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Page 1
The DNA repair protein ATM as a target in autism spectrum disorder.
Pizzamiglio L, Focchi E, Cambria C, Ponzoni L, Ferrara S, Bifari F, Desiato G, Landsberger N, Murru L, Passafaro M, Sala M, Matteoli M, Menna E, Antonucci F. Pizzamiglio L, et al. Among authors: landsberger n. JCI Insight. 2021 Feb 8;6(3):e133654. doi: 10.1172/jci.insight.133654. JCI Insight. 2021. PMID: 33373327 Free PMC article.
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 Syndrome.
Gandaglia A, Brivio E, Carli S, Palmieri M, Bedogni F, Stefanelli G, Bergo A, Leva B, Cattaneo C, Pizzamiglio L, Cicerone M, Bianchi V, Kilstrup-Nielsen C, D'Annessa I, Di Marino D, D'Adamo P, Antonucci F, Frasca A, Landsberger N. Gandaglia A, et al. Among authors: landsberger n. Mol Neurobiol. 2019 Jul;56(7):4838-4854. doi: 10.1007/s12035-018-1412-2. Epub 2018 Nov 6. Mol Neurobiol. 2019. PMID: 30402709 Free article.
The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes.
Scaramuzza L, De Rocco G, Desiato G, Cobolli Gigli C, Chiacchiaretta M, Mirabella F, Pozzi D, De Simone M, Conforti P, Pagani M, Benfenati F, Cesca F, Bedogni F, Landsberger N. Scaramuzza L, et al. Among authors: landsberger n. EMBO Mol Med. 2021 Apr 9;13(4):e12433. doi: 10.15252/emmm.202012433. Epub 2021 Mar 5. EMBO Mol Med. 2021. PMID: 33665914 Free PMC article.
Unraveling autophagic imbalances and therapeutic insights in Mecp2-deficient models.
Esposito A, Seri T, Breccia M, Indrigo M, De Rocco G, Nuzzolillo F, Denti V, Pappacena F, Tartaglione G, Serrao S, Paglia G, Murru L, de Pretis S, Cioni JM, Landsberger N, Guarnieri FC, Palmieri M. Esposito A, et al. Among authors: landsberger n. EMBO Mol Med. 2024 Nov;16(11):2795-2826. doi: 10.1038/s44321-024-00151-w. Epub 2024 Oct 14. EMBO Mol Med. 2024. PMID: 39402139 Free PMC article.
75 results