556 related articles for article (PubMed ID: 17284601)
1. Telomere dysfunction as a cause of genomic instability in Werner syndrome.
Crabbe L; Jauch A; Naeger CM; Holtgreve-Grez H; Karlseder J
Proc Natl Acad Sci U S A; 2007 Feb; 104(7):2205-10. PubMed ID: 17284601
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Defective telomere lagging strand synthesis in cells lacking WRN helicase activity.
Crabbe L; Verdun RE; Haggblom CI; Karlseder J
Science; 2004 Dec; 306(5703):1951-3. PubMed ID: 15591207
[TBL] [Abstract][Full Text] [Related]
4. Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein.
Bai Y; Murnane JP
Hum Genet; 2003 Sep; 113(4):337-47. PubMed ID: 12827497
[TBL] [Abstract][Full Text] [Related]
5. WRN at telomeres: implications for aging and cancer.
Multani AS; Chang S
J Cell Sci; 2007 Mar; 120(Pt 5):713-21. PubMed ID: 17314245
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway.
Laud PR; Multani AS; Bailey SM; Wu L; Ma J; Kingsley C; Lebel M; Pathak S; DePinho RA; Chang S
Genes Dev; 2005 Nov; 19(21):2560-70. PubMed ID: 16264192
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Utilization of Werner syndrome mouse model in studying premature aging and tumor].
Jia ST; Yang SH; Luo Y
Yi Chuan; 2009 Aug; 31(8):785-90. PubMed ID: 19689938
[TBL] [Abstract][Full Text] [Related]
12. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.
Oshima J; Sidorova JM; Monnat RJ
Ageing Res Rev; 2017 Jan; 33():105-114. PubMed ID: 26993153
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Deficient DNA repair in the human progeroid disorder, Werner syndrome.
Bohr VA
Mutat Res; 2005 Sep; 577(1-2):252-9. PubMed ID: 15916783
[TBL] [Abstract][Full Text] [Related]
15. Roles of the Werner syndrome RecQ helicase in DNA replication.
Sidorova JM
DNA Repair (Amst); 2008 Nov; 7(11):1776-86. PubMed ID: 18722555
[TBL] [Abstract][Full Text] [Related]
16. Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase.
Dhillon KK; Sidorova JM; Albertson TM; Anderson JB; Ladiges WC; Rabinovitch PS; Preston BD; Monnat RJ
DNA Repair (Amst); 2010 Jan; 9(1):11-22. PubMed ID: 19896421
[TBL] [Abstract][Full Text] [Related]
17. Introduction of a normal human chromosome 8 corrects abnormal phenotypes of Werner syndrome cells immortalized by expressing an hTERT gene.
Ariyoshi K; Suzuki K; Goto M; Oshimura M; Ishizaki K; Watanabe M; Kodama S
J Radiat Res; 2009 May; 50(3):253-9. PubMed ID: 19398855
[TBL] [Abstract][Full Text] [Related]
18. Functional role of the Werner syndrome RecQ helicase in human fibroblasts.
Dhillon KK; Sidorova J; Saintigny Y; Poot M; Gollahon K; Rabinovitch PS; Monnat RJ
Aging Cell; 2007 Feb; 6(1):53-61. PubMed ID: 17266675
[TBL] [Abstract][Full Text] [Related]
19. Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8.
Kodama S; Kashino G; Suzuki K; Takatsuji T; Okumura Y; Oshimura M; Watanabe M; Barrett JC
Cancer Res; 1998 Nov; 58(22):5188-95. PubMed ID: 9823331
[TBL] [Abstract][Full Text] [Related]
20. The Werner syndrome helicase is a cofactor for HIV-1 long terminal repeat transactivation and retroviral replication.
Sharma A; Awasthi S; Harrod CK; Matlock EF; Khan S; Xu L; Chan S; Yang H; Thammavaram CK; Rasor RA; Burns DK; Skiest DJ; Van Lint C; Girard AM; McGee M; Monnat RJ; Harrod R
J Biol Chem; 2007 Apr; 282(16):12048-57. PubMed ID: 17317667
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
