208 related articles for article (PubMed ID: 17563354)
1. Werner syndrome protein interacts functionally with translesion DNA polymerases.
Kamath-Loeb AS; Lan L; Nakajima S; Yasui A; Loeb LA
Proc Natl Acad Sci U S A; 2007 Jun; 104(25):10394-9. PubMed ID: 17563354
[TBL] [Abstract][Full Text] [Related]
2. WRN exonuclease imparts high fidelity on translesion synthesis by Y family DNA polymerases.
Yoon JH; Sellamuthu K; Prakash L; Prakash S
Genes Dev; 2024 Apr; 38(5-6):213-232. PubMed ID: 38503516
[TBL] [Abstract][Full Text] [Related]
3. WRN participates in translesion synthesis pathway through interaction with NBS1.
Kobayashi J; Okui M; Asaithamby A; Burma S; Chen BP; Tanimoto K; Matsuura S; Komatsu K; Chen DJ
Mech Ageing Dev; 2010 Jun; 131(6):436-44. PubMed ID: 20600238
[TBL] [Abstract][Full Text] [Related]
4. Functional interaction between the Werner Syndrome protein and DNA polymerase delta.
Kamath-Loeb AS; Johansson E; Burgers PM; Loeb LA
Proc Natl Acad Sci U S A; 2000 Apr; 97(9):4603-8. PubMed ID: 10781066
[TBL] [Abstract][Full Text] [Related]
5. The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer.
Compton SA; Tolun G; Kamath-Loeb AS; Loeb LA; Griffith JD
J Biol Chem; 2008 Sep; 283(36):24478-83. PubMed ID: 18596042
[TBL] [Abstract][Full Text] [Related]
6. Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage.
Machwe A; Lozada E; Wold MS; Li GM; Orren DK
J Biol Chem; 2011 Feb; 286(5):3497-508. PubMed ID: 21107010
[TBL] [Abstract][Full Text] [Related]
7. The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δ.
Kamath-Loeb AS; Shen JC; Schmitt MW; Loeb LA
J Biol Chem; 2012 Apr; 287(15):12480-90. PubMed ID: 22351772
[TBL] [Abstract][Full Text] [Related]
8. The Werner's Syndrome protein collaborates with REV1 to promote replication fork progression on damaged DNA.
Phillips LG; Sale JE
DNA Repair (Amst); 2010 Oct; 9(10):1064-72. PubMed ID: 20691646
[TBL] [Abstract][Full Text] [Related]
9. The Werner syndrome protein functions in repair of Cr(VI)-induced replication-associated DNA damage.
Liu FJ; Barchowsky A; Opresko PL
Toxicol Sci; 2009 Aug; 110(2):307-18. PubMed ID: 19487340
[TBL] [Abstract][Full Text] [Related]
10. Replication fork regression in vitro by the Werner syndrome protein (WRN): holliday junction formation, the effect of leading arm structure and a potential role for WRN exonuclease activity.
Machwe A; Xiao L; Lloyd RG; Bolt E; Orren DK
Nucleic Acids Res; 2007; 35(17):5729-47. PubMed ID: 17717003
[TBL] [Abstract][Full Text] [Related]
11. The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest.
Sidorova JM; Li N; Folch A; Monnat RJ
Cell Cycle; 2008 Mar; 7(6):796-807. PubMed ID: 18250621
[TBL] [Abstract][Full Text] [Related]
12. The Werner syndrome protein limits the error-prone 8-oxo-dG lesion bypass activity of human DNA polymerase kappa.
Maddukuri L; Ketkar A; Eddy S; Zafar MK; Eoff RL
Nucleic Acids Res; 2014 Oct; 42(19):12027-40. PubMed ID: 25294835
[TBL] [Abstract][Full Text] [Related]
13. Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing.
Kusumoto R; Dawut L; Marchetti C; Wan Lee J; Vindigni A; Ramsden D; Bohr VA
Biochemistry; 2008 Jul; 47(28):7548-56. PubMed ID: 18558713
[TBL] [Abstract][Full Text] [Related]
14. Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence.
Kamath-Loeb AS; Loeb LA; Johansson E; Burgers PM; Fry M
J Biol Chem; 2001 May; 276(19):16439-46. PubMed ID: 11279038
[TBL] [Abstract][Full Text] [Related]
15. The RAD9-RAD1-HUS1 (9.1.1) complex interacts with WRN and is crucial to regulate its response to replication fork stalling.
Pichierri P; Nicolai S; Cignolo L; Bignami M; Franchitto A
Oncogene; 2012 Jun; 31(23):2809-23. PubMed ID: 22002307
[TBL] [Abstract][Full Text] [Related]
16. Inhibition of helicase activity by a small molecule impairs Werner syndrome helicase (WRN) function in the cellular response to DNA damage or replication stress.
Aggarwal M; Sommers JA; Shoemaker RH; Brosh RM
Proc Natl Acad Sci U S A; 2011 Jan; 108(4):1525-30. PubMed ID: 21220316
[TBL] [Abstract][Full Text] [Related]
17. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
Aggarwal M; Brosh RM
Aging (Albany NY); 2009 Feb; 1(2):219-33. PubMed ID: 20157511
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Nuclear DNA helicase II (RNA helicase A) interacts with Werner syndrome helicase and stimulates its exonuclease activity.
Friedemann J; Grosse F; Zhang S
J Biol Chem; 2005 Sep; 280(35):31303-13. PubMed ID: 15995249
[TBL] [Abstract][Full Text] [Related]
20. WRN interacts physically and functionally with the recombination mediator protein RAD52.
Baynton K; Otterlei M; Bjørås M; von Kobbe C; Bohr VA; Seeberg E
J Biol Chem; 2003 Sep; 278(38):36476-86. PubMed ID: 12750383
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
