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1 ld be triggered in part through ligand-gated Glu receptors.
2 ctivates a plethora of pre- and postsynaptic Glu receptors.
3 ent antagonists of ionotropic L-glutamate (L-Glu) receptors.
4 he membrane trafficking of the AMPA receptor Glu receptor 1 (GluR1) subunit, but the role of direct p
5 tamate receptor subunits NMDA receptor 1 and Glu receptor 1 are selectively reduced in LRP1 forebrain
6 ta colocalize with the AMPA receptor subunit Glu receptor 1 but not with the GABAA receptor subunits
7 eurons consistently expressed high levels of Glu receptor 2 (GluR2) mRNA and AMPA receptors with low
8 hibit properties of Ca(2+)/Zn(2+)-permeable, Glu receptor 2 (GluR2)-lacking AMPARs before the rise in
10 antages in applications where pre-photolysis Glu receptor activation and desensitization must be mini
11 loxyaspartic acid, but not by the ionotropic Glu receptor agonists, alpha-2-amino-3-(5-methyl-3-oxo-1
12 titute for L-glutamate (L-Glu) at excitatory Glu receptors, and occurs as free D-Asp in the mammalian
14 y was designed to determine which glutamate (Glu) receptors are involved in excitatory neurotransmiss
16 hibition of Asso signaling to Fyn, Pyk2, and Glu receptors by AZD0530 was tested by brain slice assay
17 deficient in either vesicular Glu release or Glu receptor expression and could be phenocopied by muta
19 fact, we have now studied the properties of Glu receptors (GluRs) from the cerebral cortices of AD a
23 sp, which is transported but does not act at Glu receptors, induced [H+]i and [Na+]i changes that wer
25 nce indicates that at least one of the plant Glu receptor-like molecules, GLR3.4, functions as an ami
28 ad no effect, suggesting that the functional Glu receptors on the somata may be the same as those at
29 work for establishing a comprehensive map of Glu receptor populations within this major subdivision o
31 escribed phospholipase D-linked metabotropic Glu receptor to maintain the excitability of the sensory
33 uron was stimulated during a period when the Glu receptors were blocked with the antagonist DNQX.
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