Search Results - "Albizzati, Elena"

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  1. 1

    A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain by Carli, Sara, Chaabane, Linda, De Rocco, Giuseppina, Albizzati, Elena, Sormonta, Irene, Calligaro, Stefano, Bonizzi, Pietro, Frasca, Angelisa, Landsberger, Nicoletta

    Published in Neurobiology of disease (01-05-2023)
    “…Rett syndrome (RTT) is a X-linked neurodevelopmental disorder which represents the leading cause of severe incurable intellectual disability in females…”
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    Journal Article
  2. 2

    Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals by Albizzati, Elena, Florio, Elena, Miramondi, Federica, Sormonta, Irene, Landsberger, Nicoletta, Frasca, Angelisa

    Published in Frontiers in neuroscience (15-02-2022)
    “…Rett syndrome (RTT) is a neurodevelopmental disorder that represents the most common genetic cause of severe intellectual disability in females. Most patients…”
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    New Views of the DNA Repair Protein Ataxia–Telangiectasia Mutated in Central Neurons: Contribution in Synaptic Dysfunctions of Neurodevelopmental and Neurodegenerative Diseases by Briguglio, Sabrina, Cambria, Clara, Albizzati, Elena, Marcello, Elena, Provenzano, Giovanni, Frasca, Angelisa, Antonucci, Flavia

    Published in Cells (Basel, Switzerland) (30-08-2023)
    “…Ataxia–Telangiectasia Mutated (ATM) is a serine/threonine protein kinase principally known to orchestrate DNA repair processes upon DNA double-strand breaks…”
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    Journal Article
  5. 5

    Mecp2 knock-out astrocytes affect synaptogenesis by interleukin 6 dependent mechanisms by Albizzati, Elena, Breccia, Martina, Florio, Elena, Cabasino, Cecilia, Postogna, Francesca Maddalena, Grassi, Riccardo, Boda, Enrica, Battaglia, Cristina, De Palma, Clara, De Quattro, Concetta, Pozzi, Davide, Landsberger, Nicoletta, Frasca, Angelisa

    Published in iScience (15-03-2024)
    “…Synaptic abnormalities are a hallmark of several neurological diseases, and clarification of the underlying mechanisms represents a crucial step toward the…”
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    Journal Article