308 related articles for article (PubMed ID: 7663514)
1. p53 modulation of TFIIH-associated nucleotide excision repair activity.
Wang XW; Yeh H; Schaeffer L; Roy R; Moncollin V; Egly JM; Wang Z; Freidberg EC; Evans MK; Taffe BG
Nat Genet; 1995 Jun; 10(2):188-95. PubMed ID: 7663514
[TBL] [Abstract][Full Text] [Related]
2. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
Boulikas T
Anticancer Res; 1996; 16(2):693-708. PubMed ID: 8687116
[TBL] [Abstract][Full Text] [Related]
3. Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein.
Iyer N; Reagan MS; Wu KJ; Canagarajah B; Friedberg EC
Biochemistry; 1996 Feb; 35(7):2157-67. PubMed ID: 8652557
[TBL] [Abstract][Full Text] [Related]
4. Mechanism of open complex and dual incision formation by human nucleotide excision repair factors.
Evans E; Moggs JG; Hwang JR; Egly JM; Wood RD
EMBO J; 1997 Nov; 16(21):6559-73. PubMed ID: 9351836
[TBL] [Abstract][Full Text] [Related]
5. Drug-induced apoptosis is delayed and reduced in XPD lymphoblastoid cell lines: possible role of TFIIH in p53-mediated apoptotic cell death.
Robles AI; Wang XW; Harris CC
Oncogene; 1999 Aug; 18(33):4681-8. PubMed ID: 10467415
[TBL] [Abstract][Full Text] [Related]
6. Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.
Coin F; Bergmann E; Tremeau-Bravard A; Egly JM
EMBO J; 1999 Mar; 18(5):1357-66. PubMed ID: 10064601
[TBL] [Abstract][Full Text] [Related]
7. TFIIH with inactive XPD helicase functions in transcription initiation but is defective in DNA repair.
Winkler GS; Araújo SJ; Fiedler U; Vermeulen W; Coin F; Egly JM; Hoeijmakers JH; Wood RD; Timmers HT; Weeda G
J Biol Chem; 2000 Feb; 275(6):4258-66. PubMed ID: 10660593
[TBL] [Abstract][Full Text] [Related]
8. Functional interactions between p53 and the TFIIH complex are affected by tumour-associated mutations.
Léveillard T; Andera L; Bissonnette N; Schaeffer L; Bracco L; Egly JM; Wasylyk B
EMBO J; 1996 Apr; 15(7):1615-24. PubMed ID: 8612585
[TBL] [Abstract][Full Text] [Related]
9. Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.
Vermeulen W; Bergmann E; Auriol J; Rademakers S; Frit P; Appeldoorn E; Hoeijmakers JH; Egly JM
Nat Genet; 2000 Nov; 26(3):307-13. PubMed ID: 11062469
[TBL] [Abstract][Full Text] [Related]
10. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.
de Boer J; Donker I; de Wit J; Hoeijmakers JH; Weeda G
Cancer Res; 1998 Jan; 58(1):89-94. PubMed ID: 9426063
[TBL] [Abstract][Full Text] [Related]
11. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
de Boer J; van Steeg H; Berg RJ; Garssen J; de Wit J; van Oostrum CT; Beems RB; van der Horst GT; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH; Weeda G
Cancer Res; 1999 Jul; 59(14):3489-94. PubMed ID: 10416615
[TBL] [Abstract][Full Text] [Related]
12. The XPB and XPD DNA helicases are components of the p53-mediated apoptosis pathway.
Wang XW; Vermeulen W; Coursen JD; Gibson M; Lupold SE; Forrester K; Xu G; Elmore L; Yeh H; Hoeijmakers JH; Harris CC
Genes Dev; 1996 May; 10(10):1219-32. PubMed ID: 8675009
[TBL] [Abstract][Full Text] [Related]
13. Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.
Armelini MG; Muotri AR; Marchetto MC; de Lima-Bessa KM; Sarasin A; Menck CF
Cancer Gene Ther; 2005 Apr; 12(4):389-96. PubMed ID: 15650764
[TBL] [Abstract][Full Text] [Related]
14. Human xeroderma pigmentosum group D gene encodes a DNA helicase.
Sung P; Bailly V; Weber C; Thompson LH; Prakash L; Prakash S
Nature; 1993 Oct; 365(6449):852-5. PubMed ID: 8413672
[TBL] [Abstract][Full Text] [Related]
15. [Trichothiodystrophies: anomalies of the repair and transcription of genes].
Robert C; Sarasin A
Ann Dermatol Venereol; 1999 Oct; 126(10):669-71. PubMed ID: 10604001
[No Abstract] [Full Text] [Related]
16. Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast.
Wang Z; Svejstrup JQ; Feaver WJ; Wu X; Kornberg RD; Friedberg EC
Nature; 1994 Mar; 368(6466):74-6. PubMed ID: 8107888
[TBL] [Abstract][Full Text] [Related]
17. Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.
Coin F; Oksenych V; Egly JM
Mol Cell; 2007 Apr; 26(2):245-56. PubMed ID: 17466626
[TBL] [Abstract][Full Text] [Related]
18. DNA helicases, genomic instability, and human genetic disease.
van Brabant AJ; Stan R; Ellis NA
Annu Rev Genomics Hum Genet; 2000; 1():409-59. PubMed ID: 11701636
[TBL] [Abstract][Full Text] [Related]
19. The rem mutations in the ATP-binding groove of the Rad3/XPD helicase lead to Xeroderma pigmentosum-Cockayne syndrome-like phenotypes.
Herrera-Moyano E; Moriel-Carretero M; Montelone BA; Aguilera A
PLoS Genet; 2014 Dec; 10(12):e1004859. PubMed ID: 25500814
[TBL] [Abstract][Full Text] [Related]
20. Increased expression of p53 enhances transcription-coupled repair and global genomic repair of a UVC-damaged reporter gene in human cells.
Dregoesc D; Rybak AP; Rainbow AJ
DNA Repair (Amst); 2007 May; 6(5):588-601. PubMed ID: 17196445
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]