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La maladie de Parkinson en France (serveur d'exploration)

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Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found

Identifieur interne : 001540 ( PascalFrancis/Corpus ); précédent : 001539; suivant : 001541

Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found

Auteurs : G. Mercier ; J. C. Turpin ; G. Lucotte

Source :

RBID : Pascal:99-0095893

Descripteurs français

English descriptors

Abstract

We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson 5 disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0340-5354
A02 01      @0 JNRYA9
A03   1    @0 J. neurol.
A05       @2 246
A06       @2 1
A08 01  1  ENG  @1 Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found
A11 01  1    @1 MERCIER (G.)
A11 02  1    @1 TURPIN (J. C.)
A11 03  1    @1 LUCOTTE (G.)
A14 01      @1 Laboratoire de Neurogénétique Moléculaire (Service de Neurologie), Hôpital Maison Blanche 45 rue Cognacq-Jay @2 51092 Reims @3 FRA @Z 1 aut. @Z 2 aut. @Z 3 aut.
A20       @1 45-47
A21       @1 1999
A23 01      @0 ENG
A43 01      @1 INIST @2 4826 @5 354000072147530070
A44       @0 0000 @1 © 1999 INIST-CNRS. All rights reserved.
A45       @0 15 ref.
A47 01  1    @0 99-0095893
A60       @1 P
A61       @0 A
A64   1    @0 Journal of neurology
A66 01      @0 DEU
C01 01    ENG  @0 We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson 5 disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.
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 Allèle @5 06
C03 04  X  ENG  @0 Allele @5 06
C03 04  X  SPA  @0 Alelo @5 06
C03 05  X  FRE  @0 Dopamine @2 NK @2 FR @5 07
C03 05  X  ENG  @0 Dopamine @2 NK @2 FR @5 07
C03 05  X  SPA  @0 Dopamina @2 NK @2 FR @5 07
C03 06  X  FRE  @0 Transport biologique @5 08
C03 06  X  ENG  @0 Biological transport @5 08
C03 06  X  SPA  @0 Transporte biológico @5 08
C03 07  X  FRE  @0 Séquence répétée en tandem @5 09
C03 07  X  ENG  @0 Tandemly repeated sequence @5 09
C03 07  X  SPA  @0 Secuencia repetida en tandem @5 09
C03 08  X  FRE  @0 France @2 NG @5 10
C03 08  X  ENG  @0 France @2 NG @5 10
C03 08  X  GER  @0 Frankreich @2 NG @5 10
C03 08  X  SPA  @0 Francia @2 NG @5 10
C03 09  X  FRE  @0 Facteur risque @5 17
C03 09  X  ENG  @0 Risk factor @5 17
C03 09  X  SPA  @0 Factor riesgo @5 17
C03 10  X  FRE  @0 Génétique @5 18
C03 10  X  ENG  @0 Genetics @5 18
C03 10  X  SPA  @0 Genética @5 18
C03 11  X  FRE  @0 Déterminisme génétique @5 19
C03 11  X  ENG  @0 Genetic determinism @5 19
C03 11  X  SPA  @0 Determinismo genético @5 19
C03 12  X  FRE  @0 Homme @5 20
C03 12  X  ENG  @0 Human @5 20
C03 12  X  SPA  @0 Hombre @5 20
C07 01  X  FRE  @0 Europe @2 NG
C07 01  X  ENG  @0 Europe @2 NG
C07 01  X  GER  @0 Europa @2 NG
C07 01  X  SPA  @0 Europa @2 NG
C07 02  X  FRE  @0 Système nerveux pathologie @5 37
C07 02  X  ENG  @0 Nervous system diseases @5 37
C07 02  X  SPA  @0 Sistema nervioso patología @5 37
C07 03  X  FRE  @0 Système nerveux central pathologie @5 38
C07 03  X  ENG  @0 Central nervous system disease @5 38
C07 03  X  SPA  @0 Sistema nervosio central patología @5 38
C07 04  X  FRE  @0 Encéphale pathologie @5 39
C07 04  X  ENG  @0 Cerebral disorder @5 39
C07 04  X  SPA  @0 Encéfalo patología @5 39
C07 05  X  FRE  @0 Extrapyramidal syndrome @5 40
C07 05  X  ENG  @0 Extrapyramidal syndrome @5 40
C07 05  X  SPA  @0 Extrapiramidal síndrome @5 40
C07 06  X  FRE  @0 Maladie dégénérative @5 41
C07 06  X  ENG  @0 Degenerative disease @5 41
C07 06  X  SPA  @0 Enfermedad degenerativa @5 41
N21       @1 053

Format Inist (serveur)

NO : PASCAL 99-0095893 INIST
ET : Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found
AU : MERCIER (G.); TURPIN (J. C.); LUCOTTE (G.)
AF : Laboratoire de Neurogénétique Moléculaire (Service de Neurologie), Hôpital Maison Blanche 45 rue Cognacq-Jay/51092 Reims/France (1 aut., 2 aut., 3 aut.)
DT : Publication en série; Niveau analytique
SO : Journal of neurology; ISSN 0340-5354; Coden JNRYA9; Allemagne; Da. 1999; Vol. 246; No. 1; Pp. 45-47; Bibl. 15 ref.
LA : Anglais
EA : We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson 5 disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.
CC : 002B17G
FD : Parkinson maladie; Polymorphisme; Gène; Allèle; Dopamine; Transport biologique; Séquence répétée en tandem; France; Facteur risque; Génétique; Déterminisme génétique; Homme
FG : Europe; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative
ED : Parkinson disease; Polymorphism; Gene; Allele; Dopamine; Biological transport; Tandemly repeated sequence; France; Risk factor; Genetics; Genetic determinism; Human
EG : Europe; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease
GD : Frankreich
SD : Parkinson enfermedad; Polimorfismo; Gen; Alelo; Dopamina; Transporte biológico; Secuencia repetida en tandem; Francia; Factor riesgo; Genética; Determinismo genético; Hombre
LO : INIST-4826.354000072147530070
ID : 99-0095893

Links to Exploration step

Pascal:99-0095893

Le document en format XML

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<s0>Extrapiramidal síndrome</s0>
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<s5>41</s5>
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<s5>41</s5>
</fC07>
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<NO>PASCAL 99-0095893 INIST</NO>
<ET>Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found</ET>
<AU>MERCIER (G.); TURPIN (J. C.); LUCOTTE (G.)</AU>
<AF>Laboratoire de Neurogénétique Moléculaire (Service de Neurologie), Hôpital Maison Blanche 45 rue Cognacq-Jay/51092 Reims/France (1 aut., 2 aut., 3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of neurology; ISSN 0340-5354; Coden JNRYA9; Allemagne; Da. 1999; Vol. 246; No. 1; Pp. 45-47; Bibl. 15 ref.</SO>
<LA>Anglais</LA>
<EA>We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson 5 disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.</EA>
<CC>002B17G</CC>
<FD>Parkinson maladie; Polymorphisme; Gène; Allèle; Dopamine; Transport biologique; Séquence répétée en tandem; France; Facteur risque; Génétique; Déterminisme génétique; Homme</FD>
<FG>Europe; Système nerveux pathologie; Système nerveux central pathologie; Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative</FG>
<ED>Parkinson disease; Polymorphism; Gene; Allele; Dopamine; Biological transport; Tandemly repeated sequence; France; Risk factor; Genetics; Genetic determinism; Human</ED>
<EG>Europe; Nervous system diseases; Central nervous system disease; Cerebral disorder; Extrapyramidal syndrome; Degenerative disease</EG>
<GD>Frankreich</GD>
<SD>Parkinson enfermedad; Polimorfismo; Gen; Alelo; Dopamina; Transporte biológico; Secuencia repetida en tandem; Francia; Factor riesgo; Genética; Determinismo genético; Hombre</SD>
<LO>INIST-4826.354000072147530070</LO>
<ID>99-0095893</ID>
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