MovDisordV3, PubMed, Checkpoint, bibRecord, 000897

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

Identifieur interne : 000897 ( PubMed/Checkpoint ); précédent : 000896; suivant : 000898

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

Auteurs : Silke Appenzeller ; Claudia Schulte ; Sandra Thier ; Franziska Hopfner ; Manuela Pendziwiat ; Frank Papengut ; Christine Klein ; Johann Hagenah ; Meike Kasten ; Karin Srulijes ; Daniela Berg ; Thomas Gasser ; Andrew Singleton ; Günther Deuschl ; Gregor Kuhlenb Umer

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:23390085

Descripteurs français

Wicri :
- geographic : Allemagne, États-Unis.

English descriptors

KwdEn :
- Essential Tremor (genetics), Female, Genetic Association Studies, Germany, Glutamate Plasma Membrane Transport Proteins (genetics), Humans, Male, Parkinson Disease (genetics), Polymorphism, Single Nucleotide (genetics), United States.
MESH :
- chemical , genetics : Glutamate Plasma Membrane Transport Proteins.
- geographic : Germany, United States.
- genetics : Essential Tremor, Parkinson Disease, Polymorphism, Single Nucleotide.
- Female, Genetic Association Studies, Humans, Male.

DOI: 10.1002/mds.25330
PubMed: 23390085

Affiliations:

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 000A77
to stream PubMed, to step Curation: 000A77

Links to Exploration step

pubmed:23390085

Le document en format XML

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<author><name sortKey="Appenzeller, Silke" sort="Appenzeller, Silke" uniqKey="Appenzeller S" first="Silke" last="Appenzeller">Silke Appenzeller</name>
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<author><name sortKey="Schulte, Claudia" sort="Schulte, Claudia" uniqKey="Schulte C" first="Claudia" last="Schulte">Claudia Schulte</name>
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<author><name sortKey="Thier, Sandra" sort="Thier, Sandra" uniqKey="Thier S" first="Sandra" last="Thier">Sandra Thier</name>
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<author><name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
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<author><name sortKey="Pendziwiat, Manuela" sort="Pendziwiat, Manuela" uniqKey="Pendziwiat M" first="Manuela" last="Pendziwiat">Manuela Pendziwiat</name>
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<author><name sortKey="Papengut, Frank" sort="Papengut, Frank" uniqKey="Papengut F" first="Frank" last="Papengut">Frank Papengut</name>
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<author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name>
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<author><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name>
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<author><name sortKey="Kasten, Meike" sort="Kasten, Meike" uniqKey="Kasten M" first="Meike" last="Kasten">Meike Kasten</name>
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<author><name sortKey="Srulijes, Karin" sort="Srulijes, Karin" uniqKey="Srulijes K" first="Karin" last="Srulijes">Karin Srulijes</name>
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<author><name sortKey="Berg, Daniela" sort="Berg, Daniela" uniqKey="Berg D" first="Daniela" last="Berg">Daniela Berg</name>
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<author><name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
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<author><name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name>
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<author><name sortKey="Deuschl, Gunther" sort="Deuschl, Gunther" uniqKey="Deuschl G" first="Günther" last="Deuschl">Günther Deuschl</name>
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<author><name sortKey="Thier, Sandra" sort="Thier, Sandra" uniqKey="Thier S" first="Sandra" last="Thier">Sandra Thier</name>
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<author><name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
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<author><name sortKey="Pendziwiat, Manuela" sort="Pendziwiat, Manuela" uniqKey="Pendziwiat M" first="Manuela" last="Pendziwiat">Manuela Pendziwiat</name>
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<author><name sortKey="Papengut, Frank" sort="Papengut, Frank" uniqKey="Papengut F" first="Frank" last="Papengut">Frank Papengut</name>
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<author><name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name>
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<author><name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name>
</author>
<author><name sortKey="Kasten, Meike" sort="Kasten, Meike" uniqKey="Kasten M" first="Meike" last="Kasten">Meike Kasten</name>
</author>
<author><name sortKey="Srulijes, Karin" sort="Srulijes, Karin" uniqKey="Srulijes K" first="Karin" last="Srulijes">Karin Srulijes</name>
</author>
<author><name sortKey="Berg, Daniela" sort="Berg, Daniela" uniqKey="Berg D" first="Daniela" last="Berg">Daniela Berg</name>
</author>
<author><name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
</author>
<author><name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name>
</author>
<author><name sortKey="Deuschl, Gunther" sort="Deuschl, Gunther" uniqKey="Deuschl G" first="Günther" last="Deuschl">Günther Deuschl</name>
</author>
<author><name sortKey="Kuhlenb Umer, Gregor" sort="Kuhlenb Umer, Gregor" uniqKey="Kuhlenb Umer G" first="Gregor" last="Kuhlenb Umer">Gregor Kuhlenb Umer</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Female</term>
<term>Genetic Association Studies</term>
<term>Germany</term>
<term>Glutamate Plasma Membrane Transport Proteins (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Parkinson Disease (genetics)</term>
<term>Polymorphism, Single Nucleotide (genetics)</term>
<term>United States</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Glutamate Plasma Membrane Transport Proteins</term>
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<term>United States</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Essential Tremor</term>
<term>Parkinson Disease</term>
<term>Polymorphism, Single Nucleotide</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Female</term>
<term>Genetic Association Studies</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Allemagne</term>
<term>États-Unis</term>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
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<ArticleTitle>No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.</ArticleTitle>
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<ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25330</ELocationID>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Appenzeller</LastName>
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<Author ValidYN="Y"><LastName>Schulte</LastName>
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<Author ValidYN="Y"><LastName>Hagenah</LastName>
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<Author ValidYN="Y"><LastName>Kasten</LastName>
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<Agency>Intramural NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>ZO1 AG000949-06</GrantID>
<Acronym>AG</Acronym>
<Agency>NIA NIH HHS</Agency>
<Country>United States</Country>
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<PublicationTypeList><PublicationType UI="D016422">Letter</PublicationType>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Parkinsonism Relat Disord. 2007 Mar;13(2):67-76</RefSource>
<PMID Version="1">16887374</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Hum Genet. 2007 Sep;81(3):559-75</RefSource>
<PMID Version="1">17701901</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Nat Genet. 2009 Mar;41(3):277-9</RefSource>
<PMID Version="1">19182806</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Nat Genet. 2009 Dec;41(12):1308-12</RefSource>
<PMID Version="1">19915575</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1173-8</RefSource>
<PMID Version="1">20468067</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Acta Neurol Scand. 2012 Jan;125(1):1-7</RefSource>
<PMID Version="1">21470193</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neurology. 2012 Jul 17;79(3):243-8</RefSource>
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</CommentsCorrections>
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<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D020329">Essential Tremor</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010300">Parkinson Disease</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
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<tree><noCountry><name sortKey="Appenzeller, Silke" sort="Appenzeller, Silke" uniqKey="Appenzeller S" first="Silke" last="Appenzeller">Silke Appenzeller</name>
<name sortKey="Berg, Daniela" sort="Berg, Daniela" uniqKey="Berg D" first="Daniela" last="Berg">Daniela Berg</name>
<name sortKey="Deuschl, Gunther" sort="Deuschl, Gunther" uniqKey="Deuschl G" first="Günther" last="Deuschl">Günther Deuschl</name>
<name sortKey="Gasser, Thomas" sort="Gasser, Thomas" uniqKey="Gasser T" first="Thomas" last="Gasser">Thomas Gasser</name>
<name sortKey="Hagenah, Johann" sort="Hagenah, Johann" uniqKey="Hagenah J" first="Johann" last="Hagenah">Johann Hagenah</name>
<name sortKey="Hopfner, Franziska" sort="Hopfner, Franziska" uniqKey="Hopfner F" first="Franziska" last="Hopfner">Franziska Hopfner</name>
<name sortKey="Kasten, Meike" sort="Kasten, Meike" uniqKey="Kasten M" first="Meike" last="Kasten">Meike Kasten</name>
<name sortKey="Klein, Christine" sort="Klein, Christine" uniqKey="Klein C" first="Christine" last="Klein">Christine Klein</name>
<name sortKey="Kuhlenb Umer, Gregor" sort="Kuhlenb Umer, Gregor" uniqKey="Kuhlenb Umer G" first="Gregor" last="Kuhlenb Umer">Gregor Kuhlenb Umer</name>
<name sortKey="Papengut, Frank" sort="Papengut, Frank" uniqKey="Papengut F" first="Frank" last="Papengut">Frank Papengut</name>
<name sortKey="Pendziwiat, Manuela" sort="Pendziwiat, Manuela" uniqKey="Pendziwiat M" first="Manuela" last="Pendziwiat">Manuela Pendziwiat</name>
<name sortKey="Schulte, Claudia" sort="Schulte, Claudia" uniqKey="Schulte C" first="Claudia" last="Schulte">Claudia Schulte</name>
<name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name>
<name sortKey="Srulijes, Karin" sort="Srulijes, Karin" uniqKey="Srulijes K" first="Karin" last="Srulijes">Karin Srulijes</name>
<name sortKey="Thier, Sandra" sort="Thier, Sandra" uniqKey="Thier S" first="Sandra" last="Thier">Sandra Thier</name>
</noCountry>
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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.

Source :

Descripteurs français

English descriptors

Links toward previous steps (curation, corpus...)

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