QSAR models for both mutagenic potency and activity: Application to nitroarenes and aromatic amines
Author:
Publisher
Wiley
Subject
Health, Toxicology and Mutagenesis,Genetics(clinical),Epidemiology
Reference18 articles.
1. DNA sequence analysis of revertants of the hisD3052 allele of Salmonella typhimurium TA98 using the polymerase chain reaction and direct sequencing: Application to 1-nitropyrene-induced revertants
2. Quantitative structure-activity relationships: principles, and applications to mutagenicity and carcinogenicity
3. Quantitative structure-activity relationship models correctly predict the toxic and aneuploidizing properties of six halogenated methanes in Aspergillus nidulans
4. The induction of mitotic chromosome malsegregation in Aspergillus nidulans. quantitative structure activity relationship (QSAR) analysis with chlorinated aliphatic hydrocarbons
5. structure-activity relationship of genotoxic polycyclic aromatic nitro compounds: Further evidence for the importance of hydrophobicity and molecular orbital energies in genetic toxicity
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5. Extending (Q)SARs to incorporate proprietary knowledge for regulatory purposes: A case study using aromatic amine mutagenicity;Regulatory Toxicology and Pharmacology;2016-06
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