Subject Areas on Research
- A Gain-of-Function Mutation in KCNMA1 Causes Dystonia Spells Controlled With Stimulant Therapy.
- Autism and developmental disability caused by KCNQ3 gain-of-function variants.
- Expression of transgenes enriched in rare codons is enhanced by the MAPK pathway.
- Mechanism of β2AR regulation by an intracellular positive allosteric modulator.
- PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism.