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Overlapping binding sites of structurally different antiarrhythmics flecainide and propafenone in the subunit interface of potassium channel Kv2.1. , Madeja M., J Biol Chem. October 29, 2010; 285 (44): 33898-905.
Endogenous KCNE subunits govern Kv2.1 K+ channel activation kinetics in Xenopus oocyte studies. , Gordon E., Biophys J. February 15, 2006; 90 (4): 1223-31.
Modification of Kv2.1 K+ currents by the silent Kv10 subunits. , Vega-Saenz de Miera EC., Brain Res Mol Brain Res. April 7, 2004; 123 (1-2): 91-103.
Heteromeric assembly of Kv2.1 with Kv9.3: effect on the state dependence of inactivation. , Kerschensteiner D., Biophys J. July 1, 1999; 77 (1): 248-57.
Stable expression and characterization of the human brain potassium channel Kv2.1: blockade by antipsychotic agents. , Wible B., Dev Biol. June 27, 1997; 761 (1): 42-50.
Xenopus spinal neurons express Kv2 potassium channel transcripts during embryonic development. , Burger C., J Neurosci. February 15, 1996; 16 (4): 1412-21.
Susceptibility of cloned K+ channels to reactive oxygen species. , Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.