Deconstructing Sox2 Function in Brain Development and Disease

SOX2 is a transcription factor conserved throughout vertebrate evolution, whose expression marks the central nervous system from the earliest developmental stages. In humans, SOX2 mutation leads to a spectrum of CNS defects, including vision and hippocampus impairments, intellectual disability, and...

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Detalles Bibliográficos
Autores principales: Mercurio, Sara, Serra, Linda, Pagin, Miriam, Nicolis, Silvia K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139651/
https://www.ncbi.nlm.nih.gov/pubmed/35626641
http://dx.doi.org/10.3390/cells11101604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9139651/
https://www.ncbi.nlm.nih.gov/pubmed/35626641
http://dx.doi.org/10.3390/cells11101604

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