Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.
Identifieur interne : 000099 ( Ncbi/Merge ); précédent : 000098; suivant : 000100Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.
Auteurs : H. Deng [États-Unis] ; W Le ; Y. Guo ; M Huang ; W Xie ; Joseph Jankovic [États-Unis]Source :
- Neurology ; 2005.
English descriptors
- KwdEn :
- Age Factors, Aged, Comorbidity, DNA Mutational Analysis, Essential Tremor (epidemiology), Essential Tremor (ethnology), Essential Tremor (genetics), European Continental Ancestry Group, Female, Gene Frequency, Genetic Predisposition to Disease (genetics), Genetic Testing, Genetic Variation (genetics), Genotype, Humans, Male, Middle Aged, Mutation (genetics), Nerve Tissue Proteins (genetics), Parkinsonian Disorders (epidemiology), Parkinsonian Disorders (ethnology), Parkinsonian Disorders (genetics), Polymorphism, Genetic (genetics), Sex Factors.
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- epidemiology : Essential Tremor, Parkinsonian Disorders.
- ethnology : Essential Tremor, Parkinsonian Disorders.
- genetics : Essential Tremor, Genetic Predisposition to Disease, Genetic Variation, Mutation, Parkinsonian Disorders, Polymorphism, Genetic.
- Age Factors, Aged, Comorbidity, DNA Mutational Analysis, European Continental Ancestry Group, Female, Gene Frequency, Genetic Testing, Genotype, Humans, Male, Middle Aged, Sex Factors.
DOI: 10.1212/01.wnl.0000173033.32535.23
PubMed: 16116142
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000191
- to stream PubMed, to step Curation: 000191
- to stream PubMed, to step Checkpoint: 000197
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pubmed:16116142Le document en format XML
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<author><name sortKey="Deng, H" sort="Deng, H" uniqKey="Deng H" first="H" last="Deng">H. Deng</name>
<affiliation wicri:level="2"><nlm:affiliation>Department of Neurology, Baylor College of Medicine, Houston, TX 77030, USA.</nlm:affiliation>
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<wicri:regionArea>Department of Neurology, Baylor College of Medicine, Houston, TX 77030</wicri:regionArea>
<placeName><region type="state">Texas</region>
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<author><name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
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<author><name sortKey="Guo, Y" sort="Guo, Y" uniqKey="Guo Y" first="Y" last="Guo">Y. Guo</name>
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<author><name sortKey="Huang, M S" sort="Huang, M S" uniqKey="Huang M" first="M" last="Huang">M Huang</name>
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<author><name sortKey="Xie, W J" sort="Xie, W J" uniqKey="Xie W" first="W" last="Xie">W Xie</name>
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<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">Joseph Jankovic</name>
<affiliation><country>États-Unis</country>
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<author><name sortKey="Huang, M S" sort="Huang, M S" uniqKey="Huang M" first="M" last="Huang">M Huang</name>
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<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">Joseph Jankovic</name>
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<series><title level="j">Neurology</title>
<idno type="e-ISSN">1526-632X</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Age Factors</term>
<term>Aged</term>
<term>Comorbidity</term>
<term>DNA Mutational Analysis</term>
<term>Essential Tremor (epidemiology)</term>
<term>Essential Tremor (ethnology)</term>
<term>Essential Tremor (genetics)</term>
<term>European Continental Ancestry Group</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Predisposition to Disease (genetics)</term>
<term>Genetic Testing</term>
<term>Genetic Variation (genetics)</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Parkinsonian Disorders (epidemiology)</term>
<term>Parkinsonian Disorders (ethnology)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Polymorphism, Genetic (genetics)</term>
<term>Sex Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Nerve Tissue Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Essential Tremor</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="ethnology" xml:lang="en"><term>Essential Tremor</term>
<term>Parkinsonian Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Essential Tremor</term>
<term>Genetic Predisposition to Disease</term>
<term>Genetic Variation</term>
<term>Mutation</term>
<term>Parkinsonian Disorders</term>
<term>Polymorphism, Genetic</term>
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<keywords scheme="MESH" xml:lang="en"><term>Age Factors</term>
<term>Aged</term>
<term>Comorbidity</term>
<term>DNA Mutational Analysis</term>
<term>European Continental Ancestry Group</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Testing</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<Day>23</Day>
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<DateRevised><Year>2009</Year>
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<PubDate><Year>2005</Year>
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<Title>Neurology</Title>
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<ArticleTitle>Extended study of A265G variant of HS1BP3 in essential tremor and Parkinson disease.</ArticleTitle>
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<Language>eng</Language>
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<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C503777">HS1BP3 protein, human</NameOfSubstance>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020734">Parkinsonian Disorders</DescriptorName>
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<name sortKey="Le, W D" sort="Le, W D" uniqKey="Le W" first="W" last="Le">W Le</name>
<name sortKey="Xie, W J" sort="Xie, W J" uniqKey="Xie W" first="W" last="Xie">W Xie</name>
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