ライフサイエンスコーパス: desynchronize

1 to different sensitivities to glutamate, can desynchronize.

2 ial arrhythmicity, cell populations are then desynchronized.

3 mped with HF AP profiles SR Ca2+ release was desynchronized.

4 pecificity is degraded when their inputs are desynchronized.

5 ed in the upstream neurons whose activity is desynchronized.

6 ously active at baseline respond to becoming desynchronized.

7 ent manner, but their exocytosis is slow and desynchronized.

8 ate when the state of population activity is desynchronized.

9 cts are reversed when population activity is desynchronized.

10 SCN, these peripheral clocks rapidly become desynchronized.

11 ack stimulation can effectively and robustly desynchronize a network of model neurons comprising subt

12 n contrast, responses to tones and speech in desynchronized A1 were temporally precise and reliable a

13 ous GPe pacemaking, which normally serves to desynchronize activity.

14 waves contrasting with the low-voltage fast desynchronized activity of REM sleep.

15 cortex into functionally related modules, to desynchronized activity that is computationally more pow

16 : slow-wave activity (synchronous state) and desynchronized activity, that express low and high causa

17 atory activity, others highlight the role of desynchronized activity.

18 nses, but rates higher than 50Hz resulted in desynchronized activity.

19 P rules exert a strong decoupling force that desynchronizes activity.

20 in the hippocampus and olfactory bulb become desynchronized, along with the behavioral processes medi

21 Here we report that gamma networks desynchronize and theta networks synchronize during enco

22 s in peripheral tissues persisted but became desynchronized and damped in constant darkness.

23 althy mice, and find that abGCs and mGCs are desynchronized and differentially recruited by IEDs comp

24 ta oscillation developed in the LC, the mPFC desynchronized and LC-mPFC coherence increased in the th

25 dyads in immature and failing cells promoted desynchronized and slowed Ca(2+) release in these two st

26 synchronizing periodic stimulation to induce desynchronized and synchronized states, respectively.

27 r 4 d in constant light, some leaves were as desynchronized as leaves grown without any rhythmic inpu

28 With STD included in the model, the network desynchronized at frequencies above ~200 Hz, so for suff

29 w frequencies, it was largely continuous and desynchronized at high frequencies.

30 In contrast, the transmission was desynchronized at SynII(-) PV interneurons.

31 ivity in the auditory cortex is elevated and desynchronized before stimulus onset, but only if the pr

32 ts receptor, mCry1 expression was damped and desynchronized between cells.

33 ed unconsciousness, and (3) the paradoxical, desynchronized brain state in deep anesthesia contends t

34 A novel desynchronized brain state with increased spike rate var

35 h-pull interaction between synchronizing and desynchronizing brain regions better constrains seizure

36 Upon waking, GCs desynchronized, broadened their tuning and largely fired

37 ffeine can continue to exert potent cortical desynchronizing, but not behavioral, effects when PZ(Vga

38 local astrocytes, glutamate transmission was desynchronized by an alteration of the waveform and arri

39 e close or identical to one another and were desynchronized by olivary injection of the gap junction

40 hat lack of Cplx 1 significantly reduces and desynchronizes calcium-triggered synaptic transmission;

41 ally during learned non-threatening cues and desynchronize cell firing by blocking phase reset of the

42 d exhibit phase-shifted rhythms in circadian desynchronized cells.

43 ether CA1 spatial coding was altered in this desynchronized circuit, using a novel wire-free miniscop

44 is specific, not random, suggesting that the desynchronized clock cells are quickly reset in an uncon

45 lock nuclei, we now find that constant light desynchronizes clock neurons but does not compromise the

46 new study reveals how a light pulse briefly desynchronizes clock neurons in the fly brain before the

47 ehavioral and physiological arrhythmicity by desynchronizing clock cells in the SCN.

48 lidus external and suggest this approach for desynchronizing closed-loop DBS.

49 PC and neuron rhythms in both BD groups were desynchronized compared to controls.

50 xin36-deficient mice exhibited prolonged and desynchronized complex spike activity within PC microcom

51 onics devices were tested for the effects of desynchronizing constant-amplitude high-rate (5,000 Hz)

52 Second, we use desynchronizing coordinated reset stimulation and synchr

53 itory neurons were indeed more active during desynchronized cortical states with weak noise correlati

54 s can vary strongly between synchronized and desynchronized cortical states, i.e., in the presence or

55 qualitatively different in synchronized and desynchronized cortical states.

56 In this way we combine the desynchronizing delayed feedback approach with the HF DB

57 ulation of neuronal tissue that preserve the desynchronizing delayed feedback characteristics and com

58 Computationally it was shown that desynchronizing delayed feedback stimulation methods are

59 When evoked release was highly desynchronized, discrete postsynaptic events were larger

60 ns in sensory cortex, under frontal control, desynchronize during attentive preparation.

61 ind a high-dimensional subspace containing a desynchronized dynamical regime, which may optimize inpu

62 similar for all recorded animals: (1) basal desynchronized EEG before sound stimulus; (2) increase i

63 and time to recovery of righting reflex and desynchronized EEG.

64 lated network exhibits competition between a desynchronizing effect of spontaneous, cell-intrinsic bu

65 n and engagement, rewards had a long-lasting desynchronizing effect.

66 e Ca(2+)-activated potassium channels have a desynchronizing effect.

67 AR) observed in awake cortex facilitates the desynchronizing effects of inhibitory inputs upon local

68 reased RyR sensitivity partially offsets the desynchronizing effects of t-tubule disruption in heart

69 le clusters that transiently synchronize and desynchronize emerge from the complex topology of anatom

70 ep, but also during epileptiform-suppressing desynchronized episodes of waking and REM sleep supports

71 f presynaptic Ca(2+) channels, decreased and desynchronized evoked neurotransmitter release, and rend

72 chromaffin cells, we also find decreased and desynchronized evoked release, and identify a significan

73 controls flying power in Drosophila requires desynchronized firing to drive a steady wingbeat frequen

74 TRN-mediated lateral inhibition that further desynchronizes firing in the VB; and (3) powerful yet sp

75 erein the sleep/wake and behavior cycles are desynchronized from the endogenous circadian cycle, enab

76 al rhythms where sleep-wake cycles are often desynchronized from the environmental day-night changes.

77 g protocol in which the sleep-wake cycle was desynchronized from the rhythm of plasma melatonin, whic

78 ut in the VS, recent data reveal that the VS desynchronizes from the HP during epochs of burst-like P

79 se results suggest that pharmaceuticals that desynchronize FSI activity may provide a novel treatment

80 t type) contribute to their synchronizing or desynchronizing functions.

81 ollectively, our results suggest that highly desynchronized germ cell development and the maintenance

82 hat are consistent with the possibility that desynchronized growth in key cell types may contribute t

83 k connections that indicate synchronized and desynchronized hubs of neural populations.

84 l neuron (LNv) oscillations are the first to desynchronize in WLS and the last to resynchronize in WL

85 nstrated that cardiomyocyte Ca(2+)release is desynchronized in several pathological conditions.

86 firing in mouse TRN neurons that is rapidly desynchronized in thalamic networks.

87 , entrains to ambient light-dark cycles, and desynchronizes in constant bright light or upon removal

88 Desynchronizing individual axons from their local networ

89 Finally, CA1 network modeling showed that desynchronized inputs can impair the precision and stabi

90 rsed maturation of sensory nerve fibers with desynchronized inputs to the CNS also contributes to the

91 ral projections of V0s results in left-right desynchronized inspiratory motor commands in reduced bra

92 We found desynchronized interneuron firing between the CA1 and de

93 n summary, SFSS arises from an imbalance and desynchronized interplay between functional regeneration

94 ry power, increases overall firing rates and desynchronizes local neural activity.

95 ng mathematical simulations, we examined how desynchronized Lsr QS activation, arising from cell-to-c

96 We also emphasize how their synchronized, or desynchronized, mechanical behavior can lead to emerging

97 ntiphase stimulation in the same individuals desynchronized MFC-lPFC theta phase coupling and impaire

98 Next, the Erdos-Renyi network of desynchronized mixed neurons (oscillatory and excitable)

99 inhibition can shift network activity into a desynchronized mode simply by vetoing occasional RE cell

100 We also observed that the synchronized and desynchronized modulatory effect of EC stimulation was f

101 d compared them to periods of low amplitude (desynchronized) mu-alpha.

102 n of alternatively spliced cTnT variants may desynchronize myocardial contraction and contribute to t

103 duction of ectopic reprogramming factors may desynchronize natural developmental schedules.

104 ddition, differential activation of RE cells desynchronizes network activity.

105 A new paper shows that cannabinoids desynchronize neuronal assemblies without affecting aver

106 ced ANKB expression leads to hyperactive and desynchronized neuronal network activity, increased soma

107 erozygous LoF of ANK2 show a hyperactive and desynchronized neuronal network.

108 ain activation enhanced visual responses and desynchronized neuronal spiking; these changes could par

109 The behavioral effects of pharmacologically desynchronizing neuronal firing in the brain of the hone

110 to the larger communities, and a fraction of desynchronized neurons which are part of smaller communi

111 ectrical stimulation may disrupt seizures by desynchronizing neurons, but there is an uncertainty on

112 he circuits that produce stage III waves and desynchronize ON and OFF RGC firing remain obscure.

113 a highly synchronous, slow-wave state, and a desynchronized one that mimics wakefulness.

114 Blockade of ionotropic glutamate receptors desynchronized onset of action potential bursts in indiv

115 icularly during sleep induction, followed by desynchronized or decreased brain activity.

116 /alertness in cortical networks, called the "desynchronized" or "activated" state.

117 Demyelination can cause slowed, blocked, desynchronized, or paradoxically excessive spiking that

118 e ensemble of cells, and that constant light desynchronizes oscillators by maximizing VIP release.

119 Warming and overexploitation tended to desynchronize oxygen cycles from the control, particular

120 revealed that although blastomere divisions desynchronized passively, 8-cell embryos converged towar

121 We show that high-frequency stimulation can desynchronize pathologic firing patterns in populations

122 We found that high-frequency STN DBS desynchronized pathologic oscillations via the masking o

123 ies shows that a number of synchronizing and desynchronizing pathways may be involved.

124 It is less known that it desynchronizes patients with social environment.

125 the instantaneous rate of growth or decay of desynchronizing perturbations.

126 ic interneurons results in an overactive but desynchronized PFC before adolescence.

127 such that as the neuronal population becomes desynchronized, phase information becomes ambiguous.

128 ng either the amplitude or duration of IPSCs desynchronizes PIR activity in a population of TC cells.

129 to the solitary tract at area postrema level desynchronized PND from ventilation, eliminated the lung

130 Analysis of desynchronized quantal events established that the numbe

131 had fully synchronized rhythms, which could desynchronize rapidly.

132 terns of clock gene expression in the forced desynchronized rat, we propose that the vlSCN oscillator

133 em, we compared unilateral adrenalectomized, desynchronized rats that had undergone either transectio

134 enetically and neurologically intact, forced desynchronized rats to test the hypothesis that the dail

135 In the desynchronized regime, the structural plasticity decreas

136 clinical outcome, and postulate that sparing desynchronizing regions may further be beneficial.

137 e post-sleep population activity became more desynchronized relative to the pre-sleep state.

138 es of damage and repair that would otherwise desynchronize response trajectories.

139 rapid fluctuations in synchrony ranging from desynchronized responses, indicative of high alertness,

140 the sleep-wake cycle characterized by fast, desynchronized rhythms in the electroencephalogram (EEG)

141 Differences in rates of change could desynchronize seasonal species interactions within a foo

142 on, the intracellular membrane potential was desynchronized, sensory responses were enhanced, and pop

143 hronic animals, such microinjections evoke a desynchronized sleep-like state similar to natural REM s

144 any chronic disease symptomatologies involve desynchronized sleep-wake cycles, indicative of disrupte

145 By contrast, inhibitory coupling desynchronized slower, spindle-frequency responses speci

146 ting conductance are effective mechanisms to desynchronize spontaneous activity in a spatiotemporal m

147 e discriminable when evoked on a baseline of desynchronized spontaneous activity, but cortical desync

148 pondingly, decreases in the amplitude of ICa desynchronized SR Ca2+ release in control, LVH, and HF m

149 t frequency varied with cortical state, with desynchronized state activity consistent with superposit

150 reduction in response variability during the desynchronized state can be seen subcortically whereas t

151 Current-clamp recordings reveal that the desynchronized state is absent during the first 2 postna

152 tical inputs can switch barrel cortex into a desynchronized state that enables more faithful represen

153 networks undergo a transition to a much more desynchronized state that lacks a clear spatial structur

154 In many behavioral tasks, cortex enters a desynchronized state where low-frequency fluctuations in

155 ronger in the synchronized state than in the desynchronized state, and show that they can be reproduc

156 In this desynchronized state, the reduction in onset response va

157 BF stimulation induced a short-lasting desynchronized state, with sparser firing and increased

158 emporal modulations when the cortex was in a desynchronized state.

159 cur during a particular cortical state - the desynchronized state.

160 n the 'synchronized' state during sleep and 'desynchronized' state during wakefulness.

161 n the 'synchronized' state during sleep and 'desynchronized' state during waking.

162 transited through different synchronized and desynchronized states and intermittently received sensor

163 plasticity strengthens both synchronized and desynchronized states of a network.

164 states and an approximately linear system in desynchronized states.

165 e bistable and can settle in synchronized or desynchronized states.

166 g larger in synchronized states than in more desynchronized states.

167 at both frequencies promoted locomotion and desynchronized striatal network, only 10 Hz stimulation

168 increased rise and decay times, reflecting "desynchronized" SV fusion.

169 distinct local circuit features interact to desynchronize thalamic network activity.

170 Shift work or transmeridian travel can desynchronize the body's circadian rhythms from local li

171 In mice, running and whisking desynchronize the cortex and enhance sensory responses,

172 whose topological role is to synchronize or desynchronize the epileptic network.

173 by thapsigargin treatment, or in the model, desynchronized the Ca(2+) transient.

174 ll and (2) basal forebrain stimulation which desynchronized the cortical EEG.

175 ntercellular interactions, we experimentally desynchronized the development of the ALs and the ORCs b

176 nescence recordings, GABAA receptor blockade desynchronized the Fbxl3(+/+) but not the Fbxl3(Afh/Afh)

177 tential in the postganglionic nerve; it also desynchronized the firing of the remaining units.

178 at the NP decision-making and feedback tasks desynchronized the normalized alpha and beta powers of t

179 Nutrient enrichment desynchronized the oxygen dynamics and their component c

180 toxin abolished rhythms in most neurons and desynchronized the population, phenocopying the loss of

181 the presence of interleukins slows down and desynchronizes the beating of cardiomyocytes in culture.

182 ressing neurons impairs rule-shift learning, desynchronizes the gamma-frequency activity that is nece

183 from quiescence to a motor imagery task that desynchronizes the local beta rhythm) might also change

184 gus nerve has become an effective method for desynchronizing the highly coherent neural activity typi

185 udy reveals how gap junctions are the key to desynchronizing the motor neurons.

186 When local population activity is desynchronized, the correlated variability between neuro

187 cated in synchrony among SCN cells, can also desynchronize them.

188 y behavioral factors that can synchronize or desynchronize these rhythms, including light exposure, f

189 tion, being able to drive the network from a desynchronized to a synchronous state, with a progressiv

190 lumn during rest, even when neurons are in a desynchronized wake-like state prior to light stimulatio

191 hed arousal levels, it is characterized by a desynchronized, 'wake-like' EEG.

192 in harmony with the circadian clock, but can desynchronize when dopamine tone is elevated, thereby pr

193 ns in individual pacemaker neurons to become desynchronized, while Mef2 knockdown strongly dampens mo

194 we studied, gamma power rises as that region desynchronizes with gamma activity elsewhere in the brai

195 light (rLL), recognition performance becomes desynchronized, with object and visuospatial performance

196 overed, posterior beta(1)/alpha oscillations desynchronize within 0.4 to 0.7 s, consistent with optio

197 ting at 100% FI,O2 , alpha activity was less desynchronized within the temporal regions than at 21% F

198 into Per1/2 mice or rhythmic and externally desynchronized WT mice to study intestinal epithelial ce