
Publications
Articles et résultats scientifiques des équipes et collaborateurs du PGNM.
À propos
Les publications du PGNM reflètent la production scientifique des équipes et des collaborateurs du laboratoire, couvrant les mécanismes fondamentaux, les modèles de maladies, les technologies et la recherche translationnelle.
2022
Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.,
Hum Mutat 2022 Dec; 43(12): 1898-1908.
2022
Pharmacological inhibition of HDAC6 improves muscle phenotypes in dystrophin-deficient mice by downregulating TGF-β via Smad3 acetylation.,
Nat Commun 2022 Nov; 13(1): 7108.
2022
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.,
Acta Neuropathol 2022 Oct; 144(4): 707-731.
2022
Superfast excitation-contraction coupling in adult zebrafish skeletal muscle fibers.,
J Gen Physiol 2022 Sep; 154(9): .
2022
Hypothalamic-pituitary-adrenal axis activation and glucocorticoid-responsive gene expression in skeletal muscle and liver of Apc mice.,
J Cachexia Sarcopenia Muscle 2022 Jun; 13(3): 1686-1703.
2022
Mice with muscle-specific deletion of Bin1 recapitulate centronuclear myopathy and acute downregulation of dynamin 2 improves their phenotypes.,
Mol Ther 2022 Feb; 30(2): 868-880.
2022
Epigenetic Control of Muscle Stem Cells: Focus on Histone Lysine Demethylases.,
Front Cell Dev Biol 2022 ; 10(): 917771.
2022
Development of a high-throughput tailored imaging method in zebrafish to understand and treat neuromuscular diseases.,
Front Mol Neurosci 2022 ; 15(): 956582.