Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiov

Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiov

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http://www.wikidata.org/entity/Q33737606

Q33737606

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Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains.Genetic analysis of atherosclerosis and glucose homeostasis in an intercross between C57BL/6 and BALB/cJ apolipoprotein E-deficient mice.Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24 A Polymorphism in Hepatocyte Nuclear Factor 1 Alpha, rs7310409, Is Associated with Left Main Coronary Artery Disease.Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe).Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein.Pathway-Targeted Pharmacogenomics of CYP1A2 in Human Liver.Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment Associations of lipid levels susceptibility loci with coronary artery disease in Chinese population.Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels Hypocretin neuron-specific transcriptome profiling identifies the sleep modulator Kcnh4a.Integrated approach toward the discovery of glyco-biomarkers of inflammation-related diseases.Identification of novel candidate maternal serum protein markers for Down syndrome by integrated proteomic and bioinformatic analysis.Variants in MODY genes associated with maternal lipids profiles in second trimester of pregnancy.Improved Progression-Free Survival in Irinotecan-Treated Metastatic Colorectal Cancer Patients Carrying the HNF1A Coding Variant p.I27L.Systematic target function annotation of human transcription factors.A molecular case-control study of association of HNF1A gene polymorphisms (rs2259816 and rs7310409) with risk of coronary artery disease in Iranian patients.Pleiotropic effects of HNF1A rs1183910 in a population-based study of 60,283 individuals.Association of the HNF1A polymorphisms and serum lipid traits, the risk of coronary artery disease and ischemic stroke.

P2860

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P2860

Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiov

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http://www.wikidata.org/entity/Q33737606

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2009 nî lūn-bûn

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2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2009年の論文

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