Synthesis of Oligonucleotides Containing the N2-Deoxyguanosine Adduct of the Dietary Carcinogen 2-Amino-3-methylimidazo[4,5-f]quinoline
Author:
Affiliation:
1. Departments of Chemistry and Biochemistry and Center in Molecular Toxicology, Vanderbilt University, VU Station B 351822, Nashville, Tennessee 37235-1822
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx7002867
Reference87 articles.
1. HETEROCYCLIC AROMATIC AMINE METABOLISM, DNA ADDUCT FORMATION, MUTAGENESIS, AND CARCINOGENESIS
2. Heterocyclic amines: Mutagens/carcinogens produced during cooking of meat and fish
3. Human exposure to heterocyclic amine food mutagens/carcinogens: Relevance to breast cancer
4. DNA adducts of heterocyclic amine food mutagens: implications for mutagenesis and carcinogenesis
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3. Chemical Synthesis of Lesion-Containing Oligonucleotides for DNA Repair Studies;Modified Nucleic Acids in Biology and Medicine;2016
4. Base-Displaced Intercalated Conformation of the 2-Amino-3-methylimidazo[4,5-f]quinoline N2-dG DNA Adduct Positioned at the Nonreiterated G1 in the NarI Restriction Site;Chemical Research in Toxicology;2015-06-17
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