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PUBMED FOR HANDHELDS

Journal Abstract Search


205 related items for PubMed ID: 1372469

  • 21. DNA repair and replication in xeroderma pigmentosum and related disorders.
    Cleaver JE.
    Basic Life Sci; 1986; 39():425-38. PubMed ID: 3767846
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  • 22. 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; 56(1):167-74. PubMed ID: 7825573
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  • 23. 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 Jan; 14(1):9-22. PubMed ID: 10447254
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  • 24. Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.
    Kondo D, Noguchi A, Tamura H, Tsuchida S, Takahashi I, Kubota H, Yano T, Oyama C, Sawaishi Y, Moriwaki S, Takahashi T.
    Tohoku J Exp Med; 2016 Jul; 239(3):231-5. PubMed ID: 27396511
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  • 25. Xeroderma pigmentosum--bridging a gap between clinic and laboratory.
    Moriwaki S, Kraemer KH.
    Photodermatol Photoimmunol Photomed; 2001 Apr; 17(2):47-54. PubMed ID: 11338401
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  • 26. Human DNA repair disorders in dermatology: A historical perspective, current concepts and new insight.
    Moriwaki S.
    J Dermatol Sci; 2016 Feb; 81(2):77-84. PubMed ID: 26493104
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  • 27. 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; 166(1):99-111. PubMed ID: 3014327
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  • 30. 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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  • 31. 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 25; 33(7):607-10. PubMed ID: 8818951
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  • 34. 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 25; 37(2):107-16. PubMed ID: 8840721
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  • 35. Xeroderma pigmentosum-Cockayne syndrome complex.
    Natale V, Raquer H.
    Orphanet J Rare Dis; 2017 Apr 04; 12(1):65. PubMed ID: 28376890
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  • 37. Cancer in xeroderma pigmentosum and related disorders of DNA repair.
    Cleaver JE.
    Nat Rev Cancer; 2005 Jul 04; 5(7):564-73. PubMed ID: 16069818
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  • 40. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.
    Kraemer KH, Patronas NJ, Schiffmann R, Brooks BP, Tamura D, DiGiovanna JJ.
    Neuroscience; 2007 Apr 14; 145(4):1388-96. PubMed ID: 17276014
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