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Biomolecules|January 28, 2026
Selenoprotein N and SEPN1-Related Myopathies: Mechanisms, Models, and Therapeutic PerspectivesMartina Lanza, Ester Zito, Giorgia Dinoi, et al.
International Journal of Molecular Sciences|January 10, 2026
From Symptomatic Therapies to Disease-Modifying Approaches for Neuronal Sodium Channel DisordersGiorgia Dinoi, Ileana Canfora, Daniela D'Agnano, et al.
The Journal of Endocrinology|March 11, 2021
Oxtr/TRPV1 expression and acclimation of skeletal muscle to cold-stress in male miceElena Conte, Adele Romano, Michela De Bellis, et al.
Plos One|March 13, 2026
Best reference genes for unbiased normalized transcript expression in normal and dystrophic human cell models of myogenesisRaffaella Quarta, Brigida Boccanegra, Enrica Cristiano, et al.
Scientific Reports|February 3, 2016
In vivo longitudinal study of rodent skeletal muscle atrophy using ultrasonographyAntonietta Mele, Adriano Fonzino, Francesco Rana, et al.
International Journal of Molecular Sciences|September 28, 2021
A Novel <i>KCNA2</i> Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-AminopyridinePaola Imbrici, Elena Conte, Rikard Blunck, et al.
Frontiers in Pharmacology|April 8, 2020
Functional Study of Novel Bartter's Syndrome Mutations in ClC-Kb and Rescue by the Accessory Subunit Barttin Toward Personalized MedicineDalila Sahbani, Bice Strumbo, Silvana Tedeschi, et al.
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