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Journal Abstract Search

208 related items for PubMed ID: 9120013

  • 21. [Myotonic dystrophy and myotonin kinase protein gene mutation].
    Ruscák J.
    Bratisl Lek Listy; 1997 May; 98(5):274-7. PubMed ID: 9296833
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  • 22. Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.
    Winchester CL, Ferrier RK, Sermoni A, Clark BJ, Johnson KJ.
    Hum Mol Genet; 1999 Mar; 8(3):481-92. PubMed ID: 9949207
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  • 23. [Effect on gene expression of the expanded CTG repeat on 3'-untranslated region of myotonic dystrophy (DM) protein kinase].
    Furuya H, Imai N, Shiokawa K, Kira J.
    Nihon Rinsho; 1999 Apr; 57(4):932-6. PubMed ID: 10222793
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  • 24. Myotonic dystrophy and myotonic dystrophy protein kinase.
    Ueda H, Ohno S, Kobayashi T.
    Prog Histochem Cytochem; 2000 Apr; 35(3):187-251. PubMed ID: 11064921
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  • 26. Tackling the pathogenesis of RNA nuclear retention in myotonic dystrophy.
    Mastroyiannopoulos NP, Shammas C, Phylactou LA.
    Biol Cell; 2010 Jul 23; 102(9):515-23. PubMed ID: 20690904
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  • 27. Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.
    Fu YH, Friedman DL, Richards S, Pearlman JA, Gibbs RA, Pizzuti A, Ashizawa T, Perryman MB, Scarlato G, Fenwick RG.
    Science; 1993 Apr 09; 260(5105):235-8. PubMed ID: 8469976
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  • 28. Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing.
    Krahe R, Ashizawa T, Abbruzzese C, Roeder E, Carango P, Giacanelli M, Funanage VL, Siciliano MJ.
    Genomics; 1995 Jul 01; 28(1):1-14. PubMed ID: 7590731
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  • 29. Dysregulation of GSK3β-Target Proteins in Skin Fibroblasts of Myotonic Dystrophy Type 1 (DM1) Patients.
    Grande V, Hathazi D, O'Connor E, Marteau T, Schara-Schmidt U, Hentschel A, Gourdon G, Nikolenko N, Lochmüller H, Roos A.
    J Neuromuscul Dis; 2021 Jul 01; 8(4):603-619. PubMed ID: 33682722
    [Abstract] [Full Text] [Related]

  • 30. Age of onset of RNA toxicity influences phenotypic severity: evidence from an inducible mouse model of myotonic dystrophy (DM1).
    Gladman JT, Mandal M, Srinivasan V, Mahadevan MS.
    PLoS One; 2013 Jul 01; 8(9):e72907. PubMed ID: 24039817
    [Abstract] [Full Text] [Related]

  • 31. Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.
    Seznec H, Agbulut O, Sergeant N, Savouret C, Ghestem A, Tabti N, Willer JC, Ourth L, Duros C, Brisson E, Fouquet C, Butler-Browne G, Delacourte A, Junien C, Gourdon G.
    Hum Mol Genet; 2001 Nov 01; 10(23):2717-26. PubMed ID: 11726559
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  • 35. Deconstructing myotonic dystrophy.
    Tapscott SJ.
    Science; 2000 Sep 08; 289(5485):1701-2. PubMed ID: 11001736
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  • 36. Myotonic dystrophy kinase is a component of neuromuscular junctions.
    van der Ven PF, Jansen G, van Kuppevelt TH, Perryman MB, Lupa M, Dunne PW, ter Laak HJ, Jap PH, Veerkamp JH, Epstein HF.
    Hum Mol Genet; 1993 Nov 08; 2(11):1889-94. PubMed ID: 8281152
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  • 40. Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy.
    Savkur RS, Philips AV, Cooper TA.
    Nat Genet; 2001 Sep 08; 29(1):40-7. PubMed ID: 11528389
    [Abstract] [Full Text] [Related]

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