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Journal Abstract Search

197 related items for PubMed ID: 3348214

  • 21. 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
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  • 23. Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndrome.
    Theron T, Fousteri MI, Volker M, Harries LW, Botta E, Stefanini M, Fujimoto M, Andressoo JO, Mitchell J, Jaspers NG, McDaniel LD, Mullenders LH, Lehmann AR.
    Mol Cell Biol; 2005 Sep 25; 25(18):8368-78. PubMed ID: 16135823
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  • 24. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
    Oh KS, Khan SG, Jaspers NG, Raams A, Ueda T, Lehmann A, Friedmann PS, Emmert S, Gratchev A, Lachlan K, Lucassan A, Baker CC, Kraemer KH.
    Hum Mutat; 2006 Nov 25; 27(11):1092-103. PubMed ID: 16947863
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  • 25. 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 25; 41(2):87-96. PubMed ID: 16325378
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  • 26. Cross-sensitivity of certain xeroderma pigmentosum and Cockayne syndrome fibroblast strains to both ionizing radiation and ultraviolet light.
    Chan GL, Little JB.
    Mol Gen Genet; 1981 Feb 25; 181(4):562-3. PubMed ID: 6943407
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  • 27. The Cockayne syndrome--an inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA. Comparison with xeroderma pigmentosum.
    Otsuka F, Robbins JH.
    Am J Dermatopathol; 1985 Aug 25; 7(4):387-92. PubMed ID: 3842793
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  • 28. Relative repair of adenovirus damaged by sunlamp, UV and gamma-irradiation in Cockayne syndrome fibroblasts is different from that in xeroderma pigmentosum fibroblasts.
    Rainbow AJ.
    Photochem Photobiol; 1989 Aug 25; 50(2):201-7. PubMed ID: 2675138
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  • 29. 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
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  • 30. UV-enhanced reactivation of a UV-damaged reporter gene suggests transcription-coupled repair is UV-inducible in human cells.
    Francis MA, Rainbow AJ.
    Carcinogenesis; 1999 Jan 14; 20(1):19-26. PubMed ID: 9934845
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  • 32. Prenatal diagnosis of xeroderma pigmentosum and Cockayne syndrome.
    Cleaver JE, Volpe JP, Charles WC, Thomas GH.
    Prenat Diagn; 1994 Oct 14; 14(10):921-8. PubMed ID: 7534923
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  • 33. Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum.
    Evans HJ, Adams AC, Clarkson JM, German J.
    Cytogenet Cell Genet; 1978 Oct 14; 20(1-6):124-40. PubMed ID: 648171
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  • 37. U.V. enhanced reactivation of U.V.-and gamma-irradiated adenovirus in Cockayne syndrome and Xeroderma pigmentosum fibroblasts.
    Jeeves WP, Rainbow AJ.
    Int J Radiat Biol Relat Stud Phys Chem Med; 1983 Jun 14; 43(6):625-47. PubMed ID: 6343275
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  • 38. A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations.
    Itoh T, Ono T, Yamaizumi M.
    Mutat Res; 1994 May 14; 314(3):233-48. PubMed ID: 7513056
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  • 39. [Xeroderma pigmentosum (XP) : A genetic disease sheds light on UV-induced skin cancer].
    Emmert B, Hallier E, Schön MP, Emmert S.
    Hautarzt; 2011 Feb 14; 62(2):91-7. PubMed ID: 21243329
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  • 40. Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies.
    Jaspers NG.
    Cytokines Mol Ther; 1996 Jun 14; 2(2):115-9. PubMed ID: 9384696
    [Abstract] [Full Text] [Related]

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