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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Publicat a:Front Mol Neurosci
Autors principals: Vogelgesang, Steffen, Niebert, Sabine, Renner, Ute, Möbius, Wiebke, Hülsmann, Swen, Manzke, Till, Niebert, Marcus
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2017
Matèries:
Neuroscience
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5340760/
https://ncbi.nlm.nih.gov/pubmed/28337123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2017.00061
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