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Claudio Bruno

Showing results (91-100 of 302) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 17, 2019
Novel <i>TRIM32</i> mutation in sarcotubular myopathyChiara Panicucci, Monica Traverso, Serena Baratto, et al.
Pediatric Research|August 2, 2007
Fatal infantile cardiac glycogenosis with phosphorylase kinase deficiency and a mutation in the gamma2-subunit of AMP-activated protein kinaseHasan O Akman, James N Sampayo, Fiona A Ross, et al.
JIMD Reports|May 1, 2017
Mutations in GMPPB Presenting with Pseudometabolic MyopathyChiara Panicucci, Chiara Fiorillo, Francesca Moro, et al.
Clinical Neuropathology|July 20, 2021
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathiesChiara Panicucci, Serena Baratto, Lizzia Raffaghello, et al.
The American Journal of Pathology|January 12, 2002
Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiencyCarlo Minetti, Massimo Bado, Paolo Broda, et al.
Plos One|December 14, 2021
Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia GiuliaCatia Mio, Chiara Dal Secco, Stefania Marzinotto, et al.
American Journal of Physiology. Cell Physiology|September 30, 2005
Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatmentStefania Assereto, Silvia Stringara, Federica Sotgia, et al.
Chemmedchem|November 11, 2015
Stereoselective Modulation of P-Glycoprotein by Chiral Small MoleculesAlessia Carocci, Alessia Catalano, Francesco Turi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 14, 2016
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophyStefania Assereto, Rosanna Piccirillo, Serena Baratto, et al.
Biochemical and Biophysical Research Communications|February 15, 2015
Early onset cardiomyopathy associated with the mitochondrial tRNALeu((UUR)) 3271T>C MELAS mutationGiacomo Brisca, Chiara Fiorillo, Claudia Nesti, et al.
Pageof 31

Showing results (91-100 of 302) with videos related to

Sort By:
Pageof 31
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 17, 2019
Novel <i>TRIM32</i> mutation in sarcotubular myopathyChiara Panicucci, Monica Traverso, Serena Baratto, et al.
Pediatric Research|August 2, 2007
Fatal infantile cardiac glycogenosis with phosphorylase kinase deficiency and a mutation in the gamma2-subunit of AMP-activated protein kinaseHasan O Akman, James N Sampayo, Fiona A Ross, et al.
JIMD Reports|May 1, 2017
Mutations in GMPPB Presenting with Pseudometabolic MyopathyChiara Panicucci, Chiara Fiorillo, Francesca Moro, et al.
Clinical Neuropathology|July 20, 2021
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathiesChiara Panicucci, Serena Baratto, Lizzia Raffaghello, et al.
The American Journal of Pathology|January 12, 2002
Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiencyCarlo Minetti, Massimo Bado, Paolo Broda, et al.
Plos One|December 14, 2021
Local occurrence and fast spread of B.1.1.7 lineage: A glimpse into Friuli Venezia GiuliaCatia Mio, Chiara Dal Secco, Stefania Marzinotto, et al.
American Journal of Physiology. Cell Physiology|September 30, 2005
Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatmentStefania Assereto, Silvia Stringara, Federica Sotgia, et al.
Chemmedchem|November 11, 2015
Stereoselective Modulation of P-Glycoprotein by Chiral Small MoleculesAlessia Carocci, Alessia Catalano, Francesco Turi, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 14, 2016
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophyStefania Assereto, Rosanna Piccirillo, Serena Baratto, et al.
Biochemical and Biophysical Research Communications|February 15, 2015
Early onset cardiomyopathy associated with the mitochondrial tRNALeu((UUR)) 3271T>C MELAS mutationGiacomo Brisca, Chiara Fiorillo, Claudia Nesti, et al.
Pageof 31