ライフサイエンスコーパス: glutamatergic synapse

1 neuromuscular junctions, representing large glutamatergic synapses.

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

3 s the formation and functional maturation of glutamatergic synapses.

4 y contribute to the structural plasticity of glutamatergic synapses.

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

6 s in neuronal excitability and plasticity of glutamatergic synapses.

7 ucture and physiology of dendritic spines in glutamatergic synapses.

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

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

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

11 citatory neurotransmission and plasticity in glutamatergic synapses.

12 g Nmdars During The Maturation Of Tripartite Glutamatergic Synapses.

13 cytoskeleton and regulates the formation of glutamatergic synapses.

14 receptor abundance or the overall number of glutamatergic synapses.

15 re critical for the functional maturation of glutamatergic synapses.

16 temporally tunes Arc-mediated plasticity at glutamatergic synapses.

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

18 a common intrasynapse-type relationship for glutamatergic synapses.

19 element of the postsynaptic architecture of glutamatergic synapses.

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

21 ograde endocannabinoid signaling at striatal glutamatergic synapses.

22 ng proteins that are expressed in excitatory glutamatergic synapses.

23 rs morphological maturation and formation of glutamatergic synapses.

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

25 g of the functional diversity of hippocampal glutamatergic synapses.

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

27 m of structural and functional plasticity of glutamatergic synapses.

28 sistent with enhanced release probability at glutamatergic synapses.

29 t reporter synaptopHluorin preferentially at glutamatergic synapses.

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

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

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

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

34 5 expression and impaired the development of glutamatergic synapses.

35 espiratory motoneurons on both sides through glutamatergic synapses.

36 eady to quickly bind glutamate released from glutamatergic synapses.

37 critical role in regulating the stability of glutamatergic synapses.

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

39 an mediate excitotoxic cellular signaling at glutamatergic synapses.

40 etylcholine for the maturation of developing glutamatergic synapses.

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

42 ty and pruning of excitatory corticostriatal glutamatergic synapses.

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

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

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

46 ontaneous neurotransmission at GABAergic and glutamatergic synapses.

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

48 critical for the development and function of glutamatergic synapses.

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

50 nd reduce neuronal inhibitory control of CeA glutamatergic synapses.

51 nal activity-mediated feedback regulation of glutamatergic synapses.

52 rding and analysis methods at single central glutamatergic synapses.

53 contributions to signal saturation at single glutamatergic synapses.

54 oles in the nervous system, in particular at glutamatergic synapses, a potential role for Rh50 protei

55 key roles in the use-dependent adaptation of glutamatergic synapses-along the dendritic arbor.

56 This study suggested that glutamatergic synapse and axon guidance pathways were sp

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

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

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

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

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

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

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

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

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

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

67 e findings demonstrate a role for Gprasp2 in glutamatergic synapses and suggest a possible mechanism

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

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

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

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

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

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

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

75 ng at putative axo-dendritic and axo-spinous glutamatergic synapses, and intracellular labeling on th

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

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

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

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

80 Glutamatergic synapses are located mostly on dendritic s

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

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

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

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

85 anisms underlying dopaminergic modulation of glutamatergic synapses are unclear.

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

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

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

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

90 a transsynaptic adhesion protein regulating glutamatergic synapse assembly on dendrites of central n

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

92 entiation of fast excitatory transmission at glutamatergic synapses between hippocampal neurons cause

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

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

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

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

97 atic plasticity rules are well described for glutamatergic synapses but less clear for GABAergic syna

98 nderstanding of GluD1 regulation of striatal glutamatergic synapses, but also suggest possible extras

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

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

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

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

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

104 ved in ASD, in particular genes encoding for glutamatergic synapse components.

105 interneurons are recruited by activation of glutamatergic synapses comprising GluA2-containing calci

106 Many central glutamatergic synapses contain a single presynaptic acti

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

108 ipal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-us

109 sting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-us

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

111 ecessary for activity to negatively regulate glutamatergic synapse density.

112 requency coupled to a reduction in dendritic glutamatergic synapse density.

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

114 To unravel the roles of CAST/ELKS in glutamatergic synapse development and in presynaptic fun

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

116 CA1 pyramidal neurons produced no effect on glutamatergic synapse development.

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

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

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

120 he CPG2 region of SYNE1 with a mechanism for glutamatergic synapse dysfunction that could underlie su

121 We found that D2 glutamatergic synapses expressed enhanced release probab

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

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

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

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

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

127 gulate channel abundance and are involved in glutamatergic synapse formation.

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

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

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

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

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

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

134 (RhoGEF) proteins as powerful modulators of glutamatergic synapse function have also become increasi

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

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

137 At excitatory glutamatergic synapses, fusion of intracellular vesicles

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

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

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

141 Punctate nNOS appears at glutamatergic synapses in a complex with glutamate NMDA

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

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

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

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

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

147 Immature glutamatergic synapses in cultured neurons contain high-

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

149 am1 plays a unique role in the regulation of glutamatergic synapses in dentate granule neurons using

150 Glutamatergic synapses in early postnatal development tr

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

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

153 ivity-dependent long-lasting potentiation of glutamatergic synapses in LIPN neurons, while substance

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

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

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

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

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

159 s and the generation of AMPA receptor-silent glutamatergic synapses in the adult nucleus accumbens sh

160 At glutamatergic synapses in the brain, activity-dependent

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

162 endently point to the molecular diversity of glutamatergic synapses in the brain.

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

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

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

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

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

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

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

170 ptic mechanisms recruited by HA signaling at glutamatergic synapses in the NAc.

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

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

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

174 of transient synaptic potentiation (t-SP) at glutamatergic synapses in the nucleus accumbens core (NA

175 Glutamatergic synapses in the nucleus accumbens regulate

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 DA receptor-dependent synaptic plasticity of glutamatergic synapses in the prelimbic prefrontal corte

179 ructural and functional impairments occur in glutamatergic synapses in the pyramidal neurons of the a

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

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

182 3 also showed a loss of approximately 50% of glutamatergic synapses in vivo without affecting the inh

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

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

185 Glutamatergic synapses, in the CeA and throughout the br

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

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

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

189 At glutamatergic synapses, induction of associative synapti

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

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

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

198 However, glutamatergic synapses lacking either protein exhibit re

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

200 ic alpha(2)delta-2 exerts the same effect in glutamatergic synapses, leading to a mismatched localiza

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

202 At glutamatergic synapses, local endocytic recycling of AMP

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

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

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

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

207 o demonstrate that in addition to excitatory glutamatergic synapses, MOC neurons receive inhibitory G

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

209 At the glutamatergic synapse of the Drosophila larval neuromusc

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

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

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

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

214 napses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber syn

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

216 Newly formed glutamatergic synapses often lack postsynaptic AMPA-type

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

218 um and that their terminals form excitatory, glutamatergic synapses on host cortical neurons.

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

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

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

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

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

224 Glutamatergic synapses on some hippocampal GABAergic int

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

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

227 her acute stress engages these mechanisms at glutamatergic synapses onto D(1) receptor-expressing [D1

228 genous H(3) receptor signaling in the NAc at glutamatergic synapses onto D1(+)-MSNs.

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

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

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

232 t authentic and transmitted stress can prime glutamatergic synapses onto hippocampal CA1 neurons to u

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

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

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

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

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

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

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

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

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

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

243 a unique Tiam1-mediated molecular program of glutamatergic synapse regulation in dentate granule neur

244 unique RhoGEF-mediated molecular program of glutamatergic synapse regulation in dentate granule neur

245 Glutamatergic synapses rely on AMPA receptors (AMPARs) f

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

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

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

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

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

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

252 Glutamatergic synapses show large variations in strength

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

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

255 xcitatory synapse size diversity, we studied glutamatergic synapse size dynamics and diversification

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

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

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

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

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

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

262 Mounting evidence suggests numerous glutamatergic synapse subtypes exist in the brain, and t

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

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

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

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

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

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

274 At excitatory glutamatergic synapses, the immediate early gene product

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

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

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

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

279 G-protein-coupled receptor, is expressed at glutamatergic synapses throughout the mesolimbic network

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

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

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

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

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

285 een synapses.SIGNIFICANCE STATEMENT Sizes of glutamatergic synapses vary tremendously, even when form

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

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

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

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

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

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

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

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

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

295 the complex network of interacting sCAMs in glutamatergic synapses will be an important strategy for

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

297 PFC-SERT+ neurons establish glutamatergic synapses with subcortical targets, includi

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

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

300 Here, we explored GABA(B)R function at glutamatergic synapses within PV-IN-embedded microcircui