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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

118 related items for PubMed ID: 28300015

  • 41. LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene.
    Sáenz A, Leturcq F, Cobo AM, Poza JJ, Ferrer X, Otaegui D, Camaño P, Urtasun M, Vílchez J, Gutiérrez-Rivas E, Emparanza J, Merlini L, Paisán C, Goicoechea M, Blázquez L, Eymard B, Lochmuller H, Walter M, Bonnemann C, Figarella-Branger D, Kaplan JC, Urtizberea JA, Martí-Massó JF, López de Munain A.
    Brain; 2005 Apr; 128(Pt 4):732-42. PubMed ID: 15689361
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  • 42. Halofuginone promotes satellite cell activation and survival in muscular dystrophies.
    Barzilai-Tutsch H, Bodanovsky A, Maimon H, Pines M, Halevy O.
    Biochim Biophys Acta; 2016 Jan; 1862(1):1-11. PubMed ID: 26454207
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  • 47. Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
    Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS.
    Acta Neuropathol; 2008 Sep; 116(3):235-46. PubMed ID: 18392839
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  • 50. Lipid accumulation in dysferlin-deficient muscles.
    Grounds MD, Terrill JR, Radley-Crabb HG, Robertson T, Papadimitriou J, Spuler S, Shavlakadze T.
    Am J Pathol; 2014 Jun; 184(6):1668-76. PubMed ID: 24685690
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  • 51. Myotilin overexpression enhances myopathology in the LGMD1A mouse model.
    Garvey SM, Liu Y, Miller SE, Hauser MA.
    Muscle Nerve; 2008 May; 37(5):663-7. PubMed ID: 18335471
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  • 55. Lithium chloride regulates connexin43 in skeletal myoblasts in vitro: possible involvement in Wnt/beta-catenin signaling.
    Du WJ, Li JK, Wang QY, Hou JB, Yu B.
    Cell Commun Adhes; 2008 Sep; 15(3):261-71. PubMed ID: 18972237
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  • 56. Hypertrophy and atrophy inversely regulate Caveolin-3 expression in myoblasts.
    Fanzani A, Musarò A, Stoppani E, Giuliani R, Colombo F, Preti A, Marchesini S.
    Biochem Biophys Res Commun; 2007 May 25; 357(1):314-8. PubMed ID: 17418092
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  • 58. Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.
    Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S.
    Neuromuscul Disord; 2007 Feb 25; 17(2):157-62. PubMed ID: 17129727
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  • 59. Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families.
    van der Kooi AJ, Frankhuizen WS, Barth PG, Howeler CJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, van Ommen GJ, de Visser M, Bakker E, Ginjaar HB.
    Neurology; 2007 Jun 12; 68(24):2125-8. PubMed ID: 17562833
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