Induction of G.cntdot.C to A.cntdot.T transitions by the acridine half-mustard ICR-191 supports a mispairing mechanism for mutagenesis by some bulky mutagens
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00501a006
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1. Translesion synthesis of the major nitrogen mustard-induced DNA lesion by human DNA polymerase η;Biochemical Journal;2020-12-03
2. Structural and Kinetic Studies of the Effect of Guanine N7 Alkylation and Metal Cofactors on DNA Replication;Biochemistry;2018-06-29
3. N7 Methylation Alters Hydrogen-Bonding Patterns of Guanine in Duplex DNA;Journal of the American Chemical Society;2015-11-02
4. Transition-state destabilization reveals how human DNA polymerase β proceeds across the chemically unstable lesion N7-methylguanine;Nucleic Acids Research;2014-06-25
5. Frameshift mutations induced by the acridine mustard ICR-191 in embryos and in the adult gill and hepatopancreas of rpsL transgenic zebrafish;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2005-10-15
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