Ligands for Glutamate Receptors: Design and Therapeutic ProspectsHans Bräuner‐Osborne, Povl Krogsgaard‐Larsen, Jan Egebjerg et al.|Journal of Medicinal Chemistry|2000Cited by 525
Deorphanization of GPRC6A: A Promiscuous l-α-Amino Acid Receptor with Preference for Basic Amino AcidsPetrine Wellendorph, Hans Bräuner‐Osborne, Kasper B. Hansen et al.|Molecular Pharmacology|2004Cited by 209
Synthesis, Binding Affinity at Glutamic Acid Receptors, Neuroprotective Effects, and Molecular Modeling Investigation of Novel Dihydroisoxazole Amino AcidsPaola Conti, Carlo De Micheli, Francine Acher et al.|Journal of Medicinal Chemistry|2005Cited by 42
Pharmacological Characterization of Ligands at Recombinant NMDA Receptor Subtypes by Electrophysiological Recordings and Intracellular Calcium MeasurementsKasper B. Hansen, Jan Egebjerg, Hans Bräuner‐Osborne|Combinatorial Chemistry & High Throughput Screening|2008Cited by 35
Tweaking Agonist Efficacy at N-Methyl-d-aspartate Receptors by Site-Directed MutagenesisKasper B. Hansen, Hans Bräuner‐Osborne, Rasmus P. Clausen et al.|Molecular Pharmacology|2005Cited by 28