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Items: 1 to 20 of 25

2.

Camptothecin sensitivity in Werner syndrome fibroblasts as assessed by the COMET technique.

Lowe J, Sheerin A, Jennert-Burston K, Burton D, Ostler EL, Bird J, Green MH, Faragher RG.

Ann N Y Acad Sci. 2004 Jun;1019:256-9. Review.

PMID:
15247024
3.

Werner syndrome: genetic and molecular basis of a premature aging disorder.

Lebel M.

Cell Mol Life Sci. 2001 Jun;58(7):857-67. Review.

PMID:
11497235
4.

The Werner syndrome helicase-nuclease--one protein, many mysteries.

Fry M.

Sci Aging Knowledge Environ. 2002 Apr 3;2002(13):re2. Review.

PMID:
14602980
5.

Unwinding the molecular basis of the Werner syndrome.

Shen J, Loeb LA.

Mech Ageing Dev. 2001 Jul 15;122(9):921-44. Review.

PMID:
11348659
6.

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. doi: 10.1111/j.1349-7006.2008.00778.x. Epub 2008 Feb 26. Review.

7.

The Werner syndrome protein: an update.

Oshima J.

Bioessays. 2000 Oct;22(10):894-901. Review.

PMID:
10984715
8.

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
9.

WRN mutations in Werner syndrome.

Moser MJ, Oshima J, Monnat RJ Jr.

Hum Mutat. 1999;13(4):271-9. Review. Erratum in: Hum Mutat 1999;14(1):84-5.

PMID:
10220139
10.

[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
12.

Deficient DNA repair in the human progeroid disorder, Werner syndrome.

Bohr VA.

Mutat Res. 2005 Sep 4;577(1-2):252-9. Review.

PMID:
15916783
13.

[Functional analysis of yeast homologue gene associated with human DNA helicase causative syndromes].

Miyajima A.

Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 2002;(120):53-74. Review. Japanese.

PMID:
12638184
14.

Premature aging and predisposition to cancers caused by mutations in RecQ family helicases.

Furuichi Y.

Ann N Y Acad Sci. 2001 Apr;928:121-31. Review.

PMID:
11795503
15.
16.

Current advances in unraveling the function of the Werner syndrome protein.

Ozgenc A, Loeb LA.

Mutat Res. 2005 Sep 4;577(1-2):237-51. Review.

PMID:
15946710
17.

Werner syndrome and biological ageing: a molecular genetic hypothesis.

Thweatt R, Goldstein S.

Bioessays. 1993 Jun;15(6):421-6. Review.

PMID:
8357345
18.

A cascade leading to premature aging phenotypes including abnormal tumor profiles in Werner syndrome (review).

Sugimoto M.

Int J Mol Med. 2014 Feb;33(2):247-53. doi: 10.3892/ijmm.2013.1592. Epub 2013 Dec 17. Review.

PMID:
24356923
19.

Ascorbate improves metabolic abnormalities in Wrn mutant mice but not the free radical scavenger catechin.

Lebel M, Massip L, Garand C, Thorin E.

Ann N Y Acad Sci. 2010 Jun;1197:40-4. doi: 10.1111/j.1749-6632.2010.05189.x. Review.

20.

Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming.

Shimamoto A, Yokote K, Tahara H.

Front Genet. 2015 Jan 29;6:10. doi: 10.3389/fgene.2015.00010. eCollection 2015. Review.

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