BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 9618520)

  • 1. Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2.
    Winter DB; Phung QH; Umar A; Baker SM; Tarone RE; Tanaka K; Liskay RM; Kunkel TA; Bohr VA; Gearhart PJ
    Proc Natl Acad Sci U S A; 1998 Jun; 95(12):6953-8. PubMed ID: 9618520
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PMS2-deficiency diminishes hypermutation of a lambda1 transgene in young but not older mice.
    Kong Q; Maizels N
    Mol Immunol; 1999 Feb; 36(2):83-91. PubMed ID: 10378680
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications.
    Kim N; Bozek G; Lo JC; Storb U
    J Exp Med; 1999 Jul; 190(1):21-30. PubMed ID: 10429667
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hypermutation in Ig V genes from mice deficient in the MLH1 mismatch repair protein.
    Phung QH; Winter DB; Alrefai R; Gearhart PJ
    J Immunol; 1999 Mar; 162(6):3121-4. PubMed ID: 10092760
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Switch junction sequences in PMS2-deficient mice reveal a microhomology-mediated mechanism of Ig class switch recombination.
    Ehrenstein MR; Rada C; Jones AM; Milstein C; Neuberger MS
    Proc Natl Acad Sci U S A; 2001 Dec; 98(25):14553-8. PubMed ID: 11717399
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple mutations are common at mouse Aprt in genotoxin-exposed mismatch repair deficient cells.
    Shin CY; Mellon I; Turker MS
    Oncogene; 2002 Mar; 21(11):1768-76. PubMed ID: 11896608
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutagenesis in PMS2- and MSH2-deficient mice indicates differential protection from transversions and frameshifts.
    Andrew SE; Xu XS; Baross-Francis A; Narayanan L; Milhausen K; Liskay RM; Jirik FR; Glazer PM
    Carcinogenesis; 2000 Jul; 21(7):1291-5. PubMed ID: 10874005
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fixing mismatches.
    Shannon M; Weigert M
    Science; 1998 Feb; 279(5354):1159-60. PubMed ID: 9508690
    [No Abstract]   [Full Text] [Related]  

  • 10. Different mutator phenotypes in Mlh1- versus Pms2-deficient mice.
    Yao X; Buermeyer AB; Narayanan L; Tran D; Baker SM; Prolla TA; Glazer PM; Liskay RM; Arnheim N
    Proc Natl Acad Sci U S A; 1999 Jun; 96(12):6850-5. PubMed ID: 10359802
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and not with the hypermutation process.
    Frey S; Bertocci B; Delbos F; Quint L; Weill JC; Reynaud CA
    Immunity; 1998 Jul; 9(1):127-34. PubMed ID: 9697842
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hypermutability to ionizing radiation in mismatch repair-deficient, Pms2 knockout mice.
    Xu XS; Narayanan L; Dunklee B; Liskay RM; Glazer PM
    Cancer Res; 2001 May; 61(9):3775-80. PubMed ID: 11325851
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis.
    Baker SM; Bronner CE; Zhang L; Plug AW; Robatzek M; Warren G; Elliott EA; Yu J; Ashley T; Arnheim N; Flavell RA; Liskay RM
    Cell; 1995 Jul; 82(2):309-19. PubMed ID: 7628019
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair.
    Mohd AB; Palama B; Nelson SE; Tomer G; Nguyen M; Huo X; Buermeyer AB
    DNA Repair (Amst); 2006 Mar; 5(3):347-61. PubMed ID: 16338176
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Role for mismatch repair proteins Msh2, Mlh1, and Pms2 in immunoglobulin class switching shown by sequence analysis of recombination junctions.
    Schrader CE; Vardo J; Stavnezer J
    J Exp Med; 2002 Feb; 195(3):367-73. PubMed ID: 11828012
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6.
    Hegan DC; Narayanan L; Jirik FR; Edelmann W; Liskay RM; Glazer PM
    Carcinogenesis; 2006 Dec; 27(12):2402-8. PubMed ID: 16728433
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse.
    Chen PC; Dudley S; Hagen W; Dizon D; Paxton L; Reichow D; Yoon SR; Yang K; Arnheim N; Liskay RM; Lipkin SM
    Cancer Res; 2005 Oct; 65(19):8662-70. PubMed ID: 16204034
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair.
    Tomer G; Buermeyer AB; Nguyen MM; Liskay RM
    J Biol Chem; 2002 Jun; 277(24):21801-9. PubMed ID: 11897781
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.