Effects of valproate on seizure-like activity in Drosophila melanogaster with a knockdown of Ube3a in different neuronal populations as a model of Angelman Syndrome

Angelman Syndrome is a rare, genetically induced neurodevelopmental disorder. This disorder stems from a mutation or deletion of the maternal UBE3A gene. Characteristics of this disease include developmental delay, recurring seizures, and severe intellectual disabilities. We studied seizure activity...

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Detalles Bibliográficos
Autores principales: Moore, Madeline C., Taylor, Danielle T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570944/
https://www.ncbi.nlm.nih.gov/pubmed/37842098
http://dx.doi.org/10.1016/j.ebr.2023.100622

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570944/
https://www.ncbi.nlm.nih.gov/pubmed/37842098
http://dx.doi.org/10.1016/j.ebr.2023.100622

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