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Human Molecular Genetics|October 2, 2002
Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in micePatrizia D'Adamo, Hans Welzl, Stavros Papadimitriou, et al.
Molecular Neurobiology|November 8, 2018
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 SyndromeAnna Gandaglia, Elena Brivio, Sara Carli, et al.
Scientific Reports|October 8, 2016
Disruption of ArhGAP15 results in hyperactive Rac1, affects the architecture and function of hippocampal inhibitory neurons and causes cognitive deficitsValentina Zamboni, Maria Armentano, Gabriella Sarò, et al.
Brain : a Journal of Neurology|September 26, 2012
Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicityErica Butti, Marco Bacigaluppi, Silvia Rossi, et al.
Nature Communications|December 9, 2022
Neural precursor cells tune striatal connectivity through the release of IGFBPL1Erica Butti, Stefano Cattaneo, Marco Bacigaluppi, et al.
Science Immunology|November 23, 2021
Administration of aerosolized SARS-CoV-2 to K18-hACE2 mice uncouples respiratory infection from fatal neuroinvasionValeria Fumagalli, Micol Ravà, Davide Marotta, et al.
American Journal of Human Genetics|February 18, 2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephalyMaila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, et al.
Metabolism: Clinical and Experimental|December 14, 2020
Inhibiting glycolysis rescues memory impairment in an intellectual disability Gdi1-null mousePatrizia D'Adamo, Anemari Horvat, Antonia Gurgone, et al.
Scientific Reports|January 12, 2017
Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patientsAisha V Sauer, Raisa Jofra Hernandez, Francesca Fumagalli, et al.
Disease Models & Mechanisms|March 5, 2026
Development and characterization of a model of mucopolysaccharidosis type IVA for evaluating therapies targeting bone diseaseMargherita Berti, Selene Ceriotti, Ludovica Santi, et al.
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