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Colchicine: a novel positive allosteric modulator of the human 5-hydroxytryptamine3A receptor. , de Oliveira-Pierce AN., J Pharmacol Exp Ther. May 1, 2009; 329 (2): 838-47.
A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds. , Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx. , Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
Southeast Asian AE1 associated renal tubular acidosis: cation leak is a class effect. , Walsh S., Biochem Biophys Res Commun. May 15, 2009; 382 (4): 668-72.
Syndecan-1 regulates BMP signaling and dorso- ventral patterning of the ectoderm during early Xenopus development. , Olivares GH., Dev Biol. May 15, 2009; 329 (2): 338-49.
Pharmacological characteristics of the inhibition of nondepolarizing neuromuscular blocking agents at human adult muscle nicotinic acetylcholine receptor. , Jonsson Fagerlund M., Anesthesiology. June 1, 2009; 110 (6): 1244-52.
Block of HERG k channel by classic histamine h(1) receptor antagonist chlorpheniramine. , Hong HK., Korean J Physiol Pharmacol. June 1, 2009; 13 (3): 215-20.
Discovery of spiro-piperidine inhibitors and their modulation of the dynamics of the M2 proton channel from influenza A virus. , Wang J ., J Am Chem Soc. June 17, 2009; 131 (23): 8066-76.
Chemical synthesis and folding of APETx2, a potent and selective inhibitor of acid sensing ion channel 3. , Jensen JE., Toxicon. July 1, 2009; 54 (1): 56-61.
Inhibition of aquaporin-1 and aquaporin-4 water permeability by a derivative of the loop diuretic bumetanide acting at an internal pore-occluding binding site. , Migliati E., Mol Pharmacol. July 1, 2009; 76 (1): 105-12.
TWIK-1 and TREK-1 are potassium channels contributing significantly to astrocyte passive conductance in rat hippocampal slices. , Zhou M., J Neurosci. July 1, 2009; 29 (26): 8551-64.
State-dependent accessibility of the P-S6 linker of pacemaker (HCN) channels supports a dynamic pore-to-gate coupling model. , Siu CW., J Membr Biol. July 1, 2009; 230 (1): 35-47.
Quinazolindione derivatives as potent 5-HT3A receptor antagonists. , Lee BH., Bioorg Med Chem. July 1, 2009; 17 (13): 4793-6.
Effects of triterpenoids from Poria cocos Wolf on the serotonin type 3A receptor-mediated ion current in Xenopus oocytes. , Lee JH , Lee JH ., Eur J Pharmacol. August 1, 2009; 615 (1-3): 27-32.
Xhairy2 functions in Xenopus lens development by regulating p27( xic1) expression. , Murato Y., Dev Dyn. September 1, 2009; 238 (9): 2179-92.
Alternatives to animal experimentation for hormonal compounds research. , Penza M., Genes Nutr. September 1, 2009; 4 (3): 165-72.
Guanidino acids act as rho1 GABA(C) receptor antagonists. , Chebib M., Neurochem Res. October 1, 2009; 34 (10): 1704-11.
A novel fluorescent alpha-conotoxin for the study of alpha7 nicotinic acetylcholine receptors. , Hone AJ., J Neurochem. October 1, 2009; 111 (1): 80-9.
GABA analogues derived from 4-aminocyclopent-1-enecarboxylic acid. , Locock KE., Neurochem Res. October 1, 2009; 34 (10): 1698-703.
H(1) antihistamine drug promethazine directly blocks hERG K(+) channel. , Jo SH., Pharmacol Res. November 1, 2009; 60 (5): 429-37.
The actions of chloride channel blockers, barbiturates and a benzodiazepine on Caenorhabditis elegans glutamate- and ivermectin-gated chloride channel subunits expressed in Xenopus oocytes. , Bush E., Invert Neurosci. December 1, 2009; 9 (3-4): 175-84.
Functional expression of an arachnid sodium channel reveals residues responsible for tetrodotoxin resistance in invertebrate sodium channels. , Du Y., J Biol Chem. December 4, 2009; 284 (49): 33869-75.
Intein-mediated site-specific conjugation of Quantum Dots to proteins in vivo. , Charalambous A., J Nanobiotechnology. December 10, 2009; 7 9.
Species difference in the effect of grapefruit juice on intestinal absorption of talinolol between human and rat. , Shirasaka Y., J Pharmacol Exp Ther. January 1, 2010; 332 (1): 181-9.
Differential effects of ICA-27243 on cloned K(V)7 channels. , Blom SM., Pharmacology. January 1, 2010; 86 (3): 174-81.
The F-box protein Cdc4/ Fbxw7 is a novel regulator of neural crest development in Xenopus laevis. , Almeida AD., Neural Dev. January 4, 2010; 5 1.
Inhibition of human alpha4beta2 neuronal nicotinic acetylcholine receptors by volatile aromatic anesthetics depends on drug hydrophobicity. , Solt K., Anesth Analg. February 1, 2010; 110 (2): 455-60.
The human cardiac K2P3.1 ( TASK-1) potassium leak channel is a molecular target for the class III antiarrhythmic drug amiodarone. , Gierten J., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2010; 381 (3): 261-70.
Blocking effect of methylflavonolamine on human Na(V)1.5 channels expressed in Xenopus laevis oocytes and on sodium currents in rabbit ventricular myocytes. , Fan XR., Acta Pharmacol Sin. March 1, 2010; 31 (3): 297-306.
Structural and functional characterization of a novel homodimeric three-finger neurotoxin from the venom of Ophiophagus hannah (king cobra). , Roy A., J Biol Chem. March 12, 2010; 285 (11): 8302-15.
Kaitocephalin antagonism of glutamate receptors expressed in Xenopus oocytes. , Limon A., ACS Chem Neurosci. March 17, 2010; 1 (3): 175-181.
Block effect of capsaicin on hERG potassium currents is enhanced by S6 mutation at Y652. , Xing J., Eur J Pharmacol. March 25, 2010; 630 (1-3): 1-9.
Long-term consequences of Sox9 depletion on inner ear development. , Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis. , Morita H., Development. April 1, 2010; 137 (8): 1315-25.
Block of the human ether-a- go-go-related gene ( hERG) K+ channel by the antidepressant desipramine. , Hong HK., Biochem Biophys Res Commun. April 9, 2010; 394 (3): 536-41.
Atypical alpha-conotoxin LtIA from Conus litteratus targets a novel microsite of the alpha3beta2 nicotinic receptor. , Luo S., J Biol Chem. April 16, 2010; 285 (16): 12355-66.
A region of N-type Ca(2+) channel critical for blockade by the dihydropyridine amlodipine. , Miyashita Y., Eur J Pharmacol. April 25, 2010; 632 (1-3): 14-22.
Multiple mechanisms of hERG liability: K+ current inhibition, disruption of protein trafficking, and apoptosis induced by amoxapine. , Obers S., Naunyn Schmiedebergs Arch Pharmacol. May 1, 2010; 381 (5): 385-400.
B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo. , Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.
Biochemical characterization of kappaM-RIIIJ, a Kv1.2 channel blocker: evaluation of cardioprotective effects of kappaM-conotoxins. , Chen P., J Biol Chem. May 14, 2010; 285 (20): 14882-14889.
Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2. , Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
Molecular determinants of Kv1.5 channel block by diphenyl phosphine oxide-1. , Du YM., J Mol Cell Cardiol. June 1, 2010; 48 (6): 1111-20.
From genes to neural tube defects (NTDs): insights from multiscale computational modeling. , Brodland GW., HFSP J. June 1, 2010; 4 (3-4): 142-52.
[Inhibition of Jingzhaotoxin-V on Kv4.3 channel]. , Cai LJ., Sheng Li Xue Bao. June 25, 2010; 62 (3): 255-60.
MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization. , Suzuki M ., Development. July 1, 2010; 137 (14): 2329-39.
Ginsenoside Rg3 activates human KCNQ1 K+ channel currents through interacting with the K318 and V319 residues: a role of KCNE1 subunit. , Choi SH., Eur J Pharmacol. July 10, 2010; 637 (1-3): 138-47.
Alexa Fluor 546-ArIB[V11L;V16A] is a potent ligand for selectively labeling alpha 7 nicotinic acetylcholine receptors. , Hone AJ., J Neurochem. August 1, 2010; 114 (4): 994-1006.
Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR. , Sato S., Dev Biol. August 1, 2010; 344 (1): 158-71.
Aconitine blocks HERG and Kv1.5 potassium channels. , Li Y., J Ethnopharmacol. August 19, 2010; 131 (1): 187-95.
Investigations into the role of the Plasmodium falciparum SERCA (PfATP6) L263E mutation in artemisinin action and resistance. , Valderramos SG., Antimicrob Agents Chemother. September 1, 2010; 54 (9): 3842-52.