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1 and are recognized as regulatory elements of excitatory synaptic transmission.
2 ribution of the glutamate-glutamine cycle to excitatory synaptic transmission.
3  in the brain where its activation depresses excitatory synaptic transmission.
4 ne's actions on depression-like behavior and excitatory synaptic transmission.
5 mediate a slow Ca(2+)-permeable component of excitatory synaptic transmission.
6 d by ambient glutamate to regulate levels of excitatory synaptic transmission.
7 y is usually correlated with the strength of excitatory synaptic transmission.
8 tral nervous system and play a major role in excitatory synaptic transmission.
9  synaptic states to maintain the strength of excitatory synaptic transmission.
10 , whereas HDAC2 overexpression (OE) reduced, excitatory synaptic transmission.
11 rm potentiation and long-term depression, of excitatory synaptic transmission.
12 endritic spines and functional plasticity of excitatory synaptic transmission.
13 t, neuronal or synaptic structures, or basal excitatory synaptic transmission.
14 ransporters have additional roles in shaping excitatory synaptic transmission.
15 al gene expression, and deficits in cortical excitatory synaptic transmission.
16 utamate receptors that mediate a majority of excitatory synaptic transmission.
17 eptors (AMPARs) at synapses is essential for excitatory synaptic transmission.
18 ent predominantly increased postsynaptically excitatory synaptic transmission.
19 E STATEMENT Synaptic AMPARs are critical for excitatory synaptic transmission.
20  the shift is expressed by a modification of excitatory synaptic transmission.
21 y been implicated in long-term plasticity of excitatory synaptic transmission.
22 om a shift of balance between inhibitory and excitatory synaptic transmission.
23 receptors mediate the majority of vertebrate excitatory synaptic transmission.
24 sease by removing dendritic spines, sites of excitatory synaptic transmission.
25 eased the spine density to markedly increase excitatory synaptic transmission.
26 ty in hippocampal circuits, thereby reducing excitatory synaptic transmission.
27 d neuropathic pain facilitation by enhancing excitatory synaptic transmission.
28 tamate receptors (GluRs) play major roles in excitatory synaptic transmission.
29 K signaling, AMPAR membrane trafficking, and excitatory synaptic transmission.
30 e of dendritic spines--postsynaptic sites of excitatory synaptic transmission.
31 o and from synapses controls the strength of excitatory synaptic transmission.
32 ssical mushroom-head morphology, and impairs excitatory synaptic transmission.
33 t neurons show normal morphologies and basal excitatory synaptic transmission.
34 A2 is a synaptic adaptor protein involved in excitatory synaptic transmission.
35 enous neuromodulator adenosine and inhibited excitatory synaptic transmission.
36 , we report a role for opioids in modulating excitatory synaptic transmission.
37 tally with difficulty breathing and impaired excitatory synaptic transmission.
38 proteins or their binding partners regulates excitatory synaptic transmission.
39 itical for the regulation of the efficacy of excitatory synaptic transmission.
40 ion leads to short- and long-term changes in excitatory synaptic transmission.
41 d decreases both dendritic spine density and excitatory synaptic transmission.
42 ve channels that mediate a slow component of excitatory synaptic transmission.
43 ontaining, native receptors involved in fast excitatory synaptic transmission.
44 uced dendritic spine density, and diminished excitatory synaptic transmission.
45 sting that this SNARE complex is involved in excitatory synaptic transmission.
46 nc-sensitive signaling system that regulates excitatory synaptic transmission.
47 ly, the light stimuli transiently facilitate excitatory synaptic transmission.
48 tic increase in inhibitory and a decrease in excitatory synaptic transmission.
49         NMDA receptors play crucial roles in excitatory synaptic transmission.
50 Rs and their auxiliary proteins control fast excitatory synaptic transmission.
51 ptors are responsible for fast inhibitory or excitatory synaptic transmission.
52 re ligand-gated cation channels that mediate excitatory synaptic transmission.
53 nged the electrical properties and increased excitatory synaptic transmission.
54 ns in dendritic spine density and diminished excitatory synaptic transmission.
55 PA receptor levels, and thus the strength of excitatory synaptic transmission.
56 injection of JWH133 into mice also increased excitatory synaptic transmission.
57 ted ion channels that play a crucial role in excitatory synaptic transmission.
58 uronal activity to fine-tune the strength of excitatory synaptic transmission.
59 s through FSI and not via a direct effect on excitatory synaptic transmission.
60 ate uptake in astrocytes and how this shapes excitatory synaptic transmission among neurons.
61  physiological concentrations enhances basal excitatory synaptic transmission and ameliorates deficit
62 utamate receptors (AMPARs) mediate most fast excitatory synaptic transmission and are crucial for man
63 soxazole-propionate (AMPA) receptors mediate excitatory synaptic transmission and are dynamically reg
64                  AMPA receptors mediate fast excitatory synaptic transmission and are essential for s
65 receptors mediate the majority of vertebrate excitatory synaptic transmission and are therapeutic tar
66    Postsynaptic expression of parkin dampens excitatory synaptic transmission and causes a marked los
67 t this early life stressor leads to enhanced excitatory synaptic transmission and decreased levels of
68 rotein phosphatase-1 and actin and modulates excitatory synaptic transmission and dendritic spine mor
69 prevailing view, AMPA receptors mediate fast excitatory synaptic transmission and effect short-term p
70 exes of NR1 and NR2A-D subunits that mediate excitatory synaptic transmission and have a role in neur
71  ionotropic glutamate receptors that mediate excitatory synaptic transmission and have been implicate
72                                         Both excitatory synaptic transmission and network firing acti
73                                              Excitatory synaptic transmission and plasticity are crit
74  These results suggest that IgSF11 regulates excitatory synaptic transmission and plasticity through
75 l recordings show that Aph1b is required for excitatory synaptic transmission and plasticity.
76 (NMDAR) to dendritic spines is essential for excitatory synaptic transmission and plasticity.
77 euroadaptive changes in hippocampal area CA1 excitatory synaptic transmission and plasticity.
78 x 10(-7)), which is implicated in regulating excitatory synaptic transmission and plasticity.
79 rtate (NMDA) receptors (NMDARs) mediate fast excitatory synaptic transmission and play a critical rol
80 e DRN through both presynaptic inhibition of excitatory synaptic transmission and postsynaptic activa
81                       NMDA receptors mediate excitatory synaptic transmission and regulate synaptic p
82 ynchronous burst onset mediated by recurrent excitatory synaptic transmission and similar intrinsic s
83 150 (AKAP79/150) signaling complex regulates excitatory synaptic transmission and strength through te
84 d the impact of NPAS2 disruption on accumbal excitatory synaptic transmission and strength, along wit
85  enhancement of paired-pulse facilitation in excitatory synaptic transmission and stronger paired-pul
86 , these mediators have been shown to enhance excitatory synaptic transmission and suppress inhibitory
87 S-R1a activation in the hippocampus enhances excitatory synaptic transmission and synaptic plasticity
88 the AMPA receptor plays an important role in excitatory synaptic transmission and synaptic plasticity
89 e receptors (AMPARs) mediate the majority of excitatory synaptic transmission and their function impa
90 eceptors (mGluR) are important modulators of excitatory synaptic transmission and therefore potential
91 pines belies the elaborate role they play in excitatory synaptic transmission and ultimately complex
92 ltifunctional aspect of PSD-95 in regulating excitatory synaptic transmission and unveil a novel form
93 bitory synaptic transmission, an increase in excitatory synaptic transmission, and concomitant increa
94 transcripts that regulate synaptic function, excitatory synaptic transmission, and dopamine signaling
95 ignaling improves episodic memory, increases excitatory synaptic transmission, and enhances long-term
96  these paralog proteins in neurodevelopment, excitatory synaptic transmission, and plasticity.
97 ignaling pathway proteins, enhanced cortical excitatory synaptic transmission, and restored dendritic
98             AMPA receptors are important for excitatory synaptic transmission, and their antagonists
99 tate (NMDA) receptors, the main mediators of excitatory synaptic transmission, are heterotetrameric r
100 rs (AMPARs), the principal mediators of fast excitatory synaptic transmission, are specifically excha
101 the long-term potentiation and depression of excitatory synaptic transmission, are widespread phenome
102  particular, in autism and implicate reduced excitatory synaptic transmission as a potential mechanis
103 r before or after disease induction restores excitatory synaptic transmission as well as presynaptic
104  AMPA receptors play a central role in basal excitatory synaptic transmission as well as synaptic mat
105 hly expressed in the CNS and are involved in excitatory synaptic transmission, as well as synaptic pl
106 sms and in particular through degradation of excitatory synaptic transmission associated with impaire
107 sly reported a physiological role of BRI2 in excitatory synaptic transmission at both presynaptic ter
108 iological role of Itm2b in the regulation of excitatory synaptic transmission at both presynaptic ter
109 rebellar cortex, activation of CB1R inhibits excitatory synaptic transmission at parallel fiber (PF)-
110  indicate that TRPV1 activation can modulate excitatory synaptic transmission at the first sensory sy
111  well as subsequent in vivo E2 treatment, on excitatory synaptic transmission at the hippocampal CA3-
112 ecifically to the postsynaptic modulation of excitatory synaptic transmission at the larval neuromusc
113 ored the strength of pathologically weakened excitatory synaptic transmission at the stress-sensitive
114          The impaired inhibitory (as well as excitatory) synaptic transmission at frequencies associa
115                 This defect was specific for excitatory synaptic transmission, because no change in i
116  of neurosteroid E2 is to acutely potentiate excitatory synaptic transmission, but the mechanism of t
117      The neurotransmitter glutamate mediates excitatory synaptic transmission by activating ionotropi
118 postsynaptic membrane form the foundation of excitatory synaptic transmission by establishing the arc
119                  Glutamate receptors mediate excitatory synaptic transmission by forming cation chann
120      The neurotransmitter glutamate mediates excitatory synaptic transmission by gating ionotropic gl
121 siological analysis demonstrates an enhanced excitatory synaptic transmission by increasing the relea
122            Excessive levels of Abeta disrupt excitatory synaptic transmission by promoting the remova
123 ts indicate that activation of Rac1 enhances excitatory synaptic transmission by recruiting AMPARs to
124 spinal cord slices with IFN-alpha suppressed excitatory synaptic transmission by reducing the frequen
125 o exist at presynaptic terminals and reshape excitatory synaptic transmission by regulating presynapt
126                           The enhancement of excitatory synaptic transmission by TNFalpha is in fact
127  and suggest an important mechanism by which excitatory synaptic transmission can be dynamically modu
128 hese results suggest that the suppression of excitatory synaptic transmission can facilitate the appe
129                             We conclude that excitatory synaptic transmission dependent on N-type and
130   In the mammalian brain, the specificity of excitatory synaptic transmission depends on rapid diffus
131                              The strength of excitatory synaptic transmission depends partly on the n
132  1.5-fold increase in AMPA receptor-mediated excitatory synaptic transmission, dramatically altered t
133 act with neurons and blood vessels and shape excitatory synaptic transmission due to their abundant e
134  altered cytokine network, facilitated basal excitatory synaptic transmission, enhanced intrinsic neu
135 sis that an imbalance between inhibitory and excitatory synaptic transmission exists during the criti
136              Kainate receptors mediate fast, excitatory synaptic transmission for a range of inner ne
137                    In the striatum, balanced excitatory synaptic transmission from multiple sources o
138 y, demonstrating a functional segregation of excitatory synaptic transmission from neuronal morpholog
139 e we describe the impact of this mutation on excitatory synaptic transmission from parallel and climb
140 cultured mouse hippocampal neurons, recorded excitatory synaptic transmission from transfected cells,
141              Long-term potentiation (LTP) of excitatory synaptic transmission has long been considere
142             Alteration in the inhibitory and excitatory synaptic transmission (I/E) balance is a fund
143  caused by imbalances between inhibitory and excitatory synaptic transmission (I/E).
144 etwork activity by postsynaptically reducing excitatory synaptic transmission in acute and organotypi
145 xazolepropionic acid) receptors mediate fast excitatory synaptic transmission in brain and underlie a
146 , whereas both stargazin and gamma-4 rescued excitatory synaptic transmission in cerebellar granule c
147 A(-/-) mice, indicating that potentiation of excitatory synaptic transmission in DA neurons is not ne
148  of a mechanism that balances inhibitory and excitatory synaptic transmission in developing neural ci
149 uperficial DH neurons suppressed spontaneous excitatory synaptic transmission in diabetic rats in gre
150 europeptide release from sensory neurons and excitatory synaptic transmission in dorsal horn neurons,
151 docannabinoid signaling in the regulation of excitatory synaptic transmission in frontal neocortex, a
152 MPAR trafficking, silent synapse number, and excitatory synaptic transmission in hippocampal and cort
153 a galanin receptor 1-triggered depression of excitatory synaptic transmission in indirect pathway nuc
154 that alpha-BTX-sensitive nAChRs mediate fast excitatory synaptic transmission in Kenyon cells in the
155 eases intrinsic excitability and spontaneous excitatory synaptic transmission in layer V pyramidal ne
156 opic glutamate receptors, which mediate most excitatory synaptic transmission in mammalian brains.
157 naptically expressed long-term depression of excitatory synaptic transmission in medium spiny neurons
158 suggest that the drug-induced enhancement of excitatory synaptic transmission in midbrain DA neurons,
159 -type glutamate receptors (AMPARs) regulates excitatory synaptic transmission in neurons.
160 opic glutamate receptor that governs most of excitatory synaptic transmission in neurons.
161 principal glutamate receptors mediating fast excitatory synaptic transmission in neurons.
162                                              Excitatory synaptic transmission in PMDS neurons can be
163 on or potentiation of AMPA receptor-mediated excitatory synaptic transmission in prefrontal cortex py
164 at fear extinction decreases the efficacy of excitatory synaptic transmission in projections from the
165                     PACAP enhanced, however, excitatory synaptic transmission in projections from the
166 ose of natural or synthetic AAS strengthened excitatory synaptic transmission in putative ventral teg
167 rgely determines the strength of odor-evoked excitatory synaptic transmission in rat piriform cortica
168 neurons revealed no changes in inhibitory or excitatory synaptic transmission in response to PGE2 exp
169  modulation of TRPV1-mediated enhancement of excitatory synaptic transmission in response to PKC acti
170 ive forms of synaptic plasticity that reduce excitatory synaptic transmission in response to prolonge
171 s in the central nervous system that mediate excitatory synaptic transmission in response to the rele
172 ential, it is unknown whether toluene alters excitatory synaptic transmission in reward-sensitive dop
173                                 Furthermore, excitatory synaptic transmission in spinal cord slices a
174 frequency of action potentials, and enhanced excitatory synaptic transmission in spinal cord slices,
175                     Furthermore, facilitated excitatory synaptic transmission in spinal dorsal horn n
176 gs revealed severely affected inhibitory and excitatory synaptic transmission in the amygdala, hippoc
177  and emotional behavior, has dual effects on excitatory synaptic transmission in the basolateral amyg
178 annels whose function is critical for normal excitatory synaptic transmission in the brain and whose
179                              The majority of excitatory synaptic transmission in the brain occurs at
180             Glutamate receptors that mediate excitatory synaptic transmission in the brain show unusu
181 PARs) play a critical role in mediating fast excitatory synaptic transmission in the brain.
182 4 subunits that mediate the majority of fast excitatory synaptic transmission in the brain.
183 cid (AMPA) receptors mediate the majority of excitatory synaptic transmission in the brain.
184 utamate receptors (AMPARs) mediate most fast excitatory synaptic transmission in the brain.
185 a key mechanism to determine the strength of excitatory synaptic transmission in the brain.
186 nnels responsible for a majority of the fast excitatory synaptic transmission in the brain.
187 mate-gated cation channels that mediate fast excitatory synaptic transmission in the central nervous
188  channels are membrane proteins that mediate excitatory synaptic transmission in the central nervous
189 -Methyl-D-aspartate (NMDA) receptors mediate excitatory synaptic transmission in the central nervous
190  mediate a slow, Ca2+-permeable component of excitatory synaptic transmission in the central nervous
191  Glutamate receptors mediate the majority of excitatory synaptic transmission in the central nervous
192 s are ligand-gated ion channels that mediate excitatory synaptic transmission in the central nervous
193 ic glutamate receptors (iGluRs) mediate fast excitatory synaptic transmission in the central nervous
194 agues underlies much of our understanding of excitatory synaptic transmission in the central nervous
195  Ionotropic glutamate receptors mediate fast excitatory synaptic transmission in the central nervous
196  Ion channels activated by glutamate mediate excitatory synaptic transmission in the central nervous
197      Although, other forms of inhibitory and excitatory synaptic transmission in the circuit were unc
198 ) receptors (iGluRs) mediate the majority of excitatory synaptic transmission in the CNS and are esse
199                                         Fast excitatory synaptic transmission in the CNS is mediated
200  AMPA receptors mediate the majority of fast excitatory synaptic transmission in the CNS, and evidenc
201      Dendritic spines are the major sites of excitatory synaptic transmission in the CNS, and their s
202 mate receptors, which underlie a majority of excitatory synaptic transmission in the CNS, associate w
203 l membrane are the primary mediators of fast excitatory synaptic transmission in the CNS.
204 azolepropionic acid (AMPA) type mediate fast excitatory synaptic transmission in the CNS.
205  Glutamate receptors mediate the majority of excitatory synaptic transmission in the CNS.
206 ating a slow, calcium-permeable component of excitatory synaptic transmission in the CNS.
207 tion of microglia drives the facilitation of excitatory synaptic transmission in the dorsal horn, whi
208  Overall, we found that (2R,6R)-HNK enhances excitatory synaptic transmission in the hippocampus thro
209 r chaperone hsp90 (heat shock protein 90) in excitatory synaptic transmission in the hippocampus.
210                                         Fast excitatory synaptic transmission in the mammalian brain
211 s (iGluRs) that mediate the majority of fast excitatory synaptic transmission in the mammalian brain.
212 re tetrameric ion channels that mediate fast excitatory synaptic transmission in the mammalian brain.
213  receptors are the primary mediators of fast excitatory synaptic transmission in the mammalian CNS.
214  pathway-specific presynaptic enhancement of excitatory synaptic transmission in the NAc.
215                                    Most fast excitatory synaptic transmission in the nervous system i
216 utamate-gated ion channels that mediate fast excitatory synaptic transmission in the nervous system.
217  is a ligand-gated ion channel that mediates excitatory synaptic transmission in the nervous system.
218                                              Excitatory synaptic transmission in the nucleus accumben
219 -type glutamate receptors that underlie fast excitatory synaptic transmission in the SDH.
220 tioning blocked cocaine-evoked depression of excitatory synaptic transmission in the shell of the NAc
221 are involved in bi-directional regulation of excitatory synaptic transmission in the spinal cord SG r
222 R effects the expression of neuroligin 1 and excitatory synaptic transmission in the spinal cord, and
223 (2+) channels in primary sensory neurons and excitatory synaptic transmission in the spinal dorsal ho
224 o regional- and training-specific changes in excitatory synaptic transmission in the striatum.
225  have determined the actions of adenosine on excitatory synaptic transmission in the subiculum, the m
226 s are ligand-gated ion channels that mediate excitatory synaptic transmission in the vertebrate brain
227    Dendritic spines are the primary sites of excitatory synaptic transmission in the vertebrate brain
228 ndritic spines, which are the major sites of excitatory synaptic transmission in the vertebrate brain
229 tamate receptors (iGluRs) that mediate rapid excitatory synaptic transmission in the vertebrate brain
230 ant peptides in the LH to VTA projection, on excitatory synaptic transmission in the VTA and reward-s
231 ous study we showed that kisspeptin enhances excitatory synaptic transmission in these cells.
232 A, it is unknown whether leptin can modulate excitatory synaptic transmission in this brain region.
233 re we characterize the dynamic properties of excitatory synaptic transmission in two major intracorti
234     Here we report that nicotine potentiates excitatory synaptic transmission in ventral tegmental ar
235                We examined whether increased excitatory synaptic transmission in ventral tegmental ar
236 perience-dependent homeostatic plasticity of excitatory synaptic transmission in vivo.
237 hat disruption of LIS1 has direct effects on excitatory synaptic transmission independent of laminar
238                                              Excitatory synaptic transmission is accompanied by a loc
239                                              Excitatory synaptic transmission is altered during aging
240 ices of mouse somatosensory cortex show that excitatory synaptic transmission is markedly suppressed
241                                              Excitatory synaptic transmission is mediated by AMPA-typ
242 central nervous system, the majority of fast excitatory synaptic transmission is mediated by glutamat
243 mouse brain slices that alpha1-A(R)-mediated excitatory synaptic transmission is mediated by the iono
244                                              Excitatory synaptic transmission is typically studied un
245 gests the hypothesis that the suppression of excitatory synaptic transmission itself could facilitate
246 PGE2 (2 mum; 48 h) presynaptically increases excitatory synaptic transmission, leading to a hyperexci
247                Long-term depression (LTD) of excitatory synaptic transmission mediated by type 5 meta
248 d a decrease in the frequency of spontaneous excitatory synaptic transmission (mEPSCs) in neurons lac
249                          In the brain, fast, excitatory synaptic transmission occurs primarily throug
250 michannels in resting states regulates basal excitatory synaptic transmission of hippocampal CA1 pyra
251 r neuronal differentiation, and impaired the excitatory synaptic transmission of NPC-derived neurons.
252 one rats had altered inhibitory and enhanced excitatory synaptic transmission of the principal neuron
253 perience induces a persistent enhancement of excitatory synaptic transmission on NAc shell D1+ neuron
254 hol session produced enduring enhancement of excitatory synaptic transmission onto dopamine D1 recept
255 s effect is mediated by the strengthening of excitatory synaptic transmission onto dopamine neurons t
256 on of insulin into the VTA, which suppresses excitatory synaptic transmission onto dopamine neurons,
257 rd, we hypothesized that leptin can decrease excitatory synaptic transmission onto dopamine neurons.
258 that GluN2D-containing NMDARs participate in excitatory synaptic transmission onto hippocampal intern
259       Notably, fear conditioning potentiates excitatory synaptic transmission onto these long-range p
260                       Notably, we found that excitatory synaptic transmission onto these neurons was
261 t persistent long-term potentiation (LTP) of excitatory synaptic transmission onto ventral tegmental
262   Thus, enhanced CRF-induced potentiation of excitatory synaptic transmission onto VTA dopamine neuro
263 motes drug-seeking behaviors and potentiates excitatory synaptic transmission onto VTA dopamine neuro
264                 Finally, oxA/hcrt-1-mediated excitatory synaptic transmission onto VTA neurons was no
265 ial dorsal horn neurons either by increasing excitatory synaptic transmission or by decreasing inhibi
266 c Ca2+ fluxes affects spontaneous and evoked excitatory synaptic transmission or synaptic plasticity.
267       Postsynaptic kainate receptors mediate excitatory synaptic transmission over a broad range of t
268 important consequences for the regulation of excitatory synaptic transmission, plasticity, epileptoge
269              Long-term potentiation (LTP) of excitatory synaptic transmission plays a major role in m
270 la pyramidal neurons shows an attenuation of excitatory synaptic transmission, presumably because of
271 nf transcription impaired inhibitory but not excitatory synaptic transmission recorded from layer V p
272 ic glutamate receptors (iGluRs) that mediate excitatory synaptic transmission, regulate neurotransmit
273 ioral function; however, the degree to which excitatory synaptic transmission relies on the normal op
274 hermore, nerve injury persistently increased excitatory synaptic transmission (spontaneous excitatory
275  loss of synaptic AMPA receptors and reduced excitatory synaptic transmission that corresponds with i
276 ependent translation of proteins involved in excitatory synaptic transmission that in turn drives the
277 ogical studies revealed impairments in basal excitatory synaptic transmission that involved both AMPA
278                                         Fast excitatory synaptic transmission that is contingent upon
279             Among diverse factors regulating excitatory synaptic transmission, the abundance of posts
280                          As a key element in excitatory synaptic transmission, the receptor regulates
281 mulates ATP/adenosine release, and depresses excitatory synaptic transmission through activation of p
282 GABA release from A17s, regulate the flow of excitatory synaptic transmission through the rod pathway
283 uRs in the dorsal BNST induces depression of excitatory synaptic transmission through two distinct me
284  ligand-gated ion channels that mediate fast excitatory synaptic transmission throughout the central
285 utamate-gated ion channels that mediate fast excitatory synaptic transmission throughout the nervous
286         However, actions of serotonin on the excitatory synaptic transmission to LHb neurons have not
287 nipulating neurogenesis in adult mice alters excitatory synaptic transmission to mature dentate neuro
288 vestigated the effects of glucocorticoids on excitatory synaptic transmission to putative DR 5-HT neu
289                             ABSTRACT: During excitatory synaptic transmission, various structurally u
290 ence suggests that anaesthetics also inhibit excitatory synaptic transmission via a presynaptic mecha
291                 After blockade of ionotropic excitatory synaptic transmission, voltage-clamp recordin
292                             Retinogeniculate excitatory synaptic transmission was also suppressed by
293           Similar results were obtained when excitatory synaptic transmission was eliminated in a low
294                        This study shows that excitatory synaptic transmission was enhanced in the bed
295 ved on dendritic shafts, and the strength of excitatory synaptic transmission was unaffected, showing
296 f NL3 in WT or NL1 KO neurons did not affect excitatory synaptic transmission, whereas P0 knockdown o
297 s in the hippocampus for 7-10 days increases excitatory synaptic transmission, whereas short-term act
298 ptors mediates dopamine-evoked depression of excitatory synaptic transmission, which contributes to a
299 how that the protein is important for normal excitatory synaptic transmission, while its dysfunction
300 m presynaptic excitatory terminals regulated excitatory synaptic transmission within hippocampal CA3.

 
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