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Items: 1 to 20 of 100

1.

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.

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
3.

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
4.

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.

5.

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.

6.

WRN protein as a novel erythroblast immunohistochemical marker with applications for the diagnosis of Werner syndrome.

Sadahira Y, Sugihara T, Fujiwara H, Nishimura H, Suetsugu Y, Takeshita M, Okamura S, Goto M.

Virchows Arch. 2015 Mar;466(3):343-50. doi: 10.1007/s00428-014-1703-6. Epub 2014 Dec 12.

PMID:
25503078
7.

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
8.

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.

9.

The Werner syndrome protein is involved in RNA polymerase II transcription.

Balajee AS, Machwe A, May A, Gray MD, Oshima J, Martin GM, Nehlin JO, Brosh R, Orren DK, Bohr VA.

Mol Biol Cell. 1999 Aug;10(8):2655-68.

10.

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.

11.

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
12.

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
13.

Comparative aspects of the Werner syndrome gene.

Oshima J.

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

PMID:
10757074
14.

Mismatch repair in extracts of Werner syndrome cell lines.

Bennett SE, Umar A, Oshima J, Monnat RJ Jr, Kunkel TA.

Cancer Res. 1997 Jul 15;57(14):2956-60.

15.

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
16.

Functional interaction between the Werner Syndrome protein and DNA polymerase delta.

Kamath-Loeb AS, Johansson E, Burgers PM, Loeb LA.

Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4603-8.

17.

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
18.

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

Fry M.

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

PMID:
14602980
19.

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.

20.

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
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