Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
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USF1 deficiency activates brown adipose tissue and improves cardiometabolic healthSNP-SNP interactions dominate the genetic architecture of candidate genes associated with left ventricular mass in African-Americans of the GENOA study.Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.Effects of interacting networks of cardiovascular risk genes on the risk of type 2 diabetes mellitus (the CODAM study).A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study.Gene-gene interaction between APOA5 and USF1: two candidate genes for the metabolic syndromeRisk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.Gut microbiota as an epigenetic regulator: pilot study based on whole-genome methylation analysis.Two polymorphisms of USF1 gene (-202G>A and -844C>T) may be associated with hepatocellular carcinoma susceptibility based on a case-control study in Chinese Han population.Genetic association and interaction analysis of USF1 and APOA5 on lipid levels and atherosclerosisDifferential epigenetic and transcriptional response of the skeletal muscle carnitine palmitoyltransferase 1B (CPT1B) gene to lipid exposure with obesityApproaches to lipid metabolism gene identification and characterization in the postgenomic era.Unraveling the complex genetics of familial combined hyperlipidemia.Body mass index is associated with USF1 haplotype in Korean premenopausal womenPractical issues in building risk-predicting models for complex diseasesAssociation analysis of allelic variants of USF1 in coronary atherosclerosisHMGCR rs17671591 SNP Determines Lower Plasma LDL-C after Atorvastatin Therapy in Chilean Individuals.Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides.Association between single nucleotide polymorphisms of upstream transcription factor 1 (USF1) and susceptibility to papillary thyroid cancer.Significant association between upstream transcription factor 1 rs2516839 polymorphism and hepatocellular carcinoma risk: a case-control study.Association of F11 receptor gene polymorphisms with central obesity and blood pressure
P2860
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P2860
Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
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2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
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name
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@en
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@nl
type
label
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@en
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@nl
prefLabel
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@en
Variation in USF1 shows haplot ...... rosclerosis Research Study II.
@nl
P2093
P2860
P356
P1476
Variation in USF1 shows haplot ...... erosclerosis Research Study II
@en
P2093
David M Flavell
EARSII group
Jutta Palmen
Nadia Tahri-Daizadeh
Steve E Humphries
Viviane Nicaud
Wendy Putt
P2860
P304
P356
10.1093/HMG/DDH168
P577
2004-06-02T00:00:00Z