1268 related articles for article (PubMed ID: 10416615)
41. Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet light.
Lehmann AR; Arlett CF; Broughton BC; Harcourt SA; Steingrimsdottir H; Stefanini M; Malcolm A; Taylor R; Natarajan AT; Green S
Cancer Res; 1988 Nov; 48(21):6090-6. PubMed ID: 2458832
[TBL] [Abstract][Full Text] [Related]
42. 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]
43. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D.
Takayama K; Salazar EP; Lehmann A; Stefanini M; Thompson LH; Weber CA
Cancer Res; 1995 Dec; 55(23):5656-63. PubMed ID: 7585650
[TBL] [Abstract][Full Text] [Related]
44. Nucleotide excision repair syndromes: molecular basis and clinical symptoms.
Bootsma D; Weeda G; Vermeulen W; van Vuuren H; Troelstra C; van der Spek P; Hoeijmakers J
Philos Trans R Soc Lond B Biol Sci; 1995 Jan; 347(1319):75-81. PubMed ID: 7746858
[TBL] [Abstract][Full Text] [Related]
45. From a DNA helicase to brittle hair.
Winkler GS; Hoeijmakers JH
Nat Genet; 1998 Oct; 20(2):106-7. PubMed ID: 9771695
[No Abstract] [Full Text] [Related]
46. 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]
47. Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Coin F; Marinoni JC; Rodolfo C; Fribourg S; Pedrini AM; Egly JM
Nat Genet; 1998 Oct; 20(2):184-8. PubMed ID: 9771713
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. 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]
50. Repair characteristics and differentiation propensity of long-term cultures of epidermal keratinocytes derived from normal and NER-deficient mice.
Backendorf C; de Wit J; van Oosten M; Stout GJ; Mitchell JR; Borgstein AM; van der Horst GT; de Gruijl FR; Brouwer J; Mullenders LH; Hoeijmakers JH
DNA Repair (Amst); 2005 Nov; 4(11):1325-36. PubMed ID: 16182615
[TBL] [Abstract][Full Text] [Related]
51. Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients.
Dubaele S; Proietti De Santis L; Bienstock RJ; Keriel A; Stefanini M; Van Houten B; Egly JM
Mol Cell; 2003 Jun; 11(6):1635-46. PubMed ID: 12820975
[TBL] [Abstract][Full Text] [Related]
52. Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation.
George JW; Salazar EP; Vreeswijk MP; Lamerdin JE; Reardon JT; Zdzienicka MZ; Sancar A; Kadkhodayan S; Tebbs RS; Mullenders LH; Thompson LH
Mol Cell Biol; 2001 Nov; 21(21):7355-65. PubMed ID: 11585917
[TBL] [Abstract][Full Text] [Related]
53. Suppression of UV carcinogenesis by difluoromethylornithine in nucleotide excision repair-deficient Xpa knockout mice.
Rebel H; van Steeg H; Beems RB; Schouten R; de Gruijl FR; Terleth C
Cancer Res; 2002 Mar; 62(5):1338-42. PubMed ID: 11888902
[TBL] [Abstract][Full Text] [Related]
54. 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]
55. Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.
Takayama K; Salazar EP; Broughton BC; Lehmann AR; Sarasin A; Thompson LH; Weber CA
Am J Hum Genet; 1996 Feb; 58(2):263-70. PubMed ID: 8571952
[TBL] [Abstract][Full Text] [Related]
56. Relationship between UV-induced mutant p53 patches and skin tumours, analysed by mutation spectra and by induction kinetics in various DNA-repair-deficient mice.
Rebel H; Kram N; Westerman A; Banus S; van Kranen HJ; de Gruijl FR
Carcinogenesis; 2005 Dec; 26(12):2123-30. PubMed ID: 16051635
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. 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]
59. The relationship between benzo[a]pyrene-induced mutagenesis and carcinogenesis in repair-deficient Cockayne syndrome group B mice.
Wijnhoven SW; Kool HJ; van Oostrom CT; Beems RB; Mullenders LH; van Zeeland AA; van der Horst GT; Vrieling H; van Steeg H
Cancer Res; 2000 Oct; 60(20):5681-7. PubMed ID: 11059760
[TBL] [Abstract][Full Text] [Related]
60. Gene transduction in skin cells: preventing cancer in xeroderma pigmentosum mice.
Marchetto MC; Muotri AR; Burns DK; Friedberg EC; Menck CF
Proc Natl Acad Sci U S A; 2004 Dec; 101(51):17759-64. PubMed ID: 15598745
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
