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PUBMED FOR HANDHELDS

Journal Abstract Search


97 related items for PubMed ID: 3562572

  • 1. Ultraviolet hypersensitivity of Cockayne syndrome lymphoblastoid lines--the effects of exogenous beta-nicotinamide adenine dinucleotide.
    Otsuka F, Kukita A.
    Photochem Photobiol; 1986 Dec; 44(6):757-60. PubMed ID: 3562572
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  • 4. 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 Dec; 181(4):562-3. PubMed ID: 6943407
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  • 5. Roles of poly(ADP-ribose) synthesis in repair and replication in normal human, Cockayne syndrome, and xeroderma pigmentosum fibroblasts after UV irradiation.
    Fujiwara Y, Goto K, Yamamoto K, Ichihashi M.
    Princess Takamatsu Symp; 1983 Dec; 13():209-18. PubMed ID: 6418714
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  • 8. The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndrome.
    Schweiger M, Auer B, Burtscher HJ, Hirsch-Kauffmann M, Klocker H, Schneider R.
    Eur J Biochem; 1987 Jun 01; 165(2):235-42. PubMed ID: 3109898
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  • 9. Cockayne syndrome: clinicopathologic and tissue culture studies of affected siblings.
    Leech RW, Brumback RA, Miller RH, Otsuka F, Tarone RE, Robbins JH.
    J Neuropathol Exp Neurol; 1985 Sep 01; 44(5):507-19. PubMed ID: 4031953
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  • 10. Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy.
    Norris PG, Limb GA, Hamblin AS, Lehmann AR, Arlett CF, Cole J, Waugh AP, Hawk JL.
    J Invest Dermatol; 1990 Jan 01; 94(1):94-100. PubMed ID: 2295840
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  • 11. [Photosensitization and DNA repair. Possible nosologic relationship between Xeroderma pigmentosum and Cockayne's syndrome].
    Lafforet D, Dupuy JM.
    Arch Fr Pediatr; 1978 Dec 01; 35(10 Suppl):65-74. PubMed ID: 749755
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  • 12. Three complementation groups in Cockayne syndrome.
    Lehmann AR.
    Mutat Res; 1982 Dec 01; 106(2):347-56. PubMed ID: 6185841
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  • 13. Ultraviolet light-induced sister chromatid exchanges in xeroderma pigmentosum and in Cockayne's syndrome lymphocyte cell lines.
    Cheng WS, Tarone RE, Andrews AD, Whang-Peng JS, Robbins JH.
    Cancer Res; 1978 Jun 01; 38(6):1601-9. PubMed ID: 647673
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  • 14. 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 01; 41(2):87-96. PubMed ID: 16325378
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  • 15. 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 01; 37(2):107-16. PubMed ID: 8840721
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  • 16. 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 01; 39(2):346-51. PubMed ID: 3956512
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  • 17. Decrease of thymic hormone serum level in Cockayne syndrome.
    Bensman A, Dardenne M, Bach JF, Valleteau de Mouillac J, Lasfargues G.
    Pediatr Res; 1982 Feb 01; 16(2):92-4. PubMed ID: 7058086
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  • 18. 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 01; 50(2):201-7. PubMed ID: 2675138
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  • 19. 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 Aug 01; 20(1-6):124-40. PubMed ID: 648171
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  • 20. A sensitive assay for detecting hypersensitivity to ionizing radiation in lymphoblastoid lines from patients with Duchenne muscular dystrophy and primary neuronal degenerations.
    Tarone RE, Otsuka F, Robbins JH.
    J Neurol Sci; 1984 Sep 01; 65(3):367-81. PubMed ID: 6333487
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