175 related articles for article (PubMed ID: 25182132)
1. Clinical utility gene card for: Werner Syndrome--Update 2014.
Hisama FM; Kubisch C; Martin GM; Oshima J
Eur J Hum Genet; 2015 Jun; 23(6):891-. PubMed ID: 25182132
[No Abstract] [Full Text] [Related]
2. [Case report: A case of Werner syndrome with compound heterozygous mutations of WRN gene].
Tamori Y; Takahashi T; Nakajima S; Nishimoto Y; Ohno K; Takemoto M; Yokote K; Kita T; Tsutsumi M
Nihon Naika Gakkai Zasshi; 2011 Jun; 100(6):1642-4. PubMed ID: 21770289
[No Abstract] [Full Text] [Related]
3. Werner syndrome resembles normal aging.
Kyng K; Croteau DL; Bohr VA
Cell Cycle; 2009 Aug; 8(15):2323. PubMed ID: 19633413
[No Abstract] [Full Text] [Related]
4. Teaching neuroimages: a prematurely aging patient presenting with severe leukoaraiosis and stroke.
Seixas JC; Pedroso JL; Fukuda TG; de Figueiredo MM; Baiense RF; Yared JH; Ferraz HB; Barsottini OG
Neurology; 2012 May; 78(18):e113-4. PubMed ID: 22547774
[No Abstract] [Full Text] [Related]
5. 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]
6. Premature aging syndrome gene WRN genetically interacts with a topoisomerase.
Aggarwal M; Brosh RM
Cell Cycle; 2009 Jul; 8(14):2143. PubMed ID: 19587535
[No Abstract] [Full Text] [Related]
7. Syndrome-causing mutations in Werner syndrome.
Goto M
Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
[TBL] [Abstract][Full Text] [Related]
8. Werner helicase wings DNA binding.
Hoadley KA; Keck JL
Structure; 2010 Feb; 18(2):149-51. PubMed ID: 20159459
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
Friedrich K; Lee L; Leistritz DF; Nürnberg G; Saha B; Hisama FM; Eyman DK; Lessel D; Nürnberg P; Li C; Garcia-F-Villalta MJ; Kets CM; Schmidtke J; Cruz VT; Van den Akker PC; Boak J; Peter D; Compoginis G; Cefle K; Ozturk S; López N; Wessel T; Poot M; Ippel PF; Groff-Kellermann B; Hoehn H; Martin GM; Kubisch C; Oshima J
Hum Genet; 2010 Jul; 128(1):103-11. PubMed ID: 20443122
[TBL] [Abstract][Full Text] [Related]
11. The progerias.
Fossel M
J Anti Aging Med; 2003; 6(2):123-38. PubMed ID: 14614801
[No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. [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]
16. 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]
17. 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]
18. 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]
19. WRN mutations in Werner syndrome.
Moser MJ; Oshima J; Monnat RJ
Hum Mutat; 1999; 13(4):271-9. PubMed ID: 10220139
[TBL] [Abstract][Full Text] [Related]
20. [Molecular genetic analysis of Werner syndrome].
Nakura J
Nihon Ronen Igakkai Zasshi; 2001 Nov; 38(6):766-8. PubMed ID: 11774718
[No Abstract] [Full Text] [Related]
[Next] [New Search]