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PUBMED FOR HANDHELDS

Journal Abstract Search


160 related items for PubMed ID: 9639667

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  • 2. Mutagen sensitivity of human lymphoblastoid cells with a BRCA1 mutation in comparison to ataxia telangiectasia heterozygote cells.
    Speit G, Trenz K, Schütz P, Bendix R, Dörk T.
    Cytogenet Cell Genet; 2000; 91(1-4):261-6. PubMed ID: 11173867
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  • 4. Effect of caffeine in G2 on X-ray-induced chromosomal aberrations and mitotic inhibition in ataxia telangiectasia fibroblast and lymphoblastoid cells.
    Hansson K, Natarajan AT, Kihlman BA.
    Hum Genet; 1984; 67(3):329-35. PubMed ID: 6469243
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  • 7. Increased initial levels of chromosome damage and heterogeneous chromosome repair in ataxia telangiectasia heterozygote cells.
    Pandita TK, Hittelman WN.
    Mutat Res; 1994 Oct 01; 310(1):1-13. PubMed ID: 7523872
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  • 8. Modulation of chromatin conformation by the histone deacetylase inhibitor trichostatin A promotes the removal of radiation-induced lesions in ataxia telangiectasia cell lines.
    Egidi A, Filippi S, Manganello F, Lopez-Martinez W, Meschini R.
    Mutat Res Genet Toxicol Environ Mutagen; 2018 Dec 01; 836(Pt A):109-116. PubMed ID: 30389153
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  • 11. Mechanism of protection against radiation-induced DNA damage in plasmid pBR322 by caffeine.
    Kumar SS, Devasagayam TP, Jayashree B, Kesavan PC.
    Int J Radiat Biol; 2001 May 01; 77(5):617-23. PubMed ID: 11382340
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  • 12. Genome instability in ataxia telangiectasia (A-T) families: camptothecin-induced damage to replicating DNA discriminates between obligate A-T heterozygotes, A-T homozygotes and controls.
    Leonard JC, Mullinger AM, Schmidt J, Cordell HJ, Johnson RT.
    Biosci Rep; 2004 Dec 01; 24(6):617-29. PubMed ID: 16158199
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  • 14. Increased frequency of chromatid breaks in lymphocytes of heterozygotes of ataxia telangiectasia after in vitro treatment with caffeine.
    Pawlak AL, Kotecki M, Ignatowicz R.
    Mutat Res; 1990 Jun 01; 230(2):197-204. PubMed ID: 2374556
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  • 15. Elevated frequency of p53-independent apoptosis after irradiation increases levels of DNA breaks in ataxia telangiectasia lymphoblasts.
    Humar B, Müller H, Scott RJ.
    Int J Radiat Biol; 1997 Sep 01; 72(3):257-69. PubMed ID: 9298106
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  • 17. Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives.
    Claes K, Depuydt J, Taylor AM, Last JI, Baert A, Schietecatte P, Vandersickel V, Poppe B, De Leeneer K, D'Hooghe M, Vral A.
    Neuromolecular Med; 2013 Sep 01; 15(3):447-57. PubMed ID: 23632773
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  • 19. Defective modulation of double-strand break repair in ataxia telangiectasia cells by gamma radiation.
    Sikpi MO, Wang Y, Mallya SM.
    Radiat Res; 1998 Dec 01; 150(6):627-35. PubMed ID: 9840182
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  • 20. Rejoining of double strand breaks in normal human and ataxia-telangiectasia fibroblasts after exposure to 60Co gamma-rays, 241Am alpha-particles or bleomycin.
    Coquerelle TM, Weibezahn KF, Lücke-Huhle C.
    Int J Radiat Biol Relat Stud Phys Chem Med; 1987 Feb 01; 51(2):209-18. PubMed ID: 2435666
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