about
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglyceridesPolymorphism of the tryptophan hydroxylase 2 (TPH2) gene is associated with chimpanzee neuroticismAssociation of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations.ATHENA: a tool for meta-dimensional analysis applied to genotypes and gene expression data to predict HDL cholesterol levelsPrimary prevention of coronary heart disease: integration of new data, evolving views, revised goals, and role of rosuvastatin in management. A comprehensive survey.Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profileSegregation of LIPG, CETP, and GALNT2 mutations in Caucasian families with extremely high HDL cholesterol.High-density lipoprotein (HDL) particle subpopulations in heterozygous cholesteryl ester transfer protein (CETP) deficiency: maintenance of antioxidative activity.Impact of genetic variants in human scavenger receptor class B type I (SCARB1) on plasma lipid traits.Association of cholesteryl ester transfer protein genotypes with paraoxonase-1 activity, lipid profile and oxidative stress in type 2 diabetes mellitus: A study in San Luis, ArgentinaCorrecting for population structure and kinship using the linear mixed model: theory and extensions.The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans.Metabolomics and partial least square discriminant analysis to predict history of myocardial infarction of self-claimed healthy subjects: validity and feasibility for clinical practice.SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents.HDL cholesterol and bone mineral density: is there a genetic link?The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region.Beyond genome-wide association studies: the usefulness of mouse genetics in understanding the complex etiology of atherosclerosis.Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.Transgenic expression and genetic variation of Lmf1 affect LPL activity in mice and humansPopulation-Based Resequencing of LIPG and ZNF202 Genes in Subjects with Extreme HDL LevelsAssociation of Lecithin Cholesterol Acyltransferase rs5923 Polymorphism in Iranian Individuals with Extremely Low High-Density Lipoprotein Cholesterol: Tehran Lipid and Glucose Study.The SCARB1 rs5888 SNP and serum lipid levels in the Guangxi Mulao and Han populationsResequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levelsExome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended familyIdentification of Sequence Variation in the Apolipoprotein A2 Gene and Their Relationship with Serum High-Density Lipoprotein Cholesterol Levels.The combined effects of genetic variation in the SIRT1 gene and dietary intake of n-3 and n-6 polyunsaturated fatty acids on serum LDL-C and HDL-C levels: a population based studyVariations in HDL-carried miR-223 and miR-135a concentrations after consumption of dietary trans fat are associated with changes in blood lipid and inflammatory markers in healthy men - an exploratory study.Shared genetic variants between serum levels of high-density lipoprotein cholesterol and wheezing in a cohort of children from CyprusMulti-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBGGenomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study.High fat diet modifies the association of lipoprotein lipase gene polymorphism with high density lipoprotein cholesterol in an Asian Indian population.Decreased activities of apolipoprotein m promoter are associated with the susceptibility to coronary artery diseases.Comparison of direct measures of adiposity with indirect measures for assessing cardiometabolic risk factors in preadolescent girls.Do genetic variations alter the effects of exercise training on cardiovascular disease and can we identify the candidate variants now or in the future?Rationale for cholesteryl ester transfer protein inhibition.Genetics of cholesterol efflux.HDL cholesterol and cardiovascular outcomes: what is the evidence?HDL-C: clinical equipoise and vascular endothelial function.Diagnosis and management of familial dyslipoproteinemias.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Genetic causes of high and low serum HDL-cholesterol.
@ast
Genetic causes of high and low serum HDL-cholesterol.
@en
type
label
Genetic causes of high and low serum HDL-cholesterol.
@ast
Genetic causes of high and low serum HDL-cholesterol.
@en
prefLabel
Genetic causes of high and low serum HDL-cholesterol.
@ast
Genetic causes of high and low serum HDL-cholesterol.
@en
P2860
P356
P1476
Genetic causes of high and low serum HDL-cholesterol.
@en
P2093
Daphna Weissglas-Volkov
Päivi Pajukanta
P2860
P304
P356
10.1194/JLR.R004739
P577
2010-04-26T00:00:00Z