LORO, EMANUELE
LORO, EMANUELE
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.
2008 Spinazzi, Marco; Cazzola, S; Bortolozzi, Mario; Baracca, A; Loro, Emanuele; Casarin, Alberto; Solaini, G; Sgarbi, G; Casalena, G; Cenacchi, G; Malena, Adriana; Frezza, C; Carrara, F; Angelini, Corrado; Scorrano, Luca; Salviati, Leonardo; Vergani, L.
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics.
2008 Spinazzi, Marco; Cazzola, S; Bortolozzi, Mario; Baracca, A; Loro, Emanuele; Solaini, G; Sgarbi, G; Cenacchi, G; Malena, Adriana; Scorrano, Luca; Frezza, C; Angelini, Corrado; Vergani, Lodovica
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases
2013 A., Botta; Malena, Adriana; Tibaldi, Elena; L., Rocchi; Loro, Emanuele; E., Pena; L., Cenci; E., Ambrosi; M. C., Bellocchi; Pagano, MARIO ANGELO PRIMO; G., Novelli; G., Rossi; H. L., Monaco; E., Gianazza; Pantic, Boris; V., Romeo; Marin, Oriano; Brunati, ANNA MARIA; Vergani, Lodovica
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells
2010 Loro, Emanuele