ARCARI, ALESSANDRO
ARCARI, ALESSANDRO
Dipartimento di Scienze Biomediche e Cliniche
The SIRT1 activator SRT2104 exerts exercise mimetic effects and promotes Duchenne muscular dystrophy recovery
2025 M. Giovarelli, S. Zecchini, S.R. Casati, L. Lociuro, O. Gjana, L. Mollica, E. Pisanu, H.D. Mbissam, O. Cappellari, C. De Santis, A. Arcari, A. Bigot, G. Clerici, E. Catalani, S. Del Quondam, A. Andolfo, C. Braccia, M.G. Cattaneo, C. Banfi, D. Brunetti, E. Mocciaro, A. De Luca, E. Clementi, D. Cervia, C. Perrotta, C. De Palma
Cholesterol dysregulation in Rett syndrome: implications for synaptic function
2025 F. Postogna, M. Breccia, O. Roggero, F. Biella, C. Cabasino, A. Arcari, N. Giancroce, N. Landsberger, A. Frasca
Towards a new genetic player in the pathophysiology of Rett Syndrome
2024 J. Sandakly, S. Pezzini, L. Scandella, A. Arcari, E. Fraviga, D. Pozzi, M. Francolini, N. Landsberger
Reduction in cholesterol supply by Mecp2 null astrocytes contributes to synaptic defects
2024 F. Postogna, M. Breccia, O. Roggero, F. Biella, E. Albizzati, C. Cabasino, A. Arcari, D. Colombo, L. Morelli, E. Chiricozzi, N. Landsberger, A. Frasca
Deciphering the role of Hpcal4 : a potential target for Rett Syndrome ?
2024 J. Sandakly, S. Pezzini, L. Scandella, A. Arcari, D. Pozzi, M. Francolini, N. Landsberger
Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signaling
2024 D. Cervia, S. Zecchini, L. Pincigher, P. Roux-Biejat, C. Zalambani, E. Catalani, A. Arcari, S. Del Quondam, K. Brunetti, R. Ottria, S. Casati, C. Vanetti, M.C. Barbalace, C. Prata, M. Malaguti, S.R. Casati, L. Lociuro, M. Giovarelli, E. Mocciaro, S. Falcone, C. Fenizia, C. Moscheni, S. Hrelia, C. De Palma, E. Clementi, C. Perrotta
Tailored graphene nanoparticles for biomedical application: preliminary in vitro characterization of the functionality in model cell lines
2024 C. Moscheni, P. Sartori, K. Hu, S. Zecchini, L. Brambilla, A. Arcari, A. Napoli, E. Mocciaro, M. Uboldi, L. Zema, C. Perrotta, C. Castiglioni
Unravelling the role of Hpcal4 as a potential modifier gene for Rett Syndrome
2024 J. Sandakly, S. Pezzini, L. Scandella, A. Arcari, E. Fraviga, D. Pozzi, M. Francolini, N. Landsberger
Synaptic localization of HPCAL4 in neurons : looking for a role of this Ca2+ sensor in the modulation of neuronal function in health and disease
2023 L. Scandella, J. Sandakly, S. Pezzini, A. Arcari, E. Fraviga, D. Pozzi, N. Landsberger, M. Francolini
The interplay Between Hpcal4 And Mecp2 : Identification And Characterization Of A Novel Putative Target for Rett Syndrome Therapy
2023 S. Pezzini, A. Arcari, J. Sandakly, L. Scandella, M. Francolini, E. Fraviga, D. Pozzi, N. Landsberger