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Summary Anatomy Item Literature (624) Expression Attributions Wiki
XB-ANAT-1585

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Specification of ion transport cells in the Xenopus larval skin., Quigley IK., Development. February 1, 2011; 138 (4): 705-14.                                          


Quercetin Inhibits α3β4 Nicotinic Acetylcholine Receptor-Mediated Ion Currents Expressed in Xenopus Oocytes., Lee BH., Korean J Physiol Pharmacol. February 1, 2011; 15 (1): 17-22.


Molecular diversity and functional evolution of scorpion potassium channel toxins., Zhu S., Mol Cell Proteomics. February 1, 2011; 10 (2): M110.002832.


Amino acid derivatives are substrates or non-transported inhibitors of the amino acid transporter PAT2 (slc36a2)., Edwards N., Biochim Biophys Acta. January 1, 2011; 1808 (1): 260-70.                


Ginkgolide B and bilobalide block the pore of the 5-HT₃receptor at a location that overlaps the picrotoxin binding site., Thompson AJ., Neuropharmacology. January 1, 2011; 60 (2-3): 488-95.        


Quantification of the Mg2+-induced potency shift of amantadine and memantine voltage-dependent block in human recombinant GluN1/GluN2A NMDARs., Otton HJ., Neuropharmacology. January 1, 2011; 60 (2-3): 388-96.


Geminin cooperates with Polycomb to restrain multi-lineage commitment in the early embryo., Lim JW., Development. January 1, 2011; 138 (1): 33-44.                    


Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.                  


Acquisition of glial cells missing 2 enhancers contributes to a diversity of ionocytes in zebrafish., Shono T., PLoS One. January 1, 2011; 6 (8): e23746.              


The RNA-binding protein Xp54nrb isolated from a Ca²+-dependent screen is expressed in neural structures during Xenopus laevis development., Neant I., Int J Dev Biol. January 1, 2011; 55 (10-12): 923-31.        


A potent potassium channel blocker from Mesobuthus eupeus scorpion venom., Gao B., Biochimie. December 1, 2010; 92 (12): 1847-53.


Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors., Neilson KM., Dev Dyn. December 1, 2010; 239 (12): 3446-66.                                                                          


α-Conotoxin BuIA[T5A;P6O]: a novel ligand that discriminates between α6ß4 and α6ß2 nicotinic acetylcholine receptors and blocks nicotine-stimulated norepinephrine release., Azam L., FASEB J. December 1, 2010; 24 (12): 5113-23.


Aminoglycoside block of P2X2 receptors heterologously expressed in Xenopus laevis oocytes., Bongartz EV., Purinergic Signal. December 1, 2010; 6 (4): 393-403.


Open channel block of the fast transient outward K+ current by primaquine and chloroquine in rat left ventricular cardiomyocytes., Wagner M., Eur J Pharmacol. November 25, 2010; 647 (1-3): 13-20.


The effect of Δ9-tetrahydrocannabinol on 5-HT3 receptors depends on the current density., Yang KH., Neuroscience. November 24, 2010; 171 (1): 40-9.


Inhibition of thyroid hormone release from cultured amphibian thyroid glands by methimazole, 6-propylthiouracil, and perchlorate., Hornung MW., Toxicol Sci. November 1, 2010; 118 (1): 42-51.


Inhibition of TRPV1 for the treatment of sensitive skin., Kueper T., Exp Dermatol. November 1, 2010; 19 (11): 980-6.


Assessment of structurally diverse philanthotoxin analogues for inhibitory activity on ionotropic glutamate receptor subtypes: discovery of nanomolar, nonselective, and use-dependent antagonists., Frølund S., J Med Chem. October 28, 2010; 53 (20): 7441-51.


The inhibition of monocarboxylate transporter 2 (MCT2) by AR-C155858 is modulated by the associated ancillary protein., Ovens MJ., Biochem J. October 15, 2010; 431 (2): 217-25.              


Identification of selective norbornane-type aspartate analogue inhibitors of the glutamate transporter 1 (GLT-1) from the chemical universe generated database (GDB)., Luethi E., J Med Chem. October 14, 2010; 53 (19): 7236-50.


Development of a novel selective inhibitor of the Down syndrome-related kinase Dyrk1A., Ogawa Y., Nat Commun. October 5, 2010; 1 86.  


Intestinal absorption of HMG-CoA reductase inhibitor pravastatin mediated by organic anion transporting polypeptide., Shirasaka Y., Pharm Res. October 1, 2010; 27 (10): 2141-9.


Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies., Pörksen S., BMC Endocr Disord. September 23, 2010; 10 16.      


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.


Aconitine blocks HERG and Kv1.5 potassium channels., Li Y., J Ethnopharmacol. August 19, 2010; 131 (1): 187-95.


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.  


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.


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.                                                      


[Inhibition of Jingzhaotoxin-V on Kv4.3 channel]., Cai LJ., Sheng Li Xue Bao. June 25, 2010; 62 (3): 255-60.


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.


Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.                              


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.


B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo., Okuda Y., PLoS Genet. May 6, 2010; 6 (5): e1000936.                


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.


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.


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.


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.


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 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.


Kaitocephalin antagonism of glutamate receptors expressed in Xenopus oocytes., Limon A., ACS Chem Neurosci. March 17, 2010; 1 (3): 175-181.


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.


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.                  


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 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.                              


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.

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