260 related articles for article (PubMed ID: 24401204)
21. From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.
Cox LS; Faragher RG
Cell Mol Life Sci; 2007 Oct; 64(19-20):2620-41. PubMed ID: 17660942
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
Donadille B; D'Anella P; Auclair M; Uhrhammer N; Sorel M; Grigorescu R; Ouzounian S; Cambonie G; Boulot P; Laforêt P; Carbonne B; Christin-Maitre S; Bignon YJ; Vigouroux C
Orphanet J Rare Dis; 2013 Jul; 8():106. PubMed ID: 23849162
[TBL] [Abstract][Full Text] [Related]
25. The Werner syndrome protein: an update.
Oshima J
Bioessays; 2000 Oct; 22(10):894-901. PubMed ID: 10984715
[TBL] [Abstract][Full Text] [Related]
26. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes.
Maierhofer A; Flunkert J; Oshima J; Martin GM; Poot M; Nanda I; Dittrich M; Müller T; Haaf T
Aging Cell; 2019 Oct; 18(5):e12995. PubMed ID: 31259468
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A.
Kang SM; Yoon MH; Lee SJ; Ahn J; Yi SA; Nam KH; Park S; Woo TG; Cho JH; Lee J; Ha NC; Park BJ
Sci Rep; 2021 Apr; 11(1):9122. PubMed ID: 33907225
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Possible associations between successful aging and polymorphic markers in the Werner gene region.
Sild M; Koca C; Bendixen MH; Frederiksen H; McGue M; Kølvraa S; Christensen K; Nexø B
Ann N Y Acad Sci; 2006 May; 1067():309-10. PubMed ID: 16804003
[TBL] [Abstract][Full Text] [Related]
31. [An atypical case of Werner syndrome: epigenetic control and DNA damage response alterations].
Smirnova NV; Spivak NM; Pleskach NM; Zherebtsov SV; Aksenov NL; Mikhel'son VM
Tsitologiia; 2008; 50(10):868-76. PubMed ID: 19062519
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Comparative aspects of the Werner syndrome gene.
Oshima J
In Vivo; 2000; 14(1):165-72. PubMed ID: 10757074
[TBL] [Abstract][Full Text] [Related]
34. [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]
35. 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]
36. Syndrome-causing mutations in Werner syndrome.
Goto M
Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. 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]
40. Increased susceptibility to oxidative stress- and ultraviolet A-induced apoptosis in fibroblasts in atypical progeroid syndrome/atypical Werner syndrome with LMNA mutation.
Motegi S; Uchiyama A; Yamada K; Ogino S; Yokoyama Y; Perera B; Takeuchi Y; Ishikawa O
Exp Dermatol; 2016 Aug; 25 Suppl 3():20-7. PubMed ID: 27539898
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]