Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2

The RSK2 protein is a member of the RSK serine-threonine protein kinase family and is encoded by the X-linked rps6ka3 gene in human. Highly heterogeneous loss-of-function mutations affecting this gene are responsible for a severe syndromic form of cognitive impairment, Coffin-Lowry syndrome. RSK2, w...

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Detalles Bibliográficos
Autores principales: Mehmood, Tahir, Schneider, Anne, Pannetier, Solange, Hanauer, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588048/
https://www.ncbi.nlm.nih.gov/pubmed/23389038
http://dx.doi.org/10.3390/ijms14023358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588048/
https://www.ncbi.nlm.nih.gov/pubmed/23389038
http://dx.doi.org/10.3390/ijms14023358

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