Article
Cytoplasmic inter-subunit interface modulates TRPC5 activity: Molecular mechanism behind intellectual disability-related R175C mutation.
Neurobiology of disease - 15 Oct 2025
Mitro Michal, Ptáková Alexandra, Vlachová Viktorie, Zímová Lucie
Abstract excerpt
The TRPC5 (Transient Receptor Potential Canonical 5) receptor, which is highly expressed in the brain, kidney, and sensory neurons, is emerging as a pharmacological target due to its involvement in renal physiology, pain, metabolic homeostasis, and various neurodevelopmental disorders. The recently identified R175C mutation associated with intellectual disability and autism spectrum disorders has supported the...
Topics
- TRPC Cation Channels
- Intellectual Disability
- Humans
- Mutation
- HEK293 Cells
- Cytoplasm
- Animals
