FoxP1 orchestration of ASD-relevant signaling pathways in the striatum

Mutations in the transcription factor Forkhead box p1 (FOXP1) are causative for neurodevelopmental disorders such as autism. However, the function of FOXP1 within the brain remains largely uncharacterized. Here, we identify the gene expression program regulated by FoxP1 in both human neural cells an...

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Detalles Bibliográficos
Autores principales: Araujo, Daniel J., Anderson, Ashley G., Berto, Stefano, Runnels, Wesley, Harper, Matthew, Ammanuel, Simon, Rieger, Michael A., Huang, Hung-Chung, Rajkovich, Kacey, Loerwald, Kristofer W., Dekker, Joseph D., Tucker, Haley O., Dougherty, Joseph D., Gibson, Jay R., Konopka, Genevieve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617974/
https://www.ncbi.nlm.nih.gov/pubmed/26494785
http://dx.doi.org/10.1101/gad.267989.115

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