INVERNIZZI, SABRINA
INVERNIZZI, SABRINA
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
Unraveling the role of primary cilia in the pathogenesis of amyotrophic lateral sclerosis
2025 S. Invernizzi, V. Casarotto, V. Casiraghi, S. Santangelo, E. Pellegrini, P. Bossolasco, A. Ratti
Induced Pluripotent Stem Cell (iPSC)-derived Microglia for ALS modeling
2025 E. Pellegrini, C. Lattuada, S. Invernizzi, V. Casiraghi, S. Santangelo, V. Silani, A. Ratti, P. Bossolasco
Characterization of human healthy i3 lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotype
2025 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, F. Verde, N. Ticozzi, V. Silani, A. Ratti
Characterization of human healthy i3 lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotype
2025 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, F. Verde, N. Ticozzi, V. Silani, A. Ratti
Induced Pluripotent Stem Cell (iPSC)-derived Microglia and Organoids for neuronal disease modeling
2025 E. Pellegrini, C. Lattuada, S. Invernizzi, V. Casiraghi, S. Santangelo, V. Silani, A. Ratti, P. Bossolasco
Unraveling the role of NEK1 on primary cilia using mutant iPSC models
2025 S. Invernizzi, V. Casiraghi, V. Casarotto, S. Santangelo, E. Pellegrini, J. Landers, V. Silani, P. Bossolasco, A. Ratti
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Defective primary cilia in NEK1 and C9ORF72 iPSC-derived motoneurons and brain organoids
2024 S. Invernizzi, S. Santangelo, V. Casiraghi, S. Peverelli, P. Paola, Q. Angelo, V. Silani, P. Bossolasco, A. Ratti
Modeling a novel N-terminal mutation of KIF5A gene in patient-derived iPSC-motoneurons
2024 S. Invernizzi, S. Santangelo, V. Casiraghi, P. Bossolasco, C. Fallini, S. Magri, A. Poletti, V. Silani, F. Taroni, A. Ratti
Induced Pluripotent Stem Cell (iPSC)-derived Microglia for ALS modeling
2024 E. Pellegrini, C. Lattuada, S. Invernizzi, V. Casiraghi, S. Santangelo, V. Silani, A. Ratti, P. Bossolasco
Induced Pluripotent Stem Cell (iPSC)-derived Microglia for ALS modeling
2024 E. Pellegrini, C. Lattuada, S. Invernizzi, V. Casiraghi, S. Santangelo, V. Silani, A. Ratti, P. Bossolasco
Characterization of human i3 motor neurons exposed to CSF from ALS patients stratified by C9ORF72 and UNC13A genotype
2024 V. Casiraghi, E. Pellegrini, A. Brusati, S. Peverelli, S. Invernizzi, S. Santangelo, C. Colombrita, V. Silani, A. Ratti
Defective primary cilia in NEK1 and C9ORF72 iPSC-derived motoneurons and brain organoids
2024 S. Invernizzi, S. Santangelo, V. Casiraghi, S. Peverelli, P. Paola, Q. Angelo, V. Silani, P. Bossolasco, A. Ratti
NEK1 haploinsufficiency worsens DNA damage, but not defective ciliogenesis, in C9ORF72 patient-derived iPSC-motoneurons
2024 S. Santangelo, S. Invernizzi, M.N. Sorce, V. Casiraghi, S. Peverelli, A. Brusati, C. Colombrita, N. Ticozzi, V. Silani, P. Bossolasco, A. Ratti
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
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
NEK1 loss-of-function mutation impairs ciliogenesis in iPSC-motoneurons
2023 M. Nice Sorce, S. Invernizzi, C. Lattuada, S. Santangelo, V. Casiraghi, A. Brusati, A. Silva, S. Peverelli, V. Silani, P. Bossolasco, A. Ratti