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1 week ago |
biorxiv.org | Michael G Ricos |Bethan Cole |Rashid Hussain |Grigori Rychkov
AbstractObjective: Hyperactive KCNT1 potassium channels, caused by gain-of-function mutations, are associated with a range of epilepsy disorders. Patients typically experience drug-resistant seizures and in cases with infantile onset, developmental regression can follow. KCNT1-related disorders include epilepsy of infancy with migrating focal seizures and sleep related hypermotor epilepsy.
A molecular switch in RCK2 triggers sodium-dependent activation of KNa1.1 (KCNT1) potassium channels
Apr 10, 2024 |
cell.com | Bethan Cole |Antreas C. Kalli |Nadia Pilati |Autifony Srl
Results17Zhang Z. Rosenhouse-Dantsker A. Logothetis D.E. et al. The RCK2 domain uses a coordination site present in Kir channels to confer sodium sensitivity to Slo2.2 channels. J. Neurosci.
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