1. New bile acid analogs: 3α,7α-dihydroxy-7β-methyl-5β-cholanoic acid, 3α,7β-dihydroxy-7α-methyl-5β-cholanoic acid, and 3α-hydroxy-7ξ-methyl-5β-cholanoic acid;Une;J Lipid Res,1984
2. Synthesis of potential cholelitholytic agents: 3α,7α,12α-trihydroxy-7β-methyl-5β-cholanoic acid, 3α,7β,12α-trihydroxy-7α-methyl-5β-cholanoic acid, and 3α,12α-dihydroxy-7ξ-methyl-5β-cholanoic acid;Kuroki;J Lipid Res,1985
3. Metabolism of 3α,7α-dihydroxy-7β-methyl-5β-cholanoic acid and 3α,7β-dihydroxy-7β-methyl-5β-cholanoic acid in hamsters;Une;Biochim Biophys Acta,1985
4. Metabolism of the bile acid analogues, 7β-methyl-cholic acid and 7α-methyl-ursocholic acid;Kuroki;J Lipid Res,1987
5. 7-Methyl bile acids: 7β-methyl-cholic acid inhibits bacterial 7-dehydroxylation of cholic acid and chenodeoxycholic acid in the hamster;Kuroki;J Lipid Res,1987