Author:
Ikegawa Shigeo,Goto Takaaki,Mano Nariyasu,Goto Junichi
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference18 articles.
1. Conversion of 3α,7α,12α-trihydroxy-5β-cholestanoic acid into cholic acid by rat liver peroxisomes;Pederson;FEBS Lett,1980
2. Subcellular localization of 3α,7α-dihydroxy- and 3α,7α,12α-trihydroxy-5β-cholestanoyl-coenzyme A ligase(s) in rat liver;Prydz;J Lipid Res,1988
3. Identification of 3α,7α,12α-trihydroxy-5β-cholest-24-enoic acid as an intermediate in the peroxisomal conversion of 3α,7α,12α-trihydroxy-5β-cholestanoic acid to cholic acid;Farrants;Biochim Biophys Acta,1989
4. Configuration of the 3α,7α,12α-trihydroxy-5β-cholest-24-enoic acid, an intermediate in the peroxisomal conversion of 3α,7α,12α-trihydroxy-5β-cholestanoic acid to cholic acid in rat liver;Farrants;Biochem Int,1992
5. Mechanism of degradation of the steroid side chain in the formation of bile acids;Björkhem;J Lipid Res,1992
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Biliary bile acids in birds of the Cotingidae family: Taurine-conjugated (24R,25R)-3α,7α,24-trihydroxy-5β-cholestan-27-oic acid and two epimers (25R and 25S) of 3α,7α-dihydroxy-5β-cholestan-27-oic acid;Steroids;2011-09
2. Major Biliary Bile Acids of the Medaka (Oryzias latipes): 25R- and 25S-Epimers of 3α,7α,12α-Trihydroxy-5β-cholestanoic Acid;Zoological Science;2010-07
3. A new, major C27 biliary bile acid in the Red-winged tinamou (Rhynchotus rufescens):(25R)-1β,3α,7α-trihydroxy-5β-cholestan-27-oic acid;Journal of Lipid Research;2009-04
4. 3α, 7α, 12α-Trihydroxy-5β-cholestanoyl-CoA 24-hydroxylase;Class 1 · Oxidoreductases;2009
5. A mouse model for α-methylacyl-CoA racemase deficiency: adjustment of bile acid synthesis and intolerance to dietary methyl-branched lipids;Human Molecular Genetics;2004-03-11