BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

327 related articles for article (PubMed ID: 16673358)

  • 21. 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]  

  • 22. The Werner syndrome protein: an update.
    Oshima J
    Bioessays; 2000 Oct; 22(10):894-901. PubMed ID: 10984715
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. WRN helicase expression in Werner syndrome cell lines.
    Moser MJ; Kamath-Loeb AS; Jacob JE; Bennett SE; Oshima J; Monnat RJ
    Nucleic Acids Res; 2000 Jan; 28(2):648-54. PubMed ID: 10606667
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 58(22):5188-95. PubMed ID: 9823331
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Diagnosis of Werner syndrome by immunoblot analysis.
    Shimizu T; Tateishi Y; Furuichi Y; Sugimoto M; Kawabe T; Matsumoto T; Shimizu H
    Clin Exp Dermatol; 2002 Mar; 27(2):157-9. PubMed ID: 11952711
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Functional deficit associated with a missense Werner syndrome mutation.
    Tadokoro T; Rybanska-Spaeder I; Kulikowicz T; Dawut L; Oshima J; Croteau DL; Bohr VA
    DNA Repair (Amst); 2013 Jun; 12(6):414-21. PubMed ID: 23583337
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex.
    Li B; Comai L
    J Biol Chem; 2001 Mar; 276(13):9896-902. PubMed ID: 11152456
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
    Shen JC; Loeb LA
    Trends Genet; 2000 May; 16(5):213-20. PubMed ID: 10782115
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.
    Shen JC; Gray MD; Oshima J; Kamath-Loeb AS; Fry M; Loeb LA
    J Biol Chem; 1998 Dec; 273(51):34139-44. PubMed ID: 9852073
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Werner syndrome: characterization of mutations in the WRN gene in an affected family.
    Meisslitzer C; Ruppitsch W; Weirich-Schwaiger H; Weirich HG; Jabkowsky J; Klein G; Schweiger M; Hirsch-Kauffmann M
    Eur J Hum Genet; 1997; 5(6):364-70. PubMed ID: 9450180
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Solution structure of a multifunctional DNA- and protein-binding motif of human Werner syndrome protein.
    Hu JS; Feng H; Zeng W; Lin GX; Xi XG
    Proc Natl Acad Sci U S A; 2005 Dec; 102(51):18379-84. PubMed ID: 16339893
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA.
    Rodríguez-López AM; Jackson DA; Nehlin JO; Iborra F; Warren AV; Cox LS
    Mech Ageing Dev; 2003 Feb; 124(2):167-74. PubMed ID: 12633936
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The N-terminal domain of the large subunit of human replication protein A binds to Werner syndrome protein and stimulates helicase activity.
    Shen JC; Lao Y; Kamath-Loeb A; Wold MS; Loeb LA
    Mech Ageing Dev; 2003; 124(8-9):921-30. PubMed ID: 14499497
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity.
    Brosh RM; von Kobbe C; Sommers JA; Karmakar P; Opresko PL; Piotrowski J; Dianova I; Dianov GL; Bohr VA
    EMBO J; 2001 Oct; 20(20):5791-801. PubMed ID: 11598021
    [TBL] [Abstract][Full Text] [Related]  

  • 38. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects.
    Yokote K; Chanprasert S; Lee L; Eirich K; Takemoto M; Watanabe A; Koizumi N; Lessel D; Mori T; Hisama FM; Ladd PD; Angle B; Baris H; Cefle K; Palanduz S; Ozturk S; Chateau A; Deguchi K; Easwar TK; Federico A; Fox A; Grebe TA; Hay B; Nampoothiri S; Seiter K; Streeten E; Piña-Aguilar RE; Poke G; Poot M; Posmyk R; Martin GM; Kubisch C; Schindler D; Oshima J
    Hum Mutat; 2017 Jan; 38(1):7-15. PubMed ID: 27667302
    [TBL] [Abstract][Full Text] [Related]  

  • 39. p53 Modulates the exonuclease activity of Werner syndrome protein.
    Brosh RM; Karmakar P; Sommers JA; Yang Q; Wang XW; Spillare EA; Harris CC; Bohr VA
    J Biol Chem; 2001 Sep; 276(37):35093-102. PubMed ID: 11427532
    [TBL] [Abstract][Full Text] [Related]  

  • 40. WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblasts.
    Hisama FM; Chen YH; Meyn MS; Oshima J; Weissman SM
    Cancer Res; 2000 May; 60(9):2372-6. PubMed ID: 10811112
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.