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Identification of non-functional allelic variant of CYP1A2 in dogs.
Mise M, Hashizume T, Matsumoto S, Terauchi Y, Fujii T. Mise M, et al. Pharmacogenetics. 2004 Nov;14(11):769-73. doi: 10.1097/00008571-200411000-00008. Pharmacogenetics. 2004. PMID: 15564884
Characterization of substrate specificity of dog CYP1A2 using CYP1A2-deficient and wild-type dog liver microsomes.
Mise M, Hashizume T, Komuro S. Mise M, et al. Drug Metab Dispos. 2008 Sep;36(9):1903-8. doi: 10.1124/dmd.108.022301. Epub 2008 Jun 23. Drug Metab Dispos. 2008. PMID: 18573860
Polymorphic expression of CYP1A2 leading to interindividual variability in metabolism of a novel benzodiazepine receptor partial inverse agonist in dogs.
Mise M, Yadera S, Matsuda M, Hashizume T, Matsumoto S, Terauchi Y, Fujii T. Mise M, et al. Drug Metab Dispos. 2004 Feb;32(2):240-5. doi: 10.1124/dmd.32.2.240. Drug Metab Dispos. 2004. PMID: 14744947
A novel cytochrome P450 enzyme responsible for the metabolism of ebastine in monkey small intestine.
Hashizume T, Mise M, Matsumoto S, Terauchi Y, Fujii T, Imaoka S, Funae Y, Kamataki T, Miyazaki H. Hashizume T, et al. Among authors: mise m. Drug Metab Dispos. 2001 Jun;29(6):798-805. Drug Metab Dispos. 2001. PMID: 11353747
Evaluation of the potential for drug-induced liver injury based on in vitro covalent binding to human liver proteins.
Usui T, Mise M, Hashizume T, Yabuki M, Komuro S. Usui T, et al. Among authors: mise m. Drug Metab Dispos. 2009 Dec;37(12):2383-92. doi: 10.1124/dmd.109.028860. Epub 2009 Aug 31. Drug Metab Dispos. 2009. PMID: 19720731
N-Dealkylation and hydroxylation of ebastine by human liver cytochrome P450.
Hashizume T, Mise M, Terauchi Y, O L, Fujii T, Miyazaki H, Inaba T. Hashizume T, et al. Among authors: mise m. Drug Metab Dispos. 1998 Jun;26(6):566-71. Drug Metab Dispos. 1998. PMID: 9616193
Involvement of CYP2J2 and CYP4F12 in the metabolism of ebastine in human intestinal microsomes.
Hashizume T, Imaoka S, Mise M, Terauchi Y, Fujii T, Miyazaki H, Kamataki T, Funae Y. Hashizume T, et al. Among authors: mise m. J Pharmacol Exp Ther. 2002 Jan;300(1):298-304. doi: 10.1124/jpet.300.1.298. J Pharmacol Exp Ther. 2002. PMID: 11752129
Brucine as a potent inducer of CYP2B3, the third member of the CYP2B subfamily P450 in rats.
Yamada H, Minematsu Y, Nakamura T, Mise M, Fujisaki H, Oguri K. Yamada H, et al. Among authors: mise m. Biol Pharm Bull. 1996 Feb;19(2):291-3. doi: 10.1248/bpb.19.291. Biol Pharm Bull. 1996. PMID: 8850324
[Studies on PCB toxicity involving 2C subfamily cytochrome P450].
Ariyoshi N, Ito S, Okudaira A, Mise M, Matsusue K, Yamada H, Oguri K. Ariyoshi N, et al. Among authors: mise m. Fukuoka Igaku Zasshi. 1995 May;86(5):153-62. Fukuoka Igaku Zasshi. 1995. PMID: 7628802 Japanese.
Strychnine and brucine as the potent inducers of drug metabolizing enzymes in rat liver: different profiles from phenobarbital on the induction of cytochrome P450 and UDP-glucuronosyltransferase.
Fujisaki H, Mise M, Ishii Y, Yamada H, Oguri K. Fujisaki H, et al. Among authors: mise m. J Pharmacol Exp Ther. 1994 Feb;268(2):1024-31. J Pharmacol Exp Ther. 1994. PMID: 7906730
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