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Journal Abstract Search

103 related items for PubMed ID: 17336596

  • 1. Analysis of DNA repair and recombination responses in mouse cells depleted for Brca2 by SiRNA.
    Lee SA, Baker MD.
    DNA Repair (Amst); 2007 Jun 01; 6(6):809-17. PubMed ID: 17336596
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  • 3. Homozygous germ line mutation in exon 27 of murine Brca2 disrupts the Fancd2-Brca2 pathway in the homologous recombination-mediated DNA interstrand cross-links' repair but does not affect meiosis.
    Atanassov BS, Barrett JC, Davis BJ.
    Genes Chromosomes Cancer; 2005 Dec 01; 44(4):429-37. PubMed ID: 16127665
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  • 7. Lower level of BRCA2 protein in heterozygous mutation carriers is correlated with an increase in DNA double strand breaks and an impaired DSB repair.
    Arnold K, Kim MK, Frerk K, Edler L, Savelyeva L, Schmezer P, Wiedemeyer R.
    Cancer Lett; 2006 Nov 08; 243(1):90-100. PubMed ID: 16448746
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  • 8. Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice.
    Donoho G, Brenneman MA, Cui TX, Donoviel D, Vogel H, Goodwin EH, Chen DJ, Hasty P.
    Genes Chromosomes Cancer; 2003 Apr 08; 36(4):317-31. PubMed ID: 12619154
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  • 11. Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.
    Godthelp BC, van Buul PP, Jaspers NG, Elghalbzouri-Maghrani E, van Duijn-Goedhart A, Arwert F, Joenje H, Zdzienicka MZ.
    Mutat Res; 2006 Oct 10; 601(1-2):191-201. PubMed ID: 16920162
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  • 12. Strand invasion involving short tract gene conversion is specifically suppressed in BRCA2-deficient hamster cells.
    Saleh-Gohari N, Helleday T.
    Oncogene; 2004 Dec 02; 23(56):9136-41. PubMed ID: 15480413
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  • 13. Phenotypic effects of heterozygosity for a BRCA2 mutation.
    Warren M, Lord CJ, Masabanda J, Griffin D, Ashworth A.
    Hum Mol Genet; 2003 Oct 15; 12(20):2645-56. PubMed ID: 12928478
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  • 14. Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human genomic disorders.
    Sankaranarayanan K, Wassom JS.
    Mutat Res; 2005 Oct 15; 578(1-2):333-70. PubMed ID: 16084534
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  • 15. New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant.
    Tebbs RS, Hinz JM, Yamada NA, Wilson JB, Salazar EP, Thomas CB, Jones IM, Jones NJ, Thompson LH.
    DNA Repair (Amst); 2005 Jan 02; 4(1):11-22. PubMed ID: 15533833
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  • 16. BRCA2: a universal recombinase regulator.
    Thorslund T, West SC.
    Oncogene; 2007 Dec 10; 26(56):7720-30. PubMed ID: 18066084
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  • 17. BRCA1 regulates RAD51 function in response to DNA damage and suppresses spontaneous sister chromatid replication slippage: implications for sister chromatid cohesion, genome stability, and carcinogenesis.
    Cousineau I, Abaji C, Belmaaza A.
    Cancer Res; 2005 Dec 15; 65(24):11384-91. PubMed ID: 16357146
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  • 18. Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage-dependent recombination.
    Budzowska M, Jaspers I, Essers J, de Waard H, van Drunen E, Hanada K, Beverloo B, Hendriks RW, de Klein A, Kanaar R, Hoeijmakers JH, Maas A.
    EMBO J; 2004 Sep 01; 23(17):3548-58. PubMed ID: 15297881
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  • 19. Endogenous levels of Rad51 and Brca2 are required for homologous recombination and regulated by homeostatic re-balancing.
    Magwood AC, Malysewich MJ, Cealic I, Mundia MM, Knapp J, Baker MD.
    DNA Repair (Amst); 2013 Dec 01; 12(12):1122-33. PubMed ID: 24210700
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  • 20. Overexpression of Rad51 inhibits double-strand break-induced homologous recombination but does not affect gene conversion tract lengths.
    Paffett KS, Clikeman JA, Palmer S, Nickoloff JA.
    DNA Repair (Amst); 2005 Jun 08; 4(6):687-98. PubMed ID: 15878310
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