ライフサイエンスコーパス: neuronal population

1 neous neural subtypes rather than a specific neuronal population.

2 in an input-dependent manner within a single neuronal population.

3 ress-induced changes in excitability in this neuronal population.

4 average spiking rate is calculated over the neuronal population.

5 al manipulations of the latter input-defined neuronal population.

6 rtical inputs and synchronization of the STN neuronal population.

7 predominant response suppression across the neuronal population.

8 henomena of spikes triggered by an intricate neuronal population.

9 ufficient in pacing the activity of the GHRH neuronal population.

10 anscription to translation within a specific neuronal population.

11 ds associated with this infrequently studied neuronal population.

12 states are encoded by distinct hypothalamic neuronal populations.

13 rect inputs to activated versus nonactivated neuronal populations.

14 eciprocally regulates the abundance of these neuronal populations.

15 cterized by the progressive loss of specific neuronal populations.

16 abnormal bundling of neurofilaments in many neuronal populations.

17 .9 and Trpm8 are expressed in nonoverlapping neuronal populations.

18 ts are encoded through the activity of large neuronal populations.

19 tify new markers for specific progenitor and neuronal populations.

20 anscripts across nine functionally different neuronal populations.

21 er activity and NFIA expression in glial and neuronal populations.

22 e and female intruders activated overlapping neuronal populations.

23 ns can limit efficient information coding in neuronal populations.

24 neurodegeneration across various vulnerable neuronal populations.

25 behavior and is composed of many overlapping neuronal populations.

26 ric acidergic (GABAergic) plasticity in many neuronal populations.

27 on, improving the stimulus representation by neuronal populations.

28 n information from both individual cells and neuronal populations.

29 ion, and an unbalanced ratio between certain neuronal populations.

30 y spatiotemporal patterns of activity across neuronal populations.

31 lied to map input and output connectivity of neuronal populations.

32 siological response properties of diverse V1 neuronal populations.

33 could be involved in the maturation of other neuronal populations.

34 y and for high-efficiency sparse labeling of neuronal populations.

35 aling 7 (RGS7) both globally and in specific neuronal populations.

36 ion in WT vs. environments lacking different neuronal populations.

37 t tradeoffs between sensitivity and noise in neuronal populations.

38 human tissues, toxicity targets only defined neuronal populations.

39 e gain and suppressing shared variability in neuronal populations.

40 ation and in vivo genome editing in targeted neuronal populations.

41 e-varying signals through these two opponent neuronal populations.

42 Brain function involves the activity of neuronal populations.

43 hods for targeting and manipulating specific neuronal populations.

44 ements in spiking were generated in the same neuronal populations.

45 urally leads to complex dynamics in rhythmic neuronal populations.

46 ses in V1 spiking were generated in the same neuronal populations.

47 ral cortex necessary for generating expanded neuronal populations.

48 identified as one of the major itch-sensing neuronal populations.

49 ngoing and evoked activity components across neuronal populations.

50 sensors is widely used to record activity in neuronal populations.

51 ng its relevance across CNS compartments and neuronal populations.

52 ions for interpreting observed properties of neuronal populations.

53 broad GABAergic inhibition of wake-promoting neuronal populations.

54 o chemogenetically activate or inhibit these neuronal populations.

55 eously perform two-photon calcium imaging of neuronal populations across multiple areas and layers of

56 ions involve the coordinated action of large neuronal populations across multiple brain regions in bo

57 We recorded from neuronal populations across posterior cortex as mice per

58 lly and in complexes: whether particular SCN neuronal populations act as pacemakers, and if so, by wh

59 t of these data was then used to compare the neuronal populations activated by 2-deoxyglucose evoked

60 We examined functional brain circuits and neuronal populations activated by social play in adolesc

61 -dimensional linear dynamics are observed in neuronal population activity in primary motor cortex (M1

62 ypothesize that object size is inferred from neuronal population activity in V1 and predict that idio

63 In this striatal model, neuronal population activity is assumed to encode locomo

64 E STATEMENT Field potentials (FPs) can index neuronal population activity that is not evident in acti

65 tive, mechanistic interpretation of recorded neuronal population activity.

66 ures intrinsic to individual neurons or from neuronal population activity.

67 tion techniques consistently reveal that the neuronal population allows reliable decoding of both sti

68 l testing, we identified two sleep-promoting neuronal populations along a thalamo-amygdala pathway, b

69 reactivity of the infracortical white matter neuronal population, also termed white matter interstiti

70 lity within a canonical and narrowly defined neuronal population and suggests that continuous, within

71 ach to decrease or suppress Nrp1 in specific neuronal populations and at different time points during

72 coordinated, large-scale fluctuations across neuronal populations and create noise correlations that

73 Our work shows the power of using neuronal populations and decision history when relating

74 s extensive alternative splicing in specific neuronal populations and developmental time points, refl

75 microenvironment leading to massive loss of neuronal populations and increased neuroinflammation.

76 els makes distinct predictions regarding the neuronal populations and interactions underlying these e

77 ivers of a certain immune response, the same neuronal populations and neuro-mediators can exert oppos

78 phat-S immunoreactivity was observed in some neuronal populations and numerous fibers distributed thr

79 distribution of intention signaling through neuronal populations and shows how many movement paramet

80 t Nkx6.2 regulates the development of spinal neuronal populations and the formation of the spinal loc

81 nding whether these processes affect similar neuronal populations and whether they have similar effec

82 ressing parvalbumin (PV neurons), a main TRN neuronal population, and associated Wisteria floribunda

83 We link such behavior to sleep-promoting neuronal population, and demonstrate that VLPO lesion (m

84 al markers of action potentials in the local neuronal population, and showed spatially systematic pha

85 tiotemporal coordination of movement-related neuronal populations, and illustrate how those mechanism

86 The projection targets of a neuronal population are a key feature of its anatomical

87 rological disorders, where dendrites of each neuronal population are densely intermingled with cell b

88 w that task-specific representations in mPFC neuronal populations are accompanied by SWM-specific osc

89 However, only specific neuronal populations are affected.

90 imulation and the excitability properties of neuronal populations are constrained by experimental res

91 Both neuronal populations are defined by the expression of do

92 eaves unanswered the question of how enteric neuronal populations are maintained in adult guts, given

93 lidation, but CB1 receptors present in other neuronal populations are not involved.

94 While most neuronal populations are scaled-down by death, some subp

95 The intrinsic dynamics of neuronal populations are shaped by both microscale attri

96 d the optimal strategies for encoding ITD in neuronal populations are the subject of ongoing debate.

97 and suggestive of in utero depletion of this neuronal population as a consequence of Zika virus infec

98 a rich diversity of firing rates across the neuronal population as reflected in a lognormal distribu

99 urrent networks of excitatory and inhibitory neuronal populations assemble to produce robust patterns

100 shown to induce drastic synaptic changes in neuronal populations associated with reward, such as the

101 The reprogramming efficiency of different neuronal populations at any stage of development can be

102 we tested the discrimination performance of neuronal populations at five levels of the auditory syst

103 viding two-photon imaging access to cortical neuronal populations at single-cell or single dendritic

104 as enriched in excitatory and inhibitory BLA neuronal populations, but at lower levels in the extinct

105 for observing the spiking activity of large neuronal populations, but extracting the activity of eac

106 xcitatory-inhibitory ratios is adjustment of neuronal populations by cell death.

107 We used fast two-photon calcium imaging of neuronal populations (calcium indicator GCaMP6s, 10 Hz,

108 Although these neuronal populations can also promote aggressive behavio

109 hat high-quality two-photon imaging of large neuronal populations can be achieved and maintained in a

110 Spontaneous activations within neuronal populations can emerge similarly to "task-evoke

111 nd that CEA termination over the PBP and RRF neuronal populations can influence striatal circuits inv

112 arifying gene expression in narrowly defined neuronal populations can provide insight into cellular i

113 t homeobox transcription factors distinguish neuronal populations combinatorially, and exhibit extrem

114 Distinct neuronal populations containing PPCART, PPPACAP, and PPN

115 To select a movement, specific neuronal populations controlling particular features of

116 of habenular and thalamic Gpr151-expressing neuronal populations could be visualized.

117 stream processing requires identification of neuronal populations defined by their output targets.

118 Both neuronal populations display opposed seasonal variations

119 ce overall excitatory/inhibitory balance and neuronal population dynamics, which are important to moo

120 erefore, it remains unknown whether separate neuronal populations encode each of these properties or

121 A neuronal population encodes information most efficiently

122 plexed in situ gene expression revealed that neuronal populations encoding behavioral features encomp

123 We identify two neuronal populations engaged in a recurrent excitation l

124 y, while optogenetic recruitment of the same neuronal population enhances cardiac contractility and p

125 in neurons, while PI5P4Kbeta is expressed in neuronal populations, especially hippocampus and cortex.

126 The activities of neuronal populations exhibit temporal sequences that are

127 at, perhaps especially, within the striatum, neuronal populations exist in continua, with regards to

128 The sensory responses of cortical neuronal populations following training have been extens

129 urbances in metabolism, relative to glia and neuronal populations, following cerebral ischemia in a m

130 e activation with two-photon optogenetics of neuronal populations from ensembles in the visual cortex

131 ome bisulfite sequencing in neuronal and non-neuronal populations from four brain regions (anterior c

132 epresent a minority of the total neocortical neuronal population, GABAergic interneurons are highly h

133 projections promote synchrony among distant neuronal populations, giving rise to richly patterned fu

134 Although several sleep-regulating neuronal populations have been identified, little is kno

135 Here, we considered a well-defined canonical neuronal population-hippocampal CA1 pyramidal cells (CA1

136 BS in disrupting synchronization in cortical neuronal populations; however, diminishing antidromic ac

137 Among the neuronal populations implicated in sleep-wake control, t

138 oxytocin signaling in a molecularly defined neuronal population in order to modulate the behavioral

139 Here, we show that in rats, the same neuronal population in the amygdala central nucleus upda

140 Here, we have uncovered an excitatory neuronal population in the basal forebrain that is activ

141 hich has made understanding the role of this neuronal population in the CNS a challenge.

142 h the inhibitory influence on the excitatory neuronal population in the dACC of subjects with first-e

143 fish is related to oscillatory dynamics of a neuronal population in the hindbrain.

144 Collectively, these studies implicate this neuronal population in the integration and coordination

145 aken together, our results reveal a specific neuronal population in the mouse hypothalamus that serve

146 GABAergic medium spiny neurons are the main neuronal population in the striatum.

147 Despite the GABAergic neuronal population in the subplate being sparse, long-d

148 Previous studies have suggested that a CA1 neuronal population in the ventral hippocampus (VH) proj

149 ecent studies revealed a novel glutamatergic neuronal population in the VP [VP neurons expressing the

150 lation analysis reveals that activity in the neuronal population in this area appears to be related t

151 to achieve multicolor modulation of the same neuronal population in vivo.

152 on of fly lines with temporarily inactivated neuronal populations in a novel high-throughput assay de

153 The brain recruits neuronal populations in a temporally coordinated manner

154 trains, we performed comparative analysis of neuronal populations in A1 of adult (~ 10 weeks) C57BL/6

155 e in mechanisms of vulnerability of selected neuronal populations in AD and that reducing alpha-syn m

156 e in mechanisms of vulnerability of selected neuronal populations in AD and that reducing alpha-syn m

157 Herein, we characterized specific neuronal populations in an SIV-infected macaque model wi

158 , we show direct plasticity in recordings of neuronal populations in awake, behaving nonhuman primate

159 ecordings from synapses, dendrites and large neuronal populations in behaving mice and zebrafish demo

160 on (e.g., integration and segregation) among neuronal populations in cognitive functions.

161 nstruction of whole cell morphology of large neuronal populations in densely labeled brains.

162 as been devoted to measuring the activity of neuronal populations in different parts of the brain und

163 king noise decreased sound discrimination of neuronal populations in each auditory structure, but col

164 Therefore, targeting these neuronal populations in FXS and autism may be part of a

165 on are correlated with the spatial tuning of neuronal populations in healthy volunteers.

166 ed in studying the physiological function of neuronal populations in isolated retinal tissue.

167 butions of defined periaqueductal gray (PAG) neuronal populations in itch modulation in mice.

168 ect the critical role of genetically-defined neuronal populations in LS progression.

169 irect sparse labeling of genetically-defined neuronal populations in mice.

170 We then record from neuronal populations in monkey primary visual cortex (V1

171 was used to generate driver lines that label neuronal populations in patterns that, to a large but va

172 ctivate the same or distinct frequency-tuned neuronal populations in primary auditory cortex (A1), re

173 Neuronal populations in sensory cortex produce variable

174 activity of stress-responsive structures and neuronal populations in the adult brain, suggesting them

175 3 subjects (2 males, 1 female), we localized neuronal populations in the dorsal anterior insular cort

176 ventions that dissociate the activity of two neuronal populations in the GPe, elevating the activity

177 During non-rapid eye movement (NREM) sleep, neuronal populations in the mammalian forebrain alternat

178 gical recordings in mice, we have identified neuronal populations in the medial hypothalamus and brai

179 erate functional RBP-RNA maps from different neuronal populations in the mouse brain.

180 both survival and differentiation of several neuronal populations in the nervous system during develo

181 r of cellular-resolution experience-specific neuronal populations in the orbitofrontal cortex, a majo

182 We show that whereas single neurons and neuronal populations in the superficial layers conveyed

183 s issue by studying the function of multiple neuronal populations in the zebrafish hypothalamus durin

184 physiology and its relative role in distinct neuronal populations in these striatal-related diseases

185 inhibitory interactions between competitive neuronal populations in visual cortex.

186 n to affect many aspects of the responses of neuronal populations in visual cortex.

187 The fate mapped E11.5-12.5 STN neuronal population included 20% of neurons with profuse

188 der, an area that gives rise to a variety of neuronal populations including the dorsal raphe (DR) nuc

189 tures of sleep/wake states and the principal neuronal populations involved in their regulation.

190 and 2) What do we know about the neuronal populations involved?

191 The extent to which each neuronal population is affected varies between individua

192 mic regulation of plasticity thresholds in a neuronal population is critical for the formation of lon

193 vant to the amount of information encoded by neuronal populations is a crucial step toward understand

194 dulates the CRR to hypoglycemia via specific neuronal populations is currently unknown.

195 at the encoding of audiovisual stimuli in V1 neuronal populations is highly dependent on the features

196 raction algorithms in which information from neuronal populations is used to decode movement intent.

197 In Drosophila, neuronal populations located in multiple brain regions m

198 Connections between neuronal populations may be genetically hardwired or ran

199 ver, it is unknown whether activity of these neuronal populations mediates the regulation of these pr

200 gnaling pathways regulate the development of neuronal populations mediating these behaviors in divers

201 is known about how activity fluctuations of neuronal populations modulate the sensory tuning of cell

202 ctivity-dependent gene programs in different neuronal populations, Npas4 affects synaptic connections

203 The neuronal population of the subthalamic nucleus (STN) has

204 ted spontaneous activations, within the same neuronal populations of insular cortex, that emerged int

205 comprised of two uni-directionally connected neuronal populations of spiking neurons, each representi

206 es of DSB formation and repair in vulnerable neuronal populations of the brain.

207 lated between the many functionally distinct neuronal populations of the brain.

208 and distribution are restricted to specific neuronal populations of the central nervous system and t

209 rning-induced changes in distinct layers and neuronal populations of the prelimbic prefrontal cortex

210 identify the developmental origins of major neuronal populations of the ventromedial hypothalamus.

211 generated, including more than 150 distinct neuronal populations; of these, 88 are followed through

212 region of the brain, a projection pathway, a neuronal population or an individual neuron), is permane

213 Knockdown of D1 receptor subtype in whole neuronal populations or excitatory neurons in mPFC facil

214 High-frequency neuronal population oscillations (HFO, 130-180 Hz) are r

215 ration microscopy, enables the monitoring of neuronal populations over large depth ranges and can be

216 the Drosophila brain and show that different neuronal populations possess distinct RNA editing signat

217 Neuronal populations predicted, with high accuracy, whic

218 Surprisingly, two neuronal populations preferentially targeted touch domes

219 uronal data, represent a fundamental type of neuronal population processing in a variety of organisms

220 ehaviours mediated by distinct noradrenergic neuronal populations provides evidence for a modular fun

221 ons are mature and equivalent to the broader neuronal population, raising questions of how they might

222 by considering small simultaneously-recorded neuronal populations rather than individual units.

223 reflecting stronger synchronization between neuronal populations receiving mutually predictable inpu

224 orld may allow a better understanding of the neuronal populations regulating these processes, as well

225 Further, their functional roles in different neuronal populations remain to be defined.

226 Furthermore, this neuronal population remains sensitive to intrathecal NPY

227 the significance of developmentally distinct neuronal populations remains unclear.

228 To advance the measurement of distributed neuronal population representations of targeted motor ac

229 We identified spatially distributed neuronal population representations spanning the dorsal

230 zed shift of attentional modulation from the neuronal population representing the task-relevant locat

231 tent with mature neuronal function, the N398 neuronal population responded more actively with an incr

232 ip between them, we developed a model of (a) neuronal population responses and (b) transformations fr

233 The impact of these effects on neuronal population responses and network activity in se

234 Neuronal population responses can vary across trials as

235 rrays in primary motor cortex (M1) to record neuronal population responses in parkinsonian nonhuman p

236 We mapped the neuronal population responses in the hindlimb motor cort

237 is a critical lesson for those interested in neuronal population responses more generally: Descriptio

238 Analysis of neuronal population responses revealed robust choice-rel

239 Robust task-specific neuronal population responses revealed that the rat moto

240 otion, the motor cortex exhibited consistent neuronal population responses that were synchronized wit

241 Neuronal population responses to sensory stimuli are rem

242 Here we relate fluctuations in small neuronal population responses, recorded simultaneously i

243 each measure with respect to the underlying neuronal population responses.

244 nt correlated with substantial adjustment in neuronal population responses.

245 lly predictive cues (ambiguous cues) and the neuronal populations responsible for linking the predict

246 of sensory input, where gains and losses in neuronal populations results in novel output that is ult

247 Its neuronal population revealed a specialization for shape

248 on-dependent manner at the level of a single neuronal population.SIGNIFICANCE STATEMENT Because loss

249 toire of conditions that can be processed by neuronal populations.SIGNIFICANCE STATEMENT Noise, or ra

250 alization of multiple genetically identified neuronal populations so that synaptic interactions betwe

251 of the alpha oscillations modulating the two neuronal populations strongly affected the interregional

252 n VWM(6-9), which causes an overlap with the neuronal populations supporting perceptual processing(10

253 to the thalamus originating from a distinct neuronal population, tectal ganglion cells (TGCs), of th

254 etically distinct basolateral amygdala (BLA) neuronal population that drives reward behaviors and ant

255 forces to create 3D intersections of primary neuronal populations that are plated in a 2D plane.

256 ulations, whereas alpha-band rhythms inhibit neuronal populations that could interfere with movement

257 We found different neuronal populations that discharged according to a phas

258 increasing the signal-to-noise ratio of the neuronal populations that encode the attended stimulus.

259 The brainstem contains diverse neuronal populations that regulate a wide range of proce

260 Multiple hypothalamic neuronal populations that regulate energy balance have b

261 hub that contains diverse activity-specific neuronal populations that respond differentially to vari

262 ve substrate for the regeneration of certain neuronal populations that retain a growth potential over

263 Activity synchrony arises from two neuronal populations that separately encode one's own be

264 We discovered two large neuronal populations that wrap neuropils during developm

265 ns in auditory cortex and in the activity of neuronal populations, that is, in local field potentials

266 on decoding the pattern of activity across a neuronal population, the encoding properties of individu

267 Within the hypothalamic neuronal populations, the arcuate melanocortin system pl

268 ss in understanding the function of distinct neuronal populations, the parameters of connectivity tha

269 Together with a neuronal population, these cells promote de novo assembl

270 d differentially expressed genes in selected neuronal populations through fluorescence in situ hybrid

271 nent CB subtype-1 receptor (CB1R) expressing neuronal population throughout development.

272 ceptor subtype that is expressed in distinct neuronal populations throughout the CNS.

273 cts the timely generation of the appropriate neuronal population thus leading to an overall decrease

274 Understanding the contributions of each PV neuronal population to human DLPFC function requires a d

275 brief periods of excitability in oscillating neuronal populations to optimize information transmissio

276 print of the old memory to allow overlapping neuronal populations to store multiple memories.

277 se in the ability of both single neurons and neuronal populations to support discrimination of visual

278 gRP) in mice, we have demonstrated that this neuronal population tonically suppresses splanchnic SNA

279 ilters, but the retinal output also contains neuronal populations transmitting sustained signals.

280 een heterogeneity in D2R-expressing striatal neuronal populations, underlying specific D2R's function

281 TRP) channels to activate or ablate specific neuronal populations using the chemical and thermal agon

282 n each auditory structure, discrimination by neuronal populations was slightly decreased when tone-vo

283 a mean field model of an adapting, recurrent neuronal population, we find that the neocortical altern

284 line with ablated Prlr in the Nav1.8 sensory neuronal population, we show that Prlr in sensory neuron

285 e differential vulnerability of networks and neuronal populations, we focus here on what is known abo

286 Neuronal populations were classified based on fast neuro

287 In a model where both neuronal populations were connected bi-directionally, th

288 DRG neuronal populations were identified by neurofilament H-

289 bserved that rotational patterns occurred in neuronal populations when (1) there was a temporal seque

290 m governs the disinhibition of task-relevant neuronal populations, whereas the alpha-band rhythm supp

291 onlinear and may involve actions at distinct neuronal populations, which could be influenced by the b

292 rain operates as a network of interconnected neuronal populations, which display coordinated rhythmic

293 A neuronal population with a central role in puerperal cha

294 our ability to observe the activity of large neuronal populations with cellular spatial and high temp

295 Diverse neuronal populations with distinct cellular morphologies

296 ng factor to image order-of-magnitude larger neuronal populations with minimal loss in accuracy or te

297 ording technology we cannot image very large neuronal populations with simultaneously high spatial an

298 ey regulator of a previously uncharacterized neuronal population within the PVH that impinges upon mu

299 post-inspiratory phase engages a distributed neuronal population within ventral, dorsal and pontine n

300 efine and instruct the generation of diverse neuronal populations within the spinal cord.