These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
197 related articles for article (PubMed ID: 25503078)
1. WRN protein as a novel erythroblast immunohistochemical marker with applications for the diagnosis of Werner syndrome. Sadahira Y; Sugihara T; Fujiwara H; Nishimura H; Suetsugu Y; Takeshita M; Okamura S; Goto M Virchows Arch; 2015 Mar; 466(3):343-50. PubMed ID: 25503078 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Werner syndrome and mutations of the WRN and LMNA genes in France. Uhrhammer NA; Lafarge L; Dos Santos L; Domaszewska A; Lange M; Yang Y; Aractingi S; Bessis D; Bignon YJ Hum Mutat; 2006 Jul; 27(7):718-9. PubMed ID: 16786514 [TBL] [Abstract][Full Text] [Related]
4. Werner syndrome as a hereditary risk factor for exocrine pancreatic cancer: potential role of WRN in pancreatic tumorigenesis and patient-tailored therapy. Chun SG; Yee NS Cancer Biol Ther; 2010 Sep; 10(5):430-7. PubMed ID: 20657174 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. The Werner syndrome protein affects the expression of genes involved in adipogenesis and inflammation in addition to cell cycle and DNA damage responses. Turaga RV; Paquet ER; Sild M; Vignard J; Garand C; Johnson FB; Masson JY; Lebel M Cell Cycle; 2009 Jul; 8(13):2080-92. PubMed ID: 19502800 [TBL] [Abstract][Full Text] [Related]
7. A novel mutation of the WRN gene in a Chinese patient with Werner syndrome. Zhao N; Hao F; Qu T; Zuo YG; Wang BX Clin Exp Dermatol; 2008 May; 33(3):278-81. PubMed ID: 18205852 [TBL] [Abstract][Full Text] [Related]
8. 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]
10. Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas. Oshitari T; Kitahashi M; Mizuno S; Baba T; Kubota-Taniai M; Takemoto M; Yokote K; Yamamoto S; Roy S BMC Ophthalmol; 2014 Mar; 14():31. PubMed ID: 24620826 [TBL] [Abstract][Full Text] [Related]
11. The transcriptional response to distinct growth factors is impaired in Werner syndrome cells. Lutomska A; Lebedev A; Scharffetter-Kochanek K; Iben S Exp Gerontol; 2008 Sep; 43(9):820-6. PubMed ID: 18625297 [TBL] [Abstract][Full Text] [Related]
12. Transient overexpression of Werner protein rescues starvation induced autophagy in Werner syndrome cells. Maity J; Bohr VA; Laskar A; Karmakar P Biochim Biophys Acta; 2014 Dec; 1842(12 Pt A):2387-94. PubMed ID: 25257404 [TBL] [Abstract][Full Text] [Related]
13. Werner syndrome: a changing pattern of clinical manifestations in Japan (1917~2008). Goto M; Ishikawa Y; Sugimoto M; Furuichi Y Biosci Trends; 2013 Feb; 7(1):13-22. PubMed ID: 23524889 [TBL] [Abstract][Full Text] [Related]
14. A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology. Takada-Watanabe A; Yokote K; Takemoto M; Fujimoto M; Irisuna H; Honjo S; Futami K; Furuichi Y; Saito Y Geriatr Gerontol Int; 2012 Jan; 12(1):140-6. PubMed ID: 22188495 [TBL] [Abstract][Full Text] [Related]
15. Estrogen prevents senescence through induction of WRN, Werner syndrome protein. Lee SJ; Lee SH; Ha NC; Park BJ Horm Res Paediatr; 2010; 74(1):33-40. PubMed ID: 20395656 [TBL] [Abstract][Full Text] [Related]
16. Functional deficit associated with a missense Werner syndrome mutation. Tadokoro T; Rybanska-Spaeder I; Kulikowicz T; Dawut L; Oshima J; Croteau DL; Bohr VA DNA Repair (Amst); 2013 Jun; 12(6):414-21. PubMed ID: 23583337 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced. Kashino G; Kodama S; Suzuki K; Oshimura M; Watanabe M Biochem Biophys Res Commun; 2001 Nov; 289(1):111-5. PubMed ID: 11708785 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Aging stem cells. A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging. Zhang W; Li J; Suzuki K; Qu J; Wang P; Zhou J; Liu X; Ren R; Xu X; Ocampo A; Yuan T; Yang J; Li Y; Shi L; Guan D; Pan H; Duan S; Ding Z; Li M; Yi F; Bai R; Wang Y; Chen C; Yang F; Li X; Wang Z; Aizawa E; Goebl A; Soligalla RD; Reddy P; Esteban CR; Tang F; Liu GH; Belmonte JC Science; 2015 Jun; 348(6239):1160-3. PubMed ID: 25931448 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]