Source:http://linkedlifedata.com/resource/pubmed/id/11393670
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2001-6-6
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pubmed:abstractText |
Molecular variants of the angiotensinogen (AGT) and the angiotensin II type 1 receptor (ATR) genes have been associated with the risk of coronary artery disease (CAD) and myocardial infarction (MI), but data so far available are conflicting. The primary object of the paper is to verify this possible association by a rigorous, angiographically controlled study in a large sample of patients with or without multi-vessel CAD.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0263-6352
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
879-84
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:11393670-Aged,
pubmed-meshheading:11393670-Angiotensinogen,
pubmed-meshheading:11393670-Coronary Disease,
pubmed-meshheading:11393670-Female,
pubmed-meshheading:11393670-Genetic Predisposition to Disease,
pubmed-meshheading:11393670-Genetic Variation,
pubmed-meshheading:11393670-Genotype,
pubmed-meshheading:11393670-Homozygote,
pubmed-meshheading:11393670-Humans,
pubmed-meshheading:11393670-Male,
pubmed-meshheading:11393670-Middle Aged,
pubmed-meshheading:11393670-Myocardial Infarction,
pubmed-meshheading:11393670-Phenotype
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pubmed:year |
2001
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pubmed:articleTitle |
Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease.
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pubmed:affiliation |
Department of Clinical and Experimental Medicine, Chair of Internal Medicine, University of Verona, Italy. olivieri@cmib.univr.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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