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 distant brain areas derive by and large from glutamatergic neurons.

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

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

5 ponse, general growth and differentiation of glutamatergic neurons.

6 2 either removed from or expressed solely in glutamatergic neurons.

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

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

9 ion in NTS-HIF-1alpha(-/-) was restricted to glutamatergic neurons.

10 f its own receptor and synergizes with local glutamatergic neurons.

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

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

13 ional and anatomical development of cortical glutamatergic neurons.

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

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

16 d by isolated damage to developing forebrain glutamatergic neurons.

17 oor in serotonin and enriched in presumptive glutamatergic neurons.

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

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

20 from mice expressing GCaMP6, leptin excites glutamatergic neurons.

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

22 he hippocampus, where it was co-expressed in glutamatergic neurons.

23 ulates the development of both GABAergic and glutamatergic neurons.

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

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

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

27 cells by a circuit involving adrenergic and glutamatergic neurons.

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

29 ich contains predominantly VGLUT2-containing glutamatergic neurons.

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

31 not in iPSCs from individuals with SCZ or in glutamatergic neurons.

32 so encloses a subgroup of aversion-promoting glutamatergic neurons.

33 f Elavl4 translation dictates development of glutamatergic neurons.

34 OS decrease calcium transients in C. elegans glutamatergic neurons.

35 ulate the inhibitory drive on the "aversive" glutamatergic neurons.

36 ctivated FGFR3 (FGFR3(K650E)) in postmitotic glutamatergic neurons.

37 nterrogation of a subpopulation of claustral glutamatergic neurons.

38 c-1 KO mice and diminished by deleting SR in glutamatergic neurons.

39 ar hypoplasia and depletion of GABAergic and glutamatergic neurons.

40 ven forebrain reduction affecting most brain glutamatergic neurons.

41 oreover, deletion of serine racemase (SR) in glutamatergic neurons abrogated d-serine synthesis to th

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

43 he putative effect of synaptic inhibition on glutamatergic neuron activity, we studied whether gamma-

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

45 We define 15 distinct populations of glutamatergic neurons and 15 of GABAergic neurons, inclu

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

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

48 he L-type calcium influx is observed in both glutamatergic neurons and parvalbumin (PV) GABAergic int

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

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

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

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

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

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

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

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

57 inside-out radial migration of post-mitotic glutamatergic neurons, and axonal tract projections.

58 ted from Ube3a deletion in GABAergic but not glutamatergic neurons, and it was rescued by pancellular

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

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

61 Glutamatergic neurons are abundant in the Drosophila cen

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

63 We find that open chromatin regions in glutamatergic neurons are enriched for neuropsychiatric

64 Specifically, glutamatergic neurons are first primed to express transc

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

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

67 ncreases statistical power and confirms that glutamatergic neurons are most affected.

68 Glutamatergic neurons are required for the generation an

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

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

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

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

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

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

75 , recent work suggests that POA GABAergic or glutamatergic neurons capable of regulating endogenous s

76 t the novel finding that stimulation of VLPO glutamatergic neurons causes a strong increase in wakefu

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

78 ion-specific activity of ventral hippocampus glutamatergic neurons causing behaviorally diverse respo

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

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

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

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

83 Glutamatergic neurons contain free zinc packaged into ne

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

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

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

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

88 ally and genetically homogeneous subclass of glutamatergic neurons defined by the expression of the p

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

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

91 rcuit mapping, we first demonstrated that PH glutamatergic neurons directly and robustly activate HMN

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

93 show that activating MnPO/VLPO GABAergic or glutamatergic neurons does not alter anesthetic inductio

94 pathway for NREM sleep generation, in which glutamatergic neurons drive broad GABAergic inhibition o

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

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

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

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

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

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

101 astroglia and rarely in microglia; instead, glutamatergic neurons express LepR, some of which projec

102 These glutamatergic neurons express the vesicular glutamate tr

103 Optrode recording showed that pIII glutamatergic neurons expressing calcitonin gene-related

104 l of bladder and sphincter function, and its glutamatergic neurons expressing corticotropin releasing

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

106 VTA glutamatergic neurons--expressing vesicular glutamate tr

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

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

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

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

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

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

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

114 cture in four distinct populations of cells (glutamatergic neurons, GABAergic neurons, oligodendrocyt

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

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

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

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

119 tudy, we compared the projection patterns of glutamatergic neurons here with a subpopulation expressi

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

121 models of psychosis propose that hippocampal glutamatergic neuron hyperactivity drives increased stri

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

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

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

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

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

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

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

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

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

131 irectly enhances NMDAR activity on principal glutamatergic neurons in medial prefrontal cortex (mPFC)

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

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

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

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

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

137 -2 is generally considered inducible, but in glutamatergic neurons in some brain regions, including t

138 1 receptor expressed in dorsal telencephalic glutamatergic neurons in synaptic plasticity and behavio

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

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

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

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

143 On-demand optogenetic inhibition of glutamatergic neurons in the fastigial nucleus of the ce

144 ontrast, on-demand optogenetic excitation of glutamatergic neurons in the fastigial nucleus successfu

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

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

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

148 fferent drive to both GABAergic and presumed glutamatergic neurons in the mature superficial dorsal h

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

150 ibition of either cholinergic, GABAergic, or glutamatergic neurons in the medial septum/diagonal band

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

152 mistry indicated overall reduced activity of glutamatergic neurons in the mPFC of KO rats and increas

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

154 studies show that activity of GABAergic and glutamatergic neurons in the PAG is modulated in an oppo

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

156 Overall, glutamatergic neurons in the PB region project to a wide

157 We identify glutamatergic neurons in the peri-locus coeruleus (periL

158 oxytocin receptors (OXTRs) are expressed on glutamatergic neurons in the PFC, optogenetic stimulatio

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

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

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

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

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

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

165 Stimulation of glutamatergic neurons in the subfornical organ drives dr

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

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

168 e, we show that neurotensin (NTS)-expressing glutamatergic neurons in the ventrolateral PAG (vlPAG) p

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

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

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

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

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

174 he smaller population of inferior collicular glutamatergic neurons-in an otherwise Fmr1 KO mouse-elim

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

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

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

178 te that CB1 signaling especially in cortical glutamatergic neurons is essential for the development o

179 Specifically, FGF21 signaling in glutamatergic neurons is necessary for protection agains

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

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

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

183 Ndufs4 inactivation in Vglut2-expressing glutamatergic neurons leads to decreased neuronal firing

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

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

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

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

188 nsistent with models suggesting that the ARC glutamatergic neurons may play both a rapid and a slower

189 Surprisingly, PAG GABAergic neurons, but not glutamatergic neurons, may encode the aversive component

190 Both types of glutamatergic neurons (mEC LVa and LVb) as well as fast-

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

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

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

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

195 Selective deletion of IL-1R1 in glutamatergic neurons (nIL-1R1(-/-)) abrogated the stres

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

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

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

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

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

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

202 Furthermore, the deletion of Fmr1 in glutamatergic neurons of the inferior colliculus is nece

203 sociated with a diminished plasticity in the glutamatergic neurons of the infralimbic medial prefront

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

205 Conditional deletion of HIF-1alpha in glutamatergic neurons of the nucleus tractus solitarius

206 ns within the lamina terminalis-particularly glutamatergic neurons of the subfornical organ expressin

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

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

209 feelings after withdrawal that involves the glutamatergic neurons of the ventral pallidum.

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

211 2 (tethered to mCherry) was expressed in VTA glutamatergic neurons of VGluT2::Cre mice.

212 pecific CB1 deletion in dorsal telencephalic glutamatergic neurons only (Glu-CB1-KO) or in both gluta

213 r the larger population of VGlut2-expressing glutamatergic neurons or the smaller population of infer

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

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

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

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

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

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

220 tripartite synapses between cancer cells and glutamatergic neurons, presenting a rationale for brain

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

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

225 tory sleep center where different subsets of glutamatergic neurons promote NREM sleep through both lo

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

238 on of PAG GABAergic neurons or inhibition of glutamatergic neurons resulted in attenuation of scratch

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

240 ly found that CDKL5 dysfunction in forebrain glutamatergic neurons results in deficits in learning an

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

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

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

244 Constitutive Ahnak KO mice or forebrain glutamatergic neuron-selective Ahnak KO mice display a d

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 SCZ cINs, but not SCZ glutamatergic neurons, show dysregulated Oxidative Phosp

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

249 and, more moderately, by brain region, with glutamatergic neurons showing the largest regional varia

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

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 t miR-383 expression is enriched in cortical glutamatergic neurons, suggesting a unique role in these

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

255 in is evenly expressed in both GABAergic and glutamatergic neurons, suggesting the GABAergic neuron-p

256 The transient cholinergic phenotype of these glutamatergic neurons suggests a homosynaptic source of

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

258 el groups of chemosensory and mechanosensory glutamatergic neurons that detect food-related cues.

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

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

261 rocal connections with another population of glutamatergic neurons that express the peptide cholecyst

262 Our data indicate that Fmr1 deletion in glutamatergic neurons that express vesicular glutamate t

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

264 ude that activation of preoptic GABAergic or glutamatergic neurons that increase sleep or wakefulness

265 ns are inhibitory, a sub-fraction represents glutamatergic neurons that integrate into the superficia

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

267 on, as well as efferent sympathetic premotor glutamatergic neurons that regulate gastrointestinal tra

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

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

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

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

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

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

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

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

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

277 IL-17a receptor was expressed in cortical glutamatergic neurons under steady state and its genetic

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

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

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

281 The transcriptional profile of LHA glutamatergic neurons was affected by obesity, exhibitin

282 However, beta-klotho expression in glutamatergic neurons was dispensable for the effects of

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

284 thermore, selective restoration of IL-1R1 on glutamatergic neurons was sufficient to reestablish the

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

286 mine the impact of aberrant FGFR function on glutamatergic neurons, we generated a FGFR gain-of-funct

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

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

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

290 Most glutamatergic neurons were found within the periventricu

291 Encoding properties of individual LHA glutamatergic neurons were then tracked throughout obesi

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

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

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

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

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

297 Cortical OTR cells are largely glutamatergic neurons with the exception of cells in lay

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