No change in myonuclear number during muscle unloading and reloading

Bruusgaard, J. C., Egner, I. M., Larsen, T. K., Dupre-Aucouturier, S., Desplanches, D., Gundersen, K.·2012·Journal of Applied Physiology
DOI 10.1152/japplphysiol.00436.2012

Cited by (108)

Items 101–108 of 108

  1. Novel applications of flow cytometry to assess whole murine skeletal muscle and myonuclei number responses to atrophy and recovery.
    Mark R. Viggars · 2018 · Liverpool John Moores University
  2. The comparison between two high-intensity interval training protocols on skeletal muscle and satellite cell dynamics
    Cameron Sugden · 2019 · SUNScholar (Stellenbosch University)
  3. Atrophie, croissance et fonction musculaire : l'impact des leucocytes et de la triade RANK/RANKL/OPG
    Nicolas A. Dumont · 2013 · Corpus Université Laval (Université Laval)
  4. Additional file 1 of Myofiber directs macrophages IL-10-Vav1-Rac1 efferocytosis pathway in inflamed muscle following CTX myoinjury by activating the intrinsic TGF-β signaling
    Zhaohong Liao, Haiqiang Lan, Xiaoting Jian, Huang, Jingwen, Han Wang, Hu, Jijie, Hua Liao · 2024 · Figshare
  5. Mechanisms of Skeletal Muscle Mass Regulation and Muscle Memory
    Kristian Gundersen, Jo C. Bruusgaard, Einar Eftestøl · 2026 · Acta Physiologica
  6. Regulation of antioxidant defenses in the prevention of skeletal muscle deconditioning
    Coralie Arc‐Chagnaud · 2019
  7. Regenerating myofiber with activating of TGF-β signaling contributes to macrophage efferocytosis through enhancing Tregs response in inflamed muscle
    Haiqiang Lan, Xiaoting Jian, Zhaohong Liao, Yangyang Li, QiSen Wang, Jing-Wen Huang, Jijie Hu, Hua Liao · 2026 · Frontiers in Immunology
  8. Epigenetic Skeletal Muscle Memory: The Impact of Physical Activity on Aging and Post-Injury Regeneration
    Antoni Godlewski, M. Wróblewski, Julia Kuk, Magdalena Moritz, Filip Dobrak, R. Kołodziejska, Alina Woźniak · 2026 · Genes