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rdf:type |
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lifeskim:mentions |
umls-concept:C0003857,
umls-concept:C0006104,
umls-concept:C0017337,
umls-concept:C0018270,
umls-concept:C0180679,
umls-concept:C0205422,
umls-concept:C0332281,
umls-concept:C1366583,
umls-concept:C1366767,
umls-concept:C1510411,
umls-concept:C1882417
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pubmed:issue |
10
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pubmed:dateCreated |
2005-9-29
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pubmed:abstractText |
Mutations in endoglin (ENG) and activin-like kinase (ALK1) cause hereditary hemorrhagic telangiectasias, disorders characterized by pulmonary and brain arteriovenous malformations (BAVMs). We investigated whether polymorphisms in these genes are also associated with sporadic BAVM.
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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 |
http://linkedlifedata.com/resource/pubmed/chemical/ACVRL1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Activin Receptors, Type I,
http://linkedlifedata.com/resource/pubmed/chemical/Activin Receptors, Type II,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/ENG protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Vascular Cell Adhesion Molecule-1
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1524-4628
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pubmed:author |
pubmed-author:AchrolAchal SAS,
pubmed-author:BurchardEstebanE,
pubmed-author:CastroRichardR,
pubmed-author:ChoudhryShwetaS,
pubmed-author:HaConnieC,
pubmed-author:KwokPui-YanPY,
pubmed-author:LawtonMichael TMT,
pubmed-author:MarchukDouglasD,
pubmed-author:McCullochCharles ECE,
pubmed-author:PawlikowskaLudmilaL,
pubmed-author:TranMary NMN,
pubmed-author:UCSF BAVM Study Project,
pubmed-author:YoungWilliam LWL,
pubmed-author:ZaroffJonathanJ
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pubmed:issnType |
Electronic
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pubmed:volume |
36
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2278-80
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:16179574-Activin Receptors, Type I,
pubmed-meshheading:16179574-Activin Receptors, Type II,
pubmed-meshheading:16179574-Adult,
pubmed-meshheading:16179574-Antigens, CD,
pubmed-meshheading:16179574-Arteriovenous Malformations,
pubmed-meshheading:16179574-Brain,
pubmed-meshheading:16179574-Case-Control Studies,
pubmed-meshheading:16179574-Cohort Studies,
pubmed-meshheading:16179574-Female,
pubmed-meshheading:16179574-Genetic Variation,
pubmed-meshheading:16179574-Genotype,
pubmed-meshheading:16179574-Humans,
pubmed-meshheading:16179574-Male,
pubmed-meshheading:16179574-Middle Aged,
pubmed-meshheading:16179574-Models, Statistical,
pubmed-meshheading:16179574-Odds Ratio,
pubmed-meshheading:16179574-Polymorphism, Genetic,
pubmed-meshheading:16179574-Receptors, Cell Surface,
pubmed-meshheading:16179574-Transforming Growth Factor beta,
pubmed-meshheading:16179574-Vascular Cell Adhesion Molecule-1
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pubmed:year |
2005
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pubmed:articleTitle |
Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations.
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pubmed:affiliation |
Cardiovascular Research Institute, University of California, San Francisco, CA 94110, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, N.I.H., Extramural
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