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