89 related articles for article (PubMed ID: 22657828)
21. The HRDC domain oppositely modulates the unwinding activity of E. coli RecQ helicase on duplex DNA and G-quadruplex.
Teng FY; Wang TT; Guo HL; Xin BG; Sun B; Dou SX; Xi XG; Hou XM
J Biol Chem; 2020 Dec; 295(51):17646-17658. PubMed ID: 33454004
[TBL] [Abstract][Full Text] [Related]
22. Bi-directional routing of DNA mismatch repair protein human exonuclease 1 to replication foci and DNA double strand breaks.
Liberti SE; Andersen SD; Wang J; May A; Miron S; Perderiset M; Keijzers G; Nielsen FC; Charbonnier JB; Bohr VA; Rasmussen LJ
DNA Repair (Amst); 2011 Jan; 10(1):73-86. PubMed ID: 20970388
[TBL] [Abstract][Full Text] [Related]
23. Werner helicase wings DNA binding.
Hoadley KA; Keck JL
Structure; 2010 Feb; 18(2):149-51. PubMed ID: 20159459
[TBL] [Abstract][Full Text] [Related]
24. Conferring substrate specificity to DNA helicases: role of the RecQ HRDC domain.
Bernstein DA; Keck JL
Structure; 2005 Aug; 13(8):1173-82. PubMed ID: 16084389
[TBL] [Abstract][Full Text] [Related]
25. The Werner Syndrome Helicase Coordinates Sequential Strand Displacement and FEN1-Mediated Flap Cleavage during Polymerase δ Elongation.
Li B; Reddy S; Comai L
Mol Cell Biol; 2017 Feb; 37(3):. PubMed ID: 27849570
[TBL] [Abstract][Full Text] [Related]
26. Cellular dynamics and modulation of WRN protein is DNA damage specific.
Karmakar P; Bohr VA
Mech Ageing Dev; 2005 Nov; 126(11):1146-58. PubMed ID: 16087220
[TBL] [Abstract][Full Text] [Related]
27. The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta.
Harrigan JA; Wilson DM; Prasad R; Opresko PL; Beck G; May A; Wilson SH; Bohr VA
Nucleic Acids Res; 2006; 34(2):745-54. PubMed ID: 16449207
[TBL] [Abstract][Full Text] [Related]
28. Depletion of WRN enhances DNA damage in HeLa cells exposed to the benzene metabolite, hydroquinone.
Galván N; Lim S; Zmugg S; Smith MT; Zhang L
Mutat Res; 2008 Jan; 649(1-2):54-61. PubMed ID: 17875398
[TBL] [Abstract][Full Text] [Related]
29. Mechanistic insight into the interaction of BLM helicase with intra-strand G-quadruplex structures.
Chatterjee S; Zagelbaum J; Savitsky P; Sturzenegger A; Huttner D; Janscak P; Hickson ID; Gileadi O; Rothenberg E
Nat Commun; 2014 Nov; 5():5556. PubMed ID: 25418155
[TBL] [Abstract][Full Text] [Related]
30. The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage.
Jiao R; Harrigan JA; Shevelev I; Dietschy T; Selak N; Indig FE; Piotrowski J; Janscak P; Bohr VA; Stagljar I
Oncogene; 2007 May; 26(26):3811-22. PubMed ID: 17173071
[TBL] [Abstract][Full Text] [Related]
31. Werner syndrome protein prevents DNA breaks upon chromatin structure alteration.
Turaga RV; Massip L; Chavez A; Johnson FB; Lebel M
Aging Cell; 2007 Aug; 6(4):471-81. PubMed ID: 17521388
[TBL] [Abstract][Full Text] [Related]
32. Werner and Bloom helicases are involved in DNA repair in a complementary fashion.
Imamura O; Fujita K; Itoh C; Takeda S; Furuichi Y; Matsumoto T
Oncogene; 2002 Jan; 21(6):954-63. PubMed ID: 11840341
[TBL] [Abstract][Full Text] [Related]
33. DNA-dependent protein kinase (DNA-PK)-dependent cisplatin-induced loss of nucleolar facilitator of chromatin transcription (FACT) and regulation of cisplatin sensitivity by DNA-PK and FACT.
Dejmek J; Iglehart JD; Lazaro JB
Mol Cancer Res; 2009 Apr; 7(4):581-91. PubMed ID: 19372586
[TBL] [Abstract][Full Text] [Related]
34. Functional analysis of helicase and three tandem HRDC domains of RecQ in Deinococcus radiodurans.
Huang LF; Hua XT; Lu HM; Gao GJ; Tian B; Shen BH; Hua YJ
J Zhejiang Univ Sci B; 2006 May; 7(5):373-6. PubMed ID: 16615167
[TBL] [Abstract][Full Text] [Related]
35. The Werner syndrome protein confers resistance to the DNA lesions N3-methyladenine and O6-methylguanine: implications for WRN function.
Blank A; Bobola MS; Gold B; Varadarajan S; D Kolstoe D; Meade EH; Rabinovitch PS; Loeb LA; Silber JR
DNA Repair (Amst); 2004 Jun; 3(6):629-38. PubMed ID: 15135730
[TBL] [Abstract][Full Text] [Related]
36. Crystal structure of the Bloom's syndrome helicase indicates a role for the HRDC domain in conformational changes.
Newman JA; Savitsky P; Allerston CK; Bizard AH; Özer Ö; Sarlós K; Liu Y; Pardon E; Steyaert J; Hickson ID; Gileadi O
Nucleic Acids Res; 2015 May; 43(10):5221-35. PubMed ID: 25901030
[TBL] [Abstract][Full Text] [Related]
37. Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases.
Ouyang KJ; Woo LL; Ellis NA
Mech Ageing Dev; 2008; 129(7-8):425-40. PubMed ID: 18430459
[TBL] [Abstract][Full Text] [Related]
38. Structure of the RecQ C-terminal domain of human Bloom syndrome protein.
Kim SY; Hakoshima T; Kitano K
Sci Rep; 2013 Nov; 3():3294. PubMed ID: 24257077
[TBL] [Abstract][Full Text] [Related]
39. Expression and localization of Werner syndrome protein is modulated by SIRT1 and PML.
Vaitiekunaite R; Butkiewicz D; Krześniak M; Przybyłek M; Gryc A; Snietura M; Benedyk M; Harris CC; Rusin M
Mech Ageing Dev; 2007; 128(11-12):650-61. PubMed ID: 17996922
[TBL] [Abstract][Full Text] [Related]
40. Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein.
von Kobbe C; Harrigan JA; Schreiber V; Stiegler P; Piotrowski J; Dawut L; Bohr VA
Nucleic Acids Res; 2004; 32(13):4003-14. PubMed ID: 15292449
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]