Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal α-methylacyl-CoA racemase deficiency
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference28 articles.
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2. The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney;Vanhove;J. Biol. Chem.,1993
3. Further Characterization of the Peroxisomal 3-Hydroxyacyl-Coa Dehydrogenases from Rat Liver. Relationship Between the Different Dehydrogenases and Evidence That Fatty Acids and the C27 Bile Acids Di- and Tri-Hydroxycoprostanic Acids are Metabolized by Separate Multifunctional Proteins
4. Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase;Jiang;J. Biochem.,1996
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