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A cellular model for long QT syndrome. Trapping of heteromultimeric complexes consisting of truncated Kv1.1 potassium channel polypeptides and native Kv1.4 and Kv1.5 channels in the endoplasmic reticulum. , Folco E, Mathur R, Mori Y, Buckett P, Koren G., J Biol Chem. October 17, 1997; 272 (42): 26505-10.
Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241. , Suessbrich H, Schönherr R, Heinemann SH, Lang F , Busch AE., FEBS Lett. September 8, 1997; 414 (2): 435-8.
A mammalian transient type K+ channel, rat Kv1.4, has two potential domains that could produce rapid inactivation. , Kondoh S, Ishii K, Nakamura Y, Taira N., J Biol Chem. August 1, 1997; 272 (31): 19333-8.
Channel-specific effects of n-alkyl sulphate anions on three shaker-related potassium channels expressed in Xenopus oocytes. , Elliott AA, Elliott JR., Pflugers Arch. May 1, 1997; 434 (1): 132-6.
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.
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.
Characterization of the transcription unit of mouse Kv1.4, a voltage-gated potassium channel gene. , Wymore RS, Negulescu D, Kinoshita K, Kalman K, Aiyar J, Gutman GA, Chandy KG., J Biol Chem. June 28, 1996; 271 (26): 15629-34.
Functional characterization of Kv channel beta-subunits from rat brain. , Heinemann SH, Rettig J, Graack HR, Pongs O., J Physiol. June 15, 1996; 493 ( Pt 3) 625-33.
N-type inactivation in the mammalian Shaker K+ channel Kv1.4. , Lee TE, Philipson LH, Nelson DJ., J Membr Biol. June 1, 1996; 151 (3): 225-35.
Molecular and functional characterization of a rat brain Kv beta 3 potassium channel subunit. , Heinemann SH, Rettig J, Wunder F, Pongs O., FEBS Lett. December 27, 1995; 377 (3): 383-9.
C-type inactivation controls recovery in a fast inactivating cardiac K+ channel ( Kv1.4) expressed in Xenopus oocytes. , Rasmusson RL, Morales MJ, Castellino RC, Zhang Y , Campbell DL, Strauss HC., J Physiol. December 15, 1995; 489 ( Pt 3) 709-21.
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.
Alternative splicing of the human Shaker K+ channel beta 1 gene and functional expression of the beta 2 gene product. , McCormack K, McCormack T, Tanouye M, Rudy B, Stühmer W., FEBS Lett. August 14, 1995; 370 (1-2): 32-6.
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.
Time- and voltage-dependent modulation of a Kv1.4 channel by a beta-subunit (Kv beta 3) cloned from ferret ventricle. , Castellino RC, Morales MJ, Strauss HC, Rasmusson RL., Am J Physiol. July 1, 1995; 269 (1 Pt 2): H385-91.
Bi-stable block by 4-aminopyridine of a transient K+ channel ( Kv1.4) cloned from ferret ventricle and expressed in Xenopus oocytes. , Rasmusson RL, Zhang Y , Campbell DL, Comer MB, Castellino RC, Liu S , Strauss HC., J Physiol. May 15, 1995; 485 ( Pt 1) 59-71.
A novel beta subunit increases rate of inactivation of specific voltage-gated potassium channel alpha subunits. , Morales MJ, Castellino RC, Crews AL, Rasmusson RL, Strauss HC., J Biol Chem. March 17, 1995; 270 (11): 6272-7.
Molecular mechanisms of K+ channel blockade: 4-aminopyridine interaction with a cloned cardiac transient K+ ( Kv1.4) channel. , Rasmusson RL, Zhang Y , Campbell DL, Comer MB, Castellino RC, Liu S , Morales MJ, Strauss HC., Adv Exp Med Biol. January 1, 1995; 382 11-22.
Modulation of an inactivating human cardiac K+ channel by protein kinase C. , Murray KT, Fahrig SA, Deal KK, Po SS, Hu NN, Snyders DJ, Tamkun MM, Bennett PB., Circ Res. December 1, 1994; 75 (6): 999-1005.
Functional role of the NH2-terminal cytoplasmic domain of a mammalian A-type K channel. , Tseng-Crank J, Yao JA, Berman MF, Tseng GN., J Gen Physiol. December 1, 1993; 102 (6): 1057-83.
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.