Enhancement by alloxan-induced diabetes of the rate of metabolic activation of three pyrolysate carcinogens via increase in the P-448-H content in rat liver
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[1] R. Kato,et al. Metabolic activation of a protein pyrolysate promutagen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline by rat liver microsomes and purified cytochrome P-450. , 1988, Carcinogenesis.
[2] F. Gonzalez,et al. Stabilization of cytochrome P450j messenger ribonucleic acid in the diabetic rat. , 1987, Molecular endocrinology.
[3] R. Kato,et al. Suppression of levels of phenobarbital-inducible rat liver cytochrome P-450 by pituitary hormone. , 1987, The Journal of biological chemistry.
[4] D W Nebert,et al. The P450 gene superfamily: recommended nomenclature. , 1987, DNA.
[5] M. J. Coon,et al. Evidence that isoniazid and ethanol induce the same microsomal cytochrome P-450 in rat liver, an isozyme homologous to rabbit liver cytochrome P-450 isozyme 3a. , 1986, Archives of biochemistry and biophysics.
[6] S. Thorgeirsson,et al. Metabolic activation of mutagenic heterocyclic aromatic amines from protein pyrolysates. , 1986, Critical reviews in toxicology.
[7] T. Kamataki,et al. A high-spin form of cytochrome P-450 highly purified from polychlorinated biphenyl-treated rats. Catalytic characterization and immunochemical quantitation in liver microsomes. , 1983, Molecular pharmacology.
[8] T. Sugimura,et al. Isolation and characterization of active metabolites of tryptophan-pyrolysate mutagen, TRP-P-2, formed by rat liver microsomes. , 1980, Chemico-biological interactions.