RIPOLONE, MICHELA
RIPOLONE, MICHELA
DIPARTIMENTO DI BIOLOGIA (attivo dal 01/07/1979 al 26/04/2012)
Autophagy as a new therapeutic target in Duchenne muscular dystrophy
2012 C. De Palma, F. Morisi, S. Cheli, S. Pambianco, V. Cappello, M. Vezzoli, P. Rovere Querini, M. Moggio, M. Ripolone, M. Francolini, M. Sandri, E. Clementi
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy
2021 E. Mauri, D. Piga, S. Pagliarani, F. Magri, A. Manini, M. Sciacco, M. Ripolone, L. Napoli, L. Borellini, C. Cinnante, D. Cassandrini, S. Corti, N. Bresolin, G.P. Comi, A. Govoni
cAMP-Epac2-mediated activation of Rap1 in developing male germ cells : RA-RhoGAP as a possible direct down-stream effector
2009 E. Aivatiadou, M. Ripolone, F. Brunetti, G. Berruti
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders
2011 M. Ranieri, D. Ronchi, S. Orcesi, V. Spartà, A. Cosi, A. Bordoni, V. Lucchini, F. Fortunato, E. Fassone, D. Tonduti, G. Rulfi, M. Rizzuti, M. Ripolone, M. Sciacco, M. Moggio, S. Corti, S. Savasta, A. Berardinelli, P. Veggiotti, G.P. Comi
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects
2011 D. Ronchi, S. Orcesi, V. Spartà, A. Cosi, A. Bordoni, V. Lucchini, F. Fortunato, E. Fassone, D. Tonduti, G. Rulfi, M. Ranieri, M. Rizzuti, M. Ripolone, M. Sciacco, M. Moggio, S. Corti, S. Savata, A. Berardinelli, P. Veggiotti, G.P. Comi
Drp1 overexpression induces desmin disassembling and drives kinesin-1 activation promoting mitochondrial trafficking in skeletal muscle
2020 M. Giovarelli, S. Zecchini, E. Martini, M. Garre, S. Barozzi, M. Ripolone, L. Napoli, M. Coazzoli, C. Vantaggiato, P. Roux-Biejat, D. Cervia, C. Moscheni, C. Perrotta, D. Parazzoli, E. Clementi, C. De Palma
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies
2021 E. Mauri, D. Piga, A. Govoni, R. Brusa, S. Pagliarani, M. Ripolone, R. Dilena, C. Cinnante, M. Sciacco, D. Cassandrini, V. Nigro, N. Bresolin, S. Corti, G.P. Comi, F. Magri
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice
2019 J.L. Sottnik, V. Mallaredy, A. Chauca-Diaz, C. Ritterson Lew, C. Owens, G.M. Dancik, S. Pagliarani, S. Lucchiari, M. Moggio, M. Ripolone, G.P. Comi, H.F. Frierson, D. Clouthier, D. Theodorescu
Expanding the phenotypic spectrum of non-alcoholic fatty liver disease and hypertriglyceridemia
2022 M. Meroni, M. Longo, E. Paolini, G. Tria, M. Ripolone, L. Napoli, M. Moggio, A.L. Fracanzani, P. Dongiovanni
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy
2015 M. Ripolone, D. Ronchi, R. Violano, D. Vallejo, G. Fagiolari, E. Barca, V. Lucchini, I. Colombo, L. Villa, A. Berardinelli, U. Balottin, L. Morandi, M. Mora, A. Bordoni, F. Fortunato, S. Corti, D. Parisi, A. Toscano, M. Sciacco, S. Di Mauro, G.P. Comi, M. Moggio
Low anaerobic threshold and increased skeletal muscle lactate production in subjects with Huntington's Disease
2011 A. Ciammola, J. Sassone, M. Sciacco, N.E. Mencacci, M. Ripolone, C. Bizzi, C. Colciago, M. Moggio, G. Parati, V. Silani, G.G. Malfatto
mUBPy and the Hrs-STAM complex in developing male germ cells
2006 M. Ripolone, A. Favalli, G. Berruti
mUBPy in spermatogenic cells of Wobbler Mice
2007 M. Ripolone, G. Berruti
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice
2009 M. Ripolone
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy
2022 M. Ripolone, D. Velardo, S. Mondello, S. Zanotti, F. Magri, E. Minuti, S. Cazzaniga, F. Fortunato, P. Ciscato, F. Tiberio, M. Sciacco, M. Moggio, P. Bettica, G.P. Comi
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene
2006 C. Lamperti, S. Salani, G. Fagiolari, M.E. Fruguglietti, N. Grimoldi, A. Prelle, A. Bordoni, M. Ripolone, V. Crugnola, N. Bresolin, G.P. Comi
Neuropathological study of skeletal muscle, heart, liver, and brainin a neonatal form of glycogen storage disease type IV associated with a newmutation in GBE1 gene
2009 7. . Lamperti, S. Salani, S. Lucchiari, A. Bordoni, M. Ripolone, G. Fagiolari, M. Fruguglietti, V. Crugnola, C. Colombo, A. Cappellini, A. Prelle, N. Bresolin, G.P. Comi, M. Moggio
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions
2012 D. Ronchi, C. Garone, A. Bordoni, P. Gutierrez Rios, S. E. Calvo, M. Ripolone, M. Ranieri, M. Rizzuti, L. Villa, F. Magri, S. Corti, N. Bresolin, V.K. Mootha, M. Moggio, S. DiMauro, G.P. Comi, M. Sciacco
Novel missense GARS gene mutation in an Italian family with hereditary distal motor neuropathy
2005 R. Del Bo, S. Ghezzi, F. Locatelli, M. Scarlato, S. Corti, A. Prelle, G. Fagiolari, M. Ripolone, M. Moggio, M. Carpo, N. Bresolin, G.P. Comi
Oxidative defect in a large cohort of genetically-determined SMA cases
2011 A. Berardinelli, G. Fagiolari, D. Vallejo, V. Lucchini, A. Bordoni, C. Lamperti, M. Ripolone, S. Corti, U. Balottin, N. Bresolin, G. Comi, M. Sciacco, M. Moggio