- The unexpected gas-phase reactivity of the CH3OH adduct of Michler?s hydrol blue: Proton-shuttle catalysis and stepwise radical expulsions2007 | Faculty of Science
- 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 DNA2009 | Faculty of Science, First Faculty of Medicine, Faculty of Mathematics and Physics
- Mammalian peroxidases activate anticancer drug ellipticine to intermediates forming deoxyguanosine adducts in DNA identical to those found in vivo and generated from 12-hydroxyellipticine and 13-hydroxyellipticine2007 | Second Faculty of Medicine
- Human cytochrome-P450 enzymes metabolize N-(2-methoxyphenyl)hydroxylamine, a metabolite of the carcinogens o-anisidine and o-nitroanisole, thereby dictating its genotoxicity2011 | Faculty of Science
- Cytochrome P450-and peroxidase-mediated oxidation of anticancer alkaloid ellipticine dictates its anti-tumor efficiency2011 | Faculty of Science
- Formation, Persistence, and Identification of DNA Adducts Formed by the Carcinogenic Environmental Pollutant o-Anisidine in Rats2012 | Faculty of Science, Central Library of Charles University
- Activation and detoxification metabolism of urban air pollutants 2-nitrobenzanthrone and carcinogenic 3-nitrobenzanthrone by rat and mouse hepatic microsomes2012 | Faculty of Science