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Items: 1 to 20 of 75

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.

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.

3.

Analysis of helicase gene mutations in Japanese Werner's syndrome patients.

Goto M, Imamura O, Kuromitsu J, Matsumoto T, Yamabe Y, Tokutake Y, Suzuki N, Mason B, Drayna D, Sugawara M, Sugimoto M, Furuichi Y.

Hum Genet. 1997 Feb;99(2):191-3.

PMID:
9048918
4.

LMNA mutations in atypical Werner's syndrome.

Chen L, Lee L, Kudlow BA, Dos Santos HG, Sletvold O, Shafeghati Y, Botha EG, Garg A, Hanson NB, Martin GM, Mian IS, Kennedy BK, Oshima J.

Lancet. 2003 Aug 9;362(9382):440-5.

PMID:
12927431
5.

Positional cloning of the Werner's syndrome gene.

Yu CE, Oshima J, Fu YH, Wijsman EM, Hisama F, Alisch R, Matthews S, Nakura J, Miki T, Ouais S, Martin GM, Mulligan J, Schellenberg GD.

Science. 1996 Apr 12;272(5259):258-62.

PMID:
8602509
6.

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
7.
8.

Genetic analyses of two cases of Werner's syndrome.

Sogabe Y, Yasuda M, Yokoyama Y, Tamura A, Negishi I, Ohnishi K, Shinozaki T, Ishikawa O.

Eur J Dermatol. 2004 Nov-Dec;14(6):379-82.

PMID:
15564200
9.

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.

10.

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
11.

Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1.

Kawabe Y, Seki M, Seki T, Wang WS, Imamura O, Furuichi Y, Saitoh H, Enomoto T.

J Biol Chem. 2000 Jul 14;275(28):20963-6.

12.

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
13.

DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.

Suzuki N, Shimamoto A, Imamura O, Kuromitsu J, Kitao S, Goto M, Furuichi Y.

Nucleic Acids Res. 1997 Aug 1;25(15):2973-8.

14.

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
15.

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.

16.

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
17.

Physical map of the human chromosome 8p12-p21 encompassing tumor suppressor and Werner's syndrome gene loci.

Ichikawa K, Shimamoto A, Imamura O, Tokutake Y, Yamabe Y, Kitao S, Suzuki N, Sugawara K, Matsumoto T, Thomas W, Drayna D, Goto M, Sugimoto M, Sugawara M, Furuichi Y.

DNA Res. 1998 Apr 30;5(2):103-13.

PMID:
9679198
18.

[The role of Werner's syndrome gene in the genetic susceptibility to the type 2 diabetes in Chinese population].

Luo Y, Ji L, Han X.

Zhonghua Yi Xue Za Zhi. 2000 May;80(5):360-1. Chinese.

PMID:
11798788
19.

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
20.

Physical and functional interaction between p53 and the Werner's syndrome protein.

Blander G, Kipnis J, Leal JF, Yu CE, Schellenberg GD, Oren M.

J Biol Chem. 1999 Oct 8;274(41):29463-9.

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