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Results: 1 to 20 of 94

1.

Molecular biology of Werner syndrome.

Shimamoto A, Sugimoto M, Furuichi Y.

Int J Clin Oncol. 2004 Aug;9(4):288-98. Review.

PMID:
15375705
[PubMed - indexed for MEDLINE]
2.

Molecular genetics of RecQ helicase disorders.

Hanada K, Hickson ID.

Cell Mol Life Sci. 2007 Sep;64(17):2306-22. Review.

PMID:
17571213
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

Werner syndrome: entering the helicase era.

Epstein CJ, Motulsky AG.

Bioessays. 1996 Dec;18(12):1025-7. Review.

PMID:
8976161
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

Werner syndrome: genetic and molecular basis of a premature aging disorder.

Lebel M.

Cell Mol Life Sci. 2001 Jun;58(7):857-67. Review.

PMID:
11497235
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
11316787
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

SGS1, the Saccharomyces cerevisiae homologue of BLM and WRN, suppresses genome instability and homeologous recombination.

Myung K, Datta A, Chen C, Kolodner RD.

Nat Genet. 2001 Jan;27(1):113-6.

PMID:
11138010
[PubMed - indexed for MEDLINE]
10.

What can progeroid syndromes tell us about human aging?

Kipling D, Davis T, Ostler EL, Faragher RG.

Science. 2004 Sep 3;305(5689):1426-31. Review.

PMID:
15353794
[PubMed - indexed for MEDLINE]
11.

Modeling Werner Syndrome in Drosophila melanogaster: hyper-recombination in flies lacking WRN-like exonuclease.

Cox LS, Clancy DJ, Boubriak I, Saunders RD.

Ann N Y Acad Sci. 2007 Nov;1119:274-88.

PMID:
18056975
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

Human diseases deficient in RecQ helicases.

Harrigan JA, Bohr VA.

Biochimie. 2003 Nov;85(11):1185-93.

PMID:
14726023
[PubMed - indexed for MEDLINE]
15.

Telomere dysfunction as a cause of genomic instability in Werner syndrome.

Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J.

Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2205-10. Epub 2007 Feb 6.

PMID:
17284601
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

The Werner syndrome protein: an update.

Oshima J.

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

PMID:
10984715
[PubMed - indexed for MEDLINE]
17.

Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in mice.

Yamamoto ML, Reliene R, Oshima J, Schiestl RH.

Mutat Res. 2008 Sep 26;644(1-2):11-6. doi: 10.1016/j.mrfmmm.2008.06.008. Epub 2008 Jul 1.

PMID:
18639560
[PubMed - indexed for MEDLINE]
18.

Roles of the Werner syndrome protein in pathways required for maintenance of genome stability.

Brosh RM Jr, Bohr VA.

Exp Gerontol. 2002 Apr;37(4):491-506. Review.

PMID:
11830352
[PubMed - indexed for MEDLINE]
19.

Werner syndrome protein limits MYC-induced cellular senescence.

Grandori C, Wu KJ, Fernandez P, Ngouenet C, Grim J, Clurman BE, Moser MJ, Oshima J, Russell DW, Swisshelm K, Frank S, Amati B, Dalla-Favera R, Monnat RJ Jr.

Genes Dev. 2003 Jul 1;17(13):1569-74.

PMID:
12842909
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

DNA repair and mutagenesis in Werner syndrome.

Bohr VA, Souza Pinto N, Nyaga SG, Dianov G, Kraemer K, Seidman MM, Brosh RM Jr.

Environ Mol Mutagen. 2001;38(2-3):227-34.

PMID:
11746759
[PubMed - indexed for MEDLINE]

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