ライフサイエンスコーパス: burst

1 he major contributors to the first cytokinin burst.

2 se iron levels to activate a toxic oxidative burst.

3 deposits and a host reactive oxygen species burst.

4 production, and sensitivity to the oxidative burst.

5 , granularity, phagocytosis, and respiratory burst.

6 lanine (fMLP)-induced neutrophil respiratory burst.

7 ial role in modification by a sub-nanosecond burst.

8 characteristic IL-7-dependent proliferative burst.

9 (Cav1.2 plus Cav1.3) and after (Cav1.3) the burst.

10 odules evolve more slowly following an early burst.

11 th GW170817 and with a weak, short gamma-ray burst.

12 were studied for phagocytosis and oxidative burst.

13 i infections, without evidence of a mutation burst.

14 ometric observations that directly image the bursts.

15 ransients but with longer duration [Ca(2+)]i bursts.

16 tude towards short duration, lower amplitude bursts.

17 d large, bulky pseudopods with dynamic actin bursts.

18 piking events and the number of network-wide bursts.

19 lls exhibit discrete and asynchronous Ca(2+) bursts.

20 rgers as the drivers of short hard-gamma-ray bursts.

21 pen probability due to more frequent opening bursts.

22 )-are largely responsible for these activity bursts.

23 e, burst skew and amplitude of the locomotor bursts.

24 elative increase of shorter, lower amplitude bursts.

25 uously elevated, but fluctuates to give beta bursts.

26 the rhythm and replaced it by slow unstable bursting.

27 tein-level stochasticity and transcriptional bursting.

28 plant populations experiencing transposition bursts accompanied by high diversity of chromosomal site

29 -old young neurons of adult mice, that brief-burst activity in glutamatergic fibers is sufficient to

30 SN DA-like burst activity increased integrated ICa during (Cav1.2 p

31 of flying past an elevated object, the spike burst activity is modulated by the height of the object,

32 correlated with, but independent of evolving burst activity over time.

33 arkov jump process is used to drive the wind burst activity that depends on the strength of the weste

34 eness, irregular spike firing, and increased burst activity) in SNL rats.

35 by increased spontaneous spike frequency and burst activity.

36 further drop in Ca(2+) in response to theta burst activity.

37 olved in cellular responses such as neuronal bursting activity and cardiac rhythm.

38 potential depolarisation and high-frequency bursting activity at preferred whisker angles.

39 methods to show that synchronous infra-slow bursting activity in mitral cells of the mouse accessory

40 is a key determining factor for the onset of bursting activity in mouse ventricular myocytes.

41 or interspike interval variability of phasic bursting activity was affected.

42 ere temporally correlated with OS phagocytic burst after light onset.

43 However, monocyte oxidative burst after stimulation increased significantly after in

44 nefficiency of ROS scavengers to control ROS bursts after high-dose treatment with carbonyl cyanide m

45 istic, highly collimated ejecta (a gamma-ray burst afterglow).

46 essing CREB in aged animals had reduced post-burst afterhyperpolarizations, indicative of increased i

47 oriens potentiated both pathways, as did AP-bursts alone, which potentiated synaptic efficacy as wel

48 re asked to localise the position of a noise burst along the azimuth before, during, and after traini

49 ral counterparts, contributing to left-right burst alternation in the swim motor patterns.

50 gthen, whereas in Dendronotus, curare halted bursting altogether.

51 evelopmental time course of white spruce bud burst and shoot growth revealed two UGTs, PgUGT5 and PgU

52 y), to modulate human neutrophils' oxidative burst and to protect Caco-2 cells against oxidative dama

53 TBPH mutants displayed reduced motor neuron bursting and coordination during crawling and restoring

54 n fails to elicit postsynaptic complex-spike bursting and does not induce LTP at ventral SC synapses.

55 The changes in bursting and excitability were related to the altered AD

56 ic generation from gases produces attosecond bursts and enables high-harmonic spectroscopy to explore

57 Calcium bursts and hypersecretion are reversed by mutations in t

58 s, MECIII input to CA1 is crucial for ripple bursts and long-range replays specifically in quiet awak

59 in small animals showed feeding patterns of bursts and pauses, but their function is unknown.

60 but roles of neural inputs to CA1 in ripple bursts and replays are unknown.

61 e dorsal cochlear nucleus, the likelihood of bursts and the interval between their spikelets were con

62 nds of transient events, including gamma-ray bursts and tidal disruption events.

63 ons, AP properties are unchanged between LTS bursts and tonic firing and, as a result, distance-depen

64 (3-fold reduction in the proportion of long bursts), and enhanced closed dwell times (3- to 6-fold i

65 tin, CD11b upregulation, increased oxidative burst, and faster progression to apoptosis.

66 ical spindles, down-to-up transitions, theta bursts, and hippocampal sharp-wave ripples.

67 The model encapsulates burst-and-coast swimming style, speed modulation, and wa

68 that "tonic"' and low-threshold-spike (LTS) "burst" APs in both cell types are always recorded first

69 It is proposed that thalamic bursts are an adaptive response to pain that de-synchron

70 Fast radio bursts are astronomical radio flashes of unknown physica

71 etermine whether the characteristics of beta bursts are dependent on dopaminergic state.

72 Such bursts are mutagenic and thus potentially deleterious.

73 In vegetative cells, bursts are scarce but preferentially occur when cells ar

74 rection and fires action potentials in spike bursts as well as single spikes.

75 01295 reduced the E. coli-induced "oxidative burst," as well as leukocyte activation, without affecti

76 genomic analyses and reactive oxygen species burst assays to evaluate the activity of RaxX and PSY pe

77 acrophages effectively elicited an oxidative burst associated with clearance of Pneumocystis In addit

78 tening in the afterglow of a short gamma-ray burst at redshift z = 0.356, although findings indicatin

79 ple effects: (i) increasing excitability and bursting at moderate spike rates but reducing firing at

80 imulate the brain noninvasively with 50-msec bursts at a 5% duty cycle, repetition frequency of 1 Hz,

81 ynapses onto itself, in driving network-wide bursting behavior.

82 ction potential and [Ca(2+)]i alternans, and bursting behaviors.

83 rom time varying distributions mimicking the bursting behaviour of observed saltatory growth.

84 ve fungicidal activity and reduced oxidative burst, both of which improved in the presence of rhIFN-g

85 many cells would be damaged by a particular bursting bubble, or more precisely how much volume aroun

86 re mainly formed by film drops produced from bursting bubble-cap films, which become enriched with hy

87 estradiol demonstrated an enhanced oxidative burst but decreased P. aeruginosa killing and earlier ce

88 rease of neuron recruitment during epileptic bursts can lead to an increase in burst frequency at the

89 of CyaA-generated cAMP blocks the oxidative burst capacity of neutrophils by two converging mechanis

90 CAF, a process comparable to transcriptional bursting causing temporary allelic imbalance.

91 by applying a common amplitude threshold and burst characteristics were compared between the two drug

92 uding reduced l-selectin shedding, oxidative burst, chemotaxis, neutrophil extracellular trap formati

93 We show that the spike burst coding is size and speed-tuned and is selectively

94 At the timescale of a single burst, conduction delay has a non-monotonic relationship

95 ucleation, driving the dynamics of the swell-burst cycles.

96 We analyzed the killing activity, oxidative burst, cytokine production, and in vitro effects of rhIF

97 ributes to and worsens the overall oxidative burst deficits in CF MDMs compared with non-CF MDMs.

98 g differentiation accentuate transcriptional bursting due to the crowding effect of chromatin.

99 hmicity among MS neurons and fire with short burst duration (median, 38 ms) preferentially at the tro

100 ong beta bursts shifting the distribution of burst duration away from long duration with large amplit

101 , this was achieved by a selective effect on burst duration during adaptive deep brain stimulation, w

102 In Melibe, curare application caused the burst duration of the swim motor pattern to lengthen, wh

103 Importantly, the decrease in burst duration was also correlated with the motor improv

104 bthalamic nucleus increases in proportion to burst duration, consistent with progressively increasing

105 ts as neither the mean intraburst frequency, burst duration, nor interspike interval variability of p

106 logical manipulations suggest that prolonged burst durations are caused by dendritically localized Dm

107 imulation did not change the distribution of burst durations.

108 response to chitin), GO:0002679 (respiratory burst during defence response) and GO:0035556 (intracell

109 resident macrophages to maintain respiratory burst during phagocytosis via enhancing mitochondrial co

110 n factor Crz1 undergoes nuclear localization bursts during the pheromone response.

111 id diversification is characterized by early burst dynamics with decelerating morphologic rates.

112 ique topology of the AOB network, infra-slow bursting enables integration and binding of multiple che

113 and consecutive occurrence of westerly wind burst events that turned around unfavorable ocean thermo

114 ering promoted the initiation of synchronous bursting events but entailed incomplete network recruitm

115 g cortex, is a major source of the transient bursting events that are critical for brain maturation.

116 During this proliferative burst, expression of the Rag genes is transiently repres

117 nd frequency characterization of solar radio burst fine structures observed with the Low Frequency Ar

118 polarizations (AHPs); (iv) strongly enhanced burst firing and increased excitability at moderate spik

119 Hz) oscillations in somatosensory cortex and burst firing in thalamic neurons in vivo.

120 ts are involved in generating high frequency burst firing in the subiculum, but the exact nature of t

121 Burst firing induced MEF2A/D-dependent induction of the

122 with this finding, both regular-spiking and burst firing patterns were profoundly depressed in the m

123 plasticity that persistently eliminates the burst firing potential of Re neurons.

124 lasticity that eliminates the high-frequency burst firing present in many Re neurons.

125 acological inhibition of T-channels switched burst firing with lower depolarizing stimuli to regular

126 nd fully abolished hyperpolarization-induced burst firing.

127 is likely an adaptation to maintain constant burst flight capacity and induced power requirements wit

128 amage and apoptosis during the proliferation burst following IR and an impaired ability to repopulate

129 subarcsecond localization of the fast radio burst FRB 121102, the only known repeating burst source,

130 h high average controllability led to higher burst frequencies than adding the same number of self-lo

131 At adolescence (P28), an increase in burst frequency (>50 Hz) was required to gain timing-dep

132 epileptic bursts can lead to an increase in burst frequency at the network level by reducing the ref

133 Pheromone concentration modulates burst frequency in a mechanism that depends on Mid1, Fig

134 VAS was independently associated with MSNA burst frequency, cBRS and HR.

135 with the sodium ionophore monensin decreased burst frequency.

136 rollability significantly affects changes in bursting from autaptic connections.

137 y measurements of microbes ejected by bubble bursting, further supporting the assignment of BioSS mas

138 ver, the role of specific neural networks in burst generation has not been defined.

139 itational-wave source GW170817 and gamma-ray burst GRB 170817A associated with a galaxy at a distance

140 nse flashes of gamma-rays known as gamma-ray bursts (GRBs), followed by longer-lived afterglow radiat

141 So far all fast radio bursts have been detected with large single-dish telesco

142 olarimetric observations of newly discovered bursts have probed the initial afterglow phase, and show

143 However, if other fast radio bursts have similarly faint radio and optical counterpar

144 he observed spatial characteristics of radio burst images.

145 atal day 8 (P8), theta is expressed as brief bursts immediately following myoclonic twitches; by P12,

146 This short-lived burst in kinase activity links development with maternal

147 tudy for its role in enhancing the oxidative burst in patients with chronic granulomatous disease.

148 lines lack the reactive oxygen species (ROS) burst in the early stages of various stresses, as a resu

149 The normal ethylene burst in the stigma/style and petals following pollinati

150 The percentage number of longer beta bursts in a given interval is positively correlated with

151 ch the first prevents multiple transposition bursts in a given somatic cell lineage that later contri

152 Here we show that ripple bursts in CA1 and medial entorhinal cortex (MEC) are tem

153 put to CA1 during quiet awake reduced ripple bursts in CA1 and restricted the spatial coverage of rep

154 and virtual movement but appear as transient bursts in distinct high- and low-frequency bands, and it

155 ptic connections in controlling network-wide bursts in diverse cortical and subcortical regions of ma

156 cellular proteins via recording fluorescence bursts in live-cell imaging studies.

157 , or preventing the capture of unpredictable bursts in sample strength.

158 ks, probably resulting from action potential bursts in single collaterals and variable times to spike

159 inked to the presence of approximately 20 Hz bursts in SM1 and peripheral activity.

160 timing of activity and the amplitude of EMG bursts in SOD1G93A mice.

161 Chains of ripples (ripple bursts) in CA1 have been reported to co-occur with long-

162 t, a stochastic parameterization of the wind bursts including both westerly and easterly winds is cou

163 d that the frequency and duration of pumping bursts increase and the duration of long pauses diminish

164 These include acceleration-dependent initial bursts, increased dynamic response to stretch velocity i

165 The timescale and amplitude of these bursts indicate the presence of an unstable, magneticall

166 romoter elements to modulate transcriptional bursting individually allows combinatorial fine-tuning o

167 rs of coupled neurons in vitro, we show that burst-induced depression depends on calcium entry via vo

168 hese shells can relieve internal pressure by bursting intermittently, shrinking and re-growing, provi

169 action potentials, but with different inter-burst intervals.

170 Entry to and exit from an open burst is controlled by the interaction of ATP with two A

171 The phagocyte respiratory burst is crucial for innate immunity.

172 l Ca(2+) Increases in Ca(2+) driven by spike bursts last seconds; however, the increases in nerve ter

173 ated after a short latency (50 ms) following burst-like PFC electrical stimulation, and the magnitude

174 ontrast with expectation for a single "early burst" model, morphospace continued to expand following

175 somatosensory neocortex, we found that theta burst neural activity produced an unexpected long-lastin

176 change in arteriole diameter caused by theta burst neural activity.

177 bursting parameters and genes whose alleles burst non-independently.

178 nt intracellular Ca(2+) increase following a burst of action potentials.

179 ility of the second action potential in each burst of activity.

180 n of fused silica and sapphire by means of a burst of femtosecond pulses having time separation in th

181 abit of field tomatoes, resulting in a quick burst of flower production that translates to an early y

182 E1alpha deficiency in diabetes resulted in a burst of functional miRs from miR-466 and miR-200 famili

183 complex that underwent an even more dramatic burst of fusion upon Sec17p addition.

184 of a novel dishabituating stimulus (a single burst of high-intensity exercise) in male Sprague-Dawley

185 Injury to RGC axons causes a burst of intracellular superoxide, which then signals RG

186 >TTC mutation rate in Europeans, indicates a burst of mutations from about 15,000 to 2000 years ago,

187 BD treatment also attenuated the respiratory burst of neutrophils isolated from chronic plus binge al

188 e immediately after budding coincides with a burst of phosphatidylinositol-3-phosphate, distinct from

189 A substantial burst of phosphatidylinositol-4-phosphate immediately af

190 Postinjury neurogenesis occurs as a burst of proliferation that peaks in days, followed by m

191 on should be delayed until after the initial burst of proliferation, but could be beneficial during t

192 ntified: an early destructive phase, where a burst of reactive oxygen species induces loss of E-cadhe

193 An exacerbation was defined as a burst of systemic corticosteroids lasting 3 days or more

194 lso pull microscopic objects apart through a burst of their rigid tubular structure.

195 Despite inducing a strong burst of thrombin and plasmin, FXa/PCPS infusion did not

196 erminal effector cells initiated by an early burst of transcriptional activity and subsequently refin

197 lysis showed that methyl JA (MeJA) induces a burst of transcriptional activity, generating diverse ex

198 etimes sufficiently large to trigger a short burst of very high frequency (100-300 Hz) firing.

199 mber of abortive infection events, including bursting of ITs and a reduction in the number of nodules

200 ere we analyze the relative contributions to bursting of the individual core promoter elements-CCAAT,

201 Electroporation was achieved by bursts of 300-ns, 9 kV/cm pulses (50 Hz, n = 3-100) and

202 Here, we studied transposition bursts of a heat-activated retrotransposon family in Ara

203 e, whose light curve displays quasi-periodic bursts of about 30 minutes duration roughly every 2 hour

204 ed long-lasting depolarizing potentials with bursts of action potentials after synaptic stimulation.

205 We find that bursts of action potentials and local neuropeptide signa

206 in mouse primary cultures fired spontaneous bursts of action potentials.

207 atterns of single flies are characterized by bursts of activity at dawn and dusk.

208 on-contraction coupling, resulting in random bursts of Ca(2+) release probably due to Ca(2+) overload

209 ght requires the ability to efficiently fuel bursts of costly locomotion while maximizing energy cons

210 i-periodic "seasons", which include enhanced bursts of eruptions for several months, followed by quie

211 This "behavioral coupling" causes bursts of feeding activity that account for up to 68% of

212 tion of Biomolecules), that generates micros bursts of hydroxyl radicals from water, to measure chang

213 e faster than other regions, showing several bursts of rapid evolution.

214 vate innate immune signaling events, such as bursts of reactive oxygen species (ROS).

215 urons release neurohormones in long-duration bursts of secretion.

216 continuous subthreshold sine wave with short bursts of suprathreshold pulse-trains inserted at differ

217 maintain a cellular filter against decoupled bursts of transcription factor activation but mount a st

218 idly increase in copy number due to periodic bursts of transposition.

219 obabilities of initiation and termination of bursts of triggered activity that are maintained by a po

220 KOR activation increased 'bursts' of incorrect responses in the DRL task and incre

221 ritic tree compared with spikes occurring at burst onset.

222 ell type, high-frequency low-threshold spike burst or lower-frequency tonic APs undergo substantial v

223 that enhances fitness, may depend upon short bursts or complex patterns of locomotion.

224 tant plants showed a wrinkled seed coat or a burst-out embryo phenotype.

225 ut from the micropylar end, resulting in the burst-out embryo seed phenotype.

226 d by inhibitors of ROS-producing respiratory burst oxidase enzymes.

227 of the lower expression level of RESPIRATORY BURST OXIDASE HOMOLOG D (RbohD).

228 Transcripts encoding the Respiratory Burst Oxidase Homolog F, signaling components involved i

229 y captures the experimentally measured swell-burst parameters for single-component GUVs, and reveals

230 ects genes exhibiting allelic differences in bursting parameters and genes whose alleles burst non-in

231 to contribute differentially to the overall bursting pattern of the promoter during basal transcript

232 hancers to perturbation, the transcriptional bursting patterns of enhancers, and the ability of an en

233 Likewise, the transition into a burst/pause pattern results from combinations of intrins

234 STDP can bind plasticity to the mossy fiber burst phase with high temporal precision.

235 rmittent forcing that precedes switching and bursting phenomena.

236 ion potentials clustered into high-frequency bursts play distinct roles in neural computations.

237 hen accretes onto the white dwarf, producing bursts powered by the release of gravitational potential

238 trate that internally initiated GAD65LH cell bursts precede and accompany spontaneous running bouts,

239 reased unitary conductance (>/=50%), altered burst proportions (3-fold reduction in the proportion of

240 surements, gyrase relaxed overwound DNA with burst rates of approximately 100 supercoils per second (

241 in the model occurs in discrete oscillatory bursts rather than as sustained activity.

242 We measured the oxidative burst reaction in mammalian macrophages (NR8383 rat alve

243 immediate inhibitory effect on the oxidative burst reaction.

244 ncy bands, and it is not yet clear how these bursts relate to the sustained oscillation observed in r

245 ophils had an enhanced phagocyte respiratory burst relative to Nbeal2-expressing neutrophils.

246 and tri-phasic release profiles with varying burst release and lag phase.

247 strated efficacy at killing cells beyond the burst release effect.

248 er from limitations including instability, a burst release of the drug, and limited surface functiona

249 Striking behaviors include "burst" RNA nuclear export dynamics regulated by HIV-1's

250 pore size, again much smaller than the large bursts seen during drainage.

251 Brief (1 hr) periods of postsynaptic bursting selectively depressed AMPA receptor (R) synapti

252 ea) and timing (phase and skew, a measure of burst shape) when animals ran on level and inclined trea

253 e deep brain stimulation truncated long beta bursts shifting the distribution of burst duration away

254 amics of primary B-cells, but modulates both burst size and frequency in response to gamma-interferon

255 oximately 100 supercoils per second (average burst size was 6.2 supercoils).

256 was inclined, including intermuscular phase, burst skew and amplitude of the locomotor bursts.

257 During LTS bursts, somatic AP half-width increases progressively wi

258 o burst FRB 121102, the only known repeating burst source, using high-time-resolution radio interfero

259 kes have similar somatic half-widths to late burst spikes and undergo similar dendritic attenuation.

260 with increasing spike number, allowing late-burst spikes to propagate more efficiently into the dend

261 s in the thalamic reticular nucleus - paired burst spiking in coupled neurons, and mGluR-dependent te

262 Burst spiking in substantia nigra pars compacta (SNc) do

263 Thus, PPN-evoked burst spiking of SNc dopaminergic neurons in vivo may no

264 op breakup mechanisms that lead the drops to burst spontaneously into thousands of smaller droplets.

265 he synaptic response of SPNs following theta-burst stimulation (TBS) of cortical afferents.

266 Activation of vChATs with theta burst stimulation (TBS) that alleviates the decay in cho

267 hycardia on programmed right ventricular and burst stimulation and spontaneously as assessed by ECG t

268 ng-term potentiation (LTP) elicited by theta-burst stimulation in field CA1 of hippocampus.

269 Theta-burst stimulation of corticostriatal fibres produces lon

270 Except for theta-burst stimulation vs sham, similar results were obtained

271 d loss of long-term potentiation after theta-burst stimulation.

272 early onset epileptic encephalopathies with burst suppression (Ohtahara syndrome and early myoclonic

273 We confirmed burst suppression in 28 of 33 patients.

274 17 of 28 (61%) patients with confirmed early burst suppression, we identified variants predicted to b

275 TLR9 agonist induce an initial proliferative burst that is followed by apoptotic death.

276 s caused by harvesting triggers an oxidative burst that spreads throughout the cassava root, together

277 as the "hit-and-run" model and transcription bursting that could not be obtained by in vitro biochemi

278 ng) of passive muscle, including the initial burst, the dynamic response to lengthening, and rate rel

279 in are characterized by spontaneous neuronal bursts, the most common of which is the delta brush.

280 dynamic clamp restored the original rhythmic bursting, thereby affirming the roles of those synapses.

281 lications using blue light induced oxidative bursts to prime crop plants against the deleterious effe

282 ming neutrophils for an enhanced respiratory burst together with promoting granule content release co

283 Here, we use continuous theta-burst transcranial magnetic stimulation (cTBS) to test t

284 Inhibitory theta-burst Transcranial Magnetic Stimulation was applied to t

285 By combining inhibitory continuous theta-burst transcranial magnetic stimulation with model-based

286 step of the converging pathways of oxidative burst triggering.

287 This respiratory burst was associated with increased expression of cytoso

288 nocyte phagocytosis was normal and oxidative burst was augmented, suggesting that their innate antimi

289 The RGC superoxide burst was significantly reduced by intravitreal cobalami

290 The number of autapses required to induce bursting was lowered by adding autapses to high degree e

291 the short-lived closures that interrupt open bursts, was greatly increased at pHi 5.8 and 6.3.

292 Beta bursts were defined by applying a common amplitude thres

293 dow AOB mitral cells with a weak tendency to burst, which is further enhanced and stabilized by chemi

294 dynamin GTP hydrolysis occurs as stochastic bursts, which are randomly distributed relatively to the

295 prevent new initiation between transcription bursts, which may reduce noise.

296 rons were sufficient to generate oscillatory bursts with properties similar to in vivo central patter

297 are dissimilar to classical short gamma-ray bursts with ultrarelativistic jets.

298 SCALE to analyze genome-wide allele-specific bursting, with adjustment of technical variability.

299 ochastic gene expression and transcriptional bursting, with implications for regulation of pluripoten

300 ated directly with high frequency electrical bursts yielded episodic local enhancements of frequency-