Control of satellite cell function in muscle regeneration and its disruption in ageing
P Sousa-Victor, L García-Prat… - … Reviews Molecular Cell …, 2022 - nature.com
Skeletal muscle contains a designated population of adult stem cells, called satellite cells,
which are generally quiescent. In homeostasis, satellite cells proliferate only sporadically …
which are generally quiescent. In homeostasis, satellite cells proliferate only sporadically …
Inflammation in duchenne muscular dystrophy–exploring the role of neutrophils in muscle damage and regeneration
A Tulangekar, TE Sztal - Biomedicines, 2021 - mdpi.com
Duchenne muscular dystrophy (DMD) is a severe and progressive, X-linked, neuromuscular
disorder caused by mutations in the dystrophin gene. In DMD, the lack of functional …
disorder caused by mutations in the dystrophin gene. In DMD, the lack of functional …
Histological methods to assess skeletal muscle degeneration and regeneration in Duchenne muscular dystrophy
N Dubuisson, R Versele, C Planchon… - International journal of …, 2022 - mdpi.com
Duchenne muscular dystrophy (DMD) is a progressive disease caused by the loss of
function of the protein dystrophin. This protein contributes to the stabilisation of striated cells …
function of the protein dystrophin. This protein contributes to the stabilisation of striated cells …
Loss of full-length dystrophin expression results in major cell-autonomous abnormalities in proliferating myoblasts
Duchenne muscular dystrophy (DMD) affects myofibers and muscle stem cells, causing
progressive muscle degeneration and repair defects. It was unknown whether dystrophic …
progressive muscle degeneration and repair defects. It was unknown whether dystrophic …
[HTML][HTML] The therapeutic relevance of urolithins, intestinal metabolites of ellagitannin-rich food: A systematic review of in vivo studies
WK Tow, PY Chee, U Sundralingam, UD Palanisamy - Nutrients, 2022 - mdpi.com
Nutrients | Free Full-Text | The Therapeutic Relevance of Urolithins, Intestinal Metabolites of
Ellagitannin-Rich Food: A Systematic Review of In Vivo Studies Next Article in Journal Sex …
Ellagitannin-Rich Food: A Systematic Review of In Vivo Studies Next Article in Journal Sex …
Gpr18 agonist dampens inflammation, enhances myogenesis, and restores muscle function in models of Duchenne muscular dystrophy
J Dort, Z Orfi, M Fiscaletti, PM Campeau… - Frontiers in Cell and …, 2023 - frontiersin.org
Introduction: Muscle wasting in Duchenne Muscular Dystrophy is caused by myofiber
fragility and poor regeneration that lead to chronic inflammation and muscle replacement by …
fragility and poor regeneration that lead to chronic inflammation and muscle replacement by …
RhoA/ROCK signalling activated by ARHGEF3 promotes muscle weakness via autophagy in dystrophic mdx mice
Background Duchenne muscular dystrophy (DMD), caused by dystrophin deficiency, leads
to progressive and fatal muscle weakness through yet‐to‐be‐fully deciphered molecular …
to progressive and fatal muscle weakness through yet‐to‐be‐fully deciphered molecular …
Cultured myoblasts derived from rat soleus muscle show altered regulation of proliferation and myogenesis during the course of mechanical unloading
MY Komarova, SV Rozhkov, OA Ivanova… - International Journal of …, 2022 - mdpi.com
The structure and function of soleus muscle fibers undergo substantial remodeling under
real or simulated microgravity conditions. However, unloading-induced changes in the …
real or simulated microgravity conditions. However, unloading-induced changes in the …
Interplay between Pitx2 and Pax7 temporally governs specification of extraocular muscle stem cells
M Kuriki, A Korb, G Comai, S Tajbakhsh - PLoS genetics, 2024 - journals.plos.org
Gene regulatory networks that act upstream of skeletal muscle fate determinants are distinct
in different anatomical locations. Despite recent efforts, a clear understanding of the cascade …
in different anatomical locations. Despite recent efforts, a clear understanding of the cascade …
[HTML][HTML] Cellular pathogenesis of Duchenne muscular dystrophy: progressive myofibre degeneration, chronic inflammation, reactive myofibrosis and satellite cell …
P Dowling, D Swandulla… - European Journal of …, 2023 - ncbi.nlm.nih.gov
Duchenne muscular dystrophy is a highly progressive muscle wasting disease of early
childhood and characterized by complex pathophysiological and histopathological changes …
childhood and characterized by complex pathophysiological and histopathological changes …