Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals

Fragile X syndrome (FXS) is the most common form of monogenic intellectual disability and autism, caused by the absence of the functional fragile X messenger ribonucleoprotein 1 (FMRP). FXS features include increased and dysregulated protein synthesis, observed in both murine and human cells. Altere...

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Detalles Bibliográficos
Autores principales: Cencelli, Giulia, Pacini, Laura, De Luca, Anastasia, Messia, Ilenia, Gentile, Antonietta, Kang, Yunhee, Nobile, Veronica, Tabolacci, Elisabetta, Jin, Peng, Farace, Maria Giulia, Bagni, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000963/
https://www.ncbi.nlm.nih.gov/pubmed/36899894
http://dx.doi.org/10.3390/cells12050758

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000963/
https://www.ncbi.nlm.nih.gov/pubmed/36899894
http://dx.doi.org/10.3390/cells12050758

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