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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...
Autores principales: | Chojnacka, Magdalena, Beroun, Anna, Magnowska, Marta, Stawikowska, Aleksandra, Cysewski, Dominik, Milek, Jacek, Dziembowska, Magdalena, Kuzniewska, Bozena |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
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 |
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