Sfoglia per Autore
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
mUBPy and the Hrs-STAM complex in developing male germ cells
2006 M. Ripolone, A. Favalli, G. Berruti
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
mUBPy in spermatogenic cells of Wobbler Mice
2007 M. Ripolone, G. Berruti
Skin-derived stem cells transplanted into resorable guides provide functional nerve regeneration after sciatic nerve resection
2007 C. Marchesi, M. Pluderi, F. Colleoni, M. Belicchi, M. Meregalli, A. Farini, L. Draghi, M.E. Fruguglietti, M. Ripolone, M. Gavina, F. Pisati, M. Furlanetto, L. Porretti, R. Lopa, M. Battistelli, S. Corti, A. Prelle, Y. Torrente
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
mUBPY, endocytic vesicle traffic and microtubule mediated transport in acrosome biogenesis. Comparative study between wild-type and Wobbler (L967Q Vps54) mice
2009 M. Ripolone
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma
2009 M. Fruguglietti, L. Napoli, M. Sciacco, M. Ripolone, M. Serafini, N. Grimoldi, N. Bresolin, M. Moggio, A. Prelle
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
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
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
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
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
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
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
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
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.
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
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