BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 16804003)

  • 21. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
    Lebel M; Monnat RJ
    Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 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. 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]  

  • 25. The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C.
    Kamath-Loeb AS; Welcsh P; Waite M; Adman ET; Loeb LA
    J Biol Chem; 2004 Dec; 279(53):55499-505. PubMed ID: 15489508
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.
    Agrelo R; Cheng WH; Setien F; Ropero S; Espada J; Fraga MF; Herranz M; Paz MF; Sanchez-Cespedes M; Artiga MJ; Guerrero D; Castells A; von Kobbe C; Bohr VA; Esteller M
    Proc Natl Acad Sci U S A; 2006 Jun; 103(23):8822-7. PubMed ID: 16723399
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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; 14(6):379-82. PubMed ID: 15564200
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.
    Friedrich K; Lee L; Leistritz DF; Nürnberg G; Saha B; Hisama FM; Eyman DK; Lessel D; Nürnberg P; Li C; Garcia-F-Villalta MJ; Kets CM; Schmidtke J; Cruz VT; Van den Akker PC; Boak J; Peter D; Compoginis G; Cefle K; Ozturk S; López N; Wessel T; Poot M; Ippel PF; Groff-Kellermann B; Hoehn H; Martin GM; Kubisch C; Oshima J
    Hum Genet; 2010 Jul; 128(1):103-11. PubMed ID: 20443122
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lack of WRN results in extensive deletion at nonhomologous joining ends.
    Oshima J; Huang S; Pae C; Campisi J; Schiestl RH
    Cancer Res; 2002 Jan; 62(2):547-51. PubMed ID: 11809708
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Competition between the DNA unwinding and strand pairing activities of the Werner and Bloom syndrome proteins.
    Machwe A; Lozada EM; Xiao L; Orren DK
    BMC Mol Biol; 2006 Jan; 7():1. PubMed ID: 16412221
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Werner syndrome: genetic and molecular basis of a premature aging disorder.
    Lebel M
    Cell Mol Life Sci; 2001 Jun; 58(7):857-67. PubMed ID: 11497235
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.
    Oshima J; Sidorova JM; Monnat RJ
    Ageing Res Rev; 2017 Jan; 33():105-114. PubMed ID: 26993153
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Werner Syndrome as an example of inflamm-aging: possible therapeutic opportunities for a progeroid syndrome?
    Davis T; Kipling D
    Rejuvenation Res; 2006; 9(3):402-7. PubMed ID: 16859481
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Chart no 45 - WRN (RCQL3)].
    Soussi T
    Bull Cancer; 2001 Jun; 88(6):537-8. PubMed ID: 11459698
    [No Abstract]   [Full Text] [Related]  

  • 40. WRN at telomeres: implications for aging and cancer.
    Multani AS; Chang S
    J Cell Sci; 2007 Mar; 120(Pt 5):713-21. PubMed ID: 17314245
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.