Cargando…
Seizure reduction in TSC2‐mutant mouse model by an mTOR catalytic inhibitor
OBJECTIVE: Tuberous sclerosis complex (TSC) is a neurodevelopmental disorder caused by autosomal‐dominant pathogenic variants in either the TSC1 or TSC2 gene, and it is characterized by hamartomas in multiple organs, such as skin, kidney, lung, and brain. These changes can result in epilepsy, learni...
Autores principales: | Dhamne, Sameer C., Modi, Meera E., Gray, Audrey, Bonazzi, Simone, Craig, Lucas, Bainbridge, Elizabeth, Lalani, Lahin, Super, Chloe E., Schaeffer, Samantha, Capre, Ketthsy, Lubicka, Danuta, Liang, Guiqing, Burdette, Doug, McTighe, Stephanie M., Gurnani, Sarika, Vermudez, Sheryl Anne D., Curtis, Daniel, Wilson, Christopher J., Hameed, Mustafa Q., D'Amore, Angelica, Rotenberg, Alexander, Sahin, Mustafa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578885/ https://www.ncbi.nlm.nih.gov/pubmed/37545094 http://dx.doi.org/10.1002/acn3.51868 |
Ejemplares similares
-
Factors influencing the acute pentylenetetrazole‐induced seizure paradigm and a literature review
por: Yuskaitis, Christopher J., et al.
Publicado: (2021) -
Depressed glutamate transporter 1 expression in a mouse model of Dravet syndrome
por: Hameed, Mustafa Q., et al.
Publicado: (2023) -
Replicable in vivo physiological and behavioral phenotypes of the Shank3B null mutant mouse model of autism
por: Dhamne, Sameer C., et al.
Publicado: (2017) -
Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing
por: Tyburczy, Magdalena E., et al.
Publicado: (2015) -
Intramuscular Lipoma: A Review of the Literature
por: McTighe, Shane, et al.
Publicado: (2014)