Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference50 articles.
1. Cockayne syndrome—a primary defect in DNA repair, transcription, both or neither?;Friedberg;BioEssays,1996
2. Cockayne syndrome: review of 140 cases;Nance;Am. J. Med. Genet.,1992
3. The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH;Henning;Cell,1995
4. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne syndrome and preferential repair of active genes;Troelstra;Cell,1992
5. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne syndrome and xeroderma pigmentosum;Mayne;Cancer Res.,1982
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