Pathobiologic and metabolic aspects of mammary gland tumorigenesis by N-substituted aryl compounds

Author:

Malejka-Giganti D.,Ritter C. L.,Ryzewski C. N.

Publisher

Environmental Health Perspectives

Subject

Health, Toxicology and Mutagenesis,Public Health, Environmental and Occupational Health

Reference47 articles.

1. NHydroxy-2-acetylaminofluorene: a metabolite of 2-acetylaminofluorene with increased carcinogenic activity in the rat;Miller E. C.;Cancer Res.,1961

2. The N-hydroxylation of 4-acetylaminobiphenyl by the rat and dog and the strong carcinogenicity of N-hydroxy-4-acetylaminobiphenyl in the rat;Miller J. A.;Cancer Res.,1961

3. Structure-activity relationships of N-acylarylhydroxylamines in the rat;Gutmann H. R.;Cancer Res.,1970

4. The conversion of noncarcinogenic aromatic amides to carcinogenic arylhydroxamic acids by synthetic N-hydroxylation;Gutmann H. R.;Cancer Res.,1967

5. Relationship of metabolic activation of N-hydroxy-N-acylarylamines to the biological response in the liver and mammary gland of the female CD rat;Shirai T.;Cancer Res.,1981

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