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Sestina Falcone

Showing results (21-30 of 28) with videos related to

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Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.
EMBO Molecular Medicine|September 30, 2014
N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathySestina Falcone, William Roman, Karim Hnia, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2023
Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscleAdrien Morin, Amalia Stantzou, Olga N Petrova, et al.
Cells|August 13, 2025
Identification of CaVβ1 Isoforms Required for Neuromuscular Junction Formation and MaintenanceAmélie Vergnol, Aly Bourguiba, Stephanie Bauché, et al.
Biomedicines|March 6, 2021
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMDElena Gargaun, Sestina Falcone, Guilhem Solé, et al.
Brain : a Journal of Neurology|April 8, 2024
GDF5 as a rejuvenating treatment for age-related neuromuscular failureMassiré Traoré, Chiara Noviello, Amélie Vergnol, et al.
Free Radical Biology & Medicine|September 26, 2024
Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signalingDavide Cervia, Silvia Zecchini, Luca Pincigher, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Human Mutation|May 12, 2009
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological functionChiara Vantaggiato, Francesca Redaelli, Sestina Falcone, et al.
Neurogenetics|July 14, 2009
Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxinGiovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, et al.
EMBO Molecular Medicine|September 30, 2014
N-WASP is required for Amphiphysin-2/BIN1-dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathySestina Falcone, William Roman, Karim Hnia, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 3, 2023
Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscleAdrien Morin, Amalia Stantzou, Olga N Petrova, et al.
Cells|August 13, 2025
Identification of CaVβ1 Isoforms Required for Neuromuscular Junction Formation and MaintenanceAmélie Vergnol, Aly Bourguiba, Stephanie Bauché, et al.
Biomedicines|March 6, 2021
The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMDElena Gargaun, Sestina Falcone, Guilhem Solé, et al.
Brain : a Journal of Neurology|April 8, 2024
GDF5 as a rejuvenating treatment for age-related neuromuscular failureMassiré Traoré, Chiara Noviello, Amélie Vergnol, et al.
Free Radical Biology & Medicine|September 26, 2024
Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signalingDavide Cervia, Silvia Zecchini, Luca Pincigher, et al.
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