MAGRI, STEFANIA
MAGRI, STEFANIA
Universita' degli Studi di MILANO
STIP1 Homology And U-Box Containing Protein 1 (STUB1/CHIP) mutants as a key factor on TATA-box binding protein (TBP) behaviour in digenic spinocerebellar ataxia type 17 (SCA17-DI)
2023 P. Pramaggiore, S. Magri, M. Chierichetti, P. Rusmini, V. Ferrari, B. Tedesco, M. Cozzi, E. Casarotto, V. Crippa, M. Galbiati, L. Cornaggia, G. Patelli, D. Di Bella, F. Taroni, A. Poletti, R. Cristofani
Investigating the molecular mechanisms involved in KIF5A-related neurodegeneration
2022 M. Cozzi, B. Tedesco, R.M. Cristofani, V. Ferrari, E. Casarotto, M. Chierichetti, F. Mina, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, C. Gellera, S. Magri, S. Santangelo, A. Ratti, F. Taroni, A. Poletti
Identification of a new candidate gene in the insurgence of leukodystrophies
2022 A. Pezzotta, M. Spreafico, S. Magri, F. Balistreri, D. Di Bella, C. Gellera, E. Salsano, F. Taroni, A. Pistocchi
Modeling a novel N-terminal mutation of KIF5A gene in patient-derived iPSC-motoneurons
2022 S. Santangelo, P. Bossolasco, C. Fallini, S. Magri, M. Bertocchi, S. Invernizzi, D. Di Bella, D. Bardelli, C. Colombrita, V. Silani, F. Taroni, A. Ratti
Characterization of iPSC-motoneurons from a HSP patient with a novel mutation in KIF5A N-terminal region Characterization of iPSCmotoneurons from a HSP patient with a novel mutation in KIF5A N-terminal region
2022 S. Santangelo, P. Bossolasco, C. Fallini, S. Magri, M. Bertocchi, S. Invernizzi, D. Di Bella, D. Bardelli, C. Colombrita, V. Silani, F. Taroni, A. Ratti
Analysis of the autophagic response in models of KIF5A-related neurodegeneration
2021 M. Cozzi, B. Tedesco, R. Cristofani, M. Galbiati, P. Rusmini, V. Crippa, M. Piccolella, V. Ferrari, E. Casarotto, M. Chierichetti, F. Mina, C. Gellera, S. Magri, F. Taroni, A. Poletti
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations
2021 E. Abati, S. Magri, M. Meneri, G. Manenti, D. Velardo, F. Balistreri, C. Pisciotta, P. Saveri, N. Bresolin, G.P. Comi, D. Ronchi, D. Pareyson, F. Taroni, S. Corti
Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation
2018 S. Magri, V. Fracasso, M. Plumari, E. Alfei, D. Ghezzi, C. Gellera, P. Rusmini, A. Poletti, D.D. Bella, A.E. Elia, C. Pantaleoni, F. Taroni