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Journal Abstract Search

197 related items for PubMed ID: 3348214

  • 1. Ultraviolet light-induced chromosomal aberrations in cultured cells from Cockayne syndrome and complementation group C xeroderma pigmentosum patients: lack of correlation with cancer susceptibility.
    Seguin LR, Tarone RE, Liao KH, Robbins JH.
    Am J Hum Genet; 1988 Mar; 42(3):468-75. PubMed ID: 3348214
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  • 3. 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; 107(4):647-53. PubMed ID: 8823375
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  • 4. Cockayne syndrome and xeroderma pigmentosum.
    Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH.
    Neurology; 2000 Nov 28; 55(10):1442-9. PubMed ID: 11185579
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  • 5. DNA repair and replication in xeroderma pigmentosum and related disorders.
    Cleaver JE.
    Basic Life Sci; 1986 Nov 28; 39():425-38. PubMed ID: 3767846
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  • 6. Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition.
    Price FM, Parshad R, Tarone RE, Sanford KK.
    Cancer Genet Cytogenet; 1991 Nov 28; 57(1):1-10. PubMed ID: 1756475
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  • 7. Use of lymphoblastoid cell lines to evaluate the hypersensitivity to ultraviolet radiation in Cockayne syndrome.
    Otsuka F, Tarone RE, Cayeux S, Robbins JH.
    J Invest Dermatol; 1984 May 28; 82(5):480-4. PubMed ID: 6096450
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  • 8. Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
    Vermeulen W, Jaeken J, Jaspers NG, Bootsma D, Hoeijmakers JH.
    Am J Hum Genet; 1993 Jul 28; 53(1):185-92. PubMed ID: 8317483
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  • 10. 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 28; 56(1):167-74. PubMed ID: 7825573
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  • 11. Three complementation groups in Cockayne syndrome.
    Lehmann AR.
    Mutat Res; 1982 Dec 28; 106(2):347-56. PubMed ID: 6185841
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  • 12. Evidence for defective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells.
    Barrett SF, Robbins JH, Tarone RE, Kraemer KH.
    Mutat Res; 1991 Nov 28; 255(3):281-91. PubMed ID: 1719400
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  • 13. Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.
    Vélez-Cruz R, Zadorin AS, Coin F, Egly JM.
    Proc Natl Acad Sci U S A; 2013 Jan 15; 110(3):E212-20. PubMed ID: 23267107
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  • 17. 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 15; 166(1):99-111. PubMed ID: 3014327
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  • 18. Recovery from ultraviolet tight-induced depression of ribosomal RNA synthesis in normal human, xeroderma pigmentosum and Cockayne syndrome cells.
    Ayaki H, Hara R, Ikenaga M.
    J Radiat Res; 1996 Jun 15; 37(2):107-16. PubMed ID: 8840721
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  • 20. [The determination of the complementation groups for the cells of patients with xeroderma pigmentosum and the Cockayne syndrome found in Russia].
    Pleskach NM, Mikhel'son VM, Raams A, Bootsma D.
    Tsitologiia; 1996 Jun 15; 38(8):863-8. PubMed ID: 9027016
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