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4. The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair. Brosh RM; Balajee AS; Selzer RR; Sunesen M; Proietti De Santis L; Bohr VA Mol Biol Cell; 1999 Nov; 10(11):3583-94. PubMed ID: 10564257 [TBL] [Abstract][Full Text] [Related]
6. Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells. Selzer RR; Nyaga S; Tuo J; May A; Muftuoglu M; Christiansen M; Citterio E; Brosh RM; Bohr VA Nucleic Acids Res; 2002 Feb; 30(3):782-93. PubMed ID: 11809892 [TBL] [Abstract][Full Text] [Related]
7. Transcription-coupled nucleotide excision repair is coordinated by ubiquitin and SUMO in response to ultraviolet irradiation. Liebelt F; Schimmel J; Verlaan-de Vries M; Klemann E; van Royen ME; van der Weegen Y; Luijsterburg MS; Mullenders LH; Pines A; Vermeulen W; Vertegaal ACO Nucleic Acids Res; 2020 Jan; 48(1):231-248. PubMed ID: 31722399 [TBL] [Abstract][Full Text] [Related]
8. The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells. Bailey AD; Gray LT; Pavelitz T; Newman JC; Horibata K; Tanaka K; Weiner AM DNA Repair (Amst); 2012 May; 11(5):488-501. PubMed ID: 22483866 [TBL] [Abstract][Full Text] [Related]
9. The C-terminal Region and SUMOylation of Cockayne Syndrome Group B Protein Play Critical Roles in Transcription-coupled Nucleotide Excision Repair. Sin Y; Tanaka K; Saijo M J Biol Chem; 2016 Jan; 291(3):1387-97. PubMed ID: 26620705 [TBL] [Abstract][Full Text] [Related]
10. A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair. Anindya R; Mari PO; Kristensen U; Kool H; Giglia-Mari G; Mullenders LH; Fousteri M; Vermeulen W; Egly JM; Svejstrup JQ Mol Cell; 2010 Jun; 38(5):637-48. PubMed ID: 20541997 [TBL] [Abstract][Full Text] [Related]
11. The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61. Orren DK; Dianov GL; Bohr VA Nucleic Acids Res; 1996 Sep; 24(17):3317-22. PubMed ID: 8811084 [TBL] [Abstract][Full Text] [Related]
12. Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation. Lanzafame M; Branca G; Landi C; Qiang M; Vaz B; Nardo T; Ferri D; Mura M; Iben S; Stefanini M; Peverali FA; Bini L; Orioli D Nucleic Acids Res; 2021 Nov; 49(19):10911-10930. PubMed ID: 34581821 [TBL] [Abstract][Full Text] [Related]
13. Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA. Scheibye-Knudsen M; Tseng A; Borch Jensen M; Scheibye-Alsing K; Fang EF; Iyama T; Bharti SK; Marosi K; Froetscher L; Kassahun H; Eckley DM; Maul RW; Bastian P; De S; Ghosh S; Nilsen H; Goldberg IG; Mattson MP; Wilson DM; Brosh RM; Gorospe M; Bohr VA Proc Natl Acad Sci U S A; 2016 Nov; 113(44):12502-12507. PubMed ID: 27791127 [TBL] [Abstract][Full Text] [Related]
14. CSB promoter downregulation via histone H3 hypoacetylation is an early determinant of replicative senescence. Crochemore C; Fernández-Molina C; Montagne B; Salles A; Ricchetti M Nat Commun; 2019 Dec; 10(1):5576. PubMed ID: 31811121 [TBL] [Abstract][Full Text] [Related]
15. Poly(ADP-ribose) polymerase 1 (PARP1) promotes oxidative stress-induced association of Cockayne syndrome group B protein with chromatin. Boetefuer EL; Lake RJ; Dreval K; Fan HY J Biol Chem; 2018 Nov; 293(46):17863-17874. PubMed ID: 30266807 [TBL] [Abstract][Full Text] [Related]
16. Cockayne Syndrome Group B (CSB): The Regulatory Framework Governing the Multifunctional Protein and Its Plausible Role in Cancer. Spyropoulou Z; Papaspyropoulos A; Lagopati N; Myrianthopoulos V; Georgakilas AG; Fousteri M; Kotsinas A; Gorgoulis VG Cells; 2021 Apr; 10(4):. PubMed ID: 33920220 [TBL] [Abstract][Full Text] [Related]
17. Truncated Cockayne syndrome B protein represses elongation by RNA polymerase I. Lebedev A; Scharffetter-Kochanek K; Iben S J Mol Biol; 2008 Oct; 382(2):266-74. PubMed ID: 18656484 [TBL] [Abstract][Full Text] [Related]
18. Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging. Lee JH; Demarest TG; Babbar M; Kim EW; Okur MN; De S; Croteau DL; Bohr VA Nucleic Acids Res; 2019 Sep; 47(16):8548-8562. PubMed ID: 31276581 [TBL] [Abstract][Full Text] [Related]
19. Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair. Cleaver JE; Hefner E; Laposa RR; Karentz D; Marti T Neuroscience; 2007 Apr; 145(4):1300-8. PubMed ID: 17055654 [TBL] [Abstract][Full Text] [Related]
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