A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
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Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseMolecular genetics of coronary artery diseaseAdvances in the genetic basis of coronary artery diseaseStructural equation model-based genome scan for the metabolic syndrome.Search for genetic factors predisposing to atherogenic dyslipidemia.GATA2 is associated with familial early-onset coronary artery disease.Biomarkers of adiponectin: plasma protein variation and genomic DNA polymorphisms.Genetics and cardiovascular disease: Design and development of a DNA biobank.Lack of MEF2A mutations in coronary artery disease.Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components.Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci.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.Mechanisms of dexamethasone-induced disturbed sleep and fatigue in paediatric patients receiving treatment for ALLIdentifying 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 StudyGenetics talks to epigenetics? The interplay between sequence variants and chromatin structureThe mouse mahoganoid coat color mutation disrupts a novel C3HC4 RING domain proteinABCC5 transporter is a novel type 2 diabetes susceptibility gene in European and African American populations.High serum level of matrix metalloproteinase 9 and promoter polymorphism - 1562 C:T as a new risk factor for metabolic syndrome.Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.Genomics of heart failure.Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families.Novel KIF6 polymorphism increases susceptibility to type 2 diabetes mellitus and coronary heart disease in Han Chinese menLarge 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.Variations in Adipokine Genes AdipoQ, Lep, and LepR are Associated with Risk for Obesity-Related Metabolic Disease: The Modulatory Role of Gene-Nutrient Interactions.Association of adiponectin gene polymorphism with adiponectin levels and risk for insulin resistance syndrome.Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.Application of back propagation artificial neural network on genetic variants in adiponectin ADIPOQ, peroxisome proliferator-activated receptor-γ, and retinoid X receptor-α genes and type 2 diabetes risk in a Chinese Han populationRelation between ADIPOQ gene polymorphisms and type 2 diabetes in a Chinese population.Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels.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.Association of apolipoprotein A5 gene -1131T>C polymorphism with the risk of metabolic syndrome in Korean subjects.Identification of atherosclerosis-modifying genes: pathogenic insights and therapeutic potential.Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease
P2860
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P2860
A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@en
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@nl
type
label
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@en
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@nl
prefLabel
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@en
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@nl
P2093
P356
P1476
A genome-wide scan for coronar ...... he metabolic syndrome on 3q27.
@en
P2093
Balgobin V
Gunness TK
Lacquemant C
P304
P356
10.1093/HMG/10.24.2751
P577
2001-11-01T00:00:00Z