BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 10806190)

  • 1. Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1.
    Kawabe Y; Seki M; Seki T; Wang WS; Imamura O; Furuichi Y; Saitoh H; Enomoto T
    J Biol Chem; 2000 Jul; 275(28):20963-6. PubMed ID: 10806190
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Localization of the Bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: comparison with the Werner's syndrome helicase.
    Gharibyan V; Youssoufian H
    Mol Carcinog; 1999 Dec; 26(4):261-73. PubMed ID: 10569803
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functions of RecQ family helicases: possible involvement of Bloom's and Werner's syndrome gene products in guarding genome integrity during DNA replication.
    Enomoto T
    J Biochem; 2001 Apr; 129(4):501-7. PubMed ID: 11275547
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.
    Suzuki N; Shimamoto A; Imamura O; Kuromitsu J; Kitao S; Goto M; Furuichi Y
    Nucleic Acids Res; 1997 Aug; 25(15):2973-8. PubMed ID: 9224595
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases.
    Yamagata K; Kato J; Shimamoto A; Goto M; Furuichi Y; Ikeda H
    Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8733-8. PubMed ID: 9671747
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae.
    Watt PM; Hickson ID; Borts RH; Louis EJ
    Genetics; 1996 Nov; 144(3):935-45. PubMed ID: 8913739
    [TBL] [Abstract][Full Text] [Related]  

  • 7. rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest.
    Stewart E; Chapman CR; Al-Khodairy F; Carr AM; Enoch T
    EMBO J; 1997 May; 16(10):2682-92. PubMed ID: 9184215
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest.
    Constantinou A; Tarsounas M; Karow JK; Brosh RM; Bohr VA; Hickson ID; West SC
    EMBO Rep; 2000 Jul; 1(1):80-4. PubMed ID: 11256630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Roles of the Bloom's syndrome helicase in the maintenance of genome stability.
    Cheok CF; Bachrati CZ; Chan KL; Ralf C; Wu L; Hickson ID
    Biochem Soc Trans; 2005 Dec; 33(Pt 6):1456-9. PubMed ID: 16246145
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Functional analysis of yeast homologue gene associated with human DNA helicase causative syndromes].
    Miyajima A
    Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku; 2002; (120):53-74. PubMed ID: 12638184
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. The N-terminal region of Sgs1, which interacts with Top3, is required for complementation of MMS sensitivity and suppression of hyper-recombination in sgs1 disruptants.
    Ui A; Satoh Y; Onoda F; Miyajima A; Seki M; Enomoto T
    Mol Genet Genomics; 2001 Jul; 265(5):837-50. PubMed ID: 11523801
    [TBL] [Abstract][Full Text] [Related]  

  • 14. In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication.
    Sharma S; Sommers JA; Brosh RM
    Hum Mol Genet; 2004 Oct; 13(19):2247-61. PubMed ID: 15282207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1.
    Li B; Navarro S; Kasahara N; Comai L
    J Biol Chem; 2004 Apr; 279(14):13659-67. PubMed ID: 14734561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain.
    Lee JW; Kusumoto R; Doherty KM; Lin GX; Zeng W; Cheng WH; von Kobbe C; Brosh RM; Hu JS; Bohr VA
    J Biol Chem; 2005 Nov; 280(47):39627-36. PubMed ID: 16150736
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. LMNA mutations in atypical Werner's syndrome.
    Chen L; Lee L; Kudlow BA; Dos Santos HG; Sletvold O; Shafeghati Y; Botha EG; Garg A; Hanson NB; Martin GM; Mian IS; Kennedy BK; Oshima J
    Lancet; 2003 Aug; 362(9382):440-5. PubMed ID: 12927431
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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. PubMed ID: 11795503
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 11138010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.