{"date_updated":"2022-09-07T13:30:23Z","author":[{"first_name":"Hannah","last_name":"Monyer","full_name":"Monyer, Hannah"},{"id":"353C1B58-F248-11E8-B48F-1D18A9856A87","last_name":"Jonas","orcid":"0000-0001-5001-4804","first_name":"Peter M","full_name":"Jonas, Peter M"},{"full_name":"Rossier, Jean","last_name":"Rossier","first_name":"Jean"}],"user_id":"ea97e931-d5af-11eb-85d4-e6957dddbf17","editor":[{"id":"353C1B58-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5001-4804","last_name":"Jonas","first_name":"Peter M","full_name":"Jonas, Peter M"},{"last_name":"Monyer","first_name":"Hannah","full_name":"Monyer, Hannah"}],"_id":"3456","year":"1999","alternative_title":["Handbook of experimental pharmacology"],"quality_controlled":"1","doi":"10.1007/978-3-662-08022-1_9","publication_status":"published","citation":{"ista":"Monyer H, Jonas PM, Rossier J. 1999.Molecular determinants controlling functional properties of AMPARs and NMDARs in the mammalian CNS. In: Ionotropic Glutamate Receptors in the CNS. Handbook of experimental pharmacology, vol. 141, 309–339.","mla":"Monyer, Hannah, et al. “Molecular Determinants Controlling Functional Properties of AMPARs and NMDARs in the Mammalian CNS.” Ionotropic Glutamate Receptors in the CNS, edited by Peter M Jonas and Hannah Monyer, vol. 141, Springer, 1999, pp. 309–39, doi:10.1007/978-3-662-08022-1_9.","chicago":"Monyer, Hannah, Peter M Jonas, and Jean Rossier. “Molecular Determinants Controlling Functional Properties of AMPARs and NMDARs in the Mammalian CNS.” In Ionotropic Glutamate Receptors in the CNS, edited by Peter M Jonas and Hannah Monyer, 141:309–39. Springer, 1999. https://doi.org/10.1007/978-3-662-08022-1_9.","ama":"Monyer H, Jonas PM, Rossier J. Molecular determinants controlling functional properties of AMPARs and NMDARs in the mammalian CNS. In: Jonas PM, Monyer H, eds. Ionotropic Glutamate Receptors in the CNS. Vol 141. Springer; 1999:309-339. doi:10.1007/978-3-662-08022-1_9","apa":"Monyer, H., Jonas, P. M., & Rossier, J. (1999). Molecular determinants controlling functional properties of AMPARs and NMDARs in the mammalian CNS. In P. M. Jonas & H. Monyer (Eds.), Ionotropic Glutamate Receptors in the CNS (Vol. 141, pp. 309–339). Springer. https://doi.org/10.1007/978-3-662-08022-1_9","ieee":"H. Monyer, P. M. Jonas, and J. Rossier, “Molecular determinants controlling functional properties of AMPARs and NMDARs in the mammalian CNS,” in Ionotropic Glutamate Receptors in the CNS, vol. 141, P. M. Jonas and H. Monyer, Eds. Springer, 1999, pp. 309–339.","short":"H. Monyer, P.M. Jonas, J. Rossier, in:, P.M. Jonas, H. Monyer (Eds.), Ionotropic Glutamate Receptors in the CNS, Springer, 1999, pp. 309–339."},"month":"01","publication":"Ionotropic Glutamate Receptors in the CNS","scopus_import":"1","volume":141,"extern":"1","status":"public","language":[{"iso":"eng"}],"date_created":"2018-12-11T12:03:25Z","publication_identifier":{"isbn":["9783642085390"]},"title":"Molecular determinants controlling functional properties of AMPARs and NMDARs in the mammalian CNS","article_processing_charge":"No","day":"01","page":"309 - 339","intvolume":" 141","publist_id":"2931","type":"book_chapter","publisher":"Springer","oa_version":"None","date_published":"1999-01-01T00:00:00Z","abstract":[{"text":"L-a-amino-3-hydroxy-5-methyl-4-isoxazolepropionate receptors (AMPARs) and N-methyl-D-aspartate receptors (NMDARs) are the two major types of postsynaptic glutamate receptors (GluRs) that mediate excitatory synaptic transmission in the mammalian central nervous system (CNS). Both AMPARs and NMDARs are multimeric proteins, probably tetramers, formed by a variety of molecularly distinct subunits. AMPARs can be assembled from four types of subunits, termed GIuR-A, -B, -C, and -D (or, in an alternative nomenclature, G1uR1, G1uR2, GluR3, and G1uR4). Additional molecular diversity of AMPARs is generated by alternative splicing of the flip-flop module and RNA editing at the Q/R and R/G site. NMDARs are heteromers primarily assembled from NR1 subunits and NR2A, B, C, or D subunits. Various splice variants have been identified for the NR1 subunit, and a new NR3 subunit has been discovered recently. Considering all combinatorial possibilities, the molecular diversity of glutamate-receptor channels is considerable (HOLLMANN, this volume).","lang":"eng"}]}