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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.
Localization of Kv2.2 protein in Xenopus laevis embryos and tadpoles. , Gravagna NG., J Comp Neurol. October 10, 2008; 510 (5): 508-24.
VAMP2 interacts directly with the N terminus of Kv2.1 to enhance channel inactivation. , Lvov A., Pflugers Arch. September 1, 2008; 456 (6): 1121-36.
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.
Stabilizing the closed S6 gate in the Shaker Kv channel through modification of a hydrophobic seal. , Kitaguchi T., J Gen Physiol. October 1, 2004; 124 (4): 319-32.
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.
Cyclic nucleotide-gated channels. Pore topology studied through the accessibility of reporter cysteines. , Becchetti A., J Gen Physiol. September 1, 1999; 114 (3): 377-92.
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.
A new K+ channel beta subunit to specifically enhance Kv2.2 (CDRK) expression. , Fink M., J Biol Chem. October 18, 1996; 271 (42): 26341-8.
Functional characterization of Kv channel beta-subunits from rat brain. , Heinemann SH., J Physiol. June 15, 1996; 493 ( Pt 3) 625-33.
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.
Modulation by protein kinase A of a cloned rat brain potassium channel expressed in Xenopus oocytes. , Wilson GG., Pflugers Arch. September 1, 1994; 428 (2): 186-93.
Internal Na+ and Mg2+ blockade of DRK1 ( Kv2.1) potassium channels expressed in Xenopus oocytes. Inward rectification of a delayed rectifier. , Lopatin AN., J Gen Physiol. February 1, 1994; 103 (2): 203-16.
2,3-Butanedione monoxime (BDM) inhibition of delayed rectifier DRK1 ( Kv2.1) potassium channels expressed in Xenopus oocytes. , Lopatin AN., J Pharmacol Exp Ther. May 1, 1993; 265 (2): 1011-6.
A novel potassium channel with delayed rectifier properties isolated from rat brain by expression cloning. , Frech GC., Nature. August 24, 1989; 340 (6235): 642-5.