MovDisordV3, PubMed, Corpus, bibRecord, 002B11

The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.

Identifieur interne : 002B11 ( PubMed/Corpus ); précédent : 002B10; suivant : 002B12

The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.

Auteurs : Ina Schmitt ; Ullrich Wüllner ; Daniel G. Healy ; Nicholas W. Wood ; Heike Kölsch ; Reinhard Heun

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2006.

RBID : pubmed:16960859

English descriptors

KwdEn :
- Alcohol Dehydrogenase (genetics), Case-Control Studies, Codon, Terminator (genetics), DNA Mutational Analysis, Female, Gene Frequency, Genetics, Population, Germany (epidemiology), Germany (ethnology), Glycine (genetics), Great Britain (epidemiology), Great Britain (ethnology), Heterozygote, Humans, Male, Multiple System Atrophy (genetics), Mutation.
MESH :
- chemical , genetics : Alcohol Dehydrogenase, Codon, Terminator, Glycine.
- geographic , epidemiology : Germany, Great Britain.
- geographic , ethnology : Germany, Great Britain.
- genetics : Multiple System Atrophy.
- Case-Control Studies, DNA Mutational Analysis, Female, Gene Frequency, Genetics, Population, Heterozygote, Humans, Male, Mutation.

DOI: 10.1002/mds.21082
PubMed: 16960859

Links to Exploration step

pubmed:16960859

Le document en format XML

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<author><name sortKey="Schmitt, Ina" sort="Schmitt, Ina" uniqKey="Schmitt I" first="Ina" last="Schmitt">Ina Schmitt</name>
</author>
<author><name sortKey="Wullner, Ullrich" sort="Wullner, Ullrich" uniqKey="Wullner U" first="Ullrich" last="Wüllner">Ullrich Wüllner</name>
</author>
<author><name sortKey="Healy, Daniel G" sort="Healy, Daniel G" uniqKey="Healy D" first="Daniel G" last="Healy">Daniel G. Healy</name>
</author>
<author><name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W" last="Wood">Nicholas W. Wood</name>
</author>
<author><name sortKey="Kolsch, Heike" sort="Kolsch, Heike" uniqKey="Kolsch H" first="Heike" last="Kölsch">Heike Kölsch</name>
</author>
<author><name sortKey="Heun, Reinhard" sort="Heun, Reinhard" uniqKey="Heun R" first="Reinhard" last="Heun">Reinhard Heun</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.</title>
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<author><name sortKey="Wullner, Ullrich" sort="Wullner, Ullrich" uniqKey="Wullner U" first="Ullrich" last="Wüllner">Ullrich Wüllner</name>
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<author><name sortKey="Healy, Daniel G" sort="Healy, Daniel G" uniqKey="Healy D" first="Daniel G" last="Healy">Daniel G. Healy</name>
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<author><name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W" last="Wood">Nicholas W. Wood</name>
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<author><name sortKey="Kolsch, Heike" sort="Kolsch, Heike" uniqKey="Kolsch H" first="Heike" last="Kölsch">Heike Kölsch</name>
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<author><name sortKey="Heun, Reinhard" sort="Heun, Reinhard" uniqKey="Heun R" first="Reinhard" last="Heun">Reinhard Heun</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alcohol Dehydrogenase (genetics)</term>
<term>Case-Control Studies</term>
<term>Codon, Terminator (genetics)</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetics, Population</term>
<term>Germany (epidemiology)</term>
<term>Germany (ethnology)</term>
<term>Glycine (genetics)</term>
<term>Great Britain (epidemiology)</term>
<term>Great Britain (ethnology)</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Multiple System Atrophy (genetics)</term>
<term>Mutation</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Alcohol Dehydrogenase</term>
<term>Codon, Terminator</term>
<term>Glycine</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en"><term>Germany</term>
<term>Great Britain</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="ethnology" xml:lang="en"><term>Germany</term>
<term>Great Britain</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Multiple System Atrophy</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Case-Control Studies</term>
<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetics, Population</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation</term>
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<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">16960859</PMID>
<DateCreated><Year>2006</Year>
<Month>12</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted><Year>2007</Year>
<Month>02</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>21</Volume>
<Issue>11</Issue>
<PubDate><Year>2006</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.</ArticleTitle>
<Pagination><MedlinePgn>2034</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schmitt</LastName>
<ForeName>Ina</ForeName>
<Initials>I</Initials>
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<Author ValidYN="Y"><LastName>Wüllner</LastName>
<ForeName>Ullrich</ForeName>
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<Author ValidYN="Y"><LastName>Healy</LastName>
<ForeName>Daniel G</ForeName>
<Initials>DG</Initials>
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<Author ValidYN="Y"><LastName>Wood</LastName>
<ForeName>Nicholas W</ForeName>
<Initials>NW</Initials>
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<Author ValidYN="Y"><LastName>Kölsch</LastName>
<ForeName>Heike</ForeName>
<Initials>H</Initials>
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<Author ValidYN="Y"><LastName>Heun</LastName>
<ForeName>Reinhard</ForeName>
<Initials>R</Initials>
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<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType>
<PublicationType UI="D016422">Letter</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Mov Disord</MedlineTA>
<NlmUniqueID>8610688</NlmUniqueID>
<ISSNLinking>0885-3185</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D018388">Codon, Terminator</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 1.1.1.1</RegistryNumber>
<NameOfSubstance UI="D000426">Alcohol Dehydrogenase</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>TE7660XO1C</RegistryNumber>
<NameOfSubstance UI="D005998">Glycine</NameOfSubstance>
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</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000426">Alcohol Dehydrogenase</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D016022">Case-Control Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D018388">Codon, Terminator</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004252">DNA Mutational Analysis</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005787">Gene Frequency</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D005828">Genetics, Population</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" Type="Geographic" UI="D005858">Germany</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000453">epidemiology</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000208">ethnology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005998">Glycine</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" Type="Geographic" UI="D006113">Great Britain</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000453">epidemiology</QualifierName>
<QualifierName MajorTopicYN="N" UI="Q000208">ethnology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006579">Heterozygote</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D019578">Multiple System Atrophy</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D009154">Mutation</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year>
<Month>9</Month>
<Day>9</Day>
<Hour>9</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline"><Year>2007</Year>
<Month>2</Month>
<Day>21</Day>
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<Minute>0</Minute>
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<PubMedPubDate PubStatus="entrez"><Year>2006</Year>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="doi">10.1002/mds.21082</ArticleId>
<ArticleId IdType="pubmed">16960859</ArticleId>
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	Movement Disorders (revue)
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Movement Disorders (revue)

The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.

The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.

Source :

English descriptors

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