Julien Ochala
Associate Professor - Promotion Programme
ORCID: 0000-0002-6358-2920
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Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle
Roy, P., Rau, F., Ochala, Julien, Messéant, J., Fraysse, B., Lainé, J., Agbulut, O., Butler-Browne, G., Furling, D. & Ferry, A., 20 Jul 2016, In: Skeletal Muscle. 6, 1, 23.Research output: Contribution to journal › Journal article › Research › peer-review
Modulating myosin restores muscle function in a mouse model of nemaline myopathy
Lindqvist, J., Levy, Y., Pati-Alam, A., Hardeman, E. C., Gregorevic, P. & Ochala, Julien, 1 May 2016, In: Annals of Neurology. 79, 5, p. 717-725 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Myopathy-inducing mutation H40Y in ACTA1 hampers actin filament structure and function
Chan, C., Fan, J., Messer, A. E., Marston, S. B., Iwamoto, H. & Ochala, Julien, 1 Aug 2016, In: Biochimica et Biophysica Acta - Molecular Basis of Disease. 1862, 8, p. 1453-1458 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Novel myosin-based therapies for congenital cardiac and skeletal myopathies
Ochala, Julien & Sun, Y. B., 1 Oct 2016, In: Journal of Medical Genetics. 53, 10, p. 651-654 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 240294914
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Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
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60
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Myofibre hyper-contractility in horses expressing the myosin heavy chain myopathy mutation, myh1e321g
Research output: Contribution to journal › Journal article › Research › peer-review
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30
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Using nuclear envelope mutations to explore age-related skeletal muscle weakness
Research output: Contribution to journal › Journal article › Research › peer-review
Published