ライフサイエンスコーパス: glutamatergic neuron

1 ic input and output required activity of the glutamatergic neuron.

2 ar hypoplasia and depletion of GABAergic and glutamatergic neurons.

3 ven forebrain reduction affecting most brain glutamatergic neurons.

4 being more widespread and numerous than ESR1-glutamatergic neurons.

5 ing gamma-aminobutyric acid (GABA)-ergic and glutamatergic neurons.

6 d by isolated damage to developing forebrain glutamatergic neurons.

7 oor in serotonin and enriched in presumptive glutamatergic neurons.

8 el functions in dendrites and at synapses of glutamatergic neurons.

9 tor-dependent form of synaptic plasticity at glutamatergic neurons.

10 luding small, medium-sized, large, and giant glutamatergic neurons.

11 ulates the development of both GABAergic and glutamatergic neurons.

12 t mice lacking CB(1) receptors from cortical glutamatergic neurons.

13 we know little about their input from other glutamatergic neurons.

14 LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic neurons.

15 cells by a circuit involving adrenergic and glutamatergic neurons.

16 cular glutamate transporter 3 (VGLUT3) marks glutamatergic neurons.

17 ich contains predominantly VGLUT2-containing glutamatergic neurons.

18 te receptors, and formation of synapses with glutamatergic neurons.

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

20 r characteristic of progenitors for cortical glutamatergic neurons.

21 pression preferentially in VGLUT1-containing glutamatergic neurons.

22 estricting expression to specific classes of glutamatergic neurons.

23 amatergic neurons, or specific subclasses of glutamatergic neurons.

24 ctivity following KA infusion causes loss of glutamatergic neurons.

25 us and RF colocalized NPNFP and a marker for glutamatergic neurons.

26 ressed exclusively within a subpopulation of glutamatergic neurons.

27 glutamate transporter2 (VGLUT2), a marker of glutamatergic neurons.

28 ase as neurotransmitter, and is a marker for glutamatergic neurons.

29 alpha1(-/R) mice, respectively) in forebrain glutamatergic neurons.

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

31 ximately 40% GABAergic and approximately 60% glutamatergic neurons.

32 ociated with distinct subtypes of excitatory glutamatergic neurons.

33 trolled environment of dissociated, solitary glutamatergic neurons.

34 REM-on area also contains two populations of glutamatergic neurons.

35 rtical plate due to diminished production of glutamatergic neurons.

36 ly contact axon initial segments of cortical glutamatergic neurons.

37 Paradoxically, Lbx1 is also expressed in glutamatergic neurons.

38 ired for specification of, and expressed in, glutamatergic neurons.

39 rgic differentiation and induce formation of glutamatergic neurons.

40 ponse, general growth and differentiation of glutamatergic neurons.

41 2 either removed from or expressed solely in glutamatergic neurons.

42 n the application of nicotine in both DA and glutamatergic neurons.

43 tory-to-inhibitory switch in GABA actions on glutamatergic neurons.

44 of Pax6 in the development of all cerebellar glutamatergic neurons.

45 gled presence of cholinergic, GABAergic, and glutamatergic neurons.

46 ional and anatomical development of cortical glutamatergic neurons.

47 leptin-responsive GABAergic neurons, but not glutamatergic neurons, act as metabolic sensors to regul

48 rapezoid nucleus (RTN), a group of medullary glutamatergic neurons activated by extracellular brain p

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

50 agment fused to Gal4 whose expression labels glutamatergic neurons and a green fluorescent protein (G

51 exclude the expression of DNMT1 or DNMT3a in glutamatergic neurons and glia.

52 unctions exclusively in dorsal telencephalic glutamatergic neurons and investigated endocannabinoid-d

53 s, dysbindin-1 is located presynaptically in glutamatergic neurons and is reduced at these locations

54 bit similar firing properties as neighboring glutamatergic neurons and receive direct input from both

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

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

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

58 essed the excitatory hM3Dq DREADD in rat BLA glutamatergic neurons and showed that CNO acted selectiv

59 w possible to mark many, if not all, central glutamatergic neurons and synapses.

60 amic-pituitary-adrenal axis via hypothalamic glutamatergic neurons and that it may regulate other neu

61 fferentiated these iPSCs to dopamine (DA) or glutamatergic neurons and then tested their functional p

62 ecreased genesis of T-Brain-1-positive early glutamatergic neurons and, in part, to a failure to main

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

64 ng CB1 receptors selectively in GABAergic or glutamatergic neurons, and (ii) manipulating corticostri

65 itatory neural transmission, provided by the glutamatergic neurons, and the inhibitory signals from t

66 we show that lateral hypothalamic area (LHA) glutamatergic neurons, and their projections to the late

67 Glutamatergic neurons are abundant in the Drosophila cen

68 up to developing cortex where the excitatory glutamatergic neurons are born.

69 hese observations indicate that resident VTA glutamatergic neurons are likely to affect both DAergic

70 These glutamatergic neurons are located in a chemosensitive re

71 dorsal tegmental nucleus, we found that many glutamatergic neurons are maximally active during REM sl

72 Glutamatergic neurons are required for the generation an

73 al origins and relationship to other preBotC glutamatergic neurons are unknown.

74 These glutamatergic neurons are vigorously activated by CO(2)

75 ectively, these results demonstrate that LHA glutamatergic neurons are well situated to bidirectional

76 e transporters (VGluTs; specific markers for glutamatergic neurons) are expressed in forebrain sites

77 sporter 2 (VGLUT2), a marker of hypothalamic glutamatergic neurons, as well as glutamic acid decarbox

78 By embryonic day 15 a subset of Meis(+) glutamatergic neurons assumed abnormally superficial pos

79 nogaster receives extensive innervation from glutamatergic neurons at specific cardiac regions during

80 This discrepancy was specific for glutamatergic neurons, because no difference was found b

81 ive CB1 reexpression in dorsal telencephalic glutamatergic neurons but not forebrain GABAergic neuron

82 bx3 expression was restricted to a subset of glutamatergic neurons, but its absence did not affect th

83 cephalon (dTel), which generate all cortical glutamatergic neurons, but not by progenitors in the med

84 on is complex, containing both GABAergic and glutamatergic neurons, but the possible roles of these n

85 olinergic, GABAergic, and recently described glutamatergic neurons, but their specific contribution t

86 r opposite neurotransmitter release sites of glutamatergic neurons, but these release sites have hete

87 vation and suppression, respectively, of MLR glutamatergic neurons by direct and indirect pathways, w

88 i1 loss in inhibitory neurons or subcortical glutamatergic neurons causes learning deficits, while Ra

89 bustly expressed in the germinal zone of all glutamatergic neurons [cerebellar nuclear (CN) neurons,

90 act in distinct combinations in 25 different glutamatergic neuron classes to initiate and maintain ea

91 drive expression of eat-4/VGLUT in distinct glutamatergic neuron classes.

92 ing processes: (1) the placement of cortical glutamatergic neurons close to TCA clusters; (2) the reg

93 ese findings, together, demonstrate that SOM glutamatergic neurons comprise key elements of the medul

94 Glutamatergic neurons contain free zinc packaged into ne

95 likely to be glutamatergic) and suggest that glutamatergic neurons containing CRF may be part of the

96 ound that LepRb(POA) neurons are stimulatory glutamatergic neurons, contrary to prevalent models, pro

97 hat IP3R-dependent calcium transients in the glutamatergic neurons convey this signal to downstream m

98 ested that targeted apoptosis of neocortical glutamatergic neurons could trigger the generation of ne

99 eas activation of CB1R expressed in cortical glutamatergic neurons decreases cortical synchrony.

100 atment after SE is efficacious for thwarting glutamatergic neuron degeneration, alleviating interneur

101 By studying solitary glutamatergic neurons devoid of synaptic GABA input, we

102 ippocampal preparation, activation of MS-DBB glutamatergic neurons did increase the rhythmicity of hi

103 Instead, chemogenetic excitation of BLA glutamatergic neurons disrupted use of prediction error

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

105 Selective stimulation of glutamatergic neurons during the online maintenance of i

106 dy, we show that the genetic ablation of LHA glutamatergic neurons enhances caloric intake.

107 ate-induced neurotoxicity in highly enriched glutamatergic neurons (ESNs) derived from murine embryon

108 To investigate whether VTA glutamatergic neurons establish local synapses, we tagge

109 Furthermore, the activity of glutamatergic neurons exhibits a medio-lateral spatial g

110 ory neurotransmitter in the retina, and most glutamatergic neurons express one of the three known ves

111 These glutamatergic neurons express the vesicular glutamate tr

112 neurons localize mAChRs to the soma, whereas glutamatergic neurons expressed mAChRs more strongly in

113 e entorhinal cortex, the major population of glutamatergic neurons expressing Reelin in the brain.

114 gled in this region with recently discovered glutamatergic neurons expressing the vesicular glutamate

115 VTA glutamatergic neurons--expressing vesicular glutamate tr

116 elective Ube3a loss from either GABAergic or glutamatergic neurons, focusing on the development of hy

117 ast, we reveal the key importance of ESR1 in glutamatergic neurons for multiple estrogen feedback loo

118 by constructing a fate map of GABAergic and glutamatergic neurons for the 32-cell stage Xenopus embr

119 Specifically, mGluR5 is required in cortical glutamatergic neurons for the following processes: (1) t

120 ervating motoneuron lineages and required in glutamatergic neurons for walking.

121 trategy to conditionally generate excitatory glutamatergic neurons from ES cells to cure various type

122 tigation was to generate auditory nerve-like glutamatergic neurons from ES cells.

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

124 Loss of Dbx1 eliminates all glutamatergic neurons from the respiratory VLM including

125 lacks an innate potential to regenerate lost glutamatergic neurons, future strategies should concentr

126 the gene exclusively in dorsal telencephalic glutamatergic neurons (Glu-CB1 -RS) or GABAergic neurons

127 y, targeted inactivation of this receptor in glutamatergic neurons (GNs) markedly enhanced the surviv

128 In thus report, decreased Met signaling in glutamatergic neurons had no effect on excitation, but d

129 This chemogenetic excitation of BLA glutamatergic neurons had no effect on the acquisition o

130 release process at these and other central, glutamatergic neurons have shed some light on the photor

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

132 st that gene and seizure interactions in VTA glutamatergic neurons impair sociability by downregulati

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

134 Met activity downregulates GABAAreceptors on glutamatergic neurons in an insulin independent manner.

135 chemogenetic activation of BF cholinergic or glutamatergic neurons in behaving mice produced signific

136 rescued the toxicity of Abeta secreted from glutamatergic neurons in Caenorhabditis elegans.

137 ncrease sleep due to synaptic dysfunction in glutamatergic neurons in Drosophila.

138 transduced and selectively expressed in the glutamatergic neurons in either the dorsal or ventral HP

139 ESV during and after SE presented no loss of glutamatergic neurons in hippocampal cell layers, dimini

140 However, activation of glutamatergic neurons in LH inhibits feeding.

141 Knockout of mGluR5 or p11 specifically in glutamatergic neurons in mice causes depression-like beh

142 ice, we show that optogenetic stimulation of glutamatergic neurons in MnPO/OVLT drives voracious wate

143 -inhibitory switch in the actions of GABA on glutamatergic neurons in neocortical and hippocampal sli

144 that these OPCs differentiate into pyramidal glutamatergic neurons in piriform cortex.

145 ts long-term expression in VGLUT1-containing glutamatergic neurons in rat postrhinal (POR) cortex, bu

146 ter supports expression in VGLUT1-containing glutamatergic neurons in rat postrhinal (POR) cortex.

147 has the potential to influence the action of glutamatergic neurons in regulation of excitatory cardio

148 -2 is generally considered inducible, but in glutamatergic neurons in some brain regions, including t

149 1 receptor expressed in dorsal telencephalic glutamatergic neurons in synaptic plasticity and behavio

150 excitatory neurons were firmly established; glutamatergic neurons in the anterior BNST accounted for

151 entification of mouse LHX1 as a regulator of glutamatergic neurons in the brainstem.

152 three activity-dependent genes expressed by glutamatergic neurons in the cerebellar cortex (GAP-43,

153 tudy was to evaluate the functional state of glutamatergic neurons in the cerebellar cortex of patien

154 m in Drosophila highlights the prevalence of glutamatergic neurons in the CNS and presents tools for

155 leads to the incorrect specification of some glutamatergic neurons in the dorsal horn and alters the

156 ic neurons and an increase in the excitatory glutamatergic neurons in the dorsal horn of the spinal c

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

158 iginate from semilunar granule cells (SGCs), glutamatergic neurons in the inner molecular layer that

159 Our results suggest that glutamatergic neurons in the lateral PB are necessary fo

160 cally identified cholinergic, GABAergic, and glutamatergic neurons in the LDT, SubLDT, and adjoining

161 nin gene-related peptide (CGRP, a marker for glutamatergic neurons in the lPBN) neurons that project

162 e exposure triggers adaptations in layer 5/6 glutamatergic neurons in the medial prefrontal cortex (m

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

164 Here we show that glutamatergic neurons in the nucleus tractus solitarius

165 rainstem, and found a substantial input from glutamatergic neurons in the parabrachial nucleus and ad

166 gs from identified classes of inhibitory and glutamatergic neurons in the piriform cortex (PC) of mic

167 piratory-related rhythm that is generated by glutamatergic neurons in the pre-Botzinger complex (preB

168 and other investigators have suggested that glutamatergic neurons in the preBotzinger Complex (preBo

169 ral distribution and precise localization of glutamatergic neurons in the sea lamprey brainstem.

170 suggests that an increase in the activity of glutamatergic neurons in the SN allows the BG to directl

171 argely inhibitory but also consisted of some glutamatergic neurons in the spinal cord and serotonergi

172 Stimulation of glutamatergic neurons in the subfornical organ drives dr

173 at these cholinergic stimuli are conveyed to glutamatergic neurons in the ventral ganglion through mA

174 not support expression in VGLUT2-containing glutamatergic neurons in the ventral medial hypothalamus

175 is suppressed by chemogenetic activation of glutamatergic neurons in the vHPC that project to the LS

176 Here, we examined the role of MS-DBB glutamatergic neurons in theta rhythm using optogenetic

177 demonstrated a wide presence of excitatory (glutamatergic) neurons in lampreys.

178 itory (GABAergic) neurons versus excitatory (glutamatergic) neurons in the female mouse by selective

179 R specifically in GABAergic neurons, but not glutamatergic neurons, in the mPFC attenuated the antide

180 Genetic ablation of LHA glutamatergic neurons increased daily caloric intake and

181 g a selective deletion of CB1-Rs in cortical glutamatergic neurons indicated that stress-elicited LTP

182 mGluR5 is expressed in glutamatergic neurons, inhibitory neurons, and glia in v

183 ain regions, and may be colocalized in large glutamatergic neurons innervating the rat limbic system.

184 We found glutamatergic neurons innervating the VTA in almost all

185 sults show that mGluR5 signaling in cortical glutamatergic neurons is required for precisely modulati

186 bundant at the postsynaptic density (PSD) of glutamatergic neurons, is known to modulate synaptic str

187 o regulate growth and synaptic plasticity of glutamatergic neurons, its effects on basic parameters o

188 firing rates (<250 Hz) than glycinergic and glutamatergic neurons labeled in the yellow fluorescent

189 MeCP2 deficiency in glutamatergic neurons leads to early lethality, obesity,

190 Ablation of LC area glutamatergic neurons led to local PTH2R-ir loss, and ba

191 that activation of CB1 expressed in cortical glutamatergic neurons limits the cannabinoid-induced tha

192 to the fSR are glutamate-IR, indicating that glutamatergic neurons may also play an important role in

193 These results suggest that glutamatergic neurons may be hyperactive in the cerebell

194 e membrane mechanisms that reduce spiking in glutamatergic neurons may better control neuronal excita

195 tested the hypothesis that GABAergic and/or glutamatergic neurons mediate phase shifts induced by ac

196 ian brain formation, precursors of principal glutamatergic neurons migrate radially along radial glia

197 sults provide the first evidence that MS-DBB glutamatergic neurons modulate local septal circuits, wh

198 the RL and generating subsets of RL-derived glutamatergic neurons, namely neurons of the deep cerebe

199 entified in yeast modified Abeta toxicity in glutamatergic neurons of Caenorhabditis elegans and in p

200 amidal neurons, dentate gyrus granule cells, glutamatergic neurons of the basolateral amygdala, and g

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

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

203 all of these genes are strongly expressed in glutamatergic neurons of the CA1-CA3 pyramidal cell laye

204 of the maternally inherited X chromosome in glutamatergic neurons of the female cortex.

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

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

207 rgic neurons of the substantia nigra and the glutamatergic neurons of the hippocampus, cell types whi

208 ge profiles, the cholinergic, GABAergic, and glutamatergic neurons of the LDT, SubLDT, and MPPT thus

209 uring REM sleep is thought to originate from glutamatergic neurons of the sublaterodorsal nucleus (SL

210 rgic neurons of the globus pallidus (GP) and glutamatergic neurons of the subthalamic nucleus (STN) a

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

212 e find that nearly all non-catecholaminergic glutamatergic neurons of the ventrolateral medulla (VLM)

213 2 (tethered to mCherry) was expressed in VTA glutamatergic neurons of VGluT2::Cre mice.

214 , which contains primarily VGLUT1-containing glutamatergic neurons, or into the ventral medial hypoth

215 to neurons require restricting expression to glutamatergic neurons, or specific subclasses of glutama

216 om sleep in response to CO2, while medial PB glutamatergic neurons play an important role in promotin

217 y effects are mediated by GABAergic neurons; glutamatergic neurons play only a minor role.

218 ect on theta rhythms, suggesting that MS-DBB glutamatergic neurons played a role in theta generation

219 al that CB1 receptor in dorsal telencephalic glutamatergic neurons plays a sufficient role to control

220 sion, leptin signaling in GABAergic (but not glutamatergic neurons) plays a critical role in the timi

221 ation task, chemogenetic manipulation of BLA glutamatergic neurons prevented use of negative predicti

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

223 larities in the transcriptional programs for glutamatergic neuron production in the DCN and the cereb

224 Some of these LHA glutamatergic neurons project to the lateral habenula, a

225 of the CB1 receptor on dorsal telencephalic glutamatergic neurons prolonged the time course of DSE i

226 wo other social behaviors, while neighboring glutamatergic neurons promote repetitive self-grooming,

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

228 he experiments in slices suggest that MS-DBB glutamatergic neurons provide prominent excitatory input

229 Here we test whether GABAergic or glutamatergic neurons provide the intermediate pathway b

230 umin-expressing neurons (PVNs) and pyramidal glutamatergic neurons (PyrNs).

231 en during development is the adult GABAergic/glutamatergic neuron ratio first established?

232 storation of 5-HT(2A) expression to cortical glutamatergic neurons re-instated the locomotor-suppress

233 Limiting NDUFS4 loss to a subset of glutamatergic neurons recapitulates the VA hypersensitiv

234 Retinal bipolar cells are polarized glutamatergic neurons receiving direct photoreceptor inp

235 ional development of layer IV spiny stellate glutamatergic neurons receiving sensory input, mGluR5 ge

236 Descending cortical glutamatergic neurons regulate 5-HT neuronal activity in

237 These data suggest that glutamatergic neurons represent a cell type in the PBN t

238 Here, we show that Nefh-expressing glutamatergic neurons represent a major population of lo

239 receptor expression restricted to forebrain glutamatergic neurons reproduce the behavioral effects s

240 Synaptic transmission from glutamatergic neurons requires vesicular glutamate trans

241 ted with gain-of-function GlyR expression in glutamatergic neurons resulted in recurrent epileptiform

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

243 tivation of, or restoration of Cbln1 in, VTA glutamatergic neurons reverses the sociability deficits

244 trapezoid nucleus contains Phox2b-expressing glutamatergic neurons (RTN-Phox2b neurons) that regulate

245 Anterior LHA glutamatergic neurons send a functional glutamatergic pr

246 Although it is well established that many glutamatergic neurons sequester Zn(2+) within their syna

247 Glutamatergic neurons set in motion this glia-to-neuron

248 In our reduced preparation, we found that glutamatergic neurons showed no change in synaptic outpu

249 that this vector supported approximately 90% glutamatergic neuron-specific expression in postrhinal (

250 VGLUT1 promoters supported approximately 90% glutamatergic neuron-specific expression.

251 ion found in complete CB(1)(-/-) mice and in glutamatergic neuron-specific Nex-CB(1)(-/-) mice induce

252 pecific forebrain neuron subtypes, including glutamatergic neurons, striatal medium spiny neurons, an

253 In glutamatergic neurons such as granule cells of the cereb

254 the number or size of excitatory synapses in glutamatergic neurons, suggesting its synaptogenic effec

255 ation of the transverse nerve containing the glutamatergic neuron that serves the conical chamber cau

256 we report peptidergic regulation of preoptic glutamatergic neurons that contributes to temperature re

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

258 geting of the lamina III projection cells by glutamatergic neurons that express PPD, and these are li

259 contains noncholinergic noncatecholaminergic glutamatergic neurons that express the transcription fac

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

261 ll region of the VMS marginal layer contains glutamatergic neurons that innervate the main respirator

262 Hippocampal glutamatergic neurons that lack MeCP2 display a 46% redu

263 However, the VTA also has glutamatergic neurons that project to nAcc.

264 "supraolivary medulla" (SOM), which contains glutamatergic neurons that project to the spinal ventral

265 nsporter (VGLUT1) is a critical component of glutamatergic neurons that regulates GLU release.

266 In the REM-on area are two populations of glutamatergic neurons, the first of which projects to th

267 In hippocampal glutamatergic neurons, the genetic deletion of Munc13s r

268 ular glutamate transporter (VGLUT) genes for glutamatergic neurons, the neuronal glycine transporter

269 ular glutamate transporter (VGLUT) genes for glutamatergic neurons, the neuronal glycine transporter

270 e show here that the key defining feature of glutamatergic neurons, the vesicular glutamate transport

271 h Neurog1 lineages are largely restricted to glutamatergic neurons, there are multiple exceptions inc

272 gs suggest a role in reward function for VTA glutamatergic neurons through local excitatory synapses

273 DA receptors (NMDARs) and form synapses with glutamatergic neurons throughout the CNS.

274 mechanism linking increased activity of BLA glutamatergic neurons to aberrant fear.

275 the neuron-to-glia signaling process used by glutamatergic neurons to control female sexual developme

276 ly innervate and suppress the activity of LH glutamatergic neurons to control food intake.

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

278 and barley lectin was transferred from local glutamatergic neurons to GABA interneurons that surround

279 mEPSC release, and GABAergic innervation of glutamatergic neurons unveils the unclamping phenotype o

280 In particular, the signature molecule for glutamatergic neurons vesicle glutamate transporter 2 sh

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

282 ogenetics, to identify a novel population of glutamatergic neurons (VGLUT3+) in the glomerular layer

283 370 hypothalamic ventromedial nucleus (VMH) glutamatergic neurons was studied using whole-cell recor

284 t haploinsufficiency restricted to forebrain glutamatergic neurons was sufficient to disrupt cognitio

285 Aergic nature of postsynaptic targets of VTA glutamatergic neurons, we did triple immunolabeling with

286 also "W/PS-max active." Other GABAergic and glutamatergic neurons were "PS-max active," being minima

287 Conversely, some glutamatergic neurons were "W-max active," being maximal

288 Like cholinergic neurons, many GABAergic and glutamatergic neurons were also "W/PS-max active." Other

289 Most glutamatergic neurons were found within the periventricu

290 ations of dopamine (DA) or GABA VTA neurons, glutamatergic neurons were recently discovered in the VT

291 the principal sensory trigeminal nucleus are glutamatergic neurons, whereas many NPS-positive neurons

292 for gamma-aminobutyric acid (GABA)ergic and glutamatergic neurons, which are present as the most abu

293 synaptic transmission in both GABAergic and glutamatergic neurons, which has numerous implications,

294 use they lie intermingled with GABAergic and glutamatergic neurons, which might also assume these rol

295 f NeuroD1, astrocytes were reprogrammed into glutamatergic neurons, while NG2 cells were reprogrammed

296 tors mimics the MeCP2 deficiency in wildtype glutamatergic neurons, while re-expression of BDNF quant

297 netic excitation of rat basolateral amygdala glutamatergic neurons with a variety of behavioral appro

298 er-expressing progenitors generate pyramidal glutamatergic neurons within normal adult piriform corte

299 ognition memory using optogenetics to target glutamatergic neurons within the rodent mPFC specificall

300 locking task, chemogenetic excitation of BLA glutamatergic neurons yielded significant learning to a