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EMBO Molecular Medicine|March 19, 2013
Fibroadipogenic progenitors mediate the ability of HDAC inhibitors to promote regeneration in dystrophic muscles of young, but not old Mdx miceChiara Mozzetta, Silvia Consalvi, Valentina Saccone, et al.
Molecular Medicine (Cambridge, Mass.)|April 5, 2013
Preclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostatSilvia Consalvi, Chiara Mozzetta, Paolo Bettica, et al.
Cell Stem Cell|October 5, 2010
TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regenerationDaniela Palacios, Chiara Mozzetta, Silvia Consalvi, et al.
Cell Death & Disease|September 16, 2022
Non-myogenic mesenchymal cells contribute to muscle degeneration in facioscapulohumeral muscular dystrophy patientsLorena Di Pietro, Flavia Giacalone, Elvira Ragozzino, et al.
Nature Communications|September 29, 2018
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophyFabio A Iannotti, Ester Pagano, Ombretta Guardiola, et al.
EMBO Reports|August 6, 2020
HDAC inhibitors tune miRNAs in extracellular vesicles of dystrophic muscle-resident mesenchymal cellsMartina Sandonà, Silvia Consalvi, Luca Tucciarone, et al.
The EMBO Journal|November 10, 2011
Signal-dependent incorporation of MyoD-BAF60c into Brg1-based SWI/SNF chromatin-remodelling complexSonia V Forcales, Sonia Albini, Lorenzo Giordani, et al.
Genes & Development|April 1, 2014
HDAC-regulated myomiRs control BAF60 variant exchange and direct the functional phenotype of fibro-adipogenic progenitors in dystrophic musclesValentina Saccone, Silvia Consalvi, Lorenzo Giordani, et al.
Nature Communications|January 10, 2025
Aptamer-conjugated gold nanoparticles enable oligonucleotide delivery into muscle stem cells to promote regeneration of dystrophic musclesFrancesco Millozzi, Paula Milán-Rois, Arghya Sett, et al.
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