230 related articles for article (PubMed ID: 19934020)
21. A Drosophila XPD model links cell cycle coordination with neuro-development and suggests links to cancer.
Stettler K; Li X; Sandrock B; Braga-Lagache S; Heller M; Dümbgen L; Suter B
Dis Model Mech; 2015 Jan; 8(1):81-91. PubMed ID: 25431422
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Competent transcription initiation by RNA polymerase II in cell-free extracts from xeroderma pigmentosum groups B and D in an optimized RNA transcription assay.
Satoh MS; Hanawalt PC
Biochim Biophys Acta; 1997 Nov; 1354(3):241-51. PubMed ID: 9427533
[TBL] [Abstract][Full Text] [Related]
24. Codominance associated with overexpression of certain XPD mutations.
Kadkhodayan S; Coin F; Salazar EP; George JW; Egly JM; Thompson LH
Mutat Res; 2001 Mar; 485(2):153-68. PubMed ID: 11182546
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Taylor EM; Broughton BC; Botta E; Stefanini M; Sarasin A; Jaspers NG; Fawcett H; Harcourt SA; Arlett CF; Lehmann AR
Proc Natl Acad Sci U S A; 1997 Aug; 94(16):8658-63. PubMed ID: 9238033
[TBL] [Abstract][Full Text] [Related]
27. Phenotype-specific adverse effects of XPD mutations on human prenatal development implicate impairment of TFIIH-mediated functions in placenta.
Moslehi R; Kumar A; Mills JL; Ambroggio X; Signore C; Dzutsev A
Eur J Hum Genet; 2012 Jun; 20(6):626-31. PubMed ID: 22234153
[TBL] [Abstract][Full Text] [Related]
28. TFIIH central activity in nucleotide excision repair to prevent disease.
Theil AF; Häckes D; Lans H
DNA Repair (Amst); 2023 Dec; 132():103568. PubMed ID: 37977600
[TBL] [Abstract][Full Text] [Related]
29. Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS.
Horibata K; Kono S; Ishigami C; Zhang X; Aizawa M; Kako Y; Ishii T; Kosaki R; Saijo M; Tanaka K
J Hum Genet; 2015 May; 60(5):259-65. PubMed ID: 25716912
[TBL] [Abstract][Full Text] [Related]
30. The 14th Datta Lecture. TFIIH: from transcription to clinic.
Egly JM
FEBS Lett; 2001 Jun; 498(2-3):124-8. PubMed ID: 11412842
[TBL] [Abstract][Full Text] [Related]
31. Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.
Vélez-Cruz R; Zadorin AS; Coin F; Egly JM
Proc Natl Acad Sci U S A; 2013 Jan; 110(3):E212-20. PubMed ID: 23267107
[TBL] [Abstract][Full Text] [Related]
32. Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD gene.
Botta E; Nardo T; Orioli D; Guglielmino R; Ricotti R; Bondanza S; Benedicenti F; Zambruno G; Stefanini M
Hum Mutat; 2009 Mar; 30(3):438-45. PubMed ID: 19085937
[TBL] [Abstract][Full Text] [Related]
33. Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.
Frederick GD; Amirkhan RH; Schultz RA; Friedberg EC
Hum Mol Genet; 1994 Oct; 3(10):1783-8. PubMed ID: 7849702
[TBL] [Abstract][Full Text] [Related]
34. In TFIIH, XPD helicase is exclusively devoted to DNA repair.
Kuper J; Braun C; Elias A; Michels G; Sauer F; Schmitt DR; Poterszman A; Egly JM; Kisker C
PLoS Biol; 2014 Sep; 12(9):e1001954. PubMed ID: 25268380
[TBL] [Abstract][Full Text] [Related]
35. MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation.
Ito S; Tan LJ; Andoh D; Narita T; Seki M; Hirano Y; Narita K; Kuraoka I; Hiraoka Y; Tanaka K
Mol Cell; 2010 Aug; 39(4):632-40. PubMed ID: 20797633
[TBL] [Abstract][Full Text] [Related]
36. Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy.
Botta E; Nardo T; Lehmann AR; Egly JM; Pedrini AM; Stefanini M
Hum Mol Genet; 2002 Nov; 11(23):2919-28. PubMed ID: 12393803
[TBL] [Abstract][Full Text] [Related]
37. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
Weeda G; Eveno E; Donker I; Vermeulen W; Chevallier-Lagente O; Taïeb A; Stary A; Hoeijmakers JH; Mezzina M; Sarasin A
Am J Hum Genet; 1997 Feb; 60(2):320-9. PubMed ID: 9012405
[TBL] [Abstract][Full Text] [Related]
38. XPD mutations prevent TFIIH-dependent transactivation by nuclear receptors and phosphorylation of RARalpha.
Keriel A; Stary A; Sarasin A; Rochette-Egly C; Egly JM
Cell; 2002 Apr; 109(1):125-35. PubMed ID: 11955452
[TBL] [Abstract][Full Text] [Related]
39. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
Oh KS; Khan SG; Jaspers NG; Raams A; Ueda T; Lehmann A; Friedmann PS; Emmert S; Gratchev A; Lachlan K; Lucassan A; Baker CC; Kraemer KH
Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
[TBL] [Abstract][Full Text] [Related]
40. XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations.
Fan L; Fuss JO; Cheng QJ; Arvai AS; Hammel M; Roberts VA; Cooper PK; Tainer JA
Cell; 2008 May; 133(5):789-800. PubMed ID: 18510924
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
