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Items: 1 to 20 of 122

1.

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. Review.

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. doi: 10.1007/s00439-008-0562-0. Epub 2008 Sep 23. Review.

3.

The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.

Chun SG, Shaeffer DS, Bryant-Greenwood PK.

Hawaii Med J. 2011 Mar;70(3):52-5. Review.

4.

Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.

Oshima J, Hisama FM.

Gerontology. 2014;60(3):239-46. doi: 10.1159/000356030. Epub 2014 Jan 3. Review.

5.
6.

WRN at telomeres: implications for aging and cancer.

Multani AS, Chang S.

J Cell Sci. 2007 Mar 1;120(Pt 5):713-21. Review.

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. doi: 10.1111/j.1365-2230.2007.02641.x. Epub 2008 Jan 16.

PMID:
18205852
8.

[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. Review. Chinese.

PMID:
19689938
10.

Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey.

Takemoto M, Mori S, Kuzuya M, Yoshimoto S, Shimamoto A, Igarashi M, Tanaka Y, Miki T, Yokote K.

Geriatr Gerontol Int. 2013 Apr;13(2):475-81. doi: 10.1111/j.1447-0594.2012.00913.x. Epub 2012 Jul 23.

PMID:
22817610
11.

Lack of amyloid plaque formation in the central nervous system of a patient with Werner syndrome.

Mori H, Tomiyama T, Maeda N, Ozawa K, Wakasa K.

Neuropathology. 2003 Mar;23(1):51-6.

PMID:
12722926
12.

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. doi: 10.1007/s00439-010-0832-5. Epub 2010 May 5.

13.

Syndrome-causing mutations in Werner syndrome.

Goto M.

Biosci Trends. 2008 Aug;2(4):147-50.

14.

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.

PMID:
16786514
15.

First Japanese case of atypical progeroid syndrome/atypical Werner syndrome with heterozygous LMNA mutation.

Motegi S, Yokoyama Y, Uchiyama A, Ogino S, Takeuchi Y, Yamada K, Hattori T, Hashizume H, Ishikawa Y, Goto M, Ishikawa O.

J Dermatol. 2014 Dec;41(12):1047-52. doi: 10.1111/1346-8138.12657. Epub 2014 Oct 20.

PMID:
25327215
16.

Premature aging syndrome gene WRN genetically interacts with a topoisomerase.

Aggarwal M, Brosh RM Jr.

Cell Cycle. 2009 Jul 15;8(14):2143. Epub 2009 Jul 15. No abstract available.

PMID:
19587535
17.

[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 10;100(6):1642-4. Japanese. No abstract available.

PMID:
21770289
18.

Oxidative stress and antioxidant response in fibroblasts from Werner and atypical Werner syndromes.

Seco-Cervera M, Spis M, García-Giménez JL, Ibañez-Cabellos JS, Velázquez-Ledesma A, Esmorís I, Bañuls S, Pérez-Machado G, Pallardó FV.

Aging (Albany NY). 2014 Mar;6(3):231-45.

19.

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 13;104(7):2205-10. Epub 2007 Feb 6.

20.

Telomere ResQue and preservation--roles for the Werner syndrome protein and other RecQ helicases.

Opresko PL.

Mech Ageing Dev. 2008 Jan-Feb;129(1-2):79-90. Epub 2007 Oct 30. Review.

PMID:
18054793

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