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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

255 related items for PubMed ID: 32063450

  • 61.
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  • 62. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.
    Frisch R, Singleton KR, Moses PA, Gonzalez IL, Carango P, Marks HG, Funanage VL.
    Mol Genet Metab; 2001; 74(1-2):281-91. PubMed ID: 11592825
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  • 63.
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  • 65. Systemic delivery of a Peptide-linked morpholino oligonucleotide neutralizes mutant RNA toxicity in a mouse model of myotonic dystrophy.
    Leger AJ, Mosquea LM, Clayton NP, Wu IH, Weeden T, Nelson CA, Phillips L, Roberts E, Piepenhagen PA, Cheng SH, Wentworth BM.
    Nucleic Acid Ther; 2013 Apr; 23(2):109-17. PubMed ID: 23308382
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  • 66.
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  • 68. Expanded CCUG repeat RNA expression in Drosophila heart and muscle trigger Myotonic Dystrophy type 1-like phenotypes and activate autophagocytosis genes.
    Cerro-Herreros E, Chakraborty M, Pérez-Alonso M, Artero R, Llamusí B.
    Sci Rep; 2017 Jun 06; 7(1):2843. PubMed ID: 28588248
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  • 69. Bundle Branch Re-Entrant Ventricular Tachycardia: Novel Genetic Mechanisms in a Life-Threatening Arrhythmia.
    Roberts JD, Gollob MH, Young C, Connors SP, Gray C, Wilton SB, Green MS, Zhu DW, Hodgkinson KA, Poon A, Li Q, Orr N, Tang AS, Klein GJ, Wojciak J, Campagna J, Olgin JE, Badhwar N, Vedantham V, Marcus GM, Kwok PY, Deo RC, Scheinman MM.
    JACC Clin Electrophysiol; 2017 Mar 06; 3(3):276-288. PubMed ID: 29759522
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  • 70. Clinical case report atypical myopathy in a young girl with 91 CTG repeats in DM1 locus and a positive DM1 family history.
    Savić D, Keckarević D, Branković-Srećković V, Apostolski S, Todorović S, Romac S.
    Int J Neurosci; 2006 Dec 06; 116(12):1509-18. PubMed ID: 17145685
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  • 71.
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  • 72. Ventricular tachycardia: first manifestation of myotonic dystrophy.
    Cakmak N, Osmonov D, Ozcan KS, Donmez C.
    Acta Cardiol; 2011 Apr 06; 66(2):267-9. PubMed ID: 21591591
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  • 73. Does cytosine-thymine-guanine (CTG) expansion size predict cardiac events and electrocardiographic progression in myotonic dystrophy?
    Clarke NR, Kelion AD, Nixon J, Hilton-Jones D, Forfar JC.
    Heart; 2001 Oct 06; 86(4):411-6. PubMed ID: 11559681
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  • 74.
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  • 76. A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.
    Akai J, Makita N, Sakurada H, Shirai N, Ueda K, Kitabatake A, Nakazawa K, Kimura A, Hiraoka M.
    FEBS Lett; 2000 Aug 11; 479(1-2):29-34. PubMed ID: 10940383
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  • 77.
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  • 78. Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death.
    Ter Bekke RMA, Isaacs A, Barysenka A, Hoos MB, Jongbloed JDH, Hoorntje JCA, Patelski ASM, Helderman-van den Enden ATJM, van den Wijngaard A, Stoll M, Volders PGA.
    Heart Rhythm; 2017 Dec 11; 14(12):1873-1881. PubMed ID: 28782696
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  • 79.
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  • 80.
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