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The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Suppression of endogenous testosterone in young men increases serum levels of high density lipoprotein subclass lipoprotein A-I and lipoprotein(a)A von Eckardstein, S Kliesch, E Nieschlag, et al.Journal of Lipid Research|April 7, 1999
Phytanic acid is ligand and transcriptional activator of murine liver fatty acid binding proteinC Wolfrum, P Ellinghaus, M Fobker, et al.European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|January 1, 1995
Arterial and venous cytokine response to cardiopulmonary bypass for low risk CABG and relation to hemodynamicsM C Deng, M Wiedner, M Erren, et al.The Journal of Biological Chemistry|March 10, 1984
Human apolipoprotein A-I polymorphism. Identification of amino acid substitutions in three electrophoretic variants of the Münster-3 typeH J Menzel, G Assmann, S C Rall, et al.Rheumatology (Oxford, England)|August 12, 2004
Interleukin-10 promoter microsatellite polymorphisms in systemic lupus erythematosus: association with the anti-Sm immune responseH Schotte, M Gaubitz, P Willeke, et al.European Journal of Clinical Nutrition|January 18, 2007
Similar serum plant sterol responses of human subjects heterozygous for a mutation causing sitosterolemia and controls to diets enriched in plant sterols or stanolsM Kratz, F Kannenberg, E Gramenz, et al.Metabolism: Clinical and Experimental|March 21, 1998
Basal growth hormone levels in women are positively correlated with high-density lipoprotein cholesterol and apolipoprotein A-I independently of insulin-like growth factor 1 or insulinD Bänsch, C Chen-Haudenschild, A Dirkes-Kersting, et al.Diabetes|July 25, 2000
Genotype/phenotype relationships in HNF-4alpha/MODY1: haploinsufficiency is associated with reduced apolipoprotein (AII), apolipoprotein (CIII), lipoprotein(a), and triglyceride levelsD Q Shih, H M Dansky, M Fleisher, et al.The Journal of Clinical Investigation|January 1, 1991
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacitiesH Funke, A von Eckardstein, P H Pritchard, et al.Atherosclerosis|January 3, 1997
The replacement of arginine by cysteine at residue 151 in apolipoprotein A-I produces a phenotype similar to that of apolipoprotein A-IMilanoE Bruckert, A von Eckardstein, H Funke, et al.Pageof 38