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Journal Abstract Search

197 related items for PubMed ID: 3348214

  • 41. Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers.
    Spivak G, Itoh T, Matsunaga T, Nikaido O, Hanawalt P, Yamaizumi M.
    DNA Repair (Amst); 2002 Aug 06; 1(8):629-43. PubMed ID: 12509286
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  • 42. Xeroderma pigmentosum and related disorders: examining the linkage between defective DNA repair and cancer.
    Kraemer KH, Levy DD, Parris CN, Gozukara EM, Moriwaki S, Adelberg S, Seidman MM.
    J Invest Dermatol; 1994 Nov 06; 103(5 Suppl):96S-101S. PubMed ID: 7963692
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  • 43. Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells.
    Dianov GL, Houle JF, Iyer N, Bohr VA, Friedberg EC.
    Nucleic Acids Res; 1997 Sep 15; 25(18):3636-42. PubMed ID: 9278484
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  • 44. Xeroderma pigmentosum and the role of UV-induced DNA damage in skin cancer.
    van Steeg H, Kraemer KH.
    Mol Med Today; 1999 Feb 15; 5(2):86-94. PubMed ID: 10200950
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  • 45. 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 15; 56(6):1267-76. PubMed ID: 7539208
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  • 46. Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription.
    Berneburg M, Lehmann AR.
    Adv Genet; 2001 Jun 15; 43():71-102. PubMed ID: 11037299
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  • 47. 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
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  • 48. Xeroderma pigmentosum--Cockayne syndrome complex: a further case.
    Hamel BC, Raams A, Schuitema-Dijkstra AR, Simons P, van der Burgt I, Jaspers NG, Kleijer WJ.
    J Med Genet; 1996 Jul 01; 33(7):607-10. PubMed ID: 8818951
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  • 49. Xeroderma pigmentosum--bridging a gap between clinic and laboratory.
    Moriwaki S, Kraemer KH.
    Photodermatol Photoimmunol Photomed; 2001 Apr 01; 17(2):47-54. PubMed ID: 11338401
    [Abstract] [Full Text] [Related]

  • 50. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG.
    Am J Hum Genet; 2001 Aug 01; 69(2):291-300. PubMed ID: 11443545
    [Abstract] [Full Text] [Related]

  • 51. Xeroderma pigmentosum and skin cancer.
    Daya-Grosjean L.
    Adv Exp Med Biol; 2008 Aug 01; 637():19-27. PubMed ID: 19181107
    [Abstract] [Full Text] [Related]

  • 52. 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 Aug 01; 14(1):9-22. PubMed ID: 10447254
    [Abstract] [Full Text] [Related]

  • 53. 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
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  • 58. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
    Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G, Mezzina M, Sarasin A.
    Hum Mol Genet; 1999 Jun 15; 8(6):1125-33. PubMed ID: 10332046
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  • 60. Genetic complementation groups in cockayne syndrome.
    Tanaka K, Kawai K, Kumahara Y, Ikenaga M, Okada Y.
    Somatic Cell Genet; 1981 Jul 15; 7(4):445-55. PubMed ID: 7280930
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