Format
Items per page
Sort by

Send to:

Choose Destination

Results: 16

Related Articles by Review for PubMed (Select 9225981)

1.

Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.

Matsumoto T, Imamura O, Yamabe Y, Kuromitsu J, Tokutake Y, Shimamoto A, Suzuki N, Satoh M, Kitao S, Ichikawa K, Kataoka H, Sugawara K, Thomas W, Mason B, Tsuchihashi Z, Drayna D, Sugawara M, Sugimoto M, Furuichi Y, Goto M.

Hum Genet. 1997 Jul;100(1):123-30.

PMID:
9225981
2.

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
4.

Werner syndrome protein: biochemical properties and functional interactions.

Bohr VA, Cooper M, Orren D, Machwe A, Piotrowski J, Sommers J, Karmakar P, Brosh R.

Exp Gerontol. 2000 Sep;35(6-7):695-702. Review.

PMID:
11053659
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. doi: 10.1111/j.1349-7006.2008.00778.x. Epub 2008 Feb 26. Review.

PMID:
18312465
6.

Severe toxicity following induction chemotherapy for acute myelogenous leukemia in a patient with Werner's syndrome.

Seiter K, Qureshi A, Liu D, Galvin-Parton P, Arshad M, Agoliati G, Ahmed T.

Leuk Lymphoma. 2005 Jul;46(7):1091-5. Review.

PMID:
16019564
7.

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.

8.

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.

PMID:
18810497
9.

[Werner syndrome].

Goto M, Ishikawa Y.

Nihon Rinsho. 2000 Jul;58(7):1490-5. Review. Japanese.

PMID:
10921329
10.

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
11.

The Werner syndrome protein: an update.

Oshima J.

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

PMID:
10984715
12.

Roles of the Bloom's syndrome helicase in the maintenance of genome stability.

Cheok CF, Bachrati CZ, Chan KL, Ralf C, Wu L, Hickson ID.

Biochem Soc Trans. 2005 Dec;33(Pt 6):1456-9. Review.

PMID:
16246145
13.

A model for the phenotypic presentation of Werner's syndrome.

Ostler EL, Wallis CV, Sheerin AN, Faragher RG.

Exp Gerontol. 2002 Jan-Mar;37(2-3):285-92. Review.

PMID:
11772514
14.

DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders.

Mohaghegh P, Hickson ID.

Hum Mol Genet. 2001 Apr;10(7):741-6. Review.

15.

[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
16.

Functional link between Myc and the Werner gene in tumorigenesis.

Grandori C, Robinson KL, Galloway DA, Swisshelm K.

Cell Cycle. 2004 Jan;3(1):22-5. Review.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk