Julien Ochala

Julien Ochala

Associate Professor - Promotion Programme

Member of:


    1. 2013
    2. Published

      Myofilament lattice structure in presence of a skeletal myopathy-related tropomyosin mutation

      Ochala, Julien & Iwamoto, H., Aug 2013, In: Journal of Muscle Research and Cell Motility. 34, 3-4, p. 171-175 5 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    3. Published

      Skeletal and cardiac αactin isoforms differently modulate myosin cross-bridge formation and myofibre force production

      Ochala, Julien, Iwamoto, H., Ravenscroft, G., Laing, N. G. & Nowak, K. J., Nov 2013, In: Human Molecular Genetics. 22, 21, p. 4398-4404 7 p., ddt289.

      Research output: Contribution to journalJournal articleResearchpeer-review

    4. Published

      Sparing of muscle mass and function by passive loading in an experimental intensive care unit model

      Renaud, G., Llano-Diez, M., Ravara, B., Gorza, L., Feng, H. Z., Jin, J. P., Cacciani, N., Gustafson, A. M., Ochala, Julien, Corpeno, R., Li, M., Hedström, Y., Ford, G. C., Nair, K. S. & Larsson, L., Mar 2013, In: Journal of Physiology. 591, 5, p. 1385-1402 18 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    5. 2012
    6. Published

      Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb

      Kurapati, R., McKenna, C., Lindqvist, J., Williams, D., Simon, M., LeProust, E., Baker, J., Cheeseman, M., Carroll, N., Denny, P., Laval, S., Lochmüller, H., Ochala, Julien & Blanco, G., Apr 2012, In: Human Molecular Genetics. 21, 8, p. 1706-1724 19 p., ddr605.

      Research output: Contribution to journalJournal articleResearchpeer-review

    7. Published

      A myopathy-related actin mutation increases contractile function

      Lindqvist, J., Pénisson-Besnier, I., Iwamoto, H., Li, M., Yagi, N. & Ochala, Julien, May 2012, In: Acta Neuropathologica. 123, 5, p. 739-746 8 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    8. Published

      Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms

      Ochala, Julien, Gokhin, D. S., Pénisson-Besnier, I., Quijano-Roy, S., Monnier, N., Lunardi, J., Romero, N. B. & Fowler, V. M., Oct 2012, In: Human Molecular Genetics. 21, 20, p. 4473-4485 13 p., dds289.

      Research output: Contribution to journalJournal articleResearchpeer-review

    9. 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 journalJournal articleResearchpeer-review

    10. Published

      Thick and Thin Filament Proteins: Acquired and Hereditary Sarcomeric Protein Diseases

      Ochala, Julien & Larsson, L., 18 Jul 2012, Muscle: Fundamental Biology and Mechanisms of Disease. Elsevier, Vol. 1-2. p. 1023-1030 8 p.

      Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

    11. Published

      Thick and thin filament proteins: Acquired and hereditary sarcomeric protein diseases

      Ochala, Julien & Larsson, L., 2012, Muscle. Elsevier Science Inc., Vol. 2. p. 1023-1030 8 p.

      Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

    12. 2011
    13. Published

      Mechanisms underlying the sparing of masticatory versus limb muscle function in an experimental critical illness model

      Aare, S., Ochala, Julien, Norman, H. S., Radell, P., Eriksson, L. I., Göransson, H., Chen, Y. W., Hoffman, E. P. & Larsson, L., Dec 2011, In: Physiological Genomics. 43, 24, p. 1334-1350 17 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

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