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Journal Abstract Search

188 related items for PubMed ID: 39180495

  • 21. Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1.
    Azotla-Vilchis CN, Sanchez-Celis D, Agonizantes-Juárez LE, Suárez-Sánchez R, Hernández-Hernández JM, Peña J, Vázquez-Santillán K, Leyva-García N, Ortega A, Maldonado V, Rangel C, Magaña JJ, Cisneros B, Hernández-Hernández O.
    Biomolecules; 2021 Jan 26; 11(2):. PubMed ID: 33530452
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  • 23. Muscleblind-like 1 knockout mice reveal novel splicing defects in the myotonic dystrophy brain.
    Suenaga K, Lee KY, Nakamori M, Tatsumi Y, Takahashi MP, Fujimura H, Jinnai K, Yoshikawa H, Du H, Ares M, Swanson MS, Kimura T.
    PLoS One; 2012 Jan 26; 7(3):e33218. PubMed ID: 22427994
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  • 26. Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy.
    Chakraborty M, Sellier C, Ney M, Pascal V, Charlet-Berguerand N, Artero R, Llamusi B.
    Dis Model Mech; 2018 Apr 23; 11(4):. PubMed ID: 29592894
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  • 31. 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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  • 32. RNA interference targeting CUG repeats in a mouse model of myotonic dystrophy.
    Sobczak K, Wheeler TM, Wang W, Thornton CA.
    Mol Ther; 2013 Feb 01; 21(2):380-7. PubMed ID: 23183533
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  • 33. Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms.
    Meola G, Cardani R.
    Biochim Biophys Acta; 2015 Apr 01; 1852(4):594-606. PubMed ID: 24882752
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  • 34. Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features.
    Dansithong W, Wolf CM, Sarkar P, Paul S, Chiang A, Holt I, Morris GE, Branco D, Sherwood MC, Comai L, Berul CI, Reddy S.
    PLoS One; 2008 Apr 01; 3(12):e3968. PubMed ID: 19092997
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  • 35. Combinatorial effects of ion channel mis-splicing as a cause of myopathy in myotonic dystrophy.
    Nitschke L, Cooper TA.
    J Clin Invest; 2024 Jan 02; 134(1):. PubMed ID: 38165037
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  • 36. DDX6 regulates sequestered nuclear CUG-expanded DMPK-mRNA in dystrophia myotonica type 1.
    Pettersson OJ, Aagaard L, Andrejeva D, Thomsen R, Jensen TG, Damgaard CK.
    Nucleic Acids Res; 2014 Jun 02; 42(11):7186-200. PubMed ID: 24792155
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  • 37. The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.
    Botta A, Rinaldi F, Catalli C, Vergani L, Bonifazi E, Romeo V, Loro E, Viola A, Angelini C, Novelli G.
    J Med Genet; 2008 Oct 02; 45(10):639-46. PubMed ID: 18611984
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  • 38. Quercetin selectively reduces expanded repeat RNA levels in models of myotonic dystrophy.
    Mishra SK, Hicks SM, Frias JA, Vangaveti S, Nakamori M, Cleary JD, Reddy K, Berglund JA.
    bioRxiv; 2023 Feb 02. PubMed ID: 36778282
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  • 39. HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy.
    Li M, Zhuang Y, Batra R, Thomas JD, Li M, Nutter CA, Scotti MM, Carter HA, Wang ZJ, Huang XS, Pu CQ, Swanson MS, Xie W.
    Proc Natl Acad Sci U S A; 2020 Mar 10; 117(10):5472-5477. PubMed ID: 32086392
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  • 40. Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy.
    Sznajder ŁJ, Swanson MS.
    Int J Mol Sci; 2019 Jul 09; 20(13):. PubMed ID: 31323950
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