205 related articles for article (PubMed ID: 10921329)
21. Mismatch repair in extracts of Werner syndrome cell lines.
Bennett SE; Umar A; Oshima J; Monnat RJ; Kunkel TA
Cancer Res; 1997 Jul; 57(14):2956-60. PubMed ID: 9230208
[TBL] [Abstract][Full Text] [Related]
22. The Werner syndrome helicase-nuclease--one protein, many mysteries.
Fry M
Sci Aging Knowledge Environ; 2002 Apr; 2002(13):re2. PubMed ID: 14602980
[TBL] [Abstract][Full Text] [Related]
23. 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. PubMed ID: 9012406
[TBL] [Abstract][Full Text] [Related]
24. 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. PubMed ID: 10628995
[TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 8968742
[TBL] [Abstract][Full Text] [Related]
26. Deficient DNA repair in the human progeroid disorder, Werner syndrome.
Bohr VA
Mutat Res; 2005 Sep; 577(1-2):252-9. PubMed ID: 15916783
[TBL] [Abstract][Full Text] [Related]
27. Introduction of a normal human chromosome 8 corrects abnormal phenotypes of Werner syndrome cells immortalized by expressing an hTERT gene.
Ariyoshi K; Suzuki K; Goto M; Oshimura M; Ishizaki K; Watanabe M; Kodama S
J Radiat Res; 2009 May; 50(3):253-9. PubMed ID: 19398855
[TBL] [Abstract][Full Text] [Related]
28. 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. PubMed ID: 10436020
[TBL] [Abstract][Full Text] [Related]
29. Genetic cooperation between the Werner syndrome protein and poly(ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal rearrangements, and cancer in mice.
Lebel M; Lavoie J; Gaudreault I; Bronsard M; Drouin R
Am J Pathol; 2003 May; 162(5):1559-69. PubMed ID: 12707040
[TBL] [Abstract][Full Text] [Related]
30. 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. PubMed ID: 18205852
[TBL] [Abstract][Full Text] [Related]
31. [Werner syndrome].
Kato Y
Nihon Rinsho; 2002 Sep; 60 Suppl 9():834-7. PubMed ID: 12387092
[No Abstract] [Full Text] [Related]
32. 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; 104(7):2205-10. PubMed ID: 17284601
[TBL] [Abstract][Full Text] [Related]
33. p53-mediated apoptosis is attenuated in Werner syndrome cells.
Spillare EA; Robles AI; Wang XW; Shen JC; Yu CE; Schellenberg GD; Harris CC
Genes Dev; 1999 Jun; 13(11):1355-60. PubMed ID: 10364153
[TBL] [Abstract][Full Text] [Related]
34. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.
Opresko PL; Cheng WH; von Kobbe C; Harrigan JA; Bohr VA
Carcinogenesis; 2003 May; 24(5):791-802. PubMed ID: 12771022
[TBL] [Abstract][Full Text] [Related]
35. Loss of Werner syndrome protein function promotes aberrant mitotic recombination.
Prince PR; Emond MJ; Monnat RJ
Genes Dev; 2001 Apr; 15(8):933-8. PubMed ID: 11316787
[TBL] [Abstract][Full Text] [Related]
36. [Molecular genetic analysis of Werner syndrome].
Nakura J
Nihon Ronen Igakkai Zasshi; 2001 Nov; 38(6):766-8. PubMed ID: 11774718
[No Abstract] [Full Text] [Related]
37. Syndrome-causing mutations in Werner syndrome.
Goto M
Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
[TBL] [Abstract][Full Text] [Related]
38. Cloning the gene for Werner syndrome: a disease with many symptoms of premature aging.
Lombard DB; Guarente L
Trends Genet; 1996 Aug; 12(8):283-6. PubMed ID: 8783933
[No Abstract] [Full Text] [Related]
39. Molecular biology of Werner syndrome.
Shimamoto A; Sugimoto M; Furuichi Y
Int J Clin Oncol; 2004 Aug; 9(4):288-98. PubMed ID: 15375705
[TBL] [Abstract][Full Text] [Related]
40. The Werner mutation: does it lead to a "public" or "private" mechanism of aging?
Martin GM
Mol Med; 1997 Jun; 3(6):356-8. PubMed ID: 9234240
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
