ParkinsonFranceV1, Main, Curation, bibRecord, 003E79

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

Identifieur interne : 003E79 ( Main/Curation ); précédent : 003E78; suivant : 003E80

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

Auteurs : G. Mercier [France] ; J. C. Turpin [France] ; G. Lucotte [France]

Source :

Journal of neurology [ 0340-5354 ] ; 1999.

RBID : Pascal:99-0095893

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Polymorphisme, Gène, Allèle, Dopamine, Transport biologique, Séquence répétée en tandem, France, Facteur risque, Génétique, Déterminisme génétique, Homme.
Wicri :
- geographic : France.
- topic : Génétique, Homme.

English descriptors

KwdEn :
- Adult, Aged, Allele, Biological transport, Carrier Proteins (genetics), Dopamine, Dopamine Plasma Membrane Transport Proteins, Female, France, Gene, Genetic Markers, Genetic determinism, Genetics, Human, Humans, Male, Membrane Glycoproteins, Membrane Transport Proteins, Middle Aged, Minisatellite Repeats (genetics), Nerve Tissue Proteins, Parkinson Disease (blood), Parkinson Disease (genetics), Parkinson disease, Polymerase Chain Reaction, Polymorphism, Polymorphism, Genetic (genetics), Risk factor, Tandemly repeated sequence.
MESH :
- chemical , genetics : Carrier Proteins.
- blood : Parkinson Disease.
- genetics : Minisatellite Repeats, Parkinson Disease, Polymorphism, Genetic.
- Adult, Aged, Dopamine Plasma Membrane Transport Proteins, Female, Genetic Markers, Humans, Male, Membrane Glycoproteins, Membrane Transport Proteins, Middle Aged, Nerve Tissue Proteins, Polymerase Chain Reaction.

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.

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Le document en format XML

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<sourceDesc><biblStruct><analytic><title xml:lang="en">Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found.</title>
<author><name sortKey="Mercier, G" sort="Mercier, G" uniqKey="Mercier G" first="G" last="Mercier">G. Mercier</name>
<affiliation wicri:level="3"><nlm:affiliation>Laboratoire de Neurogénétique, Moléculaire (Service de Neurologie), Hôpital Maison Blanche, Reims, France.</nlm:affiliation>
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire de Neurogénétique, Moléculaire (Service de Neurologie), Hôpital Maison Blanche, Reims</wicri:regionArea>
<placeName><region type="region">Grand Est</region>
<region type="old region">Champagne-Ardenne</region>
<settlement type="city">Reims</settlement>
</placeName>
</affiliation>
</author>
<author><name sortKey="Turpin, J C" sort="Turpin, J C" uniqKey="Turpin J" first="J C" last="Turpin">J C Turpin</name>
</author>
<author><name sortKey="Lucotte, G" sort="Lucotte, G" uniqKey="Lucotte G" first="G" last="Lucotte">G. Lucotte</name>
</author>
</analytic>
<series><title level="j">Journal of neurology</title>
<idno type="ISSN">0340-5354</idno>
<imprint><date when="1999" type="published">1999</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Carrier Proteins (genetics)</term>
<term>Dopamine Plasma Membrane Transport Proteins</term>
<term>Female</term>
<term>Genetic Markers</term>
<term>Humans</term>
<term>Male</term>
<term>Membrane Glycoproteins</term>
<term>Membrane Transport Proteins</term>
<term>Middle Aged</term>
<term>Minisatellite Repeats (genetics)</term>
<term>Nerve Tissue Proteins</term>
<term>Parkinson Disease (blood)</term>
<term>Parkinson Disease (genetics)</term>
<term>Polymerase Chain Reaction</term>
<term>Polymorphism, Genetic (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Carrier Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Minisatellite Repeats</term>
<term>Parkinson Disease</term>
<term>Polymorphism, Genetic</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Dopamine Plasma Membrane Transport Proteins</term>
<term>Female</term>
<term>Genetic Markers</term>
<term>Humans</term>
<term>Male</term>
<term>Membrane Glycoproteins</term>
<term>Membrane Transport Proteins</term>
<term>Middle Aged</term>
<term>Nerve Tissue Proteins</term>
<term>Polymerase Chain Reaction</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson's 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.</div>
</front>
</TEI>
</PubMed>
</double>
</record>

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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

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

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