BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 11717399)

  • 61. Levels of H-ras codon 61 CAA to AAA mutation: response to 4-ABP-treatment and Pms2-deficiency.
    Parsons BL; Delongchamp RR; Beland FA; Heflich RH
    Mutagenesis; 2006 Jan; 21(1):29-34. PubMed ID: 16314341
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Highly elevated ultraviolet-induced mutation frequency in isolated Chinese hamster cell lines defective in nucleotide excision repair and mismatch repair proteins.
    Nara K; Nagashima F; Yasui A
    Cancer Res; 2001 Jan; 61(1):50-2. PubMed ID: 11196196
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Biallelic somatic inactivation of the mismatch repair gene MLH1 in a primary skin melanoma.
    Castiglia D; Pagani E; Alvino E; Vernole P; Marra G; Cannavò E; Jiricny J; Zambruno G; D'Atri S
    Genes Chromosomes Cancer; 2003 Jun; 37(2):165-75. PubMed ID: 12696065
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Altered somatic hypermutation and reduced class-switch recombination in exonuclease 1-mutant mice.
    Bardwell PD; Woo CJ; Wei K; Li Z; Martin A; Sack SZ; Parris T; Edelmann W; Scharff MD
    Nat Immunol; 2004 Feb; 5(2):224-9. PubMed ID: 14716311
    [TBL] [Abstract][Full Text] [Related]  

  • 65. A role for Pms2 in the prevention of tandem CC --> TT substitutions induced by ultraviolet radiation and oxidative stress.
    Shin-Darlak CY; Skinner AM; Turker MS
    DNA Repair (Amst); 2005 Jan; 4(1):51-7. PubMed ID: 15533837
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Pms2 deficiency results in increased mutation in the Hprt gene but not the Tk gene of Tk(+/-) transgenic mice.
    Dobrovolsky VN; McKinzie PB; Shaddock JG; Mittelstaedt RA; Heflich RH; Parsons BL
    Mutagenesis; 2003 Jul; 18(4):365-70. PubMed ID: 12840110
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Mismatch repair co-opted by hypermutation.
    Cascalho M; Wong J; Steinberg C; Wabl M
    Science; 1998 Feb; 279(5354):1207-10. PubMed ID: 9469811
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Signaling mismatch repair: the mechanics of an adenosine-nucleotide molecular switch.
    Fishel R; Acharya S; Berardini M; Bocker T; Charbonneau N; Cranston A; Gradia S; Guerrette S; Heinen CD; Mazurek A; Snowden T; Schmutte C; Shim KS; Tombline G; Wilson T
    Cold Spring Harb Symp Quant Biol; 2000; 65():217-24. PubMed ID: 12760035
    [No Abstract]   [Full Text] [Related]  

  • 69. Maternal effect for DNA mismatch repair in the mouse.
    Gurtu VE; Verma S; Grossmann AH; Liskay RM; Skarnes WC; Baker SM
    Genetics; 2002 Jan; 160(1):271-7. PubMed ID: 11805062
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Reassessment of the role of Mut S homolog 5 in Ig class switch recombination shows lack of involvement in cis- and trans-switching.
    Guikema JE; Schrader CE; Leus NG; Ucher A; Linehan EK; Werling U; Edelmann W; Stavnezer J
    J Immunol; 2008 Dec; 181(12):8450-9. PubMed ID: 19050263
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient in the MSH2 mismatch repair protein.
    Phung QH; Winter DB; Cranston A; Tarone RE; Bohr VA; Fishel R; Gearhart PJ
    J Exp Med; 1998 Jun; 187(11):1745-51. PubMed ID: 9607916
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Somatic hypermutation in the absence of DNA-dependent protein kinase catalytic subunit (DNA-PK(cs)) or recombination-activating gene (RAG)1 activity.
    Bemark M; Sale JE; Kim HJ; Berek C; Cosgrove RA; Neuberger MS
    J Exp Med; 2000 Nov; 192(10):1509-14. PubMed ID: 11085752
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Somatic hypermutation at A/T-rich oligonucleotide substrates shows different strand polarities in Ung-deficient or -proficient backgrounds.
    Zivojnovic M; Delbos F; Girelli Zubani G; Julé A; Alcais A; Weill JC; Reynaud CA; Storck S
    Mol Cell Biol; 2014 Jun; 34(12):2176-87. PubMed ID: 24710273
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Deficient Pms2, ERCC1, Ku86, CcOI in field defects during progression to colon cancer.
    Nguyen H; Loustaunau C; Facista A; Ramsey L; Hassounah N; Taylor H; Krouse R; Payne CM; Tsikitis VL; Goldschmid S; Banerjee B; Perini RF; Bernstein C
    J Vis Exp; 2010 Jul; (41):. PubMed ID: 20689513
    [TBL] [Abstract][Full Text] [Related]  

  • 75. The mutation spectrum of purified AID is similar to the mutability index in Ramos cells and in ung(-/-)msh2(-/-) mice.
    Larijani M; Frieder D; Basit W; Martin A
    Immunogenetics; 2005 Feb; 56(11):840-5. PubMed ID: 15650878
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Gene conversion-like sequence transfers between transgenic antibody V genes are independent of RAD54.
    D'Avirro N; Truong D; Luong M; Kanaar R; Selsing E
    J Immunol; 2002 Sep; 169(6):3069-75. PubMed ID: 12218123
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Getting rid of the PMS2 pseudogenes: mission impossible?
    Niessen RC; Kleibeuker JH; Jager PO; Sijmons RH; Hofstra RM
    Hum Mutat; 2007 Apr; 28(4):414; author reply 415. PubMed ID: 17139668
    [No Abstract]   [Full Text] [Related]  

  • 78. Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2.
    Narayanan L; Fritzell JA; Baker SM; Liskay RM; Glazer PM
    Proc Natl Acad Sci U S A; 1997 Apr; 94(7):3122-7. PubMed ID: 9096356
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Human PMS2 gene family: origin, molecular evolution, and biological implications.
    Shpakovskii DG; Shematorova EK; Shpakovskii GV
    Dokl Biochem Biophys; 2006; 408():175-9. PubMed ID: 16913423
    [No Abstract]   [Full Text] [Related]  

  • 80. Hot spot focusing of somatic hypermutation in MSH2-deficient mice suggests two stages of mutational targeting.
    Rada C; Ehrenstein MR; Neuberger MS; Milstein C
    Immunity; 1998 Jul; 9(1):135-41. PubMed ID: 9697843
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.