Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
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Structural Insights into High Density Lipoprotein: Old Models and New FactsHypercholesterolemia is associated with the apolipoprotein C-III (APOC3) genotype in children receiving HAART: an eight-year retrospective studyAssociation 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 levelsThe reverse cholesterol transport pathway improves understanding of genetic networks for fat deposition and muscle growth in beef cattleProteomic analysis allows for early detection of potential markers of metabolic impairment in very young obese children.Lipoprotein (a) concentrations, apolipoprotein (a) phenotypes, and peripheral arterial disease in three independent cohorts.Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia.Evidence for low high-density lipoprotein cholesterol levels in Australian indigenous peoples: a systematic review.Human longevity is associated with regular sleep patterns, maintenance of slow wave sleep, and favorable lipid profile.Association between Six CETP Polymorphisms and Metabolic Syndrome in Uyghur Adults from Xinjiang, China.Genetic causes of high and low serum HDL-cholesterol.Comprehensive assessment of metabolic syndrome among rural Bangladeshi womenAccounting for a quantitative trait locus for plasma triglyceride levels: utilization of variants in multiple genes.Proprotein convertases in high-density lipoprotein metabolism.Genetic association of APOB polymorphisms with variation in serum lipid profile among the Kuwait population.A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits.Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.Endothelial lipase-384A/C polymorphism is associated with acute coronary syndrome and lipid status in elderly Uygur patients in Xinjiang.Population-based resequencing of APOA1 in 10,330 individuals: spectrum of genetic variation, phenotype, and comparison with extreme phenotype approach.Re-sequencing of the APOAI promoter region and the genetic association of the -75G > A polymorphism with increased cholesterol and low density lipoprotein levels among a sample of the Kuwaiti population.Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjectsGene-gene combination effect and interactions among ABCA1, APOA1, SR-B1, and CETP polymorphisms for serum high-density lipoprotein-cholesterol in the Japanese population.Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans.Causal relevance of circulating high-density lipoprotein cholesterol with cancer: a Mendelian randomization meta-analysis.HDL cholesterol and bone mineral density: is there a genetic link?Unacylated Ghrelin is associated with the isolated low HDL-cholesterol obese phenotype independently of insulin resistance and CRP level.Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.Resequencing of LPL in African Blacks and associations with lipoprotein-lipid levelsAssociation of rs5888 SNP in the scavenger receptor class B type 1 gene and serum lipid levels.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 levelsAssessment of the environmental and genetic factors influencing prevalence of metabolic syndrome in Saudi ArabiaA Systematic Investigation of Structure/Function Requirements for the Apolipoprotein A-I/Lecithin Cholesterol Acyltransferase Interaction Loop of High-density Lipoprotein.Candidate SNP Markers of Gender-Biased Autoimmune Complications of Monogenic Diseases Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene PromotersInteraction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study.LDLR C1725T Gene Polymorphism Frequency in Type 2 Diabetes Mellitus Patients With Dyslipidemia.Lipoprotein lipase gene sequencing and plasma lipid profile.PHACTR1 and SLC22A3 gene polymorphisms are associated with reduced coronary artery disease risk in the male Chinese Han populationHigh-density lipoproteins and cardiovascular disease: 2010 update.
P2860
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P2860
Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Genetic-epidemiological eviden ...... a systematic in-depth review.
@en
Genetic-epidemiological eviden ...... a systematic in-depth review.
@nl
type
label
Genetic-epidemiological eviden ...... a systematic in-depth review.
@en
Genetic-epidemiological eviden ...... a systematic in-depth review.
@nl
prefLabel
Genetic-epidemiological eviden ...... a systematic in-depth review.
@en
Genetic-epidemiological eviden ...... a systematic in-depth review.
@nl
P2093
P2860
P1476
Genetic-epidemiological eviden ...... a systematic in-depth review.
@en
P2093
Barbara Kollerits
Florian Kronenberg
Iris M Heid
P2860
P304
P356
10.1016/J.EXGER.2008.11.003
P577
2008-11-17T00:00:00Z