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Julien Ochala

Showing results (61-70 of 103) with videos related to

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Acta Physiologica (Oxford, England)|August 21, 2023
Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutationsAlexander Sonne, Anna Katarina Antonovic, Elise Melhedegaard, et al.
American Journal of Physiology. Cell Physiology|May 22, 2023
Revisiting specific force loss in human permeabilized single skeletal muscle fibers obtained from older individualsMichaeljohn Kalakoutis, Ross D Pollock, Norman R Lazarus, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 26, 2011
Disrupted myosin cross-bridge cycling kinetics triggers muscle weakness in nebulin-related myopathyJulien Ochala, Vilma-Lotta Lehtokari, Hiroyuki Iwamoto, et al.
Nature Communications|December 9, 2020
Nuclear numbers in syncytial muscle fibers promote size but limit the development of larger myonuclear domainsAlyssa A W Cramer, Vikram Prasad, Einar Eftestøl, et al.
Experimental Physiology|March 10, 2024
Muscle fibre size and myonuclear positioning in trained and aged humansEdmund Battey, Yotam Levy, Ross D Pollock, et al.
The Journal of Physiology|May 5, 2025
Integrated single-cell functional-proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof-of-principle studyRobert A E Seaborne, Roger Moreno-Justicia, Jenni Laitila, et al.
Circulation. Heart Failure|May 6, 2026
Myosin ATPase Inhibition Relieves the Energetic Burden in Skeletal Myofibres of Patients With Heart Failure With Reduced Ejection FractionMassimiliano Ansaldo, Chahida Chaami, Simone Porcelli, et al.
Human Molecular Genetics|December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIbRamakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
Journal of Cachexia, Sarcopenia and Muscle|November 15, 2023
Ryanodine receptor type 1 content decrease-induced endoplasmic reticulum stress is a hallmark of myopathiesJeremy Vidal, Eric A Fernandez, Martin Wohlwend, et al.
Cardiovascular Diabetology|January 16, 2026
Destabilization of cardiac myosin acetylation and sequestration with type 2 diabetes mellitusMahault Mathilde Degezelle, Chahida Chaami, Christopher T A Lewis, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Acta Physiologica (Oxford, England)|August 21, 2023
Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutationsAlexander Sonne, Anna Katarina Antonovic, Elise Melhedegaard, et al.
American Journal of Physiology. Cell Physiology|May 22, 2023
Revisiting specific force loss in human permeabilized single skeletal muscle fibers obtained from older individualsMichaeljohn Kalakoutis, Ross D Pollock, Norman R Lazarus, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 26, 2011
Disrupted myosin cross-bridge cycling kinetics triggers muscle weakness in nebulin-related myopathyJulien Ochala, Vilma-Lotta Lehtokari, Hiroyuki Iwamoto, et al.
Nature Communications|December 9, 2020
Nuclear numbers in syncytial muscle fibers promote size but limit the development of larger myonuclear domainsAlyssa A W Cramer, Vikram Prasad, Einar Eftestøl, et al.
Experimental Physiology|March 10, 2024
Muscle fibre size and myonuclear positioning in trained and aged humansEdmund Battey, Yotam Levy, Ross D Pollock, et al.
The Journal of Physiology|May 5, 2025
Integrated single-cell functional-proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof-of-principle studyRobert A E Seaborne, Roger Moreno-Justicia, Jenni Laitila, et al.
Circulation. Heart Failure|May 6, 2026
Myosin ATPase Inhibition Relieves the Energetic Burden in Skeletal Myofibres of Patients With Heart Failure With Reduced Ejection FractionMassimiliano Ansaldo, Chahida Chaami, Simone Porcelli, et al.
Human Molecular Genetics|December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIbRamakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
Journal of Cachexia, Sarcopenia and Muscle|November 15, 2023
Ryanodine receptor type 1 content decrease-induced endoplasmic reticulum stress is a hallmark of myopathiesJeremy Vidal, Eric A Fernandez, Martin Wohlwend, et al.
Cardiovascular Diabetology|January 16, 2026
Destabilization of cardiac myosin acetylation and sequestration with type 2 diabetes mellitusMahault Mathilde Degezelle, Chahida Chaami, Christopher T A Lewis, et al.
Pageof 11