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	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	Block effect of capsaicin on hERG potassium currents is enhanced by S6 mutation at Y652., Xing J., Eur J Pharmacol. March 25, 2010; 630 (1-3): 1-9.
	Kaitocephalin antagonism of glutamate receptors expressed in Xenopus oocytes., Limon A., ACS Chem Neurosci. March 17, 2010; 1 (3): 175-181.
	Structural and functional characterization of a novel homodimeric three-finger neurotoxin from the venom of Ophiophagus hannah (king cobra)., Roy A., J Biol Chem. March 12, 2010; 285 (11): 8302-15.
	The human cardiac K2P3.1 (TASK-1) potassium leak channel is a molecular target for the class III antiarrhythmic drug amiodarone., Gierten J., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2010; 381 (3): 261-70.
	Blocking effect of methylflavonolamine on human Na(V)1.5 channels expressed in Xenopus laevis oocytes and on sodium currents in rabbit ventricular myocytes., Fan XR., Acta Pharmacol Sin. March 1, 2010; 31 (3): 297-306.
	Inhibition of human alpha4beta2 neuronal nicotinic acetylcholine receptors by volatile aromatic anesthetics depends on drug hydrophobicity., Solt K., Anesth Analg. February 1, 2010; 110 (2): 455-60.
	Species difference in the effect of grapefruit juice on intestinal absorption of talinolol between human and rat., Shirasaka Y., J Pharmacol Exp Ther. January 1, 2010; 332 (1): 181-9.
	Differential effects of ICA-27243 on cloned K(V)7 channels., Blom SM., Pharmacology. January 1, 2010; 86 (3): 174-81.
	Intein-mediated site-specific conjugation of Quantum Dots to proteins in vivo., Charalambous A., J Nanobiotechnology. December 10, 2009; 7 9.
	Functional expression of an arachnid sodium channel reveals residues responsible for tetrodotoxin resistance in invertebrate sodium channels., Du Y., J Biol Chem. December 4, 2009; 284 (49): 33869-75.
	The actions of chloride channel blockers, barbiturates and a benzodiazepine on Caenorhabditis elegans glutamate- and ivermectin-gated chloride channel subunits expressed in Xenopus oocytes., Bush E., Invert Neurosci. December 1, 2009; 9 (3-4): 175-84.
	H(1) antihistamine drug promethazine directly blocks hERG K(+) channel., Jo SH., Pharmacol Res. November 1, 2009; 60 (5): 429-37.
	Guanidino acids act as rho1 GABA(C) receptor antagonists., Chebib M., Neurochem Res. October 1, 2009; 34 (10): 1704-11.
	A novel fluorescent alpha-conotoxin for the study of alpha7 nicotinic acetylcholine receptors., Hone AJ., J Neurochem. October 1, 2009; 111 (1): 80-9.
	GABA analogues derived from 4-aminocyclopent-1-enecarboxylic acid., Locock KE., Neurochem Res. October 1, 2009; 34 (10): 1698-703.
	Alternatives to animal experimentation for hormonal compounds research., Penza M., Genes Nutr. September 1, 2009; 4 (3): 165-72.
	Effects of triterpenoids from Poria cocos Wolf on the serotonin type 3A receptor-mediated ion current in Xenopus oocytes., Lee JH, Lee JH., Eur J Pharmacol. August 1, 2009; 615 (1-3): 27-32.
	Chemical synthesis and folding of APETx2, a potent and selective inhibitor of acid sensing ion channel 3., Jensen JE., Toxicon. July 1, 2009; 54 (1): 56-61.
	Inhibition of aquaporin-1 and aquaporin-4 water permeability by a derivative of the loop diuretic bumetanide acting at an internal pore-occluding binding site., Migliati E., Mol Pharmacol. July 1, 2009; 76 (1): 105-12.
	TWIK-1 and TREK-1 are potassium channels contributing significantly to astrocyte passive conductance in rat hippocampal slices., Zhou M., J Neurosci. July 1, 2009; 29 (26): 8551-64.
	State-dependent accessibility of the P-S6 linker of pacemaker (HCN) channels supports a dynamic pore-to-gate coupling model., Siu CW., J Membr Biol. July 1, 2009; 230 (1): 35-47.
	Quinazolindione derivatives as potent 5-HT3A receptor antagonists., Lee BH., Bioorg Med Chem. July 1, 2009; 17 (13): 4793-6.
	Discovery of spiro-piperidine inhibitors and their modulation of the dynamics of the M2 proton channel from influenza A virus., Wang J., J Am Chem Soc. June 17, 2009; 131 (23): 8066-76.
	Pharmacological characteristics of the inhibition of nondepolarizing neuromuscular blocking agents at human adult muscle nicotinic acetylcholine receptor., Jonsson Fagerlund M., Anesthesiology. June 1, 2009; 110 (6): 1244-52.
	Block of HERG k channel by classic histamine h(1) receptor antagonist chlorpheniramine., Hong HK., Korean J Physiol Pharmacol. June 1, 2009; 13 (3): 215-20.
	Southeast Asian AE1 associated renal tubular acidosis: cation leak is a class effect., Walsh S., Biochem Biophys Res Commun. May 15, 2009; 382 (4): 668-72.
	Colchicine: a novel positive allosteric modulator of the human 5-hydroxytryptamine3A receptor., de Oliveira-Pierce AN., J Pharmacol Exp Ther. May 1, 2009; 329 (2): 838-47.
	Replication initiation complex formation in the absence of nuclear function in Xenopus., Krasinska L., Nucleic Acids Res. April 1, 2009; 37 (7): 2238-48.
	Mediolateral and rostrocaudal topographic organization of the sympathetic preganglionic cell pool in the spinal cord of Xenopus laevis., Nakano M., J Comp Neurol. March 20, 2009; 513 (3): 292-314.
	Concentration-dependent effect of naringin on intestinal absorption of beta(1)-adrenoceptor antagonist talinolol mediated by p-glycoprotein and organic anion transporting polypeptide (Oatp)., Shirasaka Y., Pharm Res. March 1, 2009; 26 (3): 560-7.
	Disruption of the IS6-AID linker affects voltage-gated calcium channel inactivation and facilitation., Findeisen F., J Gen Physiol. March 1, 2009; 133 (3): 327-43.
	Novel, potent, and selective GABAC antagonists inhibit myopia development and facilitate learning and memory., Chebib M., J Pharmacol Exp Ther. February 1, 2009; 328 (2): 448-57.
	Oxycodone is associated with dose-dependent QTc prolongation in patients and low-affinity inhibiting of hERG activity in vitro., Fanoe S., Br J Clin Pharmacol. February 1, 2009; 67 (2): 172-9.
	Regulation of antiarrhythmic drug propafenone effects on the c-type Kv1.4 potassium channel by PHo and K+., Wang Z., J Korean Med Sci. February 1, 2009; 24 (1): 84-91.
	[Effects of telmisartan on voltage-gated Kv1.3 and Kv1.5 potassium channels expressed in Xenopus oocytes]., Li MW., Zhonghua Xin Xue Guan Bing Za Zhi. February 1, 2009; 37 (2): 165-8.
	Selective noradrenaline reuptake inhibitor atomoxetine directly blocks hERG currents., Scherer D., Br J Pharmacol. January 1, 2009; 156 (2): 226-36.
	Neuronal nicotinic acetylcholine receptors are modulated by zinc., Vázquez-Gómez E., Neuropharmacology. January 1, 2009; 56 (6-7): 1035-40.
	Molecular determinants of multiple effects of nickel on NMDA receptor channels., Gavazzo P., Neurotox Res. January 1, 2009; 15 (1): 38-48.
	Inhibition of native and recombinant nicotinic acetylcholine receptors by the myristoylated alanine-rich C kinase substrate peptide., Gay EA., J Pharmacol Exp Ther. December 1, 2008; 327 (3): 884-90.
	Alpha-conotoxin Arenatus IB[V11L,V16D] [corrected] is a potent and selective antagonist at rat and human native alpha7 nicotinic acetylcholine receptors., Innocent N., J Pharmacol Exp Ther. November 1, 2008; 327 (2): 529-37.
	Opposite effects of zinc on human and rat P2X2 receptors., Tittle RK., J Neurosci. October 29, 2008; 28 (44): 11131-40.
	Development of an assay for testing the antimicrobial activity of skin peptides against the amphibian chytrid fungus (Batrachochytrium dendrobatidis) using Xenopus laevis., Gibble RE., Ecotoxicol Environ Saf. October 1, 2008; 71 (2): 506-13.
	Simvastatin inhibits catecholamine secretion and synthesis induced by acetylcholine via blocking Na+ and Ca2+ influx in bovine adrenal medullary cells., Matsuda T., J Pharmacol Exp Ther. October 1, 2008; 327 (1): 130-6.
	A novel, rapid, inhibitory effect of insulin on alpha1beta2gamma2s gamma-aminobutyric acid type A receptors., Williams DB., Neurosci Lett. September 26, 2008; 443 (1): 27-31.
	Enantiomeric propanolamines as selective N-methyl-D-aspartate 2B receptor antagonists., Tahirovic YA., J Med Chem. September 25, 2008; 51 (18): 5506-21.
	Interaction of tryptophan derivatives with SLC6A14 (ATB0,+) reveals the potential of the transporter as a drug target for cancer chemotherapy., Karunakaran S., Biochem J. September 15, 2008; 414 (3): 343-55.
	Neuronally micro-conotoxins from Conus striatus utilize an alpha-helical motif to target mammalian sodium channels., Schroeder CI., J Biol Chem. August 1, 2008; 283 (31): 21621-8.
	Two novel sodium channel inhibitors from Heriaeus melloteei spider venom differentially interacting with mammalian channel's isoforms., Billen B., Toxicon. August 1, 2008; 52 (2): 309-17.
	Intracellular Mg2+ is a voltage-dependent pore blocker of HCN channels., Vemana S., Am J Physiol Cell Physiol. August 1, 2008; 295 (2): C557-65.

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