FRASCA, ANGELISA
FRASCA, ANGELISA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
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
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
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
PURPL and NEAT1 Long Non-Coding RNAs Are Modulated in Vascular Smooth Muscle Cell Replicative Senescence
2023 C. Rossi, M. Venturin, J. Gubala, A. Frasca, A. Corsini, C. Battaglia, S. Bellosta
New Views of the DNA Repair Protein Ataxia–Telangiectasia Mutated in Central Neurons: Contribution in Synaptic Dysfunctions of Neurodevelopmental and Neurodegenerative Diseases
2023 S. Briguglio, C. Cambria, E. Albizzati, E. Marcello, G. Provenzano, A. Frasca, F. Antonucci
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
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
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
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
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
MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
2020 A. Frasca, E. Spiombi, M. Palmieri, E. Albizzati, M. Valente, A.L.B. Bergo, C. Kilstrup-Nielsen, F. Bianchi, V. Di Carlo, F. Di Cunto, N. Landsberger
Fingolimod modulates dendritic architecture in a BDNF-dependent manner
2020 A. Patnaik, E. Spiombi, A. Frasca, N. Landsberger, M. Zagrebelsky, M. Korte
Ongoing Electroencephalographic Rhythms Related to Exploratory Movements in Transgenic TASTPM Mice
2020 C. Del Percio, W. Drinkenburg, S. Lopez, M.T. Pascarelli, R. Lizio, G. Noce, R. Ferri, J.F. Bastlund, B. Laursen, D.Z. Christensen, J.T. Pedersen, G. Forloni, A. Frasca, F.M. Noe, P.F. Fabene, G. Bertini, V. Colavito, M. Bentivoglio, J. Kelley, S. Dix, F. Infarinato, A. Soricelli, F. Stocchi, J.C. Richardson, C. Babiloni
Chronic BACE-1 Inhibitor Administration in TASTPM Mice (APP KM670/671NL and PSEN1 M146V Mutation): An EEG Study
2020 S. Lopez, C. Del Percio, G. Forloni, A. Frasca, W.H. Drinkenburg, R. Lizio, G. Noce, R. Ferri, A. Soricelli, F. Stocchi, L. Vacca, R. Bordet, J.C. Richardson, C. Babiloni
A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome
2019 A. Gandaglia, E. Brivio, S. Carli, M. Palmieri, F. Bedogni, G. Stefanelli, A. Bergo, B. Leva, C. Cattaneo, L. Pizzamiglio, M. Cicerone, V. Bianchi, C. Kilstrup-Nielsen, I. D'Annessa, D. Di Marino, P. D'Adamo, F. Antonucci, A. Frasca, N. Landsberger
Aminoglycoside drugs induce efficient read-through of CDKL5 nonsense mutations, slightly restoring its kinase activity
2019 M. Fazzari, A. Frasca, F. Bifari, N. Landsberger
Splicing mutations impairing CDKL5 expression and activity can be efficiently rescued by U1snRNA-based therapy
2019 D. Balestra, D. Giorgio, M. Bizzotto, M. Fazzari, B.B. Zeev, M. Pinotti, N. Landsberger, A. Frasca
Progress in the development of in vivo redox measurements: New tools for longitudinal studies in Rett syndrome
2019 A. Frasca, F. Bedogni, N. Landsberger
Tyr120Asp mutation alters domain flexibility and dynamics of MeCP2 DNA binding domain leading to impaired DNA interaction : Atomistic characterization of a Rett syndrome causing mutation
2018 I. D'Annessa, A. Gandaglia, E. Brivio, G. Stefanelli, A. Frasca, N. Landsberger, D. Di Marino
On-going electroencephalographic rhythms related to cortical arousal in wild-type mice : the effect of aging
2017 C. Del Percio, W. Drinkenburg, S. Lopez, F. Infarinato, J.F. Bastlund, B. Laursen, J.T. Pedersen, D.Z. Christensen, G. Forloni, A. Frasca, F.M. Noã¨, M. Bentivoglio, P.F. Fabene, G. Bertini, V. Colavito, J. Kelley, S. Dix, J.C. Richardson, C. Babiloni