ライフサイエンスコーパス: temporal

1 axons to form delay lines, allowing for fine temporal analysis of signals.

2 Temporal analysis of the transcriptome and methylome fro

3 en clustering approach, we observed distinct temporal and directional patterns between the three netw

4 oherent framework for the study of spectral, temporal and functional analyses of the BG and therefore

5 We identify temporal and functional transcript co-variance that asso

6 dard-compliant spreadsheet that captures the temporal and geospatial context of each biosample.

7 ility-based models at most sites in superior temporal and inferior frontal cortices.

8 T retention most prominently in the inferior temporal and inferior parietal regions in the full cohor

9 ternate viewpoints and recent results on the temporal and mechanistic connections between hyperinsuli

10 Flow loss was more extensive in the temporal and nasal parafoveal subfields of the deep plex

11 and beta frequency within the left posterior temporal and occipital cortices in patients with the log

12 augmentation involved the bilateral superior-temporal and precentral gyri immediately following quest

13 on emission tomography scans, in the parieto-temporal and precuneus brain regions was associated with

14 r BldD to exert a multi-layer control of the temporal and spatial activity of WhiB.

15 rstanding the experimental design, including temporal and spatial alignment and interpretation of res

16 Here we compared the temporal and spatial compositions of lipids and transcri

17 s, such as individual and collective levels, temporal and spatial dimensions, content, social and geo

18 In the perspective of a temporal and spatial exploration of aquatic environments

19 ular mechanisms of cell ingression at a high temporal and spatial resolution, in this issue, Simoes e

20 For fMRI to succeed given its low temporal and spatial resolution, the neural code must be

21 Our study shows that the future temporal and spatial variation characteristics of precip

22 ascular density of the fovea, parafovea, and temporal and superior subfields.

23 Here, we identified the spatial, temporal, and amplitude characteristics of cortical resp

24 pared among these time points and the nasal, temporal, and inferior quadrants.

25 xamining modulatory influences in the middle temporal area (MT) of the macaque visual cortex, using e

26 rom early visual areas to the face-selective temporal area in individuals with early and profound dea

27 Enhanced resolution of the temporal area toward the frontal visual field may facili

28 of spatial resolving power of 8 cycles/deg (temporal area, 1,800 cells/mm(2) ), 7.7 cycles/deg (nasa

29 bited decreased activation in right superior temporal areas compared to non-amusic patients during in

30 ing into account the spatial, frequency, and temporal aspects of mid-density EEG.

31 rds (capturing individualistic, spatial, and temporal aspects of people).

32 he prevalence and incidence of PCSON and the temporal association between surgery and onset of PCSON.

33 ging at context shifts, such that successful temporal associations are more likely to be formed withi

34 Temporal autocorrelation in demographic processes is an

35 ological theory predicts that high levels of temporal autocorrelation in the environment - relatednes

36 pogenic pressures and to identify meaningful temporal baselines for biodiversity.

37 ciated with systematic differences in spatio-temporal beta-diversity patterns, leading to consistent

38 eld has investigated various features of the temporal binding window, revealing asymmetries in its si

39 We evaluated temporal cerebellar expression profiles by RNA sequencin

40 essary phenotypic plasticity for adapting to temporal changes at multiple time scales (seconds-to-min

41 tory species, such as salmon, where distinct temporal changes in growth and physiology during develop

42 Temporal changes in intratumoral TCR repertoire revealed

43 Temporal changes in MATS coverage underscore the need fo

44 ghly weathered Ultisols, and more pronounced temporal changes in soil C:N, N:P, and C:P ratios at low

45 Previous studies investigated the temporal changes in the association over a few discrete

46 also, reveals differential contributions of temporal channels across visual cortex.

47 ask for several reasons, including potential temporal character of data.

48 series of error-clamp trials to measure the temporal characteristics of the feedforward motor output

49 ly increasing gain selectively and improving temporal clarity.

50 ate platform allows the generation of binary temporal codes for efficient data encoding.

51 c mechanism to implement this process is the temporal coherence principle.

52 other models of stream segregation, such as temporal coherence, are not excluded by the present find

53 A temporal cohort effect was present.

54 ges without the need for separate spatial or temporal compensation.

55 This temporal consistency was not because of the resampling o

56 reward environment, introducing an intrinsic temporal context dependence into the neural representati

57 ts in decision making as well as spatial and temporal context effects in perception.

58 red by divisive normalization, linking these temporal context effects to spatial context effects in d

59 pattern recognition technique to recover the temporal contrast patterns and locations of the associat

60 an inducible shRNA-based system that enables temporal control of Kras expression.

61 therapy (PDT) takes advantage of the spatial-temporal control of ROS generation, the meticulous parti

62 mix) the microdroplets with high spatial and temporal control while consuming small amounts of sample

63 s that enable new levels of functionalities (temporal control, autonomous structures, motion and work

64 ratively executed with exquisite spatial and temporal control, the selective isomerization of polariz

65 photoactivated in vivo with high spatial and temporal control.

66 e DG, whereas LTP in HILs may facilitate the temporal coordination of GCs with activity patterns gove

67 We further show that the temporal correlation of the interaction shear stress det

68 d for further behavioral assays due to their temporal correlation with the behavioral changes of IJs

69 of the brain is characterized by long-range temporal correlations (LRTCs) in cortex, which are suppo

70 tween individual neural dynamics (long-range temporal correlations) of the frontocentral cortices dur

71 r ratio was higher in the bilateral superior temporal cortex (left: +10.0%; P = .03 and right: +10.8%

72 ion in the dysplasics suggests that occipito-temporal cortex specialization is driven largely by inhe

73 emispheric premotor, parietal, and posterior temporal cortices is activated even under subliminal per

74 the right hemisphere in both the insular and temporal cortices.

75 of CPC streamlines leave the prefrontal and temporal cortices.

76 ranscription factors provided evidence for a temporal coupling of replication and transcription.

77 ectly investigate the effect of major spatio-temporal couplings on light-matter interaction and revea

78 proach, which is able to handle multivariate temporal data without previous data flattening.

79 First, we show that spatial and temporal decimation techniques based on simple local ave

80 gnostic discussion was not associated with a temporal decline in either measure.

81 and loss of heart function was preceded by a temporal decrease in COX activity and copper levels in t

82 quent patterns were left and right posterior-temporal delta brushes which were associated in the left

83 dopsis thaliana at an unprecedented level of temporal detail.

84 ophic and hazardous events on Earth, yet the temporal details of post-supereruption activity, or resu

85 g with those thought to carry out model-free temporal difference (TD) learning.

86 differences (i.e., water depth) rather than temporal differences (i.e., day versus night) better-exp

87 We interpret the geochemical and temporal differences between the SE and NW lava fields t

88 s of rules for each age group to capture the temporal differences seen in the immune responses of the

89 The temporal dimension of phosphorylation effects remains no

90 also in applications of ENM to understanding temporal dimensions of niche dynamics.

91 We suggest two psychological mechanisms, temporal discounting and feeling of resource scarcity, f

92 Temporal discounting is related to regions of the brain

93 ial/temporal predictability improved spatial/temporal discrimination accuracy, but not vice versa.

94 The spatio-temporal distribution of Plasmodium parasitaemia, domina

95 fter CLP in mice and determined peaks in the temporal distribution of points of physiologic decline.

96 e were measured to ascertain the spatial and temporal distributions of nitrate transformation in the

97 opsin and rod+cone responses differed in the temporal domain, and responses to slow changes in radian

98 Temporal, dose-dependent and specific disruption of the

99 In ephemeral pond ecosystems, temporal dynamics are relatively more important than in

100 d Na(+) and Cl(-) ion concentrations and the temporal dynamics of conductivity at a range of stream s

101 Yet, the temporal dynamics of coral diseases are rarely reported.

102 how, to our knowledge, previously unreported temporal dynamics of the chronic wound microbiome.

103 Importantly, we show how the spatial and temporal effects on brain hemodynamics provide informati

104 n order to gain control over the spatial and temporal elements of fundamental cellular processes.

105 wnstream of the positive feedback, shape the temporal ERK activity profile but are dispensable for os

106 t altered neuronal network dynamics, but the temporal evolution and cellular substrates of the neuron

107 distinct chemical entities contribute to the temporal evolution and spectral shape of the continuum b

108 The inferred temporal evolution of soil moisture is remarkably consis

109 the following: (1) whether internally guided temporal expectations can dynamically and reversibly pri

110 Temporal expectations had a profound influence on workin

111 Temporal expression analyses revealed that CDX4 was expr

112 ression in known JH target tissues, in which temporal expression corresponds with periods of hormone

113 We clustered the genes by temporal expression pattern, identified transcription fa

114 The temporal expression profiles displayed by taste organoid

115 smids, 37 promoters of various strengths and temporal expression profiles, and 10 protein-localizatio

116 simple and general mechanism for conferring temporal flexibility upon sensorimotor and cognitive fun

117 , in noise backgrounds with regularly spaced temporal fluctuations, the energy-normalized signals led

118 e with both regularly and irregularly spaced temporal fluctuations.

119 foveae, a deep central fovea and a shallower temporal fovea.

120 bdivisions preferentially responding to fast temporal frequencies are more myelinated.

121 In the current study, we analyzed the temporal gene expression changes in a neuronal mRNA pool

122 a filter-based feature selection method for temporal gene expression data based on maximum relevance

123 rimary diagnosis and relapse, to investigate temporal gene expression differences and associations wi

124 tion of gaseous plumes with high spatial and temporal granularity in real-time over the skyline of Ma

125 euronal spiking activity in the human middle temporal gyrus (MTG), a cortical region supporting the s

126 modulated with the activity in the superior temporal gyrus and the angular gyrus, respectively.

127 frontal gyrus, premotor cortex, and superior temporal gyrus during a picture description task.

128 gyrus, the paracentral lobule, the superior temporal gyrus, the middle cingulate gyrus, the putamen

129 l climate change by indicating a spatial and temporal heterogeneity of vegetation change at the EOT i

130 onse to environmental variation at different temporal (i.e. seasonal to inter-decadal) scales.

131 s-modal signals may not modulate cross-modal temporal influences in short time scales.

132 functional data analysis, which utilizes the temporal information based on functional principal compo

133 ults are consistent with the hypothesis that temporal information is encoded in a widely distributed

134 How is temporal information processed in human visual cortex?

135 the micron-scale essence of the spatial and temporal instability of two-phase flow in fractured medi

136 indicating that the underlying mechanisms of temporal integration generalize across species.

137 pe-specific information recovered using such temporal integration processes.

138 This variability has been linked to the temporal irregularity of neuronal activity in the centra

139 ) than with SUVRCB (Pearson r: from 0.51 for temporal lobe [P = 0.002] to 0.82 for precuneus [P < 0.0

140 etween rather than within the visual, medial temporal lobe and default mode networks, whereas during

141 Thus, two temporal lobe areas extend the core face-processing netw

142 supported by similar interaction effects on temporal lobe cortical thickness (whole-brain voxelwise

143 The cause of mesial temporal lobe epilepsy (MTLE) is often unknown.

144 of TLE.SIGNIFICANCE STATEMENT Development of temporal lobe epilepsy (TLE) generally takes years after

145 ppocampus and neocortex of rats with chronic temporal lobe epilepsy to demonstrate that subsets of ce

146 in every two patients with pharmacoresistant temporal lobe epilepsy will not be rendered completely s

147 and propagation of temporal lobe seizures in temporal lobe epilepsy, using diffusion tensor imaging a

148 roximately one-third of patients with mesial temporal lobe epilepsy.

149 tent postoperative seizures in patients with temporal lobe epilepsy.

150 portant in the generation and propagation of temporal lobe seizures in temporal lobe epilepsy, using

151 ot be rendered completely seizure-free after temporal lobe surgery.

152 The temporal lobe was involved in 71.9% of operations.

153 ional tissue characteristics of preoperative temporal lobe white matter tracts known to be important

154 [0.11]), less severe atrophy of the lateral temporal lobe, and lower mean (SD) cerebrospinal fluid l

155 and ventral tegmental area (SN/VTA), medial temporal lobe, or subsequent memory performance.

156 pplied a virtual lesion to the left anterior temporal lobe.

157 y auditory areas and moving laterally on the temporal lobe: spectral features are found in the core o

158 Superior LPI (n = 285) and nasal/temporal LPI (n = 274) patients were matched for age (P

159 greater total energy (P < 0.001) than nasal/temporal LPIs.

160 Temporal manipulation of the in vitro environment and gr

161 aimed at studying muscle lipid profiles in a temporal manner.

162 odents have used a limited number of spectro-temporal measures to compare ultrasonic vocalizations (U

163 We propose a temporal minimum redundancy - maximum relevance (TMRMR)

164 ate a distinctly different mechanism for the temporal modulation of QD emission intensity at constant

165 d progressively more in surrounding regions, temporal modulations in a range relevant for speech anal

166 econstruction accuracy was higher for faster temporal modulations.

167 ere reconstructed more faithfully than other temporal modulations.

168 bdominal aortic aneurysm sac can be used for temporal monitoring after endovascular aortic repair, wi

169 were developed for the real-time spatial and temporal monitoring of potential wound infections.

170 bution of cortical neuron latencies and that temporal motion integration for pursuit is consistent wi

171 Although the temporal MS response at this site gives valuable field-s

172 perception and neural activity in the middle temporal (MT) area of the macaque monkey to study the ne

173 rk opens the way for the systematic study of temporal multiplex networks and we anticipate it will be

174 e in neurons is exquisitely sensitive to the temporal nature of action potential firing patterns.

175 onto-parietal control network and the fronto-temporal network.

176 surveillance systems for early detection on temporal networks.

177 t structures by using measures on static and temporal networks.

178 Despite this relatively apparent temporal niche partitioning between ancestral mammals an

179 r results suggested partial overlap of their temporal niches during crepuscular periods.

180 The daily temporal occurrence of NPF events likely caused by nucle

181 hacoemulsification whether done with a clear temporal or clear superior wound, does not affect intrao

182 No apparent temporal or dose-related changes in clinical status (spe

183 Here we describe the temporal orchestration of a series of metabolic, structu

184 iC phosphoforms generates the characteristic temporal order of KaiC phosphorylation.

185 n transcriptional states, and elucidates the temporal order, functional role and mechanistic separati

186 P, but the drug discoordinates the subsecond temporal organization of discharge among place cells.

187 However, the spatial and temporal organization of organelles within the cell rema

188 ative abundances of spider species and their temporal overlap with the pest species in tea canopy.

189 wing beyond 1 month in the nasal (P = .133), temporal (P = .376), and inferior (P = 1.000) quadrants.

190 LPI (15.8% for superior vs. 13.9% for nasal/temporal; P = 0.1) or any individual dysphotopsia sympto

191 These results suggest that disruptions of temporal parietal and sub-cortical neurogenesis during i

192 top of the hierarchy, such as the precuneus, temporal parietal junction, and medial frontal cortices,

193 works as a relay nucleus that preserves the temporal pattern of firing at high frequency.

194 e applied pattern similarity analysis on the temporal pattern of hippocampal high-frequency band acti

195 infected with IAV ex vivo exhibited the same temporal pattern of proliferation and infectious suscept

196 This temporal patterning is critical to interpreting the stim

197 or investigating the circuit-level impact of temporal patterning within a lineage.

198 the processes that give rise to spatial and temporal patterns in local community structure.

199 This 3' UTR heterogeneity directs distinct temporal patterns of translational activation or repress

200 Due to its vasculature, the temporal pole is not commonly completely lesioned in str

201 lly salient events, while abnormalities in a temporal pole-medial prefrontal cortex circuit might spe

202 and visualize this process with spatial and temporal precision in living animals.

203 The timing and temporal precision of APs when they reach each of the sy

204 t that ARHL is associated with a decrease in temporal precision of synaptic release at the first cent

205 of the functional network with unprecedented temporal precision.

206 fluence of predictions on behaviour: spatial/temporal predictability improved spatial/temporal discri

207 We provide temporal profiles of 4797 phosphopeptides, 608 of which

208 focus on average avalanche shapes, i.e., the temporal profiles of avalanches of fixed duration.

209 gion that generates sequences underlying the temporal progression of the song.

210 edness between conditions occurring in close temporal proximity - will favor populations that would o

211 be applied to at-risk individuals, in close temporal proximity to environmental impacts known to ind

212 oceanic Fe-concentrations by considering the temporal record of banded iron formations and marine red

213 ing scales are segregated by an intermediate temporal regime in the alpha band that likely reflects d

214 P = .03) and lateral (beta = -0.08, P = .03) temporal regions, subcortical white matter (beta = -0.13

215 Many environmental stimuli contain temporal regularities, a feature that can help predict f

216 urons raises questions about the spatial and temporal regulation of gene expression within neurons.

217 e field of mouse genetics for spatial and/or temporal regulation of gene function.

218 ere quantified, revealing, e.g., the precise temporal regulation of the SigB-dependent stress respons

219 iling uplift models of the plateau and their temporal relationships with the Cenozoic climatic change

220 s the amino terminus of gamma134.5 undergoes temporal replication without production of infectious vi

221 Studies to define the temporal requirements for Glut1 reveal that pre-symptoma

222 Arabidopsis (Arabidopsis thaliana) with high temporal resolution allowing for investigations of the t

223 onmental conditions as they can provide high temporal resolution and require no sample preparation.

224 Our approach offers unprecedented temporal resolution and, uniquely, physical transformati

225 ble to track the community diversity at high temporal resolution by calculating phenotypic diversity

226 g of neuronal activity with high spatial and temporal resolution deep within scattering brain tissues

227 and, by doing so, it reduces the peripheral temporal resolution in coding odor stimuli and allows fo

228 High-temporal resolution information can provide more meaning

229 We demonstrate a temporal resolution of 1.2+/-0.3 fs.

230 Taking advantage of the high spatial and temporal resolution of light control, optobiology promis

231 The temporal resolution of ultrafast electron diffraction an

232 sequencing data from budding yeast, in high temporal resolution over ca. 2.5 cycles of the short-per

233 omposite nanomaterials with high spatial and temporal resolution provides a key understanding of allo

234 l changes of biomolecules with much improved temporal resolution than the conventional method.

235 Gap detection is a measure of auditory temporal resolution that relies on the auditory cortex (

236 Light perception and temporal resolution with the implant ON were achieved in

237 erosivity is challenging as it requires high temporal resolution(<30 min) and high fidelity rainfall

238 lly relevant detection limits and high (3 s) temporal resolution, attributes suggesting that the appr

239 o-iliac/visceral arteries and the vena cava (temporal resolution, five images per second; and spatial

240 typic switch in drug-resistant bacteria with temporal resolution.

241 phenology is relatively insensitive to data temporal resolution.

242 otic chromosome structure with unprecedented temporal resolution.

243 g blocks in a noninvasive approach with high temporal resolution.

244 enabling high sensitivity to light and high temporal resolution.

245 protein function at unparalleled spatial and temporal resolutions.

246 The results were obtained using "temporal response functions," in which unique electroenc

247 zation conditions, and observe a subharmonic temporal response that is robust to external perturbatio

248 neurons are heterogeneous in selectivity and temporal responses, and are not functionally clustered.

249 atchiness, and the wide range of spatial and temporal scales at which these processes operate, obfusc

250 diverse and that embrace larger spatial and temporal scales than most experimental studies do.

251 echanisms and features that span spatial and temporal scales.

252 d to smaller females, resulting in a partial temporal segregation between sexes.

253 ide the first evidence that the frequency of temporal segregation can be modified by sensory entrainm

254 We conclude that increased temporal self-similarity (alpha) of more variable lung f

255 oupling of the peptide and [(11)C]cyanide by temporal separation of nucleophile addition.

256 Here, we characterized the temporal sequence of events leading to voltage sensor st

257 ive performance is associated with weaker FC temporal similarity together with altered switching betw

258 Temporal simultaneity provides an essential cue for inte

259 The formation of such temporal soliton bound states and their internal dynamic

260 that have lower species richness, and higher temporal species community change.

261 Importantly, biomass temporal stability is not influenced by plant species di

262 diversity, but is largely determined by the temporal stability of dominant species and asynchronous

263 of warming and altered precipitation on the temporal stability of plant community biomass in an alpi

264 studies, including non-invasive collection, temporal stability, and lower complexity relative to oth

265 n motor output mirror both the amplitude and temporal structure of the environmental perturbations.

266 such as contrast, frequency, congruency, and temporal structure.

267 n of sentinels depends on both the network's temporal structures and the infection probability of the

268 The human posterior superior temporal sulcus (pSTS), a brain region known to be impor

269 Temporal synchronization analysis was first applied to c

270 slated regions of messenger RNA requires the temporal synchronization of RNA synthesis and ligand bin

271 al changes in ADAS-cog score and left middle temporal thickness and amygdalar volume (Pone-tailed=0.0

272 s coverage is uniform, efficient modeling of temporal topic trends using time-series regression techn

273 us laevis embryos to analyze the spatial and temporal transcriptome of distinct ectodermal domains in

274 ely 1- to 4-fold coverage) from a 3,500 year temporal transect ( approximately 8,300-4,800 calibrated

275 ch potentially has wide implications for the temporal transfer of information in the brain.

276 regression adjusting for arrest factors and temporal trend.

277 Unadjusted and adjusted temporal trends for the PTOS and NTDB showed initial inc

278 Temporal trends in DNT were assessed across fourths of t

279 ditive genetic variance, and create spurious temporal trends in predicted breeding values in the abse

280 Our objective was to evaluate temporal trends in serum PFAS levels among 1257 middle-a

281 The temporal trends in soil C-N-P stoichiometry differed amo

282 lar trials has changed over time and examine temporal trends in the clinical importance of individual

283 Spatial patterns and temporal trends of nitrogen (N) and phosphorus (P) depos

284 e coding of information, and deficits in the temporal tuning of neural activity and its implication f

285 alters the baseline activity levels and the temporal tuning of the first directionally selective neu

286 This temporal uncoupling became larger in short photoperiods

287 gion and allow us to quantify the degree and temporal variability of nitrate consumption.

288 pact of fluctuating resource availability on temporal variability of the recipient community.

289 Overall, natural temporal variation in community metrics exceeded the eff

290 ling the action of methyl farnesoate through temporal variation in its expression and availability fo

291 Temporal variation was assessed by repeated measurements

292 The temporal variations of VOCs and O3 coincided with the su

293 ome key model aspects including climatic and temporal variations, how ENMs may be released into the e

294 onous presentation relative to synchronous - temporal ventriloquism - however, unlike the long-range

295 = .03 and right: +10.8%; P = .01), superior temporal white matter (left: +14.6%; P = .003 and right:

296 t active inhibitory gating, downmodulate the temporal width of LRD in slower ongoing brain activity.

297 rated that paAIP2 is useful to elucidate the temporal window of CaMKII activation required for synapt

298 The temporal window of spiking can be delicately controlled

299 This temporal window was also associated with increased theta

300 l data have generally been treated as purely temporal, with scant attention to the inherent spatial a