Impaired synaptic incorporation of AMPA receptors in a mouse model of fragile X syndrome

Fragile X syndrome (FXS) is the most common monogenetic cause of inherited intellectual disability and autism in humans. One of the well-characterized molecular phenotypes of Fmr1 KO mice, a model of FXS, is increased translation of synaptic proteins. Although this upregulation stabilizes in adultho...

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Detalles Bibliográficos
Autores principales: Chojnacka, Magdalena, Beroun, Anna, Magnowska, Marta, Stawikowska, Aleksandra, Cysewski, Dominik, Milek, Jacek, Dziembowska, Magdalena, Kuzniewska, Bozena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Molecular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665894/
https://www.ncbi.nlm.nih.gov/pubmed/38025260
http://dx.doi.org/10.3389/fnmol.2023.1258615

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665894/
https://www.ncbi.nlm.nih.gov/pubmed/38025260
http://dx.doi.org/10.3389/fnmol.2023.1258615

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