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Journal Abstract Search

111 related items for PubMed ID: 2927423

  • 21. DNA repair in human fibroblasts, as reflected by host-cell reactivation of a transfected UV-irradiated luciferase gene, is not related to donor age.
    Merkle TJ, O'Brien K, Brooks PJ, Tarone RE, Robbins JH.
    Mutat Res; 2004 Oct 04; 554(1-2):9-17. PubMed ID: 15450399
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  • 22. Transient expression of a plasmid gene, a tool to study DNA repair in human cells: defect of DNA repair in Cockayne syndrome; one thymine cyclobutane dimer is sufficient to block transcription.
    Klocker H, Schneider R, Burtscher HJ, Auer B, Hirsch-Kauffmann M, Schweiger M.
    Eur J Cell Biol; 1986 Jan 04; 39(2):346-51. PubMed ID: 3956512
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  • 23. 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
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  • 24. Incomplete complementation of the DNA repair defect in cockayne syndrome cells by the denV gene from bacteriophage T4 suggests a deficiency in base excision repair.
    Francis MA, Bagga PS, Athwal RS, Rainbow AJ.
    Mutat Res; 1997 Oct 06; 385(1):59-74. PubMed ID: 9372849
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  • 25. 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 01; 51(21):5786-93. PubMed ID: 1933849
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  • 26. Complete restoration of normal DNA repair characteristics in group F xeroderma pigmentosum cells by over-expression of transfected XPF cDNA.
    Yagi T, Matsumura Y, Sato M, Nishigori C, Mori T, Sijbers AM, Takebe H.
    Carcinogenesis; 1998 Jan 01; 19(1):55-60. PubMed ID: 9472693
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  • 28. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum.
    Madzak C, Armier J, Stary A, Daya-Grosjean L, Sarasin A.
    Carcinogenesis; 1993 Jul 01; 14(7):1255-60. PubMed ID: 8392442
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  • 29. Repair of ultraviolet B and singlet oxygen-induced DNA damage in xeroderma pigmentosum cells.
    Rünger TM, Epe B, Möller K.
    J Invest Dermatol; 1995 Jan 01; 104(1):68-73. PubMed ID: 7798643
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  • 30. UV-induced base substitution mutations in a shuttle vector plasmid propagated in group C xeroderma pigmentosum cells.
    Yagi T, Sato M, Tatsumi-Miyajima J, Takebe H.
    Mutat Res; 1992 Mar 01; 273(2):213-20. PubMed ID: 1372104
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  • 31. Replacing tryptophan-128 of T4 endonuclease V with a serine residue results in decreased enzymatic activity in vitro and in vivo.
    Valerie K.
    Nucleic Acids Res; 1995 Sep 25; 23(18):3764-70. PubMed ID: 7479008
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  • 34. Reactivation of psoralen-reacted plasmid DNA in Fanconi anemia, xeroderma pigmentosum, and normal human fibroblast cells.
    Sun Y, Moses RE.
    Somat Cell Mol Genet; 1991 May 25; 17(3):229-38. PubMed ID: 2047939
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  • 37. The repair of UV-irradiated plasmids transfected into cultured fish cells.
    Mitani H, Komura J, Shima A.
    Mutat Res; 1990 Jul 25; 236(1):77-84. PubMed ID: 2366798
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  • 38. Comparative studies of host-cell reactivation, cellular capacity and enhanced reactivation of herpes simplex virus in normal, xeroderma pigmentosum and Cockayne syndrome fibroblasts.
    Ryan DK, Rainbow AJ.
    Mutat Res; 1986 Jul 25; 166(1):99-111. PubMed ID: 3014327
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  • 39. Properties of an xeroderma pigmentosum revertant cell line expressing endonuclease V.
    Green AP, deRiel JK, Henderson E.
    Biochem Biophys Res Commun; 1993 Jan 15; 190(1):111-7. PubMed ID: 7678487
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  • 40. p53-mediated transcription induces resistance of DNA to UV inactivation.
    Huang J, Logsdon N, Schmieg FI, Simmons DT.
    Oncogene; 1998 Jul 30; 17(4):401-11. PubMed ID: 9696032
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