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Results: 1-14 |
Results: 14
Potassium channels: from scorpion venoms to high-resolution structure
Authors: Garcia, ML Gao, YD McManus, OB Kaczorowski, GJ
Citation: Ml. Garcia et al., Potassium channels: from scorpion venoms to high-resolution structure, TOXICON, 39(6), 2001, pp. 739-748
Binding of correolide to the K(v)1.3 potassium channel: Characterization of the binding domain by site-directed mutagenesis
Authors: Hanner, M Green, B Gao, YD Schmalhofer, WA Matyskiela, M Durand, DJ Felix, JP Linde, AR Bordallo, C Kaczorowski, GJ Kohler, M Garcia, ML
Citation: M. Hanner et al., Binding of correolide to the K(v)1.3 potassium channel: Characterization of the binding domain by site-directed mutagenesis, BIOCHEM, 40(39), 2001, pp. 11687-11697
Delay of intracellular calcium transients using a calcium chelator: Application to high-throughput screening of the capsaicin receptor ion channel and G-protein-coupled receptors
Authors: Grant, SK Bansal, A Mitra, A Feighner, SD Dai, G Kaczorowski, GJ Middleton, RE
Citation: Sk. Grant et al., Delay of intracellular calcium transients using a calcium chelator: Application to high-throughput screening of the capsaicin receptor ion channel and G-protein-coupled receptors, ANALYT BIOC, 294(1), 2001, pp. 27-35
Pharmacology of high-conductance, Ca2+-activated potassium channels
Authors: Garcia, ML Kaczorowski, GJ
Citation: Ml. Garcia et Gj. Kaczorowski, Pharmacology of high-conductance, Ca2+-activated potassium channels, POTASSIUM CHANNELS IN CARDIOVASCULAR BIOLOGY, 2001, pp. 219-234
Correolide, a nor-triterpenoid blocker of Shaker-type Kv1 channels elicitstwitches in guinea-pig ileum by stimulating the enteric nervous system andenhancing neurotransmitter release
Authors: Vianna-Jorge, R Oliveira, CF Garcia, ML Kaczorowski, GJ Suarez-Kurtz, G
Citation: R. Vianna-jorge et al., Correolide, a nor-triterpenoid blocker of Shaker-type Kv1 channels elicitstwitches in guinea-pig ileum by stimulating the enteric nervous system andenhancing neurotransmitter release, BR J PHARM, 131(4), 2000, pp. 772-778
Nodulisporic acid opens insect glutamate-gated chloride channels: Identification of a new high affinity modulator
Authors: Smith, MM Warren, VA Thomas, BS Brochu, RM Ertel, EA Rohrer, S Schaeffer, J Schmatz, D Petuch, BR Tang, YS Meinke, PT Kaczorowski, GJ Cohen, CJ
Citation: Mm. Smith et al., Nodulisporic acid opens insect glutamate-gated chloride channels: Identification of a new high affinity modulator, BIOCHEM, 39(18), 2000, pp. 5543-5554
Scorpion toxins and potassium channels
Authors: Garcia, ML Hanner, M Knaus, HG Slaughter, RS Kaczorowski, GJ
Citation: Ml. Garcia et al., Scorpion toxins and potassium channels, METH TOOLS, 2000, pp. 183-195
Pharmacology of voltage-gated and calcium-activated potassium channels
Authors: Kaczorowski, GJ Garcia, ML
Citation: Gj. Kaczorowski et Ml. Garcia, Pharmacology of voltage-gated and calcium-activated potassium channels, CURR OP C B, 3(4), 1999, pp. 448-458
Scorpion toxins: tools for studying K+ channels (vol 36, pg 1641, 1998)
Authors: Garcia, ML Hanner, M Kaczorowski, GJ
Citation: Ml. Garcia et al., Scorpion toxins: tools for studying K+ channels (vol 36, pg 1641, 1998), TOXICON, 37(4), 1999, pp. 701-701
Peptidyl inhibitors of shaker-type K(v)1 channels elicit twitches in guinea pig ileum by blocking K(v)1.1 at enteric nervous system and enhancing acetylcholine release
Authors: Suarez-Kurtz, G Vianna-Jorge, R Pereira, BF Garcia, ML Kaczorowski, GJ
Citation: G. Suarez-kurtz et al., Peptidyl inhibitors of shaker-type K(v)1 channels elicit twitches in guinea pig ileum by blocking K(v)1.1 at enteric nervous system and enhancing acetylcholine release, J PHARM EXP, 289(3), 1999, pp. 1517-1522
Binding of correolide to K(v)1 family potassium channels - Mapping the domains of high affinity interaction
Authors: Hanner, M Schmalhofer, WA Green, B Bordallo, C Liu, J Slaughter, RS Kaczorowski, GJ Garcia, ML
Citation: M. Hanner et al., Binding of correolide to K(v)1 family potassium channels - Mapping the domains of high affinity interaction, J BIOL CHEM, 274(36), 1999, pp. 25237-25244
WIN 17317-3, a new high-affinity probe for voltage-gated sodium channels
Authors: Wanner, SG Glossmann, H Knaus, HG Baker, R Parsons, W Rupprecht, KM Brochu, R Cohen, CJ Schmalhofer, W Smith, M Warren, V Garcia, ML Kaczorowski, GJ
Citation: Sg. Wanner et al., WIN 17317-3, a new high-affinity probe for voltage-gated sodium channels, BIOCHEM, 38(34), 1999, pp. 11137-11146
High-conductance calcium-activated potassium channels in rat brain: Pharmacology, distribution, and subunit composition
Authors: Wanner, SG Koch, RO Koschak, A Trieb, M Garcia, ML Kaczorowski, GJ Knaus, HG
Citation: Sg. Wanner et al., High-conductance calcium-activated potassium channels in rat brain: Pharmacology, distribution, and subunit composition, BIOCHEM, 38(17), 1999, pp. 5392-5400
Identification and biochemical characterization of a novel nortriterpene inhibitor of the human lymphocyte voltage-gated potassium channel, Kv1.3
Authors: Felix, JP Bugianesi, RM Schmalhofer, WA Borris, R Goetz, MA Hensens, OD Bao, JM Kayser, F Parsons, WH Rupprecht, K Garcia, ML Kaczorowski, GJ Slaughter, RS
Citation: Jp. Felix et al., Identification and biochemical characterization of a novel nortriterpene inhibitor of the human lymphocyte voltage-gated potassium channel, Kv1.3, BIOCHEM, 38(16), 1999, pp. 4922-4930
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