| Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis. |
| Balajee AS, Proietti De Santis L, Brosh RM Jr, Selzer R, Bohr VA |
| Oncogene. 2000 ; 19 (4) : 477-489. |
| PMID 10698517 |
| |
| UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells. |
| Bregman DB, Halaban R, van Gool AJ, Henning KA, Friedberg EC, Warren SL |
| Proceedings of the National Academy of Sciences of the United States of America. 1996 ; 93 (21) : 11586-11590. |
| PMID 8876179 |
| |
| The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair. |
| Brosh RM Jr, Balajee AS, Selzer RR, Sunesen M, Proietti De Santis L, Bohr VA |
| Molecular biology of the cell. 1999 ; 10 (11) : 3583-3594. |
| PMID 10564257 |
| |
| Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes. |
| Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B, Stefanini M, Vermeulen W, Hoeijmakers JH, Sarasin A |
| Carcinogenesis. 1995 ; 16 (5) : 1003-1009. |
| PMID 7767957 |
| |
| ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor. |
| Citterio E, Van Den Boom V, Schnitzler G, Kanaar R, Bonte E, Kingston RE, Hoeijmakers JH, Vermeulen W |
| Molecular and cellular biology. 2000 ; 20 (20) : 7643-7653. |
| PMID 11003660 |
| |
| Prenatal diagnosis of xeroderma pigmentosum and Cockayne syndrome. |
| Cleaver JE, Volpe JP, Charles WC, Thomas GH |
| Prenatal diagnosis. 1994 ; 14 (10) : 921-928. |
| PMID 7534923 |
| |
| 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 |
| Human molecular genetics. 1999 ; 8 (5) : 935-941. |
| PMID 10196384 |
| |
| Proneness to UV-induced apoptosis in human fibroblasts defective in transcription coupled repair is associated with the lack of Mdm2 transactivation. |
| Conforti G, Nardo T, D'Incalci M, Stefanini M |
| Oncogene. 2000 ; 19 (22) : 2714-2720. |
| PMID 10851071 |
| |
| Repair of 8-oxoguanine in DNA is deficient in Cockayne syndrome group B cells. |
| Dianov G, Bischoff C, Sunesen M, Bohr VA |
| Nucleic acids research. 1999 ; 27 (5) : 1365-1368. |
| PMID 9973627 |
| |
| Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells. |
| Dianov GL, Houle JF, Iyer N, Bohr VA, Friedberg EC |
| Nucleic acids research. 1997 ; 25 (18) : 3636-3642. |
| PMID 9278484 |
| |
| Transcription-coupled and global genome repair differentially influence UV-B-induced acute skin effects and systemic immunosuppression. |
| Garssen J, van Steeg H, de Gruijl F, de Boer J, van der Horst GT, van Kranen H, van Loveren H, van Dijk M, Fluitman A, Weeda G, Hoeijmakers JH |
| Journal of immunology (Baltimore, Md. : 1950). 2000 ; 164 (12) : 6199-6205. |
| PMID 10843671 |
| |
| Deletion of the CSB homolog, RAD26, yields Spt(-) strains with proficient transcription-coupled repair. |
| Gregory SM, Sweder KS |
| Nucleic acids research. 2001 ; 29 (14) : 3080-3086. |
| PMID 11452033 |
| |
| DNA repair. The bases for Cockayne syndrome. |
| Hanawalt PC |
| Nature. 2000 ; 405 (6785) : 415-416. |
| PMID 10839526 |
| |
| Analysis of repair and PCNA complex formation induced by ionizing radiation in human fibroblast cell lines. |
| Karmakar P, Balajee AS, Natarajan AT |
| Mutagenesis. 2001 ; 16 (3) : 225-232. |
| PMID 11320148 |
| |
| Repair and mutagenesis survey of 8-hydroxyguanine in bacteria and human cells. |
| Le Page F, Gentil A, Sarasin A |
| Biochimie. 1999 ; 81 (1-2) : 147-153. |
| PMID 10214919 |
| |
| Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome. |
| Le Page F, Kwoh EE, Avrutskaya A, Gentil A, Leadon SA, Sarasin A, Cooper PK |
| Cell. 2000 ; 101 (2) : 159-171. |
| PMID 10786832 |
| |
| Disruption of the Cockayne syndrome B gene impairs spontaneous tumorigenesis in cancer-predisposed Ink4a/ARF knockout mice. |
| Lu Y, Lian H, Sharma P, Schreiber-Agus N, Russell RG, Chin L, van der Horst GT, Bregman DB |
| Molecular and cellular biology. 2001 ; 21 (5) : 1810-1818. |
| PMID 11238917 |
| |
| Ultraviolet radiation alters the phosphorylation of RNA polymerase II large subunit and accelerates its proteasome-dependent degradation. |
| Luo Z, Zheng J, Lu Y, Bregman DB |
| Mutation research. 2001 ; 486 (4) : 259-274. |
| PMID 11516929 |
| |
| 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 |
| American journal of human genetics. 1998 ; 62 (1) : 77-85. |
| PMID 9443879 |
| |
| UV light-induced degradation of RNA polymerase II is dependent on the Cockayne's syndrome A and B proteins but not p53 or MLH1. |
| McKay BC, Chen F, Clarke ST, Wiggin HE, Harley LM, Ljungman M |
| Mutation research. 2001 ; 485 (2) : 93-105. |
| PMID 11182541 |
| |
| 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 research. 1996 ; 24 (17) : 3317-3322. |
| PMID 8811084 |
| |
| Cockayne syndrome: review of 25 cases. |
| Ozdirim E, Topçu M, Ozön A, Cila A |
| Pediatric neurology. 1996 ; 15 (4) : 312-316. |
| PMID 8972530 |
| |
| The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes. |
| Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G, Mezzina M, Sarasin A |
| Human molecular genetics. 1999 ; 8 (6) : 1125-1133. |
| PMID 10332046 |
| |
| UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II. |
| Rockx DA, Mason R, van Hoffen A, Barton MC, Citterio E, Bregman DB, van Zeeland AA, Vrieling H, Mullenders LH |
| Proceedings of the National Academy of Sciences of the United States of America. 2000 ; 97 (19) : 10503-10508. |
| PMID 10973477 |
| |
| Human cancer and DNA repair-deficient diseases. |
| Sarasin A, Stary A |
| Cancer detection and prevention. 1997 ; 21 (5) : 406-411. |
| PMID 9307843 |
| |
| Cockayne syndrome group B protein enhances elongation by RNA polymerase II. |
| Selby CP, Sancar A |
| Proceedings of the National Academy of Sciences of the United States of America. 1997 ; 94 (21) : 11205-11209. |
| PMID 9326587 |
| |
| Genetic analysis of twenty-two patients with Cockayne syndrome. |
| Stefanini M, Fawcett H, Botta E, Nardo T, Lehmann AR |
| Human genetics. 1996 ; 97 (4) : 418-423. |
| PMID 8834235 |
| |
| Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein. |
| Sunesen M, Selzer RR, Brosh RM Jr, Balajee AS, Stevnsner T, Bohr VA |
| Nucleic acids research. 2000 ; 28 (16) : 3151-3159. |
| PMID 10931931 |
| |
| Enhancement of XPG mRNA transcription by human interferon-beta in Cockayne syndrome cells with complementation group B. |
| Suzuki Y, Sugita K, Suzuki N, Kita K, Higuchi Y, Yamaura A, Kohno Y |
| International journal of molecular medicine. 1999 ; 3 (1) : 87-89. |
| PMID 9864391 |
| |
| RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62. |
| Tantin D |
| The Journal of biological chemistry. 1998 ; 273 (43) : 27794-27799. |
| PMID 9774388 |
| |
| Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes. |
| Tantin D, Kansal A, Carey M |
| Molecular and cellular biology. 1997 ; 17 (12) : 6803-6814. |
| PMID 9372911 |
| |
| Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B. |
| Troelstra C, Hesen W, Bootsma D, Hoeijmakers JH |
| Nucleic acids research. 1993 ; 21 (3) : 419-426. |
| PMID 8382798 |
| |
| The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. |
| Venema J, Mullenders LH, Natarajan AT, van Zeeland AA, Mayne LV |
| Proceedings of the National Academy of Sciences of the United States of America. 1990 ; 87 (12) : 4707-4711. |
| PMID 2352945 |
| |
| The relationship between benzo[a]pyrene-induced mutagenesis and carcinogenesis in repair-deficient Cockayne syndrome group B mice. |
| Wijnhoven SW, Kool HJ, van Oostrom CT, Beems RB, Mullenders LH, van Zeeland AA, van der Horst GT, Vrieling H, van Steeg H |
| Cancer research. 2000 ; 60 (20) : 5681-5687. |
| PMID 11059760 |
| |
| Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes. |
| Yu A, Fan HY, Liao D, Bailey AD, Weiner AM |
| Molecular cell. 2000 ; 5 (5) : 801-810. |
| PMID 10882116 |
| |
| The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex. |
| van Gool AJ, Citterio E, Rademakers S, van Os R, Vermeulen W, Constantinou A, Egly JM, Bootsma D, Hoeijmakers JH |
| The EMBO journal. 1997 ; 16 (19) : 5955-5965. |
| PMID 9312053 |
| |
| Differential role of transcription-coupled repair in UVB-induced G2 arrest and apoptosis in mouse epidermis. |
| van Oosten M, Rebel H, Friedberg EC, van Steeg H, van der Horst GT, van Kranen HJ, Westerman A, van Zeeland AA, Mullenders LH, de Gruijl FR |
| Proceedings of the National Academy of Sciences of the United States of America. 2000 ; 97 (21) : 11268-11273. |
| PMID 11005836 |
| |
| The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes. |
| van Oosterwijk MF, Versteeg A, Filon R, van Zeeland AA, Mullenders LH |
| Molecular and cellular biology. 1996 ; 16 (8) : 4436-4444. |
| PMID 8754844 |
| |
| 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 ; 89 (3) : 425-435. |
| PMID 9150142 |
| |