Zebrafish MTMR14 is required for excitation–contraction coupling, developmental motor function and the regulation of autophagy von Dowling, J.J., Low, S.E., Busta, A.S., Feldman, E.L.

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G.P.46 von Volpatti, J, Burns, A, Davidson, A.E, Roy, P, Dowling, J.J

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P9.17 Function of CCDC78 in muscle development and muscle disease von Davidson, A, Li, X, Dowling, J.J

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P.9.3 Repair of mutant nebulin transcripts by exon exchange von Laitila, J, Dowling, J.J, Pelin, K

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P.1.13 Autophagy and the pathogenesis of congenital muscular dystrophies von Horstick, E, Li, X, Moore, S, Dowling, J.J

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P.4.7 The natural history of myotubular myopathy, summary of the first year of enrollment von Amburgey, K, Julian, D, Howell, E, Britt, M, Dowling, J.J

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P.4.1 PIP kinases, muscle development, and the pathogenesis of myotubular myopathy von Reifler, A, Michele, D, Archambeau, A, Li, X, Dowling, J.J

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O.3 Identification of a novel therapeutic pathway for Duchenne muscular dystrophy through utilization of the zebrafish model sapje von Waugh, T.W, Dowling, J.J

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An investigation into the deformable characteristics of the human foot using fluoroscopic imaging von Wrbaškić, N, Dowling, J.J

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Large duplication in MTM1 associated with myotubular myopathy von Amburgey, K, Lawlor, M.W, del Gaudio, D, Cheng, Y.W, Fitzpatrick, C, Minor, A, Li, X, Aughton, D, Das, S, Beggs, A.H, Dowling, J.J

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G.P.48 von Amburgey, K, Bailey, A, Hwang, J.H, Tarnopolsky, M.A, Bönnemann, C.G, Medne, L, Mathews, K.D, Collins, J, Daube, J.R, Wellman, G.P, Callaghan, B, Vajsar, J, Yoon, G, Cohn, R, Clarke, N.F, Dowling, J.J

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P1.36 Zebrafish models of dynamin 2 – related centronuclear myopathy von Gibbs, E.M, Busta, A.S, Feldman, E.L, Dowling, J.J

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C.P.2 In silico analysis of recessive RYR1 mutations identifies novel potential disease mechanisms von Hwang, J.H, Amburgey, K, Treves, S, Zorzato, F, Dowling, J.J, Clarke, N.F

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The relationship between strength, power and ballistic performance von Wrbaškić, N, Dowling, J.J

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G.P.39 von Annoussamy, M, Landy, H, Ramsdell, D, Nelken, M, Muntoni, F, Bönnemann, C, Bharucha, D, Dowling, J.J, Amburgey, K, Lilien, C, Ollivier, G, Laporte, J, Biancalana, V, Schara, U, Cuisset, J.M, D’Amico, A, Deconinck, N, Jeannet, P.Y, Klein, A, Fluss, J, Mayer, M, Seferian, A.M, Moing, A.G. Le, Gidaro, T, Hogrel, J.Y, Mingozzi, F, Buj-Bello, A, Voit, T, Servais, L

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P1.38 Oxidative stress and RYR1-related myopathies von Dowling, J.J, McEvoy, A, Arbogast, S, Kuwada, J.Y, Ferreiro, A

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EM.P.5.05 Zebrafish models of collagen VI myopathies von Blankinship, M.J, Busta, A.S, Feldman, E.L, Dowling, J.J

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D.P.8 Expanding the clinical and genetic phenotype of TPM2-related myopathies von Dowling, J.J, Davidson, A.E, Lopez, M.E, Siddiqui, F.M, Lunt, P, Li, J.Z, Jungbluth, H, Love, S, Moore, S.A

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C.O.4 Dominant mutation in CCDC78 in a unique congenital myopathy with central nuclei and atypical cores von Davidson, A.E, Majczenko, K, Camelo-Piragua, S, Li, X, Joshi, S, Xu, J, Peng, W, Li, J.Z, Burmeister, M, Dowling, J.J

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P4.54 Increased oxidative stress and successful antioxidant treatment in a vertebrate model of RYR1 related myopathy von Dowling, J.J, Arbogast, S, McEvoy, A, Nelson, D.D, Brooks, S.V, Kuwada, J.Y, Bonnemann, C.G, Ferreiro, A

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