618 related articles for article (PubMed ID: 26993153)
1. 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]
2. Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases.
de Renty C; Ellis NA
Ageing Res Rev; 2017 Jan; 33():36-51. PubMed ID: 27238185
[TBL] [Abstract][Full Text] [Related]
3. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
Lebel M; Monnat RJ
Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
[TBL] [Abstract][Full Text] [Related]
4. The Werner syndrome protein: an update.
Oshima J
Bioessays; 2000 Oct; 22(10):894-901. PubMed ID: 10984715
[TBL] [Abstract][Full Text] [Related]
5. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis.
Muftuoglu M; Oshima J; von Kobbe C; Cheng WH; Leistritz DF; Bohr VA
Hum Genet; 2008 Nov; 124(4):369-77. PubMed ID: 18810497
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
Yokote K; Chanprasert S; Lee L; Eirich K; Takemoto M; Watanabe A; Koizumi N; Lessel D; Mori T; Hisama FM; Ladd PD; Angle B; Baris H; Cefle K; Palanduz S; Ozturk S; Chateau A; Deguchi K; Easwar TK; Federico A; Fox A; Grebe TA; Hay B; Nampoothiri S; Seiter K; Streeten E; Piña-Aguilar RE; Poke G; Poot M; Posmyk R; Martin GM; Kubisch C; Schindler D; Oshima J
Hum Mutat; 2017 Jan; 38(1):7-15. PubMed ID: 27667302
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
Shen JC; Loeb LA
Trends Genet; 2000 May; 16(5):213-20. PubMed ID: 10782115
[TBL] [Abstract][Full Text] [Related]
12. Adult progeria: a new mutation in the WRN gene.
Rocha ML; Chicharo AT; Sequeira G; Teixeira V
BMJ Case Rep; 2022 Nov; 15(11):. PubMed ID: 36396328
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
Oshima J; Hisama FM
Gerontology; 2014; 60(3):239-46. PubMed ID: 24401204
[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. Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.
Agrelo R; Cheng WH; Setien F; Ropero S; Espada J; Fraga MF; Herranz M; Paz MF; Sanchez-Cespedes M; Artiga MJ; Guerrero D; Castells A; von Kobbe C; Bohr VA; Esteller M
Proc Natl Acad Sci U S A; 2006 Jun; 103(23):8822-7. PubMed ID: 16723399
[TBL] [Abstract][Full Text] [Related]
17. Uncommon cause of cirrhosis-A case of Werner syndrome with a novel WRN mutation.
Amalnath SD; Sargolzaeiaval F; Oshima J; Baskar D
Indian J Gastroenterol; 2017 Jul; 36(4):323-325. PubMed ID: 28795391
[TBL] [Abstract][Full Text] [Related]
18. The Werner syndrome. A model for the study of human aging.
Nehlin JO; Skovgaard GL; Bohr VA
Ann N Y Acad Sci; 2000 Jun; 908():167-79. PubMed ID: 10911957
[TBL] [Abstract][Full Text] [Related]
19. The Werner syndrome protein is involved in RNA polymerase II transcription.
Balajee AS; Machwe A; May A; Gray MD; Oshima J; Martin GM; Nehlin JO; Brosh R; Orren DK; Bohr VA
Mol Biol Cell; 1999 Aug; 10(8):2655-68. PubMed ID: 10436020
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
