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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2011-1-3
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pubmed:abstractText |
chronic obstructive pulmonary disease (COPD), characterized by airflow limitation, is a disorder with high phenotypic and genetic heterogeneity. Pulmonary emphysema is a major but variable component of COPD; familial data suggest that different components of COPD, such as emphysema, may be influenced by specific genetic factors.
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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 |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1535-4970
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pubmed:author |
pubmed-author:AndersonWayneW,
pubmed-author:BakkePerP,
pubmed-author:ChoMichael HMH,
pubmed-author:CoxsonHarvey OHO,
pubmed-author:ECLIPSE Study NETT Investigators,
pubmed-author:GulsvikAmundA,
pubmed-author:HoffmanEric AEA,
pubmed-author:KongXiangyangX,
pubmed-author:LomasDavid ADA,
pubmed-author:MullerNestorN,
pubmed-author:PillaiSreekumar GSG,
pubmed-author:SilvermanEdwin KEK,
pubmed-author:WashkoGeorgeG
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
183
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
43-9
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pubmed:dateRevised |
2011-3-24
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pubmed:meshHeading |
pubmed-meshheading:20709820-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:20709820-Cytoskeletal Proteins,
pubmed-meshheading:20709820-DNA,
pubmed-meshheading:20709820-Female,
pubmed-meshheading:20709820-Follow-Up Studies,
pubmed-meshheading:20709820-Genetic Predisposition to Disease,
pubmed-meshheading:20709820-Genome-Wide Association Study,
pubmed-meshheading:20709820-Genotype,
pubmed-meshheading:20709820-Humans,
pubmed-meshheading:20709820-Male,
pubmed-meshheading:20709820-Middle Aged,
pubmed-meshheading:20709820-Polymorphism, Genetic,
pubmed-meshheading:20709820-Pulmonary Disease, Chronic Obstructive,
pubmed-meshheading:20709820-Pulmonary Emphysema,
pubmed-meshheading:20709820-Spirometry,
pubmed-meshheading:20709820-Tomography, X-Ray Computed
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pubmed:year |
2011
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pubmed:articleTitle |
Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema.
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pubmed:affiliation |
Research and Development, GlaxoSmithKline, 709 Swedeland Road, UW2230, King of Prussia, PA 19406, USA. xiangyang.q.kong@gsk.com
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pubmed:publicationType |
Journal Article,
Clinical Trial,
In Vitro,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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