pas disponibles dans des contextes à faibles revenus.</s0></fC01><fC02 i1="01" i2="X"><s0>002B11D</s0></fC02><fC02 i1="02" i2="X"><s0>002B05B02O</s0></fC02><fC02 i1="03" i2="X"><s0>002B02S02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Tuberculose</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Tuberculosis</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Pathologie de l'appareil respiratoire</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Respiratory disease</s0><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Aparato respiratorio patología</s0><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Gélose</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Agar</s0><s5>09</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Agar</s0><s5>09</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Détection</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Detection</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Detección</s0><s5>10</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Rifampicine</s0><s2>NK</s2><s2>FR</s2><s5>11</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Rifampicin</s0><s2>NK</s2><s2>FR</s2><s5>11</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Rifampicina</s0><s2>NK</s2><s2>FR</s2><s5>11</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Antibactérien</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Antibacterial agent</s0><s5>12</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Antibacteriano</s0><s5>12</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Antibiotique</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Antibiotic</s0><s5>13</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Antibiótico</s0><s5>13</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Ofloxacine</s0><s2>NK</s2><s2>FR</s2><s5>14</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Ofloxacin</s0><s2>NK</s2><s2>FR</s2><s5>14</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Ofloxacino</s0><s2>NK</s2><s2>FR</s2><s5>14</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Kanamycine</s0><s2>NK</s2><s2>FR</s2><s5>15</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Kanamycin</s0><s2>NK</s2><s2>FR</s2><s5>15</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Kanamicina</s0><s2>NK</s2><s2>FR</s2><s5>15</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>16</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>16</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Mycobacterium tuberculosis</s0><s2>NS</s2><s5>16</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Isolat</s0><s5>17</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Isolate</s0><s5>17</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Aislado</s0><s5>17</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Résistance traitement</s0><s5>18</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Treatment resistance</s0><s5>18</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Resistencia tratamiento</s0><s5>18</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Pneumologie</s0><s5>19</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Pneumology</s0><s5>19</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Neumología</s0><s5>19</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Antituberculeux</s0><s5>78</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Antituberculous agent</s0><s5>78</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Antituberculoso</s0><s5>78</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Mycobactériose</s0></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Mycobacterial infection</s0></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Micobacteriosis</s0></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Bactériose</s0></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Bacteriosis</s0></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Bacteriosis</s0></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Infection</s0></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Infección</s0></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Mycobacteriaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Mycobacteriales</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Actinomycetes</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Bactérie</s0></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Bacteria</s0></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Bacteria</s0></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0415587 INIST</NO><ET>Thin-layer agar for detection of resistance to rifampicin, ofloxacin and kanamycin in Mycobacterium tuberculosis isolates</ET><AU>MARTIN (A.); PAASCH (F.); VON GROLL (A.); FISSETTE (K.); ALMEIDA (P.); VARAINE (F.); PORTAELS (F.); PALOMINO (J.-C.)</AU><AF>Institute of Tropical Medicine, Mycobacteriology Unit/Antwerp/Belgique (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 7 aut., 8 aut.); Laboratory of Mycobacteriology, Universidade Federal do Rio Grande/Rio Grande do Sul/Brésil (3 aut., 5 aut.); Médecins Sans Frontières/Paris/France (6 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>International journal of tuberculosis and lung disease; ISSN 1027-3719; France; Da. 2009; Vol. 13; No. 10; Pp. 1301-1304; Abs. français/espagnol; Bibl. 12 ref.</SO><LA>Anglais</LA><FA>CONTEXTE: Dans les pays à faibles revenus, des méthodes économiques de détermination de la sensibilité de Mycobacterium tuberculosis aux antibiotiques sont nécessaires. OBJECTIF: Evaluer la méthode thin layer agar (culture sur agar en couche mince ; TLA) pour la détection rapide de la résistance à la rifampicine (RMP), à l'ofloxacine (OFX) et à la kanamycine (KM) dans des isolats cliniques de M. tuberculosis et de déterminer, par rapport à la méthode de référence, la sensibilité, la spécificité et la durée avant positivité de la méthode TLA. MÉTHODES: On a étudié 147 isolats cliniques de M. tuberculosis. Pour la méthode TLA, on a utilisé une boite de Pétri divisée en quatre quartiers préparée avec de l'agar 7H11 contenant les médicaments correspondants RMP, OFX et KM. Les résultats ont été comparés à la méthode gold standard MGIT960 pour la RMP et à la méthode des proportions sur agar 7H11 pour OFX et KM. RÉSULTATS: La sensibilité et la spécificité pour RMP et OFX ont été de 100% et pour KM, la sensibilité a été de 100% et la spécificité de 98,7%. L'utilisation de la plaque TLA divisée en quatre quartiers permet la détection rapide de la résistance de M. tuberculosis à l'égard des trois médicaments antituberculeux RMP, OFX et KM après une durée médiane de 10 jours. CONCLUSION: La TLA s'est avéré une méthode précise pour la détection de la résistance aux trois médicaments étudiés. Cette méthode plus rapide, d'emploi aisé, fournit une méthode alternative lorsque des techniques plus sophistiquées ne sont pas disponibles dans des contextes à faibles revenus.</FA><CC>002B11D; 002B05B02O; 002B02S02</CC><FD>Tuberculose; Pathologie de l'appareil respiratoire; Gélose; Détection; Rifampicine; Antibactérien; Antibiotique; Ofloxacine; Kanamycine; Mycobacterium tuberculosis; Isolat; Résistance traitement; Pneumologie; Antituberculeux</FD><FG>Mycobactériose; Bactériose; Infection; Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bactérie</FG><ED>Tuberculosis; Respiratory disease; Agar; Detection; Rifampicin; Antibacterial agent; Antibiotic; Ofloxacin; Kanamycin; Mycobacterium tuberculosis; Isolate; Treatment resistance; Pneumology; Antituberculous agent</ED><EG>Mycobacterial infection; Bacteriosis; Infection; Mycobacteriaceae; Mycobacteriales; Actinomycetes; Bacteria</EG><SD>Tuberculosis; Aparato respiratorio patología; Agar; Detección; Rifampicina; Antibacteriano; Antibiótico; Ofloxacino; Kanamicina; Mycobacterium tuberculosis; Aislado; Resistencia tratamiento; Neumología; Antituberculoso</SD><LO>INIST-26450.354000171106520190</LO><ID>09-0415587</ID></server></inist></record>
000D96	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Acetone Powder From Dormant Seeds of Ricinus communis L: Lipase Activity and Presence of Toxic and Allergenic Compounds</title><author><name sortKey="Cavalcanti, Elisa D C" uniqKey="Cavalcanti E">Elisa D. C. Cavalcanti</name><affiliation><inist:fA14 i1="01"><s1>Federal University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Maciel, Fabio M" uniqKey="Maciel F">Fabio M. Maciel</name><affiliation><inist:fA14 i1="02"><s1>UENF</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Villeneuve, Pierre" uniqKey="Villeneuve P">Pierre Villeneuve</name><affiliation><inist:fA14 i1="03"><s1>CIRADIAMIS</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Lago, Regina C A" uniqKey="Lago R">Regina C. A. Lago</name><affiliation><inist:fA14 i1="04"><s1>Embrapa Food Technology</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Machado, Olga L T" uniqKey="Machado O">Olga L. T. Machado</name><affiliation><inist:fA14 i1="02"><s1>UENF</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Freire, Denise M G" uniqKey="Freire D">Denise M. G. Freire</name><affiliation><inist:fA14 i1="01"><s1>Federal University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0416007</idno><date when="2007">2007</date><idno type="stanalyst">PASCAL 09-0416007 INIST</idno><idno type="RBID">Pascal:09-0416007</idno><idno type="wicri:Area/Main/Corpus">001B89</idno></publicationStmt><seriesStmt><idno type="ISSN">0273-2289</idno><title level="j" type="abbreviated">Appl. biochem. biotechnol.</title><title level="j" type="main">Applied biochemistry and biotechnology</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acetone</term><term>Albumin</term><term>Ricin</term><term>Ricinus communis</term><term>Triacylglycerol lipase</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Acétone</term><term>Triacylglycerol lipase</term><term>Albumine</term><term>Ricine</term><term>Ricinus communis</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The influence of several factors on the hydrolytic activity of lipase, present in the acetone powder from dormant castor seeds (Ricinus communis) was evaluated. The enzyme showed a marked specificity for short-chain substrates. The best reaction conditions were an acid medium, Triton X-100 as the emulsifying agent and a temperature of 30°C. The lipase activity of the acetone powder of different castor oil genotypes showed great variability and storage stability of up to 90%. The toxicology analysis of the acetone powder from genotype Nordestina BRS 149 showed a higher ricin (toxic component) content, a lower 2S albumin (allergenic compound) content, and similar allergenic potential compared with untreated seeds.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0273-2289</s0></fA01><fA02 i1="01"><s0>ABIBDL</s0></fA02><fA03 i2="1"><s0>Appl. biochem. biotechnol.</s0></fA03><fA05><s2>137-140</s2></fA05><fA08 i1="01" i2="1" l="ENG"><s1>Acetone Powder From Dormant Seeds of Ricinus communis L: Lipase Activity and Presence of Toxic and Allergenic Compounds</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Proceedings of the Twenty-Eighth Symposium on Biotechnology for Fuels and Chemicals held April 30-May 3, 2006, in Nashville, Tennessee</s1></fA09><fA11 i1="01" i2="1"><s1>CAVALCANTI (Elisa D. C.)</s1></fA11><fA11 i1="02" i2="1"><s1>MACIEL (Fabio M.)</s1></fA11><fA11 i1="03" i2="1"><s1>VILLENEUVE (Pierre)</s1></fA11><fA11 i1="04" i2="1"><s1>LAGO (Regina C. A.)</s1></fA11><fA11 i1="05" i2="1"><s1>MACHADO (Olga L. T.)</s1></fA11><fA11 i1="06" i2="1"><s1>FREIRE (Denise M. G.)</s1></fA11><fA12 i1="01" i2="1"><s1>MIELENZ (Jonathan R.)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>KLASSON (K. Thomas)</s1><s9>ed.</s9></fA12><fA12 i1="03" i2="1"><s1>ADNEY (William S.)</s1><s9>ed.</s9></fA12><fA12 i1="04" i2="1"><s1>MCMILLAN (James D.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Federal University of Rio de Janeiro</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>1 aut.</sZ><sZ>6 aut.</sZ></fA14><fA14 i1="02"><s1>UENF</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>2 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="03"><s1>CIRADIAMIS</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>3 aut.</sZ></fA14><fA14 i1="04"><s1>Embrapa Food Technology</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>4 aut.</sZ></fA14><fA15 i1="01"><s1>Oak Ridge National Laboratory</s1><s3>USA</s3><sZ>1 aut.</sZ></fA15><fA15 i1="02"><s1>Southern Regional Research Laboratory, USDA-ARS</s1><s3>USA</s3><sZ>2 aut.</sZ></fA15><fA15 i1="03"><s1>National Renewable Energy Laboratory</s1><s3>USA</s3><sZ>3 aut.</sZ><sZ>4 aut.</sZ></fA15><fA20><s1>57-65</s1></fA20><fA21><s1>2007</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>17423</s2><s5>354000170860350050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>22 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0416007</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Applied biochemistry and biotechnology</s0></fA64><fA66 i1="01"><s0>DEU</s0></fA66><fC01 i1="01" l="ENG"><s0>The influence of several factors on the hydrolytic activity of lipase, present in the acetone powder from dormant castor seeds (Ricinus communis) was evaluated. The enzyme showed a marked specificity for short-chain substrates. The best reaction conditions were an acid medium, Triton X-100 as the emulsifying agent and a temperature of 30°C. The lipase activity of the acetone powder of different castor oil genotypes showed great variability and storage stability of up to 90%. The toxicology analysis of the acetone powder from genotype Nordestina BRS 149 showed a higher ricin (toxic component) content, a lower 2S albumin (allergenic compound) content, and similar allergenic potential compared with untreated seeds.</s0></fC01><fC02 i1="01" i2="X"><s0>002A31</s0></fC02><fC02 i1="02" i2="X"><s0>215</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Acétone</s0><s2>NK</s2><s2>FX</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Acetone</s0><s2>NK</s2><s2>FX</s2><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Acetona</s0><s2>NK</s2><s2>FX</s2><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Triacylglycerol lipase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Triacylglycerol lipase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Triacylglycerol lipase</s0><s2>FE</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Albumine</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Albumin</s0><s5>10</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Albúmina</s0><s5>10</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Ricine</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Ricin</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Ricina</s0><s2>NK</s2><s5>11</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Ricinus communis</s0><s2>NS</s2><s5>13</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Ricinus communis</s0><s2>NS</s2><s5>13</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Ricinus communis</s0><s2>NS</s2><s5>13</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Carboxylic ester hydrolases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Carboxylic ester hydrolases</s0><s2>FE</s2></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Carboxylic ester hydrolases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Esterases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Esterases</s0><s2>FE</s2></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Esterases</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Hydrolases</s0><s2>FE</s2></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Euphorbiaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Euphorbiaceae</s0><s2>NS</s2></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Euphorbiaceae</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Dicotyledones</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Angiospermae</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Spermatophyta</s0><s2>NS</s2></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Symposium on Biotechnology for Fuels and Chemicals.</s1><s2>28</s2><s3>Nashville, Tennessee USA</s3><s4>2006-04-30</s4></fA30></pR></standard><server><NO>PASCAL 09-0416007 INIST</NO><ET>Acetone Powder From Dormant Seeds of Ricinus communis L: Lipase Activity and Presence of Toxic and Allergenic Compounds</ET><AU>CAVALCANTI (Elisa D. C.); MACIEL (Fabio M.); VILLENEUVE (Pierre); LAGO (Regina C. A.); MACHADO (Olga L. T.); FREIRE (Denise M. G.); MIELENZ (Jonathan R.); KLASSON (K. Thomas); ADNEY (William S.); MCMILLAN (James D.)</AU><AF>Federal University of Rio de Janeiro/Rio de Janeiro/Brésil (1 aut., 6 aut.); UENF/Rio de Janeiro/Brésil (2 aut., 5 aut.); CIRADIAMIS/Montpellier/France (3 aut.); Embrapa Food Technology/Rio de Janeiro/Brésil (4 aut.); Oak Ridge National Laboratory/Etats-Unis (1 aut.); Southern Regional Research Laboratory, USDA-ARS/Etats-Unis (2 aut.); National Renewable Energy Laboratory/Etats-Unis (3 aut., 4 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Applied biochemistry and biotechnology; ISSN 0273-2289; Coden ABIBDL; Allemagne; Da. 2007; Vol. 137-140; Pp. 57-65; Bibl. 22 ref.</SO><LA>Anglais</LA><EA>The influence of several factors on the hydrolytic activity of lipase, present in the acetone powder from dormant castor seeds (Ricinus communis) was evaluated. The enzyme showed a marked specificity for short-chain substrates. The best reaction conditions were an acid medium, Triton X-100 as the emulsifying agent and a temperature of 30°C. The lipase activity of the acetone powder of different castor oil genotypes showed great variability and storage stability of up to 90%. The toxicology analysis of the acetone powder from genotype Nordestina BRS 149 showed a higher ricin (toxic component) content, a lower 2S albumin (allergenic compound) content, and similar allergenic potential compared with untreated seeds.</EA><CC>002A31; 215</CC><FD>Acétone; Triacylglycerol lipase; Albumine; Ricine; Ricinus communis</FD><FG>Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Euphorbiaceae; Dicotyledones; Angiospermae; Spermatophyta</FG><ED>Acetone; Triacylglycerol lipase; Albumin; Ricin; Ricinus communis</ED><EG>Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Euphorbiaceae; Dicotyledones; Angiospermae; Spermatophyta</EG><SD>Acetona; Triacylglycerol lipase; Albúmina; Ricina; Ricinus communis</SD><LO>INIST-17423.354000170860350050</LO><ID>09-0416007</ID></server></inist></record>
000D97	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Bayer Bilateral Denoising on TriMedia3270</title><author><name sortKey="Phelippeau, H" uniqKey="Phelippeau H">H. Phelippeau</name><affiliation><inist:fA14 i1="01"><s1>Université Paris-Est, Labinfo, ESIEE</s1><s2>93162 Noisy-le-Grand</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>NXP Semiconductors, 2 Esplanade Anton Philips Campus Effiscience, Colombelles BP 2000 14906</s1><s2>Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Akil, M" uniqKey="Akil M">M. Akil</name><affiliation><inist:fA14 i1="01"><s1>Université Paris-Est, Labinfo, ESIEE</s1><s2>93162 Noisy-le-Grand</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Dias Rodrigues, B" uniqKey="Dias Rodrigues B">B. Dias Rodrigues</name><affiliation><inist:fA14 i1="03"><s1>Universidade Federal de Minas Gerais - UFMG</s1><s2>Belo Horizonte, Minas Gerais</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Talbot, H" uniqKey="Talbot H">H. Talbot</name><affiliation><inist:fA14 i1="01"><s1>Université Paris-Est, Labinfo, ESIEE</s1><s2>93162 Noisy-le-Grand</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bara, S" uniqKey="Bara S">S. Bara</name><affiliation><inist:fA14 i1="02"><s1>NXP Semiconductors, 2 Esplanade Anton Philips Campus Effiscience, Colombelles BP 2000 14906</s1><s2>Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0417551</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0417551 INIST</idno><idno type="RBID">Pascal:09-0417551</idno><idno type="wicri:Area/Main/Corpus">001B88</idno></publicationStmt><seriesStmt><idno type="ISSN">0277-786X</idno><title level="j" type="abbreviated">Proc. SPIE Int. Soc. Opt. Eng.</title><title level="j" type="main">Proceedings of SPIE, the International Society for Optical Engineering</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Image quality</term><term>Imagery</term><term>Implementation</term><term>Look up table</term><term>Mobile handsets</term><term>Mobile radio</term><term>Noise reduction</term><term>Optimization</term><term>Optimization method</term><term>Performance evaluation</term><term>Power consumption</term><term>Real time processing</term><term>Real time systems</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Radiocommunication service mobile</term><term>Système temps réel</term><term>Méthode optimisation</term><term>Qualité image</term><term>Imagerie</term><term>Réduction bruit</term><term>Téléphone portable</term><term>Consommation énergie électrique</term><term>Implémentation</term><term>Evaluation performance</term><term>Optimisation</term><term>Table conversion</term><term>Traitement temps réel</term><term>0130C</term><term>4230</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Digital cameras are now commonly included in several digital devices such as mobile phones. They are present everywhere and have become the principal image capturing tool. Inherent to light and semiconductors properties, sensor noise [10] continues to be an important factor of image quality [12], especially in low light conditions. Removing the noise with mathematical solutions appears thus unavoidable to obtain an acceptable image quality. However, embedded devices are limited by processing capabilities and power consumption and thus cannot make use of the full range of complex mathematical noise removing solutions. The bilateral filter [6] appears to be an interesting compromise between implementation complexity and noise removing performances. Especially, the Bayer [5] bilateral filter proposed in [I is well adapted for single sensor devices. In this paper, we simulate and optimize the Bayer bilateral filter execution on a common media-processor: the TM3270 [4] from the NXP Semiconductors TriMedia family. To do so we use the TriMedia Compilation System (TCS). We applied common optimization techniques (such as LUT, loop unrolling, convenient data type representation) as well as custom TriMedia operations. We finally propose a new Bayer bilateral filter formulation dedicated to the TM3270 architecture that yields an execution improvement of 99.6% compared to the naive version. This improvement results in real-time video processing at VGA resolution at the 350MHz clock rate.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0277-786X</s0></fA01><fA02 i1="01"><s0>PSISDG</s0></fA02><fA03 i2="1"><s0>Proc. SPIE Int. Soc. Opt. Eng.</s0></fA03><fA05><s2>7244</s2></fA05><fA08 i1="01" i2="1" l="ENG"><s1>Bayer Bilateral Denoising on TriMedia3270</s1></fA08><fA09 i1="01" i2="1" l="ENG"><s1>Real time image and video processing 2009 : 19-20 January 2009, San Jose, California, USA</s1></fA09><fA11 i1="01" i2="1"><s1>PHELIPPEAU (H.)</s1></fA11><fA11 i1="02" i2="1"><s1>AKIL (M.)</s1></fA11><fA11 i1="03" i2="1"><s1>DIAS RODRIGUES (B.)</s1></fA11><fA11 i1="04" i2="1"><s1>TALBOT (H.)</s1></fA11><fA11 i1="05" i2="1"><s1>BARA (S.)</s1></fA11><fA12 i1="01" i2="1"><s1>KEHTARNAVAZ (Nasser)</s1><s9>ed.</s9></fA12><fA12 i1="02" i2="1"><s1>CARLSOHN (Matthias F.)</s1><s9>ed.</s9></fA12><fA14 i1="01"><s1>Université Paris-Est, Labinfo, ESIEE</s1><s2>93162 Noisy-le-Grand</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>2 aut.</sZ><sZ>4 aut.</sZ></fA14><fA14 i1="02"><s1>NXP Semiconductors, 2 Esplanade Anton Philips Campus Effiscience, Colombelles BP 2000 14906</s1><s2>Caen</s2><s3>FRA</s3><sZ>1 aut.</sZ><sZ>5 aut.</sZ></fA14><fA14 i1="03"><s1>Universidade Federal de Minas Gerais - UFMG</s1><s2>Belo Horizonte, Minas Gerais</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA18 i1="01" i2="1"><s1>SPIE</s1><s3>USA</s3><s9>org-cong.</s9></fA18><fA20><s2>72440A.1-72440A.13</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA25 i1="01"><s1>SPIE</s1><s2>Bellingham, Wash.</s2></fA25><fA26 i1="01"><s0>978-0-8194-7494-0</s0></fA26><fA43 i1="01"><s1>INIST</s1><s2>21760</s2><s5>354000172971520090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>13 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0417551</s0></fA47><fA60><s1>P</s1><s2>C</s2></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Proceedings of SPIE, the International Society for Optical Engineering</s0></fA64><fA66 i1="01"><s0>USA</s0></fA66><fC01 i1="01" l="ENG"><s0>Digital cameras are now commonly included in several digital devices such as mobile phones. They are present everywhere and have become the principal image capturing tool. Inherent to light and semiconductors properties, sensor noise [10] continues to be an important factor of image quality [12], especially in low light conditions. Removing the noise with mathematical solutions appears thus unavoidable to obtain an acceptable image quality. However, embedded devices are limited by processing capabilities and power consumption and thus cannot make use of the full range of complex mathematical noise removing solutions. The bilateral filter [6] appears to be an interesting compromise between implementation complexity and noise removing performances. Especially, the Bayer [5] bilateral filter proposed in [I is well adapted for single sensor devices. In this paper, we simulate and optimize the Bayer bilateral filter execution on a common media-processor: the TM3270 [4] from the NXP Semiconductors TriMedia family. To do so we use the TriMedia Compilation System (TCS). We applied common optimization techniques (such as LUT, loop unrolling, convenient data type representation) as well as custom TriMedia operations. We finally propose a new Bayer bilateral filter formulation dedicated to the TM3270 architecture that yields an execution improvement of 99.6% compared to the naive version. This improvement results in real-time video processing at VGA resolution at the 350MHz clock rate.</s0></fC01><fC02 i1="01" i2="3"><s0>001B00A30C</s0></fC02><fC02 i1="02" i2="3"><s0>001B40B30</s0></fC02><fC03 i1="01" i2="3" l="FRE"><s0>Radiocommunication service mobile</s0><s5>03</s5></fC03><fC03 i1="01" i2="3" l="ENG"><s0>Mobile radio</s0><s5>03</s5></fC03><fC03 i1="02" i2="3" l="FRE"><s0>Système temps réel</s0><s5>11</s5></fC03><fC03 i1="02" i2="3" l="ENG"><s0>Real time systems</s0><s5>11</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Méthode optimisation</s0><s5>23</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Optimization method</s0><s5>23</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Método optimización</s0><s5>23</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Qualité image</s0><s5>41</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Image quality</s0><s5>41</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Calidad imagen</s0><s5>41</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Imagerie</s0><s5>61</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Imagery</s0><s5>61</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Imaginería</s0><s5>61</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Réduction bruit</s0><s5>62</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Noise reduction</s0><s5>62</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Reducción ruido</s0><s5>62</s5></fC03><fC03 i1="07" i2="3" l="FRE"><s0>Téléphone portable</s0><s5>63</s5></fC03><fC03 i1="07" i2="3" l="ENG"><s0>Mobile handsets</s0><s5>63</s5></fC03><fC03 i1="08" i2="3" l="FRE"><s0>Consommation énergie électrique</s0><s5>64</s5></fC03><fC03 i1="08" i2="3" l="ENG"><s0>Power consumption</s0><s5>64</s5></fC03><fC03 i1="09" i2="3" l="FRE"><s0>Implémentation</s0><s5>65</s5></fC03><fC03 i1="09" i2="3" l="ENG"><s0>Implementation</s0><s5>65</s5></fC03><fC03 i1="10" i2="3" l="FRE"><s0>Evaluation performance</s0><s5>66</s5></fC03><fC03 i1="10" i2="3" l="ENG"><s0>Performance evaluation</s0><s5>66</s5></fC03><fC03 i1="11" i2="3" l="FRE"><s0>Optimisation</s0><s5>67</s5></fC03><fC03 i1="11" i2="3" l="ENG"><s0>Optimization</s0><s5>67</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Table conversion</s0><s5>68</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Look up table</s0><s5>68</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Tabla de consulta</s0><s5>68</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Traitement temps réel</s0><s5>69</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Real time processing</s0><s5>69</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Tratamiento tiempo real</s0><s5>69</s5></fC03><fC03 i1="14" i2="3" l="FRE"><s0>0130C</s0><s4>INC</s4><s5>83</s5></fC03><fC03 i1="15" i2="3" l="FRE"><s0>4230</s0><s4>INC</s4><s5>84</s5></fC03><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA><pR><fA30 i1="01" i2="1" l="ENG"><s1>Electronic Imaging Science and Technology Symposium</s1><s3>San Jose CA USA</s3><s4>2009</s4></fA30></pR></standard><server><NO>PASCAL 09-0417551 INIST</NO><ET>Bayer Bilateral Denoising on TriMedia3270</ET><AU>PHELIPPEAU (H.); AKIL (M.); DIAS RODRIGUES (B.); TALBOT (H.); BARA (S.); KEHTARNAVAZ (Nasser); CARLSOHN (Matthias F.)</AU><AF>Université Paris-Est, Labinfo, ESIEE/93162 Noisy-le-Grand/France (1 aut., 2 aut., 4 aut.); NXP Semiconductors, 2 Esplanade Anton Philips Campus Effiscience, Colombelles BP 2000 14906/Caen/France (1 aut., 5 aut.); Universidade Federal de Minas Gerais - UFMG/Belo Horizonte, Minas Gerais/Brésil (3 aut.)</AF><DT>Publication en série; Congrès; Niveau analytique</DT><SO>Proceedings of SPIE, the International Society for Optical Engineering; ISSN 0277-786X; Coden PSISDG; Etats-Unis; Da. 2009; Vol. 7244; 72440A.1-72440A.13; Bibl. 13 ref.</SO><LA>Anglais</LA><EA>Digital cameras are now commonly included in several digital devices such as mobile phones. They are present everywhere and have become the principal image capturing tool. Inherent to light and semiconductors properties, sensor noise [10] continues to be an important factor of image quality [12], especially in low light conditions. Removing the noise with mathematical solutions appears thus unavoidable to obtain an acceptable image quality. However, embedded devices are limited by processing capabilities and power consumption and thus cannot make use of the full range of complex mathematical noise removing solutions. The bilateral filter [6] appears to be an interesting compromise between implementation complexity and noise removing performances. Especially, the Bayer [5] bilateral filter proposed in [I is well adapted for single sensor devices. In this paper, we simulate and optimize the Bayer bilateral filter execution on a common media-processor: the TM3270 [4] from the NXP Semiconductors TriMedia family. To do so we use the TriMedia Compilation System (TCS). We applied common optimization techniques (such as LUT, loop unrolling, convenient data type representation) as well as custom TriMedia operations. We finally propose a new Bayer bilateral filter formulation dedicated to the TM3270 architecture that yields an execution improvement of 99.6% compared to the naive version. This improvement results in real-time video processing at VGA resolution at the 350MHz clock rate.</EA><CC>001B00A30C; 001B40B30</CC><FD>Radiocommunication service mobile; Système temps réel; Méthode optimisation; Qualité image; Imagerie; Réduction bruit; Téléphone portable; Consommation énergie électrique; Implémentation; Evaluation performance; Optimisation; Table conversion; Traitement temps réel; 0130C; 4230</FD><ED>Mobile radio; Real time systems; Optimization method; Image quality; Imagery; Noise reduction; Mobile handsets; Power consumption; Implementation; Performance evaluation; Optimization; Look up table; Real time processing</ED><SD>Método optimización; Calidad imagen; Imaginería; Reducción ruido; Tabla de consulta; Tratamiento tiempo real</SD><LO>INIST-21760.354000172971520090</LO><ID>09-0417551</ID></server></inist></record>
000D98	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Activity of fulvestrant versus exemestane in advanced breast cancer patients with or without visceral metastases: data from the EFECT trial</title><author><name sortKey="Mauriac, Louis" uniqKey="Mauriac L">Louis Mauriac</name><affiliation><inist:fA14 i1="01"><s1>Institut Bergonié, Centre Régional de Lutte Contre le Cancer de Bordeaux et du Sud-Ouest, 229 Cours de l'Argonne</s1><s2>33076 Bordeaux</s2><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Romieu, Gilles" uniqKey="Romieu G">Gilles Romieu</name><affiliation><inist:fA14 i1="02"><s1>Centre Val D'Aurelle-Paul Lamarque</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></inist:fA14></affiliation></author><author><name sortKey="Bines, Jose" uniqKey="Bines J">José Bines</name><affiliation><inist:fA14 i1="03"><s1>Instituto Nacional de Câncer</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>3 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0417699</idno><date when="2009">2009</date><idno type="stanalyst">PASCAL 09-0417699 INIST</idno><idno type="RBID">Pascal:09-0417699</idno><idno type="wicri:Area/Main/Corpus">001B87</idno></publicationStmt><seriesStmt><idno type="ISSN">0167-6806</idno><title level="j" type="abbreviated">Breast cancer res. treat.</title><title level="j" type="main">Breast cancer research and treatment</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Advanced stage</term><term>Antineoplastic agent</term><term>Aromatase inhibitor</term><term>Biological activity</term><term>Breast cancer</term><term>Clinical trial</term><term>Comparative study</term><term>Data</term><term>Exemestane</term><term>Fulvestrant</term><term>Human</term><term>Metastasis</term><term>Patient</term><term>Viscus</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Activité biologique</term><term>Fulvestrant</term><term>Etude comparative</term><term>Exémestane</term><term>Stade avancé</term><term>Cancer du sein</term><term>Homme</term><term>Malade</term><term>Viscère</term><term>Métastase</term><term>Donnée</term><term>Essai clinique</term><term>Inhibiteur de l'aromatase</term><term>Anticancéreux</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Purpose Patients with visceral metastases (VM: lung and/or liver metastases) are generally regarded as being less responsive to hormonal therapy, and chemotherapy often becomes the default treatment. This paper reports a subgroup analysis from EFECT (The Evaluation of Faslodex versus Exemestane Clinical Trial) examining the efficacy of fulvestrant and exemestane in patients with or without VM. Methods EFECT is a randomised, double-blind, multicentre, Phase III trial in postmenopausal women with advanced breast cancer progressing or recurring after prior non-steroidal aromatase inhibitor therapy. Results Overall, approximately 57% of patients in EFECT had visceral involvement. Fulvestrant and exemestane demonstrated clinical benefit in 29.1% and 27.2% of patients with VM, respectively. Median duration of response was 13.5 vs 10.8 months and median duration of clinical benefit was 9.9 vs 8.1 months, respectively. Conclusions These results encourage the use of endocrine agents such as fulvestrant in treating patients with advanced breast cancer and VM.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0167-6806</s0></fA01><fA02 i1="01"><s0>BCTRD6</s0></fA02><fA03 i2="1"><s0>Breast cancer res. treat.</s0></fA03><fA05><s2>117</s2></fA05><fA06><s2>1</s2></fA06><fA08 i1="01" i2="1" l="ENG"><s1>Activity of fulvestrant versus exemestane in advanced breast cancer patients with or without visceral metastases: data from the EFECT trial</s1></fA08><fA11 i1="01" i2="1"><s1>MAURIAC (Louis)</s1></fA11><fA11 i1="02" i2="1"><s1>ROMIEU (Gilles)</s1></fA11><fA11 i1="03" i2="1"><s1>BINES (José)</s1></fA11><fA14 i1="01"><s1>Institut Bergonié, Centre Régional de Lutte Contre le Cancer de Bordeaux et du Sud-Ouest, 229 Cours de l'Argonne</s1><s2>33076 Bordeaux</s2><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Centre Val D'Aurelle-Paul Lamarque</s1><s2>Montpellier</s2><s3>FRA</s3><sZ>2 aut.</sZ></fA14><fA14 i1="03"><s1>Instituto Nacional de Câncer</s1><s2>Rio de Janeiro</s2><s3>BRA</s3><sZ>3 aut.</sZ></fA14><fA20><s1>69-75</s1></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>ENG</s0></fA23><fA43 i1="01"><s1>INIST</s1><s2>20699</s2><s5>354000171971390090</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>15 ref.</s0></fA45><fA47 i1="01" i2="1"><s0>09-0417699</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Breast cancer research and treatment</s0></fA64><fA66 i1="01"><s0>NLD</s0></fA66><fC01 i1="01" l="ENG"><s0>Purpose Patients with visceral metastases (VM: lung and/or liver metastases) are generally regarded as being less responsive to hormonal therapy, and chemotherapy often becomes the default treatment. This paper reports a subgroup analysis from EFECT (The Evaluation of Faslodex versus Exemestane Clinical Trial) examining the efficacy of fulvestrant and exemestane in patients with or without VM. Methods EFECT is a randomised, double-blind, multicentre, Phase III trial in postmenopausal women with advanced breast cancer progressing or recurring after prior non-steroidal aromatase inhibitor therapy. Results Overall, approximately 57% of patients in EFECT had visceral involvement. Fulvestrant and exemestane demonstrated clinical benefit in 29.1% and 27.2% of patients with VM, respectively. Median duration of response was 13.5 vs 10.8 months and median duration of clinical benefit was 9.9 vs 8.1 months, respectively. Conclusions These results encourage the use of endocrine agents such as fulvestrant in treating patients with advanced breast cancer and VM.</s0></fC01><fC02 i1="01" i2="X"><s0>002B20E02</s0></fC02><fC03 i1="01" i2="X" l="FRE"><s0>Activité biologique</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="ENG"><s0>Biological activity</s0><s5>01</s5></fC03><fC03 i1="01" i2="X" l="SPA"><s0>Actividad biológica</s0><s5>01</s5></fC03><fC03 i1="02" i2="X" l="FRE"><s0>Fulvestrant</s0><s2>NK</s2><s2>FR</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="ENG"><s0>Fulvestrant</s0><s2>NK</s2><s2>FR</s2><s5>02</s5></fC03><fC03 i1="02" i2="X" l="SPA"><s0>Fulvestrant</s0><s2>NK</s2><s2>FR</s2><s5>02</s5></fC03><fC03 i1="03" i2="X" l="FRE"><s0>Etude comparative</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="ENG"><s0>Comparative study</s0><s5>03</s5></fC03><fC03 i1="03" i2="X" l="SPA"><s0>Estudio comparativo</s0><s5>03</s5></fC03><fC03 i1="04" i2="X" l="FRE"><s0>Exémestane</s0><s2>NK</s2><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="ENG"><s0>Exemestane</s0><s2>NK</s2><s2>FR</s2><s5>04</s5></fC03><fC03 i1="04" i2="X" l="SPA"><s0>Exemestano</s0><s2>NK</s2><s2>FR</s2><s5>04</s5></fC03><fC03 i1="05" i2="X" l="FRE"><s0>Stade avancé</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="ENG"><s0>Advanced stage</s0><s5>05</s5></fC03><fC03 i1="05" i2="X" l="SPA"><s0>Estadio avanzado</s0><s5>05</s5></fC03><fC03 i1="06" i2="X" l="FRE"><s0>Cancer du sein</s0><s2>NM</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="ENG"><s0>Breast cancer</s0><s2>NM</s2><s5>06</s5></fC03><fC03 i1="06" i2="X" l="SPA"><s0>Cáncer del pecho</s0><s2>NM</s2><s5>06</s5></fC03><fC03 i1="07" i2="X" l="FRE"><s0>Homme</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="ENG"><s0>Human</s0><s5>07</s5></fC03><fC03 i1="07" i2="X" l="SPA"><s0>Hombre</s0><s5>07</s5></fC03><fC03 i1="08" i2="X" l="FRE"><s0>Malade</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="ENG"><s0>Patient</s0><s5>08</s5></fC03><fC03 i1="08" i2="X" l="SPA"><s0>Enfermo</s0><s5>08</s5></fC03><fC03 i1="09" i2="X" l="FRE"><s0>Viscère</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="ENG"><s0>Viscus</s0><s5>09</s5></fC03><fC03 i1="09" i2="X" l="SPA"><s0>Víscera</s0><s5>09</s5></fC03><fC03 i1="10" i2="X" l="FRE"><s0>Métastase</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="ENG"><s0>Metastasis</s0><s5>10</s5></fC03><fC03 i1="10" i2="X" l="SPA"><s0>Metástasis</s0><s5>10</s5></fC03><fC03 i1="11" i2="X" l="FRE"><s0>Donnée</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="ENG"><s0>Data</s0><s5>11</s5></fC03><fC03 i1="11" i2="X" l="SPA"><s0>Dato</s0><s5>11</s5></fC03><fC03 i1="12" i2="X" l="FRE"><s0>Essai clinique</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="ENG"><s0>Clinical trial</s0><s5>12</s5></fC03><fC03 i1="12" i2="X" l="SPA"><s0>Ensayo clínico</s0><s5>12</s5></fC03><fC03 i1="13" i2="X" l="FRE"><s0>Inhibiteur de l'aromatase</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="ENG"><s0>Aromatase inhibitor</s0><s5>13</s5></fC03><fC03 i1="13" i2="X" l="SPA"><s0>Inhibidor aromatase</s0><s5>13</s5></fC03><fC03 i1="14" i2="X" l="FRE"><s0>Anticancéreux</s0><s5>23</s5></fC03><fC03 i1="14" i2="X" l="ENG"><s0>Antineoplastic agent</s0><s5>23</s5></fC03><fC03 i1="14" i2="X" l="SPA"><s0>Anticanceroso</s0><s5>23</s5></fC03><fC07 i1="01" i2="X" l="FRE"><s0>Antagoniste</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="ENG"><s0>Antagonist</s0><s5>37</s5></fC07><fC07 i1="01" i2="X" l="SPA"><s0>Antagonista</s0><s5>37</s5></fC07><fC07 i1="02" i2="X" l="FRE"><s0>Antihormone</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="ENG"><s0>Antihormone</s0><s5>38</s5></fC07><fC07 i1="02" i2="X" l="SPA"><s0>Antihormona</s0><s5>38</s5></fC07><fC07 i1="03" i2="X" l="FRE"><s0>Antioestrogène</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="ENG"><s0>Antiestrogen</s0><s5>39</s5></fC07><fC07 i1="03" i2="X" l="SPA"><s0>Antiestrógeno</s0><s5>39</s5></fC07><fC07 i1="04" i2="X" l="FRE"><s0>Récepteur oestrogène</s0><s5>40</s5></fC07><fC07 i1="04" i2="X" l="ENG"><s0>Estrogen receptor</s0><s5>40</s5></fC07><fC07 i1="04" i2="X" l="SPA"><s0>Receptor estrógeno</s0><s5>40</s5></fC07><fC07 i1="05" i2="X" l="FRE"><s0>Dérivé de l'androstane</s0><s2>FR</s2><s5>41</s5></fC07><fC07 i1="05" i2="X" l="ENG"><s0>Androstane derivatives</s0><s2>FR</s2><s5>41</s5></fC07><fC07 i1="05" i2="X" l="SPA"><s0>Androstano derivado</s0><s2>FR</s2><s5>41</s5></fC07><fC07 i1="06" i2="X" l="FRE"><s0>Estrogen synthase</s0><s2>FE</s2><s5>42</s5></fC07><fC07 i1="06" i2="X" l="ENG"><s0>Estrogen synthase</s0><s2>FE</s2><s5>42</s5></fC07><fC07 i1="06" i2="X" l="SPA"><s0>Estrogen synthase</s0><s2>FE</s2><s5>42</s5></fC07><fC07 i1="07" i2="X" l="FRE"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="07" i2="X" l="ENG"><s0>Enzyme</s0><s2>FE</s2></fC07><fC07 i1="07" i2="X" l="SPA"><s0>Enzima</s0><s2>FE</s2></fC07><fC07 i1="08" i2="X" l="FRE"><s0>Inhibiteur enzyme</s0><s5>43</s5></fC07><fC07 i1="08" i2="X" l="ENG"><s0>Enzyme inhibitor</s0><s5>43</s5></fC07><fC07 i1="08" i2="X" l="SPA"><s0>Inhibidor enzima</s0><s5>43</s5></fC07><fC07 i1="09" i2="X" l="FRE"><s0>Stéroïde</s0><s5>44</s5></fC07><fC07 i1="09" i2="X" l="ENG"><s0>Steroid</s0><s5>44</s5></fC07><fC07 i1="09" i2="X" l="SPA"><s0>Esteroide</s0><s5>44</s5></fC07><fC07 i1="10" i2="X" l="FRE"><s0>Tumeur maligne</s0><s2>NM</s2><s5>45</s5></fC07><fC07 i1="10" i2="X" l="ENG"><s0>Malignant tumor</s0><s2>NM</s2><s5>45</s5></fC07><fC07 i1="10" i2="X" l="SPA"><s0>Tumor maligno</s0><s2>NM</s2><s5>45</s5></fC07><fC07 i1="11" i2="X" l="FRE"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="11" i2="X" l="ENG"><s0>Cancer</s0><s2>NM</s2></fC07><fC07 i1="11" i2="X" l="SPA"><s0>Cáncer</s0><s2>NM</s2></fC07><fC07 i1="12" i2="X" l="FRE"><s0>Pathologie de la glande mammaire</s0><s2>NM</s2><s5>46</s5></fC07><fC07 i1="12" i2="X" l="ENG"><s0>Mammary gland diseases</s0><s2>NM</s2><s5>46</s5></fC07><fC07 i1="12" i2="X" l="SPA"><s0>Glándula mamaria patología</s0><s2>NM</s2><s5>46</s5></fC07><fC07 i1="13" i2="X" l="FRE"><s0>Pathologie du sein</s0><s2>NM</s2><s5>47</s5></fC07><fC07 i1="13" i2="X" l="ENG"><s0>Breast disease</s0><s2>NM</s2><s5>47</s5></fC07><fC07 i1="13" i2="X" l="SPA"><s0>Seno patología</s0><s2>NM</s2><s5>47</s5></fC07><fC07 i1="14" i2="X" l="FRE"><s0>Récepteur hormonal</s0><s5>48</s5></fC07><fC07 i1="14" i2="X" l="ENG"><s0>Hormonal receptor</s0><s5>48</s5></fC07><fC07 i1="14" i2="X" l="SPA"><s0>Receptor hormonal</s0><s5>48</s5></fC07><fC07 i1="15" i2="X" l="FRE"><s0>Régulateur négatif sélectif du récepteur des oestrogènes</s0><s4>INC</s4><s5>86</s5></fC07><fN21><s1>299</s1></fN21><fN44 i1="01"><s1>OTO</s1></fN44><fN82><s1>OTO</s1></fN82></pA></standard><server><NO>PASCAL 09-0417699 INIST</NO><ET>Activity of fulvestrant versus exemestane in advanced breast cancer patients with or without visceral metastases: data from the EFECT trial</ET><AU>MAURIAC (Louis); ROMIEU (Gilles); BINES (José)</AU><AF>Institut Bergonié, Centre Régional de Lutte Contre le Cancer de Bordeaux et du Sud-Ouest, 229 Cours de l'Argonne/33076 Bordeaux/France (1 aut.); Centre Val D'Aurelle-Paul Lamarque/Montpellier/France (2 aut.); Instituto Nacional de Câncer/Rio de Janeiro/Brésil (3 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Breast cancer research and treatment; ISSN 0167-6806; Coden BCTRD6; Pays-Bas; Da. 2009; Vol. 117; No. 1; Pp. 69-75; Bibl. 15 ref.</SO><LA>Anglais</LA><EA>Purpose Patients with visceral metastases (VM: lung and/or liver metastases) are generally regarded as being less responsive to hormonal therapy, and chemotherapy often becomes the default treatment. This paper reports a subgroup analysis from EFECT (The Evaluation of Faslodex versus Exemestane Clinical Trial) examining the efficacy of fulvestrant and exemestane in patients with or without VM. Methods EFECT is a randomised, double-blind, multicentre, Phase III trial in postmenopausal women with advanced breast cancer progressing or recurring after prior non-steroidal aromatase inhibitor therapy. Results Overall, approximately 57% of patients in EFECT had visceral involvement. Fulvestrant and exemestane demonstrated clinical benefit in 29.1% and 27.2% of patients with VM, respectively. Median duration of response was 13.5 vs 10.8 months and median duration of clinical benefit was 9.9 vs 8.1 months, respectively. Conclusions These results encourage the use of endocrine agents such as fulvestrant in treating patients with advanced breast cancer and VM.</EA><CC>002B20E02</CC><FD>Activité biologique; Fulvestrant; Etude comparative; Exémestane; Stade avancé; Cancer du sein; Homme; Malade; Viscère; Métastase; Donnée; Essai clinique; Inhibiteur de l'aromatase; Anticancéreux</FD><FG>Antagoniste; Antihormone; Antioestrogène; Récepteur oestrogène; Dérivé de l'androstane; Estrogen synthase; Enzyme; Inhibiteur enzyme; Stéroïde; Tumeur maligne; Cancer; Pathologie de la glande mammaire; Pathologie du sein; Récepteur hormonal; Régulateur négatif sélectif du récepteur des oestrogènes</FG><ED>Biological activity; Fulvestrant; Comparative study; Exemestane; Advanced stage; Breast cancer; Human; Patient; Viscus; Metastasis; Data; Clinical trial; Aromatase inhibitor; Antineoplastic agent</ED><EG>Antagonist; Antihormone; Antiestrogen; Estrogen receptor; Androstane derivatives; Estrogen synthase; Enzyme; Enzyme inhibitor; Steroid; Malignant tumor; Cancer; Mammary gland diseases; Breast disease; Hormonal receptor</EG><SD>Actividad biológica; Fulvestrant; Estudio comparativo; Exemestano; Estadio avanzado; Cáncer del pecho; Hombre; Enfermo; Víscera; Metástasis; Dato; Ensayo clínico; Inhibidor aromatase; Anticanceroso</SD><LO>INIST-20699.354000171971390090</LO><ID>09-0417699</ID></server></inist></record>
000D99	<record><TEI xmlns:wicri="http://ticri.inpl-nancy.fr" xmlns:inist="http://www.inist.fr"><teiHeader><fileDesc><titleStmt><title xml:lang="fr" level="a">L'articulation &#34;thêmata-fond topique&#34;: fondements théoriques et application pragmatique</title><author><name sortKey="Camara Lima, Loura" uniqKey="Camara Lima L">Loura Camara Lima</name><affiliation><inist:fA14 i1="01"><s1>Université Fédérale de Mato Grosso UFMT</s1><s3>BRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation><affiliation><inist:fA14 i1="02"><s1>Centre Edgar Morin-EHESS</s1><s3>FRA</s3><sZ>1 aut.</sZ></inist:fA14></affiliation></author></titleStmt><publicationStmt><idno type="inist">09-0418176</idno><date when="2009">2009</date><idno type="stanalyst">FRANCIS 09-0418176 INIST</idno><idno type="RBID">Francis:09-0418176</idno><idno type="wicri:Area/Main/Corpus">001F86</idno></publicationStmt><seriesStmt><idno type="ISSN">0181-4095</idno><title level="j" type="abbreviated">Lang. soc. : (Paris)</title><title level="j" type="main">Langage et société : (Maison des Sciences de l'Homme)</title></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Social psychology</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Psychologie sociale</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="fr">Cet article reprend et explique les concepts de thêmata et de fond topique, dans le cadre des modèles théoriques dans lesquels ils ont été définis. Son but est double: a) démontrer que ces concepts possèdent une série de caractéristiques communes et b) expliquer les raisons qui nous conduisent à concevoir l'idée de les articuler. Du point de vue du psychologue social, l'articulation thêmata-fond topique représente un grand avantage, parce qu'elle apporte au chercheur les clés qui lui permettent d'établir une correspondance entre le niveau des représentations et le niveau des lexiques. Un exemple est donné pour illustrer cette correspondance.</div></front></TEI><inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0181-4095</s0></fA01><fA03 i2="1"><s0>Lang. soc. : (Paris)</s0></fA03><fA05><s2>129</s2></fA05><fA08 i1="01" i2="1" l="FRE"><s1>L'articulation &#34;thêmata-fond topique&#34;: fondements théoriques et application pragmatique</s1></fA08><fA11 i1="01" i2="1"><s1>CAMARA LIMA (Loura)</s1></fA11><fA14 i1="01"><s1>Université Fédérale de Mato Grosso UFMT</s1><s3>BRA</s3><sZ>1 aut.</sZ></fA14><fA14 i1="02"><s1>Centre Edgar Morin-EHESS</s1><s3>FRA</s3><sZ>1 aut.</sZ></fA14><fA20><s2>83-100, 163 [19 p.]</s2></fA20><fA21><s1>2009</s1></fA21><fA23 i1="01"><s0>FRE</s0></fA23><fA24 i1="01"><s0>eng</s0></fA24><fA43 i1="01"><s1>INIST</s1><s2>19531</s2><s5>354000171839560050</s5></fA43><fA44><s0>0000</s0><s1>© 2009 INIST-CNRS. All rights reserved.</s1></fA44><fA45><s0>1 p.1/4</s0></fA45><fA47 i1="01" i2="1"><s0>09-0418176</s0></fA47><fA60><s1>P</s1></fA60><fA61><s0>A</s0></fA61><fA64 i1="01" i2="1"><s0>Langage et société : (Maison des Sciences de l'Homme)</s0></fA64><fA66 i1="01"><s0>FRA</s0></fA66><fA68 i1="01" i2="1" l="ENG"><s1>Articulating themata and topic-ground: theoretical basis and a pragmatic application</s1></fA68><fC01 i1="01" l="FRE"><s0>Cet article reprend et explique les concepts de thêmata et de fond topique, dans le cadre des modèles théoriques dans lesquels ils ont été définis. Son but est double: a) démontrer que ces concepts possèdent une série de caractéristiques communes et b) expliquer les raisons qui nous conduisent à concevoir l'idée de les articuler. Du point de vue du psychologue social, l'articulation thêmata-fond topique représente un grand avantage, parce qu'elle apporte au chercheur les clés qui lui permettent d'établir une correspondance entre le niveau des représentations et le niveau des lexiques. Un exemple est donné pour illustrer cette correspondance.</s0></fC01><fC02 i1="01" i2="L"><s0>52422</s0><s1>III</s1></fC02><fC02 i1="02" i2="L"><s0>524</s0></fC02><fC03 i1="01" i2="L" l="FRE"><s0>Psychologie sociale</s0><s2>NI</s2><s5>01</s5></fC03><fC03 i1="01" i2="L" l="ENG"><s0>Social psychology</s0><s2>NI</s2><s5>01</s5></fC03><fN21><s1>306</s1></fN21></pA></standard><server><NO>FRANCIS 09-0418176 INIST</NO><FT>L'articulation &#34;thêmata-fond topique&#34;: fondements théoriques et application pragmatique</FT><ET>(Articulating themata and topic-ground: theoretical basis and a pragmatic application)</ET><AU>CAMARA LIMA (Loura)</AU><AF>Université Fédérale de Mato Grosso UFMT/Brésil (1 aut.); Centre Edgar Morin-EHESS/France (1 aut.)</AF><DT>Publication en série; Niveau analytique</DT><SO>Langage et société : (Maison des Sciences de l'Homme); ISSN 0181-4095; France; Da. 2009; Vol. 129; 83-100, 163 [19 p.]; Abs. anglais; Bibl. 1 p.1/4</SO><LA>Français</LA><FA>Cet article reprend et explique les concepts de thêmata et de fond topique, dans le cadre des modèles théoriques dans lesquels ils ont été définis. Son but est double: a) démontrer que ces concepts possèdent une série de caractéristiques communes et b) expliquer les raisons qui nous conduisent à concevoir l'idée de les articuler. Du point de vue du psychologue social, l'articulation thêmata-fond topique représente un grand avantage, parce qu'elle apporte au chercheur les clés qui lui permettent d'établir une correspondance entre le niveau des représentations et le niveau des lexiques. Un exemple est donné pour illustrer cette correspondance.</FA><CC>52422; 524</CC><FD>Psychologie sociale</FD><ED>Social psychology</ED><LO>INIST-19531.354000171839560050</LO><ID>09-0418176</ID></server></inist></record>