ライフサイエンスコーパス: burst

1 e to pathogens in a process called oxidative burst.

2 tion to IL-8, but did not affect respiratory burst.

3 required for suppressing the host oxidative burst.

4 tions could an FRB be associated with an SGR burst.

5 el of a TF that is synthesized in stochastic bursts.

6 that transcription occurs intermittently, in bursts.

7 n of the frequency content during ultrasound bursts.

8 ngth display a higher tendency to fire spike-bursts.

9 esponses were not time-locked to recent beta bursts.

10 mal breathing which we term deep breaths and bursts.

11 ribe the regulatory steps of transcriptional bursts.

12 otentials with the cells' propensity to fire bursts.

13 k beta synchrony anticipate episodes of beta bursting.

14 ed by unique trial-to-trial patterns of beta-bursting.

15 (-116.1 +/- 135.0 vs. -185.9 +/- 148.2 a.u. burst(-1) mmHg(-1) , P = 0.040), but not before.

16 omen than men (-2.3 +/- 1.4 vs. -3.3 +/- 1.4 bursts.100 beats(-1) mmHg(-1) , P = 0.007), while this s

17 int (burst incidence; 39 +/- 16 to 33 +/- 17 bursts.100 Hb(-1) ; P = 0.01) and diastolic operating pr

18 ive phase by emitting intense soft gamma-ray bursts(15).

19 The coincidence of FRB 200428 with an X-ray burst(9-11) favours emission models that describe synchr

20 Burst abdomen after midline laparotomy is associated wit

21 es of fascial redehiscence after surgery for burst abdomen in a study cohort (July 2014-April 2019) t

22 storical cohort and 80% of the study cohort, burst abdomen occurred after emergency laparotomy (P = 0

23 ardized surgical strategy was introduced for burst abdomen: The abdominal wall was closed using a slo

24 The combined burst acquisition rate of the pipeline is 3 Gpixel per s

25 ning positively correlated with reduced beta bursts across all tested hemispheres.

26 tions and robust duality of power-law (theta-bursts, active phase) and exponential-like (delta-bursts

27 ons, it is currently unknown whether and how burst activity, assessed in vivo during natural behavior

28 as drastically different from that of bubble-bursting aerosols from the tank experiments-suggesting a

29 cal theta activity and fired precisely timed bursts after reward and punishment.

30 However, we discovered that bursting alone cannot quantitatively recapitulate the fo

31 As a dust grain dissolves, the pockets burst and emit acoustic signals that are detected by dis

32 ll differences in the delay between the last burst and movement onset had no significant impact on ve

33 MDA receptor in these neurons, which affects bursting and plasticity, abolishes lever pressing for po

34 works revealed hyperexcitability and altered bursting and synchronicity.

35 g revealed that these regulatory strategies (bursting and the time window) respond in different ways

36 r electromagnetic pulses powered by magnetar bursts and giant flares(3,4,12,13).

37 e of a causal link between sensorimotor beta bursts and movement initiation and suggest that neurofee

38 Finally, spontaneous GPi bursts and pauses were both followed by small, slow redu

39 ed from the neighbouring fields of gamma-ray bursts and radio pulsars has also offered insights.

40 activity, examine the origin of spiking and bursting, and determine which channel types are responsi

41 scriptional process emerging from studies of bursting, and how this work contextualizes the relative

42 hibitory mechanisms that restrict excitatory bursts, and engaging wide areas of cortex.

43 nown location resided in Layer II, generated bursts, and their interspike intervals (ISIs) were typic

44 High-frequency spike-bursts are believed to be essential for this process, by

45 equired to achieve coherent radiation in SGR bursts are difficult to satisfy, and that only under ext

46 Oral corticosteroid bursts are frequently prescribed in the general adult po

47 Other engines that could produce fast radio bursts are not required, but are also not impossible.

48 These bursts are theorized to gate or permit specific motor ac

49 .SIGNIFICANCE STATEMENT High-frequency spike-bursts are thought to serve fundamental computational ro

50 x difference was observed when assessed with burst area after adjusting for carotid beta-stiffness (-

51 lder men and women, while that assessed with burst area was more sensitive as the carotid artery beca

52 Sympathetic BRS assessed with burst area was negatively (more sensitive) correlated wi

53 hile there was no difference in the range of burst area.

54 f preBotC network dynamics where inspiratory bursts arise when and only when the preBotC rhythmogenic

55 licate the occurrence and modulation of beta-bursts associated with initiation and cancellation of sa

56 Our results suggest that FRB-SGR burst associations are rare.

57 se correlations, from responses to 1 s noise bursts at 10-30 dB sensation level (dB above threshold).

58 More specifically, the Sync model uses bursts at theta frequency to flexibly bind appropriate t

59 tive oxygen species generated by respiratory burst attack iron-sulfur cluster-containing proteins, in

60 g loss at 4 weeks of age as measured by tone burst auditory brainstem responses.

61 ent cellular ROS increases or effects in MEA bursting behavior at sub-lethal dosages.

62 Moreover, when the overlap of bursts between the two STN was high, slowing was more pr

63 Bursting cholinergic neurons (Burst-BFCNs) fired synchronously, phase-locked to cortic

64 the cumulative, but recent, history of beta bursting, both locally and across basal ganglia networks

65 emission coincident with the arrivals of SGR bursts, but unfortunately we were not observing when the

66 Such phasic bursting by GABA neurons also occurred in WT mice in ass

67 The reciprocal rhythmic bursting by the pGABA and pNon-GABA neurons drove rhythm

68 ely, this finding raises doubts whether beta-bursts can be a causal mechanism of response inhibition,

69 In contrast, neither the rarely bursting cells in Layer III, nor the high-frequency burs

70 at were classically indicated as regular and bursting cells, and showed differences in the extension

71 ional neutrophil functions, like respiratory burst, chemotaxis, and phagocytosis.

72 Bursting cholinergic neurons (Burst-BFCNs) fired synchro

73 low movements are those that follow multiple bursts close to each other and bursts that are coupled a

74 The results indicate that plastic strain bursts consist of numerous individual dislocation glide

75 of TRN cell types, including state-dependent bursting, contribute to these output dynamics.

76 n (70 +/- 66 degrees , N = 89) of only a few bursts destabilize the cell-swimming direction.

77 Increased beta bursts detected in the motor cortex have also been assoc

78 d regulates the post-selection proliferative burst, differentiation and functions of iNKT cells.

79 Burst discharges (phasic firing) of dopamine-containing

80 s increased spike rates and the emergence of burst discharges reflecting network hyperexcitability.

81 n decreases striatal neuron action potential burst duration in vitro, without altering other electrop

82 in Parkinson's disease demonstrate increased burst durations relative to essential tremor patients.

83 minent theta (~4-7Hz) feature dominating the bursts during BSP in these patients.

84 The manipulation of burst dynamics may be a means of selectively improving m

85 Moreover, the bursting effects occurred only below/at, but not above,

86 ry gland typically display either spiking or bursting electrical activity, which is related to the le

87 cation glide processes, which lead to strain burst emissions in micro-scale samples.

88 at the surface until the next explosive slug-bursting event.

89 role of intermittent, transient, high-power burst events of neural activity.

90 utcomes showed either no features, transient burst features, or decreasing intraburst frequencies wit

91 Such phasic burst firing also occurs during natural attentive waking

92 Op/q mice reduces thalamic reticular nucleus burst firing and promotes rather than reduces seizure, i

93 milarly revealed cleft alkalinization during burst firing in both males and females.

94 the thalamocortical relay neurons; however, burst firing in thalamocortical relay neurons remains es

95 over, in thalamic reticular nucleus neurons, burst firing is impaired accompanied by attenuated IT.

96 We show that burst firing of mouse inner hair cells prior to hearing

97 increase of T-type calcium channel-mediated burst firing of thalamocortical neurons, though the latt

98 Q channels does not promote Cacna1g-mediated burst firing or T-type calcium current (IT) in the thala

99 Glutamate typically stimulates burst firing subsequent to this hyperpolarization in nor

100 itic excitability and smaller propensity for burst firing.

101 but these transients summated rapidly during burst firing.

102 ) is necessary to achieve the high-frequency bursting firing pattern characteristic of both types of

103 tecture of pyramidal neurons might determine burst-firing by setting the relative amount of distal ex

104 st, during rapid movement cancellation, beta-bursts first emerge over fronto-central sites typically

105 irst seconds upon hot water addition ("aroma burst"), followed by subsequent decrease in headspace (H

106 er a constant polarization angle during each burst for some repeaters(9,10) or variable polarization

107 Fast radio bursts (FRBs) are brief, bright, extragalactic radio fla

108 Fast radio bursts (FRBs) are millisecond-duration radio transients

109 Fast radio bursts (FRBs) are millisecond-duration radio transients(

110 tragalactic, millisecond-duration fast radio bursts (FRBs)(2).

111 and muscle sympathetic nerve activity (MSNA) burst frequency (+55 +/- 31%), whereas transient hyperox

112 Increases in MSNA burst frequency (time: P < 0.01, trial: p = 0.27, intera

113 ame kinetic phenomena: a coupled increase of burst frequency and amplitude.

114 n factor binding and reduces transcriptional burst frequency in a subset of gene promoters, generatin

115 pproaches, we found that the transcriptional burst frequency is modulated across the stripe to contro

116 ses (P = 0.0047), but did not attenuate MSNA burst frequency responses (P = 0.3662).

117 cients of variation for ventilatory and MSNA burst frequency responses, indicating test-retest reprod

118 tes perceived pain and pressor, but not MSNA burst frequency, responses during a CPT.

119 Consistent with BMP-dependent regulation of burst frequency, the numbers of BMP target gene transcri

120 trolled stress response is regulated via the burst frequency.

121 observations of a millisecond-duration radio burst from the Galactic magnetar SGR 1935+2154, with a f

122 magnetars are the engine powering repeating bursts from FRB sources(4-13), but no convincing evidenc

123 ng a continuous light pulse or phasically in bursts (>100 Hz) when driven by rhythmic light pulses at

124 Since firing in bursts has been associated to neuropeptide release, we h

125 led under the umbrella term 'transcriptional bursting' has received considerable interest.

126 ene regulatory mechanisms on transcriptional bursting have been studied, it remains unclear how morph

127 r-saturated ecosystems can fuel a surprising burst in shrub belowground productivity, one possible me

128 i underlies the 24-hour-based rhythms of RBC bursting in mice.

129 organization of super-enhancers (SEs) drives bursts in germline gene expression after the mitosis-to-

130 K, attenuated large-amplitude AMPAR-mediated bursts in hippocampal CA3.

131 ibution, with multiple retro-transpositional bursts in mouse evolutionary history and only one in hum

132 an facilitate volitional suppression of beta bursts in sensorimotor cortex in healthy motor control b

133 th the rate and accumulated duration of beta bursts in the contralateral motor cortex before the go-c

134 Owing to bursts in the expression of thousands of germline-specif

135 then the link between the occurrence of beta bursts in the sensorimotor cortex before the go-cue and

136 We demonstrate that bursts in theta and delta cortical rhythms exhibit compl

137 s and optogenetically induced hyperexcitable bursts in vivo were present in a cortical region distal

138 proved neutrophil function: normal oxidative burst (in 3 of 3 patients tested), corrected protein gly

139 athetic baroreflex sensitivity assessed with burst incidence was less sensitive as the carotid artery

140 Sympathetic BRS assessed with burst incidence was lower in older women than men (-2.3

141 iNO also reduced the MSNA operating point (burst incidence; 39 +/- 16 to 33 +/- 17 bursts.100 Hb(-1

142 The frequency of these discrete bursts increased progressively during the postnatal preh

143 Spike and burst indices (n/sec/channel) were computed across four

144 We further show that respiratory burst induces antibiotic tolerance in the spleen during

145 Burst occurrence and size were assessed with burst interval and area of muscle sympathetic nerve acti

146 The range of burst interval was smaller in older women than men (P =

147 that the response of burst size within each burst is augmented for the baroreflex BP control despite

148 Therefore, bursting is the single locus illustration of both gene a

149 of the polarization angle features of these bursts is consistent with a magnetospheric origin of the

150 ers from other bacterial systems, and yields bursting kinetics characteristic of eukaryotic systems.

151 activity is characterized by short-lasting, burst-like events, rather than by steady modulations.

152 activity, which is dominated by short-lived, burst-like events.

153 When the gas slug bursts, liquid is drawn up in its wake, which exsolves t

154 This facilitates translational bursting, liquidation of storage carbohydrates, increase

155 d lymphocytes, macrophages underwent a brief burst (<1 hour) of rapid phagocytosis, which was then in

156 ffects, but the risk from brief oral steroid bursts (<=14 days) is largely unknown.

157 ater may represent the single most expensive burst maneuver found in nature.

158 2 complex that mediates neutrophil oxidative burst, markedly reduced CXCL1-induced NASH and stress ki

159 amed, or FRB-like events associated with SGR bursts may have narrow spectra and characteristic freque

160 at increased synchronization denoted by beta bursting might compromise information coding capacity in

161 o fire action potentials in a high-frequency bursting mode and that this is important for peptide tra

162 The Gamma-ray Burst Monitor (GBM) on board the Fermi spacecraft provid

163 continuous encoding was more prevalent than bursting near movement initiation or termination.

164 neurons exhibit such graded changes without bursting near specific actions.

165 lastic dendritic spines of the intrinsically bursting neurons and their interaction with hyper-ramifi

166 We did not find a similar class of NW bursting neurons in L2-L4 of mouse V1.

167 Given its properties, this class of NW bursting neurons should be pivotal for the encoding and

168 y we demonstrate that small LNvs (sLNvs) are bursting neurons, and that I(h) is necessary to achieve

169 e biocatalytic reaction network coupled with burst nucleation of nanoparticles above a critical super

170 y the source of the brightest Galactic radio bursts observed on similar timescales(7).

171 cancellation of saccades, we found that beta-bursts occur too infrequently to account for the observe

172 Burst occurrence and size were assessed with burst inter

173 BP control despite the impaired response of burst occurrence in older women with greater carotid sti

174 stribution (variation) of burst size against burst occurrence was greater in women than men.

175 itical role for angiotensin II in regulating burst occurrence, and a multifunctional role for the ros

176 Single-trial analysis revealed greater burst occurrences on object individuation versus ensembl

177 eplay sequences were packaged into transient bursts occurring selectively during activation of the de

178 es in context, or event boundaries, elicit a burst of autonomic arousal, as indexed by pupil dilation

179 to the universally reported short transient burst of competent state in vitro, the naturally develop

180 A subsequent burst of DNA replication in the next mitosis generates e

181 creased phagocytosis/killing by an oxidative burst of murine neutrophils in vitro Intravital microsco

182 Notably, a postnatal burst of PACAP expression occurred in RTN neurons precis

183 driving these inflammatory responses is the burst of reactive oxygen species (ROS), with hydrogen pe

184 stimulate condensate formation, whereas the burst of RNAs produced during elongation stimulate conde

185 This burst of transposition is likely related to the activity

186 evers are the consequence of the synchronous bursting of red blood cells (RBCs) on completion of the

187 their intrinsic ability to generate rhythmic bursts of action potential.

188 With bursts of action potentials, we found that calcium respo

189 alf of the cases, additional few-millisecond bursts of an almost equiprobable CW or counterclockwise

190 Bursts of beta frequency band activity in the basal gang

191 slow periodic voltage spikes and coordinated bursts of Ca(2+) oscillations.

192 the backbones of phylogenetic trees exhibit bursts of diversification on all timescales.

193 Sawtooth waves (STW) are bursts of frontocentral slow oscillations recorded in th

194 ation is interrupted by delta/theta-periodic bursts of gamma-frequency FSI inhibition.

195 We characterized the occurrence of bursts of genome-wide loss-of-heterozygosity (LOH) in Sa

196 should be transferred through gamma-rhythmic bursts of information, resulting in a modulation of the

197 Bursts of ketamine-dependent HFO were coupled to "fast"

198 The presence of bursts of local field potential activity in the alpha, a

199 ht ions, as well as the production of strong bursts of neutrons and multi-[Formula: see text] photons

200 Plasticity can only be recovered when bursts of postsynaptic spikes are used, or when neurons

201 tions in the human cortex reflect underlying bursts of single-unit spiking activity that are organize

202 esent as scalp electroencephalographic (EEG) bursts of slow waves contrasting with the low-voltage fa

203 production from respiration instead of only bursts of stored gases.

204 logical processes responsible for punctuated bursts of structural genomic variation.

205 We show recent and rapid bursts of the three Hevea-specific LTR-retrotransposon f

206 We find that infrequent, stochastic bursts of transcription result in the co-expression of t

207 normally sighted blindfolded subjects using bursts of white noise presented frontally, laterally, or

208 Thus, an on-and-off "burst" of ClC-5 activity was crucial for preventing Cl(-

209 A convulsant, kainic acid, increased bursts only in the specifically treated networks.

210 onsist of intrinsically rhythmically active 'bursting' ORNs (bORNs) in the lobster, Panulirus argus.

211 s characterized by steady reductions of beta-bursting over bilateral sensorimotor sites.

212 ation was signified by increased phasic beta-bursting over fronto-central sites.

213 efore movement initiation and increased beta-bursting over medial frontal areas with movement cancell

214 ANCE STATEMENT The finding of increased beta-bursting over medial frontal cortex with movement cancel

215 rofeedback reflecting the occurrence of beta bursts over sensorimotor cortex quantified in real time.

216 escribed reduced frequency of transient beta-bursts over sensorimotor cortical areas before movement

217 directly bind to the promoter of RESPIRATORY BURST OXIDASE HOMOLOG 1 (RBOH1), and that RBOH1-mediated

218 e studies further identified the RESPIRATORY BURST OXIDASE HOMOLOG D (RBOHD) protein as a key player

219 aphic P wave and increased susceptibility to burst pacing-induced atrial arrhythmias.

220 putational modeling to infer transcriptional burst parameters at single-cell resolution.

221 s the T3SS to inhibit neutrophil respiratory burst, phagocytosis, and release of inflammatory cytokin

222 ely-moving mice, we explored whether and how burst propensity relates to pyramidal cell heterogeneity

223 sounds with and without overtones, sounds of burst-pulse character, graded sounds, biphonations, and

224 ynaptic dysfunction to layer V intrinsically bursting pyramidal neurons in the prefrontal cortex of m

225 s, active phase) and exponential-like (delta-bursts, quiescent phase) duration distributions, feature

226 ncy increases of bilateral sensorimotor beta-burst rates, suggesting that motor inhibition can be rap

227 by systematic spatiotemporal changes in beta-burst rates.

228 These burst-rates predicted reaction time (a relationship that

229 ed, during movement initiation, sensorimotor burst-rates steadily decreased, lateralizing just before

230 motor control, after which sensorimotor beta-bursting re-initiates.

231 low afterhyperpolarization (AHP) after spike bursts, regulating membrane excitability.

232 To investigate how beta-bursts relate to movement in male and female humans (N =

233 n vitro drug-release study showed an initial burst release (25 %) between 0-24 h and a sustained rele

234 Yet, initial burst release and optimal modulation of the release prof

235 sulphate from nanofiber exhibited an initial burst release followed by a slower release pattern.

236 mice bearing large established tumours, the burst release of annexin A5 owing to diselenide-bond cle

237 e of microparticles and mitigate the initial burst release.

238 e, lose structural integrity, and eventually burst, releasing their contents into the extracellular m

239 The microbial adaptations to the respiratory burst remain poorly understood, and establishing how the

240 ods of active nascent RNA synthesis known as bursts represent individual gene activation events in wh

241 ive microneedles allow a combinatorial rapid burst response along with slow, sustained release, respe

242 temporal epoch coincident with early visual burst responses in the SC.

243 ver distinct subsets of neurons that exhibit bursting responses specifically to a chord but neither t

244 neural activity and highlight that the theta-burst rhythm is relatively privileged in its ability to

245 Layer III neurons were only sparsely bursting (SB) and had no DAPs.

246 potential mechanisms that could support such burst sequences, it remains unclear whether these mechan

247 of gravitational-wave (GW), short gamma-ray bursts (sGRBs) or optical surveys, a large sample of kil

248 Bursts share features of chemoreflex-driven clinical bre

249 age data), suggesting that sensorimotor beta-bursting signifies an inhibited motor system, which has

250 e found that the distribution (variation) of burst size against burst occurrence was greater in women

251 tazanavir, which reduces the cellular virion burst size and hence inhibits replication only after ini

252 on muscle sympathetic nerve activity (MSNA) burst size and occurrence separately as subcomponents of

253 These data suggest that the response of burst size within each burst is augmented for the barore

254 ikely driven by random variation in parasite burst size, which is linked to the rate of host cells lo

255 trolled stress response is regulated via the burst size, while that of the sigma(54)-controlled stres

256 d noninvasive network-based continuous theta burst stimulation (cTBS) in human subjects (male and fem

257 r each of two TMS sessions, continuous theta-burst stimulation (cTBS) was applied to either a control

258 Intermittent theta-burst stimulation (iTBS) is a noninvasive brain stimulat

259 ke plasticity elicited by intermittent theta burst stimulation (iTBS) is reduced in the primary motor

260 Prolonged intermittent theta burst stimulation (piTBS) with triple doses of the stand

261 humans using network-based continuous theta burst stimulation selectively impairs behavior that requ

262 We reasoned that theta-burst stimulation would be particularly effective for im

263 cus to achieve either seizure suppression or burst suppression on continuous EEG.

264 analyses of available EEGs during prominent burst suppression patterns (BSP) present in all 3 patien

265 oscillations in the mutant mice, and reached burst-suppression pattern earlier when compared to the W

266 ork and determine how neuromodulation, short-burst tetanic microstimulation (sbTetMS), alters multire

267 llow multiple bursts close to each other and bursts that are coupled across regions.

268 ic Ca(v)3-dependent calcium events that form bursts that are stereotypic in form.

269 indicates that several long-terminal-repeat bursts that occurred from 5.7 million years ago to less

270 ed, resulting in unsuppressed host oxidative bursts that triggered immunity.

271 ts appeared as openings in quick succession (bursts) that showed no ligand concentration dependence.

272 hic growth by suppressing the host oxidative burst-the first line of plant defense.

273 spersion of a sample of localized fast radio bursts; this technique determines the electron column de

274 we further hypothesize that suppressing beta bursts through neurofeedback training can improve motor

275 We applied theta-burst TMS to LOC (and a control site) to interfere with

276 n facilitating voluntary suppression of beta bursts to speed up movement initiation.SIGNIFICANCE STAT

277 possible mechanism linking spontaneous spike bursts to tonotopic map refinement and further highlight

278 t medial-temporal cortex by delivering theta-burst transcranial magnetic stimulation (TBS) concurrent

279 Theta burst transcranial magnetic stimulation (TBS) is a poten

280 ic change to dIPL node with continuous theta-burst transcranial magnetic stimulation in a randomized,

281 aracterize and visualize how transcriptional bursting varies over time and space.

282 , we could unambiguously distinguish between bursting vesicles, which was only rarely observed (<0.01

283 Neutrophil oxidative burst was preserved in response to phorbol 12-myristate

284 Although transcriptional bursting was originally observed decades ago, only recen

285 Before movement initiation, beta-bursting was prominent at bilateral sensorimotor sites.

286 to cues prospectively triggered by STN beta bursts was slower than when responses were not time-lock

287 nts, 2 623 327 who received a single steroid burst were included.

288 Theta coupling of HFO bursts were also found in the prefrontal cortex and vent

289 Beta bursts were defined as periods exceeding the 75th percen

290 rd session, 29 soft-gamma-ray repeater (SGR) bursts were detected in gamma-ray energies.

291 Such beta-bursts were followed by short-latency increases of bilat

292 We also found beta-bursts were more common after errors, but their incidenc

293 hagocytosis, transmigration, and respiratory burst) were used to assess the effects of pre-, co- and

294 be fast-firing neurons with the capacity to burst when depolarized from a hyperpolarized membrane po

295 Bursts, which are serial taperings of respiratory depth

296 he corrective response has multiple activity bursts, which are suggested to originate from different

297 ssion of PTI-induced reactive oxygen species burst, while the full virulence activities of nuclear ta

298 ing that larger cells typically display more bursting, while the smallest cells almost always only ex

299 ported arcsecond-localized(14-18) fast radio bursts with four new localizations in host galaxies that

300 re, induced a transient but robust IFN-gamma burst within a proinflammatory cytokine/chemokine landsc