Julien Ochala
Associate Professor - Promotion Programme
- Published
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
- Published
Myosin Heavy Chain as a Novel Key Modulator of Striated Muscle Resting State
Lewis, Christopher T.A. & Ochala, Julien, 2023, In: Physiology. 38, 1, p. 3-9Research output: Contribution to journal › Review › 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
Myostatin inhibition using mrk35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice
Tinklenberg, J. A., Siebers, E. M., Beatka, M. J., Meng, H., Yang, L., Zhang, Z., Ross, J. A., Ochala, Julien, Morris, C., Owens, J. M., Laing, N. G., Nowak, K. J. & Lawlor, M. W., 15 Feb 2018, In: Human Molecular Genetics. 27, 4, p. 638-648 11 p., ddx431.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
- Published
Nemaline Myopathy-Related Skeletal Muscle α-Actin (ACTA1) Mutation, Asp286Gly, Prevents Proper Strong Myosin Binding and Triggers Muscle Weakness
Ochala, Julien, Ravenscroft, G., Laing, N. G. & Nowak, K. J., 20 Sep 2012, In: PLoS ONE. 7, 9, e45923.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
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
- 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
- Published
PGC-1α regulates myonuclear accretion after moderate endurance training
Battey, E., Furrer, R., Ross, J., Handschin, C., Ochala, Julien & Stroud, M. J., 2022, In: Journal of Cellular Physiology. 237, 1, p. 696-705Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Physical activity impacts resting skeletal muscle myosin conformation and lowers its ATP consumption
Lewis, C. T. A., Tabrizian, L., Nielsen, J., Laitila, J., Beck, T. N., Olsen, M. S., Ognjanovic, M. M., Aagaard, P., Hokken, R., Laugesen, S., Ingersen, A., Andersen, J. L., Soendenbroe, C., Helge, J. W., Dela, F., Larsen, S., Sahl, R. E., Rømer, T., Hansen, M. T., Frandsen, J. & 2 others, , 2023, In: The Journal of general physiology. 155, 7, 8 p., e202213268.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 240294914
Most downloads
-
104
downloads
Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
58
downloads
Myofibre hyper-contractility in horses expressing the myosin heavy chain myopathy mutation, myh1e321g
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
29
downloads
Using nuclear envelope mutations to explore age-related skeletal muscle weakness
Research output: Contribution to journal › Journal article › Research › peer-review
Published