Julien Ochala
Associate Professor - Promotion Programme
- 2018
SIRT1 regulates nuclear number and domain size in skeletal muscle fibers
Ross, J. A., Levy, Y., Svensson, K., Philp, A., Schenk, S. & Ochala, Julien, Sep 2018, In: Journal of Cellular Physiology. 233, 9, p. 7157-7163 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
Prelamin A causes aberrant myonuclear arrangement and results in muscle fiber weakness
Levy, Y., Ross, J. A., Niglas, M., Snetkov, V. A., Lynham, S., Liao, C., Puckelwartz, M. J., Hsu, Y., McNally, E. M., Alsheimer, M., Harridge, S. D., Young, S. G., Fong, L. G., Español, Y., Lopez-Otin, C., Kennedy, B. K., Lowe, D. A. & Ochala, Julien, 4 Oct 2018, In: JCI insight. 3, 19Research output: Contribution to journal › Journal article › Research › peer-review
Reducing dynamin 2 (DNM2) rescues DNM2-related dominant centronuclear myopathy
Buono, S., Ross, J. A., Tasfaout, H., Levy, Y., Kretz, C., Tayefeh, L., Matson, J., Guo, S., Kessler, P., Monia, B. P., Bitoun, M., Ochala, Julien, Laporte, J. & Cowling, B. S., 23 Oct 2018, In: Proceedings of the National Academy of Sciences of the United States of America. 115, 43, p. 11066-11071 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
Defining the contribution of skeletal muscle pyruvate dehydrogenase α1 to exercise performance and insulin action
Svensson, K., Dent, J. R., Tahvilian, S., Martins, V. F., Sathe, A., Ochala, Julien, Patel, M. S. & Schenk, S., Nov 2018, In: American Journal of Physiology - Endocrinology and Metabolism. 315, 5, p. E1034-E1045Research output: Contribution to journal › Journal article › Research › peer-review
Molecular consequences of the myopathy-related D286G mutation on actin function
Fan, J., Chan, C., McNamara, E. L., Nowak, K. J., Iwamoto, H. & Ochala, Julien, 1 Dec 2018, In: Frontiers in Physiology. 9, 1756.Research output: Contribution to journal › Journal article › Research › peer-review
- 2019
- Published
Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
Ross, J. A., Levy, Y., Ripolone, M., Kolb, J. S., Turmaine, M., Holt, M., Lindqvist, J., Claeys, K. G., Weis, J., Monforte, M., Tasca, G., Moggio, M., Figeac, N., Zammit, P. S., Jungbluth, H., Fiorillo, C., Vissing, J., Witting, N., Granzier, H., Zanoteli, E. & 3 others, , 2019, In: Acta Neuropathologica. 138, 3, p. 477-495 19 p.Research output: Contribution to journal › Journal article › Research › peer-review
Effect of PGC1-beta ablation on myonuclear organisation
Beedour, R., Ross, J. A., Levy, Y. & Ochala, Julien, 1 Dec 2019, In: Journal of Muscle Research and Cell Motility. 40, 3-4, p. 335-341 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2020
Candidate gene expression and coding sequence variants in Warmblood horses with myofibrillar myopathy
Williams, Z. J., Velez-Irizarry, D., Petersen, J. L., Ochala, Julien, Finno, C. J. & Valberg, S. J., 2020, (Accepted/In press) In: Equine Veterinary Journal.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Nuclear numbers in syncytial muscle fibers promote size but limit the development of larger myonuclear domains
Cramer, A. A. W., Prasad, V., Eftestøl, E., Song, T., Hansson, K. A., Dugdale, H. F., Sadayappan, S., Ochala, Julien, Gundersen, K. & Millay, D. P., 2020, In: Nature Communications. 11, 1, 14 p., 6287.Research output: Contribution to journal › Journal article › Research › peer-review
Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb
Laitila, J. M., McNamara, E. L., Wingate, C. D., Goullee, H., Ross, J. A., Taylor, R. L., Van Der Pijl, R., Griffiths, L. M., Harries, R., Ravenscroft, G., Clayton, J. S., Sewry, C., Lawlor, M. W., Ottenheijm, C. A. C., Bakker, A. J., Ochala, Julien, Laing, N. G., Wallgren-Pettersson, C., Pelin, K. & Nowak, K. J., 17 Feb 2020, In: Acta Neuropathologica Communications. 8, 1, 18.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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58
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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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29
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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