Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border
Identifieur interne : 001301 ( Istex/Corpus ); précédent : 001300; suivant : 001302Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border
Auteurs : S. M. Bardet ; I. Cobos ; E. Puelles ; M. Martínez-De-La-Torre ; L. PuellesSource :
- Journal of Comparative Neurology [ 0021-9967 ] ; 2006-12-10.
English descriptors
- KwdEn :
- BEN protein, Dlx5, Nkx2.1, Nkx2.2, Nkx6.1, Shh, calbindin, preoptic area, septum, subpallium.
Abstract
The avian lateral septal organ (LSO) is a telencephalic circumventricular specialization with liquor‐contacting neurons (Kuenzel and van Tienhoven [1982] J. Comp. Neurol. 206:293–313). We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of Dlx5 and Nkx2.1 homeobox genes, or the Shh gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for Nkx2.1, Nkx2.2, Nkx6.1, Shh, and Dlx5 mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear Dlx5‐expressing ventricular domain that surrounds the Nkx2.1‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. Neurol. 499:745–767, 2006. © 2006 Wiley‐Liss, Inc.
Url:
DOI: 10.1002/cne.21121
Links to Exploration step
ISTEX:EFD5AE4C7D99EC80DB7DA33BC8964B92A67C640BLe document en format XML
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Puelles</name><affiliation><mods:affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Journal of Comparative Neurology</title><title level="j" type="abbrev">J. Comp. 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Comp. Neurol. 206:293–313). We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of Dlx5 and Nkx2.1 homeobox genes, or the Shh gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for Nkx2.1, Nkx2.2, Nkx6.1, Shh, and Dlx5 mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear Dlx5‐expressing ventricular domain that surrounds the Nkx2.1‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. Neurol. 499:745–767, 2006. © 2006 Wiley‐Liss, Inc.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>S.M. Bardet</name><affiliations><json:string>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</json:string></affiliations></json:item><json:item><name>I. Cobos</name><affiliations><json:string>Nina Ireland Laboratory of Developmental Neurobiology, Center for Neurobiology and Psychiatry, University of California San Francisco, San Francisco, California 94143‐2611</json:string></affiliations></json:item><json:item><name>E. Puelles</name><affiliations><json:string>Institute of Neuroscience of Alicante, UMH‐CSIC, Unidad de Neurobiología del Desarrollo; Universidad Miguel Hernández, Campus de San Juan, San Juan E03550, Alicante, Spain</json:string></affiliations></json:item><json:item><name>M. Martínez‐De‐La‐Torre</name><affiliations><json:string>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</json:string></affiliations></json:item><json:item><name>L. 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Comp. Neurol. 206:293–313). We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of Dlx5 and Nkx2.1 homeobox genes, or the Shh gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for Nkx2.1, Nkx2.2, Nkx6.1, Shh, and Dlx5 mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear Dlx5‐expressing ventricular domain that surrounds the Nkx2.1‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. 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We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of Dlx5 and Nkx2.1 homeobox genes, or the Shh gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for Nkx2.1, Nkx2.2, Nkx6.1, Shh, and Dlx5 mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear Dlx5‐expressing ventricular domain that surrounds the Nkx2.1‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. Neurol. 499:745–767, 2006. © 2006 Wiley‐Liss, Inc.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>keywords</head><item><term>preoptic area</term></item><item><term>septum</term></item><item><term>subpallium</term></item><item><term>calbindin</term></item><item><term>BEN protein</term></item><item><term>Nkx2.2</term></item><item><term>Nkx6.1</term></item><item><term>Shh</term></item><item><term>Dlx5</term></item><item><term>Nkx2.1</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>article-category</head><item><term>Article</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2006-03-07">Received</change><change when="2006-06-14">Registration</change><change when="2006-12-10">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/EFD5AE4C7D99EC80DB7DA33BC8964B92A67C640B/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>Hoboken</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1096-9861</doi><issn type="print">0021-9967</issn><issn type="electronic">1096-9861</issn><idGroup><id type="product" value="CNE"></id></idGroup><titleGroup><title type="main" xml:lang="en">Journal of Comparative Neurology</title><title type="short">J. 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Neurol.</title></titleGroup></publicationMeta><publicationMeta level="part" position="50"><doi origin="wiley" registered="yes">10.1002/cne.v499:5</doi><numberingGroup><numbering type="journalVolume" number="499">499</numbering><numbering type="journalIssue">5</numbering></numberingGroup><coverDate startDate="2006-12-10">10 December 2006</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="50" status="forIssue"><doi origin="wiley" registered="yes">10.1002/cne.21121</doi><idGroup><id type="unit" value="CNE21121"></id></idGroup><countGroup><count type="pageTotal" number="23"></count></countGroup><titleGroup><title type="articleCategory">Article</title><title type="tocHeading1">Articles</title></titleGroup><copyright ownership="publisher">Copyright © 2006 Wiley‐Liss, Inc.</copyright><eventGroup><event type="manuscriptReceived" date="2006-03-07"></event><event type="manuscriptRevised" date="2006-04-27"></event><event type="manuscriptAccepted" date="2006-06-14"></event><event type="firstOnline" date="2006-10-17"></event><event type="publishedOnlineFinalForm" date="2006-10-17"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-01"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-15"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-30"></event></eventGroup><numberingGroup><numbering type="pageFirst">745</numbering><numbering type="pageLast">767</numbering></numberingGroup><correspondenceTo>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CNE.CNE21121.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="11"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="78"></count><count type="wordTotal" number="15298"></count></countGroup><titleGroup><title type="main" xml:lang="en">Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border</title><title type="short" xml:lang="en">Striatal Circumventricular Organs ABUT Pallidum</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1"><personName><givenNames>S.M.</givenNames><familyName>Bardet</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>I.</givenNames><familyName>Cobos</familyName></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af3"><personName><givenNames>E.</givenNames><familyName>Puelles</familyName></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1"><personName><givenNames>M.</givenNames><familyName>Martínez‐De‐La‐Torre</familyName></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><givenNames>L.</givenNames><familyName>Puelles</familyName></personName><contactDetails><email>puelles@um.es</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="ES" type="organization"><unparsedAffiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="US" type="organization"><unparsedAffiliation>Nina Ireland Laboratory of Developmental Neurobiology, Center for Neurobiology and Psychiatry, University of California San Francisco, San Francisco, California 94143‐2611</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="ES" type="organization"><unparsedAffiliation>Institute of Neuroscience of Alicante, UMH‐CSIC, Unidad de Neurobiología del Desarrollo; Universidad Miguel Hernández, Campus de San Juan, San Juan E03550, Alicante, Spain</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">preoptic area</keyword><keyword xml:id="kwd2">septum</keyword><keyword xml:id="kwd3">subpallium</keyword><keyword xml:id="kwd4">calbindin</keyword><keyword xml:id="kwd5">BEN protein</keyword><keyword xml:id="kwd6"><i>Nkx2.2</i></keyword><keyword xml:id="kwd7"><i>Nkx6.1</i></keyword><keyword xml:id="kwd8"><i>Shh</i></keyword><keyword xml:id="kwd9"><i>Dlx5</i></keyword><keyword xml:id="kwd10"><i>Nkx2.1</i></keyword></keywordGroup><fundingInfo><fundingAgency>Spanish Ministry of Education and Science (MEC)</fundingAgency><fundingNumber>PB2002‐3668</fundingNumber><fundingNumber>BFU2005‐09378‐C02‐01/BFI</fundingNumber></fundingInfo><fundingInfo><fundingAgency>MEC and Alicante Institute of Neuroscience (UMH‐CSIC)</fundingAgency></fundingInfo><abstractGroup><abstract type="main" xml:lang="fr"><title type="main">Abstract</title><p>The avian lateral septal organ (LSO) is a telencephalic circumventricular specialization with liquor‐contacting neurons (Kuenzel and van Tienhoven [1982] J. Comp. Neurol. 206:293–313). We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of <i>Dlx5</i> and <i>Nkx2.1</i> homeobox genes, or the <i>Shh</i> gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for <i>Nkx2.1</i>, <i>Nkx2.2</i>, <i>Nkx6.1</i>, <i>Shh</i>, and <i>Dlx5</i> mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear <i>Dlx5</i>‐expressing ventricular domain that surrounds the <i>Nkx2.1</i>‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. Neurol. 499:745–767, 2006. © 2006 Wiley‐Liss, Inc.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Striatal Circumventricular Organs ABUT Pallidum</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border</title></titleInfo><name type="personal"><namePart type="given">S.M.</namePart><namePart type="family">Bardet</namePart><affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">I.</namePart><namePart type="family">Cobos</namePart><affiliation>Nina Ireland Laboratory of Developmental Neurobiology, Center for Neurobiology and Psychiatry, University of California San Francisco, San Francisco, California 94143‐2611</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E.</namePart><namePart type="family">Puelles</namePart><affiliation>Institute of Neuroscience of Alicante, UMH‐CSIC, Unidad de Neurobiología del Desarrollo; Universidad Miguel Hernández, Campus de San Juan, San Juan E03550, Alicante, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Martínez‐De‐La‐Torre</namePart><affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">L.</namePart><namePart type="family">Puelles</namePart><affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</affiliation><affiliation>Department of Human Anatomy and Psychobiology, Medical School, University of Murcia, Murcia E30071, Spain</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2006-12-10</dateIssued><dateCaptured encoding="w3cdtf">2006-03-07</dateCaptured><dateValid encoding="w3cdtf">2006-06-14</dateValid><copyrightDate encoding="w3cdtf">2006</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">11</extent><extent unit="tables">1</extent><extent unit="references">78</extent><extent unit="words">15298</extent></physicalDescription><abstract lang="fr">The avian lateral septal organ (LSO) is a telencephalic circumventricular specialization with liquor‐contacting neurons (Kuenzel and van Tienhoven [1982] J. Comp. Neurol. 206:293–313). We studied the topological position of the chicken LSO relative to molecular borders defined previously within the telencephalic subpallium (Puelles et al. [2000] J. Comp. Neurol. 424:409–438). Differential expression of Dlx5 and Nkx2.1 homeobox genes, or the Shh gene encoding a secreted morphogen, allows distinction of striatal, pallidal, and preoptic subpallial sectors. The chicken LSO complex was characterized chemoarchitectonically from embryonic to posthatching stages, by using immunohistochemistry for calbindin, tyrosine hydroxylase, NKX2.1, and BEN proteins and in situ hybridization for Nkx2.1, Nkx2.2, Nkx6.1, Shh, and Dlx5 mRNA. Medial and lateral parts of LSO appear, respectively, at the striatal part of the septum and adjacent bottom of the lateral ventricle (accumbens), in lateral continuity with another circumventricular organ that forms along a thin subregion of the entire striatum, abutting the molecular striatopallidal boundary; we called this the “striatopallidal organ” (SPO). The SPO displays associated distal periventricular cells, which are lacking in the LSO. Moreover, the SPO is continuous caudomedially with a thin, linear ependymal specialization found around the extended amygdala and preoptic areas. This differs from SPO and LSO in some molecular aspects. We tentatively identified this structure as being composed of an “extended amygdala organ” (EAO) and a “preoptohypothalamic organ” (PHO). The position of LSO, SPO, EAO, and PHO within a linear Dlx5‐expressing ventricular domain that surrounds the Nkx2.1‐expressing pallidopreoptic domain provides an unexpected insight into possible common and differential causal mechanisms underlying their formation. J. Comp. Neurol. 499:745–767, 2006. © 2006 Wiley‐Liss, Inc.</abstract><note type="funding">Spanish Ministry of Education and Science (MEC) - No. PB2002‐3668; No. BFU2005‐09378‐C02‐01/BFI; </note><note type="funding">MEC and Alicante Institute of Neuroscience (UMH‐CSIC)</note><subject lang="en"><genre>keywords</genre><topic>preoptic area</topic><topic>septum</topic><topic>subpallium</topic><topic>calbindin</topic><topic>BEN protein</topic><topic>Nkx2.2</topic><topic>Nkx6.1</topic><topic>Shh</topic><topic>Dlx5</topic><topic>Nkx2.1</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Comparative Neurology</title></titleInfo><titleInfo type="abbreviated"><title>J. Comp. Neurol.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Article</topic></subject><identifier type="ISSN">0021-9967</identifier><identifier type="eISSN">1096-9861</identifier><identifier type="DOI">10.1002/(ISSN)1096-9861</identifier><identifier type="PublisherID">CNE</identifier><part><date>2006</date><detail type="volume"><caption>vol.</caption><number>499</number></detail><detail type="issue"><caption>no.</caption><number>5</number></detail><extent unit="pages"><start>745</start><end>767</end><total>23</total></extent></part></relatedItem><identifier type="istex">EFD5AE4C7D99EC80DB7DA33BC8964B92A67C640B</identifier><identifier type="DOI">10.1002/cne.21121</identifier><identifier type="ArticleID">CNE21121</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2006 Wiley‐Liss, Inc.</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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