نتایج جستجو برای: rs1333049
تعداد نتایج: 62 فیلتر نتایج به سال:
Cardiovascular disease (CVD) is the most common cause of morbidity and mortality globally. Despite progress being made in diagnosis treatment CVDs, one third deaths are due to CVDs. We have investigated association between rs1333049 polymorphism cyclin-dependent kinase inhibitor 2A/B (CDKN2A/B) gene with CVD outcomes a population sample recruited as part Mashhad-Stroke Heart-Atherosclerotic-Dis...
In search of genetic markers of myocardial infarction (MI) risk, which have prognostic significance for Russians, we performed a replication study of MI association with genetic variants of PCSK9 (rs562556), APOE (epsilon polymorphism, rs7412 and rs429358), LPL (rs320), MTHFR (rs1801133), eNOS (rs2070744), and the 9p21 region (rs1333049) in 405 patients with MI and 198 controls. Significant MI ...
BACKGROUND Recent genome-wide association studies have identified several genetic loci linked to coronary artery disease (CAD) and myocardial infarction (MI). The 9p21.3 locus was verified by numerous replication studies to be the first common locus for CAD and MI. In the present study, we investigated whether six single nucleotide polymorphisms (SNP) rs1333049, rs1333040, rs10757274, rs2383206...
BACKGROUND Elevated serum uric acid concentration is an independent risk factor and predictor of type 2 diabetes (T2D). Whether the uric acid-associated genes have an impact on T2D remains unclear. We aimed to investigate the effects of the uric acid-associated genes on the risk of T2D as well as glucose metabolism and insulin secretion. METHOD We recruited 2,199 normal glucose tolerance subj...
Large-scale genome-wide association studies (GWAS) have revealed that rs10757278 polymorphism (or its proxy rs1333049) on chromosome 9p21 is associated with myocardial infarction (MI) susceptibility in individuals of Caucasian ancestry. Following studies in other populations investigated this association. However, some of these studies reported weak or no significant association. Here, we reeva...
In 2007, the Wellcome Trust Case Control Consortium (WTCCC) performed a genome-wide association study in 2,000 British coronary heart disease (CHD) cases and 3,000 controls after genotyping 469,557 single nucleotide polymorphisms (SNPs). Seven variants associated with CHD were initially identified, and 5 SNPs were later found in replication studies. In the current study, the authors aimed to de...
BACKGROUND Coronary artery calcification (CAC) detected by computed tomography is a noninvasive measure of coronary atherosclerosis, which underlies most cases of myocardial infarction (MI). We sought to identify common genetic variants associated with CAC and further investigate their associations with MI. METHODS AND RESULTS Computed tomography was used to assess quantity of CAC. A meta-ana...
While atherosclerotic cardiovascular disease (ASCVD) is known to be common among modern people exposed to various risk factors, recent paleopathological studies have shown that it affected ancient populations much more frequently than expected. In 2010, we investigated a 17th century Korean female mummy with presumptive ASCVD signs. Although the resulting report was a rare and invaluable conjec...
The aim of the study was to identify a relationship between gene polymorphisms associated with developing coronary heart disease and pathogenetic features opisthorchiasis invasion. There were compared laboratory parameters assessing immune system functioning (lymphocyte immunophenotyping evaluated by flow cytometry, serum immunoglobulin cytokine concentrations, non-specific resistance indices) ...
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