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

	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.
	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.
	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.
	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.
	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.
	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.
	Determinants of potency on alpha-conotoxin MII, a peptide antagonist of neuronal nicotinic receptors., Everhart D., Biochemistry. March 16, 2004; 43 (10): 2732-7.
	Transporter-mediated renal handling of nafamostat mesilate., Li Q., J Pharm Sci. February 1, 2004; 93 (2): 262-72.
	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.
	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.
	Polyamine flux in Xenopus oocytes through hemi-gap junctional channels., Enkvetchakul D., J Physiol. November 15, 2003; 553 (Pt 1): 95-100.
	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.
	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.
	Sorcin regulates excitation-contraction coupling in the heart., Meyers MB., J Biol Chem. August 1, 2003; 278 (31): 28865-71.
	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.
	Inhibition of cloned HERG potassium channels by the antiestrogen tamoxifen., Thomas D., Naunyn Schmiedebergs Arch Pharmacol. July 1, 2003; 368 (1): 41-8.
	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.
	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.
	Solid-phase synthesis and biological activity of a thioether analogue of conotoxin G1., Bondebjerg J., Chembiochem. March 3, 2003; 4 (2-3): 186-94.
	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.
	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.
	A novel conus peptide ligand for K+ channels., Ferber M., J Biol Chem. January 24, 2003; 278 (4): 2177-83.
	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.
	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.
	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.
	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.
	Inhibition of neuronal nicotinic acetylcholine receptors by the abused solvent, toluene., Bale AS., Br J Pharmacol. October 1, 2002; 137 (3): 375-83.
	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.
	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.
	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.
	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.
	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.
	The novel diazoxide analog 3-isopropylamino-7-methoxy-4H-1,2,4-benzothiadiazine 1,1-dioxide is a selective Kir6.2/SUR1 channel opener., Dabrowski M., Diabetes. June 1, 2002; 51 (6): 1896-906.
	Flavonoid inhibition of sodium-dependent vitamin C transporter 1 (SVCT1) and glucose transporter isoform 2 (GLUT2), intestinal transporters for vitamin C and Glucose., Song J., J Biol Chem. May 3, 2002; 277 (18): 15252-60.
	From intestine to muscle: nuclear reprogramming through defective cloned embryos., Byrne JA., Proc Natl Acad Sci U S A. April 30, 2002; 99 (9): 6059-63.
	Identification of the erythrocyte Rh blood group glycoprotein as a mammalian ammonium transporter., Westhoff CM., J Biol Chem. April 12, 2002; 277 (15): 12499-502.

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