Pages that link to "Q50213041"

The following pages link to Esterification of arylhydroxylamines: evidence for a specific gene product in mutagenesis (Q50213041):

Displaying 34 items.

• DNA adduct formation and mutation induction by nitropyrenes in Salmonella and Chinese hamster ovary cells: relationships with nitroreduction and acetylation (Q28362296) (← links)
• Computer analysis of toxicological data bases: mutagenicity of aromatic amines in Salmonella tester strains (Q36489377) (← links)
• Mutagenicity and carcinogenicity of nitroarenes and their sources in the environment (Q38165869) (← links)
• Nitroreductase independent mutagenicity of 1-halogenated-2,4-dinitrobenzenes (Q38554598) (← links)
• Metabolic activation of mutagenic heterocyclic aromatic amines from protein pyrolysates (Q39733665) (← links)
• Genetic toxicity of 2-acetylaminofluorene, 2-aminofluorene and some of their metabolites and model metabolites (Q40392414) (← links)
• Identification of a Reduction Product of Aristolochic Acid: Implications for the Metabolic Activation of Carcinogenic Aristolochic Acid (Q41841343) (← links)
• Biotransformation of 1-nitropyrene to 1-aminopyrene and N-formyl-1-aminopyrene by the human intestinal microbiota (Q42217050) (← links)
• Chemistry and in vitro mutagenicity of 2-aminofluorene derivatives (Q42225248) (← links)
• The role of DNA sequence and structure of the electrophile on the mutagenicity of nitroarenes and arylamine derivatives (Q43743909) (← links)
• A QSAR investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 1. Mutagenicity of aromatic and heteroaromatic amines in Salmonella typhimurium TA98 and TA100. (Q44104976) (← links)
• New tester strains of Salmonella typhimurium highly sensitive to mutagenic nitroarenes (Q45032542) (← links)
• Influence of nitroreductase and O-acetyltransferase on the mutagenicity of substituted nitrobenzothiophenamines in Salmonella typhimurium (Q50126129) (← links)
• Synthesis, metabolism and structure-mutagenicity relationships of novel 4-nitro-(imidazoles and pyrazoles) in Salmonella typhimurium (Q50131450) (← links)
• Metabolic activation of 2- and 3-nitrodibenzopyranone isomers and related compounds by rat liver S9 and the effect of S9 on the mutational specificity of nitrodibenzopyranones (Q50135762) (← links)
• Involvement of nitroreductase andO-acetyltransferase on the mutagenicity of plant-activated benzidine and 4-aminobiphenyl (Q50136002) (← links)
• Activation and detoxification of Dinitropyrenes by cytosol and microsomes from Aroclor-pretreated rats in the Ames andumu assays (Q50136010) (← links)
• Metabolic reduction of novel 3,4-dichloro-5-nitrofurans in Salmonella typhimurium (Q50145553) (← links)
• A new Salmonella tester strain expressing a hamster acetyltransferase shows high sensitivity for arylamines (Q50158127) (← links)
• Bacterial metabolism of 2,6-dinitrotoluene with Salmonella typhimurium and mutagenicity of the metabolites of 2,6-dinitrotoluene and related compounds (Q50176925) (← links)
• Quantitative structure-activity relationship investigation of the role of hydrophobicity in regulating mutagenicity in the Ames test: 2. Mutagenicity of aromatic and heteroaromatic nitro compounds inSalmonella typhimurium TA100 (Q50181252) (← links)
• Mutagenicity of N- and O-acetyl derivatives of methyl 3,4-diphenyl-5-hydroxylamino-2-furoate and N-hydroxy-4-aminobiphenyl in Salmonella typhimurium (Q50190757) (← links)
• Comparative mutagenicity of nitrofluoranthenes in Salmonella typhimurium TA98, TA98NR, and TA98/1,8DNP6. (Q50190764) (← links)
• Disubstituted amino-, nitroso-, and nitrofluorenes: a physicochemical basis for structure-activity relationships in Salmonella typhimurium (Q50202000) (← links)
• The orientation of the nitro substituent predicts the direct-acting bacterial mutagenicity of nitrated polycyclic aromatic hydrocarbons (Q50205569) (← links)
• Mutagenic, cytotoxic, and teratogenic effects of 2-acetylaminofluorene and reactive metabolites in vitro (Q50209981) (← links)
• Evidence that nitroarene metabolites form mutagenic adducts with DNA-adenine as well as with DNA-guanine (Q50210197) (← links)
• Ultimate forms of mutagenic and carcinogenic heterocyclic amines produced by pyrolysis (Q50211078) (← links)
• Dinitro and mononitrobenzo(ghi)perylenes and mononitrocoronene are highly mutagenic in the Ames Salmonella assay (Q50212242) (← links)
• Effect of bacterial concentration on reversions induced in Salmonella typhimurium TA1538 by N-hydroxy-2-acetylaminofluorene (Q50212441) (← links)
• 5-nitroacenaphthene: A newly recognized role for the nitro function in mutagenicity (Q50212504) (← links)
• Metabolism of 2-acetylaminofluorene in the Chinese hamster ovary cell mutation assay. (Q52461550) (← links)
• Studies of 3D-quantitative structure-activity relationships on a set of nitroaromatic compounds: CoMFA, advanced CoMFA and CoMSIA (Q74680773) (← links)
• Role of Human N-Acetyltransferase 2 Genetic Polymorphism on Aromatic Amine Carcinogen-Induced DNA Damage and Mutagenicity in a Chinese Hamster Ovary Cell Mutation Assay (Q93145014) (← links)