Improvement of muscle strength in a mouse model for congenital myopathy treated with HDAC and DNA methyltransferase inhibitors von Ruiz, Alexis, Benucci, Sofia, Duthaler, Urs, Bachmann, Christoph, Franchini, Martina, Noreen, Faiza, Pietrangelo, Laura, Protasi, Feliciano, Treves, Susan, Zorzato, Francesco

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Functional characterization of RYR1 variants identified in malignant hyperthermia susceptible individuals von Noda, Yuko, Miyoshi, Hirotsugu, Benucci, Sofia, Gonzalez, Asensio, Bandschapp, Oliver, Girard, Thierry, Treves, Susan, Zorzato, Francesco

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Molecular basis of impaired extraocular muscle function in a mouse model of congenital myopathy due to compound heterozygous Ryr1 mutations von Eckhardt, Jan, Bachmann, Christoph, Benucci, Sofia, Elbaz, Moran, Ruiz, Alexis, Zorzato, Francesco, Treves, Susan

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A novel, patient-derived RyR1 mutation impairs muscle function and calcium homeostasis in mice von Benucci, Sofia, Ruiz, Alexis, Franchini, Martina, Ruggiero, Lucia, Zoppi, Dario, Sitsapesan, Rebecca, Lindsay, Chris, Pelczar, Pawel, Pietrangelo, Laura, Protasi, Feliciano, Treves, Susan, Zorzato, Francesco

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Bi-allelic expression of the RyR1 p.A4329D mutation decreases muscle strength in slow-twitch muscles in mice von Elbaz, Moran, Ruiz, Alexis, Nicolay, Sven, Tupini, Chiara, Bachmann, Christoph, Eckhardt, Jan, Benucci, Sofia, Pelczar, Pawel, Treves, Susan, Zorzato, Francesco

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