Showing results (31-40 of 282) with videos related to

Sort By:
Pageof 29
Biological & Pharmaceutical Bulletin|August 1, 1995
Stereospecific dehydrogenation of (25R)- and (25S)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acids by acyl-CoA oxidase in rat liver light mitochondrial fractionS Ikegawa, H Watanabe, T Goto, et al.
Steroids|March 1, 1995
Synthesis of 15 alpha-hydroxyestrogen 15-N-acetylglucosaminidesE Suzuki, S Namba, H Kurihara, et al.
Journal of Pharmaceutical and Biomedical Analysis|June 1, 1993
Enzyme immunoassay for 4-hydroxy-2-(4-methylphenyl)benzothiazoleS Miyairi, H Shimada, H Morita, et al.
Journal of Chromatography|October 28, 1988
Studies on steroids. CCXXXVIII. Determination of bile acids in liver tissue by gas chromatography-mass spectrometry with negative ion chemical ionization detectionJ Goto, H Miura, M Inada, et al.
Steroids|September 1, 1980
A novel immunization procedure involving pretreatment with cross-reacting steroid conjugated to a copolymer of D-glutamic acid and D-lysine for production of low cross-reactive antiseraK Tateishi, T Hamaoka, C Hayashi, et al.
Chemical & Pharmaceutical Bulletin|July 1, 1994
Analysis of conjugated bile acids in human biological fluids. Synthesis of hyodeoxycholic acid 3- and 6-glycosides and related compoundsT Iida, S Tazawa, Y Ohshima, et al.
Lipids|December 1, 1989
A method for the simultaneous analysis of unconjugated and glycine-conjugated bile acids by capillary gas-liquid chromatographyT Iida, T Itoh, K Hagiwara, et al.
Steroids|August 1, 1993
Potential bile acid metabolites. 20. A new synthetic route to stereoisomeric 3,6-dihydroxy- and 6-hydroxy-5 alpha-cholanoic acidsT Iida, T Tamaru, F C Chang, et al.
Steroids|December 1, 1990
Potential bile acid metabolites. 16. Synthesis of stereoisomeric 3 alpha,6,7,12 alpha-tetrahydroxy-5 beta-cholanoic acidsT Iida, I Komatsubara, S Yoda, et al.
Steroids|April 1, 1993
Potential bile acid metabolites. 19. The epimeric 3 alpha,6,7 beta-trihydroxy- and 3 alpha,6,7 beta,12 alpha-tetrahydroxy-5 alpha-cholanoic acidsT Iida, S Nishida, F C Chang, et al.
Pageof 29