ライフサイエンスコーパス: inhibitory input

1 from an extra synapse in the circuit shaping inhibitory input.

2 occur together with decreases (increases) in inhibitory input.

3 cedes a corresponding increase (decrease) in inhibitory input.

4 was regulated by the progressive removal of inhibitory input.

5 e final expression of functional feedforward inhibitory input.

6 ence the timing of spikes on rebound from an inhibitory input.

7 tween cell types in their laminar sources of inhibitory input.

8 region lack a substrate for strong proximal inhibitory input.

9 ly shaped by both ON and OFF pathway-derived inhibitory input.

10 embrane channels and can be stopped by brief inhibitory input.

11 re is a tight balance between excitatory and inhibitory input.

12 B, consistent with the existence of parallel inhibitory inputs.

13 ation and pitch identification, receive slow inhibitory inputs.

14 ough a 5-HT1BR-mediated suppression of local inhibitory inputs.

15 elated but precisely balanced excitatory and inhibitory inputs.

16 ll (BC) inputs and the surround from lateral inhibitory inputs.

17 dynamic interactions between excitatory and inhibitory inputs.

18 ny PCs, resulting in a continuous barrage of inhibitory inputs.

19 mportant implications for the integration of inhibitory inputs.

20 ony, they may encode signals from subsets of inhibitory inputs.

21 glia output neurons receiving excitatory and inhibitory inputs.

22 eptive fields (TRFs) of their excitatory and inhibitory inputs.

23 artment was the principal target of putative inhibitory inputs.

24 hibitory inputs or relatively broad, lateral inhibitory inputs.

25 ural circuits with correlated excitatory and inhibitory inputs.

26 nsiveness of excitatory neurons to GABAergic inhibitory inputs.

27 eceiving a complex barrage of excitatory and inhibitory inputs.

28 ducing a random background of excitatory and inhibitory inputs.

29 is under the control of both excitatory and inhibitory inputs.

30 dify structural and functional properties of inhibitory inputs.

31 ing evidence regarding the function of these inhibitory inputs.

32 scaling, and to shifts in the onset phase of inhibitory inputs.

33 Held and by additional, acoustically driven inhibitory inputs.

34 selectivity and the spatial organization of inhibitory inputs.

35 itic arbor and the pattern of excitatory and inhibitory inputs.

36 ay of dendritic excitatory inputs and axonal inhibitory inputs.

37 to measure covariation of the excitatory and inhibitory inputs a cell receives.

38 interneurons and pyramidal cells to monitor inhibitory input across a broad developmental range.

39 These effects were present with >/=10 inhibitory inputs active within 2-4 ms of each other.

40 However, it is not known how these distinct inhibitory inputs affect rod bipolar cell output and sub

41 We determined how these distinct inhibitory inputs affected rod bipolar cell output by re

42 edforward and total recurrent excitatory and inhibitory inputs all have a very weak orientation selec

43 nd precision (0-4 ms jitter) of synchrony of inhibitory inputs, along with the rates (0-100 spikes s(

44 neuron can impact the processing of afferent inhibitory input and associated behavior.

45 e a long-held view concerning the pattern of inhibitory input and provide results that agree with cur

46 n M/T cells is achieved by precisely located inhibitory input and that distance from the soma is comp

47 Regulation of GABAergic inhibitory inputs and alterations in POMC neuron activit

48 ation of the relations among stimulatory and inhibitory inputs and autonomic outputs, which, in our s

49 drenaline simultaneously reduced spontaneous inhibitory inputs and enhanced evoked inhibitory current

50 ivo, where peaks in the sound envelope drive inhibitory inputs and SPON neurons fire action potential

51 ade-like eye movements in mice elicit robust inhibitory inputs and suppress spiking of SbC-RGCs over

52 ate excitation in thalamus with their strong inhibitory inputs and thus signal to cortex by pausing a

53 stics, kinetics and timing of excitatory and inhibitory inputs, and dendrite structure.

54 uned neurons exhibit covaried excitatory and inhibitory inputs, and the relative time interval betwee

55 thermore, glycinergic ipsilateral vestibular inhibitory inputs are activated during the horizontal VO

56 o of cholecystokinin to parvalbumin-positive inhibitory inputs are also significantly higher in ACC c

57 Strong interlaminar inhibitory inputs are found, particularly for excitatory

58 We found that a neuron's excitatory and inhibitory inputs are selective for the same stimulus or

59 GCs, whereas for VS-GCs, both excitatory and inhibitory inputs are suppressed.

60 ical excitatory input as well as feedforward inhibitory input at least partially from more narrowly t

61 dels in high-conductance states and modulate inhibitory inputs at a wide range of frequencies.

62 spine density, presynaptic excitability, and inhibitory inputs at injured neurons.

63 tory inputs with long temporal durations and inhibitory inputs being more narrowly tuned than excitat

64 ition or millisecond delays in the timing of inhibitory inputs, both of which lead to a reduction in

65 l that basal dendrites are a novel source of inhibitory input, but they primarily receive excitatory

66 charge revealed a normal re-establishment of inhibitory inputs, but only partial re-establishment of

67 relates with the quantity and quality of the inhibitory input by HLA class I-specific killer cell Ig-

68 young adult mice this MF-driven polysynaptic inhibitory input can facilitate or depress in response t

69 Thus, covariation of excitatory and inhibitory inputs can be a critical determinant of the r

70 cal activity can be explained by the rate of inhibitory inputs combined with their short-term plastic

71 ons are known to receive both excitatory and inhibitory inputs, combined action of which likely regul

72 the brainstem where monaural excitatory and inhibitory inputs converge.

73 cal motor circuits depends on excitatory and inhibitory inputs converging on projection neurons in la

74 modulating the relative proportions of these inhibitory inputs could change the characteristics of ro

75 suggested that the strength and duration of inhibitory input determines the synchrony and period, re

76 e time course by which anatomically isolated inhibitory inputs develop onto maturing GCs.

77 Each dendritic arm also receives local inhibitory inputs directionally selective for inward mot

78 Both fast and slow inhibitory inputs distinctly shaped the output of rod bi

79 feedforward circuit with both excitatory and inhibitory inputs disynaptically relayed.

80 LSO neurons receive excitatory and inhibitory inputs driven by ipsilateral and contralatera

81 ory inputs driven by OFF cone bipolar cells; inhibitory inputs driven by ON cone bipolar cells; and i

82 inputs driven by ON cone bipolar cells; and inhibitory inputs driven by rod bipolar cells.

83 tion tuning profiles of their excitatory and inhibitory inputs during a post-eye-opening period when

84 ses tend to form structured territories with inhibitory inputs enriched on cell bodies and proximal d

85 equency ranges of tone-driven excitatory and inhibitory inputs first expand within a few days of the

86 otract the vibrissae receive a short latency inhibitory input, followed by synaptic excitation, from

87 uire millisecond synchrony of excitatory and inhibitory inputs for the encoding of ILDs, human and an

88 n may be held in check, at least in part, by inhibitory input from 5HT1A receptor-bearing neurons, wh

89 Second, inhibitory input from a different class of SC neuron, ho

90 eive excitatory input from bipolar cells and inhibitory input from amacrine cells (ACs).

91 es to retinal ganglion cells is regulated by inhibitory input from amacrine cells to bipolar cell (BC

92 a basal ganglia circuit wherein it receives inhibitory input from both striosomal and matrix compart

93 mall stimuli to trigger visual responses and inhibitory input from cells that prefer large, suddenly

94 We examined whether modulation of inhibitory input from gamma-aminobutyric acid (GABA) in

95 h in turn receive slowly rising and decaying inhibitory input from Ivy cells.

96 Inhibitory input from laminae III-IV was found in a subp

97 VGLUT2 on SB neurons (which have dominating inhibitory input from limb muscles), revealed very few V

98 In conclusion, RTN chemoreceptors receive an inhibitory input from myelinated lung stretch receptors,

99 e olivo-cerebellar system, receive a massive inhibitory input from Purkinje cells (PCs) of the cerebe

100 of quantal analysis, showed that the strong inhibitory input from RCs results from the large number

101 ions, the properties of neurons that receive inhibitory input from S-cones ("S-") are quite unlike th

102 The pretectum receives inhibitory input from the basal ganglia, and input from

103 These results suggest that the inhibitory input from the lateral habenula plays an impo

104 ring priming, B8 received progressively less inhibitory input from the multifunctional neurons B4/5.

105 pathway contains projections that convey an inhibitory input from the periphery to mesolimbic reward

106 ating in the amygdala, and disruption of the inhibitory input from the PFC leads to anxiety, fear, an

107 Inhibitory input from the PFC to the amygdala controls f

108 We show that GPh neurons receive inhibitory input from the striosomal compartment of the

109 nstem regions, receives prominent long-range inhibitory input from the ventral nucleus of the lateral

110 d by three deep nuclei, which receive direct inhibitory inputs from cerebellar Purkinje cells, and ex

111 t received direct excitatory and/or indirect inhibitory inputs from descending corticospinal axons.

112 pedunculopontine nucleus interact with timed inhibitory inputs from model striosomes in the ventral s

113 niscus, as well as additional excitatory and inhibitory inputs from monaural nuclei.

114 These findings suggest that inhibitory inputs from SOM+ interneurons may interact wi

115 etina relies upon highly selective wiring of inhibitory inputs from starburst amacrine cells (SACs) o

116 The CeA receives excitatory and inhibitory inputs from the basolateral nucleus (BLA) and

117 The laterodorsal tegmental nucleus receives inhibitory inputs from the contralateral dorsolateral IP

118 ubthalamic nucleus (STN) by strong GABAergic inhibitory inputs from the globus pallidus externa (GPe)

119 ing Eph receptor signaling and counteracting inhibitory inputs from the gonadal sheath cells.

120 Inhibitory inputs from the lateral septum enable separat

121 Integration of convergent excitatory and inhibitory inputs from the ON and OFF visual pathways su

122 in-signaling antagonist and by counteracting inhibitory inputs from the somatic gonadal sheath cells.

123 nucleus magnocellularis, NL neurons receive inhibitory inputs from the superior olivary nucleus (SON

124 the receptive field center and nearly purely inhibitory inputs from the surround during both stationa

125 s receive excitatory as well as polysynaptic inhibitory inputs from touch- and/or pain-sensing affere

126 g involving the potentiation of an extrinsic inhibitory input (from the amygdala or elsewhere) to CeL

127 t and later refinement of spike RFs, whereas inhibitory inputs generally reduced the size of the spik

128 locking of evoked excitatory and spontaneous inhibitory inputs had only minor effects on LSO output t

129 ance are the discoveries that excitatory and inhibitory inputs have similar frequency and intensity t

130 efore airborne sound is detectable, and that inhibitory inputs having suboptimal neural delays may th

131 hemes and the organization of excitatory and inhibitory inputs, i.e., excitatory-inhibitory balance.

132 e for the transduction of purinergic enteric inhibitory input in gastric fundus muscles.

133 Pyramidal cells receive barrages of inhibitory inputs in advance of the epileptiform wave.

134 indings on the integration of excitatory and inhibitory inputs in healthy cortical circuits and discu

135 esponsible for desynchronization: (1) shared inhibitory inputs in local VB neurons leading to asynchr

136 leads to excessive excitatory compared with inhibitory inputs in neurons extracting information abou

137 resulted in an altered balance of excitatory/inhibitory inputs in somatic and dendritic compartments.

138 mals, with a significantly greater number of inhibitory inputs in the POMC neurons in DIO rats compar

139 ant, cell type-specific temporal ordering of inhibitory inputs in which PVBC-derived perisomatic inhi

140 he fourth week of development, whereas local inhibitory inputs increase during this postnatal period.

141 he fourth week of development, whereas local inhibitory inputs increase during this postnatal period.

142 intensity increments, the temporally delayed inhibitory inputs increase monotonically in strength.

143 zes the sleep state by feeding a slow-acting inhibitory input into the arousal system and plays an im

144 sticity alters the balance of excitatory and inhibitory inputs into the muscle in a use-dependent man

145 ing pre- and postsynaptic spikes potentiated inhibitory inputs irrespective of precise temporal order

146 on; and targeted dendritic (but not somatic) inhibitory input is exquisitely suited to veto an NMDA s

147 s relatively constant, whereas the tuning of inhibitory inputs is broadened, and becomes significantl

148 The balance between excitatory and inhibitory inputs is critical for the proper functioning

149 r balance between coactivated excitatory and inhibitory inputs is often observed for individual corti

150 Although the presence of these inhibitory inputs is well established, their relative lo

151 nputs cluster at T4's dendrite shafts, while inhibitory inputs localize to the bases.

152 sisted circuit mapping (CRACM) of the entire inhibitory inputs map.

153 nges occurred in parallel for excitatory and inhibitory input maps.

154 The loss of inhibitory input may contribute to the later development

155 These results suggest that shared inhibitory input may specify horizontally clustered sist

156 neurons, and slowing and strengthening this inhibitory input may transform spindles into spike-wave

157 uration and insufficient receptive field for inhibitory input may underlie the epilepsy in lissenceph

158 Thus, in the IC, balanced excitatory and inhibitory inputs may be a general feature of synaptic c

159 emonstrate that, in the Aplysia feeding CPG, inhibitory inputs may be critical for flexible control o

160 y inputs from both A delta- and C-fibres and inhibitory inputs mediated by both fibre types.

161 ate-and-fire neuron receiving excitatory and inhibitory inputs, model fitting can be guided by prior

162 which might be caused by the surround of the inhibitory input nullifying the surround of the excitato

163 Remarkably, the spatial extent of inhibitory inputs of excitatory neurons for a given laye

164 cholinergic neurons exhibit robust proximal inhibitory inputs, of which a significant number origina

165 Second, theta-modulated inhibitory input on its own generates membrane potential

166 shown that noradrenaline (NA) increases GABA inhibitory input on to mitral cells (MCs) by exciting GC

167 arallel fiber synaptic inputs, we also found inhibitory inputs on dendritic regions with mixed ascend

168 Islet cells received primary-afferent-evoked inhibitory inputs only from A delta-fibres, while those

169 und to increase action potential-independent inhibitory input onto DMV neurons.

170 Whether inhibitory input onto inhibitory interneurons demonstrat

171 fugal projection neurons (iCFuPNs) increases inhibitory input onto the converted neurons to levels si

172 We reveal that the LH sends excitatory and inhibitory input onto VTA dopamine (DA) and GABA neurons

173 restored the disrupted balance of excitatory/inhibitory inputs onto 5-HT neurons, and reversed 5-HT h

174 The inhibitory inputs onto DSGCs are directionally tuned to

175 ctively eliminated the directional tuning of inhibitory inputs onto DSGCs by disrupting GABA release

176 retina results from patterned excitatory and inhibitory inputs onto DSGCs during motion stimuli.

177 the retina requires the asymmetric wiring of inhibitory inputs onto four subtypes of On-Off direction

178 large numbers of uncorrelated excitatory and inhibitory inputs onto individual neurons.

179 ltured neurons coincides with elimination of inhibitory inputs onto injured neurons, including those

180 To reveal the excitatory and inhibitory inputs onto interval-tuned neurons, we then e

181 ctions, and this is accompanied by a loss of inhibitory inputs onto neighboring pyramidal cells.

182 tamatergic excitatory synapses by increasing inhibitory inputs onto neurons of the dorsal intercalate

183 relies on the coregulation of excitatory and inhibitory inputs onto principal neurons.

184 oid receptor activation led to a decrease in inhibitory inputs onto the vPAG/DR dopamine neurons.

185 igured to have either cotuned excitatory and inhibitory inputs or relatively broad, lateral inhibitor

186 ectome govern this computation: an excess of inhibitory inputs over excitatory, with both being rando

187 This switch in inhibitory input polarity is controlled by the developme

188 rily within, but not between, excitatory and inhibitory input pools.

189 s scaling of the responses of excitatory and inhibitory input populations in mediating attention.

190 Conversely, the glycinergic, inhibitory input properties remained unaffected.

191 he net flow of excitability is controlled by inhibitory input provided by the many populations of loc

192 decreased the strength and spatial range of inhibitory input provided to pyramidal neurons by PV int

193 Regulation by both excitatory and inhibitory inputs provides an unexpected mechanism that

194 ased on CRH neurons; however, the excitatory/inhibitory input ratio remained constant.

195 al activation of interneurons to profile the inhibitory input received by three classes of principal

196 The delay of inhibitory input relative to excitatory input originates

197 ional connectivity, particularly in terms of inhibitory inputs, remains elusive.

198 tion via cochlear implants the proportion of inhibitory inputs resembled that of hearing animals.

199 ediated likely by feedforward excitatory and inhibitory inputs respectively greatly sharpen the spike

200 ead might be related to an excitatory and/or inhibitory input segregation.

201 promotes a remodeling of both excitatory and inhibitory inputs selectively in the deep dendritic doma

202 Thus inhibitory input shapes the temporal stimulus selectivit

203 to excitatory cells and that excitatory and inhibitory input should be correlated, in agreement with

204 In this case, inhibitory inputs substantially abbreviated a cell's spi

205 differential organization of excitatory and inhibitory inputs suggests a principle for the wiring of

206 n prevent activation of a glomerulus through inhibitory inputs targeted onto excitatory external tuft

207 tion, DTNs received a contralaterally evoked inhibitory input that preceded the excitatory input to t

208 ition, DTNs received an ipsilaterally evoked inhibitory input that was weaker, longer in latency, and

209 nes have distinct patterns of excitatory and inhibitory inputs that are related to their morphology.

210 ut how this transcription factor affects the inhibitory inputs that form on distinct domains of a neu

211 s regulated by the balance of excitatory and inhibitory inputs that impinge on it.

212 ry inputs that trigger action potentials and inhibitory inputs that promote a stable resting potentia

213 l characteristics are a likely source of the inhibitory inputs that selectivity regulate non-noxious

214 Rs have an altered balance in the excitatory/inhibitory input they receive.

215 First, theta-modulated inhibitory input to a CA1 pyramidal cell is not necessar

216 Furthermore, local inhibitory input to both classes of MSNs was negatively

217 ine decreases both GABAergic and glycinergic inhibitory input to cardiac vagal neurons, with no signi

218 leads to overnight synaptic plasticity in an inhibitory input to CeL(-) cells.

219 ous cannabinoids can thereby rapidly enhance inhibitory input to DMV neurons via VR1-mediated presyna

220 oles in auditory processing, the majority of inhibitory input to each nucleus arises from the same so

221 n result in a transient reduction of PG cell inhibitory input to ET cells.

222 ory inputs to fusiform cells and an indirect inhibitory input to fusiform cells from the granule cell

223 The inhibitory input to GnRH neurons is mostly transsynaptic

224 Despite reduced inhibitory input to granule cells, action potential and

225 f the magnitude and timing of excitatory and inhibitory input to L4 neurons.

226 t is attributable to an increase in the GABA inhibitory input to M/TCs.

227 This is followed by a reduction in inhibitory input to motor neurons.

228 These findings suggest that the direct inhibitory input to OFF parasol cells originates from ot

229 ent of interneurons dynamically enhanced the inhibitory input to olfactory bulb projection neurons an

230 These findings suggest that the inhibitory input to parasol cells conveys information ab

231 v1.2 inhibitors, secretin potently increases inhibitory input to PCs.

232 both AgRP/NPY and POMC neurons but a strong inhibitory input to POMC neurons balances the excitation

233 protraction terminator as it provides strong inhibitory input to protraction interneurons and motoneu

234 ecific mouse lines whereby the excitatory or inhibitory input to Purkinje cells (PCs) and/or PC posts

235 mplex thus enables an adaptive regulation of inhibitory input to Purkinje cells during fluctuations i

236 Dys(-/-) mice also exhibited a decreased inhibitory input to pyramidal neurons in layer V of PFC.

237 Our estimates of the excitatory and inhibitory input to single neurons indicate binocular su

238 just before the ablation and a reduction in inhibitory input to the granule cells of the dentate gyr

239 A major inhibitory input to the LC is GABAergic, arising from th

240 Here, we identify an inhibitory input to the LHb arising from a unique popula

241 ternalization results in a reduced intrinsic inhibitory input to the neurons in the baroreflex pathwa

242 l pathway in brain slices, with cortical and inhibitory input to the postsynaptic cell blocked.

243 llaterals that provided only sparse and weak inhibitory input to their neighboring MSNs.

244 pable of providing both phasic and sustained inhibitory input to their postsynaptic partners without

245 The Purkinje cells of the cerebellum provide inhibitory input to vestibular nucleus neurons, with gam

246 ization adjusts the timing of excitatory and inhibitory inputs to a neuron.

247 s to MSO neurons including the tendencies of inhibitory inputs to attenuate in response to high-frequ

248 sychogenic challenges affects excitatory and inhibitory inputs to corticotropin-releasing hormone (CR

249 hat are based, in part, on different sets of inhibitory inputs to each zone.

250 Inhibitory inputs to excitatory neurons derived largely

251 ngeal motor neurons and mixed excitatory and inhibitory inputs to glottal motor neurons.

252 The neurotransmitters responsible for inhibitory inputs to individual SG neurones are also cha

253 te cross-correlations between excitatory and inhibitory inputs to investigate correlations emerging f

254 esting that these cells are cyclically gated inhibitory inputs to Lkr neurons.

255 When recurrent excitatory and inhibitory inputs to memory neurons were balanced in str

256 N structure and on functional excitatory and inhibitory inputs to MNs.

257 hus, the use of multiple neurons to generate inhibitory inputs to motoneurons that receive concurrent

258 eover, the relative weight of excitatory and inhibitory inputs to NAc MSNs was significantly decrease

259 described how the coupling of excitatory and inhibitory inputs to neurons in the auditory cortex chan

260 nisms that establish mature distributions of inhibitory inputs to NL are not known.

261 naptic terminals to study the development of inhibitory inputs to NL between embryonic day 9 (E9) and

262 stimuli, however, could cause excitatory and inhibitory inputs to On parasol cells to increase togeth

263 igated whether CB1-expressing excitatory vs. inhibitory inputs to orexin-A-containing neurons in the

264 The data indicate that the excitatory and inhibitory inputs to orientation-selective ganglion cell

265 Thus, the transformation of inhibitory inputs to postsynaptic excitation in ET cells

266 I(h) can also transform inhibitory inputs to postsynaptic excitation.

267 Cortical gamma oscillations require strong inhibitory inputs to pyramidal neurons from the parvalbu

268 of synaptic function in both excitatory and inhibitory inputs to pyramidal neurons in CA3 of the Ts6

269 In conclusion, altered excitatory and inhibitory inputs to pyramidal neurons in the cortex in

270 zed, balanced theta-modulated excitatory and inhibitory inputs to somatically aligned, morphologicall

271 herefore, we studied long-term plasticity of inhibitory inputs to TC cells in the posterior medial nu

272 s shaped by an interaction of excitatory and inhibitory inputs to the M-cell and corresponds to the t

273 While our data suggest that the majority of inhibitory inputs to the Purkinje cell tree are associat

274 We modeled the feedforward excitatory and inhibitory inputs to these cells based on in vivo record

275 the spectrotemporal tuning of excitatory and inhibitory inputs to these cells.

276 neurons, which can drive both excitatory and inhibitory inputs to trigeminal motoneurons when optogen

277 te voltage-clamp recording of excitatory and inhibitory inputs using different holding potentials rev

278 n and replayed the slow and fast patterns of inhibitory inputs using intracortical electrical stimula

279 Laminar sources of inhibitory input varied between cell types and could not

280 bipolar cells by gap junctions, and provide inhibitory input via glycine receptor (GlyR) subunit alp

281 revealed that the frequency tuning curve of inhibitory input was broader than that of excitatory inp

282 Inhibitory input was measured by clamping voltage near 0

283 A net predominance of excitatory over inhibitory inputs was found in OT-PVN-RVLM proximal dend

284 following primary afferent stimulation when inhibitory inputs were blocked to mimic neuropathic pain

285 dal AVCN, whereas non-primary excitatory and inhibitory inputs were more common in rostral AVCN.

286 ygen to activate the neurons; GLB-5 provides inhibitory input when oxygen decreases below 21%.

287 ndirectly inhibited RTN firing by increasing inhibitory input, whereas P2Y receptor stimulation cause

288 ns arose from a wider rostrocaudal area than inhibitory inputs, whereas both excitatory and inhibitor

289 al cells was controlled principally by their inhibitory inputs, which dominated over excitation.

290 ning profiles of nonselective excitatory and inhibitory inputs, which we propose can be achieved thro

291 nctions to simultaneously reduce spontaneous inhibitory inputs while increasing evoked inhibition.

292 ns between arbor stratification and aberrant inhibitory input, while excitatory input did not vary wi

293 ntral and vertical cells exhibited GABAergic inhibitory inputs, while almost all radial cells also po

294 ( approximately 26%), and reorganization of inhibitory inputs with a relative decrease in inputs to

295 al preoptic nucleus (VLPO) shares reciprocal inhibitory inputs with wake-active neuronal nuclei, incl

296 xcitatory receptive field, but cannot reveal inhibitory inputs within the excitatory field, or show t

297 elative to its soma: (1) both excitatory and inhibitory input zones were more dorsal for neurons with

298 pecially the II/III border region, while the inhibitory input zones were mostly confined within I-II.

299 hibitory inputs, whereas both excitatory and inhibitory input zones were restricted mediolaterally.

300 orsal dendrites, and (2) excitatory, but not inhibitory, input zones were more dorsal (relative to th