G/A1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease
Identifieur interne :
003233 ( PascalFrancis/Corpus );
précédent :
003232;
suivant :
003234
G/A1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease
Auteurs : T. Xie ;
S. L. Ho ;
L. S. W. Li ;
O. C. K. MaSource :
-
Movement disorders [ 0885-3185 ] ; 1997.
RBID : Pascal:97-0321227
Descripteurs français
English descriptors
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
| pA |
| A01 | 01 | 1 | | @0 0885-3185 |
|---|
| A03 | | 1 | | @0 Mov. disord. |
|---|
| A05 | | | | @2 12 |
|---|
| A06 | | | | @2 3 |
|---|
| A08 | 01 | 1 | ENG | @1 G/A1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease |
|---|
| A11 | 01 | 1 | | @1 XIE (T.) |
|---|
| A11 | 02 | 1 | | @1 HO (S. L.) |
|---|
| A11 | 03 | 1 | | @1 LI (L. S. W.) |
|---|
| A11 | 04 | 1 | | @1 MA (O. C. K.) |
|---|
| A14 | 01 | | | @1 University Department of Medicine, University of Hong Kong, Queen Mary Hospital @3 HKG @Z 1 aut. @Z 2 aut. @Z 3 aut. |
|---|
| A14 | 02 | | | @1 Clinical Biochemistry Unit, University of Hong Kong, Queen Mary Hospital @3 HKG @Z 4 aut. |
|---|
| A20 | | | | @1 426-427 |
|---|
| A21 | | | | @1 1997 |
|---|
| A23 | 01 | | | @0 ENG |
|---|
| A43 | 01 | | | @1 INIST @2 20953 @5 354000061493640230 |
|---|
| A44 | | | | @0 0000 @1 © 1997 INIST-CNRS. All rights reserved. |
|---|
| A45 | | | | @0 7 ref. |
|---|
| A47 | 01 | 1 | | @0 97-0321227 |
|---|
| A60 | | | | @1 P @3 CC |
|---|
| A61 | | | | @0 A |
|---|
| A64 | 01 | 1 | | @0 Movement disorders |
|---|
| A66 | 01 | | | @0 USA |
|---|
| C02 | 01 | X | | @0 002B17G |
|---|
| C03 | 01 | X | FRE | @0 Parkinson maladie @5 01 |
|---|
| C03 | 01 | X | ENG | @0 Parkinson disease @5 01 |
|---|
| C03 | 01 | X | SPA | @0 Parkinson enfermedad @5 01 |
|---|
| C03 | 02 | X | FRE | @0 Polymorphisme @5 04 |
|---|
| C03 | 02 | X | ENG | @0 Polymorphism @5 04 |
|---|
| C03 | 02 | X | SPA | @0 Polimorfismo @5 04 |
|---|
| C03 | 03 | X | FRE | @0 Gène @5 05 |
|---|
| C03 | 03 | X | ENG | @0 Gene @5 05 |
|---|
| C03 | 03 | X | SPA | @0 Gen @5 05 |
|---|
| C03 | 04 | X | FRE | @0 Catechol O-methyltransferase @2 FE @5 06 @6 Catechol «O»-methyltransferase |
|---|
| C03 | 04 | X | ENG | @0 Catechol O-methyltransferase @2 FE @5 06 @6 Catechol «O»-methyltransferase |
|---|
| C03 | 04 | X | SPA | @0 Catechol O-methyltransferase @2 FE @5 06 @6 Catechol «O»-methyltransferase |
|---|
| C03 | 05 | X | FRE | @0 Allèle @5 07 |
|---|
| C03 | 05 | X | ENG | @0 Allele @5 07 |
|---|
| C03 | 05 | X | SPA | @0 Alelo @5 07 |
|---|
| C03 | 06 | X | FRE | @0 Base nucléique @5 08 |
|---|
| C03 | 06 | X | ENG | @0 Nucleic base @5 08 |
|---|
| C03 | 06 | X | SPA | @0 Base nucleica @5 08 |
|---|
| C03 | 07 | X | FRE | @0 Chinois @5 10 |
|---|
| C03 | 07 | X | ENG | @0 Chinese @5 10 |
|---|
| C03 | 07 | X | SPA | @0 Chino @5 10 |
|---|
| C03 | 08 | X | FRE | @0 Déterminisme génétique @5 17 |
|---|
| C03 | 08 | X | ENG | @0 Genetic inheritance @5 17 |
|---|
| C03 | 08 | X | SPA | @0 Determinismo genético @5 17 |
|---|
| C03 | 09 | X | FRE | @0 Facteur risque @5 18 |
|---|
| C03 | 09 | X | ENG | @0 Risk factor @5 18 |
|---|
| C03 | 09 | X | SPA | @0 Factor riesgo @5 18 |
|---|
| C03 | 10 | X | FRE | @0 Homme @5 20 |
|---|
| C03 | 10 | X | ENG | @0 Human @5 20 |
|---|
| C03 | 10 | X | SPA | @0 Hombre @5 20 |
|---|
| C07 | 01 | X | FRE | @0 Methyltransferases @2 FE |
|---|
| C07 | 01 | X | ENG | @0 Methyltransferases @2 FE |
|---|
| C07 | 01 | X | SPA | @0 Methyltransferases @2 FE |
|---|
| C07 | 02 | X | FRE | @0 Transferases @2 FE |
|---|
| C07 | 02 | X | ENG | @0 Transferases @2 FE |
|---|
| C07 | 02 | X | SPA | @0 Transferases @2 FE |
|---|
| C07 | 03 | X | FRE | @0 Enzyme |
|---|
| C07 | 03 | X | ENG | @0 Enzyme |
|---|
| C07 | 03 | X | SPA | @0 Enzima |
|---|
| C07 | 04 | X | FRE | @0 Système nerveux pathologie @5 37 |
|---|
| C07 | 04 | X | ENG | @0 Nervous system diseases @5 37 |
|---|
| C07 | 04 | X | SPA | @0 Sistema nervioso patología @5 37 |
|---|
| C07 | 05 | X | FRE | @0 Système nerveux central pathologie @5 38 |
|---|
| C07 | 05 | X | ENG | @0 Central nervous system disease @5 38 |
|---|
| C07 | 05 | X | SPA | @0 Sistema nervosio central patología @5 38 |
|---|
| C07 | 06 | X | FRE | @0 Encéphale pathologie @5 39 |
|---|
| C07 | 06 | X | ENG | @0 Cerebral disorder @5 39 |
|---|
| C07 | 06 | X | SPA | @0 Encéfalo patología @5 39 |
|---|
| C07 | 07 | X | FRE | @0 Extrapyramidal syndrome @5 40 |
|---|
| C07 | 07 | X | ENG | @0 Extrapyramidal syndrome @5 40 |
|---|
| C07 | 07 | X | SPA | @0 Extrapiramidal síndrome @5 40 |
|---|
| C07 | 08 | X | FRE | @0 Maladie dégénérative @5 41 |
|---|
| C07 | 08 | X | ENG | @0 Degenerative disease @5 41 |
|---|
| C07 | 08 | X | SPA | @0 Enfermedad degenerativa @5 41 |
|---|
| N21 | | | | @1 181 |
|---|
|
|---|
Format Inist (serveur)
| NO : | PASCAL 97-0321227 INIST |
|---|
| ET : | G/A1947 polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease |
|---|
| AU : | XIE (T.); HO (S. L.); LI (L. S. W.); MA (O. C. K.) |
|---|
| AF : | University Department of Medicine, University of Hong Kong, Queen Mary Hospital/Hong-Kong (1 aut., 2 aut., 3 aut.); Clinical Biochemistry Unit, University of Hong Kong, Queen Mary Hospital/Hong-Kong (4 aut.) |
|---|
| DT : | Publication en série; Courte communication, note brève; Niveau analytique |
|---|
| SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1997; Vol. 12; No. 3; Pp. 426-427; Bibl. 7 ref. |
|---|
| LA : | Anglais |
|---|
| CC : | 002B17G |
|---|
| FD : | Parkinson maladie; Polymorphisme; Gène; Catechol O-methyltransferase; Allèle; Base nucléique; Chinois; Déterminisme génétique; Facteur risque; Homme |
|---|
| FG : | Methyltransferases; Transferases; Enzyme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative |
|---|
| ED : | Parkinson disease; Polymorphism; Gene; Catechol O-methyltransferase; Allele; Nucleic base; Chinese; Genetic inheritance; Risk factor; Human |
|---|
| EG : | Methyltransferases; Transferases; Enzyme; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease |
|---|
| SD : | Parkinson enfermedad; Polimorfismo; Gen; Catechol O-methyltransferase; Alelo; Base nucleica; Chino; Determinismo genético; Factor riesgo; Hombre |
|---|
| LO : | INIST-20953.354000061493640230 |
|---|
| ID : | 97-0321227 |
|---|
Links to Exploration step
Pascal:97-0321227
Le document en format XML
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polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease</title><author><name sortKey="Xie, T" sort="Xie, T" uniqKey="Xie T" first="T." last="Xie">T. Xie</name>
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polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease</title><author><name sortKey="Xie, T" sort="Xie, T" uniqKey="Xie T" first="T." last="Xie">T. Xie</name>
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</inist:fA14><author><name sortKey="Ho, S L" sort="Ho, S L" uniqKey="Ho S" first="S. L." last="Ho">S. L. Ho</name>
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<sZ>3 aut.</sZ>
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<sZ>3 aut.</sZ>
</inist:fA14><author><name sortKey="Ma, O C K" sort="Ma, O C K" uniqKey="Ma O" first="O. C. K." last="Ma">O. C. K. Ma</name>
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</inist:fA14><series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="1997">1997</date>
</imprint><seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Allele</term>
<term>Catechol O-methyltransferase</term>
<term>Chinese</term>
<term>Gene</term>
<term>Genetic inheritance</term>
<term>Human</term>
<term>Nucleic base</term>
<term>Parkinson disease</term>
<term>Polymorphism</term>
<term>Risk factor</term>
</keywords><keywords scheme="Pascal" xml:lang="fr"><term>Parkinson maladie</term>
<term>Polymorphisme</term>
<term>Gène</term>
<term>Catechol O-methyltransferase</term>
<term>Allèle</term>
<term>Base nucléique</term>
<term>Chinois</term>
<term>Déterminisme génétique</term>
<term>Facteur risque</term>
<term>Homme</term>
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</fA03><fA08 i1="01" i2="1" l="ENG"><s1>G/A<sub>1947</sub>
polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease</s1><fA11 i1="01" i2="1"><s1>XIE (T.)</s1>
</fA11><fA11 i1="02" i2="1"><s1>HO (S. L.)</s1>
</fA11><fA11 i1="03" i2="1"><s1>LI (L. S. W.)</s1>
</fA11><fA11 i1="04" i2="1"><s1>MA (O. C. K.)</s1>
</fA11><fA14 i1="01"><s1>University Department of Medicine, University of Hong Kong, Queen Mary Hospital</s1>
<s3>HKG</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14><fA14 i1="02"><s1>Clinical Biochemistry Unit, University of Hong Kong, Queen Mary Hospital</s1>
<s3>HKG</s3>
<sZ>4 aut.</sZ>
</fA14><fA20><s1>426-427</s1>
</fA20><fA21><s1>1997</s1>
</fA21><fA23 i1="01"><s0>ENG</s0>
</fA23><fA43 i1="01"><s1>INIST</s1>
<s2>20953</s2>
<s5>354000061493640230</s5>
</fA43><fA44><s0>0000</s0>
<s1>© 1997 INIST-CNRS. All rights reserved.</s1>
</fA44><fA45><s0>7 ref.</s0>
</fA45><fA47 i1="01" i2="1"><s0>97-0321227</s0>
</fA47><fA60><s1>P</s1>
<s3>CC</s3>
</fA60><fA64 i1="01" i2="1"><s0>Movement disorders</s0>
</fA64><fA66 i1="01"><s0>USA</s0>
</fA66><fC02 i1="01" i2="X"><s0>002B17G</s0>
</fC02><fC03 i1="01" i2="X" l="FRE"><s0>Parkinson maladie</s0>
<s5>01</s5>
</fC03><fC03 i1="01" i2="X" l="ENG"><s0>Parkinson disease</s0>
<s5>01</s5>
</fC03><fC03 i1="01" i2="X" l="SPA"><s0>Parkinson enfermedad</s0>
<s5>01</s5>
</fC03><fC03 i1="02" i2="X" l="FRE"><s0>Polymorphisme</s0>
<s5>04</s5>
</fC03><fC03 i1="02" i2="X" l="ENG"><s0>Polymorphism</s0>
<s5>04</s5>
</fC03><fC03 i1="02" i2="X" l="SPA"><s0>Polimorfismo</s0>
<s5>04</s5>
</fC03><fC03 i1="03" i2="X" l="FRE"><s0>Gène</s0>
<s5>05</s5>
</fC03><fC03 i1="03" i2="X" l="ENG"><s0>Gene</s0>
<s5>05</s5>
</fC03><fC03 i1="03" i2="X" l="SPA"><s0>Gen</s0>
<s5>05</s5>
</fC03><fC03 i1="04" i2="X" l="FRE"><s0>Catechol O-methyltransferase</s0>
<s2>FE</s2>
<s5>06</s5>
<s6>Catechol «O»-methyltransferase</s6>
</fC03><fC03 i1="04" i2="X" l="ENG"><s0>Catechol O-methyltransferase</s0>
<s2>FE</s2>
<s5>06</s5>
<s6>Catechol «O»-methyltransferase</s6>
</fC03><fC03 i1="04" i2="X" l="SPA"><s0>Catechol O-methyltransferase</s0>
<s2>FE</s2>
<s5>06</s5>
<s6>Catechol «O»-methyltransferase</s6>
</fC03><fC03 i1="05" i2="X" l="FRE"><s0>Allèle</s0>
<s5>07</s5>
</fC03><fC03 i1="05" i2="X" l="ENG"><s0>Allele</s0>
<s5>07</s5>
</fC03><fC03 i1="05" i2="X" l="SPA"><s0>Alelo</s0>
<s5>07</s5>
</fC03><fC03 i1="06" i2="X" l="FRE"><s0>Base nucléique</s0>
<s5>08</s5>
</fC03><fC03 i1="06" i2="X" l="ENG"><s0>Nucleic base</s0>
<s5>08</s5>
</fC03><fC03 i1="06" i2="X" l="SPA"><s0>Base nucleica</s0>
<s5>08</s5>
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<s5>10</s5>
</fC03><fC03 i1="07" i2="X" l="ENG"><s0>Chinese</s0>
<s5>10</s5>
</fC03><fC03 i1="07" i2="X" l="SPA"><s0>Chino</s0>
<s5>10</s5>
</fC03><fC03 i1="08" i2="X" l="FRE"><s0>Déterminisme génétique</s0>
<s5>17</s5>
</fC03><fC03 i1="08" i2="X" l="ENG"><s0>Genetic inheritance</s0>
<s5>17</s5>
</fC03><fC03 i1="08" i2="X" l="SPA"><s0>Determinismo genético</s0>
<s5>17</s5>
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<s5>18</s5>
</fC03><fC03 i1="09" i2="X" l="ENG"><s0>Risk factor</s0>
<s5>18</s5>
</fC03><fC03 i1="09" i2="X" l="SPA"><s0>Factor riesgo</s0>
<s5>18</s5>
</fC03><fC03 i1="10" i2="X" l="FRE"><s0>Homme</s0>
<s5>20</s5>
</fC03><fC03 i1="10" i2="X" l="ENG"><s0>Human</s0>
<s5>20</s5>
</fC03><fC03 i1="10" i2="X" l="SPA"><s0>Hombre</s0>
<s5>20</s5>
</fC03><fC07 i1="01" i2="X" l="FRE"><s0>Methyltransferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="01" i2="X" l="ENG"><s0>Methyltransferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="01" i2="X" l="SPA"><s0>Methyltransferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="02" i2="X" l="FRE"><s0>Transferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="02" i2="X" l="ENG"><s0>Transferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="02" i2="X" l="SPA"><s0>Transferases</s0>
<s2>FE</s2>
</fC07><fC07 i1="03" i2="X" l="FRE"><s0>Enzyme</s0>
</fC07><fC07 i1="03" i2="X" l="ENG"><s0>Enzyme</s0>
</fC07><fC07 i1="03" i2="X" l="SPA"><s0>Enzima</s0>
</fC07><fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux pathologie</s0>
<s5>37</s5>
</fC07><fC07 i1="04" i2="X" l="ENG"><s0>Nervous system diseases</s0>
<s5>37</s5>
</fC07><fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>37</s5>
</fC07><fC07 i1="05" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>38</s5>
</fC07><fC07 i1="05" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>38</s5>
</fC07><fC07 i1="05" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>38</s5>
</fC07><fC07 i1="06" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>39</s5>
</fC07><fC07 i1="06" i2="X" l="ENG"><s0>Cerebral disorder</s0>
<s5>39</s5>
</fC07><fC07 i1="06" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>39</s5>
</fC07><fC07 i1="07" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="07" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="07" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07><fC07 i1="08" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07><fC07 i1="08" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07><fC07 i1="08" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07><fN21><s1>181</s1>
</fN21><server><NO>PASCAL 97-0321227 INIST</NO>
<ET>G/A<sub>1947</sub>
polymorphism in catechol-O-methyltransferase (COMT) gene in Parkinson's disease</ET><AU>XIE (T.); HO (S. L.); LI (L. S. W.); MA (O. C. K.)</AU>
<AF>University Department of Medicine, University of Hong Kong, Queen Mary Hospital/Hong-Kong (1 aut., 2 aut., 3 aut.); Clinical Biochemistry Unit, University of Hong Kong, Queen Mary Hospital/Hong-Kong (4 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 1997; Vol. 12; No. 3; Pp. 426-427; Bibl. 7 ref.</SO>
<LA>Anglais</LA>
<CC>002B17G</CC>
<FD>Parkinson maladie; Polymorphisme; Gène; Catechol O-methyltransferase; Allèle; Base nucléique; Chinois; Déterminisme génétique; Facteur risque; Homme</FD>
<FG>Methyltransferases; Transferases; Enzyme; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Parkinson disease; Polymorphism; Gene; Catechol O-methyltransferase; Allele; Nucleic base; Chinese; Genetic inheritance; Risk factor; Human</ED>
<EG>Methyltransferases; Transferases; Enzyme; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<SD>Parkinson enfermedad; Polimorfismo; Gen; Catechol O-methyltransferase; Alelo; Base nucleica; Chino; Determinismo genético; Factor riesgo; Hombre</SD>
<LO>INIST-20953.354000061493640230</LO>
<ID>97-0321227</ID>
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