Frasca, Angelisa

Toll-like receptor 4-dependent glial cell activation mediates the impairment in memory establishment induced by β-amyloid oligomers in an acute mouse model of Alzheimer’s disease

Balducci, C., Frasca, A., Zotti, M., La Vitola, P., Mhillaj, E., Grigoli, E., Iacobellis, M., Grandi, F., Messa, M., Colombo, L., et al. (2017) · Brain, Behavior, and Immunity

Alzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration Mechanisms

Cited by 164

AMPA receptor subunit 1 (GluR‐A) knockout mice model the glutamate hypothesis of depression

Chourbaji, S., Vogt, M. A., Fumagalli, F., Sohr, R., Frasca, A., Brandwein, C., Hörtnagl, H., Riva, M. A., Sprengel, R., & Gass, P. (2008) · The FASEB Journal

Treatment of Major DepressionNeuroscience and Neuropharmacology Research

Cited by 144

MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders

Frasca, A., Spiombi, E., Palmieri, M., Albizzati, E., Valente, M. M., Bergo, A., Leva, B., Kilstrup‐Nielsen, C., Bianchi, F., Di Carlo, V., et al. (2020) · EMBO Molecular Medicine

Genetics and Neurodevelopmental DisordersGenetic and Kidney Cyst Diseases

Cited by 46

Mecp2 knock-out astrocytes affect synaptogenesis by interleukin 6 dependent mechanisms

Albizzati, E., Breccia, M., Florio, E., Cabasino, C., Postogna, F. M., Grassi, R., Boda, E., Battaglia, C., De Palma, C., De Quattro, C., et al. (2024) · iScience

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 25

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

D'Annessa, I., Gandaglia, A., Brivio, E., Stefanelli, G., Frasca, A., Landsberger, N., & Di Marino, D. (2018) · Biochimica et Biophysica Acta (BBA) - General Subjects

Genetics and Neurodevelopmental DisordersProtein Structure and Dynamics

Cited by 18

Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals

Albizzati, E., Florio, E., Miramondi, F., Sormonta, I., Landsberger, N., & Frasca, A. (2022) · Frontiers in Neuroscience

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 12

Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway

Frasca, A., Miramondi, F., Butti, E., Indrigo, M., Balbontin Arenas, M., Postogna, F. M., Piffer, A., Bedogni, F., Pizzamiglio, L., Cambria, C., et al. (2024) · EMBO Molecular Medicine

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 9

Impaired astrocyte-to-neuron cholesterol trafficking drives synaptic dysfunction in Rett syndrome

Postogna, F. M., Giancroce, N., Cabasino, C., Biella, F., Roggero, O. M., Breccia, M., Morelli, L., Colombo, D., Arcari, A., Lunghi, G., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory)

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 1