These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 8288910)

  • 1. Hypermutable ligation of plasmid DNA ends in cells from patients with Werner syndrome.
    Rünger TM; Bauer C; Dekant B; Möller K; Sobotta P; Czerny C; Poot M; Martin GM
    J Invest Dermatol; 1994 Jan; 102(1):45-8. PubMed ID: 8288910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homologous recombination is elevated in some Werner-like syndromes but not during normal in vitro or in vivo senescence of mammalian cells.
    Cheng RZ; Murano S; Kurz B; Shmookler Reis RJ
    Mutat Res; 1990; 237(5-6):259-69. PubMed ID: 2079965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Joining of linear plasmid DNA is reduced and error-prone in Bloom's syndrome cells.
    Rünger TM; Kraemer KH
    EMBO J; 1989 May; 8(5):1419-25. PubMed ID: 2767047
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. In-vivo assessment of DNA ligation efficiency and fidelity in cells from patients with Fanconi's anemia and other cancer-prone hereditary disorders.
    Rünger TM; Sobotta P; Dekant B; Möller K; Bauer C; Kraemer KH
    Toxicol Lett; 1993 Apr; 67(1-3):309-24. PubMed ID: 8451768
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal processing of transfected plasmid DNA in cells from patients with ataxia telangiectasia.
    Rünger TM; Poot M; Kraemer KH
    Mutat Res; 1992 Nov; 293(1):47-54. PubMed ID: 1383810
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutator phenotype of Werner syndrome is characterized by extensive deletions.
    Fukuchi K; Martin GM; Monnat RJ
    Proc Natl Acad Sci U S A; 1989 Aug; 86(15):5893-7. PubMed ID: 2762303
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. The gene responsible for Werner syndrome may be a cell division "counting" gene.
    Faragher RG; Kill IR; Hunter JA; Pope FM; Tannock C; Shall S
    Proc Natl Acad Sci U S A; 1993 Dec; 90(24):12030-4. PubMed ID: 8265666
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Analysis of microsatellite instability and hypermutation of immunoglobulin variable genes in Werner syndrome.
    Rosner K; Winter DB; Skovgaard GL; Oshima J; Gearhart PJ; Bohr VA
    Mech Ageing Dev; 2001 Aug; 122(11):1121-33. PubMed ID: 11389928
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.
    Fukuchi K; Tanaka K; Kumahara Y; Marumo K; Pride MB; Martin GM; Monnat RJ
    Hum Genet; 1990 Feb; 84(3):249-52. PubMed ID: 2303247
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Essential role of limiting telomeres in the pathogenesis of Werner syndrome.
    Chang S; Multani AS; Cabrera NG; Naylor ML; Laud P; Lombard D; Pathak S; Guarente L; DePinho RA
    Nat Genet; 2004 Aug; 36(8):877-82. PubMed ID: 15235603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.
    Fukuchi K; Tanaka K; Nakura J; Kumahara Y; Uchida T; Okada Y
    Somat Cell Mol Genet; 1985 Jul; 11(4):303-8. PubMed ID: 2992100
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Immortalization of Werner syndrome and progeria fibroblasts.
    Saito H; Moses RE
    Exp Cell Res; 1991 Feb; 192(2):373-9. PubMed ID: 1671011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The Werner syndrome protein is a DNA helicase.
    Gray MD; Shen JC; Kamath-Loeb AS; Blank A; Sopher BL; Martin GM; Oshima J; Loeb LA
    Nat Genet; 1997 Sep; 17(1):100-3. PubMed ID: 9288107
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Werner syndrome: clinical evaluation of two cases and a novel mutation.
    Mansur AT; Elçioglu NH; Demirci GT
    Genet Couns; 2014; 25(2):119-27. PubMed ID: 25059010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.