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Male-transmitted transgenerational effects of the herbicide linuron on DNA methylation profiles in Xenopus tropicalis brain and testis. , Roza M, Eriksson ANM, Svanholm S, Berg C, Karlsson O., Sci Total Environ. May 1, 2024; 923 170949.
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. January 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.