Upregulation of the pathogenic transcription factor SPI1/PU.1 in tuberous sclerosis complex and focal cortical dysplasia by oxidative stress

Tuberous sclerosis complex (TSC) is a congenital disorder characterized by cortical malformations and concomitant epilepsy caused by loss‐of‐function mutations in the mTOR suppressors TSC1 or TSC2. While the underlying molecular changes caused by mTOR activation in TSC have previously been investiga...

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Detalles Bibliográficos
Autores principales: Zimmer, Till S., Korotkov, Anatoly, Zwakenberg, Susan, Jansen, Floor E., Zwartkruis, Fried J. T., Rensing, Nicholas R., Wong, Michael, Mühlebner, Angelika, van Vliet, Erwin A., Aronica, Eleonora, Mills, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412124/
https://www.ncbi.nlm.nih.gov/pubmed/33786950
http://dx.doi.org/10.1111/bpa.12949

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8412124/
https://www.ncbi.nlm.nih.gov/pubmed/33786950
http://dx.doi.org/10.1111/bpa.12949

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