The effect of single-cell knockout of Fragile X Messenger Ribonucleoprotein on synaptic structural plasticity

Fragile X Syndrome (FXS) is the best-known form of inherited intellectual disability caused by the loss-of-function mutation in a single gene. The FMR1 gene mutation abolishes the expression of Fragile X Messenger Ribonucleoprotein (FMRP), which regulates the expression of many synaptic proteins. Co...

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Detalles Bibliográficos
Autores principales: Gredell, Marie, Lu, Ju, Zuo, Yi
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/PMC10076639/
https://www.ncbi.nlm.nih.gov/pubmed/37035256
http://dx.doi.org/10.3389/fnsyn.2023.1135479

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10076639/
https://www.ncbi.nlm.nih.gov/pubmed/37035256
http://dx.doi.org/10.3389/fnsyn.2023.1135479

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