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Journal Abstract Search

285 related items for PubMed ID: 8253091

  • 1. Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
    van Vuuren AJ, Appeldoorn E, Odijk H, Yasui A, Jaspers NG, Bootsma D, Hoeijmakers JH.
    EMBO J; 1993 Sep; 12(9):3693-701. PubMed ID: 8253091
    [Abstract] [Full Text] [Related]

  • 2. Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.
    Biggerstaff M, Szymkowski DE, Wood RD.
    EMBO J; 1993 Sep; 12(9):3685-92. PubMed ID: 8253090
    [Abstract] [Full Text] [Related]

  • 3. ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.
    Brookman KW, Lamerdin JE, Thelen MP, Hwang M, Reardon JT, Sancar A, Zhou ZQ, Walter CA, Parris CN, Thompson LH.
    Mol Cell Biol; 1996 Nov; 16(11):6553-62. PubMed ID: 8887684
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

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

  • 6. Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4.
    Busch DB, van Vuuren H, de Wit J, Collins A, Zdzienicka MZ, Mitchell DL, Brookman KW, Stefanini M, Riboni R, Thompson LH, Albert RB, van Gool AJ, Hoeijmakers J.
    Mutat Res; 1997 Mar 12; 383(2):91-106. PubMed ID: 9088342
    [Abstract] [Full Text] [Related]

  • 7. Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients.
    Ahmad A, Enzlin JH, Bhagwat NR, Wijgers N, Raams A, Appledoorn E, Theil AF, J Hoeijmakers JH, Vermeulen W, J Jaspers NG, Schärer OD, Niedernhofer LJ.
    PLoS Genet; 2010 Mar 05; 6(3):e1000871. PubMed ID: 20221251
    [Abstract] [Full Text] [Related]

  • 8. Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activities.
    van Vuuren AJ, Appeldoorn E, Odijk H, Humbert S, Moncollin V, Eker AP, Jaspers NG, Egly JM, Hoeijmakers JH.
    Mutat Res; 1995 Jul 05; 337(1):25-39. PubMed ID: 7596355
    [Abstract] [Full Text] [Related]

  • 9. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Cooper PK, Nouspikel T, Clarkson SG, Leadon SA.
    Science; 1997 Feb 14; 275(5302):990-3. PubMed ID: 9020084
    [Abstract] [Full Text] [Related]

  • 10. Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5.
    O'Donovan A, Wood RD.
    Nature; 1993 May 13; 363(6425):185-8. PubMed ID: 8483505
    [Abstract] [Full Text] [Related]

  • 11. UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.
    Itoh T, Fujiwara Y, Ono T, Yamaizumi M.
    Am J Hum Genet; 1995 Jun 13; 56(6):1267-76. PubMed ID: 7539208
    [Abstract] [Full Text] [Related]

  • 12. Nucleotide excision repair. II: From yeast to mammals.
    Hoeijmakers JH.
    Trends Genet; 1993 Jun 13; 9(6):211-7. PubMed ID: 8337762
    [Abstract] [Full Text] [Related]

  • 13. DNA repair defect in xeroderma pigmentosum group C and complementing factor from HeLa cells.
    Shivji MK, Eker AP, Wood RD.
    J Biol Chem; 1994 Sep 09; 269(36):22749-57. PubMed ID: 8077226
    [Abstract] [Full Text] [Related]

  • 14. Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2.
    Scherly D, Nouspikel T, Corlet J, Ucla C, Bairoch A, Clarkson SG.
    Nature; 1993 May 13; 363(6425):182-5. PubMed ID: 8483504
    [Abstract] [Full Text] [Related]

  • 15. Mutational analysis of the human nucleotide excision repair gene ERCC1.
    Sijbers AM, van der Spek PJ, Odijk H, van den Berg J, van Duin M, Westerveld A, Jaspers NG, Bootsma D, Hoeijmakers JH.
    Nucleic Acids Res; 1996 Sep 01; 24(17):3370-80. PubMed ID: 8811092
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 56(1):167-74. PubMed ID: 7825573
    [Abstract] [Full Text] [Related]

  • 17. The COOH terminus of suppressor of stem loop (SSL2/RAD25) in yeast is essential for overall genomic excision repair and transcription-coupled repair.
    Sweder KS, Hanawalt PC.
    J Biol Chem; 1994 Jan 21; 269(3):1852-7. PubMed ID: 8294433
    [Abstract] [Full Text] [Related]

  • 18. Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
    Sijbers AM, de Laat WL, Ariza RR, Biggerstaff M, Wei YF, Moggs JG, Carter KC, Shell BK, Evans E, de Jong MC, Rademakers S, de Rooij J, Jaspers NG, Hoeijmakers JH, Wood RD.
    Cell; 1996 Sep 06; 86(5):811-22. PubMed ID: 8797827
    [Abstract] [Full Text] [Related]

  • 19. The formation of UV-induced chromosome aberrations involves ERCC1 and XPF but not other nucleotide excision repair genes.
    Chipchase MD, Melton DW.
    DNA Repair (Amst); 2002 Apr 29; 1(4):335-40. PubMed ID: 12509251
    [Abstract] [Full Text] [Related]

  • 20. Clinical symptoms and DNA repair characteristics of xeroderma pigmentosum patients from Germany.
    Thielmann HW, Popanda O, Edler L, Jung EG.
    Cancer Res; 1991 Jul 01; 51(13):3456-70. PubMed ID: 2054785
    [Abstract] [Full Text] [Related]

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