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pro vyhledávání: '"G P, Eberhart"'
Autor:
G. P. Eberhart
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 83:836-846
Autor:
M E, Brousseau, G P, Eberhart, J, Dupuis, B F, Asztalos, A L, Goldkamp, E J, Schaefer, M W, Freeman
Publikováno v:
Journal of lipid research. 41(7)
Tangier disease (TD), caused by mutations in the ATP-binding cassette 1 (ABC-1) gene, is a rare genetic disorder characterized by severe deficiency of high density lipoproteins (HDL) in the plasma, hypercatabolism of HDL, and defective apolipoprotein
Autor:
M E, Brousseau, E J, Schaefer, J, Dupuis, B, Eustace, P, Van Eerdewegh, A L, Goldkamp, L M, Thurston, M G, FitzGerald, D, Yasek-McKenna, G, O'Neill, G P, Eberhart, B, Weiffenbach, J M, Ordovas, M W, Freeman, R H, Brown, J Z, Gu
Publikováno v:
Journal of lipid research. 41(3)
Tangier disease (TD) is an autosomal co-dominant disorder in which homozygotes have a marked deficiency of high density lipoprotein (HDL) cholesterol and, in some cases, peripheral neuropathy and premature coronary heart disease (CHD). Homozygotes ar
Publikováno v:
The Journal of clinical endocrinology and metabolism. 83(3)
A 51-yr-old woman without clinical evidence of Tangier disease, but with an extremely low high density lipoprotein (HDL) cholesterol level, was studied. No defect in the major structural protein of HDL, apolipoprotein AI (apo AI), was detected. A pre
Publikováno v:
The American journal of physiology. 266(5 Pt 2)
We evaluated insulin sensitivity in epididymal adipocytes from two mouse strains shown to be either sensitive (AKR/J, n = 14) or resistant (SWR/J, n = 12) to the development of obesity when fed a high-fat diet. Half of each strain was fed a chow (CH)