1263 related articles for article (PubMed ID: 10416615)
21. Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes.
Queille S; Drougard C; Sarasin A; Daya-Grosjean L
J Invest Dermatol; 2001 Nov; 117(5):1162-70. PubMed ID: 11710928
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. Defective transcription/repair factor IIH recruitment to specific UV lesions in trichothiodystrophy syndrome.
Chiganças V; Lima-Bessa KM; Stary A; Menck CF; Sarasin A
Cancer Res; 2008 Aug; 68(15):6074-83. PubMed ID: 18676829
[TBL] [Abstract][Full Text] [Related]
24. Human cancer and DNA repair-deficient diseases.
Sarasin A; Stary A
Cancer Detect Prev; 1997; 21(5):406-11. PubMed ID: 9307843
[TBL] [Abstract][Full Text] [Related]
25. An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.
Andressoo JO; Mitchell JR; de Wit J; Hoogstraten D; Volker M; Toussaint W; Speksnijder E; Beems RB; van Steeg H; Jans J; de Zeeuw CI; Jaspers NG; Raams A; Lehmann AR; Vermeulen W; Hoeijmakers JH; van der Horst GT
Cancer Cell; 2006 Aug; 10(2):121-32. PubMed ID: 16904611
[TBL] [Abstract][Full Text] [Related]
26. Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies.
Jaspers NG
Cytokines Mol Ther; 1996 Jun; 2(2):115-9. PubMed ID: 9384696
[TBL] [Abstract][Full Text] [Related]
27. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.
Broughton BC; Steingrimsdottir H; Weber CA; Lehmann AR
Nat Genet; 1994 Jun; 7(2):189-94. PubMed ID: 7920640
[TBL] [Abstract][Full Text] [Related]
28. Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA.
de Vries A; van Oostrom CT; Hofhuis FM; Dortant PM; Berg RJ; de Gruijl FR; Wester PW; van Kreijl CF; Capel PJ; van Steeg H; Verbeek SJ
Nature; 1995 Sep; 377(6545):169-73. PubMed ID: 7675086
[TBL] [Abstract][Full Text] [Related]
29. High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A gene.
Nakane H; Takeuchi S; Yuba S; Saijo M; Nakatsu Y; Murai H; Nakatsuru Y; Ishikawa T; Hirota S; Kitamura Y
Nature; 1995 Sep; 377(6545):165-8. PubMed ID: 7675085
[TBL] [Abstract][Full Text] [Related]
30. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.
Boyle J; Ueda T; Oh KS; Imoto K; Tamura D; Jagdeo J; Khan SG; Nadem C; Digiovanna JJ; Kraemer KH
Hum Mutat; 2008 Oct; 29(10):1194-208. PubMed ID: 18470933
[TBL] [Abstract][Full Text] [Related]
31. Cell-type-specific consequences of nucleotide excision repair deficiencies: Embryonic stem cells versus fibroblasts.
de Waard H; Sonneveld E; de Wit J; Esveldt-van Lange R; Hoeijmakers JH; Vrieling H; van der Horst GT
DNA Repair (Amst); 2008 Oct; 7(10):1659-69. PubMed ID: 18634906
[TBL] [Abstract][Full Text] [Related]
32. Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation.
Kobayashi T; Uchiyama M; Fukuro S; Tanaka K
Am J Med Genet; 2002 Jul; 110(3):248-52. PubMed ID: 12116233
[TBL] [Abstract][Full Text] [Related]
33. Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
Eveno E; Bourre F; Quilliet X; Chevallier-Lagente O; Roza L; Eker AP; Kleijer WJ; Nikaido O; Stefanini M; Hoeijmakers JH
Cancer Res; 1995 Oct; 55(19):4325-32. PubMed ID: 7671243
[TBL] [Abstract][Full Text] [Related]
34. Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
Broughton BC; Berneburg M; Fawcett H; Taylor EM; Arlett CF; Nardo T; Stefanini M; Menefee E; Price VH; Queille S; Sarasin A; Bohnert E; Krutmann J; Davidson R; Kraemer KH; Lehmann AR
Hum Mol Genet; 2001 Oct; 10(22):2539-47. PubMed ID: 11709541
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Differential behaviors toward ultraviolet A and B radiation of fibroblasts and keratinocytes from normal and DNA-repair-deficient patients.
Otto AI; Riou L; Marionnet C; Mori T; Sarasin A; Magnaldo T
Cancer Res; 1999 Mar; 59(6):1212-8. PubMed ID: 10096550
[TBL] [Abstract][Full Text] [Related]
37. Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity.
Botta E; Nardo T; Broughton BC; Marinoni S; Lehmann AR; Stefanini M
Am J Hum Genet; 1998 Oct; 63(4):1036-48. PubMed ID: 9758621
[TBL] [Abstract][Full Text] [Related]
38. Functional and molecular genetic analyses of nine newly identified XPD-deficient patients reveal a novel mutation resulting in TTD as well as in XP/CS complex phenotypes.
Schäfer A; Gratchev A; Seebode C; Hofmann L; Schubert S; Laspe P; Apel A; Ohlenbusch A; Tzvetkov M; Weishaupt C; Oji V; Schön MP; Emmert S
Exp Dermatol; 2013 Jul; 22(7):486-9. PubMed ID: 23800062
[TBL] [Abstract][Full Text] [Related]
39. Tissue specific mutagenic and carcinogenic responses in NER defective mouse models.
Wijnhoven SW; Hoogervorst EM; de Waard H; van der Horst GT; van Steeg H
Mutat Res; 2007 Jan; 614(1-2):77-94. PubMed ID: 16769089
[TBL] [Abstract][Full Text] [Related]
40. Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
Mezzina M; Eveno E; Chevallier-Lagente O; Benoit A; Carreau M; Vermeulen W; Hoeijmakers JH; Stefanini M; Lehmann AR; Weber CA
Carcinogenesis; 1994 Aug; 15(8):1493-8. PubMed ID: 8055625
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
