277 related articles for article (PubMed ID: 23232694)
21. Slowly progressing nucleotide excision repair in trichothiodystrophy group A patient fibroblasts.
Theil AF; Nonnekens J; Wijgers N; Vermeulen W; Giglia-Mari G
Mol Cell Biol; 2011 Sep; 31(17):3630-8. PubMed ID: 21730288
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients.
Ueda T; Compe E; Catez P; Kraemer KH; Egly JM
J Exp Med; 2009 Dec; 206(13):3031-46. PubMed ID: 19934020
[TBL] [Abstract][Full Text] [Related]
25. Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models.
van de Ven M; Andressoo JO; van der Horst GT; Hoeijmakers JH; Mitchell JR
DNA Repair (Amst); 2012 Nov; 11(11):874-83. PubMed ID: 23046824
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. 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]
29. Nucleotide excision repair/transcription gene defects in the fetus and impaired TFIIH-mediated function in transcription in placenta leading to preeclampsia.
Moslehi R; Ambroggio X; Nagarajan V; Kumar A; Dzutsev A
BMC Genomics; 2014 May; 15():373. PubMed ID: 24885447
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. The XPD subunit of TFIIH is required for transcription-associated but not DNA double-strand break-induced recombination in mammalian cells.
Savolainen L; Cassel T; Helleday T
Mutagenesis; 2010 Nov; 25(6):623-9. PubMed ID: 20833695
[TBL] [Abstract][Full Text] [Related]
32. Metronidazole-Induced Hepatitis in a Teenager With Xeroderma Pigmentosum and Trichothiodystrophy Overlap.
Abiona A; Cordeiro N; Fawcett H; Tamura D; Khan SG; DiGiovanna JJ; Lehmann AR; Fassihi H
Pediatrics; 2021 Oct; 148(4):. PubMed ID: 34593652
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. XPD mutations in trichothiodystrophy hamper collagen VI expression and reveal a role of TFIIH in transcription derepression.
Orioli D; Compe E; Nardo T; Mura M; Giraudon C; Botta E; Arrigoni L; Peverali FA; Egly JM; Stefanini M
Hum Mol Genet; 2013 Mar; 22(6):1061-73. PubMed ID: 23221806
[TBL] [Abstract][Full Text] [Related]
36. Trichothiodystrophy view from the molecular basis of DNA repair/transcription factor TFIIH.
Hashimoto S; Egly JM
Hum Mol Genet; 2009 Oct; 18(R2):R224-30. PubMed ID: 19808800
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. Hot topics in DNA repair: the molecular basis for different disease states caused by mutations in TFIIH and XPG.
Schärer OD
DNA Repair (Amst); 2008 Feb; 7(2):339-44. PubMed ID: 18077223
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
