Cholesta-5,7,9(11)-trien-3 beta-ol found in plasma of patients with Smith-Lemli-Opitz syndrome indicates formation of sterol hydroperoxide
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference21 articles.
1. A newly recognized syndrome of multiple congenital anomalies;Smith;J. Pediatr.,1964
2. Markedly inhibited 7-dehydrocholesterol-delta 7-reductase activity in liver microsomes from Smith-Lemli-Opitz homozygotes;Shefer;J. Clin. Invest.,1995
3. Defective conversion of 7-dehydrocholesterol to cholesterol in cultured skin fibroblasts from Smith-Lemli-Opitz syndrome homozygotes;Honda;J. Lipid Res.,1995
4. Identification of 8-dehydrocholesterol (cholesta-5,8-dien-3β-ol) in patients with Smith-Lemli-Opitz syndrome;Batta;J. Lipid Res.,1995
5. Identification of 19-nor-5,7, 9 ( 10 )cholestatrien-3β-ol in patients with Smith-Lemli-Opitz syndrome;Batta;J. Lipid Res.,1995
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