ライフサイエンスコーパス: field potential

1 faces was also observed in gamma band local field potential.

2 ed in the beta oscillatory band of the local field potential.

3 changes in specific components of the local field potential.

4 he level of individual neurons and the local field potential.

5 BOLD signal and electrocorticographic (ECoG) field potential.

6 s that of rhythmic oscillations in the local field potential.

7 cted in simultaneously recorded nearby local field potential.

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

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

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

11 can aid in identifying neural generators of field potentials.

12 recorded measures of network activity, local field potentials.

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

14 d presynaptic Ca(2+) transients and striatal field potentials.

15 ectively, consistent with experimental local field potentials.

16 and soma-targeting inhibition generate these field potentials.

17 ae while simultaneously recording underlying field potentials.

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

19 Both right and left piriform cortex local field potential activities were recorded.

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

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

22 al-cortical communication, we recorded local field potential activity from retinotopically aligned re

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

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

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

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

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

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

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

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

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

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

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

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

35 he ripple-frequency oscillation in the local field potential and organize the phase-locked spiking of

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

37 tions by simultaneously recording both local field potential and single-unit activity from the basal

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

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

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

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

42 over phase relationships between oscillatory field potentials and firing rates.

43 during one stimulation train and the evoked field potentials and generated fMRI responses were measu

44 Using these criteria, averaged local field potentials and high-gamma-band power demonstrate a

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

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

47 N theta oscillatory phase synchrony of local field potentials and neocortical-theta-to-ATN-gamma cros

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

49 physiological range (1-3 mM) to record local field potentials and single cells in hippocampal slices

50 brains and used to record multiplexed local field potentials and single-unit action potentials from

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

52 statistical relationship between oscillatory field potentials and spike synchrony in: 1) simulated ne

53 s, causing robust desynchronization of local field potentials and strong decorrelation of responses b

54 the effect of peripheral inflammation on the field potentials and synaptic plasticity (LTP and LTD).

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

56 ected dopamine neurotransmission, maintained field potentials, and blocked excitotoxicity.

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

58 )-dependent afterhyperpolarization, baseline field potentials, and short-term synaptic plasticity wer

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

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

61 Hippocampal local field potentials are characterized by two mutually exclu

62 Far-field potentials are common in scar areas.

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

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

65 ns as the moving object and a periodic light-field potential as the substrate.

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

67 m cortical areas outside motor cortex; local field potentials as a source of recorded signals; somato

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

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

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

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

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

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

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

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

76 We then utilize high-density local field potential data recorded in vivo from human cortex

77 Sites with far-field potentials, defined as those that remained visible

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

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

80 HFOs occurred spontaneously in extracellular field potentials during interictal discharges (IIDs) and

81 tional magnetic resonance imaging) and local field potentials during Pavlovian fear conditioning.

82 Electrophysiological field potential dynamics are of fundamental interest in

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

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

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

86 These field potentials exhibit distinctive spatial and tempora

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

88 ciated sharp-wave-ripple events in the local field potential exhibited substructure that mapped onto

89 red off the higher part of the combined atom-field potential followed by the absorption of many photo

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

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

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

93 We recorded single cells and local field potentials from area V1 in mice head-fixed on a ru

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

95 f the subjects, we measured high gamma-range field potentials from electrocorticography arrays implan

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

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

98 We recorded local field potentials from multicontact depth electrodes impl

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

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

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

102 We recorded direct local field potentials from the human pallidum simultaneously

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

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

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

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

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

108 , we demonstrate that single units and local field potentials from the STN exhibit oscillatory entrai

109 ency oscillations (HFOs; 150-600Hz) in local field potentials generated by human hippocampal and para

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

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

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

113 nd gamma-band (40-100 Hz) power in the local field potential in the limb representations in somatosen

114 estigated their effects on hippocampal local field potentials in both anesthetized and behaving mice.

115 anced Schaffer collateral-induced excitatory field potentials in CA1 stratum radiatum.

116 We recorded spontaneous neocortical local field potentials in freely behaving infant rats during n

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

118 r anterior commissure-evoked hippocampal CA1 field potentials in strata pyramidale and radiatum and a

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

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

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

122 high-frequency ripple oscillations of local field potentials in the hippocampal CA1 area are signifi

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

124 ent with nasal respiration and with rhythmic field potentials in the olfactory bulb: hence, we called

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

126 trate that single units/multiunits and local field potentials in the primary motor (M1) cortex of non

127 TN to measure single-unit activity and local field potentials in the R6/2 transgenic mouse model of H

128 tracellular calcium (Ca(2+)i) and with local field potentials in the rat's somatosensory cortex.

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

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

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

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

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

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

135 both with Ca(2+)i and neuronal firing (local field potentials), indicating that they directly reflect

136 lations are correlated with glomerular local field potentials, indicating spontaneous local network a

137 oscillations, we have integrated oscillatory field potentials into our point process regression frame

138 Analysis of field potentials, intracellular activities, and extracel

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

140 The analysis of single trial responses of field potentials is an important tool to study brain sig

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

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

143 directional coupling with the pallidal local field potentials leading in the theta and alpha band and

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

145 uestion, we used a procedure to record local field potential (LFP) activity across the fly brain whil

146 recorded cortical electroencephalogram/local field potential (LFP) activity and intracellular activit

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

148 cally, we describe a traveling wave of local field potential (LFP) activity in cortical area V4 of ma

149 Local field potential (LFP) activity in motor cortical and bas

150 sis that distinct temporal patterns of local field potential (LFP) activity in the human limbic syste

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

152 e, we recorded EEG over the cortex and local field potential (LFP) activity in the subthalamic nucleu

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

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

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

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

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

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

159 The local field potential (LFP) captures different neural processe

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

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

162 The local field potential (LFP) in visual cortex is typically char

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

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

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

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

167 st linearly with local spiking or some local field potential (LFP) measurement.

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

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

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

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

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

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

174 Local field potential (LFP) recordings from patients with deep

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

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

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

178 g cell ensembles can be encoded in the local field potential (LFP) remains unclear.

179 Because the local field potential (LFP) represents an important link betwe

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

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

182 We measured single-neuron and local field potential (LFP) responses to visual stimuli in are

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

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

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

186 Local field potential (LFP)-related currents dominate high-fre

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

188 12-20 Hz (beta) frequency bands of the local field potential (LFP).

189 ty remains undifferentiated within the local field potential (LFP).

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

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

192 tions, we analyzed laminar profiles of local field potentials (LFPs) and concomitant multiunit activi

193 Assisted by multisite recordings of local field potentials (LFPs) and layer-specific profiling of

194 Using extracellular recordings of local field potentials (LFPs) and multiunit activity, we demon

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

196 t, for the first time, visually evoked local field potentials (LFPs) and spiking activity recorded si

197 Local field potentials (LFPs) are fluctuations of extracellula

198 ing activity and the spectral power of local field potentials (LFPs) during a task where the rhythmic

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

200 We recorded the putaminal local field potentials (LFPs) from monkeys performing a synchr

201 between the firing of single cells and local field potentials (LFPs) has received increasing attentio

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

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

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

205 , we recorded single unit activity and local field potentials (LFPs) in the middle superior temporal

206 ility and low-frequency composition of local field potentials (LFPs) offer important advantages for r

207 ound that 30-80 Hz gamma dominated CA1 local field potentials (LFPs) on the descending phase of CA1 t

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

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

210 vident in both low- and high-frequency local field potentials (LFPs) recorded on electrocorticography

211 Amygdala odor-evoked local field potentials (LFPs) via wireless electrodes were als

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

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

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

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

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

217 calization profiles, and plasticity on local field potentials (LFPs)?

218 Local fields potentials (LFPs) recorded simultaneously to cort

219 (the 'NeuroGrid') that can record both local field potentials(LFPs) and action potentials from superf

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

221 ecause of use of less locally specific local field potential measurements.

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

223 Here we recorded intracranial field potentials of 113 visually selective electrodes fr

224 Although we observed high gamma-band field potentials of similar frequency to SWRs, only the

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

226 a(+) channels, had the same frequency as the field potential oscillations associated with sharp-wave

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

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

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

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

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

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

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

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

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

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

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

238 oscillation and induces the activated local field potential pattern.

239 cellular recordings of the proximal negative field potential, pharmacologically manipulated to genera

240 (6-12 Hz) oscillatory component of the local field potential-plays a critical role in spatial navigat

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

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

243 Cortical local field potentials, power spectral density, and phase-ampl

244 wave propagation observed in the human local field potential preceding seizure termination.

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

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

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

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

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

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

251 Here we used local field potentials recorded from the midbrain of behaving

252 n in the time-varying power spectra of local field potentials recorded simultaneously in discrete bra

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

254 Field potential recording, pharmacological manipulation,

255 ographic, magnetoencephalographic, and local field potential recordings and are generally understood

256 By means of local field potential recordings and ventral hippocampal stimu

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

258 Field potential recordings at the point of wave initiati

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

260 We show, in chronic multisite local field potential recordings from rat V1, that repeated pr

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

262 To this end, we analysed local field potential recordings from the subthalamic nucleus

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

264 Local field potential recordings in visual cortex confirmed ga

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

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

267 Local field potential recordings were used to determine change

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

269 n the activity of RtN (single unit and local field potential recordings) and prefrontal cortex (PFC;

270 es in spectral signatures of dCA1-mPFC local field potential recordings, using neural mass models of

271 photometric presynaptic Ca(2+) and striatal field potential recordings, we report that relative to P

272 at therapeutic parameter settings and local field potential recordings.

273 ecognition signals by recording intracranial field potential responses from 776 electrodes in 10 epil

274 assessed in vivo by recording the MeA evoked field potential responses to stimulation of the main (n

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

276 parametric dependence on the phase of local field potential rhythms in both stimulus-unrelated backg

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

278 flected by the pronounced increase of evoked field potentials, suggesting that ASIC1a channels are ac

279 gh-amplitude gamma oscillations in the local field potential that are thought to represent the highes

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

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

282 es (SWRs) are highly synchronous oscillatory field potentials that are thought to facilitate memory c

283 same sites and (2) some electrograms are far-field potentials that can be recognized by pacing.

284 he known changes in olfactory cortical local field potentials that occur over the course of odour dis

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

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

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

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

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

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

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

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

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

294 Therefore, local field potentials were recorded from 16 hemispheres in 12

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

296 Local field potentials were recorded from the subthalamic nucl

297 Local field potentials were recorded from the subthalamic nucl

298 ld, moderate, and severe), spontaneous local field potentials were recorded throughout the sensorimot

299 Hippocampal field potentials were significantly enhanced in R192Q mi

300 er in the alpha and theta bands of PFC local field potentials, which are thought to reflect long-rang