IndraLab

Statements

KCN binds KCNA1. 4 / 4
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"Browne D, Gancher S, Nutt J, Brunt E, Smith E, Kramer P, Litt M: Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1."
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"Next, we wanted to determine whether Kv1.1 protein could form functional potassium channels in the Fezf2-GFP-positive cells."
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"Voltage‐gated Kv1.1 potassium channel α‐subunits, which are associated with sudden unexpected death in epilepsy (SUDEP) in mice, have recently come to light as important regulators of cardiac repolarization and arrhythmia susceptibility in atria (Glasscock et al., xref ; Si et al., xref )."
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"Mutations in KCN1A, the gene encoding Kv1.1, a voltage-gated neuronal potassium channel, are associated with the disorder."
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