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CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I

Abstract Background Myotonic Dystrophy type I (DM1) is the most common muscular dystrophy in adults. Previous reports have highlighted that neuromuscular junctions (NMJs) deteriorate in skeletal muscle from DM1 patients and mouse models thereof. However, the underlying pathomechanisms and their cont...

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Autori principali: Denis Falcetta, Sandrine Quirim, Ilaria Cocchiararo, Florent Chabry, Marine Théodore, Adeline Stiefvater, Shuo Lin, Lionel Tintignac, Robert Ivanek, Jochen Kinter, Markus A. Rüegg, Michael Sinnreich, Perrine Castets
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMC 2024-05-01
Serie:Skeletal Muscle
Soggetti:
Myotonic dystrophy
Neuromuscular junctions
CaMKII
Synaptic genes
Fibre type
Accesso online:https://doi.org/10.1186/s13395-024-00345-3
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