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Summary Anatomy Item Literature (101) Expression Attributions Wiki
XB-ANAT-3761

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NSrp70 is significant for embryonic growth and development, being a crucial factor for gastrulation and mesoderm induction., Lee SH., Biochem Biophys Res Commun. October 14, 2016; 479 (2): 238-244.        


Xenopus pax6 mutants affect eye development and other organ systems, and have phenotypic similarities to human aniridia patients., Nakayama T., Dev Biol. December 15, 2015; 408 (2): 328-44.                              


Inhibition of AMPA receptors by polyamine toxins is regulated by agonist efficacy and stargazin., Poulsen MH., Neurochem Res. October 1, 2014; 39 (10): 1906-13.


On-site energy supply at synapses through monocarboxylate transporters maintains excitatory synaptic transmission., Nagase M., J Neurosci. February 12, 2014; 34 (7): 2605-17.


Characterization of the insulin-like growth factor binding protein family in Xenopus tropicalis., Haramoto Y., Int J Dev Biol. January 1, 2014; 58 (9): 705-11.                                            


The orthosteric GABAA receptor ligand Thio-4-PIOL displays distinctly different functional properties at synaptic and extrasynaptic receptors., Hoestgaard-Jensen K., Br J Pharmacol. October 1, 2013; 170 (4): 919-32.


AMPA receptor/TARP stoichiometry visualized by single-molecule subunit counting., Hastie P., Proc Natl Acad Sci U S A. March 26, 2013; 110 (13): 5163-8.


Identification and evolution of molecular domains involved in differentiating the cement gland-promoting activity of Otx proteins in Xenopus laevis., Mancini P., Mech Dev. January 1, 2013; 130 (11-12): 628-39.          


α4βδ GABA(A) receptors are high-affinity targets for γ-hydroxybutyric acid (GHB)., Absalom N., Proc Natl Acad Sci U S A. August 14, 2012; 109 (33): 13404-9.


Transport properties of melanosomes along microtubules interpreted by a tug-of-war model with loose mechanical coupling., Bouzat S., PLoS One. January 1, 2012; 7 (8): e43599.                    


Modulation of human GABAA receptor function: a novel mode of action of drugs of abuse., Hondebrink L., Neurotoxicology. December 1, 2011; 32 (6): 823-7.


A new phenylalanine derivative acts as an antagonist at the AMPA receptor GluA2 and introduces partial domain closure: synthesis, resolution, pharmacology, and crystal structure., Szymańska E., J Med Chem. October 27, 2011; 54 (20): 7289-98.


Homeostatic NMDA receptor down-regulation via brain derived neurotrophic factor and nitric oxide-dependent signalling in cortical but not in hippocampal neurons., Sandoval R., J Neurochem. September 1, 2011; 118 (5): 760-72.


Functional rundown of gamma-aminobutyric acid(A) receptors in human hypothalamic hamartomas., Li G., Ann Neurol. April 1, 2011; 69 (4): 664-72.


Monitoring voltage-dependent charge displacement of Shaker B-IR K+ ion channels using radio frequency interrogation., Dharia S., PLoS One. February 4, 2011; 6 (2): e17363.          


Loss of ethanol conditioned taste aversion and motor stimulation in knockin mice with ethanol-insensitive α2-containing GABA(A) receptors., Blednov YA., J Pharmacol Exp Ther. January 1, 2011; 336 (1): 145-54.


Inhaled anesthetic responses of recombinant receptors and knockin mice harboring α2(S270H/L277A) GABA(A) receptor subunits that are resistant to isoflurane., Werner DF., J Pharmacol Exp Ther. January 1, 2011; 336 (1): 134-44.


Biostructural and pharmacological studies of bicyclic analogues of the 3-isoxazolol glutamate receptor agonist ibotenic acid., Frydenvang K., J Med Chem. December 9, 2010; 53 (23): 8354-61.


The glutamate receptor GluR5 agonist (S)-2-amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid and the 8-methyl analogue: synthesis, molecular pharmacology, and biostructural characterization., Clausen RP., J Med Chem. August 13, 2009; 52 (15): 4911-22.


Caenorhabditis elegans glutamate transporter deletion induces AMPA-receptor/adenylyl cyclase 9-dependent excitotoxicity., Mano I., J Neurochem. March 1, 2009; 108 (6): 1373-84.


Development of the proepicardium in Xenopus laevis., Jahr M., Dev Dyn. October 1, 2008; 237 (10): 3088-96.                      


How ATP inhibits the open K(ATP) channel., Craig TJ., J Gen Physiol. July 1, 2008; 132 (1): 131-44.            


Pharmacological Properties of DOV 315,090, an ocinaplon metabolite., Berezhnoy D., BMC Pharmacol. June 13, 2008; 8 11.        


The tektin family of microtubule-stabilizing proteins., Amos LA., Genome Biol. January 1, 2008; 9 (7): 229.      


A specific box switches the cell fate determining activity of XOTX2 and XOTX5b in the Xenopus retina., Onorati M., Neural Dev. June 27, 2007; 2 12.            


Antagonistic effects of TrkB and p75(NTR) on NMDA receptor currents in post-synaptic densities transplanted into Xenopus oocytes., Sandoval M., J Neurochem. June 1, 2007; 101 (6): 1672-84.


Shark rectal gland vasoactive intestinal peptide receptor: cloning, functional expression, and regulation of CFTR chloride channels., Bewley MS., Am J Physiol Regul Integr Comp Physiol. October 1, 2006; 291 (4): R1157-64.


3-hydroxypyridazine 1-oxides as carboxylate bioisosteres: a new series of subtype-selective AMPA receptor agonists., Greenwood JR., Neuropharmacology. July 1, 2006; 51 (1): 52-9.


Interleukin-1beta enhances GABAA receptor cell-surface expression by a phosphatidylinositol 3-kinase/Akt pathway: relevance to sepsis-associated encephalopathy., Serantes R., J Biol Chem. May 26, 2006; 281 (21): 14632-43.


Functional characterisation of homomeric ionotropic glutamate receptors GluR1-GluR6 in a fluorescence-based high throughput screening assay., Strange M., Comb Chem High Throughput Screen. February 1, 2006; 9 (2): 147-58.


Phosphorylation of Y14 modulates its interaction with proteins involved in mRNA metabolism and influences its methylation., Hsu IaW., J Biol Chem. October 14, 2005; 280 (41): 34507-12.


Tetrazolyl isoxazole amino acids as ionotropic glutamate receptor antagonists: synthesis, modelling and molecular pharmacology., Frølund B., Bioorg Med Chem. September 15, 2005; 13 (18): 5391-8.


Structural determinants of agonist-specific kinetics at the ionotropic glutamate receptor 2., Holm MM., Proc Natl Acad Sci U S A. August 23, 2005; 102 (34): 12053-8.


Go G-proteins mediate rapid heterologous desensitization of G-protein coupled receptors in Xenopus oocytes., Van-Ham II., J Cell Physiol. August 1, 2005; 204 (2): 455-62.


Cloning, characterization and expression of the D2 dopamine receptor from the tilapia pituitary., Levavi-Sivan B., Mol Cell Endocrinol. May 31, 2005; 236 (1-2): 17-30.


Rett syndrome: clinical review and genetic update., Weaving LS., J Med Genet. January 1, 2005; 42 (1): 1-7.


Synthesis, theoretical and structural analyses, and enantiopharmacology of 3-carboxy homologs of AMPA., Brehm L., Chirality. August 1, 2004; 16 (7): 452-66.


Regulation of gonadotropin-releasing hormone receptors by protein kinase C: inside out signalling and evidence for multiple active conformations., Caunt CJ., Endocrinology. August 1, 2004; 145 (8): 3594-602.


Partial involvement of group I metabotropic glutamate receptors in the neurotoxicity of 3-N-oxalyl-L-2,3-diaminopropanoic acid (L-beta-ODAP)., Kusama-Eguchi K., Biol Pharm Bull. July 1, 2004; 27 (7): 1052-8.


Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.        


The effects of isoflurane on desensitized wild-type and alpha 1(S270H) gamma-aminobutyric acid type A receptors., Hall AC., Anesth Analg. May 1, 2004; 98 (5): 1297-304, table of contents.


R-citalopram functionally antagonises escitalopram in vivo and in vitro: evidence for kinetic interaction at the serotonin transporter., Stórustovu Sí., Br J Pharmacol. May 1, 2004; 142 (1): 172-80.


Signaling and antiproliferative effects of type I and II gonadotropin-releasing hormone receptors in breast cancer cells., Finch AR., J Clin Endocrinol Metab. April 1, 2004; 89 (4): 1823-32.


Evidence for the involvement of GABA(A) receptor blockade in convulsions induced by cephalosporins., Sugimoto M., Neuropharmacology. September 1, 2003; 45 (3): 304-14.


Design, synthesis, and pharmacology of a highly subtype-selective GluR1/2 agonist, (RS)-2-amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic acid (Cl-HIBO)., Bjerrum EJ., J Med Chem. May 22, 2003; 46 (11): 2246-9.


(S)-2-Amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid, a potent and selective agonist at the GluR5 subtype of ionotropic glutamate receptors. Synthesis, modeling, and molecular pharmacology., Brehm L., J Med Chem. April 10, 2003; 46 (8): 1350-8.


Differences in potency and efficacy of a series of phenylisopropylamine/phenylethylamine pairs at 5-HT(2A) and 5-HT(2C) receptors., Acuña-Castillo C., Br J Pharmacol. June 1, 2002; 136 (4): 510-9.


The gonadotrophin-releasing hormone receptor: signalling, cycling and desensitisation., McArdle CA., Arch Physiol Biochem. April 1, 2002; 110 (1-2): 113-22.


Signalling, cycling and desensitisation of gonadotrophin-releasing hormone receptors., McArdle CA., J Endocrinol. April 1, 2002; 173 (1): 1-11.


The binding of lamin B receptor to chromatin is regulated by phosphorylation in the RS region., Takano M., Eur J Biochem. February 1, 2002; 269 (3): 943-53.

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