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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 |
2009-2-9
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pubmed:abstractText |
The common C34T polymorphism in the AMP deaminase-1 (AMPD1) gene results in an inactive enzyme in homozygotes for the mutated T allele. Some studies have shown an association of T allele with longer survival in heart failure (HF) and/or coronary artery disease (CAD). The aim of this study was to assess genotype-phenotype correlations in such patients, with emphasis on components of the metabolic syndrome.
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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 |
1502-7686
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pubmed:author |
pubmed-author:Binczak-KuletaAgnieszkaA,
pubmed-author:ChlubekDariuszD,
pubmed-author:CiechanowiczAndrzejA,
pubmed-author:CzyzyckaEdytaE,
pubmed-author:JakubowskaKatarzynaK,
pubmed-author:KaliszczakRobertR,
pubmed-author:Kornacewicz-JachZdzislawaZ,
pubmed-author:LoniewskaBeataB,
pubmed-author:OlszewskaMariaM,
pubmed-author:RzeuskiRyszardR,
pubmed-author:SafranowKrzysztofK,
pubmed-author:SkowronekJanuszJ,
pubmed-author:WojtarowiczAndrzejA
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pubmed:issnType |
Electronic
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
102-12
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pubmed:meshHeading |
pubmed-meshheading:18855224-AMP Deaminase,
pubmed-meshheading:18855224-Case-Control Studies,
pubmed-meshheading:18855224-Coronary Artery Disease,
pubmed-meshheading:18855224-Female,
pubmed-meshheading:18855224-Genetic Predisposition to Disease,
pubmed-meshheading:18855224-Heart Failure,
pubmed-meshheading:18855224-Humans,
pubmed-meshheading:18855224-Kidney Function Tests,
pubmed-meshheading:18855224-Male,
pubmed-meshheading:18855224-Metabolic Syndrome X,
pubmed-meshheading:18855224-Middle Aged,
pubmed-meshheading:18855224-Multivariate Analysis,
pubmed-meshheading:18855224-Natriuretic Peptide, Brain,
pubmed-meshheading:18855224-Polymorphism, Single Nucleotide,
pubmed-meshheading:18855224-Regression Analysis,
pubmed-meshheading:18855224-Waist Circumference
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pubmed:year |
2009
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pubmed:articleTitle |
Association of C34T AMPD1 gene polymorphism with features of metabolic syndrome in patients with coronary artery disease or heart failure.
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pubmed:affiliation |
Department of Biochemistry and Medical Chemistry, Pomeranian Medical University, Szczecin, Poland. chrissaf@mp.pl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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