MovDisordV3, PascalFrancis, Corpus, bibRecord, 001906

NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach

Identifieur interne : 001906 ( PascalFrancis/Corpus ); précédent : 001905; suivant : 001907

NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach

Auteurs : Daniel G. Healy ; Patrick M. Abou-Sleiman ; Kourosh R. Ahmadi ; Sonia Gandhi ; Miratul M. Muqit ; Kailash P. Bhatia ; Niall P. Quinn ; Andrew J. Lees ; Janice L. Holton ; Tamas Revesz ; Nicholas W. Wood

Source :

Movement disorders [ 0885-3185 ] ; 2006.

RBID : Pascal:07-0021725

Descripteurs français

Pascal (Inist)
- Système nerveux pathologie, Parkinson maladie, Sporadique, Voie abord, Haplotype, Marquage.

English descriptors

KwdEn :
- Haplotype, Nervous system diseases, Parkinson disease, Sporadic, Surgical approach, Tagging.

Abstract

The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A08	`01`	`1`	`ENG`	`@1 NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach`
A11	`01`	`1`		`@1 HEALY (Daniel G.)`
A11	`02`	`1`		`@1 ABOU-SLEIMAN (Patrick M.)`
A11	`03`	`1`		`@1 AHMADI (Kourosh R.)`
A11	`04`	`1`		`@1 GANDHI (Sonia)`
A11	`05`	`1`		`@1 MUQIT (Miratul M.)`
A11	`06`	`1`		`@1 BHATIA (Kailash P.)`
A11	`07`	`1`		`@1 QUINN (Niall P.)`
A11	`08`	`1`		`@1 LEES (Andrew J.)`
A11	`09`	`1`		`@1 HOLTON (Janice L.)`
A11	`10`	`1`		`@1 REVESZ (Tamas)`
A11	`11`	`1`		`@1 WOOD (Nicholas W.)`
A14	`01`			`@1 Department of Molecular Neuroscience, Institute of Neurology @2 London @3 GBR @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 5 aut. @Z 8 aut. @Z 9 aut. @Z 10 aut. @Z 11 aut.`
A14	`02`			`@1 Department of Biology, University College London @2 London @3 GBR @Z 3 aut.`
A14	`03`			`@1 Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology @2 London @3 GBR @Z 6 aut. @Z 7 aut.`
A14	`04`			`@1 Reta Lila Weston Institute for Neurological Studies, University of London @2 London @3 GBR @Z 8 aut.`
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C01	`01`		`ENG`	`@0 The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.`
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C07	`02`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 38`
C07	`02`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 38`
C07	`02`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 38`
C07	`03`	`X`	`FRE`	`@0 Maladie dégénérative @5 39`
C07	`03`	`X`	`ENG`	`@0 Degenerative disease @5 39`
C07	`03`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 39`
C07	`04`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 40`
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Format Inist (serveur)

NO :	PASCAL 07-0021725 INIST
ET :	NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach
AU :	HEALY (Daniel G.); ABOU-SLEIMAN (Patrick M.); AHMADI (Kourosh R.); GANDHI (Sonia); MUQIT (Miratul M.); BHATIA (Kailash P.); QUINN (Niall P.); LEES (Andrew J.); HOLTON (Janice L.); REVESZ (Tamas); WOOD (Nicholas W.)
AF :	Department of Molecular Neuroscience, Institute of Neurology/London/Royaume-Uni (1 aut., 2 aut., 4 aut., 5 aut., 8 aut., 9 aut., 10 aut., 11 aut.); Department of Biology, University College London/London/Royaume-Uni (3 aut.); Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology/London/Royaume-Uni (6 aut., 7 aut.); Reta Lila Weston Institute for Neurological Studies, University of London/London/Royaume-Uni (8 aut.)
DT :	Publication en série; Courte communication, note brève; Niveau analytique
SO :	Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 11; Pp. 1960-1963; Bibl. 20 ref.
LA :	Anglais
EA :	The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.
CC :	002B17; 002B17G; 002B17A03
FD :	Système nerveux pathologie; Parkinson maladie; Sporadique; Voie abord; Haplotype; Marquage
FG :	Encéphale pathologie; Extrapyramidal syndrome; Maladie dégénérative; Système nerveux central pathologie
ED :	Nervous system diseases; Parkinson disease; Sporadic; Surgical approach; Haplotype; Tagging
EG :	Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD :	Sistema nervioso patología; Parkinson enfermedad; Esporádico; Vía abordaje; Haplotipo; Marcación
LO :	INIST-20953.354000158935070220
ID :	07-0021725

Links to Exploration step

Pascal:07-0021725

Le document en format XML

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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Haplotype</term>
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<term>Parkinson disease</term>
<term>Sporadic</term>
<term>Surgical approach</term>
<term>Tagging</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Système nerveux pathologie</term>
<term>Parkinson maladie</term>
<term>Sporadique</term>
<term>Voie abord</term>
<term>Haplotype</term>
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<front><div type="abstract" xml:lang="en">The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.</div>
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<fA11 i1="04" i2="1"><s1>GANDHI (Sonia)</s1>
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<fA11 i1="05" i2="1"><s1>MUQIT (Miratul M.)</s1>
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<fA11 i1="06" i2="1"><s1>BHATIA (Kailash P.)</s1>
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<fA11 i1="07" i2="1"><s1>QUINN (Niall P.)</s1>
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<fA11 i1="08" i2="1"><s1>LEES (Andrew J.)</s1>
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<fA11 i1="09" i2="1"><s1>HOLTON (Janice L.)</s1>
</fA11>
<fA11 i1="10" i2="1"><s1>REVESZ (Tamas)</s1>
</fA11>
<fA11 i1="11" i2="1"><s1>WOOD (Nicholas W.)</s1>
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<fA14 i1="01"><s1>Department of Molecular Neuroscience, Institute of Neurology</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
<sZ>10 aut.</sZ>
<sZ>11 aut.</sZ>
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<fA14 i1="02"><s1>Department of Biology, University College London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Reta Lila Weston Institute for Neurological Studies, University of London</s1>
<s2>London</s2>
<s3>GBR</s3>
<sZ>8 aut.</sZ>
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<fA20><s1>1960-1963</s1>
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<fA21><s1>2006</s1>
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<fC01 i1="01" l="ENG"><s0>The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.</s0>
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<s5>01</s5>
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<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA"><s0>Sistema nervioso patología</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE"><s0>Parkinson maladie</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Parkinson disease</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Parkinson enfermedad</s0>
<s5>02</s5>
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<fC03 i1="03" i2="X" l="FRE"><s0>Sporadique</s0>
<s5>09</s5>
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<fC03 i1="03" i2="X" l="ENG"><s0>Sporadic</s0>
<s5>09</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Esporádico</s0>
<s5>09</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Voie abord</s0>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Surgical approach</s0>
<s5>10</s5>
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<fC03 i1="04" i2="X" l="SPA"><s0>Vía abordaje</s0>
<s5>10</s5>
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<fC03 i1="05" i2="X" l="FRE"><s0>Haplotype</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Haplotype</s0>
<s5>11</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Haplotipo</s0>
<s5>11</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Marquage</s0>
<s5>12</s5>
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<fC03 i1="06" i2="X" l="ENG"><s0>Tagging</s0>
<s5>12</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Marcación</s0>
<s5>12</s5>
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<fC07 i1="01" i2="X" l="FRE"><s0>Encéphale pathologie</s0>
<s5>37</s5>
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<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Encéfalo patología</s0>
<s5>37</s5>
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<fC07 i1="02" i2="X" l="FRE"><s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Extrapyramidal syndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>38</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>39</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>39</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Système nerveux central pathologie</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Central nervous system disease</s0>
<s5>40</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Sistema nervosio central patología</s0>
<s5>40</s5>
</fC07>
<fN21><s1>010</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
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<fN82><s1>OTO</s1>
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<ET>NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach</ET>
<AU>HEALY (Daniel G.); ABOU-SLEIMAN (Patrick M.); AHMADI (Kourosh R.); GANDHI (Sonia); MUQIT (Miratul M.); BHATIA (Kailash P.); QUINN (Niall P.); LEES (Andrew J.); HOLTON (Janice L.); REVESZ (Tamas); WOOD (Nicholas W.)</AU>
<AF>Department of Molecular Neuroscience, Institute of Neurology/London/Royaume-Uni (1 aut., 2 aut., 4 aut., 5 aut., 8 aut., 9 aut., 10 aut., 11 aut.); Department of Biology, University College London/London/Royaume-Uni (3 aut.); Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology/London/Royaume-Uni (6 aut., 7 aut.); Reta Lila Weston Institute for Neurological Studies, University of London/London/Royaume-Uni (8 aut.)</AF>
<DT>Publication en série; Courte communication, note brève; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2006; Vol. 21; No. 11; Pp. 1960-1963; Bibl. 20 ref.</SO>
<LA>Anglais</LA>
<EA>The NR4A2 gene, which may cause autosomal dominant Parkinson's disease (PD), has also been reported to be a susceptibility factor for sporadic PD. Here, we use a haplotype-tagging approach in 802 PD patients and 784 controls and demonstrate that common genetic variation, including NR4A2 haplotypes, does not influence the risk of PD in the Caucasian population.</EA>
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<ED>Nervous system diseases; Parkinson disease; Sporadic; Surgical approach; Haplotype; Tagging</ED>
<EG>Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease</EG>
<SD>Sistema nervioso patología; Parkinson enfermedad; Esporádico; Vía abordaje; Haplotipo; Marcación</SD>
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Movement Disorders (revue)

NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach

NR4A2 genetic variation in sporadic Parkinson's disease : A genewide approach

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