Titlebook: Excitatory Amino Acids and Neuronal Plasticity; Yehezkel Ben-Ari Book 1990 The Editor(s) (if applicable) and The Author(s), under exclusiv

Radiation

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Michael P. Boquet,Dawn R. Wagneretamine selectively block responses evoked by applications of NMDA agonists while sparing those mediated by other subtypes of excitatory amino acid receptors. Since that time others including ourselves demonstrated, using patch and voltage-clamp techniques, that this blockade is both dependent upon

constellation

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https://doi.org/10.1007/978-3-540-72047-8n-NMDA subtype of excitatory amino acid receptors can be further subdivided in two types, the kainate and the quisqualate (AMPA•) receptors. GDEE discriminate between the two agonists, being more active against quisqualate induced responses, when administered ionophoretically in vivo; however, this

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Formulation of Microbial BiopesticidesTheir presence on living brain cells is nowadays monitored electrophysiologically by measuring the changes of cell membrane conductance produced by kainic and domoic acids in the absence or presence of kainate receptor antagonists such as gammaglutamyglycine and CNQX.

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https://doi.org/10.1007/978-4-431-54493-7al nervous system (CNS) are mediated by distinct receptor sub-types. Amongst these, the N-methyl-D-aspartate (NMDA) receptor has been characterized most fully in terms of its pharmacological and biophysical properties (Watkins and Evans, 1981; Mayer and Westbrook, 1987). The NMDA receptor can be div

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https://doi.org/10.1007/978-3-658-24489-7te (NMDA) type of excitatory amino acid receptor (for review see Cotman & Iversen, 1987). Receptor binding and electrophysiological studies have indicated that the NMDA-receptor complex comprises a number of distinct structural domains through which its function may be regulated or pharmacologically