Cargando…
Apparent Genetic Rescue of Adult Shank3 Exon 21 Insertion Mutation Mice Tempered by Appropriate Control Experiments
SHANK3 (ProSAP2) is among the most common genes mutated in autism spectrum disorders (ASD) and is the causative gene in Phelan–McDermid syndrome (PMS). We performed genetic rescue of Shank3 mutant phenotypes in adult mice expressing a Shank3 exon 21 insertion mutation (Shank3(G)). We used a tamoxife...
Autores principales: | Speed, Haley E., Kouser, Mehreen, Xuan, Zhong, Liu, Shunan, Duong, Anne, Powell, Craig M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774147/ https://www.ncbi.nlm.nih.gov/pubmed/31451607 http://dx.doi.org/10.1523/ENEURO.0317-19.2019 |
Ejemplares similares
-
Early Restoration of Shank3 Expression in Shank3 Knock-Out Mice Prevents Core ASD-Like Behavioral Phenotypes
por: Jaramillo, Thomas C., et al.
Publicado: (2020) -
Shank Proteins Differentially Regulate Synaptic Transmission
por: Shi, Rebecca, et al.
Publicado: (2017) -
Defective Synapse Maturation and Enhanced Synaptic Plasticity in Shank2 Δex7(–/–) Mice
por: Wegener, Stephanie, et al.
Publicado: (2018) -
Unexpected Compensatory Increase in Shank3 Transcripts in Shank3 Knock-Out Mice Having Partial Deletions of Exons
por: Jin, Chunmei, et al.
Publicado: (2019) -
Restoring Shank3 in the rostral brainstem of shank3ab−/− zebrafish autism models rescues sensory deficits
por: Kozol, Robert A., et al.
Publicado: (2021)