Base-pairing properties of O-methylated bases of nucleic acids energetic and steric considerations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,Biophysics
Reference63 articles.
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3. Chemical carcinogenesis in the nervous system. Preferential accumulation of O6-methylguanine in rat brain deoxyribonucleic acid during repetitive administration of N-methyl-N-nitrosourea
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1. Structural Rationalization for the Nonmutagenic and Mutagenic Bypass of the Tobacco-Derived O4-4-(3-Pyridyl)-4-oxobut-1-yl-thymine Lesion by Human Polymerase η: A Multiscale Computational Study;Chemical Research in Toxicology;2021-04-15
2. Computational Insight into the Differential Mutagenic Patterns of O-Methylthymine Lesions;Chemical Research in Toxicology;2019-08-26
3. Synthesis, Optoelectronic Properties, Self-Association, and Base Pairing of Nucleobase-Functionalized Oligothiophenes;The Journal of Organic Chemistry;2018-09-19
4. Gilda H. Loew, Ph.D. list of publications;International Journal of Quantum Chemistry;2002
5. Mutagenic significance of proton acidities in methylated guanine and thymine bases and deoxynucleosides: a theoretical study;Journal of Molecular Structure: THEOCHEM;1997-04
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