Transcription Factor 2I Regulates Neuronal Development via TRPC3 in 7q11.23 Disorder Models

Williams syndrome (WS) and 7q11.23 duplication syndrome (Dup7q11.23) are neurodevelopmental disorders caused by the deletion and duplication, respectively, of ~ 25 protein-coding genes on chromosome 7q11.23. The general transcription factor 2I (GTF2I, protein TFII-I) is one of these proteins and has...

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Detalles Bibliográficos
Autores principales: Deurloo, Marielle H. S., Turlova, Ekaterina, Chen, Wen-Liang, Lin, You Wei, Tam, Elaine, Tassew, Nardos G., Wu, Michael, Huang, Ya-Chi, Crawley, Jacqueline N., Monnier, Philippe P., Groffen, Alexander J. A., Sun, Hong-Shuo, Osborne, Lucy R., Feng, Zhong-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477017/
https://www.ncbi.nlm.nih.gov/pubmed/30120731
http://dx.doi.org/10.1007/s12035-018-1290-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477017/
https://www.ncbi.nlm.nih.gov/pubmed/30120731
http://dx.doi.org/10.1007/s12035-018-1290-7

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