Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis. - sprookjes - yvandenbroek - TriplyDB

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.

http://www.wikidata.org/entity/Q33909617

about

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17 A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population Molecular genetics of coronary artery disease Advances in the genetic basis of coronary artery disease Aging syndrome genes and premature coronary artery disease Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains.A functionally significant polymorphism in ID3 is associated with human coronary pathology Id3 is a novel atheroprotective factor containing a functionally significant single-nucleotide polymorphism associated with intima-media thickness in humans GATA2 is associated with familial early-onset coronary artery disease.Genetic and functional association of FAM5C with myocardial infarction Additive effect of LRP8/APOER2 R952Q variant to APOE epsilon2/epsilon3/epsilon4 genotype in modulating apolipoprotein E concentration and the risk of myocardial infarction: a case-control study.Mutation in KERA identified by linkage analysis and targeted resequencing in a pedigree with premature atherosclerosis.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.A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.Apolipoprotein E receptor-2 deficiency enhances macrophage susceptibility to lipid accumulation and cell death to augment atherosclerotic plaque progression and necrosis.Identifying novel genes for atherosclerosis through mouse-human comparative genetics.A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study Genetic variants of ApoE and ApoER2 differentially modulate endothelial function.A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.Genomics of heart failure.Genome-wide linkage scan identifies two novel genetic loci for coronary artery disease: in GeneQuest families.Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.Transcription factor MEF2A mutations in patients with coronary artery disease.The power of Pasteur's quadrant: cardiovascular disease at the turn of the century.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.The genetics of heart attack EphA2 activation promotes the endothelial cell inflammatory response: a potential role in atherosclerosis Update of the G2D tool for prioritization of gene candidates to inherited diseases.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.An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MI Personalized genomic medicine: a future prerequisite for the prevention of coronary artery disease.Genetic susceptibility to myocardial infarction and coronary artery disease.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

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.

http://www.wikidata.org/entity/Q33909617

description

2004 nî lūn-bûn

@nan

2004 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի հունվարին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

Premature myocardial infarctio ...... y genomewide linkage analysis.

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Premature myocardial infarctio ...... y genomewide linkage analysis.

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type

label

Premature myocardial infarctio ...... y genomewide linkage analysis.

@ast

Premature myocardial infarctio ...... y genomewide linkage analysis.

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prefLabel

Premature myocardial infarctio ...... y genomewide linkage analysis.

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Premature myocardial infarctio ...... y genomewide linkage analysis.

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American Journal of Human Genetics

P1476

Premature myocardial infarctio ...... y genomewide linkage analysis.

@en

P2093

Erich Zirzow

http://www.w3.org/2001/XMLSchema#string

Gong-Qing Shen

http://www.w3.org/2001/XMLSchema#string

Lin Li

http://www.w3.org/2001/XMLSchema#string

Qing Wang

http://www.w3.org/2001/XMLSchema#string

Robert C Elston

http://www.w3.org/2001/XMLSchema#string

Ruth Cannata

http://www.w3.org/2001/XMLSchema#string

William J Rogers

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P2860

Atherosclerosis

A genetic polymorphism in connexin 37 as a prognostic marker for atherosclerotic plaque development

Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

Multiple connexin expression in regenerating arterial endothelial gap junctions

Individual gap junction plaques contain multiple connexins in arterial endothelium

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

The increased risk of death from ischaemic heart disease in first degree relatives of 121 men and 96 women with ischaemic heart disease.

Genetic mapping of complex traits.

Confirmation of linkage of prostate cancer aggressiveness with chromosome 19q.

A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study

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262-271

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scholarly article

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10.1086/381560

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P433

2

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P478

74

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David J Moliterno

L Kristin Newby

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2004-01-19T00:00:00Z

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8911706

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14732905

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susceptibility locus

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1181924

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