MovDisordV3, PubMed, Checkpoint, bibRecord, 000863

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.

Identifieur interne : 000863 ( PubMed/Checkpoint ); précédent : 000862; suivant : 000864

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.

Auteurs : Soraya Bardien [Afrique du Sud] ; Janine Blanckenberg ; Lize Van Der Merwe ; Matthew J. Farrer ; Owen A. Ross

Source :

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

RBID : pubmed:24014121

Descripteurs français

Wicri :
- geographic : Afrique du Sud.

English descriptors

KwdEn :
- African Continental Ancestry Group, Case-Control Studies, European Continental Ancestry Group, Female, Humans, Male, Parkinson Disease (ethnology), Parkinson Disease (genetics), Polymorphism, Single Nucleotide (genetics), Protein-Serine-Threonine Kinases (genetics), South Africa.
MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- geographic : South Africa.
- ethnology : Parkinson Disease.
- genetics : Parkinson Disease, Polymorphism, Single Nucleotide.
- African Continental Ancestry Group, Case-Control Studies, European Continental Ancestry Group, Female, Humans, Male.

DOI: 10.1002/mds.25637
PubMed: 24014121

Affiliations:

Afrique du Sud

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pubmed:24014121

Le document en format XML

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<author><name sortKey="Bardien, Soraya" sort="Bardien, Soraya" uniqKey="Bardien S" first="Soraya" last="Bardien">Soraya Bardien</name>
<affiliation wicri:level="1"><nlm:affiliation>Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, University of Stellenbosch, Cape Town, South Africa.</nlm:affiliation>
<country xml:lang="fr">Afrique du Sud</country>
<wicri:regionArea>Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, University of Stellenbosch, Cape Town</wicri:regionArea>
<wicri:noRegion>Cape Town</wicri:noRegion>
</affiliation>
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<author><name sortKey="Blanckenberg, Janine" sort="Blanckenberg, Janine" uniqKey="Blanckenberg J" first="Janine" last="Blanckenberg">Janine Blanckenberg</name>
</author>
<author><name sortKey="Van Der Merwe, Lize" sort="Van Der Merwe, Lize" uniqKey="Van Der Merwe L" first="Lize" last="Van Der Merwe">Lize Van Der Merwe</name>
</author>
<author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
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<author><name sortKey="Ross, Owen A" sort="Ross, Owen A" uniqKey="Ross O" first="Owen A" last="Ross">Owen A. Ross</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.</title>
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<affiliation wicri:level="1"><nlm:affiliation>Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, University of Stellenbosch, Cape Town, South Africa.</nlm:affiliation>
<country xml:lang="fr">Afrique du Sud</country>
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<author><name sortKey="Blanckenberg, Janine" sort="Blanckenberg, Janine" uniqKey="Blanckenberg J" first="Janine" last="Blanckenberg">Janine Blanckenberg</name>
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<author><name sortKey="Van Der Merwe, Lize" sort="Van Der Merwe, Lize" uniqKey="Van Der Merwe L" first="Lize" last="Van Der Merwe">Lize Van Der Merwe</name>
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<author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
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<author><name sortKey="Ross, Owen A" sort="Ross, Owen A" uniqKey="Ross O" first="Owen A" last="Ross">Owen A. Ross</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
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<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Parkinson Disease (ethnology)</term>
<term>Parkinson Disease (genetics)</term>
<term>Polymorphism, Single Nucleotide (genetics)</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
<term>South Africa</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein-Serine-Threonine Kinases</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>South Africa</term>
</keywords>
<keywords scheme="MESH" qualifier="ethnology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
<term>Polymorphism, Single Nucleotide</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>African Continental Ancestry Group</term>
<term>Case-Control Studies</term>
<term>European Continental Ancestry Group</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Afrique du Sud</term>
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<DateCreated><Year>2013</Year>
<Month>12</Month>
<Day>10</Day>
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<DateCompleted><Year>2014</Year>
<Month>07</Month>
<Day>29</Day>
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<DateRevised><Year>2014</Year>
<Month>12</Month>
<Day>02</Day>
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<Issue>14</Issue>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.</ArticleTitle>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bardien</LastName>
<ForeName>Soraya</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, University of Stellenbosch, Cape Town, South Africa.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Blanckenberg</LastName>
<ForeName>Janine</ForeName>
<Initials>J</Initials>
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<Author ValidYN="Y"><LastName>van der Merwe</LastName>
<ForeName>Lize</ForeName>
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<Author ValidYN="Y"><LastName>Farrer</LastName>
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<Author ValidYN="Y"><LastName>Ross</LastName>
<ForeName>Owen A</ForeName>
<Initials>OA</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>P50 NS072187</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant><GrantID>P50NS072187</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
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<PublicationTypeList><PublicationType UI="D016422">Letter</PublicationType>
<PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<ArticleDate DateType="Electronic"><Year>2013</Year>
<Month>09</Month>
<Day>06</Day>
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<MedlineJournalInfo><Country>United States</Country>
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<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>EC 2.7.11.1</RegistryNumber>
<NameOfSubstance UI="C495280">LRRK2 protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 2.7.11.1</RegistryNumber>
<NameOfSubstance UI="D017346">Protein-Serine-Threonine Kinases</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S66-70</RefSource>
<PMID Version="1">22166458</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Neurogenetics. 2006 Jul;7(3):133-8</RefSource>
<PMID Version="1">16633828</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Lancet Neurol. 2011 Oct;10(10):898-908</RefSource>
<PMID Version="1">21885347</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Science. 2009 May 22;324(5930):1035-44</RefSource>
<PMID Version="1">19407144</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Hum Mutat. 2010 May;31(5):561-8</RefSource>
<PMID Version="1">20186690</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites"><RefSource>Ann Neurol. 2008 Jul;64(1):88-92</RefSource>
<PMID Version="1">18412265</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D044465">European Continental Ancestry Group</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" Type="Geographic" UI="D013019">South Africa</DescriptorName>
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</MeshHeadingList>
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<OtherID Source="NLM">PMC3859714</OtherID>
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<affiliations><list><country><li>Afrique du Sud</li>
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<tree><noCountry><name sortKey="Blanckenberg, Janine" sort="Blanckenberg, Janine" uniqKey="Blanckenberg J" first="Janine" last="Blanckenberg">Janine Blanckenberg</name>
<name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
<name sortKey="Ross, Owen A" sort="Ross, Owen A" uniqKey="Ross O" first="Owen A" last="Ross">Owen A. Ross</name>
<name sortKey="Van Der Merwe, Lize" sort="Van Der Merwe, Lize" uniqKey="Van Der Merwe L" first="Lize" last="Van Der Merwe">Lize Van Der Merwe</name>
</noCountry>
<country name="Afrique du Sud"><noRegion><name sortKey="Bardien, Soraya" sort="Bardien, Soraya" uniqKey="Bardien S" first="Soraya" last="Bardien">Soraya Bardien</name>
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</record>

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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)

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.

Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.

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