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	Inhibition of cardiac potassium currents by pentobarbital., Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.
	The beta-lactam antibiotics, penicillin-G and cefoselis have different mechanisms and sites of action at GABA(A) receptors., Sugimoto M., Br J Pharmacol. January 1, 2002; 135 (2): 427-32.
	Schwann cells express active agrin and enhance aggregation of acetylcholine receptors on muscle fibers., Yang JF., J Neurosci. December 15, 2001; 21 (24): 9572-84.
	DCPIB is a novel selective blocker of I(Cl,swell) and prevents swelling-induced shortening of guinea-pig atrial action potential duration., Decher N., Br J Pharmacol. December 1, 2001; 134 (7): 1467-79.
	Molecular determinants of inactivation and dofetilide block in ether a-go-go (EAG) channels and EAG-related K(+) channels., Ficker E., Mol Pharmacol. December 1, 2001; 60 (6): 1343-8.
	Pharmacological differences between immunoisolated native brain and heterologously expressed rat alpha4beta2 nicotinic receptors., Truong A., Brain Res Mol Brain Res. November 30, 2001; 96 (1-2): 68-76.
	Engineered Zn(2+) switches in the gamma-aminobutyric acid (GABA) transporter-1. Differential effects on GABA uptake and currents., MacAulay N., J Biol Chem. November 2, 2001; 276 (44): 40476-85.
	Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.
	Ketamine and its preservative, benzethonium chloride, both inhibit human recombinant alpha7 and alpha4beta2 neuronal nicotinic acetylcholine receptors in Xenopus oocytes., Coates KM., Br J Pharmacol. October 1, 2001; 134 (4): 871-9.
	Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen., Phiel CJ., J Biol Chem. September 28, 2001; 276 (39): 36734-41.
	Early posterior/ventral fate specification in the vertebrate embryo., Muñoz-Sanjuán I., Dev Biol. September 1, 2001; 237 (1): 1-17.
	Pentylenetetrazole-induced inhibition of recombinant gamma-aminobutyric acid type A (GABA(A)) receptors: mechanism and site of action., Huang RQ., J Pharmacol Exp Ther. September 1, 2001; 298 (3): 986-95.
	Interaction of cations, anions, and weak base quinine with rat renal cation transporter rOCT2 compared with rOCT1., Arndt P., Am J Physiol Renal Physiol. September 1, 2001; 281 (3): F454-68.
	The Iroquois family of genes: from body building to neural patterning., Cavodeassi F., Development. August 1, 2001; 128 (15): 2847-55.
	Open channel block of HERG K(+) channels by vesnarinone., Kamiya K., Mol Pharmacol. August 1, 2001; 60 (2): 244-53.
	Effects of bis(7)-tacrine on spontaneous synaptic activity and on the nicotinic ACh receptor of Torpedo electric organ., Ros E., J Neurophysiol. July 1, 2001; 86 (1): 183-9.
	Straight-chain alcohols exhibit a cutoff in potency for the inhibition of recombinant glutamate receptor subunits., Akinshola BE., Br J Pharmacol. July 1, 2001; 133 (5): 651-8.
	Apoptotic cleavage of cytoplasmic dynein intermediate chain and p150(Glued) stops dynein-dependent membrane motility., Lane JD., J Cell Biol. June 25, 2001; 153 (7): 1415-26.
	The influence exerted by the beta(3) subunit on MVIIA omega-conotoxin binding to neuronal N-type calcium channels., Luchian T., Biochim Biophys Acta. June 6, 2001; 1512 (2): 329-34.
	The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner., Palmer S., J Cell Biol. May 28, 2001; 153 (5): 985-98.
	"Weak toxin" from Naja kaouthia is a nontoxic antagonist of alpha 7 and muscle-type nicotinic acetylcholine receptors., Utkin YN., J Biol Chem. May 11, 2001; 276 (19): 15810-5.
	Xenopus Eya1 demarcates all neurogenic placodes as well as migrating hypaxial muscle precursors., David R., Mech Dev. May 1, 2001; 103 (1-2): 189-92.
	Inhibition of m3 muscarinic acetylcholine receptors by local anaesthetics., Hollmann MW., Br J Pharmacol. May 1, 2001; 133 (1): 207-16.
	Glimepiride block of cloned beta-cell, cardiac and smooth muscle K(ATP) channels., Song DK., Br J Pharmacol. May 1, 2001; 133 (1): 193-9.
	High-affinity blockade of human ether-a-go-go-related gene human cardiac potassium channels by the novel antiarrhythmic drug BRL-32872., Thomas D., J Pharmacol Exp Ther. May 1, 2001; 297 (2): 753-61.
	Effects of mitiglinide (S 21403) on Kir6.2/SUR1, Kir6.2/SUR2A and Kir6.2/SUR2B types of ATP-sensitive potassium channel., Reimann F., Br J Pharmacol. April 1, 2001; 132 (7): 1542-8.
	KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology., Søgaard R., Am J Physiol Cell Physiol. April 1, 2001; 280 (4): C859-66.
	An N-methyl-D-aspartate receptor channel blocker with neuroprotective activity., Tai KK., Proc Natl Acad Sci U S A. March 13, 2001; 98 (6): 3519-24.
	GLC-3: a novel fipronil and BIDN-sensitive, but picrotoxinin-insensitive, L-glutamate-gated chloride channel subunit from Caenorhabditis elegans., Horoszok L., Br J Pharmacol. March 1, 2001; 132 (6): 1247-54.
	Characteristics of glycine receptors expressed by embryonic rat brain mRNAs., García-Alcocer G., Proc Natl Acad Sci U S A. February 27, 2001; 98 (5): 2781-5.
	The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K(+) channels TREK-1 and TRAAK., Meadows HJ., Dev Biol. February 16, 2001; 892 (1): 94-101.
	A conducting state with properties of a slow inactivated state in a shaker K(+) channel mutant., Olcese R., J Gen Physiol. February 1, 2001; 117 (2): 149-63.
	Importin beta is a mitotic target of the small GTPase Ran in spindle assembly., Nachury MV., Cell. January 12, 2001; 104 (1): 95-106.
	Characterization of KCNQ5/Q3 potassium channels expressed in mammalian cells., Wickenden AD., Br J Pharmacol. January 1, 2001; 132 (2): 381-4.
	Molecular characterization of taurine transport in bovine aortic endothelial cells., Qian X., Biochim Biophys Acta. December 20, 2000; 1509 (1-2): 324-34.
	Anion permeation in Ca(2+)-activated Cl(-) channels., Qu Z., J Gen Physiol. December 1, 2000; 116 (6): 825-44.
	Effects of volatile solvents on recombinant N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Cruz SL., Br J Pharmacol. December 1, 2000; 131 (7): 1303-8.
	The role of perisynaptic Schwann cells in development of neuromuscular junctions in the frog (Xenopus laevis)., Herrera AA., J Neurobiol. December 1, 2000; 45 (4): 237-54.
	Expression pattern of XIRG, a marker for non-neural ectoderm., Schmidt G., Dev Genes Evol. November 1, 2000; 210 (11): 575-8.
	Inhibition of HERG1 K(+) channels by the novel second-generation antihistamine mizolastine., Taglialatela M., Br J Pharmacol. November 1, 2000; 131 (6): 1081-8.
	Resolution, configurational assignment, and enantiopharmacology of 2-amino-3-[3-hydroxy-5-(2-methyl-2H- tetrazol-5-yl)isoxazol-4-yl]propionic acid, a potent GluR3- and GluR4-preferring AMPA receptor agonist., Vogensen SB., Chirality. November 1, 2000; 12 (10): 705-13.
	The antimalarial agent mefloquine inhibits ATP-sensitive K-channels., Gribble FM., Br J Pharmacol. October 1, 2000; 131 (4): 756-60.
	The bee venom peptide tertiapin underlines the role of I(KACh) in acetylcholine-induced atrioventricular blocks., Drici MD., Br J Pharmacol. October 1, 2000; 131 (3): 569-77.
	Potent stimulation and inhibition of the CFTR Cl(-) current by phloxine B., Bachmann A., Br J Pharmacol. October 1, 2000; 131 (3): 433-40.
	Molecular determinants of coordinated proton and zinc inhibition of N-methyl-D-aspartate NR1/NR2A receptors., Low CM., Proc Natl Acad Sci U S A. September 26, 2000; 97 (20): 11062-7.
	Mammalian ASIC2a and ASIC3 subunits co-assemble into heteromeric proton-gated channels sensitive to Gd3+., Babinski K., J Biol Chem. September 15, 2000; 275 (37): 28519-25.
	Nicotine is a potent blocker of the cardiac A-type K(+) channels. Effects on cloned Kv4.3 channels and native transient outward current., Wang H., Circulation. September 5, 2000; 102 (10): 1165-71.
	Expression of connexin 30 in Xenopus embryos and its involvement in hatching gland function., Levin M., Dev Dyn. September 1, 2000; 219 (1): 96-101.
	Functional and pharmacological characterization of human Na(+)-carnitine cotransporter hOCTN2., Wagner CA., Am J Physiol Renal Physiol. September 1, 2000; 279 (3): F584-91.
	Conantokin G is an NR2B-selective competitive antagonist of N-methyl-D-aspartate receptors., Donevan SD., Mol Pharmacol. September 1, 2000; 58 (3): 614-23.

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