Search Results - "Albizzati, Elena"
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A comprehensive longitudinal study of magnetic resonance imaging identifies novel features of the Mecp2 deficient mouse brain
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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Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals
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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MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
Published in EMBO molecular medicine (08-06-2020)“…Mutations in MECP2 cause several neurological disorders of which Rett syndrome (RTT) represents the best‐defined condition. Although mainly working as a…”
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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
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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Mecp2 knock-out astrocytes affect synaptogenesis by interleukin 6 dependent mechanisms
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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