Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome

Mutations in the X-linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder. MECP2 is a transcriptional modulator that finely regulates the expression of many genes, specifically in the central nervous system. Several studies have functionally linked the loss of MECP...

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Detalles Bibliográficos
Autores principales: Ehinger, Yann, Matagne, Valerie, Cunin, Valérie, Borloz, Emilie, Seve, Michel, Bourgoin-Voillard, Sandrine, Borges-Correia, Ana, Villard, Laurent, Roux, Jean-Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122273/
https://www.ncbi.nlm.nih.gov/pubmed/33919253
http://dx.doi.org/10.3390/ijms22094316

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122273/
https://www.ncbi.nlm.nih.gov/pubmed/33919253
http://dx.doi.org/10.3390/ijms22094316

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