ライフサイエンスコーパス: temporal

1 e greater force dysmetria but display better temporal accuracy during fast goal directed contractions

2 Here, we test whether greater temporal accuracy occurs in all individuals with SCA6, a

3 interneurons control sound-evoked responses, temporal adaptation and network dynamics in the auditory

4 ng the degradation tag (dTAG) system provide temporal advantages over genetic approaches and improved

5 To enable such temporal analysis from multimodal single-cell experiment

6 Our temporal analysis of these maps documents the single lar

7 o cutin synthesis and deposition has shown a temporal and coordinated sequence that correlates with t

8 In conclusion, a distributed network of temporal and frontal brain regions supports gamma phase

9 er enhancement, TFCE) and in FH +group (left temporal and parietal regions p<0.01, TFCE).

10 The spatio-temporal and polarisation properties of intense light is

11 Although we observed temporal and regional differences, transcriptomic change

12 ounded embryonic corneas, whilst identifying temporal and spatial changes in collagen organization du

13 Our discovery provides temporal and spatial clues of the early history of the H

14 eural stem cells (NSCs) to divide with tight temporal and spatial control to produce different daught

15 d monitoring of sharks could greatly improve temporal and spatial data used for management purposes.

16 ory included individual factors and excluded temporal and spatial factors.

17 d using optical tweezers, which enabled high temporal and spatial resolution of hydrodynamic forces.

18 research and policy interventions is the low temporal and spatial resolution of publicly available ad

19 re selection process was performed to select temporal and spectral EEG features that contribute to te

20 m amygdala, anterior cingulate, superior/mid-temporal, and middle frontal gyrus.

21 mportant purpose of filling gaps in spatial, temporal, and organismal representation, but also with a

22 to scattered lateral frontal, parietal, and temporal areas.

23 imaging (MRI) and confirmed by biopsy of the temporal artery.

24 atumoral T(R)(eg) cells; they may also allow temporal assessment of whether the fine balance between

25 m APSGN in terms of its demographic profile, temporal association with active infection and disease o

26 etween the anterolateral EC and the anterior-temporal (AT) memory network appears to drive higher tau

27 Aside from right temporal atrophy, the imaging pattern showed volume loss

28 temporal expectations and the allocation of temporal attention in the visual domain.

29 ngs provide strong evidence that cross-modal temporal biases depend on sensory experience during an e

30 This temporal cascade supports a physiological model of actio

31 .e., at a single time point) and rate-(i.e., temporal change) based demographic characteristics of sp

32 In particular, we find locus-specific temporal changes in accessibility both across megabase-l

33 Spatial and temporal changes in land cover have direct impacts on th

34 ed and controlled swine farm environments on temporal changes in the gut microbiome and resistome of

35 We describe temporal changes in the incidence, microbiology, and out

36 occurs in mycobacteria, we characterized the temporal changes in the transcriptome of synchronously r

37 evel, although control individuals exhibited temporal changes in their response times, a clear effect

38 , and demonstrated assessment of spatial and temporal changes in these parameters within calf muscles

39 gies of fossil herbivores and the associated temporal changes is one aspect of inferring paleoenviron

40 Multiple temporal characteristics of the recalled sequential acti

41 e architecture and last beyond optical pulse temporal characteristics.

42 The concentration-dependent spatio-temporal code at the output of the antenna circuits dete

43 attern of AP firing, emphasizing the role of temporal code in conveying key information about changes

44 Temporal coding quality was evaluated as vector strength

45 where it is activated following the rule of temporal colinearity.

46 Here, we describe unexpected temporal compensatory responses in biomineralization as

47 se and fall times of the elution band of the temporal component were considered as the instrumental f

48 n, we identified individual, contextual, and temporal conditions under which the interventions benefi

49 In this paper, we examine temporal confounding by generalizing derivations to allo

50 ogeneity arising from cellular types, spatio-temporal contexts and environmental stimuli.

51 Temporal control of genes is associated with specific ch

52 tics can be used to achieve quantitative and temporal control of gut bacterial metabolism in order to

53 By imposing thermal and temporal control of the orthogonal gelation methods, the

54 al agents that allow for precise spatial and temporal control over the CO release.

55 ghout the body, such molecular clocks convey temporal control to the function of organs and tissues b

56 s, trigger contents release with spatial and temporal control.

57 factor/TrkB signaling with tight spatial and temporal control.

58 cation of cellular proteins with spatial and temporal control.

59 Our findings identify temporal coordination between DSB strand exchange and ho

60 that selective attention relies on rhythmic temporal coordination between visual areas, and establis

61 The temporal correlations among these fluctuations across th

62 ues to investigate how neurons in the middle temporal cortex (MT) represent multiple stimuli that com

63 Human ventral temporal cortex (VTC) is critical for visual recognition

64 deration of the sulcal patterning in ventral temporal cortex across hominoids, as well as revise the

65 ources were identified in the right superior temporal cortex and the orbitofrontal cortex.

66 9.7 [2.6]; P = 3.0 x 10(-4)) in the inferior temporal cortex only in subjects who were diagnosed with

67 Post-mortem temporal cortex samples from Alzheimer's disease patient

68 g homology to a putative ET cluster in human temporal cortex, but with a strikingly specific regional

69 d the functional connections of the superior temporal cortex, we successfully identified the first-ep

70 -order visual regions spanning occipital and temporal cortex.

71 orbitofrontal cortex, insula, amygdala, and temporal cortex.

72 rger network to provide enhanced spatial and temporal coverage of ecological events.

73 greater than those in the other groups, and temporal CT and FAZ diameter were significantly lower (P

74 similar neurophysiological mechanisms encode temporal cues like voice-onset time (VOT), which disting

75 by selectively filtering out noise and fast temporal cues such as voicing periodicity, that are not

76 We analyzed relapse and temporal daily corticosteroid dose with and without co-a

77 -time incidence estimates that can help fill temporal data gaps resulting from surveillance reporting

78 erms of acoustic attenuation, dispersion and temporal decorrelation at typical operational ranges and

79 udinal analyses (n = 4) revealed significant temporal differences in the ratios of DRMs in the compar

80 ion, we selectively degraded the spectral or temporal dimensions of auditory sentence spectrograms to

81 sults suggest a nuanced relationship between temporal discounting and explore-exploit behavior that m

82 Delay-Discounting Questionnaire to estimate temporal discounting and the Horizon Task to quantify tw

83 atives contribute to reward decisions during temporal discounting is not clear.

84 luding short- vs. long-term sexual strategy, temporal discounting, the Arizona life history battery,

85 This temporal disparity between prepartum maturation and neon

86 after infarct and demonstrated a pattern of temporal dispersion independent of stroke location.

87 demonstrate that loss of heterozygosity and temporal dissection of mutations can be exploited to ide

88 th distinct functional properties and spatio-temporal distribution in the brain, raising the possibil

89 levels (counties) it is possible to estimate temporal diversity and farm-scale spatial diversity from

90 mprecision related to device programming and temporal drift of conductance values.

91 p consists of alternating brain states whose temporal dynamics determine whether conscious experience

92 production at the shoot apex, but the spatio-temporal dynamics of auxin gradients is unknown.

93 les of coupled climate simulations producing temporal dynamics of climate en route to stable global m

94 While spatio-temporal dynamics of clot formation are well characteriz

95 We probed the spatio-temporal dynamics of eCRF modulation using a reverse cor

96 data thus link engagement of the CRN to the temporal dynamics of episodic memory and highlight the r

97 To understand how the spatio-temporal dynamics of intracellular Mg(2+) ((i)Mg(2+)) ar

98 e use ray tracing to predict the spatial and temporal dynamics of lighting for a rendered mature Glyc

99 demonstrate that selection favorably altered temporal dynamics of plant protein digestion.

100 The temporal dynamics of spike spatial distribution were cal

101 uals have rarely been examined to verify the temporal dynamics of these biomarkers.

102 an acquire resistance to antimicrobials, the temporal dynamics of this acquisition is not well unders

103 endosomal puncta of BIK1 exhibit spatial and temporal dynamics that are distinct from those of the PR

104 Based on the spatio-temporal EEG features, we developed a system for detecti

105 protofibril-fibril interaction governs their temporal evolution and potential to exert specific toxic

106 n predicting and statistically analyzing the temporal evolution and spatial distribution of prototypi

107 bling time series experiments to monitor the temporal evolution of cell state distributions and to id

108 fire burned area, we investigated the spatio-temporal evolution of fires in Africa over 2001-2016 and

109 We examine the temporal evolution of patient state using our previously

110 The temporal evolution of the wrinkling features including w

111 be considered a marker for the formation of temporal expectations and the allocation of temporal att

112 se-dependent nature and consequences of cued temporal expectations on brain and behavior in male and

113 conclude that KSHV uses PPD to fine-tune the temporal expression of its genes by preventing their pre

114 This temporal feature allows the present D(4d)-CDMB-8 perylen

115 We propose that the temporal flexibility of a GRN is a general prerequisite

116 rn about a system's properties is to analyze temporal fluctuations in associated variables.

117 Cell fractionation revealed temporal gene regulation, in which early lytic gene expr

118 including distinctive connectivity of human temporal gray matter.

119 antly more deep inner retinal dimples in the temporal group (35%) compared with 5% in the nasal group

120 rahippocampus, thalamus, fusiform and middle temporal gyri, as well as the left and right insula, for

121 male and female) over the posterior superior temporal gyrus (pSTG), a brain area known to be importan

122 with task performance in posterior superior temporal gyrus (STGp) that was observed in healthy subje

123 ive response in the human posterior superior temporal gyrus, enhancing the efficiency of auditory spe

124 /- 1.7 mum (standard error of mean) than the temporal half at 4.1 +/- 2.1 mum (P < .001).

125 Ontario, Canada, we present the spatial and temporal heterogeneity in pathogen prevalence and intens

126 These data, capturing the spatial and temporal heterogeneity of intralesional drug PK, have ma

127 rming practices, which drive the spatial and temporal heterogeneity of life cycle environmental impac

128 t Endocardial-epicardial dissociation marked temporal heterogeneity, discordant and transitioning wav

129 tosol are challenging due to its spatial and temporal heterogeneity.

130 By investigating temporal IFN and inflammatory cytokine patterns in 32 mo

131 Our results depict the temporal impairment of vascular function over the lifesp

132 includes multiple factors, like spatial and temporal indicators.

133 nvironmental source of the specimen, spatial-temporal information and other relevant metadata, but un

134 cellular mechanism for the representation of temporal information in the human brain needed to form e

135 ns, which represents a complementary type of temporal information.

136 l dynamic component could provide additional temporal information.

137 me endpoint measurements and thus provide no temporal information.

138 We also find that the spatio-temporal interactions posited to occur during neurogenes

139 in-time" measurements, for example, can miss temporal intermittency and confound bottom-up/top-down c

140 in behavior and influences the perception of temporal intervals.

141 Temporal lags in population- and assemblage-level shifts

142 life had lower connectivity in the posterior temporal language network.

143 ng evidence points to the role of the Medial Temporal Lobe (MTL) and Medial Prefrontal Cortex (mPFC)

144 lving the orbitofrontal cortex, inferomedial temporal lobe and cerebellum.

145 future experience within neocortical-medial temporal lobe circuits.

146 nal evolutionary modifications affecting the temporal lobe connectivity pattern.

147 Mesial temporal lobe epilepsy (MTLE) is a chronic neurological

148 Individuals with temporal lobe epilepsy and normal MRI showed a similar p

149 In temporal lobe epilepsy cases, hippocampal levels of phos

150 Temporal lobe epilepsy is the most common form of epilep

151 Both amoeboid and ramified cells from mesial temporal lobe epilepsy or peritumoral cortex tissue expr

152 eralized tonic-clonic seizures in a model of temporal lobe epilepsy, and rescued cognitive impairment

153 in the hippocampus, a region associated with temporal lobe epilepsy.

154 regions for posterior cortical atrophy, left temporal lobe for logopenic progressive aphasia and medi

155 c progressive aphasia and medial and lateral temporal lobe for typical Alzheimer's disease.

156 n "process" and "representational" models of temporal lobe function is challenged.

157 on new insights into the role of the medial temporal lobe in auditory cognition.

158 sistently active neurons in the human medial temporal lobe phase lock to ongoing slow-frequency (1-7

159 wing that clear asymmetries exist within the temporal lobe structures subserving the core system and

160 Children were more often drug-free; temporal lobe surgeries had the best seizure outcomes; a

161 ial reward prediction signals in the insula, temporal lobe, and prefrontal cortex, while DA depletion

162 the right ventral frontal area and the left temporal lobe, which represented a close mirror image of

163 lateral and localized beyond the ipsilateral temporal lobe.

164 The anterior temporal lobes (ATL) have become a key brain region of i

165 gions of tau accumulation in the frontal and temporal lobes for all phenotypes and key regions of atr

166 ghlighting the importance of the spatial and temporal location of key molecular events, which may gui

167 hat constrained poetic structures serve as a temporal map for listeners to group speech contents and

168 ency in sampling can be overcome with spatio-temporal modeling to follow species density redistributi

169 le-trial ensemble recordings from the middle temporal (MT) area during perceptual-decision-making, we

170 ontrol and mutant mice before E17.5 when the temporal muscle makes attachment to the coronoid process

171 However, the temporal nature and drivers of functional adaptation rem

172 flicts, our understanding of the genetic and temporal nature of how cells respond to them is poorly e

173 In this paper, we propose a method for temporal network pattern representation and pattern chan

174 in duration and changing in time, forming a temporal network.

175 approach provides a general way not only for temporal networks but also for data stream mining in top

176 iversity, we systematically investigated the temporal neurogenesis profiles of V3 INs in the mouse sp

177 ses an anterior frontal node and a posterior temporal node connected by the white matter of the left

178 Using a temporal order judgment task, we here tested the hypothe

179 that memory recall involves reinstating this temporal order of activity.

180 ise from adaptability of cells: the relative temporal ordering of cell and molecular events was not a

181 lly, using lag analyses, we found consistent temporal ordering of fMRI signals in the cortex relative

182 l J/A transition events help to ensure their temporal ordering.

183 The design principles dictating the spatio-temporal organisation of eukaryotic cells, and in partic

184 d that bioenergetic constraints selected for temporal organisation that promotes oscillatory behaviou

185 What computations explain this hierarchical temporal organization?

186 hic hyperexcitability led to a change in the temporal pattern of AP firing, emphasizing the role of t

187 th our hypotheses, results revealed a spatio-temporal pattern of cortical activation (i.e. travelling

188 e-use, individual preference, and the spatio-temporal pattern of resources in home ranging behaviour.

189 they did not adapt to chronically presented temporal patterns in an interval-specific manner.

190 identify emerging phenomena from large-scale temporal plant phenotyping experiments.

191 l lobe and laterally in the direction of the temporal pole.

192 Atrophy of the bilateral temporal poles and the fusiform gyrus were associated wi

193 rding to their representation of the event's temporal position relative to themselves.

194 utational simulations suggest that increased temporal precision underlies both of these observations.

195 s should not be taken as specific spatial or temporal predictions of abrupt ecosystem change.

196 IAC AOD together with additional spatial and temporal predictors were used as inputs in the three fir

197 for largely transient within-breeding season temporal processes and limited spatial processes, affect

198 This suggests that age-related temporal processing deficits may develop more central to

199 However, temporal processing thresholds have seldom been explored

200 to task-evoked activations(e.g., magnitude, temporal profile) within the same populations of neurons

201 ptical approaches to measure the spatial and temporal profiles of NT and NM release in the brain usin

202 tential mechanisms underlying these distinct temporal profiles, we developed a reduced spiking model

203 that an extrinsic cue modifies an intrinsic temporal program to increase neuronal diversity.

204 and between mean ET and BLT of the inferior temporal quadrant/superior nasal quadrant (R2) were calc

205 or and inferior quadrants than the nasal and temporal quadrants.

206 To investigate the diagnostic value of the temporal radiographic changes, and the relationship to d

207 inated rather than cycle-denominated, with a temporal rate that can depend on molecular concentration

208 tract tracing methods to examine the ferret temporal region: the lateral rostral suprasylvian sulcal

209 hanges in oxy-haemoglobin in the frontal and temporal regions were quantified.

210 these findings provide new insight into the temporal regulation of genes in a cell-type specific man

211 work, we investigate this matter through the temporal regulation of initiation in a living coordinati

212 the historic LIN phenomenon but also for the temporal regulation of phage lysis in general.

213 regulators of RhoA have been identified, the temporal regulation of RhoA and the coordination of diff

214 First, we describe the temporal relationship between appetite neuron activity a

215 Here, we examine the temporal relationship between locomotor ability, brain m

216 y and XCH(4) data to investigate the spatial-temporal relationships between rice paddy area, rice pla

217 We analyzed 194 clinical S. Typhi, temporal representatives from those isolated from blood

218 Our findings define molecular and temporal requirements of the nonphotopic or photopic vis

219 erform deep transcriptomic profiling at high temporal resolution as macrophages are polarized with cy

220 nanometer spatial resolution and sub-second temporal resolution for analysis of soft matter in mater

221 n ROV photogrammetric data coupled with high temporal resolution in situ acoustic doppler current pro

222 Here, using high spatial and temporal resolution live-cell microscopy, we identified

223 l endocytic vesicles (EVs) with an unmatched temporal resolution of 2 s.

224 bulk temperature in transient systems with a temporal resolution of 50 fs and for which accurate meas

225 croscopy are able to resolve the spatial and temporal resolution of T cell receptor signaling in the

226 The high spatial and temporal resolution of the reported technique can be use

227 The temporal resolution of X-ray transient absorption experi

228 y chromatin architecture at high spatial and temporal resolution through in vivo mouse erythroid diff

229 ng state functional MRI analyses to increase temporal resolution to seconds and explore transient con

230 ined from noisy 1D and 2D NMR data with high temporal resolution, allowing further analysis by fittin

231 scle perfusion and T(2)* at 7T with improved temporal resolution, and demonstrated assessment of spat

232 imaging due to motion artefacts and limited temporal resolution, and electrophysiological studies ha

233 pecific NIR-II signals with high spatial and temporal resolution, and remarkable NIR-II image-guided

234 e experimental tools with higher spatial and temporal resolution, in situ and operando characterizati

235 ite instruments that offer finer spatial and temporal resolution.

236 mm spatial resolution and 1 frame-per-second temporal resolution.

237 amics within discrete brain networks at high temporal resolution.

238 Using high temporal-resolution proteomics, we compare the relative

239 erate at the soil profile scale and for long temporal scales (i.e. decades, centuries).

240 At the broadest temporal scales (many decades, centuries and beyond), co

241 significant neural entrainment can occur at temporal scales far longer than those commonly explored.

242 We highlight three distinct temporal scaling laws for the transport distance of exha

243 to therapeutic action, improved spatial and temporal selectivity can be achieved and subsequently ha

244 me, and the understanding of its spatial and temporal sensing at the cellular level is still an open

245 rial modes, which have well-resolved spatial-temporal separation owing to the hypebolicity of effecti

246 assessment of pathogen burden elucidated the temporal sequence of events associated with each transfu

247 by the IOL, resulting in a gap and resultant temporal shadow.

248 ions, it is critical to encode a spatial and temporal shape evolution within the initially flat shell

249 rogressed towards the monsoon season suggest temporal shifts in GRD socio-behavioural states and seas

250 ed how change in forest cover has influenced temporal shifts in populations and ecological assemblage

251 which the short-lived ones (1-10 s) are the temporal signature of a low fidelity catalytic pathway.

252 ssue (D(eff)) was determined from the spatio-temporal solute concentration profiles using an unsteady

253 However, the temporal sparsity of these measurements presents a chall

254 Using 554 temporal-spatial features of the 12-lead ECG, we train a

255 viously known as Benign Epilepsy with Centro-temporal Spikes (BECTS) or Rolandic Epilepsy, is one of

256 se persistence, productivity, abundance, and temporal stability of both mutualists and non-mutualists

257 The question of how we selectively create temporal stability of several objects remains unsolved.

258 ECSARA was tested for its temporal stability, well-to-well variability, and respon

259 ncentration differences clustering into four temporal stages, and resulting in a gradual increase in

260 d can be used to disentangle complex spectro-temporal structure and observe long-timescale organizati

261 preparations exhibited rLFPs with a similar temporal structure and thus share a similar functional n

262 present image sequences containing internal temporal structure to humans of either sex and male maca

263 ubserving the core system and that the right temporal structures mainly underpin face familiarity fee

264 Finally, our temporal studies suggest that lymphoid structures in the

265 nge in neuronal structures subject to spatio-temporal synaptic fluctuations.

266 Changes in the spatial and temporal thermal fluctuations of the particle were measu

267 Here we demonstrate a temporal topological pump that produces on-demand, robus

268 Our data show temporal transcription factors, as a group of molecules,

269 ch is an essential component in the faithful temporal transmission of sound.

270 stock, previous research has not detected a temporal trend in plastic particle concentration in the

271 .9 billion in 2014 (-6.2%, P = 0.085 for the temporal trend).

272 We aim to describe the temporal trends in age, sex, and clinical characteristic

273 There is limited data on temporal trends in wait-times and access to care for pat

274 Temporal trends indicate that concentrations of many POP

275 This disparity in temporal trends was particularly noticeable among Africa

276 or sociodemographic factors and age-adjusted temporal trends were investigated using logistic and lin

277 auses many problems, including (1) bias from temporal trends, (2) inefficiency in treatment effect es

278 n-making task with both reward asymmetry and temporal uncertainty.

279 esting-state functional connectivity using a temporal unwrapping procedure to assess the contribution

280 tive grassland by experimentally eliminating temporal variability in growing season rainfall over a w

281 Therefore, our results suggest that temporal variability in the abundances of species popula

282 rements of daily predawn and midday Psi, the temporal variability of hydraulic behavior was explored

283 ls with SCA6, and can be explained by lesser temporal variability.

284 e dominant climate variable that explains TC temporal variability.

285 uctuation in abundances around K, but higher temporal variation in beta within herds.

286 Although inter-individual and temporal variation in measures of oxidative balance were

287 After accounting for spatial and temporal variation in resources, we show that the appare

288 luctuations in the fitness function, causing temporal variation in the magnitude, but not the directi

289 d to unveil the ecological mechanisms behind temporal variation in vertebrate responses to tree diver

290 works that were sparse after controlling for temporal variation.

291 en PM(2.5) and PM(10), although considerable temporal variations existed.

292 We observed geographic and temporal variations in incidence and mortality for all 5

293 euroinflammation and discuss the spatial and temporal variations in microglial phenotypes that are ob

294 orm the basis for further investigation into temporal variations in self-harm among asylum seekers, w

295 tic monitoring is an efficient tool to study temporal variations in the occurrence and behaviour of v

296 capture 60% and 42% of the total variance of temporal variations, respectively.

297 bit high sensitivity to fast but not to slow temporal variations, whereas cone-driven responses suppl

298 t the loss in rod-driven sensitivity to slow temporal variations.

299 segments was obtained and shown to reveal a temporal waveform with a peak and trough that correlates

300 ies spawn only once per year during a narrow temporal window, sample processing is a time-limiting st