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135 related items for PubMed ID: 17141189

  • 1. A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage.
    Danoy P, Sonoda E, Lathrop M, Takeda S, Matsuda F.
    Biochem Biophys Res Commun; 2007 Jan 19; 352(3):763-8. PubMed ID: 17141189
    [Abstract] [Full Text] [Related]

  • 2. Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51.
    Silva SN, Tomar M, Paulo C, Gomes BC, Azevedo AP, Teixeira V, Pina JE, Rueff J, Gaspar JF.
    Cancer Epidemiol; 2010 Feb 19; 34(1):85-92. PubMed ID: 20004634
    [Abstract] [Full Text] [Related]

  • 3. Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination.
    Johnson RD, Liu N, Jasin M.
    Nature; 1999 Sep 23; 401(6751):397-9. PubMed ID: 10517641
    [Abstract] [Full Text] [Related]

  • 4. Collaborative roles of gammaH2AX and the Rad51 paralog Xrcc3 in homologous recombinational repair.
    Sonoda E, Zhao GY, Kohzaki M, Dhar PK, Kikuchi K, Redon C, Pilch DR, Bonner WM, Nakano A, Watanabe M, Nakayama T, Takeda S, Takami Y.
    DNA Repair (Amst); 2007 Mar 01; 6(3):280-92. PubMed ID: 17123873
    [Abstract] [Full Text] [Related]

  • 5. Homologous recombination deficiency leads to profound genetic instability in cells derived from Xrcc2-knockout mice.
    Deans B, Griffin CS, O'Regan P, Jasin M, Thacker J.
    Cancer Res; 2003 Dec 01; 63(23):8181-7. PubMed ID: 14678973
    [Abstract] [Full Text] [Related]

  • 6. Xrcc3 is recruited to DNA double strand breaks early and independent of Rad51.
    Forget AL, Bennett BT, Knight KL.
    J Cell Biochem; 2004 Oct 15; 93(3):429-36. PubMed ID: 15372620
    [Abstract] [Full Text] [Related]

  • 7. The RAD51 gene family, genetic instability and cancer.
    Thacker J.
    Cancer Lett; 2005 Mar 10; 219(2):125-35. PubMed ID: 15723711
    [Abstract] [Full Text] [Related]

  • 8. Xrcc3 induces cisplatin resistance by stimulation of Rad51-related recombinational repair, S-phase checkpoint activation, and reduced apoptosis.
    Xu ZY, Loignon M, Han FY, Panasci L, Aloyz R.
    J Pharmacol Exp Ther; 2005 Aug 10; 314(2):495-505. PubMed ID: 15843498
    [Abstract] [Full Text] [Related]

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  • 10. Genetic interactions between RAD51 and its paralogues for centrosome fragmentation and ploidy control, independently of the sensitivity to genotoxic stresses.
    Daboussi F, Thacker J, Lopez BS.
    Oncogene; 2005 May 19; 24(22):3691-6. PubMed ID: 15782136
    [Abstract] [Full Text] [Related]

  • 11. Variant XRCC3 implicated in cancer is functional in homology-directed repair of double-strand breaks.
    Araujo FD, Pierce AJ, Stark JM, Jasin M.
    Oncogene; 2002 Jun 13; 21(26):4176-80. PubMed ID: 12037675
    [Abstract] [Full Text] [Related]

  • 12. A tumour-derived mutant allele of XRCC2 preferentially suppresses homologous recombination at DNA replication forks.
    Mohindra A, Bolderson E, Stone J, Wells M, Helleday T, Meuth M.
    Hum Mol Genet; 2004 Jan 15; 13(2):203-12. PubMed ID: 14645207
    [Abstract] [Full Text] [Related]

  • 13. Polymorphism of the homologous recombination repair genes RAD51 and XRCC3 in breast cancer.
    Krupa R, Synowiec E, Pawlowska E, Morawiec Z, Sobczuk A, Zadrozny M, Wozniak K, Blasiak J.
    Exp Mol Pathol; 2009 Aug 15; 87(1):32-5. PubMed ID: 19426727
    [Abstract] [Full Text] [Related]

  • 14. Ablation of XRCC2/3 transforms immunoglobulin V gene conversion into somatic hypermutation.
    Sale JE, Calandrini DM, Takata M, Takeda S, Neuberger MS.
    Nature; 2001 Aug 30; 412(6850):921-6. PubMed ID: 11528482
    [Abstract] [Full Text] [Related]

  • 15. Single nucleotide polymorphisms of RAD51 G135C, XRCC2 Arg188His and XRCC3 Thr241Met homologous recombination repair genes and the risk of sporadic endometrial cancer in Polish women.
    Romanowicz-Makowska H, Smolarz B, Połać I, Sporny S.
    J Obstet Gynaecol Res; 2012 Jun 30; 38(6):918-24. PubMed ID: 22487057
    [Abstract] [Full Text] [Related]

  • 16. Increased risk of differentiated thyroid carcinoma with combined effects of homologous recombination repair gene polymorphisms in an Iranian population.
    Fayaz S, Karimmirza M, Tanhaei S, Fathi M, Torbati PM, Fard-Esfahani P.
    Asian Pac J Cancer Prev; 2014 Jan 30; 14(11):6727-31. PubMed ID: 24377596
    [Abstract] [Full Text] [Related]

  • 17. A homologous recombination defect affects replication-fork progression in mammalian cells.
    Daboussi F, Courbet S, Benhamou S, Kannouche P, Zdzienicka MZ, Debatisse M, Lopez BS.
    J Cell Sci; 2008 Jan 15; 121(Pt 2):162-6. PubMed ID: 18089650
    [Abstract] [Full Text] [Related]

  • 18. Dual roles for DNA polymerase eta in homologous DNA recombination and translesion DNA synthesis.
    Kawamoto T, Araki K, Sonoda E, Yamashita YM, Harada K, Kikuchi K, Masutani C, Hanaoka F, Nozaki K, Hashimoto N, Takeda S.
    Mol Cell; 2005 Dec 09; 20(5):793-9. PubMed ID: 16337602
    [Abstract] [Full Text] [Related]

  • 19. Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs.
    Takata M, Sasaki MS, Tachiiri S, Fukushima T, Sonoda E, Schild D, Thompson LH, Takeda S.
    Mol Cell Biol; 2001 Apr 09; 21(8):2858-66. PubMed ID: 11283264
    [Abstract] [Full Text] [Related]

  • 20. Differential and collaborative actions of Rad51 paralog proteins in cellular response to DNA damage.
    Yonetani Y, Hochegger H, Sonoda E, Shinya S, Yoshikawa H, Takeda S, Yamazoe M.
    Nucleic Acids Res; 2005 Apr 09; 33(14):4544-52. PubMed ID: 16093548
    [Abstract] [Full Text] [Related]

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