BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

363 related articles for article (PubMed ID: 25916843)

  • 1. Ectopic expression of RNF168 and 53BP1 increases mutagenic but not physiological non-homologous end joining.
    Zong D; Callén E; Pegoraro G; Lukas C; Lukas J; Nussenzweig A
    Nucleic Acids Res; 2015 May; 43(10):4950-61. PubMed ID: 25916843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 53BP1 mediates productive and mutagenic DNA repair through distinct phosphoprotein interactions.
    Callen E; Di Virgilio M; Kruhlak MJ; Nieto-Soler M; Wong N; Chen HT; Faryabi RB; Polato F; Santos M; Starnes LM; Wesemann DR; Lee JE; Tubbs A; Sleckman BP; Daniel JA; Ge K; Alt FW; Fernandez-Capetillo O; Nussenzweig MC; Nussenzweig A
    Cell; 2013 Jun; 153(6):1266-80. PubMed ID: 23727112
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tumors overexpressing RNF168 show altered DNA repair and responses to genotoxic treatments, genomic instability and resistance to proteotoxic stress.
    Chroma K; Mistrik M; Moudry P; Gursky J; Liptay M; Strauss R; Skrott Z; Vrtel R; Bartkova J; Kramara J; Bartek J
    Oncogene; 2017 Apr; 36(17):2405-2422. PubMed ID: 27841863
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The RNF8 and RNF168 Ubiquitin Ligases Regulate Pro- and Anti-Resection Activities at Broken DNA Ends During Non-Homologous End Joining.
    Chen BR; Wang Y; Shen ZJ; Bennett A; Hindi I; Tyler JK; Sleckman BP
    DNA Repair (Amst); 2021 Dec; 108():103217. PubMed ID: 34481157
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DNA Repair Network Analysis Reveals Shieldin as a Key Regulator of NHEJ and PARP Inhibitor Sensitivity.
    Gupta R; Somyajit K; Narita T; Maskey E; Stanlie A; Kremer M; Typas D; Lammers M; Mailand N; Nussenzweig A; Lukas J; Choudhary C
    Cell; 2018 May; 173(4):972-988.e23. PubMed ID: 29656893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The ASCIZ-DYNLL1 axis promotes 53BP1-dependent non-homologous end joining and PARP inhibitor sensitivity.
    Becker JR; Cuella-Martin R; Barazas M; Liu R; Oliveira C; Oliver AW; Bilham K; Holt AB; Blackford AN; Heierhorst J; Jonkers J; Rottenberg S; Chapman JR
    Nat Commun; 2018 Dec; 9(1):5406. PubMed ID: 30559443
    [TBL] [Abstract][Full Text] [Related]  

  • 7. REV7 counteracts DNA double-strand break resection and affects PARP inhibition.
    Xu G; Chapman JR; Brandsma I; Yuan J; Mistrik M; Bouwman P; Bartkova J; Gogola E; Warmerdam D; Barazas M; Jaspers JE; Watanabe K; Pieterse M; Kersbergen A; Sol W; Celie PHN; Schouten PC; van den Broek B; Salman A; Nieuwland M; de Rink I; de Ronde J; Jalink K; Boulton SJ; Chen J; van Gent DC; Bartek J; Jonkers J; Borst P; Rottenberg S
    Nature; 2015 May; 521(7553):541-544. PubMed ID: 25799992
    [TBL] [Abstract][Full Text] [Related]  

  • 8. RIF1 is essential for 53BP1-dependent nonhomologous end joining and suppression of DNA double-strand break resection.
    Chapman JR; Barral P; Vannier JB; Borel V; Steger M; Tomas-Loba A; Sartori AA; Adams IR; Batista FD; Boulton SJ
    Mol Cell; 2013 Mar; 49(5):858-71. PubMed ID: 23333305
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 53BP1 regulates DSB repair using Rif1 to control 5' end resection.
    Zimmermann M; Lottersberger F; Buonomo SB; Sfeir A; de Lange T
    Science; 2013 Feb; 339(6120):700-4. PubMed ID: 23306437
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Remodeling and spacing factor 1 (RSF1) deposits centromere proteins at DNA double-strand breaks to promote non-homologous end-joining.
    Helfricht A; Wiegant WW; Thijssen PE; Vertegaal AC; Luijsterburg MS; van Attikum H
    Cell Cycle; 2013 Sep; 12(18):3070-82. PubMed ID: 23974106
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regulation of DNA repair in the absence of classical non-homologous end joining.
    Kang YJ; Yan CT
    DNA Repair (Amst); 2018 Aug; 68():34-40. PubMed ID: 29929045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Roles for 53BP1 in the repair of radiation-induced DNA double strand breaks.
    Shibata A; Jeggo PA
    DNA Repair (Amst); 2020 Sep; 93():102915. PubMed ID: 33087281
    [TBL] [Abstract][Full Text] [Related]  

  • 13. RING finger nuclear factor RNF168 is important for defects in homologous recombination caused by loss of the breast cancer susceptibility factor BRCA1.
    Muñoz MC; Laulier C; Gunn A; Cheng A; Robbiani DF; Nussenzweig A; Stark JM
    J Biol Chem; 2012 Nov; 287(48):40618-28. PubMed ID: 23055523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Regulation of repair pathway choice at two-ended DNA double-strand breaks.
    Shibata A
    Mutat Res; 2017 Oct; 803-805():51-55. PubMed ID: 28781144
    [TBL] [Abstract][Full Text] [Related]  

  • 15. BARD1 reads H2A lysine 15 ubiquitination to direct homologous recombination.
    Becker JR; Clifford G; Bonnet C; Groth A; Wilson MD; Chapman JR
    Nature; 2021 Aug; 596(7872):433-437. PubMed ID: 34321663
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ING3 is required for ATM signaling and DNA repair in response to DNA double strand breaks.
    Mouche A; Archambeau J; Ricordel C; Chaillot L; Bigot N; Guillaudeux T; Grenon M; Pedeux R
    Cell Death Differ; 2019 Nov; 26(11):2344-2357. PubMed ID: 30804473
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regulation of DNA double-strand break repair pathway choice: a new focus on 53BP1.
    Zhang F; Gong Z
    J Zhejiang Univ Sci B; 2021 Jan; 22(1):38-46. PubMed ID: 33448186
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Roles for the DNA-PK complex and 53BP1 in protecting ends from resection during DNA double-strand break repair.
    Shibata A; Jeggo PA
    J Radiat Res; 2020 Sep; 61(5):718-726. PubMed ID: 32779701
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alternative end-joining and classical nonhomologous end-joining pathways repair different types of double-strand breaks during class-switch recombination.
    Cortizas EM; Zahn A; Hajjar ME; Patenaude AM; Di Noia JM; Verdun RE
    J Immunol; 2013 Dec; 191(11):5751-63. PubMed ID: 24146042
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic instability, defective spermatogenesis, immunodeficiency, and cancer in a mouse model of the RIDDLE syndrome.
    Bohgaki T; Bohgaki M; Cardoso R; Panier S; Zeegers D; Li L; Stewart GS; Sanchez O; Hande MP; Durocher D; Hakem A; Hakem R
    PLoS Genet; 2011 Apr; 7(4):e1001381. PubMed ID: 21552324
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.