296 related articles for article (PubMed ID: 22871734)
1. Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences.
Damerla RR; Knickelbein KE; Strutt S; Liu FJ; Wang H; Opresko PL
Cell Cycle; 2012 Aug; 11(16):3036-44. PubMed ID: 22871734
[TBL] [Abstract][Full Text] [Related]
2. WRN controls formation of extrachromosomal telomeric circles and is required for TRF2DeltaB-mediated telomere shortening.
Li B; Jog SP; Reddy S; Comai L
Mol Cell Biol; 2008 Mar; 28(6):1892-904. PubMed ID: 18212065
[TBL] [Abstract][Full Text] [Related]
3. Sequence-specific processing of telomeric 3' overhangs by the Werner syndrome protein exonuclease activity.
Li B; Reddy S; Comai L
Aging (Albany NY); 2009 Mar; 1(3):289-302. PubMed ID: 20157518
[TBL] [Abstract][Full Text] [Related]
4. Telomere ResQue and preservation--roles for the Werner syndrome protein and other RecQ helicases.
Opresko PL
Mech Ageing Dev; 2008; 129(1-2):79-90. PubMed ID: 18054793
[TBL] [Abstract][Full Text] [Related]
5. The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events.
Edwards DN; Machwe A; Chen L; Bohr VA; Orren DK
Nat Commun; 2015 Sep; 6():8331. PubMed ID: 26420422
[TBL] [Abstract][Full Text] [Related]
6. Cooperation of DNA-PKcs and WRN helicase in the maintenance of telomeric D-loops.
Kusumoto-Matsuo R; Opresko PL; Ramsden D; Tahara H; Bohr VA
Aging (Albany NY); 2010 May; 2(5):274-84. PubMed ID: 20519774
[TBL] [Abstract][Full Text] [Related]
7. Replication protein A stimulates the Werner syndrome protein branch migration activity.
Sowd G; Wang H; Pretto D; Chazin WJ; Opresko PL
J Biol Chem; 2009 Dec; 284(50):34682-91. PubMed ID: 19812417
[TBL] [Abstract][Full Text] [Related]
8. The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation.
Opresko PL; Sowd G; Wang H
PLoS One; 2009; 4(3):e4825. PubMed ID: 19283071
[TBL] [Abstract][Full Text] [Related]
9. TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA.
Machwe A; Xiao L; Orren DK
Oncogene; 2004 Jan; 23(1):149-56. PubMed ID: 14712220
[TBL] [Abstract][Full Text] [Related]
10. RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance.
Ghosh AK; Rossi ML; Singh DK; Dunn C; Ramamoorthy M; Croteau DL; Liu Y; Bohr VA
J Biol Chem; 2012 Jan; 287(1):196-209. PubMed ID: 22039056
[TBL] [Abstract][Full Text] [Related]
11. Role of Werner syndrome gene product helicase in carcinogenesis and in resistance to genotoxins by cancer cells.
Futami K; Ishikawa Y; Goto M; Furuichi Y; Sugimoto M
Cancer Sci; 2008 May; 99(5):843-8. PubMed ID: 18312465
[TBL] [Abstract][Full Text] [Related]
12. Telomeric repeat mutagenicity in human somatic cells is modulated by repeat orientation and G-quadruplex stability.
Damerla RR; Knickelbein KE; Kepchia D; Jackson A; Armitage BA; Eckert KA; Opresko PL
DNA Repair (Amst); 2010 Nov; 9(11):1119-29. PubMed ID: 20800555
[TBL] [Abstract][Full Text] [Related]
13. Mechanism and substrate specificity of telomeric protein POT1 stimulation of the Werner syndrome helicase.
Sowd G; Lei M; Opresko PL
Nucleic Acids Res; 2008 Aug; 36(13):4242-56. PubMed ID: 18583366
[TBL] [Abstract][Full Text] [Related]
14. Telomeric D-loops containing 8-oxo-2'-deoxyguanosine are preferred substrates for Werner and Bloom syndrome helicases and are bound by POT1.
Ghosh A; Rossi ML; Aulds J; Croteau D; Bohr VA
J Biol Chem; 2009 Nov; 284(45):31074-84. PubMed ID: 19734539
[TBL] [Abstract][Full Text] [Related]
15. Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase.
Nora GJ; Buncher NA; Opresko PL
Nucleic Acids Res; 2010 Jul; 38(12):3984-98. PubMed ID: 20215438
[TBL] [Abstract][Full Text] [Related]
16. The Werner syndrome protein suppresses telomeric instability caused by chromium (VI) induced DNA replication stress.
Liu FJ; Barchowsky A; Opresko PL
PLoS One; 2010 Jun; 5(6):e11152. PubMed ID: 20585393
[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. Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein.
Opresko PL; Laine JP; Brosh RM; Seidman MM; Bohr VA
J Biol Chem; 2001 Nov; 276(48):44677-87. PubMed ID: 11572872
[TBL] [Abstract][Full Text] [Related]
19. BLM helicase facilitates telomere replication during leading strand synthesis of telomeres.
Drosopoulos WC; Kosiyatrakul ST; Schildkraut CL
J Cell Biol; 2015 Jul; 210(2):191-208. PubMed ID: 26195664
[TBL] [Abstract][Full Text] [Related]
20. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.
Chen L; Huang S; Lee L; Davalos A; Schiestl RH; Campisi J; Oshima J
Aging Cell; 2003 Aug; 2(4):191-9. PubMed ID: 12934712
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]