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	Molecular determinants of voltage-dependent human ether-a-go-go related gene (HERG) K+ channel block., Sánchez-Chapula JA., J Biol Chem. June 28, 2002; 277 (26): 23587-95.
	Modulation of neuronal nicotinic acetylcholine receptors by mercury., Mirzoian A., J Pharmacol Exp Ther. August 1, 2002; 302 (2): 560-7.
	Energetic localization of saxitoxin in its channel binding site., Choudhary G., Biophys J. August 1, 2002; 83 (2): 912-9.
	Bertosamil blocks HERG potassium channels in their open and inactivated states., Zitron E., Br J Pharmacol. September 1, 2002; 137 (2): 221-8.
	Bupropion inhibits nicotine-evoked [(3)H]overflow from rat striatal slices preloaded with [(3)H]dopamine and from rat hippocampal slices preloaded with [(3)H]norepinephrine., Miller DK., J Pharmacol Exp Ther. September 1, 2002; 302 (3): 1113-22.
	Pharmacological characterization of Ro 63-1908 (1-[2-(4-hydroxy-phenoxy)-ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a novel subtype-selective N-methyl-D-aspartate antagonist., Gill R., J Pharmacol Exp Ther. September 1, 2002; 302 (3): 940-8.
	An N-terminal histidine regulates Zn(2+) inhibition on the murine GABA(A) receptor beta3 subunit., Dunne EL., Br J Pharmacol. September 1, 2002; 137 (1): 29-38.
	Alpha-conotoxin GIC from Conus geographus, a novel peptide antagonist of nicotinic acetylcholine receptors., McIntosh JM., J Biol Chem. September 13, 2002; 277 (37): 33610-5.
	Inhibition of recombinant K(ATP) channels by the antidiabetic agents midaglizole, LY397364 and LY389382., Proks P., Eur J Pharmacol. September 27, 2002; 452 (1): 11-9.
	Inhibition of neuronal nicotinic acetylcholine receptors by the abused solvent, toluene., Bale AS., Br J Pharmacol. October 1, 2002; 137 (3): 375-83.
	Structural and functional role of the extracellular s5-p linker in the HERG potassium channel., Liu J., J Gen Physiol. November 1, 2002; 120 (5): 723-37.
	Identification of a tyrosine in the agonist binding site of the homomeric rho1 gamma-aminobutyric acid (GABA) receptor that, when mutated, produces spontaneous opening., Torres VI., J Biol Chem. November 15, 2002; 277 (46): 43741-8.
	beta3-Adrenergic regulation of an ion channel in the heart-inhibition of the slow delayed rectifier potassium current I(Ks) in guinea pig ventricular myocytes., Bosch RF., Cardiovasc Res. December 1, 2002; 56 (3): 393-403.
	Human organic anion transporter 3 (hOAT3) can operate as an exchanger and mediate secretory urate flux., Bakhiya A., Cell Physiol Biochem. January 1, 2003; 13 (5): 249-56.
	Interactions of the C-11 hydroxyl of tetrodotoxin with the sodium channel outer vestibule., Choudhary G., Biophys J. January 1, 2003; 84 (1): 287-94.
	Inhibition of hEAG1 and hERG1 potassium channels by clofilium and its tertiary analogue LY97241., Gessner G., Br J Pharmacol. January 1, 2003; 138 (1): 161-71.
	A novel conus peptide ligand for K+ channels., Ferber M., J Biol Chem. January 24, 2003; 278 (4): 2177-83.
	Isolation, structure, and activity of GID, a novel alpha 4/7-conotoxin with an extended N-terminal sequence., Nicke A., J Biol Chem. January 31, 2003; 278 (5): 3137-44.
	Pharmacological characterization of the homomeric and heteromeric UNC-49 GABA receptors in C. elegans., Bamber BA., Br J Pharmacol. March 1, 2003; 138 (5): 883-93.
	Local anaesthetics have different mechanisms and sites of action at the recombinant N-methyl-D-aspartate (NMDA) receptors., Sugimoto M., Br J Pharmacol. March 1, 2003; 138 (5): 876-82.
	Interactions of atropine with heterologously expressed and native alpha 3 subunit-containing nicotinic acetylcholine receptors., Parker JC., Br J Pharmacol. March 1, 2003; 138 (5): 801-10.
	Dissociation of E-4031 from the HERG channel caused by mutations of an amino acid results in greater block at high stimulation frequency., Ishii K., Cardiovasc Res. March 1, 2003; 57 (3): 651-9.
	Solid-phase synthesis and biological activity of a thioether analogue of conotoxin G1., Bondebjerg J., Chembiochem. March 3, 2003; 4 (2-3): 186-94.
	Voltage-dependent profile of human ether-a-go-go-related gene channel block is influenced by a single residue in the S6 transmembrane domain., Sănchez-Chapula JA., Mol Pharmacol. May 1, 2003; 63 (5): 1051-8.
	Pharmacology of delta2 glutamate receptors: effects of pentamidine and protons., Williams K., J Pharmacol Exp Ther. May 1, 2003; 305 (2): 740-8.
	RHAMM is a centrosomal protein that interacts with dynein and maintains spindle pole stability., Maxwell CA., Mol Biol Cell. June 1, 2003; 14 (6): 2262-76.
	The antipsychotic drug chlorpromazine inhibits HERG potassium channels., Thomas D., Br J Pharmacol. June 1, 2003; 139 (3): 567-74.
	Inhibition of cloned HERG potassium channels by the antiestrogen tamoxifen., Thomas D., Naunyn Schmiedebergs Arch Pharmacol. July 1, 2003; 368 (1): 41-8.
	Toward tissue-selective pancreatic B-cells KATP channel openers belonging to 3-alkylamino-7-halo-4H-1,2,4-benzothiadiazine 1,1-dioxides., de Tullio P., J Med Chem. July 17, 2003; 46 (15): 3342-53.
	Sorcin regulates excitation-contraction coupling in the heart., Meyers MB., J Biol Chem. August 1, 2003; 278 (31): 28865-71.
	Automated Parallel Oocyte Electrophysiology Test station (POETs): a screening platform for identification of ligand-gated ion channel modulators., Shieh CC., Assay Drug Dev Technol. October 1, 2003; 1 (5): 655-63.
	Drug binding to aromatic residues in the HERG channel pore cavity as possible explanation for acquired Long QT syndrome by antiparkinsonian drug budipine., Scholz EP., Naunyn Schmiedebergs Arch Pharmacol. November 1, 2003; 368 (5): 404-14.
	Polyamine flux in Xenopus oocytes through hemi-gap junctional channels., Enkvetchakul D., J Physiol. November 15, 2003; 553 (Pt 1): 95-100.
	Recombinant baculoviruses used to study estrogen receptor function in human osteosarcoma cells., Clay WC., Assay Drug Dev Technol. December 1, 2003; 1 (6): 801-10.
	Dopamine D2-receptor activation differentially inhibits N- and R-type Ca2+ channels in Xenopus melanotrope cells., Zhang H., Neuroendocrinology. January 1, 2004; 80 (6): 368-78.
	Regulation of the epithelial Ca2+ channel TRPV5 by the NHE regulating factor NHERF2 and the serum and glucocorticoid inducible kinase isoforms SGK1 and SGK3 expressed in Xenopus oocytes., Embark HM., Cell Physiol Biochem. January 1, 2004; 14 (4-6): 203-12.
	Transporter-mediated renal handling of nafamostat mesilate., Li Q., J Pharm Sci. February 1, 2004; 93 (2): 262-72.
	Determinants of potency on alpha-conotoxin MII, a peptide antagonist of neuronal nicotinic receptors., Everhart D., Biochemistry. March 16, 2004; 43 (10): 2732-7.
	Thiol modification of cysteine 327 in the eighth transmembrane domain of the light subunit xCT of the heteromeric cystine/glutamate antiporter suggests close proximity to the substrate binding site/permeation pathway., Jiménez-Vidal M., J Biol Chem. March 19, 2004; 279 (12): 11214-21.
	Ca(2+)(cyt) negatively regulates the initiation of oocyte maturation., Sun L., J Cell Biol. April 1, 2004; 165 (1): 63-75.
	Histidine 518 in the S6-CNBD linker controls pH dependence and gating of HCN channel from sea-urchin sperm., Mistrík P., Pflugers Arch. April 1, 2004; 448 (1): 76-84.
	Salicylidene salicylhydrazide, a selective inhibitor of beta 1-containing GABAA receptors., Thompson SA., Br J Pharmacol. May 1, 2004; 142 (1): 97-106.
	Inhibition of human ether-a-go-go-related gene potassium channels by alpha 1-adrenoceptor antagonists prazosin, doxazosin, and terazosin., Thomas D., Naunyn Schmiedebergs Arch Pharmacol. May 1, 2004; 369 (5): 462-72.
	Anthraquinone polyamines: novel channel blockers to study N-methyl-D-aspartate receptors., Kashiwagi K., J Pharmacol Exp Ther. June 1, 2004; 309 (3): 884-93.
	Characterization of two novel N-methyl-D-aspartate antagonists: EAA-090 (2-[8,9-dioxo-2,6-diazabicyclo [5.2.0]non-1(7)-en2-yl]ethylphosphonic acid) and EAB-318 (R-alpha-amino-5-chloro-1-(phosphonomethyl)-1H-benzimidazole-2-propanoic acid hydrochloride)., Sun L., J Pharmacol Exp Ther. August 1, 2004; 310 (2): 563-70.
	BmBKTx1, a novel Ca2+-activated K+ channel blocker purified from the Asian scorpion Buthus martensi Karsch., Xu CQ., J Biol Chem. August 13, 2004; 279 (33): 34562-9.
	The solubilizing detergents, Tween 80 and Triton X-100 non-competitively inhibit alpha 7-nicotinic acetylcholine receptor function in Xenopus oocytes., Oz M., J Neurosci Methods. August 30, 2004; 137 (2): 167-73.
	Linopirdine blocks alpha9alpha10-containing nicotinic cholinergic receptors of cochlear hair cells., Gomez-Casati ME., J Assoc Res Otolaryngol. September 1, 2004; 5 (3): 261-9.
	Effects of the atrial antiarrhythmic drug AVE0118 on cardiac ion channels., Gögelein H., Naunyn Schmiedebergs Arch Pharmacol. September 1, 2004; 370 (3): 183-92.
	Molecular identification and characterization of three isoforms of tachykinin NK(1)-like receptors in the cane toad Bufo marinus., Liu L., Am J Physiol Regul Integr Comp Physiol. September 1, 2004; 287 (3): R575-85.

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