Peripheral Fragile X messenger ribonucleoprotein is required for the timely closure of a critical period for neuronal susceptibility in the ventral cochlear nucleus

Alterations in neuronal plasticity and critical periods are common across neurodevelopmental diseases, including Fragile X syndrome (FXS), the leading single-gene cause of autism. Characterized with sensory dysfunction, FXS is the result of gene silencing of Fragile X messenger ribonucleoprotein 1 (...

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Detalles Bibliográficos
Autores principales: Yu, Xiaoyan, Wang, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248243/
https://www.ncbi.nlm.nih.gov/pubmed/37305436
http://dx.doi.org/10.3389/fncel.2023.1186630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248243/
https://www.ncbi.nlm.nih.gov/pubmed/37305436
http://dx.doi.org/10.3389/fncel.2023.1186630

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