A social encounter drives gene expression changes linked to neuronal function, brain development, and related disorders in mice expressing the serotonin transporter Ala56 variant.

Multiple lines of evidence implicate the serotonin (5-HT) system in social function, including biomarker findings in autism spectrum disorder. In mice, knock-in of a rare Gly56Ala substitution in the serotonin transporter (SERT) causes elevated whole blood 5-HT levels, increased 5-HT clearance in th...

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發表在:Neurosci Lett
Main Authors: O’Reilly, Kally C., Anacker, Allison M. J., Rogers, Tiffany D., Forsberg, C. Gunnar, Wang, Jing, Zhang, Bing, Blakely, Randy D., Veenstra-VanderWeele, Jeremy
格式: Artigo
語言:Inglês
出版: 2020
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7440397/
https://ncbi.nlm.nih.gov/pubmed/32437898
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2020.135027
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