ライフサイエンスコーパス: inhibitory neuron

1 in excitatory neurons and other subtypes of inhibitory neuron.

2 ms in excitatory and somatostatin-expressing inhibitory neurons.

3 was found for direct synaptic input onto V1 inhibitory neurons.

4 m cells produces a network of excitatory and inhibitory neurons.

5 e putative efferent filopodial contacts onto inhibitory neurons.

6 synapses, as well as excitatory synapses on inhibitory neurons.

7 idal neurons but also a sparse population of inhibitory neurons.

8 pses on cortical excitatory and fast-spiking inhibitory neurons.

9 excitatory neurons, and 4E-BP1 and 4E-BP2 in inhibitory neurons.

10 entially expressed in excitatory compared to inhibitory neurons.

11 litude and is similar between excitatory and inhibitory neurons.

12 the HRNs mostly via transient inhibition of inhibitory neurons.

13 e the coordinated activity of excitatory and inhibitory neurons.

14 etic stimulation which predominantly targets inhibitory neurons.

15 l cells that are densely interconnected with inhibitory neurons.

16 inhibition from parvalbumin-expressing (PV) inhibitory neurons.

17 uts to the RNm targeted a region that lacked inhibitory neurons.

18 d pulse-trains stimulate both excitatory and inhibitory neurons.

19 la express SR, including both excitatory and inhibitory neurons.

20 s phenomenon is most prevalent in deep-layer inhibitory neurons.

21 regulating the subtype-specific functions of inhibitory neurons.

22 res mainly enwrapping parvalbumin-expressing inhibitory neurons.

23 precise interactions between excitatory and inhibitory neurons.

24 neuron ratio and the percentage of GABAergic inhibitory neurons.

25 the phenotype of mice lacking MeCP2 only in inhibitory neurons.

26 nd decreased excitatory synaptic response in inhibitory neurons.

27 or context that targets specific classes of inhibitory neurons.

28 ons or medial ganglionic eminence (MGE)-like inhibitory neurons.

29 horn in TOW mice, specifically in GABAergic inhibitory neurons.

30 ons may be mainly driven by the NPY-positive inhibitory neurons.

31 s that Dravet Syndrome arises from defective inhibitory neurons.

32 ar dimensions, which is modulated further by inhibitory neurons.

33 neurons in layer I, and rarely target other inhibitory neurons.

34 ion, and are detected in both excitatory and inhibitory neurons.

35 pends on interactions between excitatory and inhibitory neurons.

36 and radial glias but depleted expression in inhibitory neurons.

37 ght on mechanisms underlying neurogenesis of inhibitory neurons.

38 frontal cortex (dmPFC) across excitatory and inhibitory neurons.

39 ve direct connections to both excitatory and inhibitory neurons.

40 ilarly, whereas in V1, oxytocin targets only inhibitory neurons.

41 ly associated with projecting excitatory and inhibitory neurons.

42 ers of particular sub-classes of neocortical inhibitory neurons.

43 circuit architectures assuming non-selective inhibitory neurons.

44 gh shifts in the relative latency of Pyr and inhibitory neurons.

45 mice lacking 4E-BPs in either excitatory or inhibitory neurons.

46 ing mice lacking either protein in GABAergic inhibitory neurons.

47 tube progenitors for specification of these inhibitory neurons.

48 layer (L) 2/3 responses in V1 by driving L1 inhibitory neurons.

49 ASD-derived organoids show overproduction of inhibitory neurons.

50 reduced firing of fast-spiking, presumptive inhibitory, neurons.

51 (NPY) expression identifies a major class of inhibitory neurons, accounting for approximately one-thi

52 are notably different between excitatory and inhibitory neurons, accounting for the cell type-specifi

53 date how these motifs recruit excitatory and inhibitory neurons across cortical layers and how brain

54 ripts were expressed in young excitatory and inhibitory neurons across L2-L6.

55 simply balancing excitatory neuron activity, inhibitory neurons actively shape excitatory circuits in

56 monkey neocortex, the LFP reflects primarily inhibitory neuron activity.

57 Deletion of 4E-BP2 specifically in inhibitory neurons also prevented the ketamine-induced i

58 racellular matrix typically localized around inhibitory neurons, also surround mouse CA2 pyramidal ne

59 Inhibitory neurons, although relatively few in number, e

60 We investigated dTBI effects on inhibitory neurons and astrocytes in somatosensory and m

61 dent translational control in excitatory and inhibitory neurons and astrocytic cells to these behavio

62 eople with schizophrenia exhibit deficits in inhibitory neurons and cognition.

63 d to degrade perineuronal nets on endogenous inhibitory neurons and enhance synaptic plasticity in ho

64 ether and how their expression changes in PV inhibitory neurons and excitatory neurons track with sen

65 ive feedback mechanism operates similarly to inhibitory neurons and is essential for protecting the b

66 ruit different proportions of excitatory and inhibitory neurons and show distinct patterns of circuit

67 bicular neurons is biased by inputs from CA1 inhibitory neurons and the visual cortex, but lacks inpu

68 BA)-releasing projections target hippocampal inhibitory neurons and thus act as a disinhibitory gate

69 m synaptic interactions among excitatory and inhibitory neurons and thus provide important insight in

70 divergence of precursors for excitatory and inhibitory neurons, and an "inside-out" layer formation

71 of cortical populations into excitatory and inhibitory neurons, and for the neural oscillations that

72 While dTBI effects on inhibitory neurons appear region- and type-specific, a c

73 Although biophysical details of inhibitory neurons are becoming known, it is challenging

74 y observations in the primary visual cortex: inhibitory neurons are broadly tuned in vivo and show no

75 Excitatory and inhibitory neurons are connected into microcircuits that

76 Whereas somatostatin-expressing inhibitory neurons are driven by these large stimuli, in

77 g patterns in a cortical circuit change when inhibitory neurons are excited?

78 Inhibitory neurons are heterogeneous in the mature brain

79 In addition, inhibitory neurons are highly modulated by diverse long-

80 te subpopulations of cortical excitatory and inhibitory neurons are significantly enriched for schizo

81 nciple" of inhibitory connectivity, in which inhibitory neurons are untuned for stimulus features due

82 that GluN2B subunits on excitatory, but not inhibitory, neurons are necessary for antidepressant-lik

83 d before or after nerve injury, develop into inhibitory neurons, are activated by nociceptive primary

84 ctivity is widespread in both excitatory and inhibitory neurons as well as in oligodendrocytes and ol

85 Putative inhibitory neurons, as identified by their extracellular

86 s) and is widely expressed in excitatory and inhibitory neurons, as well as in glial cells.

87 Golgi cells are the principal inhibitory neurons at the input stage of the cerebellum,

88 s in two distinct populations of neocortical inhibitory neurons: basket cells and Martinotti cells.

89 us-evoked response profiles of pyramidal and inhibitory neurons belonging to deep and superficial lay

90 ory areas have elucidated that pyramidal and inhibitory neurons belonging to distinct layers show dis

91 are characterized by a strong implication of inhibitory neurons, both in terms of their firing rate a

92 ifferentially dysregulated in excitatory and inhibitory neurons, but, rather, because excitatory neur

93 accompany homosynaptic plasticity induced in inhibitory neurons by conventional spike-timing-dependen

94 In contrast, activation of p.Arg1872Trp in inhibitory neurons by Gad2-Cre or Dlx5/6-Cre did not ind

95 ompass neurons are thought to originate from inhibitory neurons called R neurons (also known as ring

96 equency, we found that phasic stimulation of inhibitory neurons can increase inspiratory frequency vi

97 strained recurrent network of excitatory and inhibitory neurons capable of learning predefined sequen

98 We apply this strategy to directly link inhibitory neuron cell types with their morphologies.

99 ry neuron classes and three region-invariant inhibitory neuron classes.

100 Ca(2+) responses in tadpoles, we found that inhibitory neurons cluster into two groups with opposite

101 Local inhibitory neurons control the timing of neural activity

102 differences between cortical excitatory and inhibitory neurons could predict the experimental data a

103 changes were also observed in excitatory and inhibitory neurons cultured from Cd40(-/-) mice and were

104 The changes in excitatory and inhibitory neurons cultured from Cd40(-/-) mice were mim

105 e found that deletion of 4E-BP2 in GABAergic inhibitory neurons, defined by Gad2, resulted in impairm

106 Neocortical excitatory and inhibitory neurons derive from distinct progenitor domai

107 ebrain neural progenitors and excitatory and inhibitory neurons differentiated from human pluripotent

108 te that electrical synaptic plasticity among inhibitory neurons directly interacts with the switching

109 that selective deletion of Orai1 channels in inhibitory neurons disables chemoconvulsant-induced exci

110 ine firing rates (FRs) in GC with deep-layer inhibitory neurons displaying highest FRs at baseline an

111 ommon APA preferences between excitatory and inhibitory neurons distinct from astrocytes and microgli

112 Inhibitory neurons dominate the intrinsic circuits in th

113 t unbalanced specification of excitatory and inhibitory neurons during cortical development underlies

114 paradoxical prediction: that inactivation of inhibitory neurons during one tone would decrease the re

115 ation of layer 4 excitatory and fast-spiking inhibitory neurons elicited by single thalamic stimulati

116 cortical circuitry and alterations in these inhibitory neurons, especially in the medial prefrontal

117 in DS, suggest a direct link between reduced inhibitory neuron excitability and impaired SPW-R functi

118 Experimental studies suggest that these inhibitory neurons exert some form of divisive inhibitio

119 ecific pooling of excitatory inputs and that inhibitory neurons exhibit orientation-specific noise co

120 Neocortical inhibitory neurons exhibit remarkably diverse morphology

121 It is unclear when and how inhibitory neurons express distinct structural and funct

122 n the retrotrapezoid nucleus (RTN), we found inhibitory neurons expressing the Scn1a A1783V variant a

123 Our results indicate that developing inhibitory neurons fall into distinct functional groups

124 s to major archetypal classes of neocortical inhibitory neurons, fast-spiking (FS) and non-fast-spiki

125 nt role of local excitatory input in driving inhibitory neuron firing during rhythmic states and may

126 al nervous systems, including excitatory and inhibitory neurons from several brain regions, as well a

127 antation of even a small number of embryonic inhibitory neurons from the medial ganglionic eminence (

128 oreover, in vitro glucose sensing of glucose-inhibitory neurons from the ventromedial hypothalamus wa

129 randomly connected network of excitatory and inhibitory neurons generates single-cell selectivity, pa

130 GFP-expressing inhibitory neurons (GIN), representing a fraction of mai

131 ls, the most numerous population of cortical inhibitory neurons, greatly decreases SWA and cortical f

132 Remarkably, to date only a single subtype of inhibitory neuron has been documented in the VCN, a proj

133 ic access to molecularly defined subtypes of inhibitory neurons has aided their functional characteri

134 y, molecular markers for distinct classes of inhibitory neurons have remained unknown.

135 he output synapses of parvalbumin-expressing inhibitory neurons, have only recently started to be add

136 The interplay between excitatory and inhibitory neurons imparts rich functions of the brain.

137 t runaway dynamics at excitatory synapses to inhibitory neurons imposed by Hebbian-type learning rule

138 ies revealed diverse types of excitatory and inhibitory neuron in each circumventricular organ struct

139 y 20% of A32 terminations formed synapses on inhibitory neurons in A25, notably the powerful parvalbu

140 uit based approach to understand the role of inhibitory neurons in auditory processing.

141 imary visual cortex layer 2/3 excitatory and inhibitory neurons in awake mice during passive visual s

142 tory neurons and two distinct populations of inhibitory neurons in both superficial and deep layers o

143 cting the functional roles of excitatory and inhibitory neurons in cortical circuits is a fundamental

144 CANCE STATEMENT The wiring of excitatory and inhibitory neurons in cortical circuits is key to determ

145 The roles played by cortical inhibitory neurons in experience-dependent plasticity ar

146 cific GCaMP6f expression to demonstrate that inhibitory neurons in ferret visual cortex respond robus

147 ation players, supports an emerging role for inhibitory neurons in habituation, and reveals an opposi

148 ynaptic transmission with BLA excitatory and inhibitory neurons in late infancy, events that coincide

149 A1 axons preferentially innervating specific inhibitory neurons in layer 1 and superficial layers.

150 hat the known proportion and connectivity of inhibitory neurons in layer 4 of primary visual cortex i

151 The lack of direct thalamic input to inhibitory neurons in M1 may indicate temporal differenc

152 ound that deleting Mecp2 only from GABAergic inhibitory neurons in mice replicates most of this pheno

153 rker enables precise control over a group of inhibitory neurons in monkeys.

154 1) expression in parvalbumin-expressing (PV) inhibitory neurons in mouse visual cortex.

155 NMDAR activity of excitatory and parvalbumin-inhibitory neurons in mPFC, activates Akt/mTOR signaling

156 erential and cooperative roles of SOM and PV inhibitory neurons in orchestrating specific cortical os

157 A top-down modulation of inhibitory neurons in our network provides a parsimoniou

158 is impairment appeared to critically involve inhibitory neurons in the auditory cortex called parvalb

159 dy reveals new information on excitatory and inhibitory neurons in the BNST, which will facilitate ge

160 novo translation in somatostatin-expressing inhibitory neurons in the centrolateral amygdala is nece

161 nslation in protein kinase Cdelta-expressing inhibitory neurons in the centrolateral amygdala is nece

162 ed intersectional chemogenetic strategies to inhibitory neurons in the centrolateral amygdala of mice

163 Key inhibitory neurons in the circuit lie in a column of mor

164 Excitatory and inhibitory neurons in the CNS are distinguished by sever

165 ons in A25, notably the powerful parvalbumin inhibitory neurons in the deep layers, and the disinhibi

166 ddition, the participation of excitatory and inhibitory neurons in the gamma rhythm varies across loc

167 of excitatory neurons and reduced numbers of inhibitory neurons in the hippocampus, as well as impair

168 of excitatory neurons and reduced numbers of inhibitory neurons in the hippocampus, as well as repeti

169 ated SynII function at different subtypes of inhibitory neurons in the hippocampus.

170 pal neurons that constitute one-third of the inhibitory neurons in the IC.

171 aging in freely behaving mice, we found that inhibitory neurons in the lateral hypothalamus (LH(vgat)

172 Parvalbumin-expressing inhibitory neurons in the mammalian CNS are specialized

173 ar terminals innervated excitatory relay and inhibitory neurons in the MDmc that facilitate faithful

174 sthmi pars magnocellularis (Imc), a group of inhibitory neurons in the midbrain tegmentum, is a criti

175 MDA-R hypofunction onto either excitatory or inhibitory neurons in the model.

176 We identified a novel population of inhibitory neurons in the mouse brainstem, distinguished

177 We simultaneously measured excitatory and inhibitory neurons in the posterior parietal cortex of m

178 he endocannabinoid system and those in other inhibitory neurons in the prefrontal cortex in subjects

179 alamocortical connectivity and dispersion of inhibitory neurons in the rapidly growing cortex.

180 ne the activity of individual excitatory and inhibitory neurons in the same region of the layer 2/3 m

181 he functional properties of a small group of inhibitory neurons in the vertebrate midbrain that play

182 ell recordings from layer 2/3 excitatory and inhibitory neurons in the visual cortex of awake behavin

183 However, we find that PV+ inhibitory neurons in V1 play a critical role in the exp

184 naptic inputs to parvalbumin-expressing (PV) inhibitory neurons in visual cortex.

185 modulator (PAM) elevates spiking activity of inhibitory neurons in vitro and in vivo.

186 -expressing (but not parvalbumin-expressing) inhibitory neurons increased general mRNA translation, b

187 rony at baseline, while MeCP2 dysfunction in inhibitory neurons increased susceptibility to hypersync

188 viral mimetic polyI:C, produces deficits in inhibitory neuron indices (GAD1, PVALB, SST, SSTR2 mRNAs

189 Notably, genetic deletion of 4E-BP2 in inhibitory neurons induced a reduction in baseline immob

190 , intracortical networking of excitatory and inhibitory neurons induces lateral inhibition that, thro

191 e well-documented orientation selectivity of inhibitory neurons: inhomogeneities in the orientation p

192 tic changes of three major types of cortical inhibitory neurons (INs) during a neuron-pair operant co

193 hypofunction in parvalbumin-expressing (PV+) inhibitory neurons (INs) may contribute to symptoms in p

194 ds on the correct assembly of excitatory and inhibitory neurons into neural circuits.

195 2016) show that transplantation of GABAergic inhibitory neurons into the amygdala boosts the persiste

196 the spike reliability of excitatory but not inhibitory neurons is dependent on tone frequency.

197 We find that the tuning of inhibitory neurons is inconsistent with the local non-sp

198 ms of plasticity operating in excitatory and inhibitory neurons is necessary for understanding normal

199 Inactivation of RORbeta in inhibitory neurons leads to reduced presynaptic inhibiti

200 eities in the orientation preference map for inhibitory neurons leads to spatially asymmetric inhibit

201 nitor the activity of putative pyramidal and inhibitory neurons located in deep and superficial layer

202 experimental designs targeting a majority of inhibitory neurons may be able to resolve this question.

203 nder promoters targeting a large fraction of inhibitory neurons may provide a perturbation of suffici

204 hese effects are especially prominent in the inhibitory neuron Mi4, and we show that central octopami

205 expressing and somatostatin (SOM)-expressing inhibitory neurons modulate responses in mouse visual co

206 rvated each of the three distinct classes of inhibitory neurons, most targeted neurons expressing dop

207 cortical development, newborn excitatory and inhibitory neurons must migrate over long distances to r

208 fects synaptic connections in excitatory and inhibitory neurons, neural circuit plasticity, and memor

209 dominantly in excitatory neurons compared to inhibitory neurons, not only in the entorhinal cortex, a

210 We applied this method by mapping the inhibitory neurons of mouse hippocampal area CA1, for wh

211 reveal that Lm128C cells are CaMKIIalpha(+) inhibitory neurons of parvalbumin or somatostatin subtyp

212 t CC2D1A is expressed in both excitatory and inhibitory neurons of the adult hippocampus.

213 tracing to identify inputs to excitatory and inhibitory neurons of the intermediate and deep SC.

214 al neurons that carry data to the cortex and inhibitory neurons of the thalamic reticular nucleus (TR

215 New research suggests a role for inhibitory neurons of the ventral tegmental area in the

216 trained recurrent networks of excitatory and inhibitory neurons on memories composed of varying numbe

217 ion in distinct neuronal types: Rai1 loss in inhibitory neurons or subcortical glutamatergic neurons

218 mma-aminobutyric-acid-releasing) oviposition inhibitory neurons (oviINs) mediate feed-forward inhibit

219 duced numbers of specific dorsal spinal cord inhibitory neurons, particularly those expressing Pdyn a

220 NT We demonstrate that a specific subtype of inhibitory neuron, parvalbumin-expressing (PV) basket ce

221 Inhibitory neurons play critical roles in regulating and

222 ole of de novo protein synthesis in distinct inhibitory neuron populations in the centrolateral amygd

223 ific medial prefrontal cortex excitatory and inhibitory neuron populations required for sociability t

224 Vasoactive intestinal peptide-expressing inhibitory neurons received an intermediate level of exc

225 xcitatory neurons and parvalbumin-expressing inhibitory neurons received the largest EPSPs, dominated

226 In contrast, somatostatin-expressing inhibitory neurons received very little input from eithe

227 statin-expressing and parvalbumin-expressing inhibitory neurons reduced their activity, whereas vasoa

228 Inhibitory neurons regulate the adaptation of neural cir

229 al vectors labels a subset of excitatory and inhibitory neurons related to learned lever-pressing beh

230 ect, or are complemented by other classes of inhibitory neurons, remains to be investigated.SIGNIFICA

231 albumin immunopositive WMICs, presumably all inhibitory neurons, represent ~23.1% of the total WMIC p

232 By contrast, presynaptic inhibitory neurons resided within layer 2/3 and favoured

233 n excitatory and parvalbumin (PV)-expressing inhibitory neurons, respectively.

234 e the RF selectively enhances excitatory and inhibitory neuron responses to task-irrelevant stimuli a

235 of GAB1 and GRB2 together with SHP2(D61G) in inhibitory neurons resulted in ERK activation.

236 se gain was suggested to be mediated through inhibitory neurons, resulting in the disinhibition of py

237 estigate how the three main types of retinal inhibitory neuron (RIN)--horizontal cells (HCs), inner n

238 Recurrently coupled networks of inhibitory neurons robustly generate oscillations in the

239 Inhibitory neurons showed complex, subtype-specific patt

240 Dravet inhibitory neurons showed deficits in sodium currents an

241 owed that oxytocin affects S1 excitatory and inhibitory neurons similarly, whereas in V1, oxytocin ta

242 missense mutation (A1783V) conditionally in inhibitory neurons (Slc32a1(cre/+)::Scn1a(A1783V fl/+);

243 nd a quarter in layer 4) ensheathes axons of inhibitory neurons, specifically of parvalbumin-positive

244 positive GABAergic neurons are the essential inhibitory neuron subtype necessary for gamma rhythms.

245 pe and a unique human parvalbumin-expressing inhibitory neuron subtype.

246 We sorted excitatory neurons and key inhibitory neuron subtypes from mouse brains and assesse

247 Functional characterization of distinct inhibitory neuron subtypes has not been sufficient to ex

248 ly, we discuss the idea that dysfunctions of inhibitory neuron subtypes may be responsible for variou

249 We review the emerging view that inhibitory neuron subtypes perform context-dependent mod

250 n increases synapse number in excitatory and inhibitory neurons, suggesting an instructive role and a

251 ty of the non-specific pooling principle for inhibitory neurons, suggesting different rules for funct

252 ecies conservation of regulatory elements in inhibitory neurons than in excitatory neurons.

253 thalamocortical system, gap junctions couple inhibitory neurons that are similar in their biochemical

254 ons (GINs) are a heterogeneous population of inhibitory neurons that collectively contribute to the m

255 small, yet distinct, population of cortical inhibitory neurons that express CaMKIIalpha demonstrates

256 y neurons are driven by these large stimuli, inhibitory neurons that express parvalbumin and vasoacti

257 ression was required only in amacrine cells, inhibitory neurons that innervate RGCs.

258 aptic tracing to identify two populations of inhibitory neurons that lie upstream of neurons in the p

259 a recurrent network model of excitatory and inhibitory neurons that reproduced in detail the experim

260 6 CT neurons and subnetworks of fast-spiking inhibitory neurons that reset the phase of low-frequency

261 nsist of interactions between excitatory and inhibitory neurons that result in rhythmic inhibition ca

262 ate insulin secretion by silencing a pair of inhibitory neurons that synapse with insulin-producing c

263 tiple types of interconnected excitatory and inhibitory neurons that together allow us to move, think

264 Thus, NPY neurons are a novel class of inhibitory neurons that use GABA and NPY signaling to re

265 feedback inhibition that KCs receive from an inhibitory neuron, the Giant GABAergic neuron.

266 led by explicitly considering excitatory and inhibitory neurons, their connectivity and their membran

267 citatory neurons and a subset of hippocampal inhibitory neurons (those that express somatostatin, but

268 generated, we investigated how two types of inhibitory neurons, those that express parvalbumin and s

269 sual cortex.SIGNIFICANCE STATEMENT Embryonic inhibitory neurons thrive when transplanted into postnat

270 en predominantly studied in association with inhibitory neurons throughout the brain, we describe a d

271 t Neto2 was expressed in both excitatory and inhibitory neurons throughout the fear circuit including

272 the connectivity between different types of inhibitory neuron to regulate cortical plasticity are la

273 glutamatergic signaling selectively on local inhibitory neurons to drive a functional circuit for lea

274 ndings suggest differential vulnerability of inhibitory neurons to LFPI in the different brain areas

275 ing an external current to the population of inhibitory neurons transformed the model into a type II

276 ified a highly diverse set of excitatory and inhibitory neuron types that are mostly sparse, with exc

277 Cortical inhibition is mediated by diverse inhibitory neuron types that can each play distinct role

278 ctively increasing NMDA receptor activity in inhibitory neurons using an NMDAR positive allosteric mo

279 ing a cortical model built of excitatory and inhibitory neurons, we explored a wide range of stimulat

280 to jointly and equally target excitatory and inhibitory neurons, we find a large linear regime where

281 pproach to reduce MET levels specifically in inhibitory neurons, we found that their axons are no lon

282 To extend the characterization to inhibitory neurons, we have identified three distinct su

283 form of plasticity of excitatory synapses on inhibitory neurons, weight-dependent heterosynaptic plas

284 Surprisingly, excitatory and inhibitory neurons were equally selective for the animal

285 is of our recordings confirmed that putative inhibitory neurons were indeed more active during desync

286 in Cd40(-/-) mice, whereas those of striatal inhibitory neurons were much more exuberant.

287 in cortical and cerebellar excitatory versus inhibitory neurons, where we find NOVA2 is required for,

288 edict that top-down signals primarily affect inhibitory neurons, whereas excitatory neurons are more

289 eads to the activation of dendrite-targeting inhibitory neurons which in turn suppress dendritic Ca(2

290 a network of heterogeneous canonical Class 1 inhibitory neurons which includes the sub-threshold dyna

291 mice demonstrate reduced firing of GABAergic inhibitory neurons, which are essential for the formatio

292 controlled by somatostatin-expressing (SOM) inhibitory neurons, which are excited by head movements

293 ominantly composed of fast-spiking, putative inhibitory neurons, which displayed unusually strong cou

294 Inhibitory neurons, which play a critical role in decisi

295 ntaneous MFR failed in hippocampal GABAergic inhibitory neurons, which remained hyperexcitable follow

296 immunoreactivity specifically in a subset of inhibitory neurons, which suggests that increased inhibi

297 tatory, GABAergic and parvalbumin-expressing inhibitory neurons while expression in glia was limited.

298 al class of amygdalar intercalated mass (IM) inhibitory neurons, whose wiring may help modulate auton

299 The CeL consists of mostly GABAergic inhibitory neurons with different functional and molecul

300 The selectivity of excitatory and inhibitory neurons within decision circuits and, hence,