ライフサイエンスコーパス: glutamatergic

1 ric enzymatic biosensor, we demonstrate that glutamatergic activation elevates ambient endogenous d-s

2 As the major excitatory input, glutamatergic afferents are important for control of the

3 ntia nigra; the dopamine systems themselves; glutamatergic afferents to the striatum; and one of two

4 odulation requires CB1 receptors on cortical glutamatergic afferents.

5 Unlike the rapidly acting glutamatergic agent ketamine, mGluR5-specific modulation

6 fore, we analyzed binding site densities for glutamatergic AMPA, NMDA and kainate, GABAergic GABAA ,

7 nd had an increased number of proprioceptive glutamatergic and calbindin-labeled putative Renshaw cel

8 olecular mechanisms by which EAAC1 can shape glutamatergic and dopaminergic signals and control repea

9 neurons, the PPT also includes intermingled glutamatergic and GABAergic cell populations, and the pr

10 1 neurons and larger numbers of unidentified glutamatergic and GABAergic cells.

11 Overall, glutamatergic and GABAergic innervation of newly born ne

12 entify previously undescribed sites at which glutamatergic and GABAergic inputs may stimulate and inh

13 receiving them exhibited diminished loss of glutamatergic and GABAergic neurons and greatly reduced

14 citatory and inhibitory synaptic inputs onto glutamatergic and GABAergic neurons and that the nature

15 ons are heavily apposed by axon terminals of glutamatergic and GABAergic neurons of the substantia in

16 However, the PPT nucleus also contains glutamatergic and GABAergic neurons that likely contribu

17 neurogenesis resulted in a reduced number of glutamatergic and GABAergic neurons, but the latter addi

18 tion and inhibition that was present in both glutamatergic and GABAergic neurons, whereas mice withou

19 Slice electrophysiology was used to measure glutamatergic and GABAergic strength in DMS D1- and D2-M

20 osure to addictive drugs or alcohol triggers glutamatergic and gamma-aminobutyric acidergic (GABAergi

21 f schizophrenia predicts dysfunction in both glutamatergic and gamma-aminobutyric acidergic (GABAergi

22 egulation of dopaminergic synthesis, through glutamatergic and gamma-aminobutyric acidergic pathways.

23 dies that have examined neurochemical (e.g., glutamatergic and gamma-aminobutyric acidergic) and func

24 od-brain barrier dysfunction could relate to glutamatergic and inflammatory abnormalities, which are

25 RTN neurons are glutamatergic and innervate principally the respiratory

26 ally in gamma-aminobutyric acid (GABA)ergic, glutamatergic, and catecholaminergic neurons.

27 tions, and the precise roles of cholinergic, glutamatergic, and GABAergic PPT cell groups in regulati

28 n the present study reveal that cholinergic, glutamatergic, and GABAergic PPT neurons each have disti

29 ast three different cell types (cholinergic, glutamatergic, and gamma-aminobutyric acid (GABA)ergic n

30 onal systems, specifically the dopaminergic, glutamatergic, and gamma-aminobutyric acidergic systems

31 These glutamatergic ARC projections synaptically converge with

32 in GABAergic inferior colliculus neurons and glutamatergic auditory cortical neurons supporting the p

33 LTP induced by high-frequency stimulation of glutamatergic axons, or by application of the group I mG

34 E/I is orchestrated by a diverse set of glutamatergic bipolar cells that drive DSGCs directly, a

35 nsional morphometric analysis of presynaptic glutamatergic boutons and dendritic spines was performed

36 activated by capsaicin, TRPV1 recruits more glutamatergic, but not GABAergic, terminals to OLM neuro

37 GR deletion specifically in glutamatergic, but not in GABAergic, neurons induced hyp

38 BAergic interneurons, but also from multiple glutamatergic cell types, including mature dentate granu

39 eveals a predominance of either GABAergic or glutamatergic cells within individual nuclei.

40 These findings reveal that glutamatergic, cholinergic, and GABAergic PPT neurons di

41 likely results from altered GR signaling in glutamatergic circuits of several forebrain regions, whi

42 GLYX-13 is a novel glutamatergic compound that acts as an N-methyl-D-aspart

43 id synaptogenesis and persistent increase in glutamatergic connectivity in SPNs from the shell part o

44 liciting action potentials in the absence of glutamatergic currents.

45 Although previous studies suggest glutamatergic deficits in fronto-striatal brain areas in

46 ocessing of presynaptic neurexins (Nrxns) in glutamatergic differentiation.

47 ty, and the LUC profile from sleep-promoting glutamatergic DN1s (gDN1s) paralleled daytime sleep.

48 distinguished 62 neuronal subtypes producing glutamatergic, dopaminergic or GABAergic markers for syn

49 pically affected in schizophrenia, including glutamatergic, dopaminergic, immune and antioxidant sign

50 ic-firing inhibitory lamina II interneurons, glutamatergic drive was reduced while glycinergic inhibi

51 in direct-pathway MSNs also led to increased glutamatergic drive, which is consistent with a loss of

52 a, adding converging evidence to the role of glutamatergic dysfunction in various symptoms of schizop

53 confirm that some of these mutations lead to glutamatergic dysregulation in vitro.

54 ur data empirically support that hippocampal glutamatergic elevation and resting-state network altera

55 ults in an enhanced short-term depression of glutamatergic EPSCs.

56 ar inputs evokes suprathreshold monosynaptic glutamatergic excitation in NGF interneurons and a disyn

57 both developmental stages with enrichment of glutamatergic (excitatory) processes laterally and glyci

58 the subpallial ventral telencephalon, while glutamatergic expression dominates nuclei of the pallial

59 of adult mice, that brief-burst activity in glutamatergic fibers is sufficient to induce postsynapti

60 We knocked out Ctcf postnatally in glutamatergic forebrain neurons under the control of Cam

61 many psychiatric disorders by dysregulating glutamatergic function within the prefrontal cortex (PFC

62 n of Nrxn processing by PS is deleterious to glutamatergic function.SIGNIFICANCE STATEMENT To gain in

63 We mapped the distribution of glutamatergic, GABAergic, and cholinergic neurons in the

64 occurrence and plasticity of MF simultaneous glutamatergic-GABAergic signaling onto interneurons of t

65 Targeted investigation of GRIA1, a glutamatergic gene implicated in drug-seeking behavior,

66 This glutamatergic gliotransmission is sensed by neurons of t

67 Transmission across the ARC(Glutamatergic)-->PVH(MC4R) synapse is potentiated by the

68 TRPV1 knockout mice have reduced glutamatergic innervation of OLM neurons.

69 However, the role of glutamatergic input as a whole onto dopamine neurons rem

70 studies suggested that GRPR neurons receive glutamatergic input from NMBR neurons.

71 y nucleus receive monosynaptic extra-somatic glutamatergic input from the neocortex.

72 When TRPV1 is blocked, glutamatergic input to OLM neurons is dramatically reduc

73 Our findings revealed the presence of a glutamatergic input to the MLR originating from the prim

74 that chronic cocaine use enhances excitatory glutamatergic input to these neurons, making them more s

75 eter persisted when local neural spiking and glutamatergic input were blocked, as well as during bloc

76 in the VS serve as a site of convergence for glutamatergic inputs arising from the PFC and limbic reg

77 In addition, excitable pre-OLs receive glutamatergic inputs from neighboring neurons that trigg

78 s that form Type II synapses, and long-range glutamatergic inputs from the thalamus that form Type I

79 s genetic model to directly test the role of glutamatergic inputs in dopamine-related functions.

80 Here we developed a mouse line in which glutamatergic inputs onto dopamine neurons are specifica

81 Repetitive activation of glutamatergic inputs onto HIPP cells induces long-lastin

82 activation can selectively modulate striatal glutamatergic inputs onto medium spiny neurons (MSNs).

83 Glutamatergic inputs to neurones in the inferior olive g

84 otic medication), and receives GABAergic and glutamatergic inputs.

85 It is noteworthy that glutamatergic LTD, which is known to exist on stratum lu

86 -generated synapse-like structures expressed glutamatergic marker VGluT1, pre- and post-synaptic prot

87 Cells expressing the glutamatergic markers vgluts 1-3 show primarily nonoverl

88 Stimulation of glutamatergic median preoptic area neurons produced a pr

89 with schizophrenia, suggesting that altered glutamatergic metabolite levels are associated with illn

90 2 transgenic mice, we examined the effect of glutamatergic MnPO neuron stimulation in freely behaving

91 n of separate but overlapping populations of glutamatergic MnPO neurons produces effects on drinking

92 Agents such as the glutamatergic modulator ketamine are effective in treatm

93 rapid clinical antidepressant effects of the glutamatergic modulator ketamine may be due to its abili

94 ess and molecular signaling processes (e.g., glutamatergic, monoaminergic, calcium, cyclic adenosine

95 h increased phrenic motoneuron expression of glutamatergic N-methyl-D-aspartate (NMDA) receptors and

96 Circulating autoantibodies against glutamatergic N-methyl-D-aspartate receptor (NMDAR) have

97 sing and novel targets to constrain reactive glutamatergic network rewiring in adult epilepsy.

98 ling fosters a long-lasting rearrangement of glutamatergic network that contributes to the epileptoge

99 a subpopulation of STN neurons forms a local glutamatergic network, which together with plateau poten

100 This synaptic dampening effect on glutamatergic networks suggests that increasing O-GlcNAc

101 At the glutamatergic neuromuscular junction (NMJ) synapse, we f

102 ine, and local vessel dilation is induced by glutamatergic neuron activity.

103 is important for the remodeling of aberrant glutamatergic neuronal circuits.

104 entiated using a protocol which enriched for glutamatergic neurons (hESC-neurons).

105 electively delete CB1Rs in VgluT2-expressing glutamatergic neurons (VgluT2-CB1 (-/-)) and Cre-depende

106 vidence for drug-induced neuroadaptations in glutamatergic neurons and receptors, suggested that addi

107 postsynaptic density (PSD) within excitatory glutamatergic neurons and regulate the activity of gluta

108 important regulator of synaptic function in glutamatergic neurons and serves a critical role in lear

109 was not observed when Cacna1c was deleted in glutamatergic neurons during adulthood, where the later

110 y developed a single-step method to generate glutamatergic neurons from human PSCs.

111 CDKL5 expression specifically from forebrain glutamatergic neurons impairs hippocampal-dependent memo

112 We previously found that glutamatergic neurons in the external lateral parabrachi

113 KEY POINTS: Glutamatergic neurons in the median preoptic area were s

114 ion, but not anxiety, is regulated by GRs in glutamatergic neurons of the BLA.

115 r can largely be ascribed to GR signaling in glutamatergic neurons of the BLA.

116 mice harboring loss of cacna1c in excitatory glutamatergic neurons of the forebrain (fbKO) that we ha

117 deficits in CDKL5 deficiency have origins in glutamatergic neurons of the forebrain and that loss of

118 and mice, where mutations cause deficits in glutamatergic neurons of the telencephalon-derived neoco

119 We found that photoactivation of VTA glutamatergic neurons produced robust intracranial self-

120 t embryonic deletion of Cacna1c in forebrain glutamatergic neurons promotes the manifestation of endo

121 Overexpressing FGF9 or FGF10 in cortical glutamatergic neurons results in excessive dendritic out

122 neurons that express FoxP2; and dorsolateral glutamatergic neurons that express FoxP2 in the pLC and

123 ly on VTA GABAergic neurons, but also on VTA glutamatergic neurons that express vesicular glutamate t

124 on, interneurons functionally integrate with glutamatergic neurons to form a microphysiological syste

125 in astroglial cells (but not in GABAergic or glutamatergic neurons) and postsynaptic glutamate recept

126 ven forebrain reduction affecting most brain glutamatergic neurons.

127 d in dopamine D2 receptor-expressing (D2(+)) glutamatergic neurons.

128 light-sensitive channelrhodopsin-2 into VTA glutamatergic neurons.

129 ar hypoplasia and depletion of GABAergic and glutamatergic neurons.

130 roach revealed marked impairments related to glutamatergic neurotransmission and chromatin remodeling

131 g links mitochondrial pyruvate metabolism to glutamatergic neurotransmission and establishes the MPC

132 expression levels of FGFs/FGFRs by excessive glutamatergic neurotransmission could lead to abnormal n

133 Based on the well-established role of glutamatergic neurotransmission in drug addiction, novel

134 unction of N-methyl-D-aspartate receptor and glutamatergic neurotransmission in the pathophysiology o

135 of this study were to understand the role of glutamatergic neurotransmission in the ventromedial hypo

136 minals and dendritic spines, suggesting that glutamatergic neurotransmission is unnecessary for synap

137 with pathological increases or decreases in glutamatergic neurotransmission observed in animal model

138 In hypothalamus in vitro, reduced glutamatergic neurotransmission recapitulated the repres

139 igodendrocyte differentiation, regulation of glutamatergic neurotransmission, and oxytocin receptor e

140 owever, because NMDARs contribute to overall glutamatergic neurotransmission, such loss-of-function e

141 t increased phrenic motoneuron expression of glutamatergic NMDA receptors is associated with spontane

142 .SIGNIFICANCE STATEMENT We recorded neuronal glutamatergic (NMDA and AMPA) responses in prefrontal co

143 esence of circulating autoantibodies against glutamatergic NMDAR in approximately 5% of patients with

144 alence of circulating autoantibodies against glutamatergic NMDAR in psychotic disorders remains contr

145 presence of low-titer autoantibodies against glutamatergic NMDAR in seropositive patients who cannot

146 nsists, by definition, of Phox2b-expressing, glutamatergic, non-catecholaminergic, noncholinergic neu

147 cking the receptor specifically in forebrain glutamatergic or GABAergic neurons by breeding GR(flox/f

148 al or ventral forebrain and contain cortical glutamatergic or GABAergic neurons.

149 toreceptors within reach and modulates their glutamatergic output via parallel feedback mechanisms.

150 mate/GABA co-releasing somatostatin neurons, glutamatergic parvalbumin neurons, and GABAergic parvalb

151 ll to behavior, we provide evidence of a new glutamatergic pathway activating the MLR in a graded fas

152 atric disorders and engages dopaminergic and glutamatergic pathways that regulate motivation and moto

153 urons, most hypothalamic nNOS neurons have a glutamatergic phenotype, except for nNOS neurons of the

154 Noradrenergic signaling is known to maintain glutamatergic plasticity upon reactivation of modified c

155 ificant patterning deficits, particularly in glutamatergic populations.

156 lines, we found that selective activation of glutamatergic PPT neurons induced prolonged cortical act

157 t D3 receptors define a unique population of glutamatergic principal cells in mouse PFC that largely

158 iking interneurons (FSIs) densely innervated glutamatergic projection neurons (PNs) with apparently r

159 onstrate that the activation of monosynaptic glutamatergic projections from anterior insular cortex t

160 the pedunculopontine tegmental nucleus sends glutamatergic projections to VTA dopamine neurons, and t

161 Then we quantified a set of postsynaptic glutamatergic proteins (PSD-95, GluA2, GluN1, GluN2A, Gl

162 So we studied expression of glutamatergic proteins in human V1 to determine their de

163 AIE exposure did not alter the expression of glutamatergic proteins in the adult PrL-C, there was a p

164 instatement of cocaine seeking and normalize glutamatergic proteins in the NAc of rats.

165 Here we report prolonged maturation of glutamatergic proteins, with five stages that map onto l

166 equired for the slow inhibitory component of glutamatergic PSPs and oppose temporal summation of inpu

167 pression defines a novel subclass of layer 5 glutamatergic pyramidal cell in mouse PFC (either sex).

168 on processing streams mediated by subsets of glutamatergic pyramidal cells (PCs) that receive diverse

169 balanced at the cellular level by excitatory glutamatergic pyramidal neurons and inhibitory gamma-ami

170 se regions via the excitatory projections of glutamatergic pyramidal neurons located in layer 3, whos

171 ketamine on ligand binding to a metabotropic glutamatergic receptor (mGluR5) in individuals with majo

172 be performed as evidenced by application of glutamatergic receptor antagonists, reversibly inhibitin

173 Glutamatergic receptor expression is regulated by tropom

174 The metabotropic glutamatergic receptor subtype 5 (mGluR5) may represent

175 totoxicity induced by aberrant excitation of glutamatergic receptors contributes to brain damage in s

176 his includes presynaptic inhibition of local glutamatergic release from excitatory inputs to the VS.

177 pre-synaptic segregation of cholinergic and glutamatergic release sites is also possible.

178 ld compared to Wt; elevated ROS and abnormal glutamatergic responses are detected at 14 DIV.

179 t with an FAAH inhibitor relieves sensitized glutamatergic responses in msPs and attenuates the anxie

180 sting a role for the inhibitory component of glutamatergic responses in temporal integration.

181 PKA activation potentiated MF glutamatergic responses of stratum radiatum interneurons

182 ght be treatable by medications that inhibit glutamatergic responses to drugs of abuse, drug-associat

183 Strikingly, while MF glutamatergic responses underwent LTD, the simultaneous

184 e homeostasis, and significantly reduced the glutamatergic rMF sprouting within the dentate gyrus.

185 is thought to arrive in thalamus through two glutamatergic routes called the lemniscal and paralemnis

186 We show that the glutamatergic sensory neurons AWC(ON) and ASH have disti

187 ed circuit mapping (CRACM) demonstrated that glutamatergic SI neurons frequently form functional syna

188 m lacunosum-moleculare exclusively receive a glutamatergic signal.

189 dk5-ATM signaling, possibly linking impaired glutamatergic signaling and DDR to neurodegeneration in

190 ck-driven excitation within the LHb requires glutamatergic signaling from the LH, but not from the mi

191 daptations in synaptic proteins that control glutamatergic signaling in chronically drinking monkeys.

192 implications for the nature and efficacy of glutamatergic signaling in distinct cortical areas withi

193 n important interaction between dopamine and glutamatergic signaling in midbrain dopamine neurons in

194 s identify PAR1 as an important regulator of glutamatergic signaling in the hippocampus and a possibl

195 ression of proteins regulating GABAergic and glutamatergic signaling in the prefrontal cortex.

196 ers caused by variants in key players of the glutamatergic signaling pathway.

197 g, raising the hypothesis that regulation of glutamatergic signaling represents a viable target for t

198 Light input and glutamatergic signaling to the SCN were concomitantly as

199 e rectifying several cellular adaptations in glutamatergic signaling within the brain's reward circui

200 led that AIE reduced intrinsic excitability, glutamatergic signaling, and D1 receptor modulation of t

201 aling, promotes inflammation and facilitates glutamatergic signaling, key components of opioid tolera

202 ht to be critically dependent on presynaptic glutamatergic signaling.

203 signalling were detected in the PFC and with glutamatergic signalling in the hippocampus.

204 devised a mouse genetics approach to silence glutamatergic signalling only at olivocerebellar synapse

205 ings demonstrated changes in the response to glutamatergic stimulation as well as the electrical outp

206 ive alcohol intake and withdrawal potentiate glutamatergic strength exclusively in D1-MSNs and GABAer

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

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

209 The excitatory glutamatergic synapse is the principal site of communica

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

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

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

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

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

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

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

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

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

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

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

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

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

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

224 3 also showed a loss of approximately 50% of glutamatergic synapses in vivo without affecting the inh

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

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

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

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

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

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

231 Glutamatergic synapses rely on AMPA receptors (AMPARs) f

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

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

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

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

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

237 ontaneous neurotransmission at GABAergic and glutamatergic synapses.

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

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

240 ty and pruning of excitatory corticostriatal glutamatergic synapses.

241 critical for the development and function of glutamatergic synapses.

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

243 nd reduce neuronal inhibitory control of CeA glutamatergic synapses.

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

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

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

247 nd in a MS chimeric ex vivo model, recovered glutamatergic synaptic enhancement typical of EAE/MS.

248 links into how loss of PS activity inhibits glutamatergic synaptic function in Alzheimer's disease p

249 nes in the inferior olive actively integrate glutamatergic synaptic inputs.

250 ffects on acute stress-exposed mice, through glutamatergic synaptic long-term depression (LTD), witho

251 The present study identifies a novel form of glutamatergic synaptic plasticity in VTA GABA neurons, a

252 (AMPARs) in order to selectively manipulate glutamatergic synaptic plasticity on DA neurons.

253 and memory, primarily by evoking changes in glutamatergic synaptic strength in the mesocorticolimbic

254 High-frequency dentate to CA3 glutamatergic synaptic transmission and feedforward inhi

255 on did not result in overt deficits in basal glutamatergic synaptic transmission at the mossy-fibre s

256 At the cellular level, pregabalin inhibited glutamatergic synaptic transmission differentially in WT

257 sue of the JCI, Wang and coworkers show that glutamatergic synaptic transmission onto striatal projec

258 does not affect low-frequency dentate to CA3 glutamatergic synaptic transmission.

259 olecular event in homeostatic downscaling of glutamatergic synaptic transmission.

260 ynaptic AMPA receptor expression or enhanced glutamatergic synaptogenesis.

261 underscoring the potential importance of the glutamatergic system as a target for improved therapeuti

262 Dysfunction of the glutamatergic system has been implicated in alcohol addi

263 Here we review genetic studies linking the glutamatergic system to the pathophysiology and therapeu

264 consistent with alterations in GABAergic and glutamatergic systems in patients with schizophrenia and

265 s showed hypersensitivity of corticostriatal glutamatergic terminals (lower frequency of optogenetic

266 s and neurotransmitter release at individual glutamatergic terminals by a mechanism that depends on n

267 ETATION: Hypersensitivity of corticostriatal glutamatergic terminals can constitute a main pathogenet

268 zed increased sensitivity of corticostriatal glutamatergic terminals in the rodent with brain iron de

269 2 and 3 (mGluR2/3) are key autoreceptors on glutamatergic terminals that maintain glutamate homeosta

270 in familial Alzheimer's disease, clear from glutamatergic terminals the accumulation of Nrxn C-termi

271 ate molecular layer was Glu-CB1 -RS, 53.19% (glutamatergic terminals); 2.30% (GABAergic terminals); G

272 nhibitory synapses were Glu-CB1 -RS, 21.89% (glutamatergic terminals); 2.38% (GABAergic terminals); G

273 (GABAergic terminals); GABA-CB1 -RS, 1.92% (glutamatergic terminals); 77.92% (GABAergic terminals).

274 (GABAergic terminals); GABA-CB1 -RS, 3.19% (glutamatergic terminals); 85.07% (GABAergic terminals).

275 excitatory transmission presynaptically, at glutamatergic terminals, and postsynaptically, at apical

276 ting synaptogenesis and neurotransmission at glutamatergic terminals.

277 d histone H3 hyperacetylation contributes to glutamatergic transcriptional changes that underlie addi

278 le-cell patch-clamp shows elevated levels of glutamatergic transmission and changes in AMPA receptor

279 Absence of BC1 is associated with altered glutamatergic transmission and maladaptive behavior.

280 studies revealed 2-AG modulation of amygdala glutamatergic transmission as a key synaptic correlate o

281 Ca(2+)-permeable AMPARs (CP-AMPARs) mediate glutamatergic transmission at the adult auditory hair ce

282 Because the plasticity of glutamatergic transmission from the different terminals

283 sumption and withdrawal in mice strengthened glutamatergic transmission in D1-MSNs and GABAergic tran

284 indicate that alterations in NMDA-dependent glutamatergic transmission in Tg(CJD) mice do not depend

285 (GLAST), which causes an enhancement of the glutamatergic transmission in the EAE cerebellum.

286 wn experiments that MAGUKs are essential for glutamatergic transmission in young animals and cultured

287 Blockade of glutamatergic transmission largely diminished MLR cell r

288 These results provide genetic evidence that glutamatergic transmission onto dopaminergic neurons und

289 re used for our study.SIGNIFICANCE STATEMENT Glutamatergic transmission plays critical roles in corti

290 Estradiol-negative feedback decreased glutamatergic transmission to AVPV and increased it to a

291 h feedback is mediated by demonstrating that glutamatergic transmission to these kisspeptin populatio

292 evidence for afferent-specific properties of glutamatergic transmission within the superficial dorsal

293 emoval of MAGUKs in CA1 causes reductions in glutamatergic transmission, indicating that synapses in

294 crucial components for cone to bipolar cell glutamatergic transmission, the metabotropic glutamate r

295 bln1 deletions impair sociability and weaken glutamatergic transmission.

296 imals causes rapid and lasting reductions in glutamatergic transmission.

297 that CP-AMPARs mediate a major component of glutamatergic transmission.

298 verexpression caused correlated increases in glutamatergic transmission.

299 tribution, the synaptic termination, and the glutamatergic transporter profiles of DCN A and C fibers

300 with only ipsilaterally projecting axons are glutamatergic, whereas neurons with only contralaterally