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1 e the activity of oligodendrocyte NMDARs and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
2 We tested whether alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
3 antidepressant-like effects by potentiating alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
4 Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
5 agonists of N-methyl-d-aspartic acid (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
6 alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
7 Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
8 Antagonists of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
9 c silencing through a selective reduction of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
10 (NMDAR) activity regulates the net number of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
11 nisms including Ca(2+)- and CamKII-dependent alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
12 Here we show that the NMDA-to-AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
13 or excitatory synapses that lack functional alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
14 -Na(+)/K(+)-ATPase, GluA2 subunit containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
15 or excitatory neurotransmitter in brain, and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
16 ns of neuroD2 heterozygotes including Ulip1, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
17 t .3, 1 mg/kg, or with an antagonist for the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
18 AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
19 ting dendritic spines and decreased synaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
20 Photorelease of D-aspartate did not activate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
21 Here we show that alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
22 Dynamic regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
23 ed increase in the CaMKII phosphorylation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
24 of small molecules that positively modulate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
25 receptors, but not GluA1 subunit containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
26 d by the removal of GluR2 subunit-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
27 itatory autaptic currents (eacs) mediated by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
28 This enhancement requires the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
29 As development progresses, synapses acquire alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
30 A molecular model based on alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
31 The NMDAR/alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
32 on examination of amplitude distribution of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
33 notropic glutamate receptors (iGluRs) of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
34 Instead, D2 receptor depression of both alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
35 rs demonstrated that KA killed through AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
36 ments dentate granule cell calcium-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
37 This effect was blocked by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
38 tic enhancement involves an up-regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
39 nic acid, 8Na (NF449)] reduce binding of [3H]alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
40 AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
41 ertain neuronal cells that carry Ca-permeant alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
42 cked only by joint application of glutamate [alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
43 The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
44 and detected no alterations in the ratio of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
45 ts N-methyl-D-aspartate (NMDA) receptor- and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
46 smission and is widely used as a blocker for alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
47 Here, we explored the dynamics of the TMD of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
48 Treatment of mesencephalic cultures with alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
49 Functional expression of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
50 or the opening of the GluR1Qflip channel, an alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
51 2O2, generated downstream from glutamatergic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
52 BQX), 6-cyano-7-nitroquinoxaline-2,3-dione], alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
53 like their rodent counterparts, express this alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
54 The mechanism of action of aniracetam on alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
55 kes a more rapid and complete attenuation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
56 Regulated delivery and removal of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
57 Calcium imaging showed that glutamate-, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
58 The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
59 We found that both NMDA and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
60 xetine also increases phosphorylation of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
61 BTDs) were tested for their effects on (R,S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
62 because they persist in the presence of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
63 ntagonist GYKI 53655, but are blocked by the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
64 ly stably integrated in the PSD, whereas the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
65 aptically as a functional down-regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
66 ogical behaviors of N-methyl-d-aspartate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
67 Trafficking of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
68 The expression of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
69 cognition by promoting membrane insertion of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
70 requires the activation of Ca(2+)-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
71 bination with 10 microM dizocilpine to block alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
72 in phosphatase-1 to regulate the activity of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
73 The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
74 e subunit that limits Ca(2+) permeability of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
75 irement and that DDI can be evoked solely by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
76 ity mediated by N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
77 ged glutamate was used to map the changes in alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
78 R,S-alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
79 rally have large numbers of Ca(2+)-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
80 bserved a specific increase in GluA2-lacking alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
81 atory postsynaptic currents (EPSCs), but not alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
82 amate receptors N-methyl-d-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
83 Herein, we show that GluR1-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
84 The distribution of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
85 sphodiesterase were decreased by kainate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
86 ic plasticity through the phosphorylation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
87 tain for either N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
88 Ionotropic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
89 The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
90 down-regulation of GluR2 mRNA and increased alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
91 Since oligodendrocytes express functional alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
92 participation of cholinergic muscarinic, (S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
93 n COS-7 cells phosphorylation of transfected alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
94 mistry was used to study the distribution of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
95 tive antagonist of the neuronal receptor for alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
96 with an ampakine, an allosteric modulator of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
97 In addition, GK-P3 cells express alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
98 between these NMDA receptor subunits and the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
99 -regulation of glutamate ionotropic receptor alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
100 hyl-D-aspartate (NMDA) and non-NMDA (such as alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
101 The fast component was blocked by the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
102 ssential for PKA-dependent modulation of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
103 QX 14g has 440-fold selectivity for NMDA vs alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
104 LTP increased the phosphorus-32 labeling of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
105 ons evoked by N-methyl-D-aspartate (NMDA) or alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
106 by exposure to N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
107 Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
108 aspartate (NMDA)/glycine receptors, [3H]-(S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
109 Glutamate depressed the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
110 rimarily involves the regulation of synaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
111 of N-methyl-d-aspartate receptor (NMDAR) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
112 hiadiazides such as cyclothiazide potentiate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
113 t dorsal root ganglion (DRG) neurons and the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
114 s, except for the GluR4 subunit of the (+/-)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
115 -none regulation (up or down) of clusters of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
116 of cyclothiazide on the properties of (R,S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
117 ent involves the PSD-95 scaffolding protein, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
118 ation of surface GluA1 and GluA2 subunits of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
119 Furthermore, microinjection of the NMDA or alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
120 GluA2 is a key subunit of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
121 , we show that nanoscale mobility of resting alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
122 urface Labeling in Neurons (EPSILON), to map alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
123 Here, using the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
124 how enhanced endocytosis of GluA2-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
125 -target aptamer-like direct interaction with alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
126 assium channels (VGKCs) and GluA1-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
127 and intracellular mGlu(5) activation lead to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
128 In NMDAR knockout neurons, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
129 onic-clonic seizures were also suppressed by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
130 strength through cell-surface trafficking of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
131 utamate transporter (VGlut) 1 clustering and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
132 ted wild-type mice, these compounds blocking alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
133 ndritic and somatic surface GluA1-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
134 onotropic, glutamatergic receptors, AMPARs, (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
135 ures, and displayed sustained enhancement in alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
136 lates synaptic plasticity and trafficking of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
137 ular ultrastructure regulates the opening of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
138 accompanied by a reduction of levels of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
139 overall local protein synthesis (measured as alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
140 identify new, highly effective inhibitors of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
141 We also found reduced alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
142 genes encoding N-methyl-D-aspartate (NMDA), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
143 ed with an increase in NAc spine density and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
144 ns; this increase was blocked by the NMDA or alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
145 alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
146 ing of lysosomes is correlated with synaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
147 In neurons, lysosomes regulate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
148 leus accumbens (NAc) shell calcium-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
149 -d-aspartic acid (NMDA) receptors (NMDA-Rs), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
150 mechanism involves downstream activation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
151 by direct modification of postsynaptic AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
152 e behavior in male mice, perhaps by altering alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
153 D induction and prevented NMDA-induced AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
154 o correct NMDAR hypofunction is to stimulate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
155 opic glutamate receptor 1, NMDA receptor 2A, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
156 c acetylcholine receptor superfamily (namely alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
157 ABAR) reversal potential or co-activation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
158 east some molecular targets (e.g., recycling alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
159 GluN2B N-methyl-D-aspartate (NMDA) and GluA2 alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
160 complementing prior studies implicating the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
161 cently been shown to regulate endocytosis of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
162 ted Kv1 potassium channel-complex (13%), and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
163 ly rapid activation of the highly homologous alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
164 alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
165 ity, DHPG-induced internalization of surface alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
166 vities, on gamma-aminobutyric acid (GABA)A , alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
167 post-synaptic density protein 95 (PSD95) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
168 c42 and the mobilization of GluA1-containing alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
169 Autoimmune-mediated anti-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
170 sense neuronal activity by expressing AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
171 The number of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
172 Virtually all alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
173 ctivity in the midbrain raphe nuclei through alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
174 Desensitization of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
175 glycine allosteric site of NMDA receptors or alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
176 ntly greater increase in electrically evoked alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
177 tetrahydrofuran ether class of highly potent alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
178 litis associated with antibodies against the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
179 es N-methyl-D-aspartate receptor (NMDAR) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
180 uted pyridothiadiazine dioxides belonging to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
181 l migration through its interaction with the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
182 itis [N-methyl-D-aspartate receptor (NMDAR), alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
183 luN2B, and GluN2D and has no effect on AMPA [alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
184 Three residues within the AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
185 Kainate and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
186 sing synaptic strength is the trafficking of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
187 ve allosteric modulators ("potentiators") of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
188 N-methyl-d-aspartate, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
189 s, we tested the effects of leptin on evoked alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
190 al activity-regulated pentraxin (NARP) is an alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
191 Glutamate receptors of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
192 oss of dendritic spines and loss of synaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
193 the cocaine exposure-induced enhancement of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
194 acellular signal-regulated kinase (ERK), and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
195 nt of corticosterone significantly increases alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
196 al role in mGluR-mediated internalization of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
197 ssion of an activated form of STAT5 prevents alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
198 Talampanel is a well-tolerated, oral alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
199 s N-methyl-d-aspartate (NMDA) receptor 1 and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
200 ng siRNA screening technology, we identified alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
201 Desensitization of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
202 receptor 1 (GluR1) and GluR2 subunits of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
203 thyl-d-aspartate) and KA (kainic acid)/AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
204 -methyl-D-aspartate (NMDA) receptor, and the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
205 increased anxiety correlated with increased alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
206 asticity involve the control of postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
207 t is secreted at synaptic sites and binds to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
208 We identify calcium-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
209 xcitatory neurotransmitter in the brain, and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
210 atment did not lead to an internalization of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
211 by LFS is unaffected by inhibitors of PKA or alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
212 Synaptic depression was slightly affected by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
213 A, and the clathrin-dependent endocytosis of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
214 The activity-dependent regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
215 and functional upregulation of postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
216 Ample evidence from earlier studies of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
217 alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
218 nduce nondesensitizing responses at neuronal alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
219 alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
220 Regulated endocytosis of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
221 Ionotropic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
222 Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
223 -2,3-dione (CNQX) are the most commonly used alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
224 Alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
225 iling view, N-methyl-D-aspartate (NMDA)- and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
226 igate whether synaptic scaling mediated by l-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
227 marily on two types of ionotropic receptors: alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid
228 e of astrocytes was not modified by kainate, alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic aci
229 h the glutamate receptor agonists kainate or alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic aci
230 development through selective activation of alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic aci
231 cking and activation of the GluR1 subunit of alpha-amino- 3-hydroxy-5-methyl-4-isoxazolepropionic aci
232 entials (IPSPAs and IPSPBs, respectively) on alpha-amino-3-hydroxy-5-methyl -4-isoxazolepropionic aci