269 related articles for article (PubMed ID: 17492771)
21. Genetic evidence for involvement of two distinct nonhomologous end-joining pathways in repair of topoisomerase II-mediated DNA damage.
Adachi N; Iiizumi S; So S; Koyama H
Biochem Biophys Res Commun; 2004 Jun; 318(4):856-61. PubMed ID: 15147950
[TBL] [Abstract][Full Text] [Related]
22. XRCC4 and XLF form long helical protein filaments suitable for DNA end protection and alignment to facilitate DNA double strand break repair.
Mahaney BL; Hammel M; Meek K; Tainer JA; Lees-Miller SP
Biochem Cell Biol; 2013 Feb; 91(1):31-41. PubMed ID: 23442139
[TBL] [Abstract][Full Text] [Related]
23. Cernunnos/XLF: a new player in DNA double-strand break repair.
Yano K; Morotomi-Yano K; Akiyama H
Int J Biochem Cell Biol; 2009 Jun; 41(6):1237-40. PubMed ID: 18992362
[TBL] [Abstract][Full Text] [Related]
24. Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaks.
Rothkamm K; Kühne M; Jeggo PA; Löbrich M
Cancer Res; 2001 May; 61(10):3886-93. PubMed ID: 11358801
[TBL] [Abstract][Full Text] [Related]
25. Alternative Okazaki Fragment Ligation Pathway by DNA Ligase III.
Arakawa H; Iliakis G
Genes (Basel); 2015 Jun; 6(2):385-98. PubMed ID: 26110316
[TBL] [Abstract][Full Text] [Related]
26. Yeast DNA ligase IV mutations reveal a nonhomologous end joining function of BRCT1 distinct from XRCC4/Lif1 binding.
Chiruvella KK; Renard BM; Birkeland SR; Sunder S; Liang Z; Wilson TE
DNA Repair (Amst); 2014 Dec; 24():37-45. PubMed ID: 25457772
[TBL] [Abstract][Full Text] [Related]
27. APLF promotes the assembly and activity of non-homologous end joining protein complexes.
Grundy GJ; Rulten SL; Zeng Z; Arribas-Bosacoma R; Iles N; Manley K; Oliver A; Caldecott KW
EMBO J; 2013 Jan; 32(1):112-25. PubMed ID: 23178593
[TBL] [Abstract][Full Text] [Related]
28. The embryonic lethality in DNA ligase IV-deficient mice is rescued by deletion of Ku: implications for unifying the heterogeneous phenotypes of NHEJ mutants.
Karanjawala ZE; Adachi N; Irvine RA; Oh EK; Shibata D; Schwarz K; Hsieh CL; Lieber MR
DNA Repair (Amst); 2002 Dec; 1(12):1017-26. PubMed ID: 12531011
[TBL] [Abstract][Full Text] [Related]
29. Histone H1 functions as a stimulatory factor in backup pathways of NHEJ.
Rosidi B; Wang M; Wu W; Sharma A; Wang H; Iliakis G
Nucleic Acids Res; 2008 Mar; 36(5):1610-23. PubMed ID: 18250087
[TBL] [Abstract][Full Text] [Related]
30. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.
Buck D; Moshous D; de Chasseval R; Ma Y; le Deist F; Cavazzana-Calvo M; Fischer A; Casanova JL; Lieber MR; de Villartay JP
Eur J Immunol; 2006 Jan; 36(1):224-35. PubMed ID: 16358361
[TBL] [Abstract][Full Text] [Related]
31. The pathways and outcomes of mycobacterial NHEJ depend on the structure of the broken DNA ends.
Aniukwu J; Glickman MS; Shuman S
Genes Dev; 2008 Feb; 22(4):512-27. PubMed ID: 18281464
[TBL] [Abstract][Full Text] [Related]
32. Human DNA ligases I and III, but not ligase IV, are required for microhomology-mediated end joining of DNA double-strand breaks.
Liang L; Deng L; Nguyen SC; Zhao X; Maulion CD; Shao C; Tischfield JA
Nucleic Acids Res; 2008 Jun; 36(10):3297-310. PubMed ID: 18440984
[TBL] [Abstract][Full Text] [Related]
33. Ligase I and ligase III mediate the DNA double-strand break ligation in alternative end-joining.
Lu G; Duan J; Shu S; Wang X; Gao L; Guo J; Zhang Y
Proc Natl Acad Sci U S A; 2016 Feb; 113(5):1256-60. PubMed ID: 26787905
[TBL] [Abstract][Full Text] [Related]
34. Long-term XPC silencing reduces DNA double-strand break repair.
Despras E; Pfeiffer P; Salles B; Calsou P; Kuhfittig-Kulle S; Angulo JF; Biard DS
Cancer Res; 2007 Mar; 67(6):2526-34. PubMed ID: 17363570
[TBL] [Abstract][Full Text] [Related]
35. Single-stranded DNA ligation and XLF-stimulated incompatible DNA end ligation by the XRCC4-DNA ligase IV complex: influence of terminal DNA sequence.
Gu J; Lu H; Tsai AG; Schwarz K; Lieber MR
Nucleic Acids Res; 2007; 35(17):5755-62. PubMed ID: 17717001
[TBL] [Abstract][Full Text] [Related]
36. Widespread dependence of backup NHEJ on growth state: ramifications for the use of DNA-PK inhibitors.
Singh SK; Wu W; Zhang L; Klammer H; Wang M; Iliakis G
Int J Radiat Oncol Biol Phys; 2011 Feb; 79(2):540-8. PubMed ID: 20950945
[TBL] [Abstract][Full Text] [Related]
37. DNA ligase III and DNA ligase IV carry out genetically distinct forms of end joining in human somatic cells.
Oh S; Harvey A; Zimbric J; Wang Y; Nguyen T; Jackson PJ; Hendrickson EA
DNA Repair (Amst); 2014 Sep; 21():97-110. PubMed ID: 24837021
[TBL] [Abstract][Full Text] [Related]
38. Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair.
Reid DA; Keegan S; Leo-Macias A; Watanabe G; Strande NT; Chang HH; Oksuz BA; Fenyo D; Lieber MR; Ramsden DA; Rothenberg E
Proc Natl Acad Sci U S A; 2015 May; 112(20):E2575-84. PubMed ID: 25941401
[TBL] [Abstract][Full Text] [Related]
39. DNA ligase IV and artemis act cooperatively to suppress homologous recombination in human cells: implications for DNA double-strand break repair.
Kurosawa A; Saito S; So S; Hashimoto M; Iwabuchi K; Watabe H; Adachi N
PLoS One; 2013; 8(8):e72253. PubMed ID: 23967291
[TBL] [Abstract][Full Text] [Related]
40. Dynamic assembly of end-joining complexes requires interaction between Ku70/80 and XRCC4.
Mari PO; Florea BI; Persengiev SP; Verkaik NS; Brüggenwirth HT; Modesti M; Giglia-Mari G; Bezstarosti K; Demmers JA; Luider TM; Houtsmuller AB; van Gent DC
Proc Natl Acad Sci U S A; 2006 Dec; 103(49):18597-602. PubMed ID: 17124166
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
