ライフサイエンスコーパス: excitatory neuron

1 interneurons in clusters and the same nearby excitatory neurons.

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

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

4 urons differentially amplify SSA in putative excitatory neurons.

5 cal coupling between radially aligned sister excitatory neurons.

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

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

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

9 ansient amplifying cells generating cortical excitatory neurons.

10 mice with continued mutant PS1 synthesis in excitatory neurons.

11 expression is limited almost exclusively to excitatory neurons.

12 ining increases Arc expression in subsets of excitatory neurons.

13 ficity of Syngap1 mutations within forebrain excitatory neurons.

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

15 dent cleavage of APP within cells other than excitatory neurons.

16 innervate the axon initial segment (AIS) of excitatory neurons.

17 ams of late-response genes in inhibitory and excitatory neurons.

18 -3alpha and GSK-3beta in newly born cortical excitatory neurons.

19 ic noise correlations with local and distant excitatory neurons.

20 ative inhibitory neurons than among putative excitatory neurons.

21 d hippocampus, without detectable changes in excitatory neurons.

22 ivity by repressing inhibitory synapses onto excitatory neurons.

23 nguishing between circuits of inhibitory and excitatory neurons.

24 ms consistent with pyramidal regular-spiking excitatory neurons.

25 ts in the apparently normal OS sharpening in excitatory neurons.

26 enitors generate a subpopulation of amygdala excitatory neurons.

27 ead of Pv+ cells was nearly equal to that of excitatory neurons.

28 es were elicited by stimulation of intrinsic excitatory neurons.

29 atory elements in inhibitory neurons than in excitatory neurons.

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

31 r visual stimulation, matching plasticity in excitatory neurons.

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

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

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

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

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

37 ERK/MAPK signaling in developing neocortical excitatory neurons.

38 target and directly activate inhibitory and excitatory neurons.

39 promoter that limits expression to forebrain excitatory neurons.

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

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

42 ity was relatively stable and balanced local excitatory neuron activity on a movement-by-movement bas

43 ity on a movement-by-movement basis, whereas excitatory neuron activity showed higher dynamism during

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

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

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

47 orms (types I, II, and III) are expressed in excitatory neurons, although they are also present in GA

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

49 -axonic cartridges innervate the majority of excitatory neurons and are distributed more frequently i

50 shortening the time scale of the membrane in excitatory neurons and by reducing the temporal separati

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

52 s from layer 2/3 and layer 4 visual cortical excitatory neurons and from parvalbumin-positive and som

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

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

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

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

57 with sensory information by contacting both excitatory neurons and inhibitory interneurons.

58 The neocortex contains excitatory neurons and inhibitory interneurons.

59 hese terminals innervated spines of presumed excitatory neurons and many were frequently multisynapti

60 ry neurons) as well as for pairs of putative excitatory neurons and neurons with narrow spike wavefor

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

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

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

64 gulated nuclear translocation occurs only in excitatory neurons and requires calcium influx and calci

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

66 potential activity was observed in stellate excitatory neurons and somatostatin-containing interneur

67 Cortical networks are dominated by excitatory neurons and synapses, are sparsely connected,

68 We attribute this to the number of excitatory neurons and the excitatory conductance decrea

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

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

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

72 luorescent protein to label radial clones of excitatory neurons, and in vivo two-photon calcium imagi

73 own that Celf4 is expressed predominantly in excitatory neurons, and that deficiency results in abnor

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

75 encephalon: the pallium, the major source of excitatory neurons, and the subpallium, the major source

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

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

78 The process by which excitatory neurons are generated and mature during the d

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

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

81 Biochemical studies suggest that excitatory neurons are metabolically coupled with astroc

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

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

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

85 hout the CNS, but a widely held view is that excitatory neurons are the primary (or sole) source of t

86 bventricular zones (SVZ), which give rise to excitatory neurons, are divided into distinct subtypes b

87 ut may specify horizontally clustered sister excitatory neurons as functional units in the hippocampu

88 educed action potential-driven inhibition of excitatory neurons as revealed by less frequent spontane

89 neurons with broad spike waveforms (putative excitatory neurons) as well as for pairs of putative exc

90 y neurons rather than a decreased spiking of excitatory neurons, as archaerhodopsin-3 (Arch)-mediated

91 an be ascribed to endocannabinoid control of excitatory neurons, because it was reproduced in conditi

92 ence increased maximum responses of putative excitatory neurons but had the opposite effect on maximu

93 we show that deletion of Mecp2 from cortical excitatory neurons but not forebrain inhibitory neurons

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

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

96 dominant association with spines of putative excitatory neurons, but also significant interactions wi

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

98 ng inputs to local clusters of inhibitory or excitatory neurons, but not both, using neurotropic aden

99 We suggest that LGI1 secreted from excitatory neurons, but not parvalbumin inhibitory neuro

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

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

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

103 orhinal cortex (ECII), we report clusters of excitatory neurons called island cells, which appear in

104 d evaluating mice lacking Nampt in forebrain excitatory neurons (CaMKIIalphaNampt(-/-) mice).

105 rotein kinase IIalpha (CAMKIIalpha)-positive excitatory neurons caused no significant change in V1 st

106 predominated in targeted spines of presumed excitatory neurons, consistent with their mutual activat

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

108 e mammalian cerebral cortex, a population of excitatory neurons defined by the NTSR1-Cre mouse line i

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

110 Excitatory neurons derive from progenitors in the palliu

111 Excitatory neurons derived from hiPSCs with CRISPR/Cas9-

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

113 kemia 2 (mll2/kmt2b) gene in adult forebrain excitatory neurons display impaired hippocampus-dependen

114 erating a balanced network of inhibitory and excitatory neurons during development requires precise t

115 The dynamics of excitatory neurons during the initial phase involved the

116 x, however, significant interactions between excitatory neurons (E) have been hard to detect because

117 Optogenetic depolarization of excitatory neurons either facilitated or suppressed base

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

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

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

121 The specific connections that these excitatory neurons establish with the rest of the breath

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

123 Here we show that of the two major types of excitatory neurons existing in L6, the NTSR1-Cre line se

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

125 d electrophysiological analysis, showed that excitatory neurons expressing somatostatin (SOM) include

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

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

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

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

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

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

132 naptic connectivity is highly structured and excitatory neurons form subnetworks that process related

133 s, as the specificity of connections between excitatory neurons forms the basis for the cortical cano

134 are responsible for generating a majority of excitatory neurons found in the adult neocortex.

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

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

137 g-lasting, potentially permanent, changes to excitatory neuron function in the prefrontal cortex of j

138 euron production, we quantitatively analyzed excitatory neuron genesis in the mouse neocortex using M

139 Excitatory neurons had linear, simple receptive fields t

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

141 In the mammalian cerebral cortex, excitatory neurons have been ascribed to one of two main

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

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

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

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

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

147 s (RGCs) generate layer-specific subtypes of excitatory neurons in a defined temporal sequence, in wh

148 he detailed spatial receptive fields of most excitatory neurons in a plane.

149 present the projective fields of the primary excitatory neurons in a sensory circuit.

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

151 The spatial spread of labeled excitatory neurons in AI was more than twice that found

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

153 cited interneurons in one layer (5A/LTS) and excitatory neurons in another (5B/corticospinal).

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

155 Excitatory neurons in auditory cortex, for example, adap

156 that ErbB4 localizes to dendritic spines of excitatory neurons in cortical neuronal cultures and is

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

158 In contrast, excitatory neurons in layer 4 exhibited weak excitation

159 in vivo loose-patch recordings, we found in excitatory neurons in layer 4 of mouse primary visual co

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

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

162 ch is expressed in the synaptic terminals of excitatory neurons in most nuclei of the brainstem and t

163 ry and inhibitory synaptic inputs to layer 4 excitatory neurons in mouse primary visual cortex (V1) a

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

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

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

167 ns somata situated in laminae III and V, the excitatory neurons in rat S1 were engineered to express

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

169 lin/gamma-secretase in promoting survival of excitatory neurons in the adult cerebral cortex by gener

170 rate (HR) revealing tonic inhibition of the excitatory neurons in the ARCN.

171 ar recordings in behaving mice, we find that excitatory neurons in the auditory cortex are suppressed

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

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

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

175 distinct from those in the neocortex, sister excitatory neurons in the cornu ammonis 1 region of the

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

177 Here, we show that clonally related excitatory neurons in the developing hippocampus are pro

178 e-cell voltage-clamp recordings from layer 4 excitatory neurons in the developing mouse primary visua

179 determines the balance of inhibitory versus excitatory neurons in the dorsal spinal cord.

180 We hypothesized that a subset of layer 2 excitatory neurons in the juvenile (P18 to 27) mouse whi

181 We focus on excitatory neurons in the mammalian hippocampus, one of

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

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

184 e that FGFR2 signaling expands the number of excitatory neurons in the mPFC and secondarily influence

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

186 report that evoked firing rates of binocular excitatory neurons in the primary visual cortex immediat

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

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

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

190 ior, we trained mice to report activation of excitatory neurons in visual cortex using channelrhodops

191 ne receptor selectively in mouse hippocampal excitatory neurons in vivo.

192 ) interneurons and putative principal (i.e., excitatory) neurons in freely behaving cats across perio

193 nhibitory interneurons, or CaMKII-expressing excitatory neurons, in auditory cortex of behaving mice

194 n two-neuron micronetworks consisting of two excitatory neurons, in which a neuron is connected to on

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

196 r1 has no effect on excitatory synapses onto excitatory neurons, indicating a target cell-specific fu

197 hat attenuated cAMP signaling in hippocampal excitatory neurons is a critical component underlying th

198 Axonal sprouting of excitatory neurons is frequently observed in temporal lo

199 The thermoregulatory role of hypothalamic excitatory neurons is less clear.

200 e dominant source of input to inhibitory and excitatory neurons is local in origin.

201 percentage of these intercortical inputs to excitatory neurons is somewhat higher (~20%) than to inh

202 d (3) selective deletion of Fmr1 in cortical excitatory neurons is sufficient to cause prolonged UP s

203 strate that selective ablation of ErbB4 from excitatory neurons leads to a decrease in the proportion

204 oss of the Arp2/3 subunit ArpC3 in forebrain excitatory neurons leads to an asymmetric structural pla

205 uring postnatal development in the forebrain excitatory neurons leads to higher anxiety, increased hy

206 ere that selective loss of integrin beta1 in excitatory neurons leads to reductions in the size and c

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

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

209 e results clearly demonstrate that forebrain excitatory neurons mainly use intracellular Nampt-mediat

210 Clonally related excitatory neurons maintain a coherent relationship foll

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

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

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

214 Neocortical excitatory neurons migrate radially along the glial fibe

215 nduced spine reorganization of layer (L) 2/3 excitatory neurons occurs in the distal branches of thei

216 the idea of 'canonical' connectivity between excitatory neurons of different layers within a column.

217 f zinc in glutamatergic synaptic vesicles of excitatory neurons of mammalian cerebral cortex suggests

218 in mutant mice lacking SRF in the developing excitatory neurons of neocortex and hippocampus (Srf-NEX

219 ly, its organization within the PSD of spiny excitatory neurons of neocortex and hippocampus differed

220 Complete inactivation of presenilins in excitatory neurons of the adult mouse cerebral cortex re

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

222 Cholinergic neurons are the major excitatory neurons of the enteric nervous system (ENS),

223 eceptor was overexpressed postnatally in the excitatory neurons of the forebrain areas including the

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

225 inactivation of the mutant PS1 transgene in excitatory neurons of the mouse forebrain largely rescue

226 ven at 2 mo of age, deletion of nicastrin in excitatory neurons of the postnatal forebrain using Cre

227 nificant potentiation of visual responses in excitatory neurons of the primary visual cortex in mice.

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

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

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

231 Clones of neocortical excitatory neurons originating from the same progenitor

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

233 these results suggest that MeCP2 in cortical excitatory neurons plays a critical role in the regulati

234 kout mice in which the gene was deleted from excitatory neurons postnatally.

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

236 localization to excitatory synapses between excitatory neurons, presynaptically in the granule cells

237 dies have revealed substantial insights into excitatory neuron production.

238 We conclude that some basic features of the excitatory neurons proposed to generate respiratory rhyt

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

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

241 on functional circuit mapping shows that CA2 excitatory neurons receives extensive synaptic input fro

242 Loss of MeCP2 from cortical excitatory neurons reduces the number of GABAergic synap

243 Excitatory neurons regained normal levels of response, w

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

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

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

247 In L4, a significantly larger proportion of excitatory neurons responded to light activation of thal

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

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

250 Neighboring cortical excitatory neurons show considerable heterogeneity in th

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

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

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

254 irus (CMV) promoter, and two versions of the excitatory neuron-specific Ca(2+) /calmodulin-dependent

255 we developed an adult forebrain-specific and excitatory neuron-specific conditional knock-out mouse l

256 Excitatory neuron-specific targeting was promoter-depend

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

258 cification that can guide efforts to produce excitatory neuron subtypes with increased resolution.

259 which are thought to disinhibit neighboring excitatory neurons, suggesting facilitated hippocampal a

260 neurons, which strongly inhibit neighboring excitatory neurons, suggesting gating of hippocampal out

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

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

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

264 1 receptor-mediated dendritic growth in mPFC excitatory neurons suppresses stress susceptibility.

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

266 her degree of recurrent connectivity between excitatory neurons than the microcircuit in L6.

267 toward neuronal fate and generated cortical excitatory neurons that appeared synaptically integrated

268 fear extinction silenced basal amygdala (BA) excitatory neurons that had been previously activated du

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

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

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

272 pendent plasticity are well characterized in excitatory neurons, the mechanisms that regulate this pr

273 For excitatory neurons, this late component reflected genuin

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

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

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

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

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

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

280 he real-time contribution of hippocampal CA1 excitatory neurons to remote memory and find that contex

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

282 (V1), connectivity between layer 2/3 (L2/3) excitatory neurons undergoes extensive reorganization af

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

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

285 We found that loss of RBPj in mature excitatory neurons was well tolerated, with no evidence

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

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

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

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

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

291 susceptibility to this effect than principal excitatory neurons, which are more resistant to light-in

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

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

294 types of neurons, promoting inhibition onto excitatory neurons while inducing excitation onto inhibi

295 ived convergent anatomical input from nearby excitatory neurons with a broad range of preferred orien

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

297 less possesses its equivalent in the form of excitatory neurons with input-output circuits like those

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

299 ively inactivated within postnatal forebrain excitatory neurons, with continued synthesis in all othe

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