about
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Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillationA common allele on chromosome 9 associated with coronary heart diseaseWhy did ancient people have atherosclerosis?: from autopsies to computed tomography to potential causesTEF-1 and MEF2 transcription factors interact to regulate muscle-specific promotersMammalian vestigial-like 2, a cofactor of TEF-1 and MEF2 transcription factors that promotes skeletal muscle differentiationIdentification of a novel muscle A-type lamin-interacting protein (MLIP)A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery diseasePlasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyIdentification of human homologues of the mouse mammary tumor virus receptor.IRF2BP2 is a skeletal and cardiac muscle-enriched ischemia-inducible activator of VEGFA expression.Left ventricular and myocardial function in mice expressing constitutively pseudophosphorylated cardiac troponin I.Plasma PCSK9 levels are elevated with acute myocardial infarction in two independent retrospective angiographic studiesMouse DTEF-1 (ETFR-1, TEF-5) is a transcriptional activator in alpha 1-adrenergic agonist-stimulated cardiac myocytes.9p21 and the genetic revolution for coronary artery disease.Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathwaysTrans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.Functional characterization of a promoter polymorphism that drives ACSL5 gene expression in skeletal muscle and associates with diet-induced weight lossFunctional analysis of the chromosome 9p21.3 coronary artery disease risk locus.Is atherosclerosis fundamental to human aging? Lessons from ancient mummies.Prevalence and correlates of diabetes in South asian indians in the United States: findings from the metabolic syndrome and atherosclerosis in South asians living in america study and the multi-ethnic study of atherosclerosis.Clinical and genetic association of serum ceruloplasmin with cardiovascular risk.Adiposity significantly modifies genetic risk for dyslipidemia.Mouse mammary tumor virus (MMTV)-like DNA sequences in the breast tumors of father, mother, and daughter.Personalized genomic medicine: a future prerequisite for the prevention of coronary artery disease.Large-scale association analysis identifies new risk loci for coronary artery diseaseIncreased genetic risk for obesity in premature coronary artery disease.Genetic variants influencing circulating lipid levels and risk of coronary artery disease.Recent success in the discovery of coronary artery disease genes.Genetics of coronary artery disease in the 21st century.Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion?Transcription cofactor Vgl-2 is required for skeletal muscle differentiation.Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study.Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.Partitioning the heritability of coronary artery disease highlights the importance of immune-mediated processes and epigenetic sites associated with transcriptional activity.Transcriptomic Signature of Atherosclerosis in the Peripheral Blood: Fact or Fiction?The LIM domain only 4 protein is a metabolic responsive inhibitor of protein tyrosine phosphatase 1B that controls hypothalamic leptin signaling.IRF2BP2-deficient microglia block the anxiolytic effect of enhanced postnatal care.LMO4 mRNA stability is regulated by extracellular ATP in F11 cells.TEF-1 transcription factors regulate activity of the mouse mammary tumor virus LTR.Loss of IRF2BP2 in Microglia Increases Inflammation and Functional Deficits after Focal Ischemic Brain Injury.
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P50
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1962-04-16T00:00:00Z