Julien Ochala
Associate Professor - Promotion Programme
ORCID: 0000-0002-6358-2920
1 - 5 out of 5Page size: 500
- 2015
- Published
Ryanodine receptor fragmentation and sarcoplasmic reticulum Ca2+ leak after one session of High-intensity interval exercise
Place, N., Ivarsson, N., Venckunas, T., Neyroud, D., Brazaitis, M., Cheng, A. J., Ochala, Julien, Kamandulis, S., Girard, S., Volungevičius, G., Paužas, H., Mekideche, A., Kayser, B., Martinez-Redondo, V., Ruas, J. L., Bruton, J., Truffert, A., Lanner, J. T., Skurvydas, A. & Westerblad, H., 15 Dec 2015, In: Proceedings of the National Academy of Sciences of the United States of America. 112, 50, p. 15492-15497 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
Tropomodulin 1 directly controls thin filament length in both wild-type and tropomodulin 4-deficient skeletal muscle
Gokhin, D. S., Ochala, Julien, Domenighetti, A. A. & Fowler, V. M., 15 Dec 2015, In: Development (Cambridge, England). 142, 24, p. 4351-62 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
X-ray recordings reveal how a human disease-linked skeletal muscle α-actin mutation leads to contractile dysfunction
Ochala, Julien, Ravenscroft, G., McNamara, E., Nowak, K. J. & Iwamoto, H., Dec 2015, In: Journal of Structural Biology. 192, 3, p. 331-335 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
Aberrant post-translational modifications compromise human myosin motor function in old age
Li, M., Ogilvie, H., Ochala, Julien, Artemenko, K., Iwamoto, H., Yagi, N., Bergquist, J. & Larsson, L., Apr 2015, In: Aging Cell. 14, 2, p. 228-35 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Skeletal Muscle: A Brief Review of Structure and Function
Frontera, W. R. & Ochala, Julien, 4 Mar 2015, In: Behavior Genetics. 45, 2, p. 183-195 13 p.Research output: Contribution to journal › Review › 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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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