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Antipsychotic clozapine inhibits the function of alpha7-nicotinic acetylcholine receptors. , Singhal SK., Neuropharmacology. February 1, 2007; 52 (2): 387-94.
Lead discovery and optimization of T-type calcium channel blockers. , Park JH ., Bioorg Med Chem. February 1, 2007; 15 (3): 1409-19.
Inhibition by bis(7)-tacrine of native delayed rectifier and KV1.2 encoded potassium channels. , Nie H., Neurosci Lett. January 29, 2007; 412 (2): 108-13.
3D pharmacophore based virtual screening of T-type calcium channel blockers. , Doddareddy MR., Bioorg Med Chem. January 15, 2007; 15 (2): 1091-105.
The effect of high extracellular potassium on IKr inhibition by anti-arrhythmic agents. , Lin C., Cardiology. January 1, 2007; 108 (1): 18-27.
Evidence for significant contribution of a newly identified monoamine transporter (PMAT) to serotonin uptake in the human brain. , Zhou M., Biochem Pharmacol. January 1, 2007; 73 (1): 147-54.
Cyclophane and acyclic cyclophane: novel channel blockers of N-methyl-D-aspartate receptor. , Masuko T., Neurochem Int. January 1, 2007; 50 (2): 443-9.
Niflumic acid inhibits chloride conductance of rat skeletal muscle by directly inhibiting the CLC-1 channel and by increasing intracellular calcium. , Liantonio A., Br J Pharmacol. January 1, 2007; 150 (2): 235-47.
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.
Frizzled7 mediates canonical Wnt signaling in neural crest induction. , Abu-Elmagd M., Dev Biol. October 1, 2006; 298 (1): 285-98.
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.
Characterization and function of the bHLH-O protein XHes2: insight into the mechanisms controlling retinal cell fate decision. , Sölter M., Development. October 1, 2006; 133 (20): 4097-108.
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.
Grainyhead-like 3, a transcription factor identified in a microarray screen, promotes the specification of the superficial layer of the embryonic epidermis. , Chalmers AD ., Mech Dev. September 1, 2006; 123 (9): 702-18.
Slug stability is dynamically regulated during neural crest development by the F-box protein Ppa. , Vernon AE., Development. September 1, 2006; 133 (17): 3359-70.
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.
Radial intercalation of ciliated cells during Xenopus skin development. , Stubbs JL., Development. July 1, 2006; 133 (13): 2507-15.
Induction and specification of cranial placodes. , Schlosser G ., Dev Biol. June 15, 2006; 294 (2): 303-51.
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.
The MRH protein Erlectin is a member of the endoplasmic reticulum synexpression group and functions in N-glycan recognition. , Cruciat CM., J Biol Chem. May 5, 2006; 281 (18): 12986-93.
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.
Dystroglycan is required for proper retinal layering. , Lunardi A ., Dev Biol. February 15, 2006; 290 (2): 411-20.
Ras-dva, a member of novel family of small GTPases, is required for the anterior ectoderm patterning in the Xenopus laevis embryo. , Tereshina MB., Development. February 1, 2006; 133 (3): 485-94.
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.
Msx1 and Msx2 have shared essential functions in neural crest but may be dispensable in epidermis and axis formation in Xenopus. , Khadka D., Int J Dev Biol. January 1, 2006; 50 (5): 499-502.
Tsukushi controls ectodermal patterning and neural crest specification in Xenopus by direct regulation of BMP4 and X-delta-1 activity. , Kuriyama S ., Development. January 1, 2006; 133 (1): 75-88.
Early steps in neural crest specification. , Barembaum M., Semin Cell Dev Biol. December 1, 2005; 16 (6): 642-6.
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.
An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation. , Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system. , Huang X ., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
Binding of hnRNP L to the pre-mRNA processing enhancer of the herpes simplex virus thymidine kinase gene enhances both polyadenylation and nucleocytoplasmic export of intronless mRNAs. , Guang S., Mol Cell Biol. August 1, 2005; 25 (15): 6303-13.
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.