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Nobumitsu Hanioka

Division of Environmental Chemistry

National Institute of Health Sciences

Tokyo

Japan

[email]@nihs.go.jp

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Affiliation

Division of Environmental Chemistry, National Institute of Health Sciences, Tokyo, Japan. 1998 - 2003

References

Functional characterization of three human cytochrome p450 2E1 variants with amino acid substitutions. Hanioka, N., Tanaka-Kagawa, T., Miyata, Y., Matsushima, E., Makino, Y., Ohno, A., Yoda, R., Jinno, H., Ando, M. Xenobiotica (2003) [Pubmed]
Effect of alachlor on hepatic cytochrome P450 enzymes in rats. Hanioka, N., Watanabe, K., Yoda, R., Ando, M. Drug. Chem. Toxicol (2002) [Pubmed]
Interaction of irinotecan (CPT-11) and its active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38) with human cytochrome P450 enzymes. Hanioka, N., Ozawa, S., Jinno, H., Tanaka-Kagawa, T., Nishimura, T., Ando, M., Sawada Ji, J. Drug Metab. Dispos. (2002) [Pubmed]
Determination of UDP-glucuronosyltransferase UGT1A6 activity in human and rat liver microsomes by HPLC with UV detection. Hanioka, N., Jinno, H., Tanaka-Kagawa, T., Nishimura, T., Ando, M. J. Pharm. Biomed. Anal (2001) [Pubmed]
High-performance liquid chromatographic assay for glucuronidation activity of 7-ethyl-10-hydroxycamptothecin (SN-38), the active metabolite of irinotecan (CPT-11), in human liver microsomes. Hanioka, N., Jinno, H., Nishimura, T., Ando, M., Ozawa, S., Sawada, J. Biomed. Chromatogr. (2001) [Pubmed]
Human liver UDP-glucuronosyltransferase isoforms involved in the glucuronidation of 7-ethyl-10-hydroxycamptothecin. Hanioka, N., Ozawa, S., Jinno, H., Ando, M., Saito, Y., Sawada, J. Xenobiotica (2001) [Pubmed]
Effect of 4-tert-octylphenol on cytochrome P450 enzymes in rat liver. Hanioka, N., Jinno, H., Chung, Y.S., Nishimura, T., Tanaka-Kagawa, T., Ando, M. Arch. Toxicol. (2000) [Pubmed]
Interaction of bisphenol A with rat hepatic cytochrome P450 enzymes. Hanioka, N., Jinno, H., Tanaka-Kagawa, T., Nishimura, T., Ando, M. Chemosphere (2000) [Pubmed]
Determination of cytochrome P450 1A activities in mammalian liver microsomes by high-performance liquid chromatography with fluorescence detection. Hanioka, N., Tatarazako, N., Jinno, H., Arizono, K., Ando, M. J. Chromatogr. B Biomed. Sci. Appl. (2000) [Pubmed]
In vitro metabolism of chlorotriazines: characterization of simazine, atrazine, and propazine metabolism using liver microsomes from rats treated with various cytochrome P450 inducers. Hanioka, N., Jinno, H., Tanaka-Kagawa, T., Nishimura, T., Ando, M. Toxicol. Appl. Pharmacol. (1999) [Pubmed]
Inhibition of rat hepatic cytochrome P450 activities by biodegradation products of 4-tert-octylphenol ethoxylate. Hanioka, N., Jinno, H., Chung, , Tanaka-Kagawa, T., Nishimura, T., Ando, M. Xenobiotica (1999) [Pubmed]
In vitro metabolism of simazine, atrazine and propazine by hepatic cytochrome P450 enzymes of rat, mouse and guinea pig, and oestrogenic activity of chlorotriazines and their main metabolites. Hanioka, N., Jinno, H., Tanaka-Kagawa, T., Nishimura, T., Ando, M. Xenobiotica (1999) [Pubmed]
In vitro biotransformation of atrazine by rat liver microsomal cytochrome P450 enzymes. Hanioka, N., Jinno, H., Kitazawa, K., Tanaka-Kagawa, T., Nishimura, T., Ando, M., Ogawa, K. Chem. Biol. Interact. (1998) [Pubmed]