RATTI, ANTONIA
RATTI, ANTONIA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Modeling of TDP-43 proteinopathy by chronic oxidative stress identifies rapamycin as beneficial in ALS patient-derived 2D and 3D iPSC models
2025 V. Casiraghi, M.N. Sorce, S. Santangelo, S. Invernizzi, P. Bossolasco, C. Lattuada, C. Battaglia, M. Venturin, V. Silani, C. Colombrita, A. Ratti
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data
2024 S. Saez-Atienzar, C.D.S. Souza, R. Chia, S.N. Beal, I. Lorenzini, R. Huang, J. Levy, C. Burciu, J. Ding, J.R. Gibbs, A. Jones, R. Dewan, V. Pensato, S. Peverelli, L. Corrado, J.J.F.A. van Vugt, W. van Rheenen, C. Tunca, E. Bayraktar, M. Xia, A. Iacoangeli, A. Shatunov, C. Tiloca, N. Ticozzi, F. Verde, L. Mazzini, K. Kenna, A. Al Khleifat, S. Opie-Martin, F. Raggi, M. Filosto, S.C. Piccinelli, A. Padovani, S. Gagliardi, M. Inghilleri, A. Ferlini, R. Vasta, A. Calvo, C. Moglia, A. Canosa, U. Manera, M. Grassano, J. Mandrioli, G. Mora, C. Lunetta, R. Tanel, F. Trojsi, P. Cardinali, S. Gallone, M. Brunetti, D. Galimberti, M. Serpente, C. Fenoglio, E. Scarpini, G.P. Comi, S. Corti, R. Del Bo, M. Ceroni, G.L. Pinter, F. Taroni, E.D. Bella, E. Bersano, C.J. Curtis, S.H. Lee, R. Chung, H. Patel, K.E. Morrison, J. Cooper-Knock, P.J. Shaw, G. Breen, R.J.B. Dobson, C.L. Dalgard, S.W. Scholz, A. Al-Chalabi, L.H. van den Berg, R. Mclaughlin, O. Hardiman, C. Cereda, G. Sorarù, S. D'Alfonso, S. Chandran, S. Pal, A. Ratti, C. Gellera, K. Johnson, T. Doucet-O'Hare, N. Pasternack, T. Wang, A. Nath, G. Siciliano, V. Silani, A.N. Başak, J.H. Veldink, W. Camu, J.D. Glass, J.E. Landers, A. Chiò, R. Sattler, C.E. Shaw, L. Ferraiuolo, I. Fogh, B.J. Traynor
Unleashing the potential of mRNA therapeutics for inherited neurological diseases
2024 E. Monfrini, G. Baso, D. Ronchi, M. Meneri, D. Gagliardi, L. Quetti, F. Verde, N. Ticozzi, A. Ratti, A. Di Fonzo, G.P. Comi, L. Ottoboni, S. Corti
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disorders
2024 M. Cozzi, S. Magri, B. Tedesco, G. Patelli, V. Ferrari, E. Casarotto, M. Chierichetti, P. Pramaggiore, L. Cornaggia, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, J. Mandrioli, D. Pareyson, C. Pisciotta, S. D'Arrigo, A. Ratti, L. Nanetti, C. Mariotti, E. Sarto, V. Pensato, C. Gellera, D. Di Bella, R.M. Cristofani, F. Taroni, A. Poletti
Association of APOE genotype and cerebrospinal fluid Aβ and tau biomarkers with cognitive and motor phenotype in amyotrophic lateral sclerosis
2024 A. Maranzano, F. Verde, A. Dubini, S. Torre, E. Colombo, A. Doretti, F. Gentile, A. Manini, I. Milone, A. Brusati, S. Peverelli, S. Santangelo, E.G. Spinelli, E. Torresani, D. Gentilini, S. Messina, C. Morelli, B. Poletti, F. Agosta, A. Ratti, M. Filippi, V. Silani, N. Ticozzi
One gene, many phenotypes: altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative and neurodevelopmental disorders
2024 M. Cozzi, S. Magri, B. Tedesco, G. Patelli, V. Ferrari, E. Casarotto, M. Chierichetti, P. Pramaggiore, L. Cornaggia, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, J. Mandrioli, D. Pareyson, C. Pisciotta, S. D'Arrigo, A. Ratti, L. Nanetti, C. Mariotti, E. Sarto, V. Pensato, C. Gellera, D. Di Bella, R. Cristofani, F. Taroni, A. Poletti
Quantification of serum TDP-43 and neurofilament light chain in patients with amyotrophic lateral sclerosis stratified by UNC13A genotype
2024 V. Casiraghi, I. Milone, A. Brusati, S. Peverelli, A. Doretti, B. Poletti, L. Maderna, C. Morelli, N. Ticozzi, V. Silani, F. Verde, A. Ratti
Shaping the Neurovascular Unit Exploiting Human Brain Organoids
2024 M. Rizzuti, V. Melzi, L. Brambilla, L. Quetti, L. Sali, L. Ottoboni, M. Meneri, A. Ratti, F. Verde, N. Ticozzi, G.P. Comi, S. Corti, E. Abati
PTBP1 mediates Sertoli cell actin cytoskeleton organization by regulating alternative splicing of actin regulators
2024 Y. Wang, U. Chembazhi, D. Yee, S. Chen, J. J, Y. Wang, K. Nguyen, P. Lin, A. Ratti, R. Hess, H. Qiao, C. Ko, J. Yang, A. Kalsotra, W. Mei
Distribution of the C9orf72 hexanucleotide repeat expansion in healthy subjects: a multicenter study promoted by the Italian IRCCS network of neuroscience and neurorehabilitation
2024 E. Giardina, P. Mandich, R. Ghidoni, N. Ticozzi, G. Rossi, C. Fenoglio, F.D. Tiziano, F. Esposito, S. Capellari, B. Nacmias, R. Mineri, R. Campopiano, L. Di Pilla, F. Sammarone, S. Zampatti, C. Peconi, F. De Angelis, I. Palmieri, C. Galandra, E. Nicodemo, P. Origone, F. Gotta, C. Ponti, R. Nicsanu, L. Benussi, S. Peverelli, A. Ratti, M. Ricci, G. Di Fede, S. Magri, M. Serpente, S. Lattante, T. Domi, P. Carrera, E. Saltimbanco, S. Bagnoli, A. Ingannato, A. Albanese, F. Tagliavini, R. Lodi, C. Caltagirone, S. Gambardella, E.M. Valente, V. Silani
Exploiting the role of CSF NfL, CHIT1, and miR-181b as potential diagnostic and prognostic biomarkers for ALS
2024 D. Gagliardi, M. Rizzuti, P. Masrori, D. Saccomanno, R. Del Bo, L. Sali, M. Meneri, S. Scarcella, I. Milone, N. Hersmus, A. Ratti, N. Ticozzi, V. Silani, K. Poesen, P. Van Damme, G.P. Comi, S. Corti, F. Verde
U1 snRNA as a novel RNA-based therapeutic approach to modulate C9ORF72 pathology in patient-derived iPSC-motoneurons
2023 S. Invernizzi, S. Santangelo, E. Bussani, G. Romano, C. Colombrita, V. Casiraghi, M. Nice Sorce, P. Bossolasco, V. Silani, F. Pagani, A. Ratti
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis
2023 A. Manini, V. Casiraghi, A. Brusati, A. Maranzano, F. Gentile, E. Colombo, R. Bonetti, S. Peverelli, S. Invernizzi, D. Gentilini, S. Messina, F. Verde, B. Poletti, I. Fogh, C. Morelli, V. Silani, A. Ratti, N. Ticozzi
Influence of kidney function and CSF/serum albumin ratio on plasma Aβ42 and Aβ40 levels measured on a fully automated platform in patients with Alzheimer’s disease
2023 F. Verde, I. Milone, A. Dubini, C. Colombrita, A. Perego, F. Solca, A. Maranzano, E. Ciusani, B. Poletti, A. Ratti, E. Torresani, V. Silani, N. Ticozzi
Exploring epigenetic drift and rare epivariations in amyotrophic lateral sclerosis by epigenome-wide association study
2023 A. Brusati, S. Peverelli, L. Calzari, C. Tiloca, V. Casiraghi, M.N. Sorce, S. Invernizzi, E. Carbone, R. Cavagnola, F. Verde, V. Silani, N. Ticozzi, A. Ratti, D. Gentilini
Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis
2023 F. Verde, I. Milone, E. Colombo, A. Maranzano, F. Solca, S. Torre, A. Doretti, F. Gentile, A. Manini, R. Bonetti, S. Peverelli, S. Messina, L. Maderna, C. Morelli, B. Poletti, A. Ratti, V. Silani, N. Ticozzi
Human motor neurons derived from induced pluripotent stem cells are susceptible to SARS-CoV-2 infection
2023 G. Cappelletti, C. Colombrita, F. Limanaqi, S. Invernizzi, M. Garziano, C. Vanetti, C. Moscheni, S. Santangelo, S. Zecchini, D. Trabattoni, V. Silani, M. Clerici, A. Ratti, M. Biasin
Molecular mechanisms in KIF5A-related neurodegeneration
2023 M. Cozzi, B. Tedesco, V. Ferrari, E. Casarotto, M. Chierichetti, P. Pramaggiore, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, C. Gellera, S. Magri, S. Santangelo, A. Ratti, R. Cristofani, F. Taroni, A. Poletti
Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene
2023 S. Santangelo, P. Bossolasco, S. Magri, C. Colombrita, S. Invernizzi, C. Gellera, L. Nanetti, D. Di Bella, V. Silani, F. Taroni, A. Ratti
Rapamycin reverts TDP-43 splicing defects and mislocalization in human in vitro models of TDP-43 proteinopathy
2023 V. Casiraghi, C. Colombrita, S. Santangelo, S. Invernizzi, M.N. Sorce, P. Bossolasco, V. Silani, A. Ratti