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Drug Metabolism and Disposition: the Biological Fate of Chemicals|September 25, 1999
Isoform-selective metabolism of mianserin by cytochrome P-450 2DT Chow, T Hiroi, S Imaoka, et al.
Biochemical Pharmacology|June 9, 1992
Expression of hepatic microsomal cytochrome P450s as altered by uremiaS Ikemoto, S Imaoka, N Hayahara, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 1, 1997
Effect of phenobarbital on the pharmacokinetics of lidocaine, monoethylglycinexylidide and 3-hydroxylidocaine in the rat: correlation with P450 isoform levelsT Nakamoto, Y Oda, S Imaoka, et al.
Biochemical Pharmacology|June 15, 1997
Specific binding of 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl propyl) piperazine (GBR-12935), an inhibitor of the dopamine transporter, to human CYP2D6T Hiroi, S Imaoka, T Chow, et al.
Research Communications in Molecular Pathology and Pharmacology|April 2, 1998
cis-Diamminedichloroplatinum induces peroxisomes as well as CYP4A1 in rat kidneyM Nakamura, S Imaoka, E Tanaka, et al.
Clinical & Experimental Metastasis|May 1, 1997
Identification and characterization of motility stimulating factor secreted from pancreatic cancer cells: role in tumor invasion and metastasisY Sakurai, T Sawada, Y S Chung, et al.
Endocrinology|August 23, 2001
Progesterone oxidation by cytochrome P450 2D isoforms in the brainT Hiroi, W Kishimoto, T Chow, et al.
Carcinogenesis|December 1, 1993
Increased CYP1A2 content and capacity to activate Glu-P-1 and Trp-P-2 in liver microsomes of scorbutic ODS ratsT Mori, R Kitamura, S Imaoka, et al.
Research Communications in Chemical Pathology and Pharmacology|February 1, 1989
Form-specific degradation of cytochrome P-450 by lipid peroxidation in rat liver microsomesM Kitada, M Komori, H Ohi, et al.
Biochemical Pharmacology|August 17, 1993
Changes in amounts of cytochrome P450 isozymes and levels of catalytic activities in hepatic and renal microsomes of rats with streptozocin-induced diabetesN Shimojo, T Ishizaki, S Imaoka, et al.
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