236 related articles for article (PubMed ID: 9443879)
1. Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.
Mallery DL; Tanganelli B; Colella S; Steingrimsdottir H; van Gool AJ; Troelstra C; Stefanini M; Lehmann AR
Am J Hum Genet; 1998 Jan; 62(1):77-85. PubMed ID: 9443879
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis.
Balajee AS; Proietti De Santis L; Brosh RM; Selzer R; Bohr VA
Oncogene; 2000 Jan; 19(4):477-89. PubMed ID: 10698517
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity.
Colella S; Nardo T; Mallery D; Borrone C; Ricci R; Ruffa G; Lehmann AR; Stefanini M
Hum Mol Genet; 1999 May; 8(5):935-41. PubMed ID: 10196384
[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. Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome.
Calmels N; Botta E; Jia N; Fawcett H; Nardo T; Nakazawa Y; Lanzafame M; Moriwaki S; Sugita K; Kubota M; Obringer C; Spitz MA; Stefanini M; Laugel V; Orioli D; Ogi T; Lehmann AR
J Med Genet; 2018 May; 55(5):329-343. PubMed ID: 29572252
[TBL] [Abstract][Full Text] [Related]
8. Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein.
Sunesen M; Selzer RR; Brosh RM; Balajee AS; Stevnsner T; Bohr VA
Nucleic Acids Res; 2000 Aug; 28(16):3151-9. PubMed ID: 10931931
[TBL] [Abstract][Full Text] [Related]
9. Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair.
Zhang X; Horibata K; Saijo M; Ishigami C; Ukai A; Kanno S; Tahara H; Neilan EG; Honma M; Nohmi T; Yasui A; Tanaka K
Nat Genet; 2012 May; 44(5):593-7. PubMed ID: 22466612
[TBL] [Abstract][Full Text] [Related]
10. Novel missense mutations in a conserved loop between ERCC6 (CSB) helicase motifs V and VI: Insights into Cockayne syndrome.
Wilson BT; Lochan A; Stark Z; Sutton RE
Am J Med Genet A; 2016 Mar; 170(3):773-6. PubMed ID: 26749132
[TBL] [Abstract][Full Text] [Related]
11. Identification and Characterization of a Novel Recurrent
Zayoud K; Kraoua I; Chikhaoui A; Calmels N; Bouchoucha S; Obringer C; Crochemore C; Najjar D; Zarrouk S; Miladi N; Laugel V; Ricchetti M; Turki I; Yacoub-Youssef H
Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946871
[TBL] [Abstract][Full Text] [Related]
12. Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome.
Horibata K; Iwamoto Y; Kuraoka I; Jaspers NG; Kurimasa A; Oshimura M; Ichihashi M; Tanaka K
Proc Natl Acad Sci U S A; 2004 Oct; 101(43):15410-5. PubMed ID: 15486090
[TBL] [Abstract][Full Text] [Related]
13. Cockayne syndrome type II in a Druze isolate in Northern Israel in association with an insertion mutation in ERCC6.
Falik-Zaccai TC; Laskar M; Kfir N; Nasser W; Slor H; Khayat M
Am J Med Genet A; 2008 Jun; 146A(11):1423-9. PubMed ID: 18446857
[TBL] [Abstract][Full Text] [Related]
14. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V; Dalloz C; Durand M; Sauvanaud F; Kristensen U; Vincent MC; Pasquier L; Odent S; Cormier-Daire V; Gener B; Tobias ES; Tolmie JL; Martin-Coignard D; Drouin-Garraud V; Heron D; Journel H; Raffo E; Vigneron J; Lyonnet S; Murday V; Gubser-Mercati D; Funalot B; Brueton L; Sanchez Del Pozo J; Muñoz E; Gennery AR; Salih M; Noruzinia M; Prescott K; Ramos L; Stark Z; Fieggen K; Chabrol B; Sarda P; Edery P; Bloch-Zupan A; Fawcett H; Pham D; Egly JM; Lehmann AR; Sarasin A; Dollfus H
Hum Mutat; 2010 Feb; 31(2):113-26. PubMed ID: 19894250
[TBL] [Abstract][Full Text] [Related]
15. Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition.
van der Horst GT; van Steeg H; Berg RJ; van Gool AJ; de Wit J; Weeda G; Morreau H; Beems RB; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH
Cell; 1997 May; 89(3):425-35. PubMed ID: 9150142
[TBL] [Abstract][Full Text] [Related]
16. Two Cockayne Syndrome patients with a novel splice site mutation - clinical and metabolic analyses.
Sanchez-Roman I; Lautrup S; Aamann MD; Neilan EG; Østergaard JR; Stevnsner T
Mech Ageing Dev; 2018 Oct; 175():7-16. PubMed ID: 29944916
[TBL] [Abstract][Full Text] [Related]
17. Phenotypic consequences of mutations in the conserved motifs of the putative helicase domain of the human Cockayne syndrome group B gene.
Muftuoglu M; Selzer R; Tuo J; Brosh RM; Bohr VA
Gene; 2002 Jan; 283(1-2):27-40. PubMed ID: 11867210
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress.
Kristensen U; Epanchintsev A; Rauschendorf MA; Laugel V; Stevnsner T; Bohr VA; Coin F; Egly JM
Proc Natl Acad Sci U S A; 2013 Jun; 110(25):E2261-70. PubMed ID: 23733932
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
