Abstract Estrogen had been found to be negatively associated with serum triglyceride (TG) levels. Apolipoprotein A5 (APOA5), a novel member of apolipoprotein family, was reported to have a strong ability to decrease serum concentrations of TG. Clinical data found concentrations of APOA5 were higher in woman than that in men, and the negative relationship between APOA5 and TG levels was more significant in woman. These suggests APOA5 may involve in estrogen actions. Therefore, we hypothesize estrogen up-regulates serum concentrations of APOA5 and subsequently decreases serum TG levels. We will design the following experiments to test this hypothesis. (1) We will treat wild and APOA5-defeted ovariectomized hamster with or without estrogen to ...
Objective—Cholesterol and lipoprotein metabolism display pronounced gender differences. Premenopausa...
Genistein (GEN) has been shown to significantly inhibit hepatic triglyceride accretion triggered by ...
The antiatherogenic property of estrogens is mediated via at least two mechanisms: first by affectin...
Apolipoprotein M (apoM) is present predominantly in high-density lipoprotein (HDL) in human plasma, ...
We have shown mouse to be an useful animal model for studies on the estrogen-mediated synthesis and ...
The apolipoprotein AV gene (APOA5) is a key determinant of plasma triglyceride levels, a major risk ...
Hypertriglyceridemia is an independent risk factor forcoronary heart disease.1 Apolipoproteins that ...
Apolipoprotein A5 (APOA5) is a newly described member of the apolipoprotein gene family whose initi...
Elevated plasma triglyceride (TG) is a major and independent risk factor for cardiovascular disease....
2001, is part of the apolipoprotein family (APOA1/C3/ A4). Apo A-V is encoded by the APOA5 gene, whi...
A5 (ApoA5) is fast gaining attention as a key regulator of serum triglyceride concentrations. An Apo...
Context: Growth hormone (GH) stimulates hepatic synthesis of very-low-density lipoproteins (VLDL), w...
Background: We have previously demonstrated that estrogen could significantly enhance expression of ...
The APOA5 gene encoding apolipoprotein A-V (a 366amino acid protein), present in minute amounts in V...
Abstract Apolipoprotein A5 (apoA5) has been identified to play an important role in lipid metabolism...
Objective—Cholesterol and lipoprotein metabolism display pronounced gender differences. Premenopausa...
Genistein (GEN) has been shown to significantly inhibit hepatic triglyceride accretion triggered by ...
The antiatherogenic property of estrogens is mediated via at least two mechanisms: first by affectin...
Apolipoprotein M (apoM) is present predominantly in high-density lipoprotein (HDL) in human plasma, ...
We have shown mouse to be an useful animal model for studies on the estrogen-mediated synthesis and ...
The apolipoprotein AV gene (APOA5) is a key determinant of plasma triglyceride levels, a major risk ...
Hypertriglyceridemia is an independent risk factor forcoronary heart disease.1 Apolipoproteins that ...
Apolipoprotein A5 (APOA5) is a newly described member of the apolipoprotein gene family whose initi...
Elevated plasma triglyceride (TG) is a major and independent risk factor for cardiovascular disease....
2001, is part of the apolipoprotein family (APOA1/C3/ A4). Apo A-V is encoded by the APOA5 gene, whi...
A5 (ApoA5) is fast gaining attention as a key regulator of serum triglyceride concentrations. An Apo...
Context: Growth hormone (GH) stimulates hepatic synthesis of very-low-density lipoproteins (VLDL), w...
Background: We have previously demonstrated that estrogen could significantly enhance expression of ...
The APOA5 gene encoding apolipoprotein A-V (a 366amino acid protein), present in minute amounts in V...
Abstract Apolipoprotein A5 (apoA5) has been identified to play an important role in lipid metabolism...
Objective—Cholesterol and lipoprotein metabolism display pronounced gender differences. Premenopausa...
Genistein (GEN) has been shown to significantly inhibit hepatic triglyceride accretion triggered by ...
The antiatherogenic property of estrogens is mediated via at least two mechanisms: first by affectin...