How Can Proteomics Help to Elucidate the Pathophysiological Crosstalk in Muscular Dystrophy and Associated Multi-System Dysfunction?
P Dowling, C Trollet, E Negroni, D Swandulla… - Proteomes, 2024 - mdpi.com
This perspective article is concerned with the question of how proteomics, which is a core
technique of systems biology that is deeply embedded in the multi-omics field of modern …
technique of systems biology that is deeply embedded in the multi-omics field of modern …
Characterization of disease-specific alterations in metabolites and effects of mesenchymal stromal cells on dystrophic muscles
Y Nitahara-Kasahara, G Posadas-Herrera… - Frontiers in Cell and …, 2024 - frontiersin.org
Introduction Duchenne muscular dystrophy (DMD) is a genetic disorder caused by mutations
in the dystrophin-encoding gene that leads to muscle necrosis and degeneration with …
in the dystrophin-encoding gene that leads to muscle necrosis and degeneration with …
Differential metabolic secretion between muscular dystrophy mouse-derived spindle cell sarcomas and rhabdomyosarcomas drives tumor type development
ETE Niba, H Awano, N Nishimura… - … of Physiology-Cell …, 2024 - journals.physiology.org
The dystrophin gene (Dmd) is recognized for its significance in Duchenne muscular
dystrophy (DMD), a lethal and progressive skeletal muscle disease. Some patients with …
dystrophy (DMD), a lethal and progressive skeletal muscle disease. Some patients with …
[HTML][HTML] Evaluation of Creatine Monohydrate Supplementation on the Gastrocnemius Muscle of Mice with Muscular Dystrophy: A Preliminary Study
VAR Fernandes, GP Dos Santos, A Iatecola… - …, 2025 - pmc.ncbi.nlm.nih.gov
Background/Objectives: Duchenne muscular dystrophy (DMD) is a genetic disease
characterized by a lack of dystrophin caused by mutations in the DMD gene, and some …
characterized by a lack of dystrophin caused by mutations in the DMD gene, and some …