ASSERETO, STEFANIA
ASSERETO, STEFANIA
100009 - Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili
Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene.
2018-01-01 Fiorillo, C; D'Apice, Mr; Trucco, F; Murdocca, M; Spitalieri, P; Assereto, S; Baratto, S; Morcaldi, G; Minetti, C; Sangiuolo, F; Novelli, G.
Clinical and molecular consequences of exon 78 deletion in DMD gene
2018-01-01 Traverso, Monica; Assereto, Stefania; Baratto, Serena; Iacomino, Michele; Pedemonte, Marina; Diana, Maria Cristina; Ferretti, Marta; Broda, Paolo; Minetti, Carlo; Gazzerro, Elisabetta; Madia, Francesca; Bruno, Claudio; Zara, Federico; Fiorillo, Chiara
Early onset cardiomyopathy associated with the mitochondrial tRNALeu(UUR) 3271T>C MELAS mutation
2015-01-01 Brisca, G.; Fiorillo, C.; Nesti, C.; Trucco, F.; Derchi, M.; Andaloro, A.; Assereto, S.; Morcaldi, G.; Pedemonte, M.; Minetti, C.; Santorelli, F. M.; Bruno, C.
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations
2012-01-01 Canafoglia, L.; Gennaro, E.; Capovilla, G.; Gobbi, G.; Boni, A.; Beccaria, F.; Viri, M.; Michelucci, R.; Agazzi, P.; Assereto, S.; Coviello, D. A.; Di Stefano, M.; Rossi Sebastiano, D.; Franceschetti, S.; Zara, F.
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis.
2015-01-01 Gazzerro, E; Baldassari, S; Assereto, S; Fruscione, F; Pistorio, A; Panicucci, C; Volpi, S; Perruzza, L; Fiorillo, C; Minetti, C; Traggiai, E; Grassi, F; Bruno, C.
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I.
2014-01-01 Assereto, Stefania; Robbiano, A; Di Rocco, M; Rossi, A; Cassandrini, D; Panicucci, C; Brigati, Giorgia; Biancheri, R; Bruno, C; Minetti, Carlo; Trucks, H; Sander, T; Zara, Federico; Gazzerro, E.
The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy
2019-01-01 Gazzerro, E; Baratto, S; Assereto, S; Baldassari, S; Panicucci, C; Raffaghello, L; Scudieri, P; De Battista, D; Fiorillo, C; Volpi, S; Chaabane, L; Malnati, M; Messina, G; Bruzzone, S; Traggiai, E; Grassi, F; Minetti, C; Bruno, C
The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane.
2016-01-01 Baskin, Jm; Wu, X; Christiano, R; Oh, Ms; Schauder, Cm; Gazzerro, E; Messa, M; Baldassari, S; Assereto, Stefania; Biancheri, R; Zara, F; Minetti, Carlo; Raimondi, A; Simons, M; Walther, Tc; Reinisch, Km; De Camilli, P.
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy
2016-01-01 Assereto, Stefania; Piccirillo, Rosanna; Baratto, Serena; Scudieri, Paolo; Fiorillo, Chiara; Massacesi, Manuela; Traverso, Monica; Galietta, LUIS JUAN VICENTE; Bruno, Claudio; Minetti, Carlo; Zara, Federico; Gazzerro, Elisabetta
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene. | 1-gen-2018 | Fiorillo, C; D'Apice, Mr; Trucco, F; Murdocca, M; Spitalieri, P; Assereto, S; Baratto, S; Morcaldi, G; Minetti, C; Sangiuolo, F; Novelli, G. | |
| Clinical and molecular consequences of exon 78 deletion in DMD gene | 1-gen-2018 | Traverso, Monica; Assereto, Stefania; Baratto, Serena; Iacomino, Michele; Pedemonte, Marina; Diana, Maria Cristina; Ferretti, Marta; Broda, Paolo; Minetti, Carlo; Gazzerro, Elisabetta; Madia, Francesca; Bruno, Claudio; Zara, Federico; Fiorillo, Chiara | |
| Early onset cardiomyopathy associated with the mitochondrial tRNALeu(UUR) 3271T>C MELAS mutation | 1-gen-2015 | Brisca, G.; Fiorillo, C.; Nesti, C.; Trucco, F.; Derchi, M.; Andaloro, A.; Assereto, S.; Morcaldi, G.; Pedemonte, M.; Minetti, C.; Santorelli, F. M.; Bruno, C. | |
| Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations | 1-gen-2012 | Canafoglia, L.; Gennaro, E.; Capovilla, G.; Gobbi, G.; Boni, A.; Beccaria, F.; Viri, M.; Michelucci, R.; Agazzi, P.; Assereto, S.; Coviello, D. A.; Di Stefano, M.; Rossi Sebastiano, D.; Franceschetti, S.; Zara, F. | |
| Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis. | 1-gen-2015 | Gazzerro, E; Baldassari, S; Assereto, S; Fruscione, F; Pistorio, A; Panicucci, C; Volpi, S; Perruzza, L; Fiorillo, C; Minetti, C; Traggiai, E; Grassi, F; Bruno, C. | |
| Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I. | 1-gen-2014 | Assereto, Stefania; Robbiano, A; Di Rocco, M; Rossi, A; Cassandrini, D; Panicucci, C; Brigati, Giorgia; Biancheri, R; Bruno, C; Minetti, Carlo; Trucks, H; Sander, T; Zara, Federico; Gazzerro, E. | |
| The danger signal extracellular ATP is involved in the immunomediated damage of α-sarcoglycan deficient muscular dystrophy | 1-gen-2019 | Gazzerro, E; Baratto, S; Assereto, S; Baldassari, S; Panicucci, C; Raffaghello, L; Scudieri, P; De Battista, D; Fiorillo, C; Volpi, S; Chaabane, L; Malnati, M; Messina, G; Bruzzone, S; Traggiai, E; Grassi, F; Minetti, C; Bruno, C | |
| The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane. | 1-gen-2016 | Baskin, Jm; Wu, X; Christiano, R; Oh, Ms; Schauder, Cm; Gazzerro, E; Messa, M; Baldassari, S; Assereto, Stefania; Biancheri, R; Zara, F; Minetti, Carlo; Raimondi, A; Simons, M; Walther, Tc; Reinisch, Km; De Camilli, P. | |
| The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy | 1-gen-2016 | Assereto, Stefania; Piccirillo, Rosanna; Baratto, Serena; Scudieri, Paolo; Fiorillo, Chiara; Massacesi, Manuela; Traverso, Monica; Galietta, LUIS JUAN VICENTE; Bruno, Claudio; Minetti, Carlo; Zara, Federico; Gazzerro, Elisabetta |