266 related articles for article (PubMed ID: 15650764)
1. 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]
2. 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]
3. 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]
4. 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]
5. Transcription by RNA polymerase II: a process linked to DNA repair.
Chalut C; Moncollin V; Egly JM
Bioessays; 1994 Sep; 16(9):651-5. PubMed ID: 7980491
[TBL] [Abstract][Full Text] [Related]
6. Clinical, genetic and DNA repair studies on a consecutive series of patients with xeroderma pigmentosum.
Pawsey SA; Magnus IA; Ramsay CA; Benson PF; Giannelli F
Q J Med; 1979 Apr; 48(190):179-210. PubMed ID: 504548
[TBL] [Abstract][Full Text] [Related]
7. Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndrome.
Broughton BC; Thompson AF; Harcourt SA; Vermeulen W; Hoeijmakers JH; Botta E; Stefanini M; King MD; Weber CA; Cole J
Am J Hum Genet; 1995 Jan; 56(1):167-74. PubMed ID: 7825573
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes.
Carreau M; Eveno E; Quilliet X; Chevalier-Lagente O; Benoit A; Tanganelli B; Stefanini M; Vermeulen W; Hoeijmakers JH; Sarasin A
Carcinogenesis; 1995 May; 16(5):1003-9. PubMed ID: 7767957
[TBL] [Abstract][Full Text] [Related]
12. p53 modulation of TFIIH-associated nucleotide excision repair activity.
Wang XW; Yeh H; Schaeffer L; Roy R; Moncollin V; Egly JM; Wang Z; Freidberg EC; Evans MK; Taffe BG
Nat Genet; 1995 Jun; 10(2):188-95. PubMed ID: 7663514
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Reduced capacity to repair irradiated adenovirus in fibroblasts from xeroderma pigmentosum heterozygotes.
Rainbow AJ
Cancer Res; 1980 Nov; 40(11):3945-9. PubMed ID: 7471045
[TBL] [Abstract][Full Text] [Related]
16. Ribosomal protein S3 associates with the TFIIH complex and positively regulates nucleotide excision repair.
Park YJ; Kim SH; Kim TS; Lee SM; Cho BS; Seo CI; Kim HD; Kim J
Cell Mol Life Sci; 2021 Apr; 78(7):3591-3606. PubMed ID: 33464383
[TBL] [Abstract][Full Text] [Related]
17. Construction of a recombinant adenovirus containing the denV gene from bacteriophage T4 which can partially restore the DNA repair deficiency in xeroderma pigmentosum fibroblasts.
Colicos MA; Haj-Ahmad Y; Valerie K; Henderson EE; Rainbow AJ
Carcinogenesis; 1991 Feb; 12(2):249-55. PubMed ID: 1704821
[TBL] [Abstract][Full Text] [Related]
18. Development and field-test validation of an assay for DNA repair in circulating human lymphocytes.
Athas WF; Hedayati MA; Matanoski GM; Farmer ER; Grossman L
Cancer Res; 1991 Nov; 51(21):5786-93. PubMed ID: 1933849
[TBL] [Abstract][Full Text] [Related]
19. The human DNA repair gene, ERCC2 (XPD), corrects ultraviolet hypersensitivity and ultraviolet hypermutability of a shuttle vector replicated in xeroderma pigmentosum group D cells.
Gözükara EM; Parris CN; Weber CA; Salazar EP; Seidman MM; Watkins JF; Prakash L; Kraemer KH
Cancer Res; 1994 Jul; 54(14):3837-44. PubMed ID: 8033104
[TBL] [Abstract][Full Text] [Related]
20. Gamma-ray-enhanced reactivation of irradiated adenovirus in Xeroderma pigmentosum and Cockayne syndrome fibroblasts.
Jeeves WP; Rainbow AJ
Radiat Res; 1983 Jun; 94(3):480-98. PubMed ID: 6856785
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]