LANDSBERGER, NICOLETTA
LANDSBERGER, NICOLETTA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
Mecp2 knock-out astrocytes affect synaptogenesis by Interleukin 6 dependent mechanisms
2024 E. Albizzati, M. Breccia, E.M. Florio, C. Cabasino, F.M. Postogna, R. Grassi, E. Boda, C. Battaglia, C. DE PALMA, C. De Quattro, D. Pozzi, N. Landsberger, A. Frasca
Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway
2024 A. Frasca, F. Miramondi, E. Butti, M. Indrigo, M. BALBONTIN ARENAS, F.M. Postogna, A. Piffer, F. Bedogni, L. Pizzamiglio, C. Cambria, U. Borello, F. Antonucci, G. Martino, N. Landsberger
Unravelling the role of Hpcal4 as a potential modifier gene for Rett Syndrome
2024 J. Sandakly, S. Pezzini, L. Scandella, A. Arcari, E. Fraviga, D. Pozzi, M. Francolini, N. Landsberger
Advanced genetic therapies for the treatment of Rett syndrome: state of the art and future perspectives
2023 M. Palmieri, D. Pozzer, N. Landsberger
A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain
2023 S. Carli, L. Chaabane, G. De Rocco, E. Albizzati, I. Sormonta, S. Calligaro, P. Bonizzi, A. Frasca, N. Landsberger
Synaptic localization of HPCAL4 in neurons : looking for a role of this Ca2+ sensor in the modulation of neuronal function in health and disease
2023 L. Scandella, J. Sandakly, S. Pezzini, A. Arcari, E. Fraviga, D. Pozzi, N. Landsberger, M. Francolini
The interplay Between Hpcal4 And Mecp2 : Identification And Characterization Of A Novel Putative Target for Rett Syndrome Therapy
2023 S. Pezzini, A. Arcari, J. Sandakly, L. Scandella, M. Francolini, E. Fraviga, D. Pozzi, N. Landsberger
The detrimental effect of Mecp2 null astrocytes on synapses: exploring the molecular mechanisms to find novel druggable targets for Rett syndrome
2023 E. Albizzati, E.M. Florio, M. Breccia, C. Cabasino, D. Pozzi, E. Boda, C. Battaglia, C. DE PALMA, Concetta De Quattro, N. Landsberger, A. Frasca
Neural precursor/stem cell-based therapy for Rett syndrome
2023 A. Frasca, F. Miramondi, M. Balbontin, M. Indrigo, E. Butti, U. Borello, F. Bedogni, G. Martino, N. Landsberger
Neural Precursor Cells as a potential therapeutic approach for Rett Syndrome: identification of the involved molecular mechanisms
2023 M. BALBONTIN ARENAS, F. Miramondi, E. Butti, G. Martino, A. Frasca, N. Landsberger
Complex CDKL5 translational regulation and its potential role in CDKL5 deficiency disorder
2023 V. Ruggiero, C. Fagioli, S. de Pretis, V. Di Carlo, N. Landsberger, D. Zacchetti
MeCP2 deficiency in astrocytes alters synaptogenesis: new insights on Rett syndrome
2023 M. Breccia, E. Albizzati, E. Florio, C. Cabasino, D. Pozzi, E. Boda, C. Battaglia, C. De Palma, C. De Quattro, N. Landsberger, A. Frasca
Not Just Loss-of-Function Variations: Identification of a Hypermorphic Variant in a Patient With a CDKL5 Missense Substitution
2022 A. Frasca, E. Pavlidou, M. Bizzotto, Y. Gao, D. Balestra, M. Pinotti, H.A. Dahl, N.D. Mazarakis, N. Landsberger, M. Kinali
MeCP2 deficiency in astrocytes alters synaptogenesis: new insights on Rett syndrome
2022 E. Albizzati, E.M. Florio, M. Breccia, C. Cabasino, D. Pozzi, C. DE PALMA, N. Landsberger, A. Frasca
Neural precursor/stem cell-based therapy for Rett syndrome
2022 A. Frasca, F. Miramondi, E. Butti, M. Indrigo, G. DE ROCCO, F. Bedogni, G. Martino, N. Landsberger
Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals
2022 E. Albizzati, E. Florio, F. Miramondi, I. Sormonta, N. Landsberger, A. Frasca
Pharmacological modulation of neuronal activity for the treatment of Rett syndrome
2022 G. De Rocco, L. Scaramuzza, M. Indrigo, N. Landsberger
The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes
2021 L. Scaramuzza, G. De Rocco, G. Desiato, C. Cobolli Gigli, M. Chiacchiaretta, F. Mirabella, D. Pozzi, M. De Simone, P. Conforti, M. Pagani, F. Benfenati, F. Cesca, F. Bedogni, N. Landsberger
In vivo magnetic resonance spectroscopy in the brain of Cdkl5 null mice reveals a metabolic profile indicative of mitochondrial dysfunctions
2021 S. Carli, L. Chaabane, C. Butti, C. De Palma, P. Aimar, C. Salio, A. Vignoli, M. Giustetto, N. Landsberger, A. Frasca
The DNA repair protein ATM as target in autism spectrum disorder
2020 L. Pizzamiglio, E. Focchi, C. Cambria, L. Ponzoni, S. Ferrara, F. Bifari, G. Desiato, N. Landsberger, L. Murru, M. Passafaro, M. Sala, M. Matteoli, E. Menna, F. Antonucci