豊吉一美 | Gifu Pharmaceutical University

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著作論文

Influence of Microsomal and Cytosolic Fractions from the Liver of 4 Animal Species and Man on the Mutagenicity of Carcinogenic Aminoazo Dyes and Nature of the Mutagenicity-Enhancing Factor in the Cytosol from Rat Liver
A Role of Alkaline Phosphatase in Phosphate Transport
Aryl Hydroxylation of Aminoazo Dyes and 3-Acetaminotoluene by Several Model Systems
Studies on Carcinogenic Azo Dyes. VII. Changes in the Hepatic Activities of 3'-Me-DAB Metabolism by Rat, Mouse, and Hamster during the Repeated Administration of 3'-Me-DAB
Carcinogenic Azo Dyes. XVIII. Syntheses of Azo Dyes related to 3'-Hydroxymethyl-4-(dimethylamino) azobenzene, a New Potent Hepatocarcinogen
Studies on Carcinogenic Azo Dyes. VI. Effect of Factors Influencing Drug Metabolism on the NIH Shift during Hydroxylations of 4-Dimethylamino-3'-methylazobenzene and 3-Methylacetanilide
Absorption, Distribution, and Excretion of Suprofen in Mice of Both Sexes
Carcinogenic Azo Dyes. XII. Detection of New Metabolites of Aminoazo Dyes by Rat Liver
Carcinogenic Azo Dyes. XI. Analysis of Biliary and Urinary Metabolites of 3'-Methyl-4-(methylamino) azobenzene in Rat
Aryl Hydroxylation of 3-Methylacetanilide [4-^H] by Several Model Systems
Studies on Carcinogenic Azo Dyes. V. The NIH Shift during the Aryl Hydroxylation of 3'-Methyl-4-(dimethylamino) azobenzene and 3-Methylacetanilide by the Rat
Studies on Carcinogenic Azo Dyes. III. Retention of Tritium during Enzymatic Hydroxylation of 3'-Methyl-4-dimethylaminoazobenzene (4'-^3H, or 5'-^3H) or Chemical Substitutions of the Related Compound, and the Effect of the Repeated Administration of This

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