ライフサイエンスコーパス: glutamatergic synapse

1 e measurements at the calyx of Held, a giant glutamatergic synapse.

2 houses the postsynaptic terminal of a single glutamatergic synapse.

3 and maintenance of long-term potentiation of glutamatergic synapses.

4 receptors (AMPARs) to postsynaptic sites of glutamatergic synapses.

5 cytoskeleton and regulates the formation of glutamatergic synapses.

6 receptor abundance or the overall number of glutamatergic synapses.

7 re critical for the functional maturation of glutamatergic synapses.

8 temporally tunes Arc-mediated plasticity at glutamatergic synapses.

9 e (METH) exposure causes neuroadaptations at glutamatergic synapses.

10 a common intrasynapse-type relationship for glutamatergic synapses.

11 element of the postsynaptic architecture of glutamatergic synapses.

12 nd a complex interaction with ethanol at CeA glutamatergic synapses.

13 ograde endocannabinoid signaling at striatal glutamatergic synapses.

14 rs morphological maturation and formation of glutamatergic synapses.

15 the postsynaptic density (PSD) of excitatory glutamatergic synapses.

16 rane-associated m2 receptors were located at glutamatergic synapses.

17 m of structural and functional plasticity of glutamatergic synapses.

18 ontaneous neurotransmission at GABAergic and glutamatergic synapses.

19 sistent with enhanced release probability at glutamatergic synapses.

20 t reporter synaptopHluorin preferentially at glutamatergic synapses.

21 aturation of adult-born GCs and formation of glutamatergic synapses.

22 r the synaptic action of IL-1beta on central glutamatergic synapses.

23 (NLG1), a postsynaptic adhesion molecule at glutamatergic synapses.

24 ell as cell culture, increases the number of glutamatergic synapses.

25 5 expression and impaired the development of glutamatergic synapses.

26 espiratory motoneurons on both sides through glutamatergic synapses.

27 eady to quickly bind glutamate released from glutamatergic synapses.

28 critical role in regulating the stability of glutamatergic synapses.

29 te most of the fast postsynaptic response at glutamatergic synapses.

30 ic synapses and an in vivo LTD of excitatory glutamatergic synapses.

31 of long-term depression at cortico-accumbal glutamatergic synapses.

32 ion of proteins required for potentiation of glutamatergic synapses.

33 ghtly coupled to formation and maturation of glutamatergic synapses.

34 tic efficacy and triggers a proliferation of glutamatergic synapses.

35 long-term potentiation (LTP) at hippocampal glutamatergic synapses.

36 critical for the development and function of glutamatergic synapses.

37 evoked neurotransmitter release at cortical glutamatergic synapses.

38 tes the function and stability of excitatory glutamatergic synapses.

39 ty and pruning of excitatory corticostriatal glutamatergic synapses.

40 of Rac1's control of actin polymerization at glutamatergic synapses.

41 nd reduce neuronal inhibitory control of CeA glutamatergic synapses.

42 nal activity-mediated feedback regulation of glutamatergic synapses.

43 rding and analysis methods at single central glutamatergic synapses.

44 contributions to signal saturation at single glutamatergic synapses.

45 ls' brains have reduced dendritic spines and glutamatergic synapses.

46 s the formation and functional maturation of glutamatergic synapses.

47 y contribute to the structural plasticity of glutamatergic synapses.

48 h are critical for the development of mature glutamatergic synapses.

49 s in neuronal excitability and plasticity of glutamatergic synapses.

50 ucture and physiology of dendritic spines in glutamatergic synapses.

51 nown whether Shisa7 has a functional role in glutamatergic synapses.

52 's specific sites or mechanisms of action at glutamatergic synapses.

53 m is persistently altered by the activity of glutamatergic synapses.

54 he kinetics of NMDA and non-NMDA currents at glutamatergic synapses.

55 citatory neurotransmission and plasticity in glutamatergic synapses.

56 n neuron, indicative of decreased numbers of glutamatergic synapses.

57 g Nmdars During The Maturation Of Tripartite Glutamatergic Synapses.

58 shown to reduce the strength of excitatory (glutamatergic) synapses.

59 atio of NMDA receptor subunit composition at glutamatergic synapses, a rejuvenation to a composition

60 However, how glutamatergic synapses acquire AMPA-Rs with distinct kin

61 determine whether plasticity will occur at a glutamatergic synapse and confer long-term potentiation

62 suppression at ventral hippocampal-amygdala glutamatergic synapses and amygdala-specific 2-AG deplet

63 nts in NRG2 KOs are augmented at hippocampal glutamatergic synapses and are more sensitive to ifenpro

64 Here we present the pattern of glutamatergic synapses and cell bodies in the late larva

65 g of the factors that gate the maturation of glutamatergic synapses and complex behavior.

66 ic proteins discriminate among 4 subtypes of glutamatergic synapses and GABAergic synapses.

67 y (PCP) pathway, are localized at developing glutamatergic synapses and interact with key synaptic pr

68 naptic PTPRD promotes the differentiation of glutamatergic synapses and interacts with SLITRK3.

69 known as GluR4, which is found on excitatory glutamatergic synapses and is important for learning and

70 k1) decreases the number of cortico-striatal glutamatergic synapses and of D1 and D2 dopamine recepto

71 trate a common thread in the organization of glutamatergic synapses and suggest a link between genes

72 ulfate is critical for normal functioning of glutamatergic synapses and that its deficiency mediates

73 onal mechanism of rhythm generation in which glutamatergic synapses and the short-term depression of

74 We first present a brief overview of glutamatergic synapses and then explore the genetic and

75 nterneuron, pyramidal neuron, single CA3-CA1 glutamatergic synapse, and astrocytes, we found that int

76 te fast excitatory postsynaptic responses at glutamatergic synapses, and are involved in various form

77 ference RNAs to eliminate both proteins from glutamatergic synapses, and find that they are essential

78 d presynaptic and postsynaptic maturation of glutamatergic synapses, and implicate presynaptic alpha7

79 nts, PlexinA2-/- mice show an increase in GC glutamatergic synapses, and we show that Sema5A and Plex

80 alterations in the strength of an individual glutamatergic synapse are often accompanied by changes i

81 Likewise in the adult CNS, glutamatergic synapses are abundant throughout all major

82 A subset of central glutamatergic synapses are coordinately pruned and matur

83 Early in development, when glutamatergic synapses are initially forming, waves of e

84 m potentiation (LTP) and depression (LTD) at glutamatergic synapses are intensively investigated proc

85 Glutamatergic synapses are located mostly on dendritic s

86 to the periphery of the terminals, in which glutamatergic synapses are located, but also was present

87 In excitatory neurons, most glutamatergic synapses are made on the heads of dendriti

88 hieved with phasic NE release, provided only glutamatergic synapses are modulated.

89 meable AMPA receptors (CP-AMPARs) at central glutamatergic synapses are of special interest because o

90 Early in development, however, when glutamatergic synapses are only beginning to form, nicot

91 At early developmental stages, glutamatergic synapses are sparse, immature and function

92 1 receptor (CB(1)R)-dependent depression at glutamatergic synapses are sufficient to induce long-ter

93 everal molecules in regulating plasticity of glutamatergic synapses are translationally elevated in t

94 anisms underlying dopaminergic modulation of glutamatergic synapses are unclear.

95 Thus far, these glutamatergic synapses are well recognized for showing a

96 To begin filling this gap, SNc glutamatergic synapses arising from pedunculopotine nucl

97 nesis, and point to the Trio-Rac1 pathway at glutamatergic synapses as a possible key point of conver

98 Recent evidence implicates glutamatergic synapses as key pathogenic sites in psychi

99 show that hilar mossy cells provide initial glutamatergic synapses as well as disynaptic GABAergic i

100 ve decreased density of dendritic spines and glutamatergic synapses, as well as impaired dendritic gr

101 cause changes in the strength of subsets of glutamatergic synapses at multiple locations, including

102 y illustrates for the first time how a tonic glutamatergic synapse avoids postsynaptic receptor desen

103 We mapped the spatial organization of glutamatergic synapses between layer 5 pyramidal cells b

104 During the first postnatal month glutamatergic synapses between layer 5 pyramidal cells i

105 Here we show that the tonic glutamatergic synapses between photoreceptors and rod-do

106 cdh-gammaC5 is present in some GABAergic and glutamatergic synapses both pre- and postsynaptically; 2

107 At glutamatergic synapses, both long-term potentiation (LTP

108 ut mice exhibit loss of approximately 50% of glutamatergic synapses, but not inhibitory synapses, in

109 ARs) modulate release and plasticity at many glutamatergic synapses, but the specificity of their exp

110 efine the kinetics of synaptic depression at glutamatergic synapses by controlling the size of the ve

111 egative regulator to confine the strength of glutamatergic synapses by downregulating the expression

112 oted long-term depression of corticostriatal glutamatergic synapses, by suppressing regulator of G pr

113 These results reveal that glutamatergic synapses can instruct plasticity at electr

114 ults demonstrate that astrocytes adjacent to glutamatergic synapses can release glutamine in a tempor

115 Many central glutamatergic synapses contain a single presynaptic acti

116 observed that many, but not all, interneuron glutamatergic synapses contain AMPA receptors that are G

117 ychiatric pathogenesis by reducing spine and glutamatergic synapse density downstream of GSK3 in the

118 ecessary for activity to negatively regulate glutamatergic synapse density.

119 n the inner and outer plexiform layers after glutamatergic synapses depolarize TH cell dendrites in t

120 se results imply that normal activity-driven glutamatergic synapse development is impaired by perturb

121 d its ligand FLRT3 play an important role in glutamatergic synapse development.

122 tract (ST) relay homeostatic information via glutamatergic synapses directly to second-order neurons

123 Here we show that activation of glutamatergic synapses drives long-term depression of el

124 To better understand the function of glutamatergic synapses during development, we made whole

125 ha7-nAChRs unexpectedly promote formation of glutamatergic synapses during development.

126 We found that D2 glutamatergic synapses expressed enhanced release probab

127 NRG1 also is present at a subset of glutamatergic synapses expressing the vesicular glutamat

128 n synaptic and extrasynaptic compartments at glutamatergic synapses, focusing on AMPA and NMDA recept

129 st in part from the insertion of AMPARs into glutamatergic synapses following chronic reductions in n

130 r data show that Piccolo is not required for glutamatergic synapse formation but does influence presy

131 neuromodulation regulates activity-dependent glutamatergic synapse formation in the developing striat

132 iven activity shapes bipolar-->ganglion cell glutamatergic synapse formation, beginning around the ti

133 t the opposing roles of Celsr3 and Vangl2 in glutamatergic synapse formation.

134 els result in aberrant neurite outgrowth and glutamatergic synapse formation.

135 ptic mechanisms of cholinergic modulation at glutamatergic synapses formed by parallel fiber axons on

136 ion, and our data reveal that Wnt5a inhibits glutamatergic synapses formed via Celsr3.

137 unipolar brush cells (UBC) receive a single glutamatergic synapse from a mossy fiber (MF), which mak

138 the mouse barrel cortex, NG2 cells received glutamatergic synapses from thalamocortical fibers and p

139 of the recycling endosome protein GRASP1 in glutamatergic synapse function and animal behavior.

140 animal models supporting a role for aberrant glutamatergic synapse function in the etiology of intell

141 the most promising candidate genes affecting glutamatergic synapse function, highlighting the likely

142 At excitatory glutamatergic synapses, fusion of intracellular vesicles

143 the GABAergic synapses and 25 +/- 2% of the glutamatergic synapses had colocalizing septin 11 cluste

144 At glutamatergic synapses, high and low activity of AMPA re

145 f Held to characterize NO modulation at this glutamatergic synapse in the auditory pathway.

146 Held is a giant nerve terminal that forms a glutamatergic synapse in the auditory pathway.

147 e normal structural maturation of Drosophila glutamatergic synapses in a developmental role that is n

148 ation and is implicated in the regulation of glutamatergic synapses in autism spectrum disorder (ASD)

149 ith morphological and functional deficits at glutamatergic synapses in both humans and rodents.

150 The m2 receptors were also enriched at glutamatergic synapses in both motoneuronal perikarya an

151 S14 (RGS14-KO) and now express robust LTP at glutamatergic synapses in CA2 neurons with no impact on

152 Immature glutamatergic synapses in cultured neurons contain high-

153 ections are enough to trigger adaptations at glutamatergic synapses in D(1)-expressing MSNs, which, a

154 Glutamatergic synapses in early postnatal development tr

155 wever, little is known about the role of CEm glutamatergic synapses in fear regulation and anxiety-li

156 litation is completely blocked in excitatory glutamatergic synapses in hippocampal autaptic cultures.

157 However, whereas key plasticity occurs at glutamatergic synapses in mammals, the neurochemistry of

158 major transmitter reception compartments of glutamatergic synapses in most principal neurons of the

159 SCs significantly decreased, suggesting that glutamatergic synapses in NG2(+) cells undergo a maturat

160 ly mediated by time-dependent adaptations at glutamatergic synapses in nucleus accumbens (NAc).

161 phy to delineate the organization of PSDs at glutamatergic synapses in rat hippocampal cultures.

162 in the development of presynaptic muting at glutamatergic synapses in rat hippocampal neurons.

163 tability of these cocaine-induced changes at glutamatergic synapses in the accumbens shell by utilizi

164 At glutamatergic synapses in the brain, activity-dependent

165 spines are the postsynaptic compartments of glutamatergic synapses in the brain.

166 oid receptors and eCB synthetic machinery at glutamatergic synapses in the CeA and find that CeA neur

167 ynaptic expression of betaARs in a subset of glutamatergic synapses in the cerebral cortex.

168 The maturation of glutamatergic synapses in the CNS is regulated by NMDA r

169 ession (LTD) has been studied extensively at glutamatergic synapses in the CNS.

170 long with prominent functional impairment of glutamatergic synapses in the hippocampus and medial pre

171 Selective strengthening of specific glutamatergic synapses in the mammalian hippocampus is c

172 AMPA receptor (AMPAR) plasticity at glutamatergic synapses in the mesoaccumbal dopaminergic

173 t changes in neuroplasticity at the level of glutamatergic synapses in the nucleus accumbens (NAc).

174 Cocaine induces plasticity at glutamatergic synapses in the nucleus accumbens (NAc).

175 We further demonstrate that glutamatergic synapses in the nucleus accumbens are pote

176 eeking involves impairments in plasticity at glutamatergic synapses in the nucleus accumbens.

177 nknown and we hypothesized that they involve glutamatergic synapses in the nucleus tractus solitarius

178 group I mGluRs by transmitter spillover from glutamatergic synapses in the rat accumbens.

179 eased levels of AMPA receptor (AMPAR)-silent glutamatergic synapses in this projection, accompanied b

180 3 also showed a loss of approximately 50% of glutamatergic synapses in vivo without affecting the inh

181 To determine how NL1 influences the state of glutamatergic synapses in vivo, we compared the synaptic

182 ynaptically and ER-evoked calcium release at glutamatergic synapses in young AD transgenic mice.

183 Glutamatergic synapses, in the CeA and throughout the br

184 tation and enhanced short term depression of glutamatergic synapses, indicating a difference in trans

185 -frequency stimulation (1 Hz, 15 min) of the glutamatergic synapses induced heterosynaptic LTD of GAB

186 iously that postsynaptic TrkC functions as a glutamatergic synapse-inducing (synaptogenic) cell adhes

187 At glutamatergic synapses, induction of associative synapti

188 Manipulating presynaptic K(+) at a glutamatergic synapse influenced quantal size, indicatin

189 Although repetitive activity of glutamatergic synapses initiates the eCB mobilization re

190 The development of glutamatergic synapses involves changes in the number an

191 The excitatory glutamatergic synapse is the principal site of communica

192 The concentration of glutamate within the glutamatergic synapse is tightly regulated by the excita

193 f N-methyl-d-aspartate receptors (NMDARs) at glutamatergic synapses is essential for certain forms of

194 Their role within glutamatergic synapses is not completely understood.

195 riate transmission of nerve impulses through glutamatergic synapses is required throughout the brain

196 ntribution to the long-term stabilization of glutamatergic synapses is unknown.

197 ank3, which encodes a scaffolding protein at glutamatergic synapses, is a genetic risk factor for aut

198 pulation restored NMDAR-mediated currents at glutamatergic synapses, it did not rescue GluN2B loss of

199 However, glutamatergic synapses lacking either protein exhibit re

200 tro data, that astrocytes provide lactate to glutamatergic synapses ("lactate shuttle").

201 dritic spine maturation, and that defects at glutamatergic synapses likely contribute to the behavior

202 At the parallel fibre-Purkinje cell glutamatergic synapse, little or no Ca(2+) entry takes p

203 een many electrophysiological studies of MSN glutamatergic synapses, little is known about how cortic

204 At glutamatergic synapses, local endocytic recycling of AMP

205 reased or defective OPHN1 signaling prevents glutamatergic synapse maturation and causes loss of syna

206 in regulating the timing of neuronal growth, glutamatergic synapse maturation and cortical circuit fu

207 proposed to underlie the observed defects of glutamatergic synapse maturation and function and to aff

208 NMDAR)-dependent signaling regulates central glutamatergic synapse maturation and has been implicated

209 endogenous d-serine release, which promotes glutamatergic synapse maturation and stabilizes axonal s

210 Central glutamatergic synapses may express AMPA-sensitive glutam

211 At excitatory glutamatergic synapses, NMDA receptors (NMDARs) have a f

212 At the glutamatergic synapse of the Drosophila larval neuromusc

213 activity evokes astrocytic Ca(2+) signals at glutamatergic synapses of adult mice.

214 esynaptic and postsynaptic Nav expression in glutamatergic synapses of CH and SR supporting neurotran

215 We compared the densities of glutamatergic synapses of granule cells (GCs) generated

216 influences the quantitative rule of STDP at glutamatergic synapses of hippocampal neurons.

217 Here, we investigate Parkin's role at glutamatergic synapses of rat hippocampal neurons.

218 f transmission during locomotive behavior at glutamatergic synapses of the Drosophila larval neuromus

219 Newly formed glutamatergic synapses often lack postsynaptic AMPA-type

220 Spine loss appeared with mislocation of glutamatergic synapses on dendritic shafts and a reducti

221 asting, experience-dependent potentiation of glutamatergic synapses on hypocretin neurons in mice fol

222 In MCHR1 KO mice, the efficacy of glutamatergic synapses on hypocretin/orexin neurons is p

223 e, implicate ErbB4 as a selective marker for glutamatergic synapses on inhibitory interneurons.

224 Many glutamatergic synapses on interneurons involved in feedb

225 of transient synaptic potentiation (t-SP) at glutamatergic synapses on medium spiny neurons (MSNs) in

226 To determine the source of early glutamatergic synapses on newborn GCs in adult mice, we

227 ent synaptic potentiation (t-SP) of cortical glutamatergic synapses on nucleus accumbens core medium

228 ceptor subunit composition and regulation of glutamatergic synapses on PV(+) and SOM(+) interneurons.

229 Glutamatergic synapses on some hippocampal GABAergic int

230 spiny neurons (MSNs) are more sensitive than glutamatergic synapses on the same cells to endocannabin

231 Postsynaptic remodeling of glutamatergic synapses on ventral striatum (vSTR) medium

232 nd that demyelinated axons formed functional glutamatergic synapses onto adult-born NG2(+) oligodendr

233 onfirmed that ribbon-containing endings made glutamatergic synapses onto DA cells processes in S3 and

234 uption of AKAP-PKA anchoring does not affect glutamatergic synapses onto DA neurons, suggesting that

235 r they mediate long-term depression (LTD) of glutamatergic synapses onto excitatory and inhibitory ne

236 is supported by long-lasting modification of glutamatergic synapses onto perisomatic inhibitory inter

237 contrast, we show that maturation of silent glutamatergic synapses onto principal neurons was suffic

238 e found that augmented maternal care reduced glutamatergic synapses onto stress-sensitive hypothalami

239 Because plasticity of glutamatergic synapses onto VTA neurons can encode predi

240 asing UBE3A in the nucleus downregulates the glutamatergic synapse organizer Cbln1, which is needed f

241 nes belonging to the postsynaptic density at glutamatergic synapses, particularly components of the N

242 logy of depression and demonstrated that the glutamatergic synapse presents multiple targets for deve

243 ngs suggest that the elimination of immature glutamatergic synapses proceeds normally in the absence

244 In single neurons, glutamatergic synapses receiving distinct afferent input

245 ate the selective loss of GABAergic--but not glutamatergic--synapses, reduced GABA release, and a shi

246 ine relative availability at rat hippocampal glutamatergic synapses regulate the trafficking and syna

247 Glutamatergic synapses rely on AMPA receptors (AMPARs) f

248 round awakening--may ensure that hippocampal glutamatergic synapses remain fully responsive and able

249 their localization and function at specific glutamatergic synapses remain unknown.

250 siological role of vesicular zinc at central glutamatergic synapses remains poorly understood.

251 f MCU-dependent mitochondrial Ca2+ uptake at glutamatergic synapses rescues the altered neurotransmit

252 t types associated with synaptic vesicles in glutamatergic synapses revealed by electron microscope t

253 maging of developing Drosophila melanogaster glutamatergic synapses revealed that the Unc13B isoform

254 Glutamatergic synapses show large variations in strength

255 Drosophila neuromuscular junction (NMJ) is a glutamatergic synapse, similar in composition and functi

256 Thus, E2 acutely potentiates glutamatergic synapses similarly in both sexes, but dist

257 ansgenic mice to show how dopamine regulates glutamatergic synapses specific to the striatonigral and

258 neurons precludes long-term potentiation of glutamatergic synapses specifically by preventing activi

259 at long-term plasticity at subthalamo-nigral glutamatergic synapses (STN-SNr) sculpting the activity

260 could act in a paracrine fashion to suppress glutamatergic synapse strength by triggering removal of

261 e that glutamate secreted via xCT suppresses glutamatergic synapse strength by triggering removal of

262 iation studies, indicate that alterations in glutamatergic synapse structure and function represent a

263 between MRs and an epigenetic control of the glutamatergic synapse that underlies susceptibility to s

264 increase in the number of VGluT1(+) neuronal glutamatergic synapses that are ensheathed by processes

265 y a unique, previously unrecognized, role at glutamatergic synapses that are important for learning a

266 ribed, but also promotes the presence of new glutamatergic synapses that contain only NMDA receptors-

267 Deletion of Rab3a results in glutamatergic synapses that have a compromised responsiv

268 Plastic changes in glutamatergic synapses that lead to endurance of drug cr

269 a major postsynaptic scaffolding protein of glutamatergic synapses that regulates synaptic strength

270 fficient to trigger sustained changes on VTA glutamatergic synapses that resemble activity-dependent

271 but provide a substantial proportion of the glutamatergic synapses that the cells receive (over a th

272 the trapezoid body (MNTB) through the giant glutamatergic synapse, the calyx of Held.

273 on result from interactions with colocalized glutamatergic synapses, the activity of which leads to t

274 In the postsynaptic density of glutamatergic synapses, the discs large (DLG)-membrane-a

275 eed, disrupted plasticity at corticostriatal glutamatergic synapses, the gateway of the BG, is correl

276 At excitatory glutamatergic synapses, the immediate early gene product

277 dvantage of the large size of a rat auditory glutamatergic synapse--the calyx of Held--and combined v

278 GluA1 subunit and NMDA receptor subunits at glutamatergic synapses, these results suggest a developm

279 aptic plasticity mediated through actions at glutamatergic synapses; those in the second class impact

280 e of KCC2 in the development and function of glutamatergic synapses through mechanisms that remain po

281 Regulation of a key component of glutamatergic synapses through RoR2 provides a mechanism

282 s (NMDARs) mediate a slow EPSC at excitatory glutamatergic synapses throughout the brain.

283 in vivo causes a disproportionate number of glutamatergic synapses to be localized on dendritic shaf

284 e Drosophila neuromuscular junction, a model glutamatergic synapse, to characterize the role of Shank

285 ynaptic plasticity with respect to mammalian glutamatergic synapses, to address these issues through

286 ve, although protein loss suggests a role in glutamatergic synapse transmission and overexpression st

287 e (i.e., mostly thalamostriatal) axo-spinous glutamatergic synapses using a 3D electron microscopic a

288 targeted gene transfer across a neocortical glutamatergic synapse, using as the model the projection

289 Moreover, the number and function of glutamatergic synapses was unaffected by MEN1 knockdown,

290 gs from the calyx of Held, a giant mammalian glutamatergic synapse, we found that changes in presynap

291 reted from presynaptic neurons, localizes to glutamatergic synapses, where it associates with postsyn

292 so expressed in the postsynaptic membrane of glutamatergic synapses, where their activation and regul

293 dala are enriched in synapses and located to glutamatergic synapses, where they selectively control s

294 arval ventral nerve cord neuropil is rich in glutamatergic synapses, which are primarily located near

295 re-organization of the neuropil surrounding glutamatergic synapses, which is associated with faster

296 ate phase of long-term potentiation (LTP) at glutamatergic synapses, which is thought to underlie lon

297 g-term depression (eCB-LTD) at adult central glutamatergic synapses, while another form of presynapti

298 ' NMDAR-Ab prevent long-term potentiation at glutamatergic synapses, while leaving NMDAR-mediated cal

299 -Phox2b neurons establish classic excitatory glutamatergic synapses with pre-Botzinger complex neuron

300 ions suggest that VGluT3-expressing ACs form glutamatergic synapses with W3 ganglion cells, and targe

301 ation in rats generated AMPA receptor-silent glutamatergic synapses within both infralimbic (IL) and