ライフサイエンスコーパス: frequency band

1 d can be opposite in nature depending on the frequency band.

2 of the incident intensity) across a 3.1 GHz frequency band.

3 hronized firing of cortical neurons in gamma-frequency band.

4 es were weighted by their coherence within a frequency band.

5 n infants between 9 and 25 weeks in the beta frequency band.

6 y, demonstrating a perceptual tuning to this frequency band.

7 networks seen during sleep and in the gamma frequency band.

8 brain oscillatory activity in the alpha/beta frequency band.

9 ack inhibition, pyramidal cells in the gamma frequency band.

10 ated by sounds within a distinctly different frequency band.

11 eased rhythmic network activity in the gamma-frequency band.

12 y constrained distribution of power for each frequency band.

13 e not concentrated at any particular spatial frequency band.

14 cement when attending to the least-preferred frequency band.

15 the reduction of power elicited in the gamma frequency band.

16 ithin a 200-650 ms time-window and a 4-55 Hz frequency band.

17 75 g/kg) decreased the power in the 16-32 Hz frequency band.

18 ngth of brain-muscle signal coupling at beta frequency band.

19 s of a sniff, and maximally within the theta frequency band.

20 oscillatory activity in the slow (0.5-4 Hz) frequency band.

21 n principle possible, at least over a narrow frequency band.

22 y motor EEG activity to dominate in the beta frequency band.

23 ancing thalamocortical communication in this frequency band.

24 ssment revealed no prominent increase at any frequency band.

25 al field potential oscillations in the alpha frequency band.

26 d activity and loss of bursts in the spindle frequency band.

27 erence (ITPC) measure for the theta and beta frequency bands.

28 rtex, and medial temporal areas in different frequency bands.

29 ross cortical networks and spanning multiple frequency bands.

30 ilure via oscillatory synchrony in different frequency bands.

31 ctivity between muscles at multiple distinct frequency bands.

32 and motor preparation in the alpha and beta frequency bands.

33 nd rIFC was found in both the alpha and beta frequency bands.

34 n in the alpha (8-14 Hz) and beta (15-30 Hz) frequency bands.

35 een the DHPC-Amyg and Fctx-DHPC in the theta frequency bands.

36 underlying the power modulations in specific frequency bands.

37 omenon relates to neuronal activity in other frequency bands.

38 ivity are less clear, especially in specific frequency bands.

39 importance of interactions between different frequency bands.

40 al tuning amplifies selected combinations of frequency bands.

41 ditory populations are sensitive to multiple frequency bands.

42 ment spatial extent, spatial resolution, and frequency bands.

43 d by decomposing the LFP into nonoverlapping frequency bands.

44 a contribution from contrast in more distant frequency bands.

45 nantly led by activity in the cortex in both frequency bands.

46 e reductions in the evoked activity in these frequency bands.

47 ldren had brain oscillations in intermingled frequency bands.

48 Bursting enhances resonance in two distinct frequency bands.

49 o the change of spatial structure than other frequency bands.

50 ic elastic wave transmission in multiple low frequency bands.

51 in the theta- (4-8 Hz) and gamma- (30-90 Hz) frequency bands.

52 s prevalent in the delta- (1-4 Hz) and gamma-frequency bands.

53 ic behavioural states and more classical EEG frequency bands.

54 ode phase synchronization across several LFP frequency bands.

55 osaic of spectral interrelationships between frequency bands.

56 coherence within theta and beta oscillatory frequency bands.

57 ntly in the delta-, alpha-, beta-, and gamma-frequency bands.

58 en all electrode combinations for difference frequency bands.

59 ct time scales in the theta, beta, and gamma frequency bands.

60 wer spectrum analyses in pre-established low-frequency bands.

61 istinct peaks in the theta, alpha, and gamma frequency bands.

62 stronger when integrating oscillations over frequency bands.

63 ted to I.Q. especially in the alpha and beta frequency bands.

64 neural phase in the delta, theta, and alpha frequency bands.

65 n different regions is reflected in distinct frequency bands.

66 ts in different functional brain systems and frequency bands.

67 strongly entrains EEG slow waves in a narrow frequency band (0.75-1.5 Hz) only when thalamic T-type c

68 lculated and divided into the following four frequency bands: 0.01-0.027 Hz, 0.027-0.073 Hz, 0.073-0.

69 ifically, we observe sensitivity to multiple frequency bands (1) at exactly one octave distance from

70 nning temporal window) across four different frequency bands (1, 2, 4, and 6 kHz).

71 us induces oscillations in the gamma-to-beta frequency band (13-100 Hz) and can induce long-term pote

72 e has characteristic alterations in the beta frequency band (13-30 Hz) in the basal ganglia-thalamoco

73 Corticomuscular coherence in the beta frequency band (15-30 Hz) has been demonstrated in both

74 nal networks operating in the classical beta frequency band, 15-30 Hz.

75 is (large ground finch), singing in the same frequency band (2-4 kHz), colonized Daphne in 1983 and i

76 y increased power in a multiple of slow-wave frequency bands (2-4 Hz and 4-6 Hz) in the parietal cort

77 stability of the EEG power in the slow-wave frequency bands (2-4 Hz, 4-6 Hz, and 6-8 Hz) of adolesce

78 preferentially synchronized in the high beta frequency band (~20-30 Hz) in response to somatosensory

79 BCs primarily occurred within the low gamma frequency band (25-50 Hz).

80 Furthermore, LFP oscillations in the gamma frequency band (30-80 Hz) are amplitude modulated in pha

81 ally, rhythmic network activity in the gamma-frequency band (30-80 Hz) was significantly decreased in

82 ound that neuronal oscillations in the gamma frequency band (30-80 Hz) were preferentially disrupted

83 with local population activity in the gamma frequency band (30-80 Hz).

84 cortical neuronal oscillations in the gamma frequency band (30-80 Hz, gamma oscillations) have been

85 ar field activity primarily within the theta frequency band (4-12 Hz).

86 Neural activity in the theta-frequency band (4-8 Hz) was enhanced before presentation

87 terion performance, is specific to the gamma frequency band (65-85 Hz), and is independent of changes

88 with a single prominent peak in the 4-12 Hz frequency band (7.7 +/- 0.1 Hz, n = 60).

89 is preferentially synchronized in the alpha frequency band (~7-12 Hz) in response to auditory stimul

90 ent response component within the high gamma frequency band (75-150 Hz) was identified.

91 5 degrees, multispectral images across the X frequency band (8 GHz-12 GHz), and a time resolution of

92 e spatial distribution of power in the alpha frequency band (8-12 Hz) can be used to decode the conte

93 essed by means of EEG coherence in the alpha frequency band (8-12 Hz).

94 ed characteristic temporal patterns for each frequency band across consciousness and anesthesia.

95 on the temporal pattern of hippocampal high-frequency band activity in single hippocampal contacts.

96 ly registers specific electrical oscillatory frequency band activity, suggesting that fMRI may be abl

97 ce on choice, whereas power in task-specific frequency bands affected the encoding of sensory evidenc

98 ding and persist across different states and frequency bands (albeit with slightly different characte

99 enhance theta rhythm and suppress peri-theta frequency bands, allowing theta oscillations to dominate

100 he degree of behavioral modulation by either frequency band alone.

101 comprises a shift in relative power from low-frequency bands (alpha and beta) to the gamma band.

102 r patterns of information flow in the higher-frequency bands (alpha1, alpha2, and beta band), dominat

103 Besides traditional frequency-band analysis, we also presented a new individ

104 omagnetic fields is not confined to a narrow frequency band and birds tested far from sources of elec

105 was observed specifically in the 20-40-hertz frequency band and specifically between the distal part

106 vity abnormalities in ASD were the mediating frequency band and whether the network included frontal

107 e identified significant interaction between frequency bands and groups in the inferior occipital gyr

108 on of resting-state oscillations in multiple frequency bands and in the timing-error sequences.

109 We examined reinstatement in individual frequency bands and individual electrodes and found that

110 activity across theta, alpha, beta and gamma frequency bands and show that their activation likely im

111 easures correlated with ASD severity in some frequency bands and spatially specific subnetworks.

112 ffects in terms of the perceptually relevant frequency bands and state parameters (phase/power).

113 increased neuronal synchrony across several frequency bands and the emergence of theta-gamma couplin

114 hip between neural oscillations in different frequency bands and the maintenance of information in wo

115 Oscillatory activities across multiple frequency bands and their cross-frequency interactions w

116 s both subjects and sensors that varied over frequency bands and was more pronounced in controls than

117 significantly by 1.5-fold across the entire frequency band, and phase shifted ~5 degrees at frequenc

118 therapy owing to its tight focal spot, broad frequency band, and stable excitation with minimal ultra

119 ting devices usually occurs only in a narrow frequency band, and the asymmetric frequencies are alway

120 s transient bursts in distinct high- and low-frequency bands, and it is not yet clear how these burst

121 triggered by step onsets, sine waves in two frequency bands, and noise.

122 was a greater right IFG response in the beta frequency band ( approximately 16 Hz) for successful ver

123 In 'go' trials, LFP activity in the beta frequency band ( approximately 20 Hz) decreased prior to

124 zed by excessive synchronization in the beta frequency band ( approximately 20Hz) throughout basal ga

125 graded activation profiles evoked by single-frequency bands are correlated with attentionally driven

126 Rhythmic activity in the beta frequency band, around 20 Hz, has been reported in recen

127 ng inputs oscillate incoherently in the same frequency band as the target, communication accuracy is

128 generate population rhythms within the same frequency bands as neocortex suggests that they act as a

129 a computational model to show that the beta1 frequency band, as found in rat association cortex, has

130 gnals are similar and differ only in a small frequency band at 2 kHz present in the chirping species.

131 another and with instrumental records in the frequency bands at which they overlap.

132 alent in the motor system occurs in the beta frequency band, at about 20 Hz.

133 ions used for imaging and analysis (0.1-1 Hz frequency band), autofluorescence and hemodynamic effect

134 rk, we implement such a profile over a broad frequency band based on a novel idea of space-frequency

135 fter the target onset, and a decrease of all frequency bands before response followed by an increase

136 Although two principal frequency bands--beta (15-30 Hz) and gamma (60-90 Hz)--h

137 , we show coherent oscillations in the delta frequency band between parietal and frontal cortices dur

138 In both, pure optical rotation occurs in a frequency band between two transmission minima, where al

139 stence of Ferrell-Berreman (FB) modes within frequency bands bounded by points of ZGV with the goal t

140 that attention is not related to any single frequency band but that each network has a distinct osci

141 Hz) cyclical modulations in LFP power in all frequency bands but with large and variable phase differ

142 is the promotion of reactivity in the gamma frequency band, but it remains unclear whether the latte

143 ivity patterns in ASD are driven by specific frequency bands, by spatial network properties, or by so

144 All of these frequency bands can be theoretically predicted to realiz

145 wing detection of temperature variability in frequency bands characteristic of the AMO over the past

146 ctroencephalogram (EEG) changes in the theta-frequency band correlated with inferior communication pe

147 ining the neuronal correlate of specific HFO frequency bands could improve electroencephalographic an

148 to maintain oscillatory activity in specific frequency bands could thus result in the information ove

149 served spectral patterns among the canonical frequency bands (delta 0-3 Hz, theta 3-7 Hz, alpha 7-13

150 e examined brain activity in three different frequency bands: delta, theta, and alpha.

151 While healthy subjects exhibited a specific, frequency band-dependent, large-scale neural organizatio

152 ersistent pattern of connections that form a frequency-band-dependent network template, and a set of

153 These results suggest that a metastable, frequency-band-dependent scaffold of brain connectivity

154 The various frequency bands determine the dynamic gating regimes ena

155 physiological oscillatory activity within a frequency band dictated by the rhythm of the stimulation

156 zation at a 3-9 Hz theta and a 12-30 Hz beta frequency band during the delay and preparation periods

157 nd primary sensory neocortex occurs in these frequency bands during inattention.

158 so showed less attenuation of power at these frequency bands during rest-to-task transition.

159 mal to center fundamental tones at different frequency bands during the call series.

160 Neural-phase effects were specific to the frequency bands entrained by the rhythmic stimulation.

161 -band changes in the EEG without predefining frequency bands, evidence was found for transient freque

162 ipal components analysis derived data-driven frequency bands evoked power.

163 avioral comodulation by neural phase in both frequency bands exceeded the degree of behavioral modula

164 e global and highly coherent; moreover, this frequency band exhibited a striking increase in anterior

165 OPs in the ERG of primates fall in two frequency bands: fast OPs with a peak frequency around 1

166 The lens can work within a certain frequency band for which the ratio between the bandwidth

167 we observe a graded shift of power to higher-frequency bands for BAs further removed from the primary

168 nnectivity both within and between classical frequency bands ([Formula: see text], [Formula: see text

169 The thermal (emitted) infrared frequency bands, from 20-40 THz and 60-100 THz, are best

170 display functional interactions in the lower frequency bands, gamma-band activity in the alert monkey

171 dimensions and material parameters to create frequency band gaps are examined.

172 that supports the formation of wide and low-frequency band gaps, while simultaneously reducing their

173 erturbative theoretical model predicting the frequency band-gaps of periodic plates with sinusoidal c

174 ased after eye-opening, especially in higher frequency bands (>30 Hz).

175 Oscillatory activity in the beta frequency band has been shown to be modulated during the

176 Rhythmic neuronal activity of multiple frequency bands has been described in many brain areas a

177 ucleus, with those drives in the higher beta frequency band having much shorter net delays to subthal

178 Maps were created independently for a high-frequency band (HFB) (76-100 Hz) and a low-frequency ban

179 ortical response strength as indexed by high-frequency band (HFB) activity (70-150 Hz) amplitude reve

180 cortical activity is well-indexed by higher-frequency bands [high-gamma band (Hgamma): 80-150 Hz].

181 e suboptimal for in vivo characterization of frequency bands higher than 1-3 Hz.

182 D children showed less EEG power in very low frequency bands (i.e., .02-.2Hz).

183 mented via synchronized activity in the beta frequency band in a right IFG/basal ganglia network, wit

184 tions of brain oscillations in the EEG alpha frequency band in posterior cortex can dissociate curren

185 The high-frequency band in spectral analysis of heart rate variab

186 ad higher neuronal oscillations in the delta frequency band in the 100 Schizophrenia patients as comp

187 line availability on hippocampal oscillatory frequency bands in 12 month-old male and female rats.

188 ociated with cognitive deficits in different frequency bands in 25 PP-MS patients (12 M, mean age 50.

189 ntracranial current density for standard EEG frequency bands in 82 unmedicated adults with MDD, using

190 connectivity and variability across multiple frequency bands in brain networks underlying cognitive d

191 Oscillations are observed at various frequency bands in continuous-valued neural recordings l

192 icular domain of visual perception, specific frequency bands in different brain regions and networks,

193 (1) increased ERO energy in delta and theta frequency bands in Fctx, (2) reduced gamma ERO energy in

194 fied by using root mean square (RMS) for two-frequency bands in five horizontal and four vertical loc

195 00-900 Hz were found to be the most reliable frequency bands in healthy children.

196 atory activity in the low-beta and low-gamma frequency bands in sensory detection, perception, and re

197 ssociated with increased activity in the low-frequency bands in the electroencephalogram (EEG).

198 esynchronization extending across a wide low-frequency band including delta, theta, and alpha.

199 It has been suggested that different frequency bands index distinct canonical computations.

200 riable across patients in terms of areas and frequency bands involved, and in direction of power chan

201 pagation of sensory information use distinct frequency bands is an appealing assumption for which evi

202 brain regions overtly synchronize in narrow frequency bands is critical for understanding disease pr

203 thin the alpha (8-12 Hz) and beta (15-25 Hz) frequency bands is modulated during actual and imagined

204 The functional significance of these frequency bands is supported by the variation in the str

205 erfect synchronization, observed in the beta frequency band, is believed to be related to the hypokin

206 These data support the concept that each frequency-band lamina in the ICC may comprise several fu

207 rganization of the SG-to-CN projections into frequency band laminae is clearly evident despite severe

208 h-frequency band (HFB) (76-100 Hz) and a low-frequency band (LFB) (8-32 Hz) for several different mov

209 recordings are typically separated into two frequency bands: local field potentials (LFPs) (a circui

210 SOM cell spiking reduces the spontaneous low-frequency band (<30-Hz) oscillations and selectively red

211 Activity in these slow frequency bands may reflect a neural substrate for corti

212 ions, the envelope, after decomposition into frequency bands, may be enhanced by sparse transformatio

213 Within the alpha frequency band, misclassification analysis produced evid

214 ng working memory (WM), specific oscillatory frequency bands modulate in space and time.

215 in malignant musculoskeletal tumours at the frequency band of 0.073-0.198 Hz.

216 tions were significantly coherent in a broad frequency band of 5-30 Hz.

217 0.9; p = 0.02) and relative power of a high frequency band of heart rate variability (adjusted odds

218 Change in the high-frequency band of heart rate variability, an estimate of

219 ew model naturally accounts for the observed frequency band of hiss, its incoherent nature, its day-n

220 Power in the theta-frequency band of the local field potentials also decrea

221 al sector was carried primarily in the theta frequency band of the response.

222 king masker energy is added well outside the frequency band of the target, and comodulated with the o

223 ed robust coupling between the high- and low-frequency bands of ongoing electrical activity in the hu

224 tedly recurred since its conception: limited frequency bands of operation.

225 k speed of 2.45 GHz to satisfy the principal frequency bands of smart phones such as those for cellul

226 esponses and the amplitude and power in most frequency bands of the evoked LFPs and reduced the rostr

227 nd to correlate preferentially with specific frequency bands of the LFP, it is still unclear whether

228 piking to 3-7 Hz (theta) and 12-20 Hz (beta) frequency bands of the local field potential (LFP).

229 We found deviance-related responses in both frequency bands over lateral temporal and inferior front

230 nce of strong signal power increases in some frequency bands over the course of sleep deprivation may

231 increase of 43% in the power of the 12-25 Hz frequency band (P = 0.007).

232 l correlates with the power coherence in low-frequency bands, particularly the delta band.

233 Brain oscillations across all frequency bands play a key role for memory formation.

234 t that the oscillatory activity in the alpha frequency band plays a central role in the active storag

235 functional architecture were alterations in frequency band power, variance, covariance, and phase-po

236 al and expected picture interval in the high-frequency band predicted picture-naming latencies.

237 hippocampus we found more power in the high-frequency band prior to high-expected pictures than weak

238 independent of changes in the theta or beta frequency band range.

239 onstrated oscillations in the alpha and beta frequency bands, reactive to self-paced movement.

240 EMG-EMG coherence in the beta and gamma frequency bands recorded from tibialis anterior muscle i

241 Therefore, the HFO frequency band reflects a range of firing dynamics of hi

242 y in neural processing, in particular in low-frequency bands, regardless of whether the deviant tone

243 studied via echo revivals, occurs in narrow-frequency bands related to differences in Larmor precess

244 ent: the variation in sound pressure in each frequency band, relative to the mean pressure.

245 amplitudes, in the approximately 150-200 Hz frequency band, reliably reflect spatial constellations

246 lish in male and female listeners that human frequency-band-selective attention drives activation in

247 bility, within and across multiple entrained frequency bands, shapes the effective neural processing

248 udy, we investigated whether these different frequency bands show a differential relation with the la

249 of corticomuscular coherence in the 20-40 Hz frequency band showed a significantly larger coherence f

250 s network's activity confirmed that no other frequency band showed equivalent results.

251 The exploratory SWRs showed peak frequency bands similar to those of quiescent SWRs, and

252 P phase and amplitude was independent within frequency bands, since the joint information exhibited n

253 d significantly greater power in the highest frequency band (slow-3: 0.073-0.198 Hz) after ingestion

254 neous neural activity in the three different frequency bands (slow-5:0.01-0.027 Hz; slow-4:0.027-0.08

255 detect gaps depended on different numbers of frequency bands--sometimes one, sometimes two, and somet

256 stribution was studied as a function of four frequency bands, spanning the full BOLD bandwidth.

257 NAC DBS produce distinct region-specific and frequency band-specific changes in LFP oscillations.

258 ariate pattern misclassification analysis of frequency band-specific local topographical patterns in

259 es have suggested the relation of particular frequency bands such as theta (4-8 Hz), alpha (8-14 Hz),

260 e Anterior Cingulate Cortex (ACC) in the low frequency band suggesting the presence of a cortical net

261 ation between delta, theta, alpha1 and gamma frequency bands that is significantly stronger in the ti

262 s in EEG amplitude and power in all analyzed frequency bands that occurred simultaneously with cerebr

263 Changes in the number of frequency bands that predict perception are a hallmark o

264 raction-dependent distributions of energy in frequency bands that span the range of vibrotactile sens

265 d enhanced intertrial coherence in the theta frequency band, the LDN corresponded to a period of even

266 Unlike coherence in the higher frequency bands, the distribution of the phase at peak t

267 onveyed only by the speech ENVs from several frequency bands; the speech TFS within each band was rep

268 e LFP phase coupling was decreased for lower frequency bands (theta and alpha) but slightly increased

269 leptiform spikes, the relative power of five frequency bands (theta, alpha, beta, low gamma, and high

270 Pe and SNr shifted from the pathological low-frequency band to the stimulation frequency during high-

271 nd the analysis of ITD representation across frequency bands to a large neural population, we employe

272 Neurons could synchronize in different frequency bands to form assemblies operating in differen

273 G frequency range in SWS, and left other EEG frequency bands unchanged.

274 orary research indicates that the alpha-beta frequency band underlies top-down control, whereas the g

275 notably, there are sudden jumps between two frequency bands used for either echolocation or communic

276 asonic hearing to minimize congestion in the frequency bands used for sound communication and to incr

277 fference (P = .002) was found in one of four frequency bands used to analyze the cochlear response; h

278 le (125-250 Hz) and fast ripple (250-500 Hz) frequency bands using intracranial recordings from 12 pa

279 rom tibialis anterior muscle in the 20-40 Hz frequency band was also significantly larger for the 9-2

280 s period, the oscillatory phase in the theta frequency band was informative about both task processin

281 vely during task performance times when each frequency band was most strongly modulated, and only aft

282 of representational area gain for the signal frequency band was significantly positively correlated w

283 retrieval this difference in timing between frequency bands was absent.

284 is end, functional connectivity in different frequency bands was assessed with phase locking value in

285 We found that ERD within both frequency bands was consistently stronger, arose faster,

286 The delta spectral power relative to higher frequency bands was highest for secondarily generalized

287 wer in high- (60-150 Hz) and low- (25-40 Hz) frequency bands was significantly correlated with arm mo

288 oscillations in the delta, theta, and gamma frequency bands, we compared the D1- and D2-dopamine-rec

289 Based on connectivity within canonical frequency bands, we found that patient networks had redu

290 Power decreases in the beta frequency band were consistently observed following audi

291 interrupted, and asynchronously interrupted frequency bands were constructed that constituted speech

292 OPs in two distinct frequency bands were discriminated in the monkey mfERG:

293 In addition, all frequency bands were significantly different between NRE

294 t role for synchronous activity in the delta frequency band when large-scale, distant cortical networ

295 nt oscillatory synchronization at restricted frequency bands, whereas synchronized oscillatory neuron

296 x to integrative frontal areas in the higher-frequency bands, which is mirrored by a theta band anter

297 amplified local neural synchrony in the beta frequency band while others either suppressed it or did

298 narrow band amplifiers operating in the VHF frequency band with power gains as high as 14 dB.

299 ANOVA was conducted for each frequency band with the following two factors: the locat

300 oscillations in both the 3.1-Hz and 5.075-Hz frequency bands, with the best performance occurring whe