Analysis of the Serotonergic System in a Mouse Model of Rett Syndrome Reveals Unusual Upregulation of Serotonin Receptor 5b

Mutations in the transcription factor methyl-CpG-binding-protein 2 (MeCP2) cause a delayed-onset neurodevelopmental disorder known as Rett syndrome (RTT). Although alteration in serotonin levels have been reported in RTT patients, the molecular mechanisms underlying these defects are not well unders...

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Detalles Bibliográficos
Autores principales: Vogelgesang, Steffen, Niebert, Sabine, Renner, Ute, Möbius, Wiebke, Hülsmann, Swen, Manzke, Till, Niebert, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340760/
https://www.ncbi.nlm.nih.gov/pubmed/28337123
http://dx.doi.org/10.3389/fnmol.2017.00061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340760/
https://www.ncbi.nlm.nih.gov/pubmed/28337123
http://dx.doi.org/10.3389/fnmol.2017.00061

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