RIPOLONE, MICHELA
RIPOLONE, MICHELA
DIPARTIMENTO DI BIOLOGIA (attivo dal 01/07/1979 al 26/04/2012)
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls
2023 F. Magri, L. Napoli, M. Ripolone, P. Ciscato, M. Moggio, S. Corti, G.P. Comi, M. Sciacco, S. Zanotti
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant
2023 M. Rimoldi, F. Magri, S. Antognozzi, M. Ripolone, S. Salani, D. Piga, L. Bertolasi, S. Zanotti, P. Ciscato, F. Fortunato, M. Moggio, S. Corti, G.P. Comi, D. Ronchi
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene
2023 S. Zanotti, M. Ripolone, L. Napoli, D. Velardo, S. Salani, P. Ciscato, S. Priori, D. Kukavica, A. Mazzanti, L. Diamanti, E. Vegezzi, M. Moggio, S. Corti, G. Comi, M. Sciacco
MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization
2023 M. Ripolone, S. Zanotti, L. Napoli, D. Ronchi, P. Ciscato, G.P. Comi, M. Moggio, M. Sciacco
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
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
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
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
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
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
Purkinje cell COX deficiency and mtDNA depletion in an animal model of spinocerebellar ataxia type 1
2018 M. Ripolone, V. Lucchini, D. Ronchi, G. Fagiolari, A. Bordoni, F. Fortunato, S. Mondello, S. Bonato, M. Meregalli, Y. Torrente, S. Corti, G.P. Comi, M. Moggio, M. Sciacco.
Reversal of Defective Mitochondrial Biogenesis in Limb-Girdle Muscular Dystrophy 2D by Independent Modulation of Histone and PGC-1α Acetylation
2016 S. Pambianco, M. Giovarelli, C. Perrotta, S. Zecchini, D. Cervia, I. Di Renzo, C. Moscheni, M. Ripolone, R. Violano, M. Moggio, M.T. Bassi, P.L. Puri, L. Latella, E. Clementi, C. De Palma
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
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
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
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
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
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
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
USP8, a regulator of endosomal sorting, is involved in mouse acrosome biogenesis through interaction with the spermatid ESCRT-0 complex and microtubules
2010 G. Berruti, M. Ripolone, M. Ceriani