Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo

How the loss of fragile X mental retardation protein (FMRP) in different brain cell types, especially in non-neuron glial cells, induces fragile X syndrome (FXS) phenotypes has just begun to be understood. In the current study, we generated inducible astrocyte-specific Fmr1 conditional knock-out mic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:J Neurosci
Hauptverfasser: Higashimori, Haruki, Schin, Christina S., Chiang, Ming Sum R., Morel, Lydie, Shoneye, Temitope A., Nelson, David L., Yang, Yongjie
Format: Artigo
Sprache:Inglês
Veröffentlicht: Society for Neuroscience 2016
Schlagworte:
Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4938857/
https://ncbi.nlm.nih.gov/pubmed/27383586
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1069-16.2016
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge