Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
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The APOA5 Trp19 allele is associated with metabolic syndrome via its association with plasma triglyceridesAnalysis of sequence variability in the CART gene in relation to obesity in a Caucasian populationGender-specific association of a perilipin gene haplotype with obesity risk in a white populationChromosome 4q25, microsomal transfer protein gene, and human longevity: novel data and a meta-analysis of association studies.A study of the relationships between KLF2 polymorphisms and body weight control in a French population.Analysis of common PTPN1 gene variants in type 2 diabetes, obesity and associated phenotypes in the French populationComputation of haplotypes on SNPs subsets: advantage of the "global method".A new JAVA interface implementation of THESIAS: testing haplotype effects in association studies.Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control studyThe 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.Fibrinogen beta variants confer protection against coronary artery disease in a Greek case-control studySELP and SELPLG genetic variation is associated with cell surface measures of SELP and SELPLG: the Atherosclerosis Risk in Communities Carotid MRI StudyAssociation of common variants in JAK2 gene with reduced risk of metabolic syndrome and related disorders.Genetics of coronary heart disease with reference to ApoAI-CIII-AIV gene region.Study of the impact of perilipin polymorphisms in a French population.Pharmacogenomics of adrenoceptors.Common TGFβ2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma.An evolutionary history of the selectin gene cluster in humans.Specific P-selectin and P-selectin glycoprotein ligand-1 genotypes/haplotypes are associated with risk of incident CHD and ischemic stroke: the Atherosclerosis Risk in Communities (ARIC) studyA Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.Molecular genetics of myocardial infarctionSialic acids in human health and disease.Pharmacogenomic association of nonsynonymous SNPs in SIGLEC12, A1BG, and the selectin region and cardiovascular outcomes.Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery diseaseHaplotype associations with quantitative traits in the presence of complex multilocus and heterogeneous effects.Molecular and functional characterization of polymorphisms in the secreted phospholipase A2 group X gene: relevance to coronary artery diseaseAdhesion molecule polymorphisms and pulse wave velocity in American youth.Peroxisome proliferator-activated receptor gamma polymorphisms and coronary heart disease.The adhesion mediated by the P-selectin P-selectin glycoprotein ligand-1 (PSGL-1) couple is stronger for shorter PSGL-1 variants.Automated detection of informative combined effects in genetic association studies of complex traits.Polymorphisms of inflammatory markers and risk of essential hypertension in Tatars from Russia.Soluble P-selectin, SELP polymorphisms, and atherosclerotic risk in European-American and African-African young adults: the Coronary Artery Risk Development in Young Adults (CARDIA) Study.SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease.Polymorphism R92Q of the tumour necrosis factor receptor 1 gene is associated with myocardial infarction and carotid intima-media thickness--the ECTIM, AXA, EVA and GENIC Studies.Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.Polymorphisms in the P-selectin (CD62P) and P-selectin glycoprotein ligand-1 (PSGL-1) genes and coronary heart disease.An SNP in the adiponectin gene is associated with decreased serum adiponectin levels and risk for impaired glucose tolerance.Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions.Association between liver X receptor alpha gene polymorphisms and risk of metabolic syndrome in French populations.Selectin haplotypes and the risk of venous thrombosis: influence of linkage disequilibrium with the factor V Leiden mutation.
P2860
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P2860
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@en
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@nl
type
label
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@en
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@nl
prefLabel
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@en
Specific haplotypes of the P-selectin gene are associated with myocardial infarction.
@nl
P2093
P50
P356
P1476
Specific haplotypes of the P-selectin gene are associated with myocardial infarction
@en
P2093
François Cambien
Jean-Louis Golmard
Laurence Tiret
Nadia Tahri
P304
P356
10.1093/HMG/11.17.2015
P577
2002-08-01T00:00:00Z