ライフサイエンスコーパス: synchronization

1 or untreated with androgen after cell-cycle synchronization.

2 ause of progressive neuronal recruitment and synchronization.

3 rareal coactivation is subserved by neuronal synchronization.

4 vitro 4-aminopyridine model of epileptiform synchronization.

5 on, consistent with progressively increasing synchronization.

6 ime course of low-frequency (1-5 Hz) sensory synchronization.

7 ation of local activity and interareal phase synchronization.

8 dynamical properties of networks that favor synchronization.

9 dk1 activity represent a possible process of synchronization.

10 ucleus at a short latency following receptor synchronization.

11 and conditional V3 CINs promoting left-right synchronization.

12 ate spatial patterns of local and interareal synchronization.

13 control, decorrelation, and gamma-frequency synchronization.

14 namics, network topology, and uncertainty in synchronization.

15 ub cells" transiently supporting CA3 network synchronization.

16 e biomolecules without the need for ensemble synchronization.

17 ct pathway is required for hippocampal theta synchronization.

18 o control excitation to prevent epileptiform synchronization.

19 stimulation and was associated with stronger synchronization.

20 1 phase, which was further confirmed by cell synchronization.

21 work more connected and homogeneous enhances synchronization.

22 CC2 influences GABAergic control of neuronal synchronization.

23 of GABAergic interneurons and neural network synchronization.

24 chromatin without the need for cell culture synchronization.

25 tion involves different mechanisms of rhythm synchronization.

26 cal phases and the onset of various types of synchronization.

27 used a delay of delta (2-4 Hz) frontocentral synchronization.

28 ic Ca release achieved a sufficient level of synchronization.

29 ere analysed to explore the cortico-cortical synchronization.

30 es for clusters where neurons increase their synchronization.

31 se the power of delta-band (1-4 Hz) cortical synchronization.

32 ences by beta-band ( approximately 14-18 Hz) synchronization.

33 rs effective controllability for network (de)synchronization.

34 ntal cortex via enhanced low-frequency phase synchronization.

35 n influences are mediated by alpha-beta band synchronization.

36 disorders characterized by abnormal neuronal synchronization.

37 th an increase in local and interhemispheric synchronization.

38 considered a condition for functional neural synchronization.

39 rmation in the relative phase differences at synchronization.

40 in a demanding WM task and large-scale brain synchronization.

41 are critical to regulate phase relations and synchronization.

42 emispheres, was evidenced by bilateral phase synchronization.

43 hibitory balance and high-frequency neuronal synchronization.

44 lay a causal role in the control of cortical synchronizations.

45 de outline-slide preparation and worm growth synchronization (15 min), mounting (20 min), image acqui

46 17%; poor relaxation 13-21%; poor ventilator synchronization 8-17%; and overall optimum sedation 45-7

47 amplitude coupling and inter-electrode phase synchronization across several LFP frequency bands.

48 Integrating 4D SPIM imaging with synchronization algorithm demonstrated that coinjection

49 brafish embryos with a retrospective cardiac synchronization algorithm for four-dimensional reconstru

50 lambda indices, which quantify the degree of synchronization among communities and along time, respec

51 ntensities, we observe regions of high-order synchronization, analogous to Arnold Tongues in dynamica

52 Temporal synchronization analysis was first applied to capture th

53 n the controls covaried with occipital alpha synchronization and activity in right prefrontal cortice

54 yte culture usually require complex parasite synchronization and addition of stimulating and/or inhib

55 rgic systems, contribute to enhanced network synchronization and an improved signal-to-noise ratio.

56 insights into the molecular control of brain synchronization and are revolutionizing our understandin

57 mplex interaction that is required for rapid synchronization and Ca(2+) cooperativity of vesicle rele

58 excitability correlates with changes in EEG synchronization and cognitive performance.

59 for statistical problems motivated by graph synchronization and community detection in networks.

60 novel oscillatory framework that integrates synchronization and desynchronization mechanisms to expl

61 Specifically, we argue that the synchronization and desynchronization reflect a division

62 riety of phenomena, including self-organized synchronization and dynamical phase transitions.

63 nce, modes of auditory-motor timing, such as synchronization and entrainment, are experimentally trac

64 cterize the processes underscoring excessive synchronization and its termination.

65 ive phonemes showed smaller and faster phase synchronization and less spectral power in the theta ran

66 Cell cycle synchronization and live-cell time-lapse observation are

67 nation of long-range, within-frequency phase synchronization and local cross-frequency PAC.

68 mbination of long-range, low-frequency phase synchronization and local cross-frequency phase-amplitud

69 We generalize this to synchronization and offer a sequence of constructions th

70 oss of dopamine is associated with increased synchronization and oscillatory activity in the subthala

71 The synchronization and percolation are associated to abrupt

72 suggests also self-organized ways to control synchronization and percolation in natural and social sy

73 with respect to high levels of motor cortex synchronization and reduction of cortical synchronizatio

74 ermine the neuron's response to stimuli, its synchronization and resonance properties and, ultimately

75 p between the GPe and striatum that promotes synchronization and rhythmicity.

76 ctions of AUT00063 in vivo improved auditory synchronization and supported more accurate decoding of

77 Here we explore systems in which both synchronization and swarming occur together.

78 several recording techniques are related to synchronization and that behavioral state may affect the

79 ity is necessary for the emergence of strong synchronization and the amplification and propagation of

80 vioural rhythms that emerge from such social synchronization and the underlying evolutionary and ecol

81 ndex to quantify the global cortico-cortical synchronization and to obtain topographic differentiatio

82 erties of in-phase, out-of-phase, anti-phase synchronizations and phase-locking, dynamically mimickin

83 elays in cell division and led to cell-cycle synchronization, and (ii) whether a bacterium would surv

84 Hz) and gamma-band ( approximately 60-80 Hz) synchronization, and feedback influences by beta-band (

85 activity, temporally precise and widespread synchronization, and memory consolidation; therefore, th

86 ompare the respiratory pattern, variability, synchronization, and neuromuscular coupling within compa

87 lectronic circuits, we study the inter-layer synchronization as a function of the removed links.

88 ivity have identified global levels of phase synchronization as measures that characterize normal lev

89 We find that FEF and ACC showed prominent synchronization at a 3-9 Hz theta and a 12-30 Hz beta fr

90 hallenged theories assuming widespread gamma synchronization at a fixed common frequency.

91 Here we achieve all-optical synchronization at the soft X-ray free-electron laser FL

92 ion and subsequent motor response, transient synchronization between auditory and motor regions was o

93 ormance can induce modulation of the resting synchronization between brain regions.

94 insonism are characterized by increased beta synchronization between cortical and subcortical areas.

95 f mobility-selected ions, greatly easing the synchronization between different analyzing stages.

96 Comparing this synchronization between different attention conditions r

97 onal communication relies upon the transient synchronization between distinct low-frequency (<80 Hz)

98 y considering the advantages of tail-beating synchronization between neighbors, which we have also ch

99 campus and ventral striatum showed increased synchronization between neuronal firing and local field

100 In this study, low-frequency phase synchronization between prefrontal and temporal cortex c

101 wer during SO up-phases, and led to stronger synchronization between SO and spindle power fluctuation

102 dicating specific difficulties in long-range synchronization between the hemispheres.

103 ception of stiffness and that TMS alters the synchronization between the two signals causing lasting

104 lower and, irrespective of visual isolation, synchronization between these ultradian rhythms was obse

105 ion, as type II neurons are more amenable to synchronization by mutual excitation.

106 ex synchronization and reduction of cortical synchronization by subthalamic DBS, providing an explana

107 ergic activity limits this uncontrolled beta synchronization by terminating long duration beta bursts

108 and despite 24-h environmental cues, social synchronization can generate far more diverse behavioura

109 We hypothesized that reduced neural synchronization caused by disruption of neural signal pr

110 of nodes to lose synchronization, leading to synchronization collapse for the entire network.

111 onstrate the generality of the phenomenon of synchronization collapse using a variety of complex netw

112 We found that the synchronization communities relate to previously defined

113 Measures of LFP synchronization confirmed and computer simulations detai

114 diffusion models of rhythmic timing during a synchronization-continuation tapping task (SCT).

115 potentials (LFPs) from monkeys performing a synchronization-continuation task (SCT) and a serial rea

116 music and dance, have been studied using the synchronization-continuation task (SCT), where subjects

117 Gamma-band synchronization coordinates brief periods of excitabilit

118 Ventilator synchronization correlated with Behavioral Pain Scale (r

119 ures stand at the crossroads of all neuronal synchronization disorders in the developing and aging br

120 endothelial cells driving branching, whilst synchronization drives vessel expansion.

121 er cortical space than in Ctrl mice, however synchronization during evoked responses induced by whisk

122 nism originating the observed spatiotemporal synchronization dynamics by using a network model of pha

123 istability and delayed complex networks with synchronization dynamics.

124 also summarize the current studies of animal synchronization, engaging an evolutionary perspective on

125 studies addressing rhythm, meter, movement, synchronization, entrainment, the perception of groove,

126 eriority in stability and self-correction of synchronization errors.

127 Cell cycle synchronization experiments indicated that mitosis parti

128 ssion, GJ formation and myocyte connectivity/synchronization for labour.

129 who vocalized longer also elicited stronger synchronization from the adult.

130 ween basal bodies display markedly different synchronization from the wild type.

131 So far, the study of such inter-layer synchronization has been restricted to the case in which

132 Reversible synchronization has no effect on pluripotency or differe

133 Synchronization, however, was not limited to local neura

134 Externally induced synchronization improved performance when cognitive dema

135 Thus, synchronization improves spatial resolution and sensitiv

136 Here we show that synchronization in 2D and 3D neuronal networks is signif

137 tually resecting putative control regions on synchronization in a validated model of the human epilep

138 antly increased left-hemispheric theta phase synchronization in AP compared with non-AP musicians.

139 ecific patterns of abnormal global and local synchronization in ASD.

140 cent attempts to elucidate the role of brain synchronization in defensive responses to threat.

141 ve closed-loop techniques for the control of synchronization in ensembles of interacting oscillators.

142 ter population responses and disrupts neural synchronization in large-scale networks, leading to abno

143 reflect the lack of capacity for predictive synchronization in monkeys, or lack of motivation to exh

144 20 ms) central peak was observed for EMG-EMG synchronization in older infants.

145 ut to address the motor network activity and synchronization in Parkinson's disease and its modulatio

146 ls of global and nonspecific fluctuation and synchronization in scale-free population activity also v

147 or pinpointing brain regions that facilitate synchronization in the epileptic network.

148 , these properties include global zero-phase synchronization in the gamma band, the phase-restriction

149 Furthermore, movement leads to exaggerated synchronization in the low beta band specifically within

150 tive attention is controlled by the rhythmic synchronization in the prefrontal cortex (PFC) and its c

151 e investigated which principles govern gamma synchronization in the presence of input-dependent frequ

152 ocampus coordinating neocortical activity by synchronization in the theta range is common among theor

153 the integration of sensory functions, while synchronization in theta/alpha bands supports the regula

154 temporal patterns of resting state neuronal synchronizations in primary progressive aphasia syndrome

155 underlying odor-elicited neural oscillatory synchronization increased information transmission rates

156 dows, we developed an extension of the phase synchronization index to quantify the global cortico-cor

157 t to their contributions to the global phase synchronization index.

158 Cell cycle synchronization indicated that the shift in subcellular

159 physical systems in which self-assembly and synchronization interact.

160 Inter-layer synchronization is a dynamical process occurring in mult

161 dicates that the performance of this optical synchronization is limited primarily by the free-electro

162 new node can cause a group of nodes to lose synchronization, leading to synchronization collapse for

163 Surprisingly, we find that global neural synchronization levels decrease during brain evolution,

164 epilepsy patient and uncover that explosive synchronization-like transition occurs around the clinic

165 r the optimal gain that produces the maximum synchronization margin allows us to compare the synchron

166 optimal number of neighbours with a maximum synchronization margin is demonstrated.

167 tochastic uncertainty, allows us to define a synchronization margin.

168 crepancy is due to a voltage-dependent spike-synchronization mechanism inherent in networks of spikin

169 rmation in humans relies on a theta-specific synchronization mechanism.

170 ulation paradigm, which exploits these power synchronization mechanisms.

171 dicate that deficits in ripples and neuronal synchronization occur before overt deficits in place fie

172 Synchronization occurs in many natural and technological

173 Synchronization occurs with MR ratio ~ 14% and volume ~

174 Synchronization of 2D real-time imaging with patient ECG

175 timulation relatively selectively suppressed synchronization of activity between the subthalamic nucl

176 Different levels of cross-tissue synchronization of age-related gene expression changes a

177 The observations support the hypothesis that synchronization of alpha oscillations across a wide neur

178 In low light, the synchronization of behavioral rhythms relies on either C

179 sue-specific peripheral clocks allow for the synchronization of biological processes with diurnal cyc

180 lier Tubes (PMT) can be used to describe the synchronization of bioluminescent activity of abyssopela

181 Synchronization of Ca wave initiation and triggered acti

182 Due to synchronization of Ca(2+) releases during the action pot

183 Light is the major stimulus for the synchronization of circadian clocks with day-night cycle

184 Hence the role of nAChRs in the synchronization of cortical activity during slow-wave sl

185 lized spike-wave seizures involving abnormal synchronization of cortical and underlying thalamic circ

186 fewer multipeak waves, indicating increased synchronization of cortical neurons in aging, opposite t

187 (5-bromo-2-deoxyuridine) staining following synchronization of cultures by serum starvation.

188 The synchronization of death between individuals suggests a

189 Synchronization of DESI (sDESI) with the ion injection p

190 Generally, synchronization of DESI with IT improves performance and

191 Our results show that synchronization of DESI with the IT of an LTQ Orbitrap-X

192 omic and bibliomic data, enable quantitative synchronization of disparate data types.

193 expression of Dll4, leads to Notch dependent synchronization of Dll4 fluctuations within clusters, bo

194 g in neuronal networks relies on the precise synchronization of ensembles of neurons, coordinated by

195 ed attentional processing, while optogenetic synchronization of FS-PV neurons at gamma frequencies ha

196 ion of attention was characterized by strong synchronization of FS-PV neurons, increased gamma oscill

197 tion is proposed to arise from the selective synchronization of functionally specialized but widely d

198 OS production, and disturbed circadian clock synchronization of glucose and lipid metabolism.

199 and insulin but also to enhance/suppress the synchronization of hormone secretions between islets und

200 s associated with PISO are flawed due to non-synchronization of lattice temperatures and carrier temp

201 CC and FEF circuits coordinate through phase synchronization of local field potential and neural spik

202 While diffusion is too slow for synchronization of mitosis across large spatial scales,

203 Whereas N-type VGCCs contribute only to the synchronization of multivesicular release, P/Q-type VGCC

204 Effective labour contractions require synchronization of myometrial cells through gap junction

205 The synchronization of native state motions as they transiti

206 mic activities are associated with increased synchronization of neuronal firing patterns in the hippo

207 gamma coupling are associated with increased synchronization of neurons within the mPFC.

208 Specifically, synchronization of new leaf growth with dry season litte

209 The synchronization of nonlinear systems connected over larg

210 nning tool - DIET ASSESS & PLAN could enable synchronization of nutrition surveillance across countri

211 s low-frequency variability emerges from the synchronization of ocean anomalies in all basins via glo

212 Understanding the synchronization of oscillations across space is fundamen

213 We also highlight recent evidence for synchronization of oscillations between prefrontal corte

214 ABAA inhibition observed during task-related synchronization of oscillations in inhibitory interneuro

215 In ecology, long-range synchronization of oscillations in spatial populations m

216 et eliminates ultrarapid ephaptic inhibitory synchronization of Purkinje cell firing.

217 gions of messenger RNA requires the temporal synchronization of RNA synthesis and ligand binding-depe

218 pendent network sufficient condition for the synchronization of scalar nonlinear systems with stochas

219 on will be illustrated, with emphasis on the synchronization of secretin administration and MR image

220 n, suppressing PV cell activity elevates the synchronization of spontaneous activity across a broad f

221 The synchronization of stochastic coupled oscillators is a c

222 ected using VBA data processing based on the synchronization of the isotope signals.

223 their TAs' reuse results from the mechanical synchronization of the leading and trailing cells' protr

224 Synchronization of the molecular geometry across several

225 ulation, as heterogeneity facilitates the de-synchronization of the phases in the disease cycle of th

226 ned previously, the network topology driving synchronization of the SCN has not been elucidated.

227 ification of hyperdirect cortical inputs and synchronization of the STN neuronal population.

228 A single irradiation dose also caused synchronization of thymopoiesis, with a periodic thymocy

229 on how climate variation affects large-scale synchronization of tree masting.

230 he transition from incoherence to long-range synchronization of two-cycle oscillations in noisy spati

231 h the preBotC acts as a master clock for the synchronization of vibrissa, pad, and snout movements, a

232 nout movements, as well as for the bilateral synchronization of whisking.

233 The prevailing assumption is that synchronization on distances longer than the dispersal s

234 cognition with WM via the reliance of neural synchronization on propagation of neural signals.SIGNIFI

235 es representative of global cortical network synchronization or desynchronization.

236 usually in the context of a single state of synchronization or lack thereof.

237 h multiple regressions, and the reduction of synchronization over the right prefrontal area showed a

238 ceived pro-social priming, inducing in their synchronization partner greater feelings of connectednes

239 s (n = 45) or healthy controls (n = 45), and synchronization partners (n = 90), was assessed with a h

240 tently approximates the temporal and spatial synchronization patterns of the empirical data, and reve

241 The networks are revealed by analysis of the synchronization patterns with the use of an oscillatory

242 y a decrease in beta oscillations during the synchronization phase, to finally rebound during the con

243 an examination of percolation, diffusion or synchronization phenomena in multilayer networks.

244 One such synchronization phenomenon, dynamic mode locking, occurs

245 f voluntary movement: the post-movement beta synchronization (PMBS).

246 poral organization could be reduced to basic synchronization principles of weakly coupled oscillators

247 responsible for a possible chemically driven synchronization process.

248 le neuron network or its relationship to the synchronization processes that are essential for its for

249 Pause beginning synchronization produced better time-locking of nuclear

250 ts, indicative of the degree of local neural synchronization, progressively increased with burst dura

251 chronization margin allows us to compare the synchronization properties of various complex network to

252 xtended periods of postperformance beta-band synchronization reflect primarily the modulated densitie

253 Moreover, local synchronization reflected in occipitocerebellar beta-ban

254 Significant areas of overlap occur between synchronization regimes, with the bundle intermittently

255 of cortical network fragmentation and global synchronization, respectively.

256 Examination of the network synchronization revealed that the identified rich-club c

257 he basis of changes in firing rate or firing synchronization/rhythmicity.

258 Reactivation-related synchronization showed distinct peaks in the theta, alph

259 rk of nonlinear oscillators can maintain its synchronization stability as it expands.

260 the combination of PAC and long-range phase synchronization subserves enhanced large-scale brain com

261 opology resulted spatially organized partial synchronization such that there was a synchrony gradient

262 Within these regions, beta/gamma phase-synchronization supports the integration of sensory func

263 plets, the intraclass correlation (ICC), the synchronization surface ICC is measured on >25,000 cells

264 The synchronization surface provides evidence that cells com

265 Using a floral synchronization system and a SHATTERPROOF2 (SHP2) domain

266 namic neural response features including the synchronization, temporal patterning, and short-term pla

267 nection between WM microstructure and neural synchronization that is critical for cognitive processin

268 sult in the abnormal neuronal activation and synchronization that underlies seizures.

269 e, the fundamental mathematical principle of synchronization through instantaneous frequency modulati

270 Considerable work indicates oscillatory synchronization through phase alignment is a major agent

271 lar photoreceptors are sufficient to mediate synchronization through the NORPA pathway.

272 e capacity for predictive and tempo-flexible synchronization to a beat, but that only certain vocal l

273 Predictive and tempo-flexible synchronization to an auditory beat is a fundamental com

274 nt immunofluorescence and computational cell synchronization to determine the temporal dynamics of ke

275 dentifies a top-down pathway that uses gamma synchronization to guide the activity of subcortical net

276 ptor 25a (IR25a) is required for behavioural synchronization to low-amplitude temperature cycles.

277 at gamma range frequencies, while resisting synchronization to lower input frequencies.

278 rainment and provide evidence linking neural synchronization to the perception of pulse, a widely deb

279 We here study explosive synchronization transitions and network activity propaga

280 ociation (UVPD) fragmentation, complete with synchronization triggering to make it compatible with li

281 s with poor limb relaxation, poor ventilator synchronization, unnecessary deep sedation, agitation, a

282 rovides evidence that cells communicate, and synchronization varies with genotype.

283 trodes arrays, we show that neuronal network synchronization was altered in MECP2dup-derived neurons.

284 tion, under certain experimental conditions, synchronization was essential to acquire distinct MS ima

285 demonstrated that the cortico-cortical phase synchronization was largely dominated by genuine neurona

286 -duration (40-50 ms) central peak of EMG-EMG synchronization was observed for infants younger than 9

287 CA1-PFC synchronization was stronger during awake SWRs, and spat

288 Global aspects of integration and synchronization were also rebalanced.

289 Observed changes in synchronization were reproduced in a computational model

290 re, a particularly sensitive phase of social synchronization where pair members potentially compromis

291 V2b interneurons resulted in flexor-extensor synchronization, whereas selective inactivation of only

292 imulus is subserved by interareal gamma-band synchronization, whereas top-down influences are mediate

293 ve documented the effects of climate-induced synchronization, which could remove temporal barriers be

294 V2b interneurons led to the flexor-extensor synchronization, while inactivation of V1 interneurons d

295 We analyzed gamma synchronization with respect to phase-locking, phase-rel

296 constitutes a complex process that requires synchronization with the physiological state of the host

297 such bidecadal variability exhibits a robust synchronization, with a maximum in Atlantic Meridional O

298 ing both local power and interregional phase synchronization within a posterior parietal network.

299 pable to resolve contractile waves and their synchronization within maturing, unlabeled induced pluri

300 ntal cortex by increased low-frequency phase synchronization within the theta/alpha band.