351 related articles for article (PubMed ID: 27922005)
41. Repair of protein-linked DNA double strand breaks: Using the adenovirus genome as a model substrate in cell-based assays.
Lamarche BJ; Orazio NI; Goben B; Meisenhelder J; You Z; Weitzman MD; Hunter T
DNA Repair (Amst); 2019 Feb; 74():80-90. PubMed ID: 30583959
[TBL] [Abstract][Full Text] [Related]
42. Telomere-Internal Double-Strand Breaks Are Repaired by Homologous Recombination and PARP1/Lig3-Dependent End-Joining.
Doksani Y; de Lange T
Cell Rep; 2016 Nov; 17(6):1646-1656. PubMed ID: 27806302
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. CtIP-Mediated Fork Protection Synergizes with BRCA1 to Suppress Genomic Instability upon DNA Replication Stress.
Przetocka S; Porro A; Bolck HA; Walker C; Lezaja A; Trenner A; von Aesch C; Himmels SF; D'Andrea AD; Ceccaldi R; Altmeyer M; Sartori AA
Mol Cell; 2018 Nov; 72(3):568-582.e6. PubMed ID: 30344097
[TBL] [Abstract][Full Text] [Related]
45. The Deubiquitylating Enzyme USP4 Cooperates with CtIP in DNA Double-Strand Break End Resection.
Liu H; Zhang H; Wang X; Tian Q; Hu Z; Peng C; Jiang P; Wang T; Guo W; Chen Y; Li X; Zhang P; Pei H
Cell Rep; 2015 Oct; 13(1):93-107. PubMed ID: 26387952
[TBL] [Abstract][Full Text] [Related]
46. DNA repair kinetics in SCID mice Sertoli cells and DNA-PKcs-deficient mouse embryonic fibroblasts.
Ahmed EA; Vélaz E; Rosemann M; Gilbertz KP; Scherthan H
Chromosoma; 2017 Mar; 126(2):287-298. PubMed ID: 27136939
[TBL] [Abstract][Full Text] [Related]
47. Subtelomeric regions in mammalian cells are deficient in DNA double-strand break repair.
Miller D; Reynolds GE; Mejia R; Stark JM; Murnane JP
DNA Repair (Amst); 2011 May; 10(5):536-44. PubMed ID: 21466975
[TBL] [Abstract][Full Text] [Related]
48. Pharmacological targeting of differential DNA repair, radio-sensitizes WRN-deficient cancer cells in vitro and in vivo.
Gupta P; Saha B; Chattopadhyay S; Patro BS
Biochem Pharmacol; 2021 Apr; 186():114450. PubMed ID: 33571504
[TBL] [Abstract][Full Text] [Related]
49. Neddylation inhibits CtIP-mediated resection and regulates DNA double strand break repair pathway choice.
Jimeno S; Fernández-Ávila MJ; Cruz-García A; Cepeda-García C; Gómez-Cabello D; Huertas P
Nucleic Acids Res; 2015 Jan; 43(2):987-99. PubMed ID: 25567988
[TBL] [Abstract][Full Text] [Related]
50. The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2.
Opresko PL; Otterlei M; Graakjaer J; Bruheim P; Dawut L; Kølvraa S; May A; Seidman MM; Bohr VA
Mol Cell; 2004 Jun; 14(6):763-74. PubMed ID: 15200954
[TBL] [Abstract][Full Text] [Related]
51. Exonuclease function of human Mre11 promotes deletional nonhomologous end joining.
Zhuang J; Jiang G; Willers H; Xia F
J Biol Chem; 2009 Oct; 284(44):30565-73. PubMed ID: 19744924
[TBL] [Abstract][Full Text] [Related]
52. AUNIP/C1orf135 directs DNA double-strand breaks towards the homologous recombination repair pathway.
Lou J; Chen H; Han J; He H; Huen MSY; Feng XH; Liu T; Huang J
Nat Commun; 2017 Oct; 8(1):985. PubMed ID: 29042561
[TBL] [Abstract][Full Text] [Related]
53. Werner Syndrome Protein and DNA Replication.
Mukherjee S; Sinha D; Bhattacharya S; Srinivasan K; Abdisalaam S; Asaithamby A
Int J Mol Sci; 2018 Nov; 19(11):. PubMed ID: 30400178
[TBL] [Abstract][Full Text] [Related]
54. WRN is recruited to damaged telomeres via its RQC domain and tankyrase1-mediated poly-ADP-ribosylation of TRF1.
Sun L; Nakajima S; Teng Y; Chen H; Yang L; Chen X; Gao B; Levine AS; Lan L
Nucleic Acids Res; 2017 Apr; 45(7):3844-3859. PubMed ID: 28158503
[TBL] [Abstract][Full Text] [Related]
55. Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in
Emerson CH; Lopez CR; Ribes-Zamora A; Polleys EJ; Williams CL; Yeo L; Zaneveld JE; Chen R; Bertuch AA
Genetics; 2018 May; 209(1):115-128. PubMed ID: 29500182
[TBL] [Abstract][Full Text] [Related]
56. The DNA damage response at dysfunctional telomeres, and at interstitial and subtelomeric DNA double-strand breaks.
Muraki K; Murnane JP
Genes Genet Syst; 2018 Jan; 92(3):135-152. PubMed ID: 29162774
[TBL] [Abstract][Full Text] [Related]
57. Vitamin C alters the amount of specific endoplasmic reticulum associated proteins involved in lipid metabolism in the liver of mice synthesizing a nonfunctional Werner syndrome (Wrn) mutant protein.
Aumailley L; Roux-Dalvai F; Kelly I; Droit A; Lebel M
PLoS One; 2018; 13(3):e0193170. PubMed ID: 29494634
[TBL] [Abstract][Full Text] [Related]
58. Phosphorylated CtIP Functions as a Co-factor of the MRE11-RAD50-NBS1 Endonuclease in DNA End Resection.
Anand R; Ranjha L; Cannavo E; Cejka P
Mol Cell; 2016 Dec; 64(5):940-950. PubMed ID: 27889449
[TBL] [Abstract][Full Text] [Related]
59. POT1 inhibits the efficiency but promotes the fidelity of nonhomologous end joining at non-telomeric DNA regions.
Yu Y; Tan R; Ren Q; Gao B; Sheng Z; Zhang J; Zheng X; Jiang Y; Lan L; Mao Z
Aging (Albany NY); 2017 Dec; 9(12):2529-2543. PubMed ID: 29227966
[TBL] [Abstract][Full Text] [Related]
60. Werner syndrome protein: functions in the response to DNA damage and replication stress in S-phase.
Cheng WH; Muftuoglu M; Bohr VA
Exp Gerontol; 2007 Sep; 42(9):871-8. PubMed ID: 17587522
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]