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The Journal of Biological Chemistry|October 24, 2006
A mouse model for monitoring calpain activity under physiological and pathological conditionsMarc Bartoli, Nathalie Bourg, Daniel Stockholm, et al.
Human Molecular Genetics|February 16, 2010
Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transferWilliam Lostal, Marc Bartoli, Nathalie Bourg, et al.
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.
STAR Protocols|April 3, 2026
Protocol for monitoring cytoplasmic Ca<sup>2+</sup> dynamics using Fura Red-AM on a Zeiss Axio Observer microscopeSabrina Beaumier, Marc Bartoli
The FEBS Journal|September 24, 2010
A new pathway encompassing calpain 3 and its newly identified substrate cardiac ankyrin repeat protein is involved in the regulation of the nuclear factor-κB pathway in skeletal muscleLydie Laure, Nathalie Danièle, Laurence Suel, 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.
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.
Human Molecular Genetics|February 7, 2008
Mannosidase I inhibition rescues the human alpha-sarcoglycan R77C recurrent mutationMarc Bartoli, Evelyne Gicquel, Laetitia Barrault, et al.
Medecine Sciences : M/S|May 2, 2020
[CRISPR-Cas9 for muscle dystrophies]Océane Ballouhey, Marc Bartoli, Nicolas Levy
Methods in Molecular Biology (Clifton, N.J.)|July 28, 2025
Restoration of Dysferlin After Exon 32 Skipping in Patient CellsFlorian Barthélémy, Sébastien Courrier, Marc Bartoli
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