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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.
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.
(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.
Resolution, absolute stereochemistry and molecular pharmacology of the enantiomers of ATPA. , Stensbøl TB., Eur J Pharmacol. September 10, 1999; 380 (2-3): 153-62.
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., Chirality. January 1, 1999; 11 (10): 752-9.
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., Mol Pharmacol. March 1, 1998; 53 (3): 590-6.