Syntaxin 1B Mediates Berberine’s Roles in Epilepsy-Like Behavior in a Pentylenetetrazole-Induced Seizure Zebrafish Model

Epilepsy is a neuronal dysfunction syndrome characterized by transient and diffusely abnormal discharges of neurons in the brain. Previous studies have shown that mutations in the syntaxin 1b (stx1b) gene cause a familial, fever-associated epilepsy syndrome. It is unclear as to whether the stx1b gen...

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Detalles Bibliográficos
Autores principales: Zheng, Yang-Min, Chen, Bo, Jiang, Jian-Dong, Zhang, Jing-Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275243/
https://www.ncbi.nlm.nih.gov/pubmed/30534049
http://dx.doi.org/10.3389/fnmol.2018.00378

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275243/
https://www.ncbi.nlm.nih.gov/pubmed/30534049
http://dx.doi.org/10.3389/fnmol.2018.00378

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