Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality-Reference-Cited by-同舟云学术

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Neurodevelopmental defects in Dravet syndrome Scn1a+/− mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortality

Published:2025-04 Issue: Volume:207 Page:106853
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Pizzamiglio Lara,Capitano Fabrizio,Rusina Evgeniia,Fossati Giuliana,Menna Elisabetta,Léna Isabelle,Antonucci Flavia,Mantegazza Massimo

Funder

Ministero dell'Università e della Ricerca

French National Research Agency

Publisher

Elsevier BV

Reference98 articles.

1. SCN1B-linked early infantile developmental and epileptic encephalopathy;Aeby;Ann. Clin. Transl. Neurol.,2019

2. Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome;Almog;Neurobiol. Dis.,2021

3. KCC2 regulates dendritic spine formation in a brain-region specific and BDNF dependent manner;Awad;Cereb. Cortex,2018

4. Enhanced phosphorylation of p53 by ATM in response to DNA damage;Banin;Science,1998

5. Optimising Golgi-cox staining for use with perfusion-fixed brain tissue validated in the zQ175 mouse model of Huntington’s disease;Bayram-Weston;J. Neurosci. Methods,2016

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Emerging Insights into the Pathogenic Mechanisms of Dravet Syndrome;Neurochemical Research;2025-06-26

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