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Journal Abstract Search

144 related items for PubMed ID: 3762565

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  • 3. 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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  • 6. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
    Riou L, Zeng L, Chevallier-Lagente O, Stary A, Nikaido O, Taïeb A, Weeda G, Mezzina M, Sarasin A.
    Hum Mol Genet; 1999 Jun 01; 8(6):1125-33. PubMed ID: 10332046
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  • 7. 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 01; 255(3):281-91. PubMed ID: 1719400
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  • 8. DNA sequence dependence of closely opposed cyclobutyl pyrimidine dimers induced by UV radiation.
    Lam LH, Reynolds RJ.
    Mutat Res; 1987 Jun 01; 178(2):167-76. PubMed ID: 3587252
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  • 9. DNA excision repair in cell extracts from human cell lines exhibiting hypersensitivity to DNA-damaging agents.
    Hansson J, Keyse SM, Lindahl T, Wood RD.
    Cancer Res; 1991 Jul 01; 51(13):3384-90. PubMed ID: 2054778
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  • 15. 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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  • 16. Inherited defects in DNA repair and susceptibility to DNA-damaging agents.
    Hansson J.
    Toxicol Lett; 1992 Dec 15; 64-65 Spec No():141-8. PubMed ID: 1471167
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  • 17. 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 15; 16(5):1003-9. PubMed ID: 7767957
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  • 18. Fibroblasts from patients with Fanconi's anemia are not deficient in excision of thymine dimer.
    Klocker H, Burtscher HJ, Auer B, Hirsch-Kauffmann M, Schweiger M.
    Eur J Cell Biol; 1985 May 15; 37():240-2. PubMed ID: 4029168
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  • 19. Repair in ribosomal RNA genes is deficient in xeroderma pigmentosum group C and in Cockayne's syndrome cells.
    Christians FC, Hanawalt PC.
    Mutat Res; 1994 Apr 15; 323(4):179-87. PubMed ID: 7512688
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