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	NSC348884, a nucleophosmin inhibitor disrupts oligomer formation and induces apoptosis in human cancer cells., Qi W., Oncogene. July 10, 2008; 27 (30): 4210-20.
	Inhibition of cardiac hERG potassium channels by tetracyclic antidepressant mianserin., Scherer D., Naunyn Schmiedebergs Arch Pharmacol. July 1, 2008; 378 (1): 73-83.
	Is TEA an inhibitor for human Aquaporin-1?, Müller EM., Pflugers Arch. July 1, 2008; 456 (4): 663-9.
	Identification of a new urate and high affinity nicotinate transporter, hOAT10 (SLC22A13)., Bahn A., J Biol Chem. June 13, 2008; 283 (24): 16332-41.
	Cyclothiazide: a subunit-specific inhibitor of GABAC receptors., Xie A., J Physiol. June 1, 2008; 586 (11): 2743-52.
	Gambierol, a toxin produced by the dinoflagellate Gambierdiscus toxicus, is a potent blocker of voltage-gated potassium channels., Cuypers E., Toxicon. May 1, 2008; 51 (6): 974-83.
	Ethanol inhibits functional activity of the human intestinal dipeptide transporter hPepT1 expressed in Xenopus oocytes., Li K., Alcohol Clin Exp Res. May 1, 2008; 32 (5): 777-84.
	An extracellular Cu2+ binding site in the voltage sensor of BK and Shaker potassium channels., Ma Z., J Gen Physiol. May 1, 2008; 131 (5): 483-502.
	Kadsuracoccinic acids A-C, ring-A seco-lanostane triterpenes from Kadsura coccinea and their effects on embryonic cell division of Xenopus laevis., Li H., J Nat Prod. April 1, 2008; 71 (4): 739-41.
	Antimalarial drugs inhibit human 5-HT(3) and GABA(A) but not GABA(C) receptors., Thompson AJ., Br J Pharmacol. April 1, 2008; 153 (8): 1686-96.
	Hypotonic stimuli enhance proton-gated currents of acid-sensing ion channel-1b., Ugawa S., Biochem Biophys Res Commun. March 14, 2008; 367 (3): 530-4.
	Modulation of voltage-gated Na+ and K+ channels by pumiliotoxin 251D: a "joint venture" alkaloid from arthropods and amphibians., Vandendriessche T., Toxicon. March 1, 2008; 51 (3): 334-44.
	Ion binding in the open HCN pacemaker channel pore: fast mechanisms to shape "slow" channels., Lyashchenko AK., J Gen Physiol. March 1, 2008; 131 (3): 227-43.
	Rohon-Beard sensory neurons are induced by BMP4 expressing non-neural ectoderm in Xenopus laevis., Rossi CC., Dev Biol. February 15, 2008; 314 (2): 351-61.
	Characterization of a novel psi-conotoxin from Conus parius Reeve., Lluisma AO., Toxicon. February 1, 2008; 51 (2): 174-80.
	Protriptyline block of the human ether-à-go-go-related gene (HERG) K+ channel., Jo SH., Life Sci. January 30, 2008; 82 (5-6): 331-40.
	Extracellular acidification and hyperkalemia induce changes in HERG inhibition by ibutilide., Lin C., Cardiology. January 1, 2008; 110 (3): 209-16.
	The additive effects of the active component of grapefruit juice (naringenin) and antiarrhythmic drugs on HERG inhibition., Lin C., Cardiology. January 1, 2008; 110 (3): 145-52.
	Convergence of a head-field selector Otx2 and Notch signaling: a mechanism for lens specification., Ogino H., Development. January 1, 2008; 135 (2): 249-58.
	Defining an inhibitory domain in the alpha-subunit of the epithelial sodium channel., Carattino MD., Am J Physiol Renal Physiol. January 1, 2008; 294 (1): F47-52.
	The role of glial cells in the formation and maintenance of the neuromuscular junction., Feng Z., Ann N Y Acad Sci. January 1, 2008; 1132 19-28.
	Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis., Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
	Effects of resveratrol, a grape polyphenol, on catecholamine secretion and synthesis in cultured bovine adrenal medullary cells., Shinohara Y., Biochem Pharmacol. December 3, 2007; 74 (11): 1608-18.
	Anticholinergic antiparkinson drug orphenadrine inhibits HERG channels: block attenuation by mutations of the pore residues Y652 or F656., Scholz EP., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2007; 376 (4): 275-84.
	Nafamostat mesilate reversibly blocks acid-sensing ion channel currents., Ugawa S., Biochem Biophys Res Commun. November 9, 2007; 363 (1): 203-8.
	The endogenous cannabinoid anandamide inhibits cromakalim-activated K+ currents in follicle-enclosed Xenopus oocytes., Oz M., J Pharmacol Exp Ther. November 1, 2007; 323 (2): 547-54.
	Transport of butyryl-L-carnitine, a potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB(0,+)., Srinivas SR., Am J Physiol Gastrointest Liver Physiol. November 1, 2007; 293 (5): G1046-53.
	Tripeptides of RS1 (RSC1A1) inhibit a monosaccharide-dependent exocytotic pathway of Na+-D-glucose cotransporter SGLT1 with high affinity., Vernaleken A., J Biol Chem. September 28, 2007; 282 (39): 28501-13.
	Molecular mapping of the binding site for a blocker of hyperpolarization-activated, cyclic nucleotide-modulated pacemaker channels., Cheng L., J Pharmacol Exp Ther. September 1, 2007; 322 (3): 931-9.
	Identification of cysteines in rat organic cation transporters rOCT1 (C322, C451) and rOCT2 (C451) critical for transport activity and substrate affinity., Sturm A., Am J Physiol Renal Physiol. September 1, 2007; 293 (3): F767-79.
	How old genes make a new head: redeployment of Six and Eya genes during the evolution of vertebrate cranial placodes., Schlosser G., Integr Comp Biol. September 1, 2007; 47 (3): 343-59.
	Bacterial expression, NMR, and electrophysiology analysis of chimeric short/long-chain alpha-neurotoxins acting on neuronal nicotinic receptors., Lyukmanova EN., J Biol Chem. August 24, 2007; 282 (34): 24784-91.
	Targeting of retinal axons requires the metalloproteinase ADAM10., Chen YY., J Neurosci. August 1, 2007; 27 (31): 8448-56.
	Lobeline, a potential pharmacotherapy for drug addiction, binds to mu opioid receptors and diminishes the effects of opioid receptor agonists., Miller DK., Drug Alcohol Depend. July 10, 2007; 89 (2-3): 282-91.
	Phosphonic acid analogs of GABA through reductive dealkylation of phosphonic diesters with lithium trialkylborohydrides., Chowdhury S., Bioorg Med Chem Lett. July 1, 2007; 17 (13): 3745-8.
	Partial agonist and neuromodulatory activity of S 24795 for alpha7 nAChR responses of hippocampal interneurons., Lopez-Hernandez G., Neuropharmacology. July 1, 2007; 53 (1): 134-44.
	The antimalarial drugs quinine, chloroquine and mefloquine are antagonists at 5-HT3 receptors., Thompson AJ., Br J Pharmacol. July 1, 2007; 151 (5): 666-77.
	Verapamil blocks HERG channel by the helix residue Y652 and F656 in the S6 transmembrane domain., Duan JJ., Acta Pharmacol Sin. July 1, 2007; 28 (7): 959-67.
	Integrated microsystem for non-invasive electrophysiological measurements on Xenopus oocytes., Dahan E., Biosens Bioelectron. June 15, 2007; 22 (12): 3196-202.
	Effects of dextrorotatory morphinans on brain Na+ channels expressed in Xenopus oocytes., Lee JH, Lee JH., Eur J Pharmacol. June 14, 2007; 564 (1-3): 7-17.
	The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.
	Cloning and developmental expression of the Xenopus Nkx6 genes., Zhao S., Dev Genes Evol. June 1, 2007; 217 (6): 477-83.
	Isolation of the first toxin from the scorpion Buthus occitanus israelis showing preference for Shaker potassium channels., Kozminsky-Atias A., FEBS Lett. May 29, 2007; 581 (13): 2478-84.
	W-7 modulates Kv4.3: pore block and Ca2+-calmodulin inhibition., Qu YJ., Am J Physiol Heart Circ Physiol. May 1, 2007; 292 (5): H2364-77.
	Point mutations at the local anesthetic receptor site modulate the state-dependent block of rat Na v1.4 sodium channels by pyrazoline-type insecticides., Silver KS., Neurotoxicology. May 1, 2007; 28 (3): 655-63.
	The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.
	Modulation of ERG channels by XE991., Elmedyb P., Basic Clin Pharmacol Toxicol. May 1, 2007; 100 (5): 316-22.
	Role of homologous ASP334 and GLU319 in human non-gastric H,K- and Na,K-ATPases in cardiac glycoside binding., Radkov R., Biochem Biophys Res Commun. April 27, 2007; 356 (1): 142-6.
	A novel gene, BENI is required for the convergent extension during Xenopus laevis gastrulation., Homma M., Dev Biol. March 1, 2007; 303 (1): 270-80.
	Identification of ginsenoside interaction sites in 5-HT3A receptors., Lee BH., Neuropharmacology. March 1, 2007; 52 (4): 1139-50.

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