Apolipoprotein AV (apoAV) overexpression causes a decrease in plasma triglyceride (TG) levels, while deficiency of apoAV causes hypertriglyceridemia in both men and mice. However, contrary to what would be expected, plasma apoAV and TG levels in humans are positively correlated. To address this apparent paradox, we determined plasma apoAV levels in various mouse models with median TG levels ranging from 30 mg/dl in wild-type mice to 2089 mg/dl in glycosylphosphatidylinositol-anchored HDL binding protein 1-deficient mice. The data show that apoAV and TG levels are positively correlated in mice (r = +0.798, P < 0.001). In addition, we show that LPL gene transfer caused a simultaneous decrease in TG and apoAV in LPL-deficient mice. The comb...
ObjectiveApolipoprotein A-V (apoA-V) is a low-abundance plasma protein that modulates triacylglycero...
Clinical and epidemiological investigations confirm that patients with loss-of-function mutations (R...
Objective - Mutations in LPL or APOC2 genes are recognized causes of inherited forms of severe hyper...
Apolipoprotein AV (apoAV) overexpression causes a decrease in plasma triglyceride (TG) levels, while...
Hypertriglyceridemia is an independent risk factor forcoronary heart disease.1 Apolipoproteins that ...
ApoAV has been discovered recently as a novel modifier of triglyceride (TG) metabolism, but the path...
The apolipoprotein APOA5 gene, a member of the gene cluster on chromosome 11q23 that includes APOA1,...
Both the apolipoprotein A5 and C3 genes have repeatedly been shown to play an important role in dete...
Both the apolipoprotein A5 and C3 genes have repeatedly been shown to play an important role in det...
ApoAV has been discovered recently as a novel modifier of triglyceride (TG) metabolism, but the path...
Apolipoprotein E2 (apoE2)-associated hyperlipidemia is characterized by a disturbed clearance of apo...
Elevated plasma triglyceride (TG) is a major and independent risk factor for cardiovascular disease....
The APOA5 gene encoding apolipoprotein A-V (a 366amino acid protein), present in minute amounts in V...
We have generated transgenic mice expressing the human apo-lipoprotein CII (apoCI) gene under the tr...
APOA5 encodes a novel apolipoprotein (apo A-V) which appears to be a modulator of plasma triglycerid...
ObjectiveApolipoprotein A-V (apoA-V) is a low-abundance plasma protein that modulates triacylglycero...
Clinical and epidemiological investigations confirm that patients with loss-of-function mutations (R...
Objective - Mutations in LPL or APOC2 genes are recognized causes of inherited forms of severe hyper...
Apolipoprotein AV (apoAV) overexpression causes a decrease in plasma triglyceride (TG) levels, while...
Hypertriglyceridemia is an independent risk factor forcoronary heart disease.1 Apolipoproteins that ...
ApoAV has been discovered recently as a novel modifier of triglyceride (TG) metabolism, but the path...
The apolipoprotein APOA5 gene, a member of the gene cluster on chromosome 11q23 that includes APOA1,...
Both the apolipoprotein A5 and C3 genes have repeatedly been shown to play an important role in dete...
Both the apolipoprotein A5 and C3 genes have repeatedly been shown to play an important role in det...
ApoAV has been discovered recently as a novel modifier of triglyceride (TG) metabolism, but the path...
Apolipoprotein E2 (apoE2)-associated hyperlipidemia is characterized by a disturbed clearance of apo...
Elevated plasma triglyceride (TG) is a major and independent risk factor for cardiovascular disease....
The APOA5 gene encoding apolipoprotein A-V (a 366amino acid protein), present in minute amounts in V...
We have generated transgenic mice expressing the human apo-lipoprotein CII (apoCI) gene under the tr...
APOA5 encodes a novel apolipoprotein (apo A-V) which appears to be a modulator of plasma triglycerid...
ObjectiveApolipoprotein A-V (apoA-V) is a low-abundance plasma protein that modulates triacylglycero...
Clinical and epidemiological investigations confirm that patients with loss-of-function mutations (R...
Objective - Mutations in LPL or APOC2 genes are recognized causes of inherited forms of severe hyper...