Showing results (21-30 of 62) with videos related to
Sort By:
Pageof 7
Biomolecules|January 28, 2026
Selenoprotein N and SEPN1-Related Myopathies: Mechanisms, Models, and Therapeutic PerspectivesMartina Lanza, Ester Zito, Giorgia Dinoi, et al.Frontiers in Pharmacology|June 6, 2020
Changes in Expression and Cellular Localization of Rat Skeletal Muscle ClC-1 Chloride Channel in Relation to Age, Myofiber Phenotype and PKC ModulationElena Conte, Adriano Fonzino, Antonio Cibelli, 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.Experimental Neurology|May 15, 2021
Increased sarcolemma chloride conductance as one of the mechanisms of action of carbonic anhydrase inhibitors in muscle excitability disordersConcetta Altamura, Adriano Fonzino, Nancy Tarantino, 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.Plos One|November 13, 2024
Determination of qPCR reference genes suitable for normalizing gene expression in a novel model of Duchenne muscular dystrophy, the D2-mdx mouseBrigida Boccanegra, Roberta Lenti, Paola Mantuano, 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.Pageof 7