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235 related items for PubMed ID: 23071719

  • 1. Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues.
    Bourn RL, De Biase I, Pinto RM, Sandi C, Al-Mahdawi S, Pook MA, Bidichandani SI.
    PLoS One; 2012; 7(10):e47085. PubMed ID: 23071719
    [Abstract] [Full Text] [Related]

  • 2. The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model.
    Ezzatizadeh V, Pinto RM, Sandi C, Sandi M, Al-Mahdawi S, Te Riele H, Pook MA.
    Neurobiol Dis; 2012 Apr; 46(1):165-71. PubMed ID: 22289650
    [Abstract] [Full Text] [Related]

  • 3. MutLα heterodimers modify the molecular phenotype of Friedreich ataxia.
    Ezzatizadeh V, Sandi C, Sandi M, Anjomani-Virmouni S, Al-Mahdawi S, Pook MA.
    PLoS One; 2014 Apr; 9(6):e100523. PubMed ID: 24971578
    [Abstract] [Full Text] [Related]

  • 4. DNA mismatch repair complex MutSβ promotes GAA·TTC repeat expansion in human cells.
    Halabi A, Ditch S, Wang J, Grabczyk E.
    J Biol Chem; 2012 Aug 24; 287(35):29958-67. PubMed ID: 22787155
    [Abstract] [Full Text] [Related]

  • 5. Disease-associated repeat instability and mismatch repair.
    Schmidt MHM, Pearson CE.
    DNA Repair (Amst); 2016 Feb 24; 38():117-126. PubMed ID: 26774442
    [Abstract] [Full Text] [Related]

  • 6. MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
    Tomé S, Holt I, Edelmann W, Morris GE, Munnich A, Pearson CE, Gourdon G.
    PLoS Genet; 2009 May 24; 5(5):e1000482. PubMed ID: 19436705
    [Abstract] [Full Text] [Related]

  • 7. Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.
    Gomes-Pereira M, Fortune MT, Ingram L, McAbney JP, Monckton DG.
    Hum Mol Genet; 2004 Aug 15; 13(16):1815-25. PubMed ID: 15198993
    [Abstract] [Full Text] [Related]

  • 8. Role of mismatch repair enzymes in GAA·TTC triplet-repeat expansion in Friedreich ataxia induced pluripotent stem cells.
    Du J, Campau E, Soragni E, Ku S, Puckett JW, Dervan PB, Gottesfeld JM.
    J Biol Chem; 2012 Aug 24; 287(35):29861-72. PubMed ID: 22798143
    [Abstract] [Full Text] [Related]

  • 9. The GAA triplet-repeat is unstable in the context of the human FXN locus and displays age-dependent expansions in cerebellum and DRG in a transgenic mouse model.
    Clark RM, De Biase I, Malykhina AP, Al-Mahdawi S, Pook M, Bidichandani SI.
    Hum Genet; 2007 Jan 24; 120(5):633-40. PubMed ID: 17024371
    [Abstract] [Full Text] [Related]

  • 10. E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence.
    Bourn RL, Rindler PM, Pollard LM, Bidichandani SI.
    Mutat Res; 2009 Feb 10; 661(1-2):71-7. PubMed ID: 19046977
    [Abstract] [Full Text] [Related]

  • 11. 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 10; 27(12):2402-8. PubMed ID: 16728433
    [Abstract] [Full Text] [Related]

  • 12. Diverse effects of individual mismatch repair components on transcription-induced CAG repeat instability in human cells.
    Lin Y, Wilson JH.
    DNA Repair (Amst); 2009 Aug 06; 8(8):878-85. PubMed ID: 19497791
    [Abstract] [Full Text] [Related]

  • 13. Replication-independent instability of Friedreich's ataxia GAA repeats during chronological aging.
    Neil AJ, Hisey JA, Quasem I, McGinty RJ, Hitczenko M, Khristich AN, Mirkin SM.
    Proc Natl Acad Sci U S A; 2021 Feb 02; 118(5):. PubMed ID: 33495349
    [Abstract] [Full Text] [Related]

  • 14. Mismatch repair genes expression defects & association with clinicopathological characteristics in colorectal carcinoma.
    Kaur G, Masoud A, Raihan N, Radzi M, Khamizar W, Kam LS.
    Indian J Med Res; 2011 Aug 02; 134(2):186-92. PubMed ID: 21911971
    [Abstract] [Full Text] [Related]

  • 15. Replication in mammalian cells recapitulates the locus-specific differences in somatic instability of genomic GAA triplet-repeats.
    M Rindler P, Clark RM, Pollard LM, De Biase I, Bidichandani SI.
    Nucleic Acids Res; 2006 Aug 02; 34(21):6352-61. PubMed ID: 17142224
    [Abstract] [Full Text] [Related]

  • 16. Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer.
    Truninger K, Menigatti M, Luz J, Russell A, Haider R, Gebbers JO, Bannwart F, Yurtsever H, Neuweiler J, Riehle HM, Cattaruzza MS, Heinimann K, Schär P, Jiricny J, Marra G.
    Gastroenterology; 2005 May 02; 128(5):1160-71. PubMed ID: 15887099
    [Abstract] [Full Text] [Related]

  • 17. Large expansion of CTG•CAG repeats is exacerbated by MutSβ in human cells.
    Nakatani R, Nakamori M, Fujimura H, Mochizuki H, Takahashi MP.
    Sci Rep; 2015 Jun 05; 5():11020. PubMed ID: 26047474
    [Abstract] [Full Text] [Related]

  • 18. Elevated levels of the mismatch repair protein PMS2 are associated with prostate cancer.
    Norris AM, Woodruff RD, D'Agostino RB, Clodfelter JE, Scarpinato KD.
    Prostate; 2007 Feb 01; 67(2):214-25. PubMed ID: 17044039
    [Abstract] [Full Text] [Related]

  • 19. Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
    Haraldsdottir S, Hampel H, Tomsic J, Frankel WL, Pearlman R, de la Chapelle A, Pritchard CC.
    Gastroenterology; 2014 Dec 01; 147(6):1308-1316.e1. PubMed ID: 25194673
    [Abstract] [Full Text] [Related]

  • 20. Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma.
    Hall G, Clarkson A, Shi A, Langford E, Leung H, Eckstein RP, Gill AJ.
    Pathology; 2010 Dec 01; 42(5):409-13. PubMed ID: 20632815
    [Abstract] [Full Text] [Related]

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