Stereoselective Covalent Binding of Anti-benzo(a)pyrene Diol Epoxide to DNA Conformation of Enantiomer Adducts
Author:
Publisher
Informa UK Limited
Subject
Molecular Biology,General Medicine,Structural Biology
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
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4. Evidence for the Binding of Polynuclear Aromatic Hydrocarbons to the Nucleic Acids of Mouse Skin : Relation between Carcinogenic Power of Hydrocarbons and their Binding to Deoxyribonucleic Acid
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1. NMR Solution Structures of Stereoisomeric Covalent Polycyclic Aromatic Carcinogen−DNA Adducts: Principles, Patterns, and Diversity;Chemical Research in Toxicology;1997-02-01
2. Identification of a Novel, N7-Deoxyguanosine Adduct as the Major DNA Adduct Formed by a Non-Bay-Region Diol Epoxide of Benzo[a]pyrene with Low Mutagenic Potential;Biochemistry;1994-03-15
3. Sequence dependence of benzo[a]pyrene diol epoxide-DNA adduct conformer distribution: A study by laser-induced fluorescence/polyacrylamide gel electrophoresis;Chemical Research in Toxicology;1994-01
4. Separation and identification of DNA-carcinogen adduct conformers by polyacrylamide gel electrophoresis with laser-induced fluorescence detection;Analytical Chemistry;1992-12-01
5. Influence of benzo[a]pyrenediol epoxide chirality on solution conformations of DNA covalent adducts: the (-)-trans-anti-[BP]G.cntdot.C adduct structure and comparison with the (+)-trans-anti[BP]G.cntdot.C enantiomer;Biochemistry;1992-07-16
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