ParkinsonFranceV1, PubMed, Corpus, bibRecord, 000A82

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Identifieur interne : 000A82 ( PubMed/Corpus ); précédent : 000A81; suivant : 000A83

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Auteurs : Suzanne Lesage ; Christel Condroyer ; Ebba Lohman ; André Troiano ; François Tison ; François Viallet ; Philippe Damier ; Christine Tranchant ; Marie Vidhaillet ; Anne-Marie Ouvrard-Hernandez ; Alexandra Dürr ; Alexis Brice

Source :

Neurobiology of aging [ 1558-1497 ] ; 2010.

RBID : pubmed:20004041

English descriptors

KwdEn :
- Adult, Aged, Aged, 80 and over, Carrier Proteins (genetics), Family Health, Female, Follow-Up Studies, France, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Parkinson Disease (genetics), Young Adult.
MESH :
- chemical , genetics : Carrier Proteins.
- geographic : France.
- genetics : Parkinson Disease.
- Adult, Aged, Aged, 80 and over, Family Health, Female, Follow-Up Studies, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Middle Aged, Young Adult.

Abstract

Meeus et al. (2009) reported no pathogenic mutations in a comprehensive genetic analysis of the entire GRB10-interacting GYF protein-2 gene (GIGYF2) in a Belgian series of both familial and sporadic patients with Parkinson's disease (PD). Although we initially proposed that GIGYF2 corresponds to the PARK11 locus, in familial PD, we found no causative variations in a follow-up study in which GIGYF2 was screened in an independent series of 185 patients with autosomal dominant PD, mostly of French origin. Together, these results do not support a major role of GIGYF2 in PD.

DOI: 10.1016/j.neurobiolaging.2009.06.008
PubMed: 20004041

Links to Exploration step

pubmed:20004041

Le document en format XML

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<author><name sortKey="Lesage, Suzanne" sort="Lesage, Suzanne" uniqKey="Lesage S" first="Suzanne" last="Lesage">Suzanne Lesage</name>
<affiliation><nlm:affiliation>INSERM, UMR_S975 (Formerly UMR_S679), Hôpital de la Salpêtrière, Paris, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Condroyer, Christel" sort="Condroyer, Christel" uniqKey="Condroyer C" first="Christel" last="Condroyer">Christel Condroyer</name>
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<author><name sortKey="Lohman, Ebba" sort="Lohman, Ebba" uniqKey="Lohman E" first="Ebba" last="Lohman">Ebba Lohman</name>
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<author><name sortKey="Troiano, Andre" sort="Troiano, Andre" uniqKey="Troiano A" first="André" last="Troiano">André Troiano</name>
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<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
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<author><name sortKey="Viallet, Francois" sort="Viallet, Francois" uniqKey="Viallet F" first="François" last="Viallet">François Viallet</name>
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<author><name sortKey="Damier, Philippe" sort="Damier, Philippe" uniqKey="Damier P" first="Philippe" last="Damier">Philippe Damier</name>
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<author><name sortKey="Tranchant, Christine" sort="Tranchant, Christine" uniqKey="Tranchant C" first="Christine" last="Tranchant">Christine Tranchant</name>
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<author><name sortKey="Vidhaillet, Marie" sort="Vidhaillet, Marie" uniqKey="Vidhaillet M" first="Marie" last="Vidhaillet">Marie Vidhaillet</name>
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<author><name sortKey="Ouvrard Hernandez, Anne Marie" sort="Ouvrard Hernandez, Anne Marie" uniqKey="Ouvrard Hernandez A" first="Anne-Marie" last="Ouvrard-Hernandez">Anne-Marie Ouvrard-Hernandez</name>
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<author><name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Dürr">Alexandra Dürr</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.</title>
<author><name sortKey="Lesage, Suzanne" sort="Lesage, Suzanne" uniqKey="Lesage S" first="Suzanne" last="Lesage">Suzanne Lesage</name>
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<author><name sortKey="Condroyer, Christel" sort="Condroyer, Christel" uniqKey="Condroyer C" first="Christel" last="Condroyer">Christel Condroyer</name>
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<author><name sortKey="Troiano, Andre" sort="Troiano, Andre" uniqKey="Troiano A" first="André" last="Troiano">André Troiano</name>
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<author><name sortKey="Tison, Francois" sort="Tison, Francois" uniqKey="Tison F" first="François" last="Tison">François Tison</name>
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<author><name sortKey="Viallet, Francois" sort="Viallet, Francois" uniqKey="Viallet F" first="François" last="Viallet">François Viallet</name>
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<author><name sortKey="Damier, Philippe" sort="Damier, Philippe" uniqKey="Damier P" first="Philippe" last="Damier">Philippe Damier</name>
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<author><name sortKey="Tranchant, Christine" sort="Tranchant, Christine" uniqKey="Tranchant C" first="Christine" last="Tranchant">Christine Tranchant</name>
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<author><name sortKey="Vidhaillet, Marie" sort="Vidhaillet, Marie" uniqKey="Vidhaillet M" first="Marie" last="Vidhaillet">Marie Vidhaillet</name>
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<author><name sortKey="Ouvrard Hernandez, Anne Marie" sort="Ouvrard Hernandez, Anne Marie" uniqKey="Ouvrard Hernandez A" first="Anne-Marie" last="Ouvrard-Hernandez">Anne-Marie Ouvrard-Hernandez</name>
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<author><name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Dürr">Alexandra Dürr</name>
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<author><name sortKey="Brice, Alexis" sort="Brice, Alexis" uniqKey="Brice A" first="Alexis" last="Brice">Alexis Brice</name>
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<series><title level="j">Neurobiology of aging</title>
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<term>Family Health</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>France</term>
<term>Genetic Predisposition to Disease</term>
<term>Genome-Wide Association Study</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (genetics)</term>
<term>Young Adult</term>
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<term>Aged</term>
<term>Aged, 80 and over</term>
<term>Family Health</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Genetic Predisposition to Disease</term>
<term>Genome-Wide Association Study</term>
<term>Humans</term>
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<front><div type="abstract" xml:lang="en">Meeus et al. (2009) reported no pathogenic mutations in a comprehensive genetic analysis of the entire GRB10-interacting GYF protein-2 gene (GIGYF2) in a Belgian series of both familial and sporadic patients with Parkinson's disease (PD). Although we initially proposed that GIGYF2 corresponds to the PARK11 locus, in familial PD, we found no causative variations in a follow-up study in which GIGYF2 was screened in an independent series of 185 patients with autosomal dominant PD, mostly of French origin. Together, these results do not support a major role of GIGYF2 in PD.</div>
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	La maladie de Parkinson en France (serveur d'exploration)
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La maladie de Parkinson en France (serveur d'exploration)

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki