Cargando…
Infant and adult SCA13 mutations differentially affect Purkinje cell excitability, maturation, and viability in vivo
Mutations in KCNC3, which encodes the Kv3.3 K(+) channel, cause spinocerebellar ataxia 13 (SCA13). SCA13 exists in distinct forms with onset in infancy or adulthood. Using zebrafish, we tested the hypothesis that infant- and adult-onset mutations differentially affect the excitability and viability...
Autores principales: | Hsieh, Jui-Yi, Ulrich, Brittany N, Issa, Fadi A, Lin, Meng-chin A, Brown, Brandon, Papazian, Diane M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386905/ https://www.ncbi.nlm.nih.gov/pubmed/32644043 http://dx.doi.org/10.7554/eLife.57358 |
Ejemplares similares
-
Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish
por: Hsieh, Jui-Yi, et al.
Publicado: (2014) -
Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)
por: Figueroa, Karla P., et al.
Publicado: (2011) -
Early molecular layer interneuron hyperactivity triggers Purkinje neuron degeneration in SCA1
por: Pilotto, Federica, et al.
Publicado: (2023) -
Anti-Excitotoxic Effects of N-Butylidenephthalide Revealed by Chemically Insulted Purkinje Progenitor Cells Derived from SCA3 iPSCs
por: Yang, Hsin-Han, et al.
Publicado: (2022) -
Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development
por: Issa, Fadi A., et al.
Publicado: (2012)