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Genotoxic mechanisms for the carcinogenicity of the environmental pollutants and carcinogens o-anisidine and 2-nitroanisole follow from adducts generated by their metabolite N-(2-methoxyphenyl)hydroxylamine with deoxyguanosine in DNA Cover

Genotoxic mechanisms for the carcinogenicity of the environmental pollutants and carcinogens o-anisidine and 2-nitroanisole follow from adducts generated by their metabolite N-(2-methoxyphenyl)hydroxylamine with deoxyguanosine in DNA

Interdisciplinary Toxicology
Volume 2 (2009): Issue 1 (March 2009)
By: Marie Stiborová,  Karel Naiman,  Markéta Martínková,  Václav Martínek,  Martina Svobodová,  Heinz Schmeiser and  Eva Frei  
Open Access
|Jun 2009

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DOI: https://doi.org/10.2478/v10102-009-0004-4 | Journal eISSN: 1337-9569 | Journal ISSN: 1337-6853
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Language: English
Page range: 24 - 27
Published on: Jun 19, 2009
Published by: Slovak Academy of Sciences, Institute of Experimental Pharmacology & Toxicology, Centre of Experimental Medicine
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
Keywords:
carcinogens,
-anisidine,
2-nitroanisole,
-(2-methoxyphenyl)hydroxylamine,
metabolism,
DNA adducts,
cancer
Related subjects:
Medicine,
Clinical medicine,
Pharmacology, toxicology

© 2009 Marie Stiborová, Karel Naiman, Markéta Martínková, Václav Martínek, Martina Svobodová, Heinz Schmeiser, Eva Frei, published by Slovak Academy of Sciences, Institute of Experimental Pharmacology & Toxicology, Centre of Experimental Medicine
This work is licensed under the Creative Commons License.

Volume 2 (2009): Issue 1 (March 2009)