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552 related items for PubMed ID: 9716445

  • 1. Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.
    Ellison AR, Nouspikel T, Jaspers NG, Clarkson SG, Gruenert DC.
    Exp Cell Res; 1998 Aug 25; 243(1):22-8. PubMed ID: 9716445
    [Abstract] [Full Text] [Related]

  • 2. 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 25; 12(4):389-96. PubMed ID: 15650764
    [Abstract] [Full Text] [Related]

  • 3. Characterization of three XPG-defective patients identifies three missense mutations that impair repair and transcription.
    Schäfer A, Schubert S, Gratchev A, Seebode C, Apel A, Laspe P, Hofmann L, Ohlenbusch A, Mori T, Kobayashi N, Schürer A, Schön MP, Emmert S.
    J Invest Dermatol; 2013 Jul 25; 133(7):1841-9. PubMed ID: 23370536
    [Abstract] [Full Text] [Related]

  • 4. Increased expression of p53 enhances transcription-coupled repair and global genomic repair of a UVC-damaged reporter gene in human cells.
    Dregoesc D, Rybak AP, Rainbow AJ.
    DNA Repair (Amst); 2007 May 01; 6(5):588-601. PubMed ID: 17196445
    [Abstract] [Full Text] [Related]

  • 5. Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stress.
    Soltys DT, Rocha CR, Lerner LK, de Souza TA, Munford V, Cabral F, Nardo T, Stefanini M, Sarasin A, Cabral-Neto JB, Menck CF.
    Hum Mutat; 2013 Mar 01; 34(3):481-9. PubMed ID: 23255472
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 60(2):431-8. PubMed ID: 10667598
    [Abstract] [Full Text] [Related]

  • 7. Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.
    Thorel F, Constantinou A, Dunand-Sauthier I, Nouspikel T, Lalle P, Raams A, Jaspers NG, Vermeulen W, Shivji MK, Wood RD, Clarkson SG.
    Mol Cell Biol; 2004 Dec 15; 24(24):10670-80. PubMed ID: 15572672
    [Abstract] [Full Text] [Related]

  • 8. Xeroderma pigmentosum and molecular cloning of DNA repair genes.
    Boulikas T.
    Anticancer Res; 1996 Dec 15; 16(2):693-708. PubMed ID: 8687116
    [Abstract] [Full Text] [Related]

  • 9. DNA damage in transcribed genes induces apoptosis via the JNK pathway and the JNK-phosphatase MKP-1.
    Hamdi M, Kool J, Cornelissen-Steijger P, Carlotti F, Popeijus HE, van der Burgt C, Janssen JM, Yasui A, Hoeben RC, Terleth C, Mullenders LH, van Dam H.
    Oncogene; 2005 Nov 03; 24(48):7135-44. PubMed ID: 16044158
    [Abstract] [Full Text] [Related]

  • 10. 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 06; 252(5):550-62. PubMed ID: 7563073
    [Abstract] [Full Text] [Related]

  • 11. Roles of XPG and XPF/ERCC1 endonucleases in UV-induced immunostaining of PCNA in fibroblasts.
    Miura M, Nakamura S, Sasaki T, Takasaki Y, Shiomi T, Yamaizumi M.
    Exp Cell Res; 1996 Jul 10; 226(1):126-32. PubMed ID: 8660947
    [Abstract] [Full Text] [Related]

  • 12. Increased ultraviolet sensitivity and chromosomal instability related to P53 function in the xeroderma pigmentosum variant.
    Cleaver JE, Afzal V, Feeney L, McDowell M, Sadinski W, Volpe JP, Busch DB, Coleman DM, Ziffer DW, Yu Y, Nagasawa H, Little JB.
    Cancer Res; 1999 Mar 01; 59(5):1102-8. PubMed ID: 10070969
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 20(4):340-7. PubMed ID: 9433478
    [Abstract] [Full Text] [Related]

  • 14. Enhanced transformation of xeroderma pigmentosum variant cells by ultraviolet light-irradiated simian virus 40.
    Hall JD, Tokuno SI.
    Cancer Res; 1979 Oct 01; 39(10):4064-8. PubMed ID: 225015
    [Abstract] [Full Text] [Related]

  • 15. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
    Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH.
    J Invest Dermatol; 1996 Oct 01; 107(4):647-53. PubMed ID: 8823375
    [Abstract] [Full Text] [Related]

  • 16. Impaired jun-NH2-terminal kinase activation by ultraviolet irradiation in fibroblasts of patients with Cockayne syndrome complementation group B.
    Dhar V, Adler V, Lehmann A, Ronai Z.
    Cell Growth Differ; 1996 Jun 01; 7(6):841-6. PubMed ID: 8780897
    [Abstract] [Full Text] [Related]

  • 17. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.
    Nouspikel T, Lalle P, Leadon SA, Cooper PK, Clarkson SG.
    Proc Natl Acad Sci U S A; 1997 Apr 01; 94(7):3116-21. PubMed ID: 9096355
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 59(14):3489-94. PubMed ID: 10416615
    [Abstract] [Full Text] [Related]

  • 19. A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy.
    Cleaver JE, Thompson LH, Richardson AS, States JC.
    Hum Mutat; 1999 Jul 15; 14(1):9-22. PubMed ID: 10447254
    [Abstract] [Full Text] [Related]

  • 20. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome.
    Itoh T.
    J Dermatol Sci; 2006 Feb 15; 41(2):87-96. PubMed ID: 16325378
    [Abstract] [Full Text] [Related]

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