Papers associated with

Limit to papers also referencing gene:

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 ???pagination.result.next???

Sort Newest To Oldest

Sort Oldest To Newest

	Association of Kv1.5 and Kv1.3 contributes to the major voltage-dependent K+ channel in macrophages., Vicente R., J Biol Chem. December 8, 2006; 281 (49): 37675-85.
	The flounder organic anion transporter fOat has sequence, function, and substrate specificity similarity to both mammalian Oat1 and Oat3., Aslamkhan AG., Am J Physiol Regul Integr Comp Physiol. December 1, 2006; 291 (6): R1773-80.
	Ancillary subunits and stimulation frequency determine the potency of chromanol 293B block of the KCNQ1 potassium channel., Bett GC., J Physiol. November 1, 2006; 576 (Pt 3): 755-67.
	Functional demonstration of the ability of a primary spermatogonium as a stem cell by tracing a single cell destiny in Xenopus laevis., Kawasaki T., Dev Growth Differ. October 1, 2006; 48 (8): 525-35.
	Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers., Ku IW., Bioorg Med Chem Lett. October 1, 2006; 16 (19): 5244-8.
	In vitro modulation of HERG channels by organochlorine solvent trichlormethane as potential explanation for proarrhythmic effects of chloroform., Scholz EP., Toxicol Lett. August 20, 2006; 165 (2): 156-66.
	GABA-site antagonism and pentobarbital actions do not depend on the alpha-subunit type in the recombinant rat GABA receptor., Rahman M., Acta Physiol (Oxf). August 1, 2006; 187 (4): 479-88.
	The epithelial Na+ channel is inhibited by a peptide derived from proteolytic processing of its alpha subunit., Carattino MD., J Biol Chem. July 7, 2006; 281 (27): 18901-7.
	Atypical tetracyclic antidepressant maprotiline is an antagonist at cardiac hERG potassium channels., Kiesecker C., Naunyn Schmiedebergs Arch Pharmacol. June 1, 2006; 373 (3): 212-20.
	Blockade of HERG human K+ channels and IKr of guinea-pig cardiomyocytes by the antipsychotic drug clozapine., Lee SY., Br J Pharmacol. June 1, 2006; 148 (4): 499-509.
	A comparative study of the action of tolperisone on seven different voltage dependent sodium channel isoforms., Hofer D., Eur J Pharmacol. May 24, 2006; 538 (1-3): 5-14.
	Interaction with sigma(1) protein, but not N-methyl-D-aspartate receptor, is involved in the pharmacological activity of donepezil., Maurice T., J Pharmacol Exp Ther. May 1, 2006; 317 (2): 606-14.
	Analyses of dose-response curves to compare the antimicrobial activity of model cationic alpha-helical peptides highlights the necessity for a minimum of two activity parameters., Rautenbach M., Anal Biochem. March 1, 2006; 350 (1): 81-90.
	Drug binding interactions in the inner cavity of HERG channels: molecular insights from structure-activity relationships of clofilium and ibutilide analogs., Perry M., Mol Pharmacol. February 1, 2006; 69 (2): 509-19.
	Four novel tarantula toxins as selective modulators of voltage-gated sodium channel subtypes., Bosmans F., Mol Pharmacol. February 1, 2006; 69 (2): 419-29.
	The receptor site of the spider toxin PcTx1 on the proton-gated cation channel ASIC1a., Salinas M., J Physiol. January 15, 2006; 570 (Pt 2): 339-54.
	Enantiomers of cis-constrained and flexible 2-substituted GABA analogues exert opposite effects at recombinant GABA(C) receptors., Crittenden DL., Bioorg Med Chem. January 15, 2006; 14 (2): 447-55.
	Molecular identification and functional characterization of a temperature-sensitive transient receptor potential channel (TRPM8) from canine., Liu Y., Eur J Pharmacol. January 13, 2006; 530 (1-2): 23-32.
	Block of hERG channel by ziprasidone: biophysical properties and molecular determinants., Su Z., Biochem Pharmacol. January 12, 2006; 71 (3): 278-86.
	Inhibitory modulation of ATP-sensitive potassium channels by gallate-ester moiety of (-)-epigallocatechin-3-gallate., Baek WK., Biochem Pharmacol. November 25, 2005; 70 (11): 1560-7.
	CaMKII tethers to L-type Ca2+ channels, establishing a local and dedicated integrator of Ca2+ signals for facilitation., Hudmon A., J Cell Biol. November 7, 2005; 171 (3): 537-47.
	The beta subunit increases the ginkgolide B sensitivity of inhibitory glycine receptors., Kondratskaya EL., Neuropharmacology. November 1, 2005; 49 (6): 945-51.
	Evans blue is a specific antagonist of the human epithelial Na+ channel delta-subunit., Yamamura H., J Pharmacol Exp Ther. November 1, 2005; 315 (2): 965-9.
	Characteristics of ginsenoside Rg3-mediated brain Na+ current inhibition., Lee JH, Lee JH., Mol Pharmacol. October 1, 2005; 68 (4): 1114-26.
	A single residue in the S6 transmembrane domain governs the differential flecainide sensitivity of voltage-gated potassium channels., Herrera D., Mol Pharmacol. August 1, 2005; 68 (2): 305-16.
	The dietary polyphenol ellagic acid is a potent inhibitor of hOAT1., Whitley AC., Drug Metab Dispos. August 1, 2005; 33 (8): 1097-100.
	Zinc activates TREK-2 potassium channel activity., Kim JS., J Pharmacol Exp Ther. August 1, 2005; 314 (2): 618-25.
	The effects of the tramadol metabolite O-desmethyl tramadol on muscarinic receptor-induced responses in Xenopus oocytes expressing cloned M1 or M3 receptors., Nakamura M., Anesth Analg. July 1, 2005; 101 (1): 180-6, table of contents.
	Mutation of the pore glutamate affects both cytoplasmic and external dequalinium block in the rat olfactory CNGA2 channel., Qu W., Eur Biophys J. July 1, 2005; 34 (5): 442-53.
	Inhibition of human ether-a-go-go-related gene K+ channel and IKr of guinea pig cardiomyocytes by antipsychotic drug trifluoperazine., Choi SY., J Pharmacol Exp Ther. May 1, 2005; 313 (2): 888-95.
	Transport of the natural sweetener stevioside and its aglycone steviol by human organic anion transporter (hOAT1; SLC22A6) and hOAT3 (SLC22A8)., Srimaroeng C., J Pharmacol Exp Ther. May 1, 2005; 313 (2): 621-8.
	Molecular dissection of tropisetron, an alpha7 nicotinic acetylcholine receptor-selective partial agonist., Papke RL., Neurosci Lett. April 22, 2005; 378 (3): 140-4.
	ZW10 links mitotic checkpoint signaling to the structural kinetochore., Kops GJ., J Cell Biol. April 11, 2005; 169 (1): 49-60.
	Marine alkaloids (-)-pictamine and (-)-lepadin B block neuronal nicotinic acetylcholine receptors., Tsuneki H., Biol Pharm Bull. April 1, 2005; 28 (4): 611-4.
	Relapsing diabetes can result from moderately activating mutations in KCNJ11., Gloyn AL., Hum Mol Genet. April 1, 2005; 14 (7): 925-34.
	The effects of the neurosteroids: pregnenolone, progesterone and dehydroepiandrosterone on muscarinic receptor-induced responses in Xenopus oocytes expressing M1 and M3 receptors., Horishita T., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2005; 371 (3): 221-8.
	Contrasting the effects of nifedipine on subtypes of endogenous and recombinant T-type Ca2+ channels., Shcheglovitov A., Biochem Pharmacol. March 1, 2005; 69 (5): 841-54.
	The acetylcholinesterase inhibitor BW284c51 is a potent blocker of Torpedo nicotinic AchRs incorporated into the Xenopus oocyte membrane., Olivera-Bravo S., Br J Pharmacol. January 1, 2005; 144 (1): 88-97.
	Class Ia anti-arrhythmic drug ajmaline blocks HERG potassium channels: mode of action., Kiesecker C., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2004; 370 (6): 423-35.
	Block of wild-type and inactivation-deficient human ether-a-go-go-related gene K+ channels by halofantrine., Sánchez-Chapula JA., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2004; 370 (6): 484-91.
	Analysis of the effects of halothane on Gi-coupled muscarinic M2 receptor signaling in Xenopus oocytes using a chimeric G alpha protein., Minami K., Pharmacology. November 1, 2004; 72 (3): 205-12.
	A noncompetitive, sequential mechanism for inhibition of rat alpha4beta2 neuronal nicotinic acetylcholine receptors by carbamate pesticides., Smulders CJ., Toxicol Sci. November 1, 2004; 82 (1): 219-27.
	Inhibitory profile of SEA0400 [2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline] assessed on the cardiac Na+-Ca2+ exchanger, NCX1.1., Lee C, Lee C., J Pharmacol Exp Ther. November 1, 2004; 311 (2): 748-57.
	The dietary flavonoids apigenin and (-)-epigallocatechin gallate enhance the positive modulation by diazepam of the activation by GABA of recombinant GABA(A) receptors., Campbell EL., Biochem Pharmacol. October 15, 2004; 68 (8): 1631-8.
	Automated higher-throughput compound screening on ion channel targets based on the Xenopus laevis oocyte expression system., Pehl U., Assay Drug Dev Technol. October 1, 2004; 2 (5): 515-24.
	State-dependent trapping of flecainide in the cardiac sodium channel., Ramos E., J Physiol. October 1, 2004; 560 (Pt 1): 37-49.
	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.
	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.

???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 ???pagination.result.next???