BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 16673358)

  • 61. The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. Online.
    Vidal V; Bay JO; Champomier F; Grancho M; Beauville L; Glowaczower C; Lemery D; Ferrara M; Bignon YJ
    Hum Mutat; 1998; 11(5):413-4. PubMed ID: 10206685
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Analyses of the interaction of WRNIP1 with Werner syndrome protein (WRN) in vitro and in the cell.
    Kawabe Y; Seki M; Yoshimura A; Nishino K; Hayashi T; Takeuchi T; Iguchi S; Kusa Y; Ohtsuki M; Tsuyama T; Imamura O; Matsumoto T; Furuichi Y; Tada S; Enomoto T
    DNA Repair (Amst); 2006 Jul; 5(7):816-28. PubMed ID: 16769258
    [TBL] [Abstract][Full Text] [Related]  

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

  • 64. Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein.
    Opresko PL; Laine JP; Brosh RM; Seidman MM; Bohr VA
    J Biol Chem; 2001 Nov; 276(48):44677-87. PubMed ID: 11572872
    [TBL] [Abstract][Full Text] [Related]  

  • 65. 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]  

  • 66. Functional link between Myc and the Werner gene in tumorigenesis.
    Grandori C; Robinson KL; Galloway DA; Swisshelm K
    Cell Cycle; 2004 Jan; 3(1):22-5. PubMed ID: 14657658
    [TBL] [Abstract][Full Text] [Related]  

  • 67. 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]  

  • 68. 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]  

  • 69. 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]  

  • 70. Nucleolar localization of the Werner syndrome protein in human cells.
    Marciniak RA; Lombard DB; Johnson FB; Guarente L
    Proc Natl Acad Sci U S A; 1998 Jun; 95(12):6887-92. PubMed ID: 9618508
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Syndrome-causing mutations in Werner syndrome.
    Goto M
    Biosci Trends; 2008 Aug; 2(4):147-50. PubMed ID: 20103920
    [TBL] [Abstract][Full Text] [Related]  

  • 72. 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]  

  • 73. Crystal structure of the HRDC domain of human Werner syndrome protein, WRN.
    Kitano K; Yoshihara N; Hakoshima T
    J Biol Chem; 2007 Jan; 282(4):2717-28. PubMed ID: 17148451
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Homologous recombination resolution defect in werner syndrome.
    Saintigny Y; Makienko K; Swanson C; Emond MJ; Monnat RJ
    Mol Cell Biol; 2002 Oct; 22(20):6971-8. PubMed ID: 12242278
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase.
    Dhillon KK; Sidorova JM; Albertson TM; Anderson JB; Ladiges WC; Rabinovitch PS; Preston BD; Monnat RJ
    DNA Repair (Amst); 2010 Jan; 9(1):11-22. PubMed ID: 19896421
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Werner syndrome protein contains three structure-specific DNA binding domains.
    von Kobbe C; Thomä NH; Czyzewski BK; Pavletich NP; Bohr VA
    J Biol Chem; 2003 Dec; 278(52):52997-3006. PubMed ID: 14534320
    [TBL] [Abstract][Full Text] [Related]  

  • 77. TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA.
    Machwe A; Xiao L; Orren DK
    Oncogene; 2004 Jan; 23(1):149-56. PubMed ID: 14712220
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products.
    Goto M; Yamabe Y; Shiratori M; Okada M; Kawabe T; Matsumoto T; Sugimoto M; Furuichi Y
    Hum Genet; 1999 Oct; 105(4):301-7. PubMed ID: 10543396
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Search and insights into novel genetic alterations leading to classical and atypical Werner syndrome.
    Oshima J; Hisama FM
    Gerontology; 2014; 60(3):239-46. PubMed ID: 24401204
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Werner protein recruits DNA polymerase delta to the nucleolus.
    Szekely AM; Chen YH; Zhang C; Oshima J; Weissman SM
    Proc Natl Acad Sci U S A; 2000 Oct; 97(21):11365-70. PubMed ID: 11027336
    [TBL] [Abstract][Full Text] [Related]  

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