Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
about
Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese populationNovel tumor necrosis factor-responsive mammalian neutral sphingomyelinase-3 is a C-tail-anchored proteinThe SLC6A14 gene shows evidence of association with obesityMutation of MEF2A in an inherited disorder with features of coronary artery diseaseMolecular genetics of coronary artery diseaseAdvances in the genetic basis of coronary artery diseaseGATA2 is associated with familial early-onset coronary artery disease.Genetics and cardiovascular disease: Design and development of a DNA biobank.Lack of MEF2A mutations in coronary artery disease.Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.Genomewide linkage analysis for internal carotid artery intimal medial thickness: evidence for linkage to chromosome 12.Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.Identifying novel genes for atherosclerosis through mouse-human comparative genetics.A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart StudyGenome-wide association study of coronary artery disease.Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart diseaseGenomic approaches to coronary artery diseaseGenomics of heart failure.Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia.Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes.Transcription factor MEF2A mutations in patients with coronary artery disease.Genetic evaluation for coronary artery disease.Epistatic interaction between variations in the angiotensin I converting enzyme and angiotensin II type 1 receptor genes in relation to extent of coronary atherosclerosis.VAMP-8 gene variant is associated with increased risk of early myocardial infarction.Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.Distinctive Clinical Profile of Blacks Versus Whites Presenting With Sudden Cardiac Arrest.Genetic and genomic insights into the molecular basis of atherosclerosis.Identification of shared genetic susceptibility locus for coronary artery disease, type 2 diabetes and obesity: a meta-analysis of genome-wide studies.Genetic susceptibility to myocardial infarction and coronary artery disease.Integrative genomics in cardiovascular medicineIdentification of atherosclerosis-modifying genes: pathogenic insights and therapeutic potential.Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery diseaseGenes, diet and public health.Molecular genetics of myocardial infarctionIdentifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism.Genetic variation and atherosclerosis.Molecular signatures of cardiovascular disease risk: potential for test development and clinical application.
P2860
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P2860
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Two loci on chromosomes 2 and ...... lement populations of Finland.
@ast
Two loci on chromosomes 2 and ...... lement populations of Finland.
@en
Two loci on chromosomes 2 and ...... lement populations of Finland.
@nl
type
label
Two loci on chromosomes 2 and ...... lement populations of Finland.
@ast
Two loci on chromosomes 2 and ...... lement populations of Finland.
@en
Two loci on chromosomes 2 and ...... lement populations of Finland.
@nl
prefLabel
Two loci on chromosomes 2 and ...... lement populations of Finland.
@ast
Two loci on chromosomes 2 and ...... lement populations of Finland.
@en
Two loci on chromosomes 2 and ...... lement populations of Finland.
@nl
P2093
P2860
P50
P356
P1476
Two loci on chromosomes 2 and ...... lement populations of Finland.
@en
P2093
Kareinen A
Pajukanta P
Peltonen L
Rönnemaa T
P2860
P304
P356
10.1086/316902
P407
P577
2000-11-13T00:00:00Z