Papers associated with kcna2

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	The inhibitory effect of the antipsychotic drug haloperidol on HERG potassium channels expressed in Xenopus oocytes., Suessbrich H, Schönherr R, Heinemann SH, Attali B, Lang F, Busch AE., Br J Pharmacol. March 1, 1997; 120 (5): 968-74.
	A potassium-channel toxin from the sea anemone Bunodosoma granulifera, an inhibitor for Kv1 channels. Revision of the amino acid sequence, disulfide-bridge assignment, chemical synthesis, and biological activity., Cotton J, Crest M, Bouet F, Alessandri N, Gola M, Forest E, Karlsson E, Castañeda O, Harvey AL, Vita C, Ménez A., Eur J Biochem. February 15, 1997; 244 (1): 192-202.
	Quinidine enhances and suppresses Kv1.2 from outside and inside the cell, respectively., Tseng GN, Zhu B, Ling S, Yao JA., J Pharmacol Exp Ther. November 1, 1996; 279 (2): 844-55.
	Effects of charybdotoxin on K+ channel (KV1.2) deactivation and inactivation kinetics., Sprunger LK, Stewig NJ, O'Grady SM., Eur J Pharmacol. October 31, 1996; 314 (3): 357-64.
	Novel effects of dendrotoxin homologues on subtypes of mammalian Kv1 potassium channels expressed in Xenopus oocytes., Robertson B, Owen D, Stow J, Butler C, Newland C., FEBS Lett. March 25, 1996; 383 (1-2): 26-30.
	Xenopus spinal neurons express Kv2 potassium channel transcripts during embryonic development., Burger C, Ribera AB., J Neurosci. February 15, 1996; 16 (4): 1412-21.
	Susceptibility of cloned K+ channels to reactive oxygen species., Duprat F, Guillemare E, Romey G, Fink M, Lesage F, Lazdunski M, Honore E., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.
	Suppression of two cloned smooth muscle-derived delayed rectifier potassium channels by cholinergic agonists and phorbol esters., Vogalis F, Ward M, Horowitz B., Mol Pharmacol. December 1, 1995; 48 (6): 1015-23.
	Microheterogeneity in heteromultimeric assemblies formed by Shaker (Kv1) and Shaw (Kv3) subfamilies of voltage-gated K+ channels., Shahidullah M, Hoshi N, Yokoyama S, Higashida H., Proc Biol Sci. September 22, 1995; 261 (1362): 309-17.
	Slow inactivation conserved in heteromultimeric voltage-dependent K+ channels between Shaker (Kv1) and Shaw (Kv3) subfamilies., Shahidullah M, Hoshi N, Yokoyama S, Kawamura T, Higashida H., FEBS Lett. September 11, 1995; 371 (3): 307-10.
	Antiarrhythmic and bradycardic drugs inhibit currents of cloned K+ channels, KV1.2 and KV1.4., Yamagishi T, Ishii K, Taira N., Eur J Pharmacol. August 4, 1995; 281 (2): 151-9.
	Block by 4-aminopyridine of a Kv1.2 delayed rectifier K+ current expressed in Xenopus oocytes., Russell SN, Publicover NG, Hart PJ, Carl A, Hume JR, Sanders KM, Horowitz B., J Physiol. December 15, 1994; 481 ( Pt 3) 571-84.
	Receptor-mediated modulation of rat KV1.2 in Xenopus oocytes., Murakoshi H, Ishii K, Nunoki K, Taira N., Eur J Pharmacol. August 16, 1994; 268 (3): 451-4.
	Cloning and expression of a Kv1.2 class delayed rectifier K+ channel from canine colonic smooth muscle., Hart PJ, Overturf KE, Russell SN, Carl A, Hume JR, Sanders KM, Horowitz B., Proc Natl Acad Sci U S A. October 15, 1993; 90 (20): 9659-63.
	Heteromultimeric assembly of human potassium channels. Molecular basis of a transient outward current?, Po S, Roberds S, Snyders DJ, Tamkun MM, Bennett PB., Circ Res. June 1, 1993; 72 (6): 1326-36.
	Absence of effects of class III antiarrhythmic agents on cloned cardiac K channels., Yamagishi T, Ishii K, Taira N., Jpn J Pharmacol. April 1, 1993; 61 (4): 371-3.
	Effects of the level of mRNA expression on biophysical properties, sensitivity to neurotoxins, and regulation of the brain delayed-rectifier K+ channels Kv1.2., Guillemare E, Honoré E, Pradier L, Lesage F, Schweitz H, Attali B, Barhanin J, Lazdunski M., Biochemistry. December 15, 1992; 31 (49): 12463-8.

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