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Items: 1 to 20 of 223

1.

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
2.

Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8.

Kodama S, Kashino G, Suzuki K, Takatsuji T, Okumura Y, Oshimura M, Watanabe M, Barrett JC.

Cancer Res. 1998 Nov 15;58(22):5188-95.

3.

Comparative aspects of the Werner syndrome gene.

Oshima J.

In Vivo. 2000 Jan-Feb;14(1):165-72.

PMID:
10757074
4.

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
5.

Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene.

Wang L, Ogburn CE, Ware CB, Ladiges WC, Youssoufian H, Martin GM, Oshima J.

Genetics. 2000 Jan;154(1):357-62.

6.

The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.

Shen JC, Loeb LA.

Trends Genet. 2000 May;16(5):213-20. Review.

PMID:
10782115
7.

The spectrum of WRN mutations in Werner syndrome patients.

Huang S, Lee L, Hanson NB, Lenaerts C, Hoehn H, Poot M, Rubin CD, Chen DF, Yang CC, Juch H, Dorn T, Spiegel R, Oral EA, Abid M, Battisti C, Lucci-Cordisco E, Neri G, Steed EH, Kidd A, Isley W, Showalter D, Vittone JL, Konstantinow A, Ring J, Meyer P, Wenger SL, von Herbay A, Wollina U, Schuelke M, Huizenga CR, Leistritz DF, Martin GM, Mian IS, Oshima J.

Hum Mutat. 2006 Jun;27(6):558-67.

8.

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Yu CE, Oshima J, Wijsman EM, Nakura J, Miki T, Piussan C, Matthews S, Fu YH, Mulligan J, Martin GM, Schellenberg GD.

Am J Hum Genet. 1997 Feb;60(2):330-41.

9.

[Werner syndrome].

Goto M, Ishikawa Y.

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

PMID:
10921329
10.

WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.

Chen L, Huang S, Lee L, Davalos A, Schiestl RH, Campisi J, Oshima J.

Aging Cell. 2003 Aug;2(4):191-9.

PMID:
12934712
11.

Homozygous and compound heterozygous mutations at the Werner syndrome locus.

Oshima J, Yu CE, Piussan C, Klein G, Jabkowski J, Balci S, Miki T, Nakura J, Ogihara T, Ells J, Smith M, Melaragno MI, Fraccaro M, Scappaticci S, Matthews J, Ouais S, Jarzebowicz A, Schellenberg GD, Martin GM.

Hum Mol Genet. 1996 Dec;5(12):1909-13.

PMID:
8968742
12.

Preferential expression of an intact WRN gene in Werner syndrome cell lines in which a normal chromosome 8 has been introduced.

Kashino G, Kodama S, Suzuki K, Oshimura M, Watanabe M.

Biochem Biophys Res Commun. 2001 Nov 23;289(1):111-5.

PMID:
11708785
13.

Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

Prince PR, Emond MJ, Monnat RJ Jr.

Genes Dev. 2001 Apr 15;15(8):933-8.

14.

The Werner syndrome protein: an update.

Oshima J.

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

PMID:
10984715
15.

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.

PMID:
16804003
16.

A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay.

Müller FB, Tsianakas A, Kuwert C, Korge BP, Hunzelmann N.

Br J Dermatol. 2005 May;152(5):1030-2.

PMID:
15888165
17.

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.

PMID:
18205852
18.

Diverse dealings of the Werner helicase/nuclease.

Cheng WH, Bohr VA.

Sci Aging Knowledge Environ. 2003 Aug 6;2003(31):PE22.

PMID:
12904570
19.

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. Review.

20.
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