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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
2010-12-2
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pubmed:abstractText |
The thyroid stimulating hormone receptor (TSHR) gene is an established susceptibility locus for Graves' disease (GD), with recent studies refining association to two single nucleotide polymorphisms (SNPs), rs179247 and rs12101255, within TSHR intron 1.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1932-6203
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pubmed:author |
pubmed-author:BednarczukTomaszT,
pubmed-author:BrandOliver JOJ,
pubmed-author:FranaszczykMariaM,
pubmed-author:FranklynJayne AJA,
pubmed-author:GoughStephen C LSC,
pubmed-author:Jarz?bBarbaraB,
pubmed-author:Jurecka-LubienieckaBeataB,
pubmed-author:KaramatMuhammad AMA,
pubmed-author:KrajewskiPawe?P,
pubmed-author:KulaDorotaD,
pubmed-author:P?oskiRafa?R,
pubmed-author:SimmondsMatthew JMJ
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pubmed:issnType |
Electronic
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
e15512
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pubmed:meshHeading |
pubmed-meshheading:21124799-Case-Control Studies,
pubmed-meshheading:21124799-Cohort Studies,
pubmed-meshheading:21124799-European Continental Ancestry Group,
pubmed-meshheading:21124799-Female,
pubmed-meshheading:21124799-Gene Frequency,
pubmed-meshheading:21124799-Genetic Predisposition to Disease,
pubmed-meshheading:21124799-Genotype,
pubmed-meshheading:21124799-Graves Disease,
pubmed-meshheading:21124799-Great Britain,
pubmed-meshheading:21124799-Haplotypes,
pubmed-meshheading:21124799-Humans,
pubmed-meshheading:21124799-Introns,
pubmed-meshheading:21124799-Linkage Disequilibrium,
pubmed-meshheading:21124799-Logistic Models,
pubmed-meshheading:21124799-Male,
pubmed-meshheading:21124799-Poland,
pubmed-meshheading:21124799-Polymorphism, Single Nucleotide,
pubmed-meshheading:21124799-Receptors, Thyrotropin,
pubmed-meshheading:21124799-Risk Factors
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pubmed:year |
2010
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pubmed:articleTitle |
Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.
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pubmed:affiliation |
Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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