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Molecular Therapy : the Journal of the American Society of Gene Therapy|November 18, 2005
Safety and efficacy of AAV-mediated calpain 3 gene transfer in a mouse model of limb-girdle muscular dystrophy type 2AMarc Bartoli, Carinne Roudaut, Samia Martin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 31, 2024
Knockdown of calpain1 in lumbar motoneurons reduces spasticity after spinal cord injury in adult ratsMarjorie Kerzonkuf, Jérémy Verneuil, Cécile Brocard, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Novel Pathogenic Variants in a French Cohort Widen the Mutational Spectrum of GNE MyopathyMathieu Cerino, Svetlana Gorokhova, Anthony Béhin, et al.
Clinical Immunology (Orlando, Fla.)|July 8, 2024
Store-operated calcium entry dysfunction in CRAC channelopathy: Insights from a novel STIM1 mutationBenedicte Alary, Pascal Cintas, Corentin Claude, et al.
Clinical Genetics|March 18, 2021
A novel bi-allelic loss-of-function mutation in STIM1 expands the phenotype of STIM1-related diseasesAlexandra Salvi, Cristina Skrypnyk, Nathalie Da Silva, et al.
Biochimica Et Biophysica Acta|September 29, 2009
Calcium-dependent plasma membrane repair requires m- or mu-calpain, but not calpain-3, the proteasome, or caspasesRonald L Mellgren, Katsuya Miyake, Irina Kramerova, et al.
Molecular Biology Reports|September 23, 2021
First characterization of congenital myasthenic syndrome type 5 in North AfricaRochdi Khaoula, Mathieu Cerino, Nathalie Da Silva, et al.
Skeletal Muscle|February 19, 2013
A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactomeGaëlle Blandin, Sylvie Marchand, Karine Charton, et al.
Cell Communication and Signaling : CCS|November 22, 2025
Zinc binding to a conserved motif in STIM1 induces clustering and SOCE activationBenedicte Alary, Viktoriia E Baksheeva, Sabrina Beaumier, et al.
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