Julien Ochala
Associate Professor - Promotion Programme
ORCID: 0000-0002-6358-2920
11 - 15 out of 15Page size: 10
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Predominant myosin superrelaxed state in canine myocardium with naturally occurring dilated cardiomyopathy
Ochala, Julien, Lewis, Christopher T.A. , Beck, T., Iwamoto, H., Hessel, A. L., Campbell, K. S. & Pyle, W. G., 2023, In: American journal of physiology. Heart and circulatory physiology. 325, 3, p. H585-H591Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The dawn of the functional genomics era in muscle physiology
Seaborne, Robert Arthur Elliston & Ochala, Julien, 15 Apr 2023, In: Journal of Physiology. 601, 8, p. 1343-1352Research output: Contribution to journal › Review › Research › peer-review
- Published
Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations
Sonne, A., Antonovic, A. K., Thomsen, Elise Julie Melhedegaard, Akter, F., Andersen, J. L., Jungbluth, H., Witting, N., Vissing, John, Zanoteli, E., Fornili, A. & Ochala, Julien, 2023, In: Acta Physiologica. 239, 2, 14 p., e14035.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Myosin post-translational modifications and function in the presence of myopathy-linked truncating MYH2 mutations
Sonne, A., Peverelli, L., Hernandez-Lain, A., Domínguez-González, C., Andersen, J. L., Milone, M., Beggs, A. H. & Ochala, Julien, 2023, In: American journal of physiology. Cell physiology. 324, 3, p. C769–C776 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ryanodine receptor type 1 content decrease-induced endoplasmic reticulum stress is a hallmark of myopathies
Vidal, J., Fernandez, E. A., Wohlwend, M., Laurila, P. P., Lopez-Mejia, A., Ochala, Julien, Lobrinus, A. J., Kayser, B., Lopez-Mejia, I. C., Place, N. & Zanou, N., 2023, In: Journal of Cachexia, Sarcopenia and Muscle. 14, 6, p. 2882-2897Research 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
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Myofibre hyper-contractility in horses expressing the myosin heavy chain myopathy mutation, myh1e321g
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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
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