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Arteriosclerosis, Thrombosis, and Vascular Biology|January 15, 1999
Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiencyM Marcil, L Yu, L Krimbou, et al.Human Genetics|July 1, 1995
Evidence for a cholesterol-lowering gene in a French-Canadian kindred with familial hypercholesterolemiaC Sass, L M Giroux, Y Ma, et al.Metabolism: Clinical and Experimental|December 1, 1991
High-density lipoprotein particles in octogenariansG Luc, J M Bard, S Lussier-Cacan, et al.Journal of Lipid Research|October 1, 1987
Enzyme-linked immunosorbent assay for human plasma apolipoprotein BJ M Ordovas, J P Peterson, P Santaniello, et al.Lancet (London, England)|May 22, 1993
Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemiaS Moorjani, M Roy, A Torres, et al.The Journal of Nutrition|September 1, 1989
Postprandial changes in the plasma concentration of alpha- and gamma-tocopherol in human subjects fed a fat-rich meal supplemented with fat-soluble vitaminsM Meydani, J S Cohn, J B Macauley, et al.Atherosclerosis|August 1, 1989
Lipoprotein composition changes induced by fenofibrate in dysbetalipoproteinemia type IIIS Lussier-Cacan, J M Bard, L Boulet, et al.Annals of Medicine|April 1, 1991
A phenocopy of type III dysbetalipoproteinemia occurring in a candidate family for a putative apo E receptor defectJ Davignon, J Dallongeville, G Roederer, et al.Arteriosclerosis (Dallas, Tex.)|January 1, 1989
Apolipoprotein E2(Arg158----Cys) frequency in a hyperlipidemic French-Canadian population of apolipoprotein E2/2 subjects. Determination by synthetic oligonucleotide probesK H Weisgraber, Y M Newhouse, J M Taylor, et al.Journal of Lipid Research|September 1, 1990
Comparison of deuterated leucine, valine, and lysine in the measurement of human apolipoprotein A-I and B-100 kineticsA H Lichtenstein, J S Cohn, D L Hachey, et al.Pageof 22