Associated Papers
A common structural component for β-subunit mediated modulation of slow inactivation in different KV channels.
Strutz-Seebohm N et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology, 2013
The molecular basis of high-affinity binding of the antiarrhythmic compound vernakalant (RSD1235) to Kv1.5 channels.
Eldstrom J et al.
Molecular Pharmacology, 2007
Block by internal Mg2+ causes voltage-dependent inactivation of Kv1.5.
Claydon TW et al.
European Biophysics Journal : Ebj, 2006
A single residue in the S6 transmembrane domain governs the differential flecainide sensitivity of voltage-gated potassium channels.
Herrera D et al.
Molecular Pharmacology, 2005
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