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The potassium channel MBK1 ( Kv1.1) is expressed in the mouse retina. , Klumpp DJ, Farber DB, Bowes C, Song EJ, Pinto LH., Cell Mol Neurobiol. December 1, 1991; 11 (6): 611-22.
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.
Primary sensory neurons express a Shaker-like potassium channel gene. , Ribera AB , Nguyen DA., J Neurosci. November 1, 1993; 13 (11): 4988-96.
Pursuing the voltage sensor of a voltage-gated mammalian potassium channel. , Tytgat J, Nakazawa K, Gross A, Hess P., J Biol Chem. November 15, 1993; 268 (32): 23777-9.
Aminopyridine block of Kv1.1 potassium channels expressed in mammalian cells and Xenopus oocytes. , Castle NA, Fadous S, Logothetis DE, Wang GK., Mol Pharmacol. June 1, 1994; 45 (6): 1242-52.
Reversal of rectification and alteration of selectivity and pharmacology in a mammalian Kv1.1 potassium channel by deletion of domains S1 to S4. , Tytgat J, Vereecke J, Carmeliet E., J Physiol. November 15, 1994; 481 ( Pt 1) 7-13.
4-Aminopyridine binding and slow inactivation are mutually exclusive in rat Kv1.1 and Shaker potassium channels. , Castle NA, Fadous SR, Logothetis DE, Wang GK., Mol Pharmacol. December 1, 1994; 46 (6): 1175-81.
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.
Transmembrane segments critical for potassium channel function. , Van de Voorde A, Tytgat J., Biochem Biophys Res Commun. April 26, 1995; 209 (3): 1094-101.
The alpha-dendrotoxin footprint on a mammalian potassium channel. , Tytgat J, Debont T, Carmeliet E, Daenens P., J Biol Chem. October 20, 1995; 270 (42): 24776-81.
Xenopus spinal neurons express Kv2 potassium channel transcripts during embryonic development. , Burger C, Ribera AB ., J Neurosci. February 15, 1996; 16 (4): 1412-21.
Effect of isosorbiddinitrate on exogenously expressed slowly activating K+ channels and endogenous K+ channels in Xenopus oocytes. , Busch AE, Kopp HG, Waldegger S, Samarzija I, Süssbrich H, Raber G, Kunzelmann K , Ruppersberg JP, Lang F ., J Physiol. March 15, 1996; 491 ( Pt 3) 735-41.
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.
Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole. , Suessbrich H, Waldegger S, Lang F , Busch AE., FEBS Lett. April 29, 1996; 385 (1-2): 77-80.
Mechanism of action of the epileptogenic drug pentylenetetrazol on a cloned neuronal potassium channel. , Madeja M, Musshoff U, Lorra C, Pongs O, Speckmann EJ., Dev Biol. May 25, 1996; 722 (1-2): 59-70.
Molecular cloning of a glibenclamide-sensitive, voltage-gated potassium channel expressed in rabbit kidney. , Yao X, Chang AY, Boulpaep EL, Segal AS, Desir GV., J Clin Invest. June 1, 1996; 97 (11): 2525-33.
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.
Do voltage-gated Kv1.1 and inward rectifier Kir2.1 potassium channels form heteromultimers? , Tytgat J, Buyse G, Eggermont J, Droogmans G, Nilius B, Daenens P., FEBS Lett. July 29, 1996; 390 (3): 280-4.
Specific blockade of slowly activating I(sK) channels by chromanols -- impact on the role of I(sK) channels in epithelia. , Suessbrich H, Bleich M, Ecke D, Rizzo M, Waldegger S, Lang F , Szabo I, Lang HJ, Kunzelmann K , Greger R, Busch AE., FEBS Lett. November 4, 1996; 396 (2-3): 271-5.
Phosphorylation of a K+ channel alpha subunit modulates the inactivation conferred by a beta subunit. Involvement of cytoskeleton. , Levin G, Chikvashvili D, Singer-Lahat D, Peretz T, Thornhill WB, Lotan I., J Biol Chem. November 15, 1996; 271 (46): 29321-8.
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.
Effect of lanthanum on voltage-dependent gating of a cloned mammalian neuronal potassium channel. , Tytgat J, Daenens P., Dev Biol. February 28, 1997; 749 (2): 232-7.
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.
Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channels. , Kharrat R, Mansuelle P, Sampieri F, Crest M, Oughideni R, Van Rietschoten J, Martin-Eauclaire MF, Rochat H, El Ayeb M., FEBS Lett. April 14, 1997; 406 (3): 284-90.
Inactivation of a voltage-dependent K+ channel by beta subunit. Modulation by a phosphorylation-dependent interaction between the distal C terminus of alpha subunit and cytoskeleton. , Jing J, Peretz T, Singer-Lahat D, Chikvashvili D, Thornhill WB, Lotan I., J Biol Chem. May 30, 1997; 272 (22): 14021-4.
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 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.
Effect of fluoxetine on a neuronal, voltage-dependent potassium channel ( Kv1.1). , Tytgat J, Maertens C, Daenens P., Br J Pharmacol. December 1, 1997; 122 (7): 1417-24.
kappa-Conotoxin PVIIA is a peptide inhibiting the shaker K+ channel. , Shon KJ, Stocker M, Terlau H, Stühmer W, Jacobsen R, Walker C, Grilley M, Watkins M, Hillyard DR, Gray WR, Olivera BM., J Biol Chem. January 2, 1998; 273 (1): 33-8.
Cyclosporin A selectively reduces the functional expression of Kir2.1 potassium channels in Xenopus oocytes. , Chen H , Kubo Y, Hoshi T, Heinemann SH., FEBS Lett. February 6, 1998; 422 (3): 307-10.
Activation of a metabotropic glutamate receptor and protein kinase C reduce the extent of inactivation of the K+ channel Kv1.1/Kvbeta1.1 via dephosphorylation of Kv1.1. , Levy M, Jing J, Chikvashvili D, Thornhill WB, Lotan I., J Biol Chem. March 13, 1998; 273 (11): 6495-502.
Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency. , Zerr P, Adelman JP, Maylie J., J Neurosci. April 15, 1998; 18 (8): 2842-8.
Toxin and subunit specificity of blocking affinity of three peptide toxins for heteromultimeric, voltage-gated potassium channels expressed in Xenopus oocytes. , Hopkins WF., J Pharmacol Exp Ther. June 1, 1998; 285 (3): 1051-60.
Site directed mutants of Noxiustoxin reveal specific interactions with potassium channels. , Martínez F, Muñoz-Garay C, Gurrola G, Darszon A, Possani LD, Becerril B., FEBS Lett. June 16, 1998; 429 (3): 381-4.
Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel. , Zerr P, Adelman JP, Maylie J., FEBS Lett. July 24, 1998; 431 (3): 461-4.
A snake toxin inhibitor of inward rectifier potassium channel ROMK1. , Imredy JP, Chen C , MacKinnon R., Biochemistry. October 20, 1998; 37 (42): 14867-74.
Selective peptide antagonist of the class E calcium channel from the venom of the tarantula Hysterocrates gigas. , Newcomb R, Szoke B, Palma A, Wang G, Chen X, Hopkins W, Cong R, Miller J , Urge L, Tarczy-Hornoch K, Loo JA, Dooley DJ, Nadasdi L, Tsien RW, Lemos J, Miljanich G., Biochemistry. November 3, 1998; 37 (44): 15353-62.
Open channel block and open channel destabilization: contrasting effects of phenol, TEA+ and local anaesthetics on Kv1.1 K+ channels. , Elliott AA, Harrold JA, Newman JP, Elliott JR., Toxicol Lett. November 23, 1998; 100-101 277-85.
Transplanting the N-terminus from Kv1.4 to Kv1.1 generates an inwardly rectifying K+ channel. , Chanda B, Tiwari JK, Varshney A, Mathew MK., Neuroreport. February 5, 1999; 10 (2): 237-41.
Fast inactivation of a brain K+ channel composed of Kv1.1 and Kvbeta1.1 subunits modulated by G protein beta gamma subunits. , Jing J, Chikvashvili D, Singer-Lahat D, Thornhill WB, Reuveny E, Lotan I., EMBO J. March 1, 1999; 18 (5): 1245-56.
Ile-177 and Ser-180 in the S1 segment are critically important in Kv1.1 channel function. , Mathur R, Zhou J, Babila T, Koren G., J Biol Chem. April 23, 1999; 274 (17): 11487-93.
Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy. , Spauschus A, Eunson L, Hanna MG, Kullmann DM., Ann N Y Acad Sci. April 30, 1999; 868 442-6.
Identification of residues in dendrotoxin K responsible for its discrimination between neuronal K+ channels containing Kv1.1 and 1.2 alpha subunits. , Wang FC, Bell N, Reid P, Smith LA, McIntosh P, Robertson B, Dolly JO., Eur J Biochem. July 1, 1999; 263 (1): 222-9.
Protein kinase C inhibits Kv1.1 potassium channel function. , Boland LM, Jackson KA., Am J Physiol. July 1, 1999; 277 (1): C100-10.
Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K(+) channel function. , D'Adamo MC, Imbrici P, Sponcichetti F, Pessia M., FASEB J. August 1, 1999; 13 (11): 1335-45.
Voltage sensitivity and gating charge in Shaker and Shab family potassium channels. , Islas LD, Sigworth FJ ., J Gen Physiol. November 1, 1999; 114 (5): 723-42.
Role of disulfide bonds in the structure and potassium channel blocking activity of ShK toxin. , Pennington MW, Lanigan MD, Kalman K, Mahnir VM, Rauer H, McVaugh CT, Behm D, Donaldson D, Chandy KG, Kem WR, Norton RS., Biochemistry. November 2, 1999; 38 (44): 14549-58.
Modal behavior of the Kv1.1 channel conferred by the Kvbeta1.1 subunit and its regulation by dephosphorylation of Kv1.1. , Singer-Lahat D, Dascal N , Lotan I., Pflugers Arch. December 1, 1999; 439 (1-2): 18-26.
Inhibition of neuronal KV potassium currents by the antidepressant drug, fluoxetine. , Yeung SY, Millar JA, Mathie A., Br J Pharmacol. December 1, 1999; 128 (7): 1609-15.
Distribution in rat brain of binding sites of kaliotoxin, a blocker of Kv1.1 and Kv1.3 alpha-subunits. , Mourre C, Chernova MN, Martin-Eauclaire MF, Bessone R, Jacquet G, Gola M, Alper SL, Crest M., J Pharmacol Exp Ther. December 1, 1999; 291 (3): 943-52.