LEO1 is a partner for Cockayne syndrome protein B (CSB) in response to transcription-blocking DNA damage
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Title
LEO1 is a partner for Cockayne syndrome protein B (CSB) in response to transcription-blocking DNA damage
Authors
Keywords
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Journal
NUCLEIC ACIDS RESEARCH
Volume 49, Issue 11, Pages 6331-6346
Publisher
Oxford University Press (OUP)
Online
2021-06-04
DOI
10.1093/nar/gkab458
References
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Related references
Note: Only part of the references are listed.- Current and emerging roles of Cockayne syndrome group B (CSB) protein
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- Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair
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- Regulation of the RNAPII Pool Is Integral to the DNA Damage Response
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- The cooperative action of CSB, CSA, and UVSSA target TFIIH to DNA damage-stalled RNA polymerase II
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- A C. elegans model for neurodegeneration in Cockayne syndrome
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- Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging
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- Nucleic Acid Binding Activity of Human Cockayne Syndrome B Protein and Identification of Ca2+ as a Novel Metal Cofactor
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