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Journal of Inherited Metabolic Disease|November 20, 1998
Accurate detection of Smith-Lemli-Opitz syndrome carriers by measurement of the rate of reduction of the ergosterol C-7 double bond in cultured skin fibroblastsM Honda, G S Tint, S Shefer, et al.Metabolism: Clinical and Experimental|July 1, 1994
Deficient ileal 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in sitosterolemia: sitosterol is not a feedback inhibitor of intestinal cholesterol biosynthesisL B Nguyen, G Salen, S Shefer, et al.Gastroenterology|October 1, 1995
Treatment of the cholesterol biosynthetic defect in Smith-Lemli-Opitz syndrome reproduced in rats by BM 15.766G Xu, G Salen, S Shefer, et al.Journal of Lipid Research|June 1, 1996
Abnormal cholesterol biosynthesis in the Smith-Lemli-Opitz syndromeG Salen, S Shefer, A K Batta, et al.Metabolism: Clinical and Experimental|November 1, 1994
Regulation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase activity in the rat ileum: effects of bile acids and lovastatinL B Nguyen, S Shefer, G Salen, et al.The Journal of Clinical Investigation|April 1, 1990
Feedback regulation of bile-acid synthesis in the rat. Differing effects of taurocholate and tauroursocholateS Shefer, L Nguyen, G Salen, et al.Digestive Diseases and Sciences|December 1, 1989
Gallstone dissolution therapy with ursodiol. Efficacy and safetyG SalenJournal of Clinical Gastroenterology|January 1, 1988
Clinical perspective on the treatment of gallstones with ursodeoxycholic acidG SalenLipids|December 1, 1978
Biosynthesis of chenodeoxycholic acid: side-chain hydroxylation of 5 beta-cholestane-3 alpha, 7 alpha-diol by subcellular fractions of guinea pig liverN Hoshita, S Shefer, F W Cheng, et al.Hepatology (Baltimore, Md.)|August 1, 1996
Blocking late cholesterol biosynthesis inhibits the growth of transplanted Morris hepatomas (7288CTC) in ratsG Xu, G Salen, M Lea, et al.Pageof 26