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Journal Abstract Search

263 related items for PubMed ID: 7513056

  • 1. 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; 314(3):233-48. PubMed ID: 7513056
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  • 6. [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 May; 38(8):863-8. PubMed ID: 9027016
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  • 7. Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genes.
    Carreau M, Eveno E, Quilliet X, Chevalier-Lagente O, Benoit A, Tanganelli B, Stefanini M, Vermeulen W, Hoeijmakers JH, Sarasin A.
    Carcinogenesis; 1995 May; 16(5):1003-9. PubMed ID: 7767957
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  • 10. 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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  • 12. Incomplete complementation of the DNA repair defect in cockayne syndrome cells by the denV gene from bacteriophage T4 suggests a deficiency in base excision repair.
    Francis MA, Bagga PS, Athwal RS, Rainbow AJ.
    Mutat Res; 1997 Oct 28; 385(1):59-74. PubMed ID: 9372849
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  • 14. Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A.
    Itoh T, Shiomi T, Shiomi N, Harada Y, Wakasugi M, Matsunaga T, Nikaido O, Friedberg EC, Yamaizumi M.
    Mutat Res; 1996 Feb 15; 362(2):167-74. PubMed ID: 8596535
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  • 15. Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
    Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA.
    Am J Hum Genet; 1992 Apr 15; 50(4):677-89. PubMed ID: 1372469
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  • 16. Cockayne syndrome in two adult siblings.
    Miyauchi H, Horio T, Akaeda T, Asada Y, Chang HR, Ishizaki K, Ikenaga M.
    J Am Acad Dermatol; 1994 Feb 15; 30(2 Pt 2):329-35. PubMed ID: 8294592
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  • 17. Cockayne syndrome without typical clinical manifestations including neurologic abnormalities.
    Miyauchi-Hashimoto H, Akaeda T, Maihara T, Ikenaga M, Horio T.
    J Am Acad Dermatol; 1998 Oct 15; 39(4 Pt 1):565-70. PubMed ID: 9777763
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  • 18. 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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