Conformation and Pairing Properties of an <i>O</i><sup>6</sup>-Methyl-2′-deoxyguanosine-Directed Benzimidazole Nucleoside Analog in Duplex DNA-Reference-Cited by-同舟云学术

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Conformation and Pairing Properties of an O⁶-Methyl-2′-deoxyguanosine-Directed Benzimidazole Nucleoside Analog in Duplex DNA

Published:2022-08-16 Issue:10 Volume:35 Page:1903-1913
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Kellum Andrew H.¹,Pallan Pradeep S.²,Nilforoushan Arman³,Sturla Shana J.³^ORCID,Stone Michael P.¹²^ORCID,Egli Martin²^ORCID

Affiliation:

1. Department of Chemistry, Vanderbilt University, College of Arts and Science, Nashville, Tennessee 37235, United States

2. Department of Biochemistry, Vanderbilt University, School of Medicine, Nashville, Tennessee 37232, United States

3. Department of Health Sciences and Technology, ETH Zürich, Zurich 8092, Switzerland

Funder

U.S. Department of Health and Human Services

NRSA Institutional Training

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.chemrestox.2c00165

Reference51 articles.

1. Possible Relevance of O–6 Alkylation of Deoxyguanosine to the Mutagenicity and Carcinogenicity of Nitrosamines and Nitrosamides

2. DNA Methylation Damage: Formation, Repair and Biological Consequences

3. Alkylation damage in DNA and RNA—repair mechanisms and medical significance

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1. Dedication of 35-year Chemical Research in Toxicology Anniversary to Founding Editor Larry Marnett;Chemical Research in Toxicology;2022-10-17

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