ライフサイエンスコーパス: excitatory neuron

1 h (GR)(80) gradually accumulates in cortical excitatory neurons.

2 ion, such as GAB1 and GRB2, were enriched in excitatory neurons.

3 neurons control the output and plasticity of excitatory neurons.

4 icity at different timescales in hippocampal excitatory neurons.

5 ronger during non-REM sleep among deep-layer excitatory neurons.

6 ve cues in distinct, intermingled sets of BA excitatory neurons.

7 sinhibition unmasks more excitatory input to excitatory neurons.

8 ells (hiPSCs) can rapidly produce high-yield excitatory neurons.

9 interneurons in clusters and the same nearby excitatory neurons.

10 target and directly activate inhibitory and excitatory neurons.

11 ine and movement-related activity in layer 4 excitatory neurons.

12 ed a mouse overexpressing Ube3a isoform 2 in excitatory neurons.

13 as lowered by adding autapses to high degree excitatory neurons.

14 ic noise correlations with local and distant excitatory neurons.

15 atory elements in inhibitory neurons than in excitatory neurons.

16 ually antagonistic fbRF and ffRF, similar to excitatory neurons.

17 y a loss of inter-areal connectivity between excitatory neurons.

18 r visual stimulation, matching plasticity in excitatory neurons.

19 change mainly to long-range coupling between excitatory neurons.

20 ortance of Nav1.1 in human inhibitory versus excitatory neurons.

21 is, thus enhancing PV neuronal inhibition to excitatory neurons.

22 urons, and the Thy1, expressed in putatively excitatory neurons.

23 nsitive fluorophore GCaMP in layer 2/3 and 5 excitatory neurons.

24 ERK/MAPK signaling in developing neocortical excitatory neurons.

25 promoter that limits expression to forebrain excitatory neurons.

26 ss movement-related activity in layer 4 (L4) excitatory neurons.

27 ons (PV-INs) through inhibition of principal excitatory neurons.

28 istence of selective pools of inhibitory and excitatory neurons.

29 urons differentially amplify SSA in putative excitatory neurons.

30 cal coupling between radially aligned sister excitatory neurons.

31 ge and release of glutamate from synapses of excitatory neurons.

32 onal network, which is primarily composed of excitatory neurons.

33 ansient amplifying cells generating cortical excitatory neurons.

34 n by the differential spatial recruitment of excitatory neurons.

35 rain regions, than the overall population of excitatory neurons.

36 ll layers of A25, mostly targeting spines of excitatory neurons.

37 Kcna1 (encoding Kv1.1) in mouse hippocampal excitatory neurons.

38 with maximal enrichment in cortical layer V excitatory neurons.

39 from NMDA-R hypofunction predominantly onto excitatory neurons.

40 expressing interneurons and disinhibit local excitatory neurons.

41 ivity of SOM neurons leads to suppression of excitatory neurons.

42 PV interneuron activity and disinhibition of excitatory neurons.

43 n of GABA and hyperactivation of neighboring excitatory neurons.

44 d feed-forward inhibition of visual cortical excitatory neurons.

45 tch recordings of optogenetically identified excitatory neurons.

46 ogeneous, comprising a mix of inhibitory and excitatory neurons.

47 ergic inhibitory, and putative glutamatergic excitatory neurons.

48 likely to be modulated by IEDs than putative excitatory neurons (19 of 157 vs 31 of 571).

49 from the soma the targets were mostly other excitatory neurons, about half of these being other HVC(

50 stablished that, instead of simply balancing excitatory neuron activity, inhibitory neurons actively

51 in FS neuron activity and an increase in L4 excitatory neuron activity.

52 ustained decreases in synaptic inhibition to excitatory neurons, along with reduced synaptic excitati

53 d or receptor that laterally disperse sister excitatory neurons also disrupt preferential electrical

54 sal exerts a feedback pull-push influence on excitatory neurons-an inversion of the canonical push-pu

55 numerous MCHS-related phenotypes, including excitatory neuron and microglia gene expression changes.

56 ces eIF2alpha phosphorylation in hippocampal excitatory neurons and a subset of hippocampal inhibitor

57 These findings indicate that excitatory neurons and astrocytes are organized into dis

58 ix metalloprotease-9, increases branching of excitatory neurons and concomitantly attenuates the peri

59 iscriminated between putative inhibitory and excitatory neurons and found that the inhibitory st-LFP

60 The neocortex contains glutamatergic excitatory neurons and gamma-aminobutyric acid (GABA)erg

61 in the human developing brain, especially in excitatory neurons and glial cells, but shows a more res

62 reatest dysregulation occurred in deep layer excitatory neurons and immature oligodendrocyte precurso

63 le the probability of firing in postsynaptic excitatory neurons and in SOM, but not FS, interneurons.

64 these cells receive inputs from deeper-layer excitatory neurons and inhibitory interneurons in the fi

65 at CR cells receive inputs from deeper-layer excitatory neurons and inhibitory interneurons in the fi

66 We sorted excitatory neurons and key inhibitory neuron subtypes fr

67 induced pluripotent stem cell (iPSC)-induced excitatory neurons and lower motor neurons, iPSC-derived

68 tosensory cortex that synapses with cervical excitatory neurons and modulates the lumbar locomotor ne

69 report that bursts enhanced the responses of excitatory neurons and of inhibitory interneurons that p

70 at is markedly distinct from that induced in excitatory neurons and other subtypes of inhibitory neur

71 We found that excitatory neurons and parvalbumin-expressing inhibitory

72 ant epilepsy-and record activity of putative excitatory neurons and parvalbumin-positive GABAergic ne

73 eriods and demostrate enriched expression in excitatory neurons and radial glias but depleted express

74 velopment, decreased dendritic complexity of excitatory neurons and reduced numbers of inhibitory neu

75 velopment, decreased dendritic complexity of excitatory neurons and reduced numbers of inhibitory neu

76 We obtained whole-cell recordings from excitatory neurons and somatostatin- and parvalbumin-pos

77 signatures both for the regular-spiking (RS) excitatory neurons and the fast-spiking (FS) inhibitory

78 found that synaptic signaling of upper-layer excitatory neurons and the molecular state of microglia

79 nstrate that BLA afferents directly activate excitatory neurons and two distinct populations of inhib

80 tivity of the drugs is mediated by 4E-BP2 in excitatory neurons, and 4E-BP1 and 4E-BP2 in inhibitory

81 Calbindin and Lmx1b, which are expressed by excitatory neurons, and found that more than half (58%)

82 increased synaptic release preferentially in excitatory neurons, and hence the perturbation of the ex

83 iking in inhibitory and decreases spiking in excitatory neurons, and increases signal-to-noise ratio

84 radial glia, intermediate progenitor cells, excitatory neurons, and interneurons isolated from mid-g

85 l IP, which contains a mix of inhibitory and excitatory neurons, and the dorsomedial IP, which is exc

86 voked firing of regular spiking, presumptive excitatory, neurons, and a reduced firing of fast-spikin

87 Thus, BLA excitatory neurons are a highly heterogenous collection

88 Excitatory neurons are derived from the dorsal telenceph

89 Here we show, in rats, that excitatory neurons are disproportionately affected.

90 In striking contrast, excitatory neurons are far more common (by a factor of 1

91 ting that inhibitory cortical connections to excitatory neurons are generally localized within the sa

92 during embryonic neurogenesis, a period when excitatory neurons are generated from progenitors.

93 Many excitatory neurons are generated through a two-step proc

94 primarily affect inhibitory neurons, whereas excitatory neurons are more sensitive to stimulus specif

95 Excitatory neurons are preferentially impaired in early

96 titde (VIP)-expressing interneurons, whereas excitatory neurons are recruited several seconds later.

97 Connections between the two types of excitatory neurons are sparse, and local processing of h

98 atory and inhibitory synaptic connections to excitatory neurons are spatially organized on a layer-by

99 ates that CaMKIIalpha is not as specific for excitatory neurons as commonly believed.

100 n-of-function mutation of SCN8A and identify excitatory neurons as critical targets for therapeutic i

101 rons, and an "inside-out" layer formation of excitatory neurons as seen in other species.

102 to generate brain-wide maps of the input to excitatory neurons as well as three inhibitory interneur

103 matin changes occurring in mouse hippocampal excitatory neurons at different time points after synchr

104 eus RNA sequencing reveals selective loss of excitatory neurons at disease end-stage, which is charac

105 er, in the absence of TBR2, clonally related excitatory neurons become more laterally dispersed and t

106 e genes include markers of L2/3, L5b, and L6 excitatory neurons but not glial or inhibitory markers,

107 lencephalon divide asymmetrically to produce excitatory neurons, but also indirectly to produce neuro

108 C is highly expressed in developing cortical excitatory neurons, but its role in their development re

109 ferential electrical coupling between sister excitatory neurons, but not that between RGP and newborn

110 M) facilitated visual responses in layer 2/3 excitatory neurons by approximately 20%.

111 are differentially regulated in hippocampal excitatory neurons by exposing mice to an environment wi

112 hat selective deletion of SIRT1 in forebrain excitatory neurons causes depression-like phenotypes in

113 cell-type set containing two region-specific excitatory neuron classes and three region-invariant inh

114 the presynaptic input neurons to individual excitatory neuron clones as a unit that constitutes func

115 s on the selective synaptic communication of excitatory neuron clones in the sensory area that provid

116 au accumulation takes place predominantly in excitatory neurons compared to inhibitory neurons, not o

117 ptor signaling system both on inhibitory and excitatory neurons controls functional and structural sy

118 Genetic deletion of the Agrn gene in excitatory neurons decreases NSPCs proliferation and inc

119 eletion of 4E-BP2 in forebrain glutamatergic excitatory neurons, defined by Camk2a, or in astrocytes,

120 lts into a compartmental model of developing excitatory neurons demonstrated that all ASD variants, r

121 ndromic repeats (CRISPR) techniques in human excitatory neurons, demonstrating that CDK5RAP3, STRAP a

122 Clones of excitatory neurons derived from a common progenitor have

123 Excitatory neurons derived from hiPSCs with CRISPR/Cas9-

124 evealed feature-specific suppression between excitatory neurons, despite the presence of highly speci

125 ish early transcriptomic differences between excitatory neurons destined to give rise to broad "proto

126 ated fused organoid models of inhibitory and excitatory neuron development, which can now achieve fun

127 Finally, a conditional BIN1 knockout in excitatory neurons did not alter BACE1, APP, C-terminal

128 Continued MET expression in cortical excitatory neurons disrupted synaptic protein profiles,

129 ediated chemogenetic activation of forebrain excitatory neurons during postnatal life (P2-14), but no

130 enhanced Gq-mediated signaling in forebrain excitatory neurons during postnatal life can evoke persi

131 q-signaling-mediated activation of forebrain excitatory neurons during the critical postnatal window

132 Optogenetic depolarization of excitatory neurons either facilitated or suppressed base

133 eletion of Mef2c in cortical and hippocampal excitatory neurons (Emx1-lineage) produces a dramatic re

134 rneurons reduced movement-related spiking in excitatory neurons, enhancing selectivity for touch-rela

135 n contrast to the transient participation of excitatory neurons, ensemble measurements dominated by i

136 which mainly inhibit perisomatic regions of excitatory neurons, exhibited a gradual increase in axon

137 On the other hand, excitatory neurons expressing CaMKIIalpha displayed no s

138 ted in obese mice, and induction of Cadm1 in excitatory neurons facilitated weight gain while exacerb

139 ched and whole-cell recordings revealed that excitatory neuron firing slightly preceded interneuron f

140 ng interneurons (FSIs) control the timing of excitatory neuron firing via somatic inhibition and gene

141 for the restoration of sensory processing in excitatory neurons following peripheral nerve injuries.

142 , the spatial extent of inhibitory inputs of excitatory neurons for a given layer closely mirrors tha

143 ng neural precursor cells in the SVZ produce excitatory neurons for each cortical layer in the neocor

144 biting SOM neurons, which leads to relief of excitatory neurons from suppression.

145 However, excitatory neurons from the Emx-Cre; Clock(flox/flox) mo

146 )-derived forebrain neurons and Ngn2-induced excitatory neurons, from two independent SZ patient coho

147 g significant enrichments of autism risk and excitatory neuron genes.

148 ignificant alterations in gene expression in excitatory neurons, glia and other cell types.

149 We found that a local patch of excitatory neurons has a large diversity of contrast tun

150 We found that only a fraction of excitatory neurons homeostatically recover activity afte

151 It is likely that excitatory neurons horizontally disperse in other gyrenc

152 rojections to paraventricular thalamus (PVT) excitatory neurons immediately (in 2 to 3 seconds) evoke

153 s of the PDE4A5 isoform in mouse hippocampal excitatory neurons impairs a long-lasting form of hippoc

154 input received by three classes of principal excitatory neuron in the anterior piriform cortex.

155 ne-scale spatial and circuit organization of excitatory neurons in addition to enhancing neurogenesis

156 forebrain (Oxtr(-/-)) or CA2/CA3a-restricted excitatory neurons in adult male mice impaired the persi

157 We tested this by optogenetically activating excitatory neurons in alert macaque primary visual corte

158 Two-photon imaging showed that many excitatory neurons in auditory cortex were suppressed du

159 Excitatory neurons in auditory cortex, for example, adap

160 nia and bipolar disorder are concentrated in excitatory neurons in cortical layers II-III, IV, and V,

161 radial columns of laminar microcircuits, and excitatory neurons in different V1 laminae exhibit disti

162 Deleting ngr1 in excitatory neurons in L4, but not in L2/3, L5, or L6, pr

163 nhibitory inputs are found, particularly for excitatory neurons in layers 2/3 and 5.

164 d inhibitory synaptic laminar connections to excitatory neurons in layers 2/3-6 of the mouse visual c

165 sion of nrg1,2,3,4 and erbB1,2,3,4 in PV and excitatory neurons in mouse visual cortex.

166 tor subtype in whole neuronal populations or excitatory neurons in mPFC facilitates the induction of

167 and their newborn progeny and between sister excitatory neurons in ontogenetic radial clones at the e

168 cal role in enhancing response properties of excitatory neurons in primary visual cortex (V1) during

169 role of dopamine D1 receptor subtype in mPFC excitatory neurons in suppressing stress susceptibility.

170 Layer (L) 4 excitatory neurons in the barrel cortex, the major targe

171 een afferent pathways, PV-INs, and principal excitatory neurons in the basolateral amygdala.

172 An autorhythmic population of excitatory neurons in the brainstem pre-Botzinger comple

173 itic spines, the postsynaptic compartment of excitatory neurons in the CNS.

174 Selective inactivation of excitatory neurons in the dACC not only increased omissi

175 Mossy cells are excitatory neurons in the dentate hilus that regulate de

176 urons made synapses on the dendrites of host excitatory neurons in the DG and the CA1 subfield of the

177 ther, these results suggest that stimulating excitatory neurons in the fastigial nucleus may be a pro

178 tify the transcriptional profile of immature excitatory neurons in the human amygdala between 4-15 ye

179 Here we interrogate a unique class of excitatory neurons in the hypothalamic arcuate nucleus (

180 on of eukaryotic initiation factor 2alpha in excitatory neurons in the LA enhanced memory strength bu

181 n synthesis inhibition pan-neuronally and in excitatory neurons in the lateral amygdala (LA) impaired

182 istinct, spatially segregated populations of excitatory neurons in the mouse BLA that participate in

183 ditionally deleted (cKO) Top1 in postmitotic excitatory neurons in the mouse cerebral cortex and hipp

184 we examined the activity of layer 2/3 (L2/3) excitatory neurons in the mouse primary visual cortex (V

185 Here we show that feedback projections onto excitatory neurons in the mouse primary visual cortex ge

186 ion and increases dendritic spine density on excitatory neurons in the OFC.

187 We show that a subset of excitatory neurons in the pre-locus coeruleus express pr

188 resentation, we performed calcium imaging of excitatory neurons in the primary visual cortex (V1) of

189 a suggest CR expression is not restricted to excitatory neurons in the SDH.

190 e layer-by-layer synaptic wiring diagrams of excitatory neurons in the visual cortex.

191 and VGLUT2 identify distinct populations of excitatory neurons in visual brain structures across mam

192 Adding more autaptic connections to excitatory neurons increased the number of spiking event

193 Using small molecule differentiation into excitatory neurons, induced pluripotent stem cell-derive

194 Thus, the fast intrinsic adaptation of excitatory neurons is not sufficient to account for the

195 These results suggest that SIRT1 in mPFC excitatory neurons is required for normal neuronal excit

196 In contrast, nrg1 expression by excitatory neurons is unchanged at P28 and P104 followin

197 Conditional deletion of Cc2d1a (cKO) from excitatory neurons leads to impaired performance in obje

198 Adding an adaptation current to excitatory neurons leads to spontaneous alternations bet

199 explained by a decrease in coupling between excitatory neurons located in distinct brain areas.

200 homogeneous population of central cell-like excitatory neurons located in lamina II of the superfici

201 Clonally related excitatory neurons maintain a coherent relationship foll

202 This restricts inhibition of excitatory neurons, maintaining them in a state that is

203 optogenetic activation of subfornical organ excitatory neurons, marked by the expression of the tran

204 lpha has traditionally been considered as an excitatory neuron marker, our single-cell sequencing res

205 We propose that excitatory neurons may branch their leading process as a

206 ceptor subtype and related signaling in mPFC excitatory neurons mediate acute stress-induced dendriti

207 s studies revealed that MeCP2 dysfunction in excitatory neurons mediated elevated synchrony at baseli

208 conditionally delete Cc2d1a exclusively from excitatory neurons of male mouse forebrain to examine it

209 NMDAR PAM AGN-241751 and identify GluN2B on excitatory neurons of mPFC as initial cellular trigger u

210 beta-adrenergic signaling exclusively within excitatory neurons of the basolateral amygdala.

211 Excitatory neurons of the cerebral cortex migrate radial

212 show that selective deletion of Gtf2i in the excitatory neurons of the forebrain caused neuroanatomic

213 on conditions, elevation of S-SCAM levels in excitatory neurons of the forebrain was sufficient to in

214 Excitatory neurons of the mammalian cerebral cortex are

215 ective inactivation of APP family members in excitatory neurons of the postnatal forebrain results in

216 in populations, such as cortical layer (L) 4 excitatory neurons of the primary somatosensory (S1) bar

217 Excitatory neurons on average suppressed other neurons a

218 this length scale, basal-ganglia-projecting excitatory neurons, on average, fire at a specific phase

219 Activation of monSTIM1 in either excitatory neurons or astrocytes of mice brain is able t

220 BLA afferents either selectively activating excitatory neurons or driving a compound response consis

221 yndrome and control iPSCs into telencephalic excitatory neurons or medial ganglionic eminence (MGE)-l

222 Chemogenetic inhibition of excitatory neurons or pharmacologically strengthening GA

223 heir major excitatory input, the oviposition excitatory neurons (oviENs).

224 sion of bidirectionally connected inhibitory-excitatory neuron pairs.SIGNIFICANCE STATEMENT Many stru

225 This finding suggests that dACC excitatory neurons play a principal role in modulating a

226 at cerebellar BDNF is derived primarily from excitatory neurons--precerebellar nuclei/spinal cord neu

227 ression of E4 by stem-cell-derived forebrain excitatory neurons predisposes neurons to calcium dysreg

228 to be due to the block of sodium channels on excitatory neurons, primarily Na(V)1.6 and Na(V)1.2.

229 dies have revealed substantial insights into excitatory neuron production.

230 In the mammalian neocortex, excitatory neurons provide excitation in both columnar a

231 by lineage relationships among locally born excitatory neurons, raising the intriguing possibility t

232 and inhibitory neurons, but, rather, because excitatory neurons rely more heavily on inhibition to co

233 ory synaptic inputs in relation to principal excitatory neurons remains incomplete, and it is unclear

234 Deletion of miR-132/212 from forebrain excitatory neurons replicates the binocular matching def

235 onditional Mef2c heterozygosity in forebrain excitatory neurons reproduced a subset of the Mef2c-Het

236 In contrast, L4 excitatory neurons responded mainly to touch.

237 Vm oscillations coincided with visual cues, excitatory neuron responses to preferred cues were signi

238 addition our analysis allows an estimate of excitatory neuron-restricted precursors (about 10) that

239 in vivo whole-cell patch-clamp recording of excitatory neurons revealed variation in the amplitudes

240 interaction with SHP2(D61G), selectively in excitatory neurons, reversed SHP2(D61G)-mediated deficit

241 s), which mainly inhibit distal dendrites of excitatory neurons, showed a decrease in axonal boutons

242 sory deprivation, whereas nrg3 expression by excitatory neurons shows changes depending on the age an

243 We find that synaptic input sources of excitatory neurons span the radial columns of laminar mi

244 Presynaptic excitatory neurons spanned layers 2/3 and 4 and were dis

245 tory markers, confirming Arc-dVenus to be an excitatory neuron-specific but non-layer-specific activi

246 ia adeno-associated viral vectors, driven by excitatory neuron-specific promoter elements, to manipul

247 Excitatory neuron-specific targeting was promoter-depend

248 could lead to increased synaptic release in excitatory neurons, steering neuronal circuits towards e

249 Methylation signatures identified a layer 6 excitatory neuron subtype and a unique human parvalbumin

250 GAP-43 protein was primarily located in excitatory neurons, suggesting its functional significan

251 a reduction in synaptic inhibition onto all excitatory neurons, suggesting that both synaptic mechan

252 increased spontaneous inhibitory currents in excitatory neurons, suggesting that mPFC-BLA circuit mat

253 1 receptor-mediated dendritic growth in mPFC excitatory neurons suppresses stress susceptibility.

254 We describe a group of excitatory neurons, termed Odd neurons, which are import

255 Because the thalamus is composed of excitatory neurons that are devoid of local recurrent ex

256 for selective subnetworks of inhibitory and excitatory neurons that are shaped by experience to supp

257 or cell-specific manipulation, we discovered excitatory neurons that induce nausea-related behaviors,

258 The diverse subtypes of excitatory neurons that populate the neocortex are born

259 s strong homology to extratelencephalic (ET) excitatory neurons that project to subcerebral targets.

260 evelopment in the mammalian brain, groups of excitatory neurons that receive similar sensory informat

261 We conclude that the human PL contains excitatory neurons that remain immature for decades, a p

262 external tufted cells (ETCs), the two major excitatory neurons that transmit glomerular output.

263 use primary visual cortex (V1) as well as L4 excitatory neurons, the main bottom-up source, and long-

264 For excitatory neurons, this late component reflected genuin

265 However, a subpopulation of excitatory neurons thought to mediate behavioral output

266 ory and inhibitory synaptic inputs to single excitatory neurons throughout cortical layers 2/3-6 in t

267 The late component in excitatory neurons thus shares time course, deviance det

268 ly correlated activity with other recovering excitatory neurons, thus forming a subnetwork of recover

269 hibition caused by reduced responsiveness of excitatory neurons to GABAergic inhibitory inputs.

270 n mice deficient in Met activity in cortical excitatory neurons to gain insights into aberrant somato

271 epend on inhibition that paces assemblies of excitatory neurons to produce alternating temporal windo

272 s the cellular and regional vulnerability of excitatory neurons to tau pathology.

273 d by increased periods of firing in pools of excitatory neurons, together with asymmetrical associati

274 ression changes in PV inhibitory neurons and excitatory neurons track with sensory perturbation.

275 Restriction of p.Arg1872Trp expression to excitatory neurons using Emx1-Cre recapitulated seizures

276 tion, nuclear pore defects and cell death in excitatory neurons via the complement activation pathway

277 As in excitatory neurons, voltage-gated Ca(2+) influx through

278 niature inhibitory post-synaptic currents in excitatory neurons was consistent with impaired post-syn

279 orsal lateral geniculate nucleus input to V1 excitatory neurons was found, there was no evidence of d

280 ion selectivity of layer (L)2/3, but not L4, excitatory neurons was sharpened in the presence of soun

281 ypes and circuit diagram of clonally related excitatory neurons, we performed multi-cell patch clamp

282 Large excitatory neurons were born in the first wave, and smal

283 Laminar-specific synaptic wiring diagrams of excitatory neurons were constructed on the basis of circ

284 The presence and distribution of excitatory neurons were firmly established; glutamatergi

285 rons remained locomotion responsive, SST and excitatory neurons were largely non-responsive.

286 The dendrites of hippocampal excitatory neurons were markedly stunted in Cd40(-/-) mi

287 In contrast, in somatosensory cortex (S1), excitatory neurons were mostly stellate and SOM(+) inter

288 escued by a Nav1.1 transgene, whereas Dravet excitatory neurons were normal.

289 Nearly all excitatory neurons were pyramidal and all somatostatin-p

290 to be expressed during mid-gestation and in excitatory neurons, whereas neurodegenerative-disorder r

291 PV interneuron activity and disinhibition of excitatory neurons, which are known hallmarks of cortica

292 Direct photoactivation of excitatory neurons, which did not change tone-evoked res

293 composed of multiple types of inhibitory and excitatory neurons, which form sophisticated microcircui

294 ic complexity and spine density in forebrain excitatory neurons, which may underlie the altered synap

295 el of a synaptically connected population of excitatory neurons with [Formula: see text] and [Formula

296 Results show autaptic connections to excitatory neurons with high average controllability led

297 ha 0.4 promoter as the best choice to target excitatory neurons with rAAVs.

298 cted precursors (about 10) that generate the excitatory neurons within a cortical column.

299 The relative recruitment of inhibitory and excitatory neurons within an area controls the gain of n

300 fferentiated into pure cultures of forebrain excitatory neurons without contamination from other cell