Cargando…
The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellum
The Moonwalker (Mwk) mouse is a model of dominantly inherited cerebellar ataxia caused by a gain-of-function mutation in the transient receptor potential (TRP) channel TRPC3. Here, we report impairments in dendritic growth and synapse formation early on during Purkinje cell development in the Mwk ce...
Autores principales: | Dulneva, Anna, Lee, Sheena, Oliver, Peter L., Di Gleria, Katalin, Kessler, Benedikt M., Davies, Kay E., Becker, Esther B. E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4476454/ https://www.ncbi.nlm.nih.gov/pubmed/25908616 http://dx.doi.org/10.1093/hmg/ddv150 |
Ejemplares similares
-
The Moonwalker Mouse: New Insights into TRPC3 Function, Cerebellar Development, and Ataxia
por: Becker, Esther B. E.
Publicado: (2014) -
Modeling Suggests TRPC3 Hydrogen Bonding and Not Phosphorylation
Contributes to the Ataxia Phenotype of the Moonwalker Mouse
por: Hanson, Sonya M., et al.
Publicado: (2015) -
Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia
por: Becker, Esther B. E., et al.
Publicado: (2011) -
Moonwalk with Your Eyes: A Pocket Field Guide
por: Plotner, Tammy
Publicado: (2010) -
TRPC channel lipid specificity and mechanisms of lipid regulation
por: Beech, David J., et al.
Publicado: (2009)