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329 related items for PubMed ID: 20935170

  • 1. 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]

  • 2. Somatic CTG*CAG repeat instability in a mouse model for myotonic dystrophy type 1 is associated with changes in cell nuclearity and DNA ploidy.
    van den Broek WJ, Wansink DG, Wieringa B.
    BMC Mol Biol; 2007 Jul 23; 8():61. PubMed ID: 17645799
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation.
    De Temmerman N, Seneca S, Van Steirteghem A, Haentjens P, Van der Elst J, Liebaers I, Sermon KD.
    Mol Hum Reprod; 2008 Jul 20; 14(7):405-12. PubMed ID: 18577525
    [Abstract] [Full Text] [Related]

  • 5. DNA mismatch repair in trinucleotide repeat instability.
    Guo J, Chen L, Li GM.
    Sci China Life Sci; 2017 Oct 20; 60(10):1087-1092. PubMed ID: 29075942
    [Abstract] [Full Text] [Related]

  • 6. MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.
    Franck S, Barbé L, Ardui S, De Vlaeminck Y, Allemeersch J, Dziedzicka D, Spits C, Vanroye F, Hilven P, Duqué G, Vermeesch JR, Gheldof A, Sermon K.
    Hum Mol Genet; 2021 Jan 06; 29(21):3566-3577. PubMed ID: 33242073
    [Abstract] [Full Text] [Related]

  • 7. 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 06; 5(5):e1000482. PubMed ID: 19436705
    [Abstract] [Full Text] [Related]

  • 8. Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.
    Manley K, Shirley TL, Flaherty L, Messer A.
    Nat Genet; 1999 Dec 06; 23(4):471-3. PubMed ID: 10581038
    [Abstract] [Full Text] [Related]

  • 9. Fen1 does not control somatic hypermutability of the (CTG)(n)*(CAG)(n) repeat in a knock-in mouse model for DM1.
    van den Broek WJ, Nelen MR, van der Heijden GW, Wansink DG, Wieringa B.
    FEBS Lett; 2006 Oct 02; 580(22):5208-14. PubMed ID: 16978612
    [Abstract] [Full Text] [Related]

  • 10. Disease-associated repeat instability and mismatch repair.
    Schmidt MHM, Pearson CE.
    DNA Repair (Amst); 2016 Feb 02; 38():117-126. PubMed ID: 26774442
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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 Jun 05; 9(2):e1003280. PubMed ID: 23468640
    [Abstract] [Full Text] [Related]

  • 13. Huntington's disease--like 2 is associated with CUG repeat-containing RNA foci.
    Rudnicki DD, Holmes SE, Lin MW, Thornton CA, Ross CA, Margolis RL.
    Ann Neurol; 2007 Mar 05; 61(3):272-82. PubMed ID: 17387722
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
    de Haro M, Al-Ramahi I, De Gouyon B, Ukani L, Rosa A, Faustino NA, Ashizawa T, Cooper TA, Botas J.
    Hum Mol Genet; 2006 Jul 01; 15(13):2138-45. PubMed ID: 16723374
    [Abstract] [Full Text] [Related]

  • 16. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
    Savić D, Rakocvic-Stojanovic V, Keckarevic D, Culjkovic B, Stojkovic O, Mladenovic J, Todorovic S, Apostolski S, Romac S.
    Hum Mutat; 2002 Feb 01; 19(2):131-9. PubMed ID: 11793472
    [Abstract] [Full Text] [Related]

  • 17. A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage.
    Jackson SM, Whitworth AJ, Greene JC, Libby RT, Baccam SL, Pallanck LJ, La Spada AR.
    Gene; 2005 Feb 28; 347(1):35-41. PubMed ID: 15715978
    [Abstract] [Full Text] [Related]

  • 18. Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
    Braida C, Stefanatos RK, Adam B, Mahajan N, Smeets HJ, Niel F, Goizet C, Arveiler B, Koenig M, Lagier-Tourenne C, Mandel JL, Faber CG, de Die-Smulders CE, Spaans F, Monckton DG.
    Hum Mol Genet; 2010 Apr 15; 19(8):1399-412. PubMed ID: 20080938
    [Abstract] [Full Text] [Related]

  • 19. Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability.
    Ueki J, Nakamori M, Nakamura M, Nishikawa M, Yoshida Y, Tanaka A, Morizane A, Kamon M, Araki T, Takahashi MP, Watanabe A, Inagaki N, Sakurai H.
    Sci Rep; 2017 Feb 13; 7():42522. PubMed ID: 28211918
    [Abstract] [Full Text] [Related]

  • 20. Instability in the transmission of the myotonic dystrophy CTG repeat in human oocytes and preimplantation embryos.
    Dean NL, Tan SL, Ao A.
    Fertil Steril; 2006 Jul 13; 86(1):98-105. PubMed ID: 16716318
    [Abstract] [Full Text] [Related]

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