MALENA, ADRIANA
MALENA, ADRIANA
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.
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes
2017 Milioto, Carmelo; Malena, Adriana; Maino, Eleonora; Polanco, Maria J.; Marchioretti, Caterina; Borgia, Doriana; Gomes Pereira, Marcelo; Blaauw, Bert; Lieberman, Andrew P.; Venturini, Roberta; Plebani, Mario; Sambataro, Fabio; Vergani, Lodovica; Pegoraro, Elena; Sorar, Gianni; Pennuto, Maria; Pennuto, Maria; Soraru', Gianni; Sambataro, Fabio
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
Functional and molecular responses to stress conditions in heteroplasmic MELAS (3243) RD cybrids.
2006 Vergani, Lodovica; Emanuele, Loro; Malena, Adriana; Silvia, Cazzorla
Functional and molecular responses to stress conditions in heteroplasmic MELAS 3243 RD cybrids.
2006 Malena, Adriana; Emanuele, Loro; Silvia, Cazzola; Andrea, Marchetto; Vergani, Lodovica
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients
2017 Borgia, Doriana; Malena, Adriana; Spinazzi, Marco; Andrea Desbats, Maria; Salviati, Leonardo; Russell, Aaron P; Miotto, Giovanni; Tosatto, Laura; Pegoraro, Elena; Sorarù, Gianni; Pennuto, Maria; Vergani, Lodovica; Miotto, Giovanni
INHIBITION OF MITOCHONDRIAL FISSION FAVOURS MUTANT OVER WILD-TYPE MITOCHONDRIAL DNA
2009 Malena, Adriana; Loro, E; DI RE, M; Holt, Ji; 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
Mitochondrial DNA heteroplasmy in muscle cybrids harbouring A3243G Melas mutation
2008 Malena, Adriana
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA.
2016 Malena, Adriana; Pantic, Boris; Borgia, Doriana; Sgarbi, G; Solaini, G; Holt, Ij; Spinazzola, A; Perissinotto, Egle; Sandri, Marco; Baracca, A; Vergani, Lodovica
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.
2010 Loro, E; Rinaldi, F; Malena, Adriana; Masiero, E; Novelli, G; Angelini, Corrado; Romeo, V; Sandri, Marco; Botta, A; Vergani, Lodovica
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts
2016 Pantic, Boris; Borgia, Doriana; Giunco, Silvia; Malena, Adriana; Kiyono, Tohru; Salvatori, Sergio; DE ROSSI, Anita; Giardina, Emiliano; Sangiuolo, Federica; Pegoraro, Elena; Vergani, Lodovica; Botta, Annalisa