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553 related items for PubMed ID: 23468640

  • 1. MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice.
    Tomé S, Manley K, Simard JP, Clark GW, Slean MM, Swami M, Shelbourne PF, Tillier ER, Monckton DG, Messer A, Pearson CE.
    PLoS Genet; 2013; 9(2):e1003280. PubMed ID: 23468640
    [Abstract] [Full Text] [Related]

  • 2. A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease.
    Aldous SG, Smith EJ, Landles C, Osborne GF, Cañibano-Pico M, Nita IM, Phillips J, Zhang Y, Jin B, Hirst MB, Benn CL, Bond BC, Edelmann W, Greene JR, Bates GP.
    Brain; 2024 May 03; 147(5):1784-1798. PubMed ID: 38387080
    [Abstract] [Full Text] [Related]

  • 3. Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
    Pinto RM, Dragileva E, Kirby A, Lloret A, Lopez E, St Claire J, Panigrahi GB, Hou C, Holloway K, Gillis T, Guide JR, Cohen PE, Li GM, Pearson CE, Daly MJ, Wheeler VC.
    PLoS Genet; 2013 Oct 03; 9(10):e1003930. PubMed ID: 24204323
    [Abstract] [Full Text] [Related]

  • 4. Transcription elongation and tissue-specific somatic CAG instability.
    Goula AV, Stys A, Chan JP, Trottier Y, Festenstein R, Merienne K.
    PLoS Genet; 2012 Oct 03; 8(11):e1003051. PubMed ID: 23209427
    [Abstract] [Full Text] [Related]

  • 5. Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease.
    O'Reilly D, Belgrad J, Ferguson C, Summers A, Sapp E, McHugh C, Mathews E, Boudi A, Buchwald J, Ly S, Moreno D, Furgal R, Luu E, Kennedy Z, Hariharan V, Monopoli K, Yang XW, Carroll J, DiFiglia M, Aronin N, Khvorova A.
    Mol Ther; 2023 Jun 07; 31(6):1661-1674. PubMed ID: 37177784
    [Abstract] [Full Text] [Related]

  • 6. Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.
    Du J, Campau E, Soragni E, Jespersen C, Gottesfeld JM.
    Hum Mol Genet; 2013 Dec 20; 22(25):5276-87. PubMed ID: 23933738
    [Abstract] [Full Text] [Related]

  • 7. Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liver.
    Lee JM, Pinto RM, Gillis T, St Claire JC, Wheeler VC.
    PLoS One; 2011 Dec 20; 6(8):e23647. PubMed ID: 21897851
    [Abstract] [Full Text] [Related]

  • 8. Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
    Dragileva E, Hendricks A, Teed A, Gillis T, Lopez ET, Friedberg EC, Kucherlapati R, Edelmann W, Lunetta KL, MacDonald ME, Wheeler VC.
    Neurobiol Dis; 2009 Jan 20; 33(1):37-47. PubMed ID: 18930147
    [Abstract] [Full Text] [Related]

  • 9. 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 20; 5(5):e1000482. PubMed ID: 19436705
    [Abstract] [Full Text] [Related]

  • 10. Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.
    Goula AV, Berquist BR, Wilson DM, Wheeler VC, Trottier Y, Merienne K.
    PLoS Genet; 2009 Dec 20; 5(12):e1000749. PubMed ID: 19997493
    [Abstract] [Full Text] [Related]

  • 11. Disease-associated repeat instability and mismatch repair.
    Schmidt MHM, Pearson CE.
    DNA Repair (Amst); 2016 Feb 20; 38():117-126. PubMed ID: 26774442
    [Abstract] [Full Text] [Related]

  • 12. Loss of TDP-43 promotes somatic CAG repeat expansion in Huntington's disease knock-in mice.
    Bai D, Zhu L, Jia Q, Duan X, Chen L, Wang X, Hou J, Jiang G, Yang S, Li S, Li XJ, Yin P.
    Prog Neurobiol; 2023 Aug 20; 227():102484. PubMed ID: 37315918
    [Abstract] [Full Text] [Related]

  • 13. Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.
    Wheeler VC, Dion V.
    J Huntingtons Dis; 2021 Aug 20; 10(1):123-148. PubMed ID: 33579861
    [Abstract] [Full Text] [Related]

  • 14. Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice.
    Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, Gillis T, Lopez E, Myers RH, MacDonald ME, Wheeler VC.
    Hum Mol Genet; 2006 Jun 15; 15(12):2015-24. PubMed ID: 16687439
    [Abstract] [Full Text] [Related]

  • 15. Age-, tissue- and length-dependent bidirectional somatic CAG•CTG repeat instability in an allelic series of R6/2 Huntington disease mice.
    Larson E, Fyfe I, Morton AJ, Monckton DG.
    Neurobiol Dis; 2015 Apr 15; 76():98-111. PubMed ID: 25662336
    [Abstract] [Full Text] [Related]

  • 16. Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
    van den Broek WJ, Nelen MR, Wansink DG, Coerwinkel MM, te Riele H, Groenen PJ, Wieringa B.
    Hum Mol Genet; 2002 Jan 15; 11(2):191-8. PubMed ID: 11809728
    [Abstract] [Full Text] [Related]

  • 17. Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation.
    Seriola A, Spits C, Simard JP, Hilven P, Haentjens P, Pearson CE, Sermon K.
    Hum Mol Genet; 2011 Jan 01; 20(1):176-85. PubMed ID: 20935170
    [Abstract] [Full Text] [Related]

  • 18. Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice.
    Kovalenko M, Dragileva E, St Claire J, Gillis T, Guide JR, New J, Dong H, Kucherlapati R, Kucherlapati MH, Ehrlich ME, Lee JM, Wheeler VC.
    PLoS One; 2012 Jan 01; 7(9):e44273. PubMed ID: 22970194
    [Abstract] [Full Text] [Related]

  • 19. The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeats.
    Goula AV, Pearson CE, Della Maria J, Trottier Y, Tomkinson AE, Wilson DM, Merienne K.
    Biochemistry; 2012 May 08; 51(18):3919-32. PubMed ID: 22497302
    [Abstract] [Full Text] [Related]

  • 20. Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age.
    Mason AG, Tomé S, Simard JP, Libby RT, Bammler TK, Beyer RP, Morton AJ, Pearson CE, La Spada AR.
    Hum Mol Genet; 2014 Mar 15; 23(6):1606-18. PubMed ID: 24191263
    [Abstract] [Full Text] [Related]

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