ライフサイエンスコーパス: neuronal population

1 average spiking rate is calculated over the neuronal population.

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

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

4 ition reflecting the overall activity of the neuronal population.

5 s in how information is distributed over the neuronal population.

6 logy, with autism reflecting a less "social" neuronal population.

7 re activated such that they reconstitute the neuronal population.

8 e not been fully characterized in a purified neuronal population.

9 rtical inputs and synchronization of the STN neuronal population.

10 predominant response suppression across the neuronal population.

11 henomena of spikes triggered by an intricate neuronal population.

12 ns can limit efficient information coding in neuronal populations.

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

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

15 Brain function involves the activity of neuronal populations.

16 hods for targeting and manipulating specific neuronal populations.

17 urally leads to complex dynamics in rhythmic neuronal populations.

18 neurodegeneration across various vulnerable neuronal populations.

19 tion between replicating and quiescent fetal neuronal populations.

20 the amount of information encoded in sensory neuronal populations.

21 y correlated between these task-co-activated neuronal populations.

22 behavior and is composed of many overlapping neuronal populations.

23 racellular Cl(-) level, within heterogeneous neuronal populations.

24 y interactions between orientation-selective neuronal populations.

25 us consists of distinct regions with diverse neuronal populations.

26 nt firing patterns are regulated in specific neuronal populations.

27 formation arising from the activity of large neuronal populations.

28 re affected by prior experience in selective neuronal populations.

29 tion of MHC-I by gamma-interferon than other neuronal populations.

30 ce of persistent firing patterns in specific neuronal populations.

31 e effective connectivity between interacting neuronal populations.

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

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

34 on, improving the stimulus representation by neuronal populations.

35 n information from both individual cells and neuronal populations.

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

37 y spatiotemporal patterns of activity across neuronal populations.

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

39 siological response properties of diverse V1 neuronal populations.

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

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

42 e and female intruders activated overlapping neuronal populations.

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

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

45 t tradeoffs between sensitivity and noise in neuronal populations.

46 human tissues, toxicity targets only defined neuronal populations.

47 e gain and suppressing shared variability in neuronal populations.

48 entrainment of sensorimotor and associative neuronal populations, acquired through learning, could b

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

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

51 on of behavior are guided by the activity of neuronal populations across multiple frontal cortical ar

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

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

54 ding (4-8 Hz) and increased prefrontal local neuronal population activity (high gamma amplitude, 80-1

55 hematical model consistent with the observed neuronal population activity and determine analytically

56 circuit function, in terms of both the local neuronal population activity at the site of activation a

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

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

59 One of the striking manifestations of neuronal population activity is that of rhythmic oscilla

60 otically driven magnocellular neurosecretory neuronal population activity leads to a predominant nitr

61 Two-photon imaging of neuronal population activity showed that prolonged expos

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

63 also be estimated and accounted for based on neuronal population activity.

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

65 known, nor is clear the identity of specific neuronal populations affected.

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

67 ythms provide a mechanism to select relevant neuronal populations, although the relative contribution

68 ently, if the CB1 receptor is lost in either neuronal population, an allostatic shift will occur lead

69 ed high efficacy in protecting the remaining neuronal population and restoring motor function.

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

71 mitter glutamate, used partially by the same neuronal population and thus probably mediating the resp

72 tation and inhibition of firing in specified neuronal populations and artifact-free recording of firi

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

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

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

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

77 FoxO1-dependent transcription from different neuronal populations and multiple hypothalamic regions,

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

79 g and reproductive neuropeptide synthesizing neuronal populations and suggest a potential pathway tha

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

81 g the susceptible age, predicting vulnerable neuronal populations, and devising mitigating strategies

82 semi-rhythmic activity produced by aggregate neuronal populations, and organized spatiotemporal pheno

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

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

85 Furthermore, we can show that distinct neuronal populations are activated for the visual cue an

86 Hypothalamic neuronal populations are central regulators of energy ho

87 hysiological and morphological properties of neuronal populations are crucial for the appropriate fun

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

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

90 e found that DAMB overexpression in specific neuronal populations arrested development of the fly and

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

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

93 We imaged the activity of the same layer 2/3 neuronal populations as mice learned to discriminate two

94 tudied the evolution of activity in cortical neuronal populations, as well as the Granger causal inte

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

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

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

98 an efficient intersectional means to target neuronal populations based on cell type and projection p

99 is too strong, spike timing within the local neuronal population becomes too synchronous; when oscill

100 hat the temporal dynamics of a heterogeneous neuronal population brings about complementary informati

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

102 racterized by the progressive loss of select neuronal populations, but the prodeath genes mediating t

103 the preferential activation of different M1 neuronal populations by applying transcranial magnetic s

104 We characterize these functionally distinct neuronal populations by comparing their electrophysiolog

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

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

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

108 emonstrated that the patterns of activity in neuronal populations can vary strongly between synchroni

109 y map a measured brain volume in search of a neuronal population code with a specific geometry.

110 pproach to assess the noise tolerance of the neuronal population code.

111 Neuronal population codes are increasingly being investi

112 How noise affects neuronal population coding is poorly understood.

113 multiple targets, the relative activities of neuronal populations compete for the selection of a sacc

114 whereas reduction of mHTT expression in both neuronal populations consistently ameliorates all behavi

115 Distinct neuronal populations containing PPCART, PPPACAP, and PPN

116 As neuronal populations contribute to multiple representati

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

118 on baseline firing, at least three types of neuronal populations could be distinguished.

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

120 eless deep brain stimulation of well-defined neuronal populations could facilitate the study of intac

121 e dynamics and function of local circuits of neuronal populations dedicated to a common task, such as

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

123 he ability to replenish its neuronal and non-neuronal populations due to the presence of germinal bas

124 cortex demonstrate interrogation of the same neuronal population during different behavioral states a

125 es assembly formation in rat basal forebrain neuronal populations during a selective attention task.

126 enabling direct visualization of TMS-induced neuronal population dynamics.

127 ifying the neuronal configuration in which a neuronal population encodes given information can serve

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

129 ow the temporal structure of the activity of neuronal populations, exemplified by brain rhythms, can

130 and the Gq-coupled M3-DREADD within the same neuronal population facilitated the sequential and bidir

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

132 ack of objective criteria to distinguish one neuronal population from another.

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

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

135 ynchronized activation of the ARN kisspeptin neuronal population generates pulses of LH.

136 Shared, trial-to-trial variability in neuronal populations has a strong impact on the accuracy

137 ternal segment of the globus pallidus (GPe), neuronal populations have been defined using molecular,

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

139 Similar changes were observed in identified neuronal populations imaged repeatedly over days.

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

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

142 NK1IP -n were seen to constitute a large neuronal population in the cc and had a distribution sim

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

144 neuronal numbers after a loss of 40% of the neuronal population in the DRG.

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

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

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

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

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

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

151 The brain recruits neuronal populations in a temporally coordinated manner

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

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

154 Vice-versa, neuronal populations in anterior/ventral auditory region

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

156 ed novel marker genes that characterize rare neuronal populations in both mouse and zebrafish.

157 and applied it to simultaneous recordings of neuronal populations in cortical areas V1 and V2 of the

158 In vivo Ca2+ imaging of neuronal populations in deep cortical layers has remaine

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

160 , even without execution, modulates relevant neuronal populations in early visual areas.

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

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

163 e remodeling could apply to other vulnerable neuronal populations in neurodegenerative disease.

164 inuous, precise optical control of firing in neuronal populations in order to disentangle causally re

165 Cell replacement for restoring neuronal populations in Parkinson's disease has been dem

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

167 Specifically, our fMRI results suggest that neuronal populations in posterior/dorsal auditory region

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

169 on calcium imaging to record the activity of neuronal populations in primary visual cortex of awake m

170 rvations indicate that shared variability of neuronal populations in sensory cortex can be largely ex

171 l and powerful tools to investigate discrete neuronal populations in the brain.

172 in receptors (IRs) are expressed in discrete neuronal populations in the central nervous system, incl

173 ic interactions occur among IC local circuit neuronal populations in the control of regional cardiac

174 lation analyses to large-scale recordings of neuronal populations in the cornu ammonis 1 (CA1) and CA

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

176 ctional manipulations, we find that distinct neuronal populations in the MeA control different social

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

178 ), we genetically reduced mHTT expression in neuronal populations in the striatum, cortex or both.

179 ess of visual stimuli, but it is unknown how neuronal populations in this area process detected and u

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

181 ecord the activity of ever larger and denser neuronal populations in vivo.

182 epertoires of synaptic adhesion molecules in neuronal populations in vivo.

183 nal ensembles ( approximately 4-13% of total neuronal population) in the nucleus accumbens core, dors

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

185 for the acquisition of CTA, but the specific neuronal populations involved are unknown.

186 is directly related to the disinhibition of neuronal populations involved in the computations of mov

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

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

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

190 f electrical activity in genetically defined neuronal populations is a long-standing goal in neurosci

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

192 the ontogeny of these critical hypothalamic neuronal populations is largely unknown.

193 memory, but the relationship between the two neuronal populations is not fully understood.

194 udies in which visualization of CaMKIIalpha- neuronal populations is required.

195 wever, to what extent individual neurons and neuronal populations maintain internal firing properties

196 tion and temporal response profiles of these neuronal populations match that of its constituting indi

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

198 During development these two neuronal populations migrate from distinct progenitor zo

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

200 Because the neuronal populations most vulnerable in PD are character

201 associated with the degeneration of several neuronal populations, most notably CA3 pyramidal neurons

202 n the suprachiasmatic nucleus (SCN), yet the neuronal population necessary for the generation of time

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

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

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

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

207 ffectively silenced, in different excitatory neuronal populations of the hippocampus.

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

209 ity or excitability of single neurons, local neuronal populations or "assemblies," and/or multiple re

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

211 ain GABA neurons, but not from several other neuronal populations or from astrocytes, decreased wheel

212 The response of a neuronal population over a space of inputs depends on th

213 showed functional similarity to neighboring neuronal populations over spatial distances resembling m

214 Neuronal populations predicted, with high accuracy, whic

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

216 r is evident both for simulated data and for neuronal population recordings from macaque primary visu

217 we report that blocking the activity of this neuronal population reduces alcohol intake.

218 ivity was observed in the entire cholinergic neuronal population regardless of age or Alzheimer's dis

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

220 It is now clear that many neuronal populations release more than one classical neu

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

222 by spatiotemporal activity patterns in these neuronal populations remains poorly understood.

223 the significance of developmentally distinct neuronal populations remains unclear.

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

225 on and locomotion, are comprised of discrete neuronal populations residing within the brainstem and s

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

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

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

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

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

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

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

233 e then used multielectrode arrays to measure neuronal population responses to those same images in vi

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

235 onstrated by recordings of single neuron and neuronal population responses.

236 nt correlated with substantial adjustment in neuronal population responses.

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

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

239 Its neuronal population revealed a specialization for shape

240 mplex adult populations with the early brain neuronal populations revealed in developmental studies o

241 Moreover, neuronal populations showed consistencies in activation

242 gic/inhibitory and glutamatergic/excitatory) neuronal populations, so the activation of one and/or an

243 Sporadic coherence events between neuronal population spike counts and LFPs were observed

244 In the primary motor cortex of PD patients, neuronal population spiking is excessively synchronized

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

246 However, neuronal populations subject to stochastic fluctuations

247 hat are often misfolded or malfunctioning in neuronal populations subserving overt NDD symptomology.

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

249 Sensory hair cells in the cochlea, like most neuronal populations that are postmitotic, terminally di

250 about the output of these pacemakers, as the neuronal populations that are targeted by pacemaker axon

251 The rhombic lip gives rise to neuronal populations that contribute to cerebellar, prop

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

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

254 The neuronal populations that govern circadian rhythms are d

255 red in concert to generate these specialized neuronal populations that help connect us to our environ

256 These observations support the idea that neuronal populations that integrate information about en

257 cursors not only differentiate into discrete neuronal populations that mediate energy balance (POMC a

258 ids such as morphine, but the MOR-expressing neuronal populations that mediate the distinct opiate ef

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 e used functional MRI adaptation to identify neuronal populations that represent color categories irr

262 al input, reconstructed using simulations of neuronal populations that reproduce natural spiking resp

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

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

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

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

267 gamma oscillations and synchrony of cortical neuronal populations, thought to be the signature of hig

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

269 rade-off may govern the modulation tuning of neuronal populations throughout the auditory cortex.

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

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

272 We and others have previously investigated neuronal populations to study how bioenergetic parameter

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

274 pocampal contextual information by cingulate neuronal populations, to inform choices in a task-phase-

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

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

277 es have been mapped to specific hypothalamic neuronal populations using cell type-specific knockout e

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

279 tive ablation of the leptin receptor in each neuronal population: Vgat-Cre;Lepr(lox/lox) and Vglut2-C

280 ference; however, the average phase of local neuronal populations was similar through the depth of la

281 variability reflects factors shared across a neuronal population, we analyzed the activity of many si

282 hmC influences gene expression in an in vivo neuronal population, we assessed the patterning and func

283 cular genetic approaches to target different neuronal populations, we find that the gamma lobes of th

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

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

286 ASP-immunoreactive neuronal populations were rather similar as the glutamat

287 Other neuronal populations were unaffected.

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

289 r (nAChR) subtypes are expressed in specific neuronal populations, which are involved in numerous neu

290 hought to mediate the dynamic interaction of neuronal populations, which is essential for information

291 antagonist, MK801, to a molecularly defined neuronal population with the cell-type-selectivity of ge

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

293 e local neural responses by stimulating both neuronal populations with identical stimuli presented sy

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

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

296 However, the identification of distinct neuronal populations within a given brain region is ofte

297 ith connectivity deficits involving specific neuronal populations within cortical and basal ganglia c

298 s circuit dynamics in large, densely sampled neuronal populations within slices of mouse primary audi

299 The sizes of different neuronal populations within the CNS are precisely contro

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