FOXG1 Regulates PRKAR2B Transcriptionally and Posttranscriptionally via miR200 in the Adult Hippocampus

Rett syndrome is a complex neurodevelopmental disorder that is mainly caused by mutations in MECP2. However, mutations in FOXG1 cause a less frequent form of atypical Rett syndrome, called FOXG1 syndrome. FOXG1 is a key transcription factor crucial for forebrain development, where it maintains the b...

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Detalles Bibliográficos
Autores principales: Weise, Stefan C., Arumugam, Ganeshkumar, Villarreal, Alejandro, Videm, Pavankumar, Heidrich, Stefanie, Nebel, Nils, Dumit, Verónica I., Sananbenesi, Farahnaz, Reimann, Viktoria, Craske, Madeline, Schilling, Oliver, Hess, Wolfgang R., Fischer, Andre, Backofen, Rolf, Vogel, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647430/
https://www.ncbi.nlm.nih.gov/pubmed/30539330
http://dx.doi.org/10.1007/s12035-018-1444-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647430/
https://www.ncbi.nlm.nih.gov/pubmed/30539330
http://dx.doi.org/10.1007/s12035-018-1444-7

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