Repair of APOBEC3G-Mutated Retroviral DNA In Vivo Is Facilitated by the Host Enzyme Uracil DNA Glycosylase 2
Author:
Affiliation:
1. Department of Microbiology and Immunology, University of Illinois at Chicago College of Medicine, Chicago, Illinois, USA
Abstract
Funder
HHS | NIH | National Institute of Allergy and Infectious Diseases
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Link
https://journals.asm.org/doi/pdf/10.1128/JVI.01244-21
Reference51 articles.
1. Guidelines for Naming Nonprimate APOBEC3 Genes and Proteins
2. The Biochemistry of Somatic Hypermutation
3. DNA repair mechanisms in dividing and non-dividing cells
4. Generation, Biological Consequences and Repair Mechanisms of Cytosine Deamination in DNA
5. Mitochondrial base excision repair of uracil and AP sites takes place by single-nucleotide insertion and long-patch DNA synthesis
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