Histone deacetylation regulates nucleotide excision repair through an interaction with the XPC protein
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Multidisciplinary
Reference96 articles.
1. Real-time tracking of parental histones reveals their contribution to chromatin integrity following DNA damage;Adam;Mol. Cell,2016
2. SUMOylation of xeroderma pigmentosum group C protein regulates DNA damage recognition during nucleotide excision repair;Akita;Sci. Rep.,2015
3. Peptide-N-glycanases and DNA repair proteins, Xp-C/Rad4, are, respectively, active and inactivated enzymes sharing a common transglutaminase fold;Anantharaman;Hum. Mol. Genet.,2001
4. Stable binding of human XPC complex to irradiated DNA confers strong discrimination for damaged sites;Batty;J. Mol. Biol.,2000
5. Biochemical and structural domain analysis of xeroderma pigmentosum complementation group C protein;Bunick;Biochemistry,2006
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1. Histone H3 mutations and their impact on genome stability maintenance;Biochemical Society Transactions;2024-09-09
2. New facets in the chromatin-based regulation of genome maintenance;DNA Repair;2024-08
3. New Discoveries on Protein Recruitment and Regulation during the Early Stages of the DNA Damage Response Pathways;International Journal of Molecular Sciences;2024-01-30
4. Fluorescence-microscopy-based assay assessing regulatory mechanisms of global genome nucleotide excision repair in cultured cells;STAR Protocols;2023-09
5. Lesion recognition by XPC, TFIIH and XPA in DNA excision repair;Nature;2023-04-19
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