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Summary Expression Phenotypes Gene Literature (52) GO Terms (5) Nucleotides (56) Proteins (31) Interactants (45) Wiki
XB--6050068

Papers associated with grik2



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Structure and assembly mechanism for heteromeric kainate receptors., Kumar J, Schuck P, Mayer ML., Neuron. July 28, 2011; 71 (2): 319-31.


Kaitocephalin antagonism of glutamate receptors expressed in Xenopus oocytes., Limon A, Reyes-Ruiz JM, Vaswani RG, Chamberlin AR, Miledi R., ACS Chem Neurosci. March 17, 2010; 1 (3): 175-181.


The glutamate receptor subunit delta2 is capable of gating its intrinsic ion channel as revealed by ligand binding domain transplantation., Schmid SM, Kott S, Sager C, Huelsken T, Hollmann M., Proc Natl Acad Sci U S A. June 23, 2009; 106 (25): 10320-5.


Arabidopsis thaliana glutamate receptor ion channel function demonstrated by ion pore transplantation., Tapken D, Hollmann M., J Mol Biol. October 31, 2008; 383 (1): 36-48.


Different structural requirements for functional ion pore transplantation suggest different gating mechanisms of NMDA and kainate receptors., Villmann C, Hoffmann J, Werner M, Kott S, Strutz-Seebohm N, Nilsson T, Hollmann M., J Neurochem. October 1, 2008; 107 (2): 453-65.


Block of kainate receptor desensitization uncovers a key trafficking checkpoint., Priel A, Selak S, Lerma J, Stern-Bach Y., Neuron. December 21, 2006; 52 (6): 1037-46.


Investigation via ion pore transplantation of the putative relationship between glutamate receptors and K+ channels., Hoffmann J, Villmann C, Werner M, Hollmann M., Mol Cell Neurosci. December 1, 2006; 33 (4): 358-70.


Crystal structures of the kainate receptor GluR5 ligand binding core dimer with novel GluR5-selective antagonists., Mayer ML, Ghosal A, Dolman NP, Jane DE., J Neurosci. March 15, 2006; 26 (11): 2852-61.


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


Functional significance of the kainate receptor GluR6(M836I) mutation that is linked to autism., Strutz-Seebohm N, Korniychuk G, Schwarz R, Baltaev R, Ureche ON, Mack AF, Ma ZL, Hollmann M, Lang F, Seebohm G., Cell Physiol Biochem. January 1, 2006; 18 (4-5): 287-94.


Tetrazolyl isoxazole amino acids as ionotropic glutamate receptor antagonists: synthesis, modelling and molecular pharmacology., Frølund B, Greenwood JR, Holm MM, Egebjerg J, Madsen U, Nielsen B, Bräuner-Osborne H, Stensbøl TB, Krogsgaard-Larsen P., Bioorg Med Chem. September 15, 2005; 13 (18): 5391-8.


Glucocorticoid adrenal steroids and glucocorticoid-inducible kinase isoforms in the regulation of GluR6 expression., Strutz-Seebohm N, Seebohm G, Shumilina E, Mack AF, Wagner HJ, Lampert A, Grahammer F, Henke G, Just L, Skutella T, Hollmann M, Lang F., J Physiol. June 1, 2005; 565 (Pt 2): 391-401.


Functional analysis of Caenorhabditis elegans glutamate receptor subunits by domain transplantation., Strutz-Seebohm N, Werner M, Madsen DM, Seebohm G, Zheng Y, Walker CS, Maricq AV, Hollmann M., J Biol Chem. November 7, 2003; 278 (45): 44691-701.


A role for extracellular Na+ in the channel gating of native and recombinant kainate receptors., Paternain AV, Cohen A, Stern-Bach Y, Lerma J., J Neurosci. September 24, 2003; 23 (25): 8641-8.


(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, Greenwood JR, Hansen KB, Nielsen B, Egebjerg J, Stensbøl TB, Bräuner-Osborne H, Sløk FA, Kronborg TT, Krogsgaard-Larsen P., J Med Chem. April 10, 2003; 46 (8): 1350-8.


Kainate-binding proteins are rendered functional ion channels upon transplantation of two short pore-flanking domains from a kainate receptor., Strutz N, Villmann C, Breitinger HG, Werner M, Wenthold RJ, Kizelsztein P, Teichberg VI, Hollmann M., J Biol Chem. December 13, 2002; 277 (50): 48035-42.


Does acetaldehyde mediate ethanol action in the central nervous system?, Mascia MP, Maiya R, Borghese CM, Lobo IA, Hara K, Yamakura T, Gong DH, Beckstead MJ., Alcohol Clin Exp Res. November 1, 2001; 25 (11): 1570-5.


Structural similarities between glutamate receptor channels and K(+) channels examined by scanning mutagenesis., Panchenko VA, Glasser CR, Mayer ML., J Gen Physiol. April 1, 2001; 117 (4): 345-60.                


Identification of domains and amino acids involved in GLuR7 ion channel function., Strutz N, Villmann C, Thalhammer A, Kizelsztein P, Eisenstein M, Teichberg VI, Hollmann M., J Neurosci. January 15, 2001; 21 (2): 401-11.


Electrophysiological characterization of CGP68730A a N-methyl-D-aspartate antagonist acting at the strychnine-insensitive glycine site., Pozza MF, Zimmerman K, Bischoff S, Lingenhöhl K., Prog Neuropsychopharmacol Biol Psychiatry. May 1, 2000; 24 (4): 647-70.


In vitro and in vivo characterization of conantokin-R, a selective NMDA receptor antagonist isolated from the venom of the fish-hunting snail Conus radiatus., White HS, McCabe RT, Armstrong H, Donevan SD, Cruz LJ, Abogadie FC, Torres J, Rivier JE, Paarmann I, Hollmann M, Olivera BM., J Pharmacol Exp Ther. January 1, 2000; 292 (1): 425-32.


Amino acid substitutions in the pore of rat glutamate receptors at sites influencing block by polyamines., Panchenko VA, Glasser CR, Partin KM, Mayer ML., J Physiol. October 15, 1999; 520 Pt 2 337-57.


Resolution, absolute stereochemistry and molecular pharmacology of the enantiomers of ATPA., Stensbøl TB, Borre L, Johansen TN, Egebjerg J, Madsen U, Ebert B, Krogsgaard-Larsen P., Eur J Pharmacol. September 10, 1999; 380 (2-3): 153-62.


Investigation by ion channel domain transplantation of rat glutamate receptor subunits, orphan receptors and a putative NMDA receptor subunit., Villmann C, Strutz N, Morth T, Hollmann M., Eur J Neurosci. May 1, 1999; 11 (5): 1765-78.


Acute effects of ethanol on kainate receptors with different subunit compositions., Valenzuela CF, Cardoso RA., J Pharmacol Exp Ther. March 1, 1999; 288 (3): 1199-206.


Lectin-induced inhibition of desensitization of the kainate receptor GluR6 depends on the activation state and can be mediated by a single native or ectopic N-linked carbohydrate side chain., Everts I, Petroski R, Kizelsztein P, Teichberg VI, Heinemann SF, Hollmann M., J Neurosci. February 1, 1999; 19 (3): 916-27.


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.


Acute effects of ethanol on recombinant kainate receptors: lack of role of protein phosphorylation., Valenzuela CF, Cardoso RA, Lickteig R, Browning MD, Nixon KM., Alcohol Clin Exp Res. September 1, 1998; 22 (6): 1292-9.


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.


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.


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.


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.


Selective actions of a detergent on ligand-gated ion channels expressed in Xenopus oocytes., Machu TK, Mihic SJ, Dildy-Mayfield JE., J Pharmacol Exp Ther. January 1, 1998; 284 (1): 32-6.


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. November 1, 1997; 36 (11-12): 1489-501.


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.


Actions of long chain alcohols on GABAA and glutamate receptors: relation to in vivo effects., Dildy-Mayfield JE, Mihic SJ, Liu Y, Deitrich RA, Harris RA., Br J Pharmacol. May 1, 1996; 118 (2): 378-84.


Structure and pharmacological properties of a molluscan glutamate-gated cation channel and its likely role in feeding behavior., Stühmer T, Amar M, Harvey RJ, Bermudez I, van Minnen J, Darlison MG., J Neurosci. May 1, 1996; 16 (9): 2869-80.


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.


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.


A unitary non-NMDA receptor short subunit from Xenopus: DNA cloning and expression., Ishimaru H, Kamboj R, Ambrosini A, Henley JM, Soloviev MM, Sudan H, Rossier J, Abutidze K, Rampersad V, Usherwood PN, Bateson AN, Barnard EA., Recept Channels. January 1, 1996; 4 (1): 31-49.


Negative allosteric modulation of wild-type and mutant AMPA receptors by GYKI 53655., Partin KM, Mayer ML., Mol Pharmacol. January 1, 1996; 49 (1): 142-8.


Structural determinants of allosteric regulation in alternatively spliced AMPA receptors., Partin KM, Bowie D, Mayer ML., Neuron. April 1, 1995; 14 (4): 833-43.


Ethanol inhibits kainate responses of glutamate receptors expressed in Xenopus oocytes: role of calcium and protein kinase C., Dildy-Mayfield JE, Harris RA., J Neurosci. April 1, 1995; 15 (4): 3162-71.


Agonist selectivity of glutamate receptors is specified by two domains structurally related to bacterial amino acid-binding proteins., Stern-Bach Y, Bettler B, Hartley M, Sheppard PO, O'Hara PJ, Heinemann SF., Neuron. December 1, 1994; 13 (6): 1345-57.


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 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.


Ca2+ permeability of unedited and edited versions of the kainate selective glutamate receptor GluR6., Egebjerg J, Heinemann SF., Proc Natl Acad Sci U S A. January 15, 1993; 90 (2): 755-9.


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.


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.


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.

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