Landsberger, Nicoletta

Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model

Ricciardi, S., Boggio, E. M., Grosso, S., Lonetti, G., Forlani, G., Stefanelli, G., Calcagno, E., Morello, N., Landsberger, N., Biffo, S., et al. (2011) · Human Molecular Genetics

Genetics and Neurodevelopmental DisordersPI3K/AKT/mTOR signaling in cancer

Cited by 223

Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms

Bedogni, F., Cobolli Gigli, C., Pozzi, D., Rossi, R. L., Scaramuzza, L., Rossetti, G., Pagani, M., Kilstrup-Nielsen, C., Matteoli, M., & Landsberger, N. (2016) · Cerebral Cortex

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 84

Rett syndrome and the urge of novel approaches to study MeCP2 functions and mechanisms of action

Bedogni, F., Rossi, R. L., Galli, F., Cobolli Gigli, C., Gandaglia, A., Kilstrup-Nielsen, C., & Landsberger, N. (2014) · Neuroscience & Biobehavioral Reviews

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 51

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 related studies benefit from the use of CD1 as genetic background

Cobolli Gigli, C., Scaramuzza, L., Gandaglia, A., Bellini, E., Gabaglio, M., Parolaro, D., Kilstrup-Nielsen, C., Landsberger, N., & Bedogni, F. (2016) · PLOS ONE

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 37

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