159 related articles for article (PubMed ID: 25605938)
21. 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]
22. 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]
23. Trichothiodystrophy: from basic mechanisms to clinical implications.
Stefanini M; Botta E; Lanzafame M; Orioli D
DNA Repair (Amst); 2010 Jan; 9(1):2-10. PubMed ID: 19931493
[TBL] [Abstract][Full Text] [Related]
24. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
Berneburg M; Clingen PH; Harcourt SA; Lowe JE; Taylor EM; Green MH; Krutmann J; Arlett CF; Lehmann AR
Cancer Res; 2000 Jan; 60(2):431-8. PubMed ID: 10667598
[TBL] [Abstract][Full Text] [Related]
25. Fibroblast extracellular matrix gene expression in response to keratinocyte-releasable stratifin.
Ghaffari A; Li Y; Karami A; Ghaffari M; Tredget EE; Ghahary A
J Cell Biochem; 2006 May; 98(2):383-93. PubMed ID: 16440305
[TBL] [Abstract][Full Text] [Related]
26. A history of TFIIH: two decades of molecular biology on a pivotal transcription/repair factor.
Egly JM; Coin F
DNA Repair (Amst); 2011 Jul; 10(7):714-21. PubMed ID: 21592869
[TBL] [Abstract][Full Text] [Related]
27. Overexpression of matrix metalloproteinase 1 in dermal fibroblasts from DNA repair-deficient/cancer-prone xeroderma pigmentosum group C patients.
Fréchet M; Warrick E; Vioux C; Chevallier O; Spatz A; Benhamou S; Sarasin A; Bernerd F; Magnaldo T
Oncogene; 2008 Sep; 27(39):5223-32. PubMed ID: 18469853
[TBL] [Abstract][Full Text] [Related]
28. Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes.
Coin F; Marinoni JC; Egly JM
Pathol Biol (Paris); 1998 Nov; 46(9):679-80. PubMed ID: 9885814
[No Abstract] [Full Text] [Related]
29. 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]
30. Mutations in the general transcription factor TFIIH result in beta-thalassaemia in individuals with trichothiodystrophy.
Viprakasit V; Gibbons RJ; Broughton BC; Tolmie JL; Brown D; Lunt P; Winter RM; Marinoni S; Stefanini M; Brueton L; Lehmann AR; Higgs DR
Hum Mol Genet; 2001 Nov; 10(24):2797-802. PubMed ID: 11734544
[TBL] [Abstract][Full Text] [Related]
31. New clinico-genetic classification of trichothiodystrophy.
Morice-Picard F; Cario-André M; Rezvani H; Lacombe D; Sarasin A; Taïeb A
Am J Med Genet A; 2009 Sep; 149A(9):2020-30. PubMed ID: 19681155
[TBL] [Abstract][Full Text] [Related]
32. Solution structure and self-association properties of the p8 TFIIH subunit responsible for trichothiodystrophy.
Vitorino M; Coin F; Zlobinskaya O; Atkinson RA; Moras D; Egly JM; Poterszman A; Kieffer B
J Mol Biol; 2007 Apr; 368(2):473-80. PubMed ID: 17350038
[TBL] [Abstract][Full Text] [Related]
33. Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes.
Dumaz N; Duthu A; Ehrhart JC; Drougard C; Appella E; Anderson CW; May P; Sarasin A; Daya-Grosjean L
Mol Carcinog; 1997 Dec; 20(4):340-7. PubMed ID: 9433478
[TBL] [Abstract][Full Text] [Related]
34. Mutations in TFIIH causing trichothiodystrophy are responsible for defects in ribosomal RNA production and processing.
Nonnekens J; Perez-Fernandez J; Theil AF; Gadal O; Bonnart C; Giglia-Mari G
Hum Mol Genet; 2013 Jul; 22(14):2881-93. PubMed ID: 23562818
[TBL] [Abstract][Full Text] [Related]
35. A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A.
Giglia-Mari G; Coin F; Ranish JA; Hoogstraten D; Theil A; Wijgers N; Jaspers NG; Raams A; Argentini M; van der Spek PJ; Botta E; Stefanini M; Egly JM; Aebersold R; Hoeijmakers JH; Vermeulen W
Nat Genet; 2004 Jul; 36(7):714-9. PubMed ID: 15220921
[TBL] [Abstract][Full Text] [Related]
36. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells.
Marionnet C; Benoit A; Benhamou S; Sarasin A; Stary A
J Mol Biol; 1995 Oct; 252(5):550-62. PubMed ID: 7563073
[TBL] [Abstract][Full Text] [Related]
37. TTDA: big impact of a small protein.
Theil AF; Hoeijmakers JH; Vermeulen W
Exp Cell Res; 2014 Nov; 329(1):61-8. PubMed ID: 25016283
[TBL] [Abstract][Full Text] [Related]
38. p8/TTDA overexpression enhances UV-irradiation resistance and suppresses TFIIH mutations in a Drosophila trichothiodystrophy model.
Aguilar-Fuentes J; Fregoso M; Herrera M; Reynaud E; Braun C; Egly JM; Zurita M
PLoS Genet; 2008 Nov; 4(11):e1000253. PubMed ID: 19008953
[TBL] [Abstract][Full Text] [Related]
39. Effects of basic fibroblast growth factor on the expression of extracellular matrix and matrix metalloproteinase-1 in wound healing.
Xie J; Bian H; Qi S; Xu Y; Tang J; Li T; Liu X
Clin Exp Dermatol; 2008 Mar; 33(2):176-82. PubMed ID: 18257838
[TBL] [Abstract][Full Text] [Related]
40. Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
Kobayashi T; Kuraoka I; Saijo M; Nakatsu Y; Tanaka A; Someda Y; Fukuro S; Tanaka K
Hum Mutat; 1997; 9(4):322-31. PubMed ID: 9101292
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]