Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.
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Lipoprotein-associated phospholipase A2 prognostic role in atherosclerotic complicationsGenetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles.Evolution of genetic and genomic features unique to the human lineage.TAP1 I333V gene polymorphism and type 1 diabetes mellitus: a meta-analysis of 2248 cases.Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemiaElevated PLA2G7 gene promoter methylation as a gender-specific marker of aging increases the risk of coronary heart disease in females.Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.Association between polymorphisms in phospholipase A2 genes and the plasma triglyceride response to an n-3 PUFA supplementation: a clinical trialLipoprotein-associated phospholipase A2 and risk of incident cardiovascular disease in a multi-ethnic cohort: The multi ethnic study of atherosclerosis.Modulation of oxidative stress, inflammation, and atherosclerosis by lipoprotein-associated phospholipase A2MARV: a tool for genome-wide multi-phenotype analysis of rare variants.Lipoprotein associated phospholipase A2 activity, apolipoprotein C3 loss-of-function variants and cardiovascular disease: The Atherosclerosis Risk In Communities StudyAn association study between genetic polymorphisms related to lipoprotein-associated phospholipase A(2) and coronary heart disease.A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations.From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary DiseaseAssociations of MDR1, TBXA2R, PLA2G7, and PEAR1 genetic polymorphisms with the platelet activity in Chinese ischemic stroke patients receiving aspirin therapy.A previously unreported impact of a PLA2G7 gene polymorphism on the plasma levels of lipoprotein-associated phospholipase A2 activity and mass.Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.Functional genomics of the human high-density lipoprotein receptor scavenger receptor BI: an old dog with new tricks.Effect of the R92H and A379V genotypes of platelet-activating factor acetylhydrolase on its enzyme activity, oxidative stress and metabolic profile in Chinese women with polycystic ovary syndrome.Small dense low-density lipoprotein-cholesterol concentrations predict risk for coronary heart disease: the Atherosclerosis Risk In Communities (ARIC) study.Association between the MLX interacting protein-like, BUD13 homolog and zinc finger protein 259 gene polymorphisms and serum lipid levels.New therapies for coronary artery disease: genetics provides a blueprint.Critical appraisal of inflammatory markers in cardiovascular risk stratification.Mendelian Randomization Analyses for Selection of Therapeutic Targets for Cardiovascular Disease Prevention: a Note of Circumspection.The effects of PPARγ on the regulation of the TOMM40-APOE-C1 genes cluster.The Relevance of Genomic Signatures at Adhesion GPCR Loci in Humans.Lipoprotein-associated phospholipase A2, and subsequent cardiovascular events and mortality among patients with coronary heart disease.Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.Associations between four types of single-nucleotide polymorphisms in PLA2G7 gene and clinical atherosclerosis: a meta-analysis.Effects of apoC1 genotypes on the hormonal levels, metabolic profile and PAF-AH activity in Chinese women with polycystic ovary syndrome.Associations of platelet-activating factor acetylhydrolase (PAF-AH) gene polymorphisms with circulating PAF-AH levels and risk of coronary heart disease or blood stasis syndrome in the Chinese Han population.Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.
P2860
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P2860
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Eight genetic loci associated ...... five community-based studies.
@ast
Eight genetic loci associated ...... five community-based studies.
@en
type
label
Eight genetic loci associated ...... five community-based studies.
@ast
Eight genetic loci associated ...... five community-based studies.
@en
prefLabel
Eight genetic loci associated ...... five community-based studies.
@ast
Eight genetic loci associated ...... five community-based studies.
@en
P2093
P2860
P50
P356
P1476
Eight genetic loci associated ...... five community-based studies.
@en
P2093
Alexandre F R Stewart
Christie M Ballantyne
Heide A Stirnadel-Farrant
Jacqueline C M Witteman
Jeanenne J Nelson
Jennifer F Yamamoto
Jens Baumert
John F Keaney
João Daniel Fontes
P2860
P304
P356
10.1093/EURHEARTJ/EHR372
P50
P577
2011-10-14T00:00:00Z