ライフサイエンスコーパス: oscillation

1 or, which provides the feedback required for oscillation.

2 . 2.5 cycles of the short-period respiratory oscillation.

3 agement of the circuitry that produces gamma oscillations.

4 trainment of SPN firing to parkinsonian beta oscillations.

5 interactions between slow and fast neuronal oscillations.

6 ng information in the brain based on coupled oscillations.

7 he amplitude of endothelial cytosolic Ca(2+) oscillations.

8 to functional outputs such as bistability or oscillations.

9 cant effect on the properties of the calcium oscillations.

10 pplying a DBS-like input we suppressed these oscillations.

11 d robustness of the fission yeast cell cycle oscillations.

12 hances NMDA receptor-dependent early network oscillations.

13 her forebrain structures is enabled by theta oscillations.

14 s visually induced changes in beta and gamma oscillations.

15 vity was modulated by the phase of the alpha oscillations.

16 l hours into regular low-frequency (0.03 Hz) oscillations.

17 such as switching behaviour, bistability or oscillations.

18 is orchestrated by means of prefrontal theta oscillations.

19 the role of the cortex and thalamus in these oscillations.

20 nist concentration for intracellular calcium oscillations.

21 late effects of EFS-induced cellular calcium oscillations.

22 ility in period and amplitude of single-cell oscillations.

23 lict by switching from in-phase to antiphase oscillations.

24 cillations, and a decrease in theta and beta oscillations.

25 ) GABAergic input coordinates cortical theta oscillations.

26 ns, that limits population sizes and reduces oscillations.

27 p between specific TW durations and specific oscillations.

28 neration and information processing of theta oscillations.

29 t resets the phase of low-frequency cortical oscillations.

30 ced, and they disparately engaged in network oscillations.

31 atures are usually required to observe these oscillations.

32 te unaltered and only slightly reduced theta oscillations.

33 ERK activity profile but are dispensable for oscillations.

34 exerted feedback control of the visual alpha oscillations.

35 cal to allow for development of robust gamma oscillations.

36 y neurons in orchestrating specific cortical oscillations.

37 5 Hz) develop, distinct from concurrent slow oscillations (0.1-1 Hz).

38 ement ceases, coherent thalamocortical delta oscillations (1-5 Hz) develop, distinct from concurrent

39 Beta oscillations (15-29Hz) are among the most prominent sign

40 Previous studies have suggested that gamma oscillations (30-80 Hz) measured in human visual cortex

41 ctral properties on the EEG, including alpha oscillations (8-12 Hz), Slow Wave Oscillations (SWO, 0.1

42 ent of cell types; and (iii) 10-20 Hz damped oscillations across retinal layers.

43 ntrollable deformation of the droplet and/or oscillation along the vortex axis.

44 Alpha-band oscillations also carried clear information about the lo

45 Coherent oscillations also occur within individual brain regions,

46 econnections with the Atlantic Multi-decadal Oscillation (AMO).

47 ing and phasing of the Atlantic Multidecadal Oscillation (AMO).

48 xplained by the remote Atlantic multidecadal oscillation (AMO).

49 llatory system, it leads to the decay of the oscillation amplitude.

50 We show that fast narrowband oscillations, an important feature of population activit

51 le a competing interaction between a 6-12 Hz oscillation and a fear-associated 3-6 Hz oscillation wit

52 elated to warm phases of the Pacific Decadal Oscillation and the Oceanic Nino Index, an indicator of

53 higher temperatures (>100 degrees C), RHEED oscillations and AFM data indicate a transition to a ste

54 and sarcomere length 2.15 mum), small 4 kHz oscillations and determining the relation between half-s

55 hesized that entrainment would align ongoing oscillations and drive them toward the stimulation frequ

56 mporal and spatial processing, such as theta oscillations and grid cell firing.

57 s on the presence of approximately 20 Hz SM1 oscillations and needs not rely on feedback from the per

58 sequencing relationships affect neocortical oscillations and neuronal responses is poorly understood

59 through Orai1-mediated intracellular Ca(2+) oscillations and reveal a possible molecular basis for z

60 e and classical network states such as theta oscillations and sharp-wave ripples.

61 The coupled interaction between slow-wave oscillations and sleep spindles during non-rapid-eye-mov

62 nimodipine) on airway contraction and Ca(2+) oscillations and SOCE-mediated Ca(2+) influx in ASMCs wi

63 analysis of the relationship between spindle oscillations and spindle position relative to the cortex

64 ensitive to external signals such as glucose oscillations and stress cues.

65 f maturational changes in neurophysiological oscillations and synchrony, rather than disturbances in

66 nositol 1,4,5-trisphosphate-mediated calcium oscillations and the up-regulation of the transcription

67 Gamma oscillations and their regulation by NMDA receptors can

68 ibitory neural activity that regulates alpha oscillations and visual information processing.

69 membrane determines the dynamics of nuclear oscillations and, in essence, dynein activity.

70 en specific features of sleep (e.g., network oscillations) and sleep-dependent plasticity has been di

71 pulation activity, a small increase in gamma oscillations, and a decrease in theta and beta oscillati

72 d a functional balance of gamma-band network oscillations, and allowed treated eFSE rats to encode an

73 I injury improved synaptic plasticity, brain oscillations, and learning behavior.

74 others where the populations exhibit damped oscillations, and still others where one population is d

75 North Atlantic Oscillation (NAO) and Arctic Oscillation (AO) indices.

76 CO2 concentrations and the El Nino-Southern Oscillation are well known, the magnitude of the correla

77 This system was used to demonstrate that oscillations are a collective property of PSM cells that

78 cally resistant epilepsy, we find that theta oscillations are a distinct electrophysiological signatu

79 Gamma oscillations are associated with enhanced attentional ca

80 In airway smooth muscle cells, these Ca(2+) oscillations are caused by cyclic Ca(2+) release from th

81 It is not clear, however, how alpha oscillations are controlled and how they interact with t

82 saccadic preparation and visual sensitivity oscillations are coupled and the coupling might be instr

83 In modeling, two features of alpha oscillations are critical to account for the observed ef

84 Plasma insulin oscillations are known to have physiological importance

85 gs, both sustained potentials and alpha-band oscillations are present during the delay period of work

86 f memory have argued that large-scale neural oscillations are reinstated to support successful memory

87 These oscillations are related to local spiking activity and t

88 junctions (NMJs), where low-frequency Ca(2+) oscillations are required for synaptic refinement and th

89 In situations where stable oscillations are required, the energy dissipated by the

90 Two of these oscillations are shown to arise from three- and two-dime

91 Beta frequency oscillations are shown to require pallido-striatal feedb

92 Beta and gamma oscillations are the dominant oscillatory activity in th

93 We demonstrated that high frequency oscillations are the major determinants for priming, tri

94 citability.SIGNIFICANCE STATEMENT Alpha-band oscillations are thought to reflect cortical excitabilit

95 Oscillations are ubiquitous in the brain, and they can p

96 Gamma oscillations arise in the subthalamic-globus pallidus fe

97 case study for understanding how beta/gamma oscillations arise.

98 ed both beta and gamma local field potential oscillations as well as synchrony of inhibitory signals

99 ing phase-shifted, antiphase or synchronized oscillations, as well as stable steady-state population

100 adening, and complex intensity variation and oscillation at twice the phonon frequency for the valenc

101 at rhythmic sensory events can entrain brain oscillations at different frequencies, how learning and

102 ERCA level will enable intracellular calcium oscillations at low agonist concentrations whereas lower

103 onding to the coupling of individual plasmon oscillations at medium- and substrate-related diffractio

104 ctions in neural networks result in cortical oscillations at the beat frequency, and that such entrai

105 ACS has recently been shown to induce neural oscillations at the frequency stimulated.

106 m accounts for the graded emergence of gamma oscillations at the stimulation site while retaining pro

107 that the dynamics of the ET network support oscillations at the tremor frequency and the application

108 o reflected in the visual responses; the LFP oscillation became more entrained by visual stimulation

109 e in single-unit activity and stronger gamma oscillations began to emerge.

110 delay, these clusters abruptly disperse and oscillation begins, alternating between clustering and d

111 We postulated that alpha oscillations, believed to exert active inhibitory gating

112 tions within active neuronal assemblies.Slow oscillations between cortical Up and Down states are a d

113 damental differences across species in these oscillations between humans and rodents.

114 ioral findings, increased synchronized theta oscillations between V2L and basolateral amygdala, a phy

115 mic range for signal integration and network oscillation by the ACC.

116 ectrons into vibrating surface atoms, phonon oscillations can be observed on the atomic scale.

117 lis biofilm communities undergoing metabolic oscillations can become coupled through electrical signa

118 econd (delta frequency) timescales, cortical oscillations can entrain spiking activity throughout the

119 w, for the first time, that low-frequency Vm oscillations can significantly modulate sensory signal p

120 Here, we show that these theta oscillations carry predictive information about timed re

121 trough of both CA1 theta and slow irregular oscillations, coincident with highest hippocampal excita

122 In humans, 8-12 Hz alpha oscillations constitute the strongest deviation from 1/f

123 ve device applications, especially if the MR oscillation could materialize at higher temperature by m

124 angshanensis during the Pleistocene climatic oscillations could have been the cause of the overlap.

125 gation, in which the phase of ongoing neural oscillations determines whether two stimuli are integrat

126 uring this pre-micturition interval, a theta oscillation developed in the LC, the mPFC desynchronized

127 sistance oscillations, the magnetoresistance oscillations do not modify the giant magnetoresistance,

128 hosen to allow observation of fixed cortical oscillations driven by contextual (but missing) sensory

129 Mechanical dampening of resonant oscillations due to the presence of shear forces between

130 We also uncovered a new type of oscillation during recovery from H2O2 challenge.

131 endogenous alpha-band ( approximately 10 Hz) oscillations during a selective visuospatial attention t

132 ved neurobiological characteristics of theta oscillations during ambulatory spatial navigation, while

133 the globus pallidus leads to transient beta oscillations during behavior.SIGNIFICANCE STATEMENT Tran

134 the cholinergic contributions to prefrontal oscillations during cue detection in rats.

135 cisely controlled with the number of current oscillations during potentiostatic deposition of the imp

136 ch as solar radiation and the North Atlantic Oscillation, during the late Holocene.

137 havior.SIGNIFICANCE STATEMENT Transient beta oscillations emerge in the normal functioning cortico-ba

138 The oscillations enable us to probe the surface structure.

139 The El Nino-Southern Oscillation (ENSO) and the variability in the Pacific su

140 The evolution of the El Nino-Southern Oscillation (ENSO) during the Holocene remains uncertain

141 The El Nino Southern Oscillation (ENSO) has significant impact on global clim

142 the equatorial Pacific and El Nino-Southern Oscillation (ENSO) variability after 2000 are documented

143 ability associated with the El Nino/Southern Oscillation (ENSO).

144 g activity, whereas delta-frequency cortical oscillations entrain spiking activity throughout the ent

145 ed a range of functions such as bistability, oscillation, feedback, and logic capabilities.

146 delta, theta, and low-gamma oscillations followed the nonlinear variation of compreh

147 pping, highlighting the importance of neural oscillations for the interaction between visual and memo

148 The histograms of the many single ion oscillation frequencies have resolved peaks that corresp

149 sed in astrocytes tripled astrocytic calcium oscillation frequency in both the preBotzinger complex a

150 the beat frequency, and that such entrained oscillations give rise to the percept of a beat or a pul

151 Brief epochs of beta oscillations have been implicated in sensorimotor contro

152 Motor cortical beta oscillations have been reported for decades, yet their b

153 membrane potential accompanying the calcium oscillations have no significant effect on the propertie

154 We find that, in PD, M1 beta oscillations have sharp, asymmetric, nonsinusoidal featu

155 ime scale, changes switch-like behavior into oscillations having a period of 1 hour or longer.

156 the source of tip-focussed cytosolic Ca(2+) oscillations: Hechtian adhesion between the plasma membr

157 s regulates MSDR by regulating the molecular oscillation in DN1 neurons.

158 Some data implicate a cell-autonomous oscillation in gene expression, while others strongly su

159 Correlative evidence suggests that the daily oscillation in global protein accumulation depends on a

160 This feature entails a relaxation oscillation in polariton condensate formation, resulting

161 istical description of heterogeneous calcium oscillations in a dynamic environment.

162 ign of sea level-driven glacial/interglacial oscillations in biogeochemical fluxes at and near the oc

163 The structure of these oscillations in both cortex and thalamus closely paralle

164 ositol trisphosphate often evokes repetitive oscillations in cytosolic Ca(2+) .

165 ylation and dephosphorylation in response to oscillations in cytosolic calcium.

166 The record displays major oscillations in deep-sea temperature and Antarctic ice v

167 lishes the ability of sperm to induce Ca(2+) oscillations in eggs.

168 ns, we report the classical analogue of Rabi oscillations in ensemble-averaged spins of a ferromagnet

169 count for complex patterns of transient beta oscillations in healthy animals.

170 f image that elicits larger narrowband gamma oscillations in healthy visual cortex is also more likel

171 The role of neuronal oscillations in human somatosensory perception is curren

172 erved during task-related synchronization of oscillations in inhibitory interneuronal circuits, suppo

173 tied to experimental work, we show that the oscillations in membrane potential accompanying the calc

174 on and suggest a crucial role for prefrontal oscillations in metacognitive performance.

175 eaction-diffusion simulations predict robust oscillations in modeled cyanobacterial cells provided th

176 Oscillations in neural activity play a critical role in

177 onstrate that a computational model for beta oscillations in Parkinson's disease (PD) can also accoun

178 oreover, it has not been shown whether lipid oscillations in peripheral tissues are driven by diurnal

179 ntrain to time-varying signals to keep their oscillations in phase with the day-night rhythm.

180 stigated whether the involvement of neuronal oscillations in processing accelerated speech also relat

181 s challenged that view by showing that theta oscillations in rodent V1 may come to convey timed expec

182 d significant cortical entrainment to visual oscillations in sign language <5 Hz, peaking at [Formula

183 n this paper, we report sustained glycolytic oscillations in single cells without the need for cyanid

184 Theta frequency oscillations in the 6- to 10-Hz range dominate the roden

185 rol appears to be established dynamically by oscillations in the alpha (8-13 Hz) and beta (13-18 Hz)

186 ing hypercapnic challenge, increases calcium oscillations in the chemosensitive parafacial respirator

187 or the first time, that modulations of brain oscillations in the EEG alpha frequency band in posterio

188 orks of inhibitory neurons robustly generate oscillations in the gamma band.

189 Theta oscillations in the hippocampus orchestrate such timing

190 processing involving the generation of theta oscillations in the hippocampus.

191 nment, supporting a critical role of ongoing oscillations in the integration/segregation of informati

192 Theta oscillations in the local field potential (LFP) of V1 ha

193 s of the tree and leading to global coherent oscillations in the network.

194 e while retaining propagating waves of gamma oscillations in the non-stimulated tissue.

195 insic environmental changes such as climatic oscillations in the Quaternary or by intrinsic biologica

196 ranule cells (GCs) can generate synchronized oscillations in the rodent olfactory bulb.

197 olar surface quantum Hall effect and quantum oscillations in the Seebeck and Nernst effect.

198 ding evidence for a critical role of ongoing oscillations in the temporal organization of perception.

199 In parallel, synchronous oscillations in the theta and gamma bands between the BL

200 cortex is an important driver of gamma-band oscillations in the vStr and associated limbic areas.SIG

201 ircuitry is not a major contributor to gamma oscillations in the vStr LFP and that piriform cortex is

202 is of arterial waveform that extracts hidden oscillations in the waveform that we called intrinsic fr

203 k model, we demonstrate that the synchronous oscillations in these assemblies emerge from interplay b

204 thus elucidating a behavioral role for theta oscillations in V1 and extending our understanding of th

205 sults suggest that states of decreased alpha oscillations increase the global baseline excitability o

206 th V1 delta (0.5-4 Hz) and spindle (7-15 Hz) oscillations increased, with neurons most responsive to

207 cell line and modified the cytosolic Ca(2+) oscillations induced by the sodium/calcium exchanger NCX

208 , hippocampal ripples, and the cortical slow oscillations-is thought to be critical for memory consol

209 oon (ISM) shows quasi-rhythmic intraseasonal oscillations (ISO) manifested as alternate 'active' phas

210 erstood, much less is known about tipping of oscillations (limit cycles) though this dynamics are the

211 It has been hypothesized that slow rs-fMRI oscillations (<0.1 Hz) are driven by underlying electrop

212 nd not just somatic inhibition, SOM-mediated oscillations may expand the computational power of gamma

213 y little is known about how slow hemodynamic oscillations measured with fMRI relate to electrophysiol

214 ns, gridded climate data, and North Atlantic Oscillation (NAO) and Arctic Oscillation (AO) indices.

215 database) and data on the Northern Atlantic Oscillation (NAO), we show that in the last 60 years bot

216 ote the negative phase of the North Atlantic Oscillation (NAO-).

217 cale atmospheric circulation (North Atlantic Oscillation, NAO).

218 We speculated that low-frequency oscillations observed in the granular layer may provide

219 Moreover, these oscillations occurred when animals were in high and low

220 cause of ET is unknown, however pathological oscillations of a network of a number of brain regions a

221 namics are systematically embedded in visual oscillations of contrast sensitivity that fluctuate rhyt

222 such metal nanostructures feature collective oscillations of electrons (plasmons), providing huge ele

223 atures (TDW) close to 200 K via the coherent oscillations of its collective modes, which is reminisce

224 rved high coherence, intact NVC, between the oscillations of SctO2 and aEEG in the frequency range of

225 Of interest, these ingredients power the oscillations of the anaphase spindle in budding yeast, b

226 waves in ME antennas stimulate magnetization oscillations of the ferromagnetic thin film, which resul

227 ng pH offers a new way to measure glycolytic oscillations on individual cells.

228 r photonic bandgap resonators, we drive Rabi oscillations on nuclear spins exclusively using electric

229 lassic hippocampal network states like theta oscillations or sharp-wave ripples.

230 .g., higher temperature, large-scale climate oscillations) or whether they are more sensitive to glob

231 ated with unprecedented quantum Little-Parks oscillations originating from the interference of superc

232 ne channels is also necessary to sustain the oscillations over longer times.

233 werful typhoons) in negative Pacific Decadal Oscillation (PDO) years, as well as with sea-level-rise

234 r interactions that control the frequency of oscillations, population variability, and dynamical stab

235 ociated with an increase in theta- and gamma-oscillation power and cross-frequency coupling in dorsal

236 transpiration, along with the North Atlantic Oscillation, predicted variation in selection across pla

237 In contrast, alpha-band oscillations primarily carry location information, consi

238 ortex, where low-frequency (0.01 Hz) calcium oscillations refine topographic maps.

239 ndings support the idea that posterior alpha oscillations represent a state of increased processing o

240 Sustained Ca(2+) oscillations require a Ca(2+) influx to replenish Ca(2+)

241 neous biological variations induce irregular oscillations (resonance "strength") rises profoundly as

242 aps, LRTC in the delta, theta, and low-gamma oscillations resumed the low levels observed for intelli

243 of the Hall effect and the Shubnikov-de Haas oscillations revealed that the Fermi surface of this com

244 ivity in the 30-90 Hz range and a narrowband oscillation seen in mice at frequencies close to 60 Hz.

245 ation is a likely mechanism for rescuing the oscillations seen in islets from mice deficient in K(ATP

246 or a brain-wide change in individual network oscillations, shared by all patients, is largely equivoc

247 When compared to R oscillations, significantly better outcomes were observe

248 iarity with sound objects, whereas beta-band oscillation signifies involvement of the action-percepti

249 Cortical slow oscillations (SO; 0.5-1 Hz) and thalamocortical spindle

250 e hallmarked by electroencephalographic slow oscillations (SOs), appears of particular relevance here

251 e source, enabling the future use of natural oscillation sources such as electromagnetic radiation.

252 input is decreased, leading to synchronized oscillations spanning d delta to beta frequencies; (2) t

253 l energy supply is removed, the amplitude of oscillations start to decay immediately, since there is

254 plitude coupling between HPC theta and gamma oscillations strongly and specifically increased in RSC

255 The phase and amplitude analysis of the oscillation suggests that it arises from the wavepacket

256 ding alpha oscillations (8-12 Hz), Slow Wave Oscillations (SWO, 0.1-1.5 Hz), and dose-dependent phase

257 And also, the forced oscillation technique (FOT) is a noninvasive method that

258 ired lung mechanics determined by the forced oscillation technique and plethysmography.

259 e superposition enhances a later part of the oscillation that is normally damped; when this enhanceme

260 g in the context of the synchronized network oscillations that are abnormally exaggerated in cortical

261 ciated with stereotyped electrophysiological oscillations that are thought to reflect profound disrup

262 ose addition to immobilized cells induced pH oscillations that could be imaged with fluorescent senso

263 found visually evoked stereotyped 3-5 Hz Vm oscillations that disrupt excitatory responsiveness to v

264 physiological agent that triggers the Ca(2+) oscillations that normally initiate embryogenesis.

265 Circadian rhythms are biological oscillations that schedule daily changes in physiology.

266 ther from a movement onset state during beta oscillations that were neurofeedback-induced or naturall

267 attenuation of contralateral alpha (8-14 Hz) oscillations that, moreover, predicted working memory ac

268 stigated the sources of the narrowband gamma oscillation, the factors modulating its strength, and it

269 ay between flashes matches the period of the oscillation, the superposition enhances a later part of

270 ual subject scaling exponents of delta/theta oscillations, the greater the comprehension of the faste

271 sence of radiation-induced magnetoresistance oscillations, the magnetoresistance oscillations do not

272 e dependence, scale-free properties of alpha oscillations themselves, and a modulation of baseline le

273 mics by which the system reaches limit cycle oscillations, thereby gaining information on the key par

274 at flicker may also entrain endogenous brain oscillations, thereby modulating cognitive processes sup

275 he spatiotemporal coordination of NREM sleep oscillations therefore represent one pathway explaining

276 d maturation thus culminate with FA traction oscillation to drive efficient FA mechanosensing.

277 ed zones undergoing coordinated pole-to-pole oscillation to help ensure that the cytokinetic division

278 Some studies link beta oscillations to changes in underlying neural activity, b

279 We used sensory entrainment to align neural oscillations to different frequencies and then character

280 Next, we test for entrainment of neural oscillations to visual change in sign language, using el

281 spindles induced in-phase with cortical slow oscillation up-states, but not out-of-phase-induced spin

282 Decoupling of spiking to slow oscillations using optogenetic methods eliminated rescal

283 The frequency of the AFM oscillations varies in the range of 0.1-2.0 THz with the

284 (OAI) of hyporheic zones subjected to redox oscillations, VC is degraded via coexisting aerobic ethe

285 chia coli in the form of plasmid copy number oscillations via a modular design that can be readily ad

286 ntrol that show simultaneous growth and size oscillations, we create a minimal theoretical framework

287 These results were confirmed when perceptual oscillations were characterized in the time domain with

288 Concurrent alpha-beta oscillations were observed over parieto-occipital region

289 Lipid metabolite oscillations were strongly attenuated upon siRNA-mediate

290 pecific to the gamma band as lower frequency oscillations were suppressed consistently across daily n

291 We recorded stereotyped 3-5 Hz Vm oscillations where the Vm baseline hyperpolarized as the

292 Cortical cognitive processing involves gamma oscillations, which support memory, attention, cognitive

293 is shown successfully to damp pathologic eye oscillations while allowing normal saccadic shifts of ga

294 then characterized the resultant perceptual oscillation with a temporal dense sampling of the integr

295 OMVs induced irregular Ca(2+) oscillations with a decreased frequency in cardiomyocyte

296 al variability due to ENSO (El-Nino/Southern Oscillation), with more events under La-Nina and less un

297 Hz oscillation and a fear-associated 3-6 Hz oscillation within the BLA.

298 n is proportional to the frequency of Ca(2+) oscillations within airway smooth muscle cells (ASMCs).

299 engineering strategy that can support stable oscillations without supplying external energy to compen

300 oduced a reduction in the frequency of theta oscillations, without affecting the slope of the non-lin