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Summary Expression Phenotypes Gene Literature (110) GO Terms (5) Nucleotides (168) Proteins (72) Interactants (158) Wiki
XB-GENEPAGE-995620

Papers associated with gria1



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Molecular cloning and functional expression of glutamate receptor subunit genes., Boulter J, Hollmann M, O'Shea-Greenfield A, Hartley M, Deneris E, Maron C, Heinemann S., Science. August 31, 1990; 249 (4972): 1033-7.

Functional expression from cloned cDNAs of glutamate receptor species responsive to kainate and quisqualate., Sakimura K, Bujo H, Kushiya E, Araki K, Yamazaki M, Meguro H, Warashina A, Numa S, Mishina M., FEBS Lett. October 15, 1990; 272 (1-2): 73-80.

Cloning of a novel glutamate receptor subunit, GluR5: expression in the nervous system during development., Bettler B, Boulter J, Hermans-Borgmeyer I, O'Shea-Greenfield A, Deneris ES, Moll C, Borgmeyer U, Hollmann M, Heinemann S., Neuron. November 1, 1990; 5 (5): 583-95.

Homomeric GluR1 excitatory amino acid receptors expressed in Xenopus oocytes., Dawson TL, Nicholas RA, Dingledine R., Mol Pharmacol. December 1, 1990; 38 (6): 779-84.

Electrophysiological and pharmacological properties of GluR1, a subunit of a glutamate receptor-channel expressed in Xenopus oocytes., Lambolez B, Curutchet P, Stinnakre J, Bregestovski P, Rossier J, Prado de Carvalho L., Neurosci Lett. February 11, 1991; 123 (1): 69-72.

Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition., Hollmann M, Hartley M, Heinemann S., Science. May 10, 1991; 252 (5007): 851-3.

Cloning of a cDNA for a glutamate receptor subunit activated by kainate but not AMPA., Egebjerg J, Bettler B, Hermans-Borgmeyer I, Heinemann S., Nature. June 27, 1991; 351 (6329): 745-8.

A chimeric glutamate receptor subunit: discrete changes modify the properties of the channel., Bochet P, Dutriaux A, Lambolez B, Nalivaiko E, Rossier J, Prado de Carvalho L., Biochem Biophys Res Commun. June 28, 1991; 177 (3): 1183-7.

A single amino acid residue determines the Ca2+ permeability of AMPA-selective glutamate receptor channels., Mishina M, Sakimura K, Mori H, Kushiya E, Harabayashi M, Uchino S, Nagahari K., Biochem Biophys Res Commun. October 31, 1991; 180 (2): 813-21.

In the GluR1 glutamate receptor subunit a glutamine to histidine point mutation suppresses inward rectification but not calcium permeability., Curutchet P, Bochet P, Prado de Carvalho L, Lambolez B, Stinnakre J, Rossier J., Biochem Biophys Res Commun. February 14, 1992; 182 (3): 1089-93.

Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors., Sun W, Ferrer-Montiel AV, Schinder AF, McPherson JP, Evans GA, Montal M., Proc Natl Acad Sci U S A. February 15, 1992; 89 (4): 1443-7.

Calcium influx through subunits GluR1/GluR3 of kainate/AMPA receptor channels is regulated by cAMP dependent protein kinase., Keller BU, Hollmann M, Heinemann S, Konnerth A., EMBO J. March 1, 1992; 11 (3): 891-6.

Structural determinants of barium permeation and rectification in non-NMDA glutamate receptor channels., Dingledine R, Hume RI, Heinemann SF., J Neurosci. October 1, 1992; 12 (10): 4080-7.

N-acetylaspartylglutamate acts as an agonist upon homomeric NMDA receptor (NMDAR1) expressed in Xenopus oocytes., Sekiguchi M, Wada K, Wenthold RJ., FEBS Lett. October 26, 1992; 311 (3): 285-9.

Agonist- and subunit-dependent potentiation of glutamate receptors by a nootropic drug aniracetam., Tsuzuki K, Takeuchi T, Ozawa S., Brain Res Mol Brain Res. November 1, 1992; 16 (1-2): 105-10.

Expression of neurotransmitter receptors by mRNAs from neurons developing in vitro: a Xenopus oocyte expression study., Wahl P, Ragsdale D, Schousboe A, Miledi R., J Neurochem. January 1, 1993; 60 (1): 57-65.

Identification of a subunit-specific antagonist of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate/kainate receptor channels., Keller BU, Blaschke M, Rivosecchi R, Hollmann M, Heinemann SF, Konnerth A., Proc Natl Acad Sci U S A. January 15, 1993; 90 (2): 605-9.

Neurotransmitter receptors and voltage-dependent Ca2+ channels encoded by mRNA from the adult corpus callosum., Matute C, Miledi R., Proc Natl Acad Sci U S A. April 15, 1993; 90 (8): 3270-4.

Are chimeric kainate/N-methyl-D-aspartate receptors expressed in Xenopus oocytes from mammalian and amphibian RNA?, Brackley PT, Usherwood PN., J Pharmacol Exp Ther. May 1, 1993; 265 (2): 910-9.

A single amino acid determines the subunit-specific spider toxin block of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate receptor channels., Blaschke M, Keller BU, Rivosecchi R, Hollmann M, Heinemann S, Konnerth A., Proc Natl Acad Sci U S A. July 15, 1993; 90 (14): 6528-32.

Selective antagonism of native and cloned kainate and NMDA receptors by polyamine-containing toxins., Brackley PT, Bell DR, Choi SK, Nakanishi K, Usherwood PN., J Pharmacol Exp Ther. September 1, 1993; 266 (3): 1573-80.

Cyclothiazide potentiates agonist responses at human AMPA/kainate receptors expressed in oocytes., Sharp RL, May PC, Mayne NG, Snyder YM, Burnett JP., Eur J Pharmacol. January 1, 1994; 266 (1): R1-2.

Subunit-specific enhancement of glutamate receptor responses by zinc., Dreixler JC, Leonard JP., Brain Res Mol Brain Res. March 1, 1994; 22 (1-4): 144-50.

Activation of protein kinase C inhibits kainate-induced currents in oocytes expressing glutamate receptor subunits., Dildy-Mayfield JE, Harris RA., J Neurochem. April 1, 1994; 62 (4): 1639-42.

A deletion in the second cytoplasmic loop of GluR3 produces a dominant negative mutant of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor., Sekiguchi M, Doi K, Zhu WS, Watase K, Yokotani N, Wada K, Wenthold RJ., J Biol Chem. May 20, 1994; 269 (20): 14559-65.

N-glycosylation site tagging suggests a three transmembrane domain topology for the glutamate receptor GluR1., Hollmann M, Maron C, Heinemann S., Neuron. December 1, 1994; 13 (6): 1331-43.

Identification of a Ca2+/calmodulin-dependent protein kinase II regulatory phosphorylation site in non-N-methyl-D-aspartate glutamate receptors., Yakel JL, Vissavajjhala P, Derkach VA, Brickey DA, Soderling TR., Proc Natl Acad Sci U S A. February 28, 1995; 92 (5): 1376-80.

Molecular design of the N-methyl-D-aspartate receptor binding site for phencyclidine and dizolcipine., Ferrer-Montiel AV, Sun W, Montal M., Proc Natl Acad Sci U S A. August 15, 1995; 92 (17): 8021-5.

New developments in the molecular pharmacology of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate and kainate receptors., Fletcher EJ, Lodge D., Pharmacol Ther. January 1, 1996; 70 (1): 65-89.

CDNA cloning of chick brain alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors reveals conservation of structure, function and post-transcriptional processes with mammalian receptors., Paperna T, Lamed Y, Teichberg VI., Brain Res Mol Brain Res. February 1, 1996; 36 (1): 101-13.

Anesthetics produce subunit-selective actions on glutamate receptors., Dildy-Mayfield JE, Eger EI, Harris RA., J Pharmacol Exp Ther. March 1, 1996; 276 (3): 1058-65.

Pentameric subunit stoichiometry of a neuronal glutamate receptor., Ferrer-Montiel AV, Montal M., Proc Natl Acad Sci U S A. April 2, 1996; 93 (7): 2741-4.

A venus flytrap mechanism for activation and desensitization of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors., Mano I, Lamed Y, Teichberg VI., J Biol Chem. June 28, 1996; 271 (26): 15299-302.

A single tryptophan on M2 of glutamate receptor channels confers high permeability to divalent cations., Ferrer-Montiel AV, Sun W, Montal M., Biophys J. August 1, 1996; 71 (2): 749-58.

Thiocyanate ions inhibit AMPA-activated currents in recombinant non-NMDA receptors expressed in Xenopus laevis oocytes: the role of the GluR2 subunit., Eugène D, Moss SJ, Smart TG., Eur J Neurosci. September 1, 1996; 8 (9): 1983-93.

Pharmacological differentiation between neuronal and recombinant glutamate receptor channels expressed in Xenopus oocytes., Blaschke M, Gremmels D, Everts I, Weigand E, Heinemann SF, Hollmann M, Keller BU., Neuropharmacology. January 1, 1997; 36 (11-12): 1489-501.

Effects of external calcium on zinc modulation of AMPA receptors., Dreixler JC, Leonard JP., Dev Biol. March 28, 1997; 752 (1-2): 170-4.

Comparison of the agonist binding site of homomeric, heteromeric, and chimeric GluR1(o) and GluR3(o) AMPA receptors., Banke TG, Schousboe A, Pickering DS., J Neurosci Res. July 15, 1997; 49 (2): 176-85.

A serum factor potentiates ACh and AMPA receptor currents via differential signal transduction pathways., Nishizaki T, Matsuoka T, Nomura T, Sumikawa K., Biochem Biophys Res Commun. September 18, 1997; 238 (2): 565-8.

Kainate binding proteins possess functional ion channel domains., Villmann C, Bull L, Hollmann M., J Neurosci. October 15, 1997; 17 (20): 7634-43.

Benzyl-polyamines: novel, potent N-methyl-D-aspartate receptor antagonists., Igarashi K, Shirahata A, Pahk AJ, Kashiwagi K, Williams K., J Pharmacol Exp Ther. November 1, 1997; 283 (2): 533-40.

Block of open channels of recombinant AMPA receptors and native AMPA/kainate receptors by adamantane derivatives., Magazanik LG, Buldakova SL, Samoilova MV, Gmiro VE, Mellor IR, Usherwood PN., J Physiol. December 15, 1997; 505 ( Pt 3) 655-63.

Structural determinants of the blocker binding site in glutamate and NMDA receptor channels., Ferrer-Montiel AV, Merino JM, Planells-Cases R, Sun W, Montal M., Neuropharmacology. January 1, 1998; 37 (2): 139-47.

A tetrameric subunit stoichiometry for a glutamate receptor-channel complex., Mano I, Teichberg VI., Neuroreport. January 26, 1998; 9 (2): 327-31.

Antagonist properties of a phosphono isoxazole amino acid at glutamate R1-4 (R,S)-2-amino-3-(3-hydroxy-5-methyl-4-isoxazolyl)propionic acid receptor subtypes., Wahl P, Anker C, Traynelis SF, Egebjerg J, Rasmussen JS, Krogsgaard-Larsen P, Madsen U., Mol Pharmacol. March 1, 1998; 53 (3): 590-6.

Pharmacological detection of AMPA receptor heterogeneity by use of two allosteric potentiators in rat hippocampal cultures., Sekiguchi M, Takeo J, Harada T, Morimoto T, Kudo Y, Yamashita S, Kohsaka S, Wada K., Br J Pharmacol. April 1, 1998; 123 (7): 1294-303.

The methylglutamate, SYM 2081, is a potent and highly selective agonist at kainate receptors., Donevan SD, Beg A, Gunther JM, Twyman RE., J Pharmacol Exp Ther. May 1, 1998; 285 (2): 539-45.

Effects of the abused solvent toluene on recombinant N-methyl-D-aspartate and non-N-methyl-D-aspartate receptors expressed in Xenopus oocytes., Cruz SL, Mirshahi T, Thomas B, Balster RL, Woodward JJ., J Pharmacol Exp Ther. July 1, 1998; 286 (1): 334-40.

Neurosteroid modulation of recombinant ionotropic glutamate receptors., Yaghoubi N, Malayev A, Russek SJ, Gibbs TT, Farb DH., Dev Biol. August 24, 1998; 803 (1-2): 153-60.

Resolution, absolute stereochemistry, and enantiopharmacology of the GluR1-4 and GluR5 antagonist 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid., Møller EH, Egebjerg J, Brehm L, Stensbøl TB, Johansen TN, Madsen U, Krogsgaard-Larsen P., Chirality. January 1, 1999; 11 (10): 752-9.

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