Regulation of WRN Helicase Activity in Human Base Excision Repair
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference45 articles.
1. Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations
2. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.
3. Junction of RecQ Helicase Biochemistry and Human Disease
4. Werner syndrome diploid fibroblasts are sensitive to 4‐nitroquinoline‐N‐oxide and 8‐methoxypsoralen: implications for the disease phenotype
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1. WRN helicase and mismatch repair complexes independently and synergistically disrupt cruciform DNA structures;The EMBO Journal;2022-12-21
2. The Relevance of G-Quadruplexes for DNA Repair;International Journal of Molecular Sciences;2021-11-22
3. Action-at-a-distance mutations at 5′-GpA-3′ sites induced by oxidised guanine in WRN-knockdown cells;Mutagenesis;2021-07-17
4. WRN modulates translation by influencing nuclear mRNA export in HeLa cancer cells;BMC Molecular and Cell Biology;2020-10-14
5. Endogenous oxidized DNA bases and APE1 regulate the formation of G-quadruplex structures in the genome;Proceedings of the National Academy of Sciences;2020-05-13
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