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Results: 13

1.

Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Saha B, Lessel D, Nampoothiri S, Rao AS, Hisama FM, Peter D, Bennett C, Nürnberg G, Nürnberg P, Martin GM, Kubisch C, Oshima J.

Mol Genet Genomic Med. 2013 May 1;1(1):7-14.

PMID:
23936869
[PubMed]
Free PMC Article
2.

Mutant huntingtin impairs Ku70-mediated DNA repair.

Enokido Y, Tamura T, Ito H, Arumughan A, Komuro A, Shiwaku H, Sone M, Foulle R, Sawada H, Ishiguro H, Ono T, Murata M, Kanazawa I, Tomilin N, Tagawa K, Wanker EE, Okazawa H.

J Cell Biol. 2010 May 3;189(3):425-43. doi: 10.1083/jcb.200905138.

PMID:
20439996
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Werner syndrome gene variants in human sarcomas.

Hsu JJ, Kamath-Loeb AS, Glick E, Wallden B, Swisshelm K, Rubin BP, Loeb LA.

Mol Carcinog. 2010 Feb;49(2):166-74. doi: 10.1002/mc.20586.

PMID:
19824023
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Mechanism of Werner DNA helicase: POT1 and RPA stimulates WRN to unwind beyond gaps in the translocating strand.

Ahn B, Lee JW, Jung H, Beck G, Bohr VA.

PLoS One. 2009;4(3):e4673. doi: 10.1371/journal.pone.0004673. Epub 2009 Mar 5.

PMID:
19262689
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

PMID:
16673358
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Werner Syndrome.

Chen L, Oshima J.

J Biomed Biotechnol. 2002;2(2):46-54.

PMID:
12488583
[PubMed - as supplied by publisher]
Free PMC Article
7.

WRN helicase expression in Werner syndrome cell lines.

Moser MJ, Kamath-Loeb AS, Jacob JE, Bennett SE, Oshima J, Monnat RJ Jr.

Nucleic Acids Res. 2000 Jan 15;28(2):648-54.

PMID:
10606667
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization.

Shiratori M, Sakamoto S, Suzuki N, Tokutake Y, Kawabe Y, Enomoto T, Sugimoto M, Goto M, Matsumoto T, Furuichi Y.

J Cell Biol. 1999 Jan 11;144(1):1-9.

PMID:
9885239
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Structure and function of the human Werner syndrome gene promoter: evidence for transcriptional modulation.

Wang L, Hunt KE, Martin GM, Oshima J.

Nucleic Acids Res. 1998 Aug 1;26(15):3480-5.

PMID:
9671808
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Nucleolar localization of the Werner syndrome protein in human cells.

Marciniak RA, Lombard DB, Johnson FB, Guarente L.

Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6887-92.

PMID:
9618508
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A.

Shen JC, Gray MD, Oshima J, Loeb LA.

Nucleic Acids Res. 1998 Jun 15;26(12):2879-85.

PMID:
9611231
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Genetics and the pathobiology of ageing.

Martin GM.

Philos Trans R Soc Lond B Biol Sci. 1997 Dec 29;352(1363):1773-80. Review.

PMID:
9460060
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The Werner mutation: does it lead to a "public" or "private" mechanism of aging?

Martin GM.

Mol Med. 1997 Jun;3(6):356-8. Review. No abstract available.

PMID:
9234240
[PubMed - indexed for MEDLINE]
Free PMC Article

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