ライフサイエンスコーパス: field potential

1 en-level dependent (BOLD) signal and surface field potential.

2 ctive units with an associated event-related field potential.

3 BOLD signal and electrocorticographic (ECoG) field potential.

4 have previously reported an FN in the local field potential.

5 can aid in identifying neural generators of field potentials.

6 ae while simultaneously recording underlying field potentials.

7 l spikes reliably and does not measure local field potentials.

8 ectively, consistent with experimental local field potentials.

9 and soma-targeting inhibition generate these field potentials.

10 band increase in the power spectrum of local field potentials.

11 recorded measures of network activity, local field potentials.

12 the phase of oscillatory activities in local field potentials.

13 , in both the spiking activity and the local field potentials.

14 ded single- and multiunit activity and local field potentials across V1 layers of awake mice (both se

15 er small animals, slow oscillations of local field potential activity are driven at the rate of breat

16 ronization between neuronal firing and local field potential activity during cued compared with uncue

17 or memory, we recorded single cell and local field potential activity from the CA1 region of the hipp

18 vidence for respiratory entrainment of local field potential activity in human piriform cortex, amygd

19 The presence of bursts of local field potential activity in the alpha, and even more so,

20 To this end we recorded local field potential activity in the subthalamic nucleus of 1

21 demonstrate that coherent spiking and local field potential activity is generated by stimulation-evo

22 wave ripples (SWRs) are high-frequency local field potential activity patterns characteristic for the

23 We sampled spiking and local field potential activity simultaneously from multiple si

24 ral hippocampus, as well as continuous local-field-potential activity.

25 Inferring putative synaptic currents from field potentials advances our ability to study neural pr

26 n components of the extracellular electrical field potential affects the efficiency of place cell map

27 re detected in real time from cortical local field potentials, after which DCS was applied.

28 accompanied by a reduction in event-related field potential amplitude.

29 Here, using single-unit and local field potential analyses, we explored MDT function durin

30 xplored narrowband oscillations in the local field potential and broadband power increases.

31 ied electrophysiological recordings of local field potential and extracellular K(+) concentration, im

32 inate through phase synchronization of local field potential and neural spiking activity in macaque m

33 We used optical imaging, MRI, and field potential and potassium electrode recordings in mi

34 ion, we demonstrate stable 128-channel local field potential and single-unit recordings from multiple

35 Using simultaneous local field potential and unit recordings in NR, HPC, and mPFC

36 iatum of male Wistar rats was examined using field potential and unit recordings, local inhibition, n

37 rding in awake behaving mice and concomitant field potential and whole-cell recordings in slice prepa

38 We captured local field potentials and action-potentials while mice engage

39 atio based on the spectral exponent of local field potentials and bioenergetics based on the activity

40 Results show both resting-state field potentials and CBF were depressed after cocaine ad

41 rocircuit contribution to intracranial local field potentials and EEG.

42 y of neuronal populations, that is, in local field potentials and magnetic fields.

43 To this end, we obtained local field potentials and multiunit activity recordings in Te

44 oelectrode array (NeuroGrid) to record local field potentials and neural spiking across the dorsal co

45 to consciousness by directly recording local field potentials and single neuron activity in a functio

46 and we demonstrated stable multiplexed local field potentials and single-unit recordings in mouse bra

47 lated with low-frequency oscillations in the field potentials and spikes at the theta (8 Hz) band, an

48 device enabled long-term recordings of local field potentials and the real-time cancellation of stimu

49 aim in the present study was to record local field potentials and unit activity from these two struct

50 defined as high-frequency power in the local field potential) and gamma-band activity evoked by brief

51 d stability of LEAP, its relationship to the field potential, and its efficacy for quantifying AP mor

52 were more phase-locked to spindle-band local field potential, and synchrony across units peaked durin

53 s, voltage traces, spike raster plots, local field potentials, and information theoretic measures.

54 of the cortical site measured with broadband field potentials, and less so with event related potenti

55 arly axonal volley and later spinal synaptic field potentials, and used the slope of the relationship

56 atistical scores are derived, using the mean-field potentials approach, for describing the different

57 Coherent neural spiking and local field potentials are believed to be signatures of the bi

58 Far-field potentials are common in scar areas.

59 Our results suggest that field potentials are mostly generated by a pathway in de

60 GNIFICANCE STATEMENT Extracellular voltages (field potentials) are a common measure of brain activity

61 s pattern as a template, and using the local field potential as a simultaneous and independent measur

62 Previous studies recorded local field potentials as a measure of synaptic activity toget

63 s possibly important on the genesis of local field potentials, as well as on the cable properties of

64 o be controlled by oscillations in the local field potentials at frequencies traditionally associated

65 We used the accuracy of local field potential-based classification of the limb to be m

66 ter similarity in the pattern of hippocampal field potentials between pre-picture interval and expect

67 tivity of neurons and synapses that generate field potentials, but this "inverse problem" is not easi

68 ke timing and the oscillatory phase in local field potentials-but not changes in spike rate-were pred

69 We combined it with assessment of local field potentials by electrophysiological recordings, cer

70 Motor processes are accompanied by prominent field potential changes in the beta-frequency band (15-2

71 oundly reduced spontaneous hippocampal local field potentials, comparable in magnitude to infusions o

72 s allowed us to compare the pathway-specific field potentials corresponding to the gamma-paced CA3 ou

73 differences in spectral features, unit-local field potential coupling, and information theoretic char

74 spike-field coherence in multichannel local field potential data can be analyzed using the gedCFC fr

75 Simultaneously recorded single-unit local field potential did not provide a good match, demonstrat

76 y recording single-neuron activity and local field potentials directly in the functionally interconne

77 as a time dependent drug-induced increase in field potential duration in the cardiac compartment in r

78 range dominate the rodent hippocampal local field potential during translational movement, suggestin

79 multiple electrodes to record BG spiking and field potentials during normal sleep and in 1-methyl-4-p

80 Local field potential dynamics allowed accurate prediction of

81 Electrophysiological field potential dynamics are of fundamental interest in

82 Extracellular field potentials (EFPs) are an important source of infor

83 us signals across four scales: spikes, local field potential, electrocorticogram (ECoG), and EEG, and

84 phase-amplitude coupling, we recorded local field potentials/electrocorticography from hand motor an

85 performed chronic recordings of evoked local field potentials (eLFPs) in A1 of head-fixed female rats

86 (2) the amplitude of the postsynaptic local field potential elicited near the interneuron by spikes

87 displayed unusually strong coupling to local field potential even before seizures.

88 Ketamine depressed local field potentials evoked in the OFC by excitatory thalami

89 These field potentials exhibit distinctive spatial and tempora

90 ional networks of coherent spiking and local field potentials exhibit frequency-specific spatiotempor

91 rrant further assessment of the use of local field potentials for closed-loop neuromodulation for OCD

92 ways through the laminar distribution of the field potential (FP) generators underlying spontaneous a

93 al synaptic responses.SIGNIFICANCE STATEMENT Field potentials (FPs) can index neuronal population act

94 However, although field potentials (FPs) may reflect the synaptic currents

95 By simultaneously recording local field potential from both the dorsal hippocampus and ana

96 ecorded high spatial and temporal resolution field potentials from both the inferior frontal gyrus an

97 ecorded scalp electroencephalogram and local field potentials from deep brain stimulation electrodes

98 ovement and disease state, we recorded local field potentials from hand sensorimotor cortex using sub

99 We recorded local field potentials from implanted electrodes while subject

100 We recorded spikes and local field potentials from laminar electrodes in five cortica

101 n human magnetoencephalography, and in local field potentials from mice performing a detection task.

102 We recorded local field potentials from multicontact depth electrodes impl

103 decision-making task while we recorded local field potentials from multiple brain structures.

104 us extracellular action potentials and local field potentials from the dorsal CA1 pyramidal cell laye

105 Here, we recorded neuronal firing and local field potentials from the medial entorhinal cortex of fr

106 ive neurostimulation system, we record local field potentials from the NAc of mice and a human antici

107 ile simultaneously recording respiration and field potentials from the olfactory bulb (OB) and hippoc

108 Here we directly recorded local field potentials from the OrbitoFrontal Cortex (OFC) in

109 tegory task while recording spikes and local field potentials from the PFC and PPC with multiple elec

110 We recorded local field potentials from the subthalamic nucleus (STN) in 1

111 We recorded local field potentials from the ventral intermediate nucleus o

112 y uncovering the laminar distribution of the field potential generators underlying the dominant delta

113 d was most prominent in high frequency local field potentials (>30 Hz), followed by local spiking act

114 frequency (4-8 Hz) fluctuations of the local field potential have long been implicated in learning an

115 requency (300-900 Hz) component of the local field potential (HF-LFP), believed to reflect local spik

116 ophysiologic recordings of hippocampal local field potential in both male and female mice demonstrate

117 gamma (40-110 Hz) oscillations of the local field potential in mammals have both been linked to odor

118 yramidal neuron membrane potential and local field potential in mice running on a linear treadmill.

119 ne the responses of single neurons and local field potentials in human neurosurgical patients in two

120 Local field potentials in monkey motor cortex revealed charact

121 ology) in healthy participants and STN local field potentials in Parkinson's patients during a task i

122 chopathological information carried by local field potentials in the BNST has not yet been described.

123 he ipsilateral hindlimb in awake rats evoked field potentials in the C1 zone in the copula pyramidis

124 We recorded single-unit activity and local field potentials in the dorsomedial PFC (dmPFC) of male

125 e addressed this question by recording local field potentials in the Drosophila central complex, a br

126 bjects affect the frequency content of local field potentials in the human brain.

127 ed single units in the MDT, as well as local field potentials in the MDT, piriform cortex (PCX), and

128 sess experience-dependent changes in dentate field potentials in the presence and absence of neurogen

129 Here, we record local field potentials in the primary auditory cortex of rats

130 We study brainstem field potentials in the region of the medial superior ol

131 We recorded local field potentials in the subthalamic nucleus (STN) and sc

132 e dorsal lateral geniculate and of the local field potentials in their recipient zone in primary visu

133 During the task, we measured local field potentials in three patients with depth electrodes

134 We tested this prediction by recording local field potentials in two ferrets after administration of

135 nd behavioral levels, including evoked local field potentials, increased hippocampal cFos expression,

136 nd beta (15-35 Hz) oscillations of the local field potential indicate different neural firing statist

137 of high broadband activity in human cortical field potentials indicates local processing and has repe

138 Analysis of field potentials, intracellular activities, and extracel

139 eural activity, but proper interpretation of field potentials is a long-standing challenge.

140 tly correlated with corresponding changes in field potential latencies and their precision.

141 e increasing their precision; subtraction of field potential latencies from SLC latencies revealed a

142 and to decode gripping force based on local field potential (LFP) activities recorded from the subth

143 ed for 10 min, can induce seizure-like local field potential (LFP) activity in both anaesthetized and

144 We recorded spiking and local field potential (LFP) activity in the PPC while two rhes

145 lking task to compare synchronized STN local field potential (LFP) activity with activity in motor co

146 We also recorded local field potential (LFP) activity within the primary motor

147 analyze delta-band (1-4 Hz) rhythms in local field potential (LFP) activity, in multielectrode record

148 ch through a delay epoch, and used the local field potential (LFP) along with simultaneously recorded

149 With paired local field potential (LFP) and intracellular recordings and c

150 ed the spontaneous and visual-elicited local field potential (LFP) and multi-unit activity (MUA) in t

151 We analyzed local field potential (LFP) and spiking from the prefrontal co

152 However, coherence and spike-local field potential (LFP) coupling between the two structure

153 characterized single-unit activity and local field potential (LFP) dynamics in the S1, primary visual

154 and neuronal activity underlying these local field potential (LFP) events remains unclear.

155 relation between the thresholds of the local field potential (LFP) for aDBS and apLDF, the extent of

156 ike the electroencephalogram (EEG) and local field potential (LFP) in bulk brain matter, and analysis

157 ed extracellular unit activity and the local field potential (LFP) in premotor and prefrontal cortex

158 The cortical local field potential (LFP) is a common measure of population

159 The local field potential (LFP) is generated by large populations

160 euronal ensembles with the hippocampal local field potential (LFP) is reflected in dynamic calcium ac

161 tation of the extracellularly recorded local field potential (LFP) is still not fully established.

162 The local field potential (LFP) is thought to reflect a temporal r

163 rtical assemblies could be recorded as local field potential (LFP) measurements.

164 currently unknown; even the spread of local field potential (LFP) obtained from microelectrodes is d

165 Theta oscillations in the local field potential (LFP) of V1 have been found to convey te

166 Local field potential (LFP) oscillations recorded from deep br

167 bnormal low beta (8-15 Hz) spiking and local field potential (LFP) oscillations resonate across the B

168 ugh temporal organization reflected in local field potential (LFP) oscillations.

169 We have identified a specific local field potential (LFP) pattern generated in the PrL corte

170 n sharp-wave ripples (SWRs), which are local field potential (LFP) patterns in hippocampal CA1 that i

171 Using concurrent hippocampal local field potential (LFP) recordings and functional MRI (fMR

172 We used in vivo neuron and local field potential (LFP) recordings from the ventral telenc

173 We studied local field potential (LFP) recordings in PD subjects undergoi

174 Using multi-channel local field potential (LFP) recordings in primary somatosensor

175 We perform local field potential (LFP) recordings on flies spontaneously

176 Because the local field potential (LFP) reflects the total activity across

177 Prior studies have reported "local" field potential (LFP) responses to faces in the macaque

178 ial-by-trial behavioural improvements, local field potential (LFP) responses to stimuli detected insi

179 Here, we measured changes in local field potential (LFP) responses to ventral hippocampal s

180 been recent debate as to whether this local field potential (LFP) rhythm reflects internal processin

181 data about the information carried by local field potential (LFP) signals in this area during obsess

182 nsolidation, and also exhibit distinct local field potential (LFP) signatures during memory consolida

183 We used the local field potential (LFP) spectrogram to characterize sleep

184 he use of the extracellularly recorded local field potential (LFP) to investigate neural network acti

185 , increases in gamma band power in the local field potential (LFP), and increases calcium signals in

186 mperometric recording of local pO2 and local field potential (LFP)-related currents during seizures i

187 nsory responsive, as is the gamma band local field potential (LFP).

188 erates synchronous oscillations of the Local Field Potential (LFP).

189 power have been well characterized in local field potential (LFP; obtained from microelectrodes), an

190 a continuous spatiotemporal profile of local field potentials (LFP) and multi-unit activity (MUA) bef

191 We measured local field potentials (LFP) and multi-unit activity (MUA) in

192 performed extracellular recordings of local field potentials (LFP) and multi-unit activity along the

193 ctivity in the LGN simultaneously with local field potentials (LFP) in primary visual cortex, in sufe

194 ous phases of trials) of low frequency local field potentials (LFP) in visual area MT of macaque monk

195 o measurable signatures in behavior or local field potentials (LFP).

196 itude of a high-frequency component of local field potentials (LFP).

197 atial and temporal scales by recording local field potentials (LFPs) and action potentials (multiunit

198 enchmark, we assessed rat pup cortical local field potentials (LFPs) and behaviors exposed to adversi

199 The relationship between mesoscopic local field potentials (LFPs) and single-neuron firing in the

200 We recorded local field potentials (LFPs) and spikes in two monkeys traine

201 device's ability to chronically record local field potentials (LFPs) at implanted DBS leads was valid

202 c behavior of cortical and hippocampal local field potentials (LFPs) during slow-wave sleep-related t

203 l functional connectivity by recording local field potentials (LFPs) during spontaneous behavioral tr

204 Local field potentials (LFPs) encode visual information via va

205 d and spontaneous spiking activity and local field potentials (LFPs) from monkey spinal cord in order

206 generate propagating wave patterns in local field potentials (LFPs) in a movement-sensitive area of

207 we measured the phase and amplitude of local field potentials (LFPs) in electrode array recordings fr

208 troencephalograms (EEGs) in humans and local field potentials (LFPs) in nonhuman primates and rodents

209 the effects of DAA and DAQ on rhythmic local field potentials (LFPs) occurring in the degenerating re

210 Oscillations in local field potentials (LFPs) provide fingerprints of such net

211 Local field potentials (LFPs) recorded from the human and rode

212 elta; spindles), we recorded units and local field potentials (LFPs) simultaneously in the limbic tha

213 To reveal the question, local field potentials (LFPs) was recorded and analyzed in two

214 oherence between striatum and amygdala local field potentials (LFPs) were found to couple these struc

215 is sufficient to generate macroscopic local field potentials (LFPs), and if so, respiratory (r) LFPs

216 racranial electroencephalogram (iEEG), local field potentials (LFPs), and single-unit activity in pat

217 etrics on different frequency bands of local field potentials (LFPs), and the relationship of dynamic

218 PPN local field potentials (LFPs), recorded while patients perform

219 both high-resolution BOLD at 9.4 T and local field potentials (LFPs), using 98-channel microelectrode

220 Local field potentials (LFPs), which represent the electrophys

221 network activity that is reflected in local field potentials (LFPs).

222 patch-clamp recordings and synchronous local field potentials (LFPs).

223 Local fields potentials (LFPs) recorded simultaneously to cort

224 BF) and neurophysiological recordings (local field potentials, LFPs).

225 tragranular) and recording modalities (local field potential) most likely affected by V2 connections,

226 ma-band (40-80 Hz) oscillations in the local field potential of non-human primate motor cortex.

227 Short-term recordings of extracellular field potentials of spontaneously beating cardiomyocytes

228 The measured extracellular field potentials, or neurophonics, were strongly ITD tun

229 This local field potential oscillation occurred in short bouts (app

230 es (SPW-Rs), which consist of high-frequency field potential oscillations (ripples, 100-260 Hz) super

231 tracellular detection of low-frequency local field potential oscillations and high-frequency action p

232 KO reduced both beta and gamma local field potential oscillations as well as synchrony of inh

233 reased noise correlations and stronger local field potential oscillations in the alpha frequency band

234 to prediction violations is encoded by local field potential oscillations in the gamma band (>30 Hz),

235 mpact of nicotine on unit activity and local field potential oscillations in the PFC of behaving rats

236 Additionally, the power of local field potential oscillations in the theta and gamma freq

237 Local field potential oscillations reflect temporally coordina

238 oride concentrations leading to seizure-like field potential oscillations.

239 ity to recruit recurrent inhibition, entrain field-potential oscillations and more importantly in the

240 us measurement of behavioural kinematics and field potential parameters of C-start startle responses

241 us measurement of behavioural kinematics and field potential parameters of C-start startle responses

242 Quantification of SLC kinematics and field potential parameters revealed that, apart from the

243 from their latencies, SLC kinematics and SLC field potential parameters were intensity independent.

244 crease the presentation rate of the selected field potential pattern across training.

245 We have identified a specific local field potential pattern generated in the prelimbic corte

246 (6-12 Hz) oscillatory component of the local field potential-plays a critical role in spatial navigat

247 ividual neuronal outputs and the mean, local field potential (population activity) accompany these ch

248 ity and a low theta/delta ratio in the local field potential power spectrum.

249 D abrogated the enhanced intracortical local field potential power, including the delta and theta rhy

250 r signaling is reflected in gamma-band local field potentials, presumably serving to efficiently inte

251 tural counterpart, amplitude and dV/dtmax of field potential progressively increased during the cours

252 Extracellular voltage recordings (Ve ; field potentials) provide an accessible view of in vivo

253 nsient and a sustained gamma rhythm in local field potential recorded from the primary visual cortex.

254 ated time-frequency representations of local field potential recorded simultaneously in the primary a

255 yzed the emergence of beta activity in local field potentials recorded from olfactory, sensorimotor a

256 heta-gamma cross-frequency coupling of local field potentials recorded from the mEC of freely moving

257 We have extracted from local field potentials recorded simultaneously from multiple l

258 Using local field potential recording in awake behaving mice and con

259 We used simultaneous local field potential recordings and widefield imaging of a ge

260 We present the first local field potential recordings directly comparing bicycling

261 Here, by using in vivo wireless local field potential recordings during working memory process

262 of rest and button presses, leading to local field potential recordings from 19 (15 participants) STN

263 performed high-density single unit and local field potential recordings from hippocampi of behaving r

264 , we examined electrocorticographic cortical field potential recordings from the human nonprimary aud

265 s, preclinical evidence from slice and local field potential recordings has shown that central cannab

266 Local field potential recordings in rodent striatum show dopam

267 Local field potential recordings in visual cortex confirmed ga

268 Here, we used local field potential recordings obtained from 10 patients wit

269 Laminar multiunit activity and local field potential recordings of neural activity were perfo

270 an STG, we use high-density cortical surface field potential recordings while participants listened t

271 Using in vivo local field potential recordings, we observed dampened oscilla

272 Degeneration-induced local field potentials remain a major challenge common to all

273 deficits (volume, neurogenesis, c-Fos, local field potential) required combined chronic high corticos

274 However, analysis of the local field potential revealed a marked sensitization of theta

275 Spectral analysis of STN local field potentials revealed elevated beta power during REM

276 electrode arrays to record respiratory local field potentials (rLFPs) from 196-364 electrode sites wi

277 est that the brain state identified by local field potential spectrum is not stationary but changes s

278 ntiation (LTP) had a higher threshold in LPP field potential studies but not in voltage clamped neuro

279 activity, and we infer that features of the field potential that are uncorrelated with BOLD arise la

280 tions (sharp-waves) in the hippocampal local field potential that co-occur with high-frequency (>80 H

281 reduced activity and flattening of the local field potential that resolved within minutes.

282 g of MFC neurons to amygdala and hippocampus field potentials, thereby enabling the routing of memori

283 ident in grid cell firing rate and the local field potential theta frequency.

284 changes in a proposed speed signal by local field potential theta frequency.

285 ubthreshold theta oscillations than to local field potential theta oscillations.

286 tion on single-neuron firing rates and local field potentials; this mechanistic insight explains prev

287 tal network displayed population-based local field potential transient deflections (LFP spikes) whose

288 We concurrently measured cortical field potentials via thinned-skull electroencephalograph

289 xtinction (EE), when freezing was maximal, a field potential was evoked in the PAG by the auditory fe

290 ecoding accuracy of ECoG compared with local field potential was not because of differences in low-le

291 on coupled neural synchrony in dentate local field potentials was reduced in X-irradiated mice, espec

292 Results Oscillatory local field potentials were captured with cortical recordings.

293 and the precision in the latency of the SLC field potentials were linearly correlated to the latenci

294 tielectrode recordings of spike activity and field potentials were made in male rats as they performe

295 Spike activity and local field potentials were recorded during task performance s

296 Spontaneous field potentials were recorded from hippocampus of pre-p

297 Local field potentials were recorded from prelimbic (PL) and i

298 Local field potentials were recorded from the subthalamic nucl

299 Local field potentials were recorded from the subthalamic nucl

300 eously tracked eye movements and hippocampal field potentials while neurosurgical patients performed