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Journal Abstract Search

526 related items for PubMed ID: 30118588

  • 1. Furamidine Rescues Myotonic Dystrophy Type I Associated Mis-Splicing through Multiple Mechanisms.
    Jenquin JR, Coonrod LA, Silverglate QA, Pellitier NA, Hale MA, Xia G, Nakamori M, Berglund JA.
    ACS Chem Biol; 2018 Sep 21; 13(9):2708-2718. PubMed ID: 30118588
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  • 3. (CTG)n repeat-mediated dysregulation of MBNL1 and MBNL2 expression during myogenesis in DM1 occurs already at the myoblast stage.
    André LM, van Cruchten RTP, Willemse M, Wansink DG.
    PLoS One; 2019 Sep 21; 14(5):e0217317. PubMed ID: 31116797
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  • 5. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
    Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA.
    J Cell Sci; 2005 Jul 01; 118(Pt 13):2923-33. PubMed ID: 15961406
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  • 8. Phenylbutazone induces expression of MBNL1 and suppresses formation of MBNL1-CUG RNA foci in a mouse model of myotonic dystrophy.
    Chen G, Masuda A, Konishi H, Ohkawara B, Ito M, Kinoshita M, Kiyama H, Matsuura T, Ohno K.
    Sci Rep; 2016 Apr 29; 6():25317. PubMed ID: 27126921
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  • 9. Small molecule kinase inhibitors alleviate different molecular features of myotonic dystrophy type 1.
    Wojciechowska M, Taylor K, Sobczak K, Napierala M, Krzyzosiak WJ.
    RNA Biol; 2014 Apr 29; 11(6):742-54. PubMed ID: 24824895
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  • 10. Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2.
    Carpentier C, Ghanem D, Fernandez-Gomez FJ, Jumeau F, Philippe JV, Freyermuth F, Labudeck A, Eddarkaoui S, Dhaenens CM, Holt I, Behm-Ansmant I, Marmier-Gourrier N, Branlant C, Charlet-Berguerand N, Marie J, Schraen-Maschke S, Buée L, Sergeant N, Caillet-Boudin ML.
    Biochim Biophys Acta; 2014 Apr 29; 1842(4):654-64. PubMed ID: 24440524
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  • 15. Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).
    Santoro M, Modoni A, Masciullo M, Gidaro T, Broccolini A, Ricci E, Tonali PA, Silvestri G.
    Exp Mol Pathol; 2010 Oct 29; 89(2):158-68. PubMed ID: 20685272
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  • 16. In silico discovery of substituted pyrido[2,3-d]pyrimidines and pentamidine-like compounds with biological activity in myotonic dystrophy models.
    González ÀL, Konieczny P, Llamusi B, Delgado-Pinar E, Borrell JI, Teixidó J, García-España E, Pérez-Alonso M, Estrada-Tejedor R, Artero R.
    PLoS One; 2017 Oct 29; 12(6):e0178931. PubMed ID: 28582438
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  • 17. Calcitriol increases MBNL1 expression and alleviates myotonic dystrophy phenotypes in HSALR mouse models.
    Huang K, Wang DD, Hu WB, Zeng WQ, Xu X, Li QX, Bi FF, Yang H, Qiu J.
    J Transl Med; 2022 Dec 12; 20(1):588. PubMed ID: 36510245
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  • 18. Rescue of Scn5a mis-splicing does not improve the structural and functional heart defects of a DM1 heart mouse model.
    Nitschke L, Hu RC, Miller AN, Cooper TA.
    Hum Mol Genet; 2024 Oct 07; 33(20):1789-1799. PubMed ID: 39126705
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  • 19. 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
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  • 20. Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy.
    Lueck JD, Mankodi A, Swanson MS, Thornton CA, Dirksen RT.
    J Gen Physiol; 2007 Jan 01; 129(1):79-94. PubMed ID: 17158949
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