ライフサイエンスコーパス: oscillation

1 justed ensemble-mean forecast North Atlantic Oscillation.

2 l forcing rather than any intrinsic internal oscillation.

3 ggests the influence of the El Nino/Southern Oscillation.

4 s in the correct phase of the quasi biennial oscillation.

5 ma band activity nested within a delta/theta oscillation.

6 with a positive phase of the North Atlantic Oscillation.

7 tic-induced hypnosis and underlying neuronal oscillations.

8 tivity promote channel opening and intensify oscillations.

9 power of cholinergically induced slow gamma oscillations.

10 driving dynamical gene expression, including oscillations.

11 frequency did not entrain ultralow-frequency oscillations.

12 ted by the synchronisation of ongoing neural oscillations.

13 buffer in the SR enhances the appearance of oscillations.

14 with a role in generating cardiorespiratory oscillations.

15 with a gradual increase in the coherent beta oscillations.

16 n the induction mechanisms of cortical gamma oscillations.

17 of brain activity - namely the frequency of oscillations.

18 the actively beating cilia can entrain cilia oscillations.

19 the transition from in-phase to out-of-phase oscillations.

20 s were observed in protein expression during oscillations.

21 integration engages top-down theta and beta oscillations.

22 icity, cortical processing, brain states and oscillations.

23 pecific memories associated with local sleep oscillations.

24 negativity' response and transiently induced oscillations.

25 dilation and attenuation of occipital alpha oscillations.

26 lectrical activity and cytosolic free Ca(2+) oscillations.

27 model struggled to predict extreme and fast oscillations.

28 s reuniens at the UP state onset during slow oscillations.

29 n, yet ORAI1 is dispensable in generation of oscillations.

30 subcircuits within the phase space of theta oscillations.

31 ivity was associated with a decrease in slow oscillations (0.1-2 Hz) throughout the cortex, and spont

32 ortical gamma connectivity (25-155 Hz), slow oscillations (0.5-1 Hz), and complexity (<175 Hz).

33 ecrease pathological basal ganglia (BG) beta oscillations (10-17 Hz in primates), suggesting that bet

34 Studies have shown that gamma oscillations (30-100 Hz) are relevant for neurocircuit f

35 Here, a small voltage potential oscillation across a newly designed electro-chemical cat

36 Our results implicate theta oscillations across the MTL as a common neurophysiologic

37 tion (ENSO), the North Atlantic Multidecadal Oscillation (AMO), and tropical cyclone counts (TC).

38 Strong decrease of oscillation amplitude A is observed with the tilt: [Form

39 ability peaks, an effect that increases with oscillation amplitude, establishing a functional link be

40 methods in detecting rhythms with decreasing oscillation amplitudes and in recovering phase shift.

41 opy is applied to assess the symmetry of the oscillation and evaluated subjectively.

42 ciated both with increased narrow-band theta oscillations and a broad-band tilt of the power spectrum

43 beta inhibition reverses both abnormal gamma oscillations and behavioral deficits with high correlati

44 SK3A knockdown, also reversed abnormal gamma oscillations and behavioral deficits.

45 g rest, trisomic mice showed increased theta oscillations and cross-frequency coupling in the PFC and

46 -frequency domain to assess stimulus-induced oscillations and cross-layer phase synchrony.

47 ating the influence of color on visual gamma oscillations and how these observations may relate to lo

48 nt decrease (p < 0.001) in the power of slow oscillations and increase (p < 0.001) in cortical comple

49 of ryanodine receptor 2 (RyR2)-mediated Ca2+ oscillations and inositol 1,4,5-triphosphate receptor (I

50 flectivity measurements yield extensive Laue oscillations and Kiessig thickness fringes for films gro

51 blish dissociable roles for prefrontal theta oscillations and parietal alpha oscillations in the cont

52 splayed two preferred firing phases in theta oscillations and preferentially participated in reverse

53 reaches the rear, inducing transient GTPase oscillations and RhoA activity spikes.

54 that the prevention of gene pairing disrupts oscillations and segmentation, and the linkage of her1 a

55 walls is driven by low-frequency arteriolar oscillations and suggest that age-related reduction of t

56 Typically, oscillations and synchronization take place concurrently

57 lls within the beta-cell network drive islet oscillations and that electrically silencing or opticall

58 with anticipatory states of attenuated alpha oscillations and the CNV.

59 ntity, as follows: attenuation of alpha-band oscillations and the contingent negative variation (CNV)

60 demonstrated using the examples of nonlinear oscillations and the Kepler problem.

61 ency interactions between finely tuned gamma oscillations and the stimulation frequency may suggest a

62 so need to preserve or enhance cortical slow oscillations and their coordination with thalamic spindl

63 ST(+) interneurons in slow hippocampal gamma oscillations, and further suggest that intense activatio

64 The amplitude, the frequency of oscillations, and the DW velocity depend on the number o

65 NOX4 silencing suppressed Ca(2+) oscillations, and the patch-clamped K(ATP) channel opene

66 a functional E/I ratio (fE/I) from neuronal oscillations, and validate it in healthy subjects and ch

67 ehavior increases the parameter region where oscillations appear and provides a gradual transition fr

68 Gamma oscillations are a prominent activity pattern in the cer

69 s subjects supporting a model by which theta oscillations are excitatory to neural activity, and alph

70 are excitatory to neural activity, and alpha oscillations are inhibitory.

71 humans have indicated that hippocampal theta oscillations are lower in frequency and less prevalent t

72 Because such oscillations are nonvocal in most nonhuman primates, the

73 Intriguingly, oscillations are not linked to translational control, as

74 ms regulating slow (<1 Hz) forms of thalamic oscillations are not well understood.

75 In conclusion, sleep oscillations are promising targets for improving memory

76 These oscillations are reminiscent of sleep slow waves (SW) an

77 When baseline oscillations are weak, the stimulated area exhibits enha

78 reducing physiological tremor by suppressing oscillations around 10 Hz.

79 our results identify and characterize alpha oscillations as a cortical signature of representations

80 or example, the magnitudes of sensory-evoked oscillations, as measured by auditory steady-state respo

81 he firing rate of cortical neurons and gamma oscillations, as well as improved cognition.

82 Here, we show that a Plk4 oscillation at the base of the growing centriole initiat

83 revious research has suggested that neuronal oscillations at different frequency bands are associated

84 Inter-areal synchronization of neuronal oscillations at frequencies below ~100 Hz is a pervasive

85 ing virtual movement, we observe hippocampal oscillations at multiple frequencies from 2 to 14 Hz.

86 Thus, vLGN can engage its targets using oscillation-based and conventional rate codes.

87 Although oscillation-based FC is classically defined relative to

88 In conclusion, the spatial organization of oscillation-based FC is largely stable over cognitive st

89 es of distributed spatial patterns show that oscillation-based FC is omnipresent, occurring even in t

90 Thus, the issue of whether oscillation-based FC is primarily shaped by cognitive st

91 ctional connectivity of neural oscillations (oscillation-based FC) is thought to afford dynamic infor

92 During oscillations between 30 degrees C and 37 degrees C, cell

93 easure projection analyses to compare neural oscillations between individuals with cLBP who experienc

94 unctional connectivity (FC) of resting-state oscillations between pairs of 330 cortical regions and 1

95 as canonical chromothripsis profiles display oscillations between two copy-number states, a considera

96 .e., structure and meaning) organizes neural oscillations beyond the timescale and rhythmicity of the

97 0) and k(tr) to control values and abolished oscillations, but phosphorylated (p)-rC0C7-sc did not co

98 We also observe slower ~3 Hz oscillations, but these signals are more prevalent in th

99 We found greater attenuation of alpha oscillations by tVNS than by sham stimulation.

100 dissociation between 2-5 Hz and 5-9 Hz theta oscillations, by which power increases in 2-5 Hz oscilla

101 athematical modeling indicates that the Plk4 oscillation can be generated by a time-delayed negative

102 air bundle stiffness, and spontaneous bundle oscillation can occur within seconds after Ca(2+) chelat

103 ally how bistability, biphasic responses and oscillations can be generated by minimal augmentations t

104 These cortical gamma oscillations can be indexed by the gamma-band auditory s

105 sion whereas the induction of cortical gamma oscillations can reduce amyloid load and improve cogniti

106 en blood flow signals and respiratory and PB oscillations clearly demonstrate contrasting origins of

107 ulated right-lateralized fronto-visual theta oscillations compared to those observed in left fronto-v

108 The frequency of these oscillations corresponds to the strength of the antiferr

109 by the blood, and vasomotion-like 0.1-0.3 Hz oscillations could also be generated.

110 With intact cortex, theta and gamma oscillations could be reliably elicited in V1 and V4 whe

111 c mice, we reveal how stimulus evoked Ca(2+) oscillations couple to contractions in basal epithelial

112 asound imaging to quantify transverse muscle oscillations (deep-superficial displacement of the muscl

113 NNs induces a decrease in gamma activity, an oscillation dependent on PV+ cells, in the mPFC of anest

114 TATEMENT The generation of hippocampal gamma oscillations depends on synchronized inhibition provided

115 ndings suggest that low-frequency arteriolar oscillations drive drainage of solutes.

116 otivating research to understand how climate oscillations drive host health and disease.

117 yet to be direct in vivo measures of muscle oscillations during locomotion.

118 t produce an action tremor by causing signal oscillations during movement.

119 at state anxiety alters the dynamics of beta oscillations during reward processing, thereby impairing

120 hase lock to ongoing slow-frequency (1-7 Hz) oscillations during WM maintenance.

121 , 2016, 2020; Martin and Doumas, 2017) where oscillations encode endogenously generated linguistic co

122 k between variations in the El Nino-Southern Oscillation (ENSO) and GMSL.

123 oss frequently occur during El Nino-Southern Oscillation (ENSO) events originating in the Eastern Tro

124 Forecasting the El Nino-Southern Oscillation (ENSO) has been a subject of vigorous resear

125 The El Nino Southern Oscillation (ENSO) is highly dependent on coupled atmosp

126 El Nino-Southern Oscillation (ENSO) is the dominant interseasonal-interan

127 The El Nino-Southern Oscillation (ENSO) shapes global climate patterns yet it

128 cale oscillations including El Nino Southern Oscillation (ENSO), North Atlantic Oscillation (NAO), an

129 lopmental region (MDR), the El Nino-Southern Oscillation (ENSO), the North Atlantic Multidecadal Osci

130 El Nino-Southern Oscillation (ENSO), which is one of the main drivers of

131 ies, the "Blob" and extreme El Nino Southern Oscillation (ENSO).

132 ch occurred during the 2015 El Nino Southern Oscillation event.

133 vibrational spectral weight associated to Ag oscillations evolving into stochastic decaying fluctuati

134 These oscillations exhibited a significant phase reset that al

135 signalling controls the phase and period of oscillations, expanding the role of this pathway beyond

136 tors in the regime of large-amplitude steady oscillations experimentally and as well theoretically.

137 sical model to simulate different vocal fold oscillations, extended the openly available BAGLS datase

138 -mediated augmentation of spike-like calcium oscillations first promoted stable expression of ASCL-1

139 tively associated with lagged North Atlantic Oscillation for seals at NR and (b) positively associate

140 rence in a band containing regions' baseline oscillation frequencies.

141 des a brief, but pronounced, prolactin peak, oscillation frequency remains stable.

142 tability, speed, and coherence of cell cycle oscillation, from which the different vital phases of th

143 e-operated Ca(2+) entry, on cytosolic Ca(2+) oscillations generated by receptor stimulation or on CRA

144 ded behavior, but it is unclear whether this oscillation has causal significance.

145 Our data suggest that gamma oscillations have a role in the pathophysiology of the a

146 Gamma oscillations have been argued to support visual percepti

147 In contrast, faster activities and oscillations have been considered to be largely local-ci

148 Spontaneous neural oscillations have emerged as a key predictor of trial-to

149 ve control; however, whether distinct neural oscillations have similar or different functions for cog

150 Oscillations have traditionally been studied at the neur

151 High frequency oscillations (HFOs) are newer biomarkers for epileptogen

152 generalization is linked to decreased alpha oscillation in medial frontal channels.

153 display circadian rhythmicity resulting from oscillation in the genes involved in AS and APA.

154 tofrontal cortex (OFC), there is a prominent oscillation in the theta frequency (4-8 Hz) during rewar

155 ted dusk, and are superimposed on daily 24 h oscillations in [Ca(2+) ](cyt) .

156 precipitation was obtained accompanied by pH oscillations in a well-stirred, closed reactor.

157 The data indicate that metabolic oscillations in acetogen gas fermentation are controlled

158 making it capable of producing physiological oscillations in addition to the epileptiform activity.

159 clear phenotypic heterogeneity of circadian oscillations in clonal cell populations to investigate t

160 ion and increases the power of ex vivo gamma oscillations in conventionally housed mice.

161 In humans, gamma oscillations in cortical motor areas reflect asynchronou

162 muscarinic receptor-mediated high-frequency oscillations in cortical regions.

163 attention tasks, but it is unclear if neural oscillations in insects are selectively correlated to di

164 ous proteins subject to cell cycle-dependent oscillations in levels and organization.

165 Since immune cells display oscillations in numbers and function throughout the day,

166 oscillations in prefrontal cortex and alpha oscillations in parietal cortex, respectively.

167 ression task demands designed to drive theta oscillations in prefrontal cortex and alpha oscillations

168 ng viral lattice assembly and recapitulating oscillations in protein expression levels for a circadia

169 Beta frequency oscillations in scalp electroencephalography (EEG) recor

170 l1 function is necessary for daily molecular oscillations in skin fibroblasts and liver slices.

171 Circadian oscillations in spontaneous action potential firing in t

172 Modulations of oscillations in the alpha to beta range in task-relevant

173 rontal theta oscillations and parietal alpha oscillations in the control of internally maintained WM

174 sal linked to the occurrence of synchronized oscillations in the electroencephalogram (EEG).

175 onal-translational feedback loops, producing oscillations in the expressions of genes and proteins to

176 d that LOB was correlated with low-frequency oscillations in the field potentials and spikes at the t

177 Neuronal oscillations in the frontal cortex have been hypothesize

178 We found that ripple oscillations in the human cortex reflect underlying burs

179 puts arriving at the excitable phase of beta oscillations in the motor cortex are known to lead to mu

180 nied with more prominent delta and theta EEG oscillations in the mutant mice, and reached burst-suppr

181 Sleep oscillations in the neocortex and hippocampus are critic

182 ssociated with low-frequency, high-amplitude oscillations in the peri-infarct zone in both rodents an

183 tionally, the power of local field potential oscillations in the theta and gamma frequency bands, whi

184 ) that specific microbiota members show 24-h oscillations in their relative abundance and identified

185 e SC, but not dLGN, visual stimuli entrained oscillations in vLGN, perhaps reflecting shared strategi

186 c surface temperature anomalies coexist with oscillations in wave direction, which indicates the infl

187 by climate, one must account for large-scale oscillations including El Nino Southern Oscillation (ENS

188 tal and avertin, but both still showed daily oscillations independent of biological sex.

189 The Pacific Decadal Oscillation index showed a positive correlation with the

190 al role in mediating the regenerative Ca(2+) oscillations induced by physiological receptor activatio

191 Concomitantly, task-associated gamma band oscillations induced by trains of auditory stimuli, or e

192 d periodic and long-lived electron cyclotron oscillations inside the magnetic field of the objective

193 onto this scaffold in order to turn such jaw oscillations into vocalized syllables.

194 Cortical tremor is a fine rhythmic oscillation involving distal upper limbs, linked to incr

195 but under high dopaminergic tone, this beta oscillation is interrupted by delta/theta-periodic burst

196 improved, suggesting that the North Atlantic Oscillation is not driven solely by Atlantic multidecada

197 A hallmark of healthy vocal fold oscillation is the symmetric motion of the left and righ

198 e disruption of pathologically enhanced beta oscillations is considered one of the key mechanisms med

199 The robustness of these oscillations is determined by the amount of calsequestri

200 A component of these oscillations is generated centrally, with respiratory ne

201 ffect of critical illness on gene expression oscillations is unknown.

202 that allows quantification of the vocal fold oscillation, is more commonly employed in research due t

203 In between, calcium oscillations may appear.

204 Neural oscillations may be a key signature for focal object ind

205 nked to an increase in intracellular calcium oscillation mediated by ryanodine receptor (RyR).

206 d by the frequency of the star's fundamental oscillation mode (f-mode).

207 multivariate analysis, and spindle and slow oscillation morphology and coupling.

208 The North Atlantic Oscillation (NAO) is the major atmospheric mode that con

209 Southern Oscillation (ENSO), North Atlantic Oscillation (NAO), and Pacific Decadal Oscillation (PDO)

210 cillation (PDO) index and North Pacific Gyre Oscillation (NPGO) index have changed over multidecadal

211 sis in V1 revealed that both theta and gamma oscillations occurred primarily in the supragranular lay

212 linked 26 metabolic pathways to the diurnal oscillation of gut bacteria.

213 in addition to its role in driving circadian oscillations of [Ca(2+) ] in the cytosol and chloroplast

214 ightings are capable of producing sinusoidal oscillations of any frequency and phase, adding to the g

215 f the clock pathway that regulates circadian oscillations of gene expression.

216 Here, we report phase-coherent oscillations of out-of-plane magnetoresistance in the la

217 MS cooling decreased theta frequency oscillations of place cells and reduced distance-time co

218 put may modulate synchrony and low-frequency oscillations of SNr neurons, which we confirm using opto

219 (2020) reveal that inverse oscillations of synaptic inhibition and excitation lead

220 'artificial' confounding, including cyclical oscillations of the 'dirty-cage/excrement microbiome', w

221 , rotation and amorphization-crystallization oscillations of the Au clusters.

222 ion from the qubit by recording quantum Rabi oscillations of the qubit through single-photon detectio

223 ll as those of the mouse(4)-recapitulate the oscillations of the segmentation clock.

224 both magnitude and frequency in the measured oscillations of the soleus muscle; one of the main human

225 smatched the expected underlying task-driven oscillations of the targeted region.

226 nockout mice, both tissues exhibited 24-hour oscillations of the transcriptome, proteome, and phospho

227 st that beneficial effects of cortical gamma oscillations on Alzheimer's disease pathology can depend

228 The net fluidic flow due to the bubble oscillation orients the microrobot's axisymmetric axis p

229 These oscillations originate from an Fe-ligand stretching vibr

230 of a two-band t-J model reveal that the THz oscillations originate from the interplay between local

231 Functional connectivity of neural oscillations (oscillation-based FC) is thought to afford

232 itability, mu (9-14 Hz), and beta (15-25 Hz) oscillations over sensorimotor cortex.

233 Arabidopsis transcriptome, finding that the oscillation patterns of different transcripts of multitr

234 conditions mapping onto the Pacific Decadal Oscillation (PDO) index and North Pacific Gyre Oscillati

235 antic Oscillation (NAO), and Pacific Decadal Oscillation (PDO).

236 re found to be driven by the Pacific Decadal Oscillation (PDO).

237 yered delafossites PdCoO(2) and PtCoO(2) The oscillation period is equivalent to that determined by t

238 le-flux tunnelling (flux qubit(8)) and phase oscillations (phase qubit(9) or transmon(10)).

239 These findings suggest that cortical gamma oscillations play a beneficial role in modulating the LT

240 individual slow wave slope and frontal fast oscillation power.

241 a ramp-up in the number of neocortical slow oscillations preceding spasms, which was also observed i

242 appear to favor an effect of tDCS on neural oscillations rather than spiking, and findings that tDCS

243 el-treated rats exhibited a robust circadian oscillation, reaching the nadir during the daytime (inac

244 of conductances may underlie voltage/Ca(2+) oscillations, recognizing that zG layer self-renewal and

245 waves (STW) are bursts of frontocentral slow oscillations recorded in the scalp electroencephalogram

246 d signals arrive unaligned to the receiver's oscillation, reducing signal transfer.

247 Local field potential oscillations reflect temporally coordinated neuronal ens

248 Core clock gene mRNA oscillations remained mostly unaffected but rhythmic Klf

249 ffect of this tidally induced biogeochemical oscillation remains poorly understood, limiting the effe

250 R acts locally or globally on cortical sleep oscillations remains unknown.

251 general role, high- and low-frequency theta oscillations, respectively, may reflect spatial and non-

252 orm for ultrasound imaging to examine muscle oscillation responses to impact forces induced by change

253 These oscillations resulted from complex ocean-atmosphere inte

254 ith out-of-phase transverse and longitudinal oscillations, resulting in trochoidal, or cartwheeling,

255 sc was less effective at damping contractile oscillations, results suggest that spontaneous oscillato

256 l systems theory, including multi-stability, oscillations, robustness and stochasticity, are critical

257 nable the CA3 circuit to generate fast gamma oscillations.SIGNIFICANCE STATEMENT The generation of hi

258 Moreover, patients expressed slow oscillations (SOs), and SO-fast spindle coupling was obs

259 -band tilt of the power spectrum; (ii) theta oscillations specifically support associative memory, wh

260 y the ensemble members with a North Atlantic Oscillation sufficiently close to the variance-adjusted

261 y, decreasing the interpulse interval led to oscillation suppression.

262 ivo to determine if neural activity, network oscillations, synaptic transmission, and/or synaptic pla

263 n was measured by a spirogram and the forced oscillation technique.

264 ctive and phase locked to 30- to 80-Hz gamma oscillations than other neuron types.

265 dulate frontal midline theta (FMT) and alpha oscillations that are linked with marked alterations in

266 ross species, mediated by Quaternary climate oscillations that have facilitated a dynamic of isolatio

267 ssociated with increased beta (20- to 30-Hz) oscillations that selectively locked onto temporal featu

268 asets revealed distinct functions from those oscillations that were harmonic, suggesting purposeful b

269 t of nonrapid eye movement (NREM) sleep beta oscillations that were synchronized across the BG and ce

270 noise variability, transient overshoots and oscillations, that have so far escaped a common, princip

271 the total variability) of the North Atlantic Oscillation (the leading mode of variability in North At

272 n of layer 2/3 pyramidal neurons drives fast oscillations throughout development, yet the acceleratio

273 al theta, we examine the properties of theta oscillations throughout the anterior-posterior length of

274 eep or to GAs is characterized by: (a) delta oscillations throughout the cortex; (b) marked reduction

275 The presence of Laue oscillations throughout the self-assembly provided atomi

276 m mobile-carrier conduction and bound-charge oscillation to the ac conductivity are equivalent in a m

277 w fluctuations change from local independent oscillations to a homogeneous bulk behaviour.

278 that noise can amplify and sustain transient oscillations to the fixed point, giving rise to quasiper

279 d seasonality, links to the El Nino-Southern Oscillation, triggering processes and impacts on ocean p

280 ystems corresponds to high and low frequency oscillations typically seen in blood pressure and heart

281 the ability to detect distinct amplitudes of oscillations via image processing.

282 2 and 0.018 Hz where this very low-frequency oscillation (VLFO) was hypothesized to be generated by t

283 eurons (SPNs) are capable of generating beta oscillations, we show that networks of striatal fast-spi

284 cts on memory performance and cortical sleep oscillations were not observed when unilateral olfactory

285 iated with delta oscillations, whereas theta oscillations were observed when the number of rules incr

286 d during this stage three millennial climate oscillations were recorded.

287 Further, gamma oscillations were similarly tuned in LFP and ECoG to sti

288 llations, by which power increases in 2-5 Hz oscillations were uniquely linked with successful associ

289 vel of abstraction was associated with delta oscillations, whereas theta oscillations were observed w

290 Circadian rhythms are endogenous 24-h oscillations which regulate physiological processes incl

291 ss the latter also in the context of Friedel oscillations, which we argue might promote CDW formation

292 ngth of LH optogenetic responses and network oscillations, which were consistent with ultra-sparse in

293 dependent reduction of intracellular calcium oscillations, while other caged inositol pyrophosphates

294 ur model FSI network produces low gamma band oscillations, while under high dopaminergic tone the FSI

295 spikes of some cells in vLGN displayed gamma oscillations whose phase and strength varied with stimul

296 of DNA length whereas kunloop showed a clear oscillation with a period close to the helical turn of D

297 Rather than one hippocampal theta oscillation with a single general role, high- and low-fr

298 CFS and PAC networks coupled theta and alpha oscillations with higher frequencies in large-scale netw

299 Evolution of the oscillations with temperature T shows that the parameter

300 imited conditions and results in respiratory oscillations (YROs).