Apolipoprotein multigene family: tandem organization of human apolipoprotein AI, CIII, and AIV genes
about
Lipoprotein genotype and conserved pathway for exceptional longevity in humansApolipoprotein C3 SstI polymorphism and triglyceride levels in Asian IndiansIntestinal apolipoprotein AI gene transcription is regulated by multiple distinct DNA elements and is synergistically activated by the orphan nuclear receptor, hepatocyte nuclear factor 4An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphismsAntagonism between apolipoprotein AI regulatory protein 1, Ear3/COUP-TF, and hepatocyte nuclear factor 4 modulates apolipoprotein CIII gene expression in liver and intestinal cellsStructure, evolution, and polymorphisms of the human apolipoprotein A4 gene (APOA4)Nonsynonymous polymorphic sites in the apolipoprotein (apo) A-IV gene are associated with changes in the concentration of apo B- and apo A-I-containing lipoproteins in a normal populationInhibition of renal permeability towards albumin: a new function of apolipoproteins with possible pathogenetic relevance in focal glomerulosclerosis.The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.The genetics of serum lipid responsiveness to dietary interventions.Can novel Apo A-I polymorphisms be responsible for low HDL in South Asian immigrants?The SP1 sites of the human apoCIII enhancer are essential for the expression of the apoCIII gene and contribute to the hepatic and intestinal expression of the apoA-I gene in transgenic miceApolipoprotein A1 polymorphisms and risk of coronary artery disease: a meta-analysis.High density lipoprotein deficiency with xanthomas. A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene.Orphan nuclear hormone receptor Rev-erbalpha regulates the human apolipoprotein CIII promoter.Intestinal expression of human apolipoprotein A-IV in transgenic mice fails to influence dietary lipid absorption or feeding behavior.A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocation.A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.DNA inversion within the apolipoproteins AI/CIII/AIV-encoding gene cluster of certain patients with premature atherosclerosisThe common apolipoprotein A-1 polymorphism -75A>G is associated with ethnic differences in recurrent coronary events after recovery from an acute myocardial infarction.Monogenic causes of elevated HDL cholesterol and implications for development of new therapeutics.Apolipoprotein C3 genetic polymorphisms are associated with lipids and coronary artery disease in a Chinese population.Metabolic syndrome in South Asian immigrants: more than low HDL requiring aggressive management.Gene polymorphism and coronary risk factors in Indian population.A human mannose-binding protein is an acute-phase reactant that shares sequence homology with other vertebrate lectinsApoA-IV: current and emerging roles in intestinal lipid metabolism, glucose homeostasis, and satietyVariation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian children.Haplotypes identified by DNA restriction-fragment-length polymorphisms in the A-1 C-III A-IV gene region and hypertriglyceridemia.The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genesGenetic determination of plasma apolipoprotein AI in a population-based sample.Effect of apolipoprotein C3 genetic polymorphisms on serum lipid levels and the risk of intracerebral hemorrhage.Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels.Apolipoprotein A-IV regulates chylomicron metabolism-mechanism and function.Effect of apolipoprotein A1 genetic polymorphisms on lipid profiles and the risk of coronary artery disease.Apolipoprotein A-IV: a protein intimately involved in metabolism.African origin of human-specific polymorphic Alu insertions.Apolipoprotein A1 -75 G/A and +83 C/T polymorphisms and renal cancer risk.The use of PCR in diagnosing lipoprotein disorders.Single nucleotide polymorphisms of APOA1 gene and their relationship with serum apolipoprotein A-I concentrations in the native population of AssamDifferent cis-acting DNA elements control expression of the human apolipoprotein AI gene in different cell types.
P2860
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P2860
Apolipoprotein multigene family: tandem organization of human apolipoprotein AI, CIII, and AIV genes
description
1985 nî lūn-bûn
@nan
1985 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@ast
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@en
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@nl
type
label
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@ast
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@en
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@nl
prefLabel
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@ast
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@en
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@nl
P2860
P356
P1476
Apolipoprotein multigene famil ...... rotein AI, CIII, and AIV genes
@en
P2093
S K Karathanasis
P2860
P304
P356
10.1073/PNAS.82.19.6374
P407
P577
1985-10-01T00:00:00Z