ライフサイエンスコーパス: lapse

1 ug craving and stress-induced initial heroin lapse.

2 level, number of days abstinent, relapse, or lapse.

3 ite pattern was observed for those who later lapsed.

4 ention abilities and reduce the frequency of lapses.

5 ring paradigm designed to elicit attentional lapses.

6 In this paper, OPM is adapted to allow time-lapse 3-D imaging of 3-D biological cultures in commerci

7 Time-lapse 3-D imaging of multicellular spheroids expressing

8 We used time-lapse 3D imaging and quantitative image analysis to dete

9 Time-lapse AFM imaging, in solution, show that over time, oli

10 FN fibrillogenesis visualized by time-lapse AFM thus provides new structural and mechanistic i

11 Here, we use single-cell time-lapse analyses to reveal that mycobacterial cell populat

12 ime point against the control (0 h) and time-lapse analysis by comparing each time point with the pre

13 Time-lapse analysis revealed that OHCs isolated from WT anima

14 Time lapse and live cell images of human cells expressing flu

15 Time to lapse and relapse were examined with Cox regressions; lo

16 Here we use wide-field time-lapse and three-dimensional structured illumination micr

17 Marker, time-lapse and ultrastructural studies indicated that oligode

18 idual differences in frequency of behavioral lapsing and intraindividual temporal fluctuations in res

19 ne cotinine level, number of days abstinent, lapse, and relapse were not observed between groups (all

20 These 'neuronal lapses' are evident on a trial-by-trial basis when compa

21 bination of fluorescence microscopy and time-lapse atomic force microscopy (AFM) to visualize initial

22 bination of fluorescence microscopy and time-lapse atomic force microscopy (AFM) to visualize initial

23 Using time-lapse atomic force microscopy, we analyzed the morpholog

24 tory (never screened, regularly screened, or lapsed attender) using data from a population-based case

25 ladaptive electrophysiological precursors of lapsing attention by acting selectively on top-down endo

26 ced known electrophysiological precursors of lapsing attention over different time scales.

27 posed cascade was addressed by means of time-lapse automated fluorescence microscopy, electron micros

28 Here, we report a time-lapse-based bright-field imaging analysis system that al

29 lifetime, age at presentation, and the time lapse between surgery and the first AT episode varied am

30 most astrocytes appeared dormant during time-lapse calcium imaging, a subgroup displayed persistent,

31 Here we combine time-lapse, complete chromosomal assessment and single-cell R

32 This protocol describes multichannel time-lapse confocal imaging of anchor-cell invasion in live C

33 ng a membrane-permeant PI3P derivative, time-lapse confocal imaging, electrophysiology, as well as kn

34 We used multiphoton and time-lapse confocal microscopy to monitor intracellular pH an

35 In this work, we exploit live-cell time-lapse confocal reflectance microscopy and image correlat

36 This is consistent with time-lapse crystallographic structures following insertion of

37 Recent time-lapse crystallographic studies of DNA polymerases have i

38 Here we use time-lapse crystallography to follow 8-oxo-dGTP insertion opp

39 Using kinetics and time-lapse crystallography, we evaluated how a model DNA poly

40 nexpected features revealed recently in time-lapse crystallography.

41 mbination of computational modeling and time-lapse data analysis provides a general way to examine th

42 CI relies on quantitative phase imaging time-lapse data and, as such, functions in label-free mode, w

43 The time-lapse data indicate that the same cells are differential

44 tract quantitative information from the time lapse data.

45 nt and track neuronal morphodynamics in time-lapse datasets.

46 Time-lapse electrical resistivity imaging (ERI) was used to m

47 Here, using time-lapse embryonic imaging, genetics, protein-interaction,

48 Viewed by time-lapse epi-fluorescence microscopy, monocytes appeared to

49 Utilizing time-lapse epifluorescence microscopy, we observed that the m

50 Time-lapse ex vivo imaging revealed a drastic elimination of

51 llowed us to study chitin deposition in time lapse experiments and by using it we have identified une

52 tion and tracking of cells in long-term time-lapse experiments has emerged as a powerful method to un

53 ted within the scientific community for time-lapse experiments, and combining them with simple graph-

54 ng tracking parameters for high-content time-lapse experiments.

55 me fluorescent imaging (zone adjustable time-lapse fluorescence image processor) and separation contr

56 pically, the approximate time frame for time-lapse fluorescence imaging of mt-Keima is 20 h for livin

57 Unexpectedly, we find using time-lapse fluorescence imaging that cdc-42 is not required f

58 der, and probed their expressions using time-lapse fluorescence microscopy and single-molecule fluore

59 Microfluidics coupled to quantitative time-lapse fluorescence microscopy is transforming our abilit

60 Here, using time-lapse fluorescence microscopy to examine PhoP-dependent

61 combination of microfluidic devices and time-lapse fluorescence microscopy to track oscillations in c

62 In this study, time-lapse fluorescence microscopy was used to investigate th

63 We used live-cell time-lapse fluorescence microscopy, followed by 3D rendering,

64 Using time-lapse fluorescence microscopy, we carried out an in-dept

65 may account for otherwise unexplained memory lapses following trauma.

66 Furthermore, time-lapse force measurements showed that these cells migrate

67 apse, but the clonidine group took longer to lapse (hazard ratio=0.67, 95% CI=0.45-1.00).

68 pes, detect symmetry-breaking events in time-lapse image data, and quantify the time-dependent correl

69 imental and modeling approach that uses time-lapse imagery to directly relate burrow formation to res

70 eage Mapper, an open-source tracker for time-lapse images of biological cells, colonies, and particle

71 demonstrated by kymographs derived from time-lapse images of FtsZ ladder formation.

72 uorescence signals from single-molecule time-lapse images of individual Escherichia coli cells.

73 n vivo two-photon microscopy to produce time-lapse images of serotonin axons in the neocortex of the

74 The analysis of time-lapse images showing cells dividing to produce clones of

75 Localization and time-lapse imaging analysis reveals that MAP7 is enriched at

76 Time-lapse imaging and analysis of reporter transgenics show

77 Time-lapse imaging and fate mapping demonstrate that the dors

78 e, we performed atomic force microscopy time-lapse imaging and mechanical mapping of actin in the cor

79 Time-lapse imaging and mutagenesis studies further establish

80 Time-lapse imaging and scanning electron microscopy revealed

81 e archaeal cells to enable quantitative time-lapse imaging and single-cell analysis, which would be u

82 The software enabled time-lapse imaging and the use of temporally varying characte

83 imension, facilitating high-resolution, time-lapse imaging and tracking of individual cells.

84 This study used a novel, prolonged time-lapse imaging approach to continuously track the behavio

85 Using a time-lapse imaging assay, we found that developing amacrine c

86 Time-lapse imaging assays also revealed the essential roles o

87 Using a complementary combination of time-lapse imaging by fluorescence confocal microscopy and se

88 Results indicate that use of continuous time-lapse imaging can distinguish cellular heterogeneity wit

89 le-cell resolution from high-throughput time-lapse imaging data, especially, the interactions between

90 In vivo time-lapse imaging demonstrated that local TH first increased

91 Time-lapse imaging demonstrated that SEC3a and SEC8 were high

92 elivered fluorescent probes and in vivo time-lapse imaging in a mouse model of demyelination to inves

93 Through 3D time-lapse imaging in a secreting organ, we show that F-actin

94 on and two-photon microscopy, including time-lapse imaging in light-sheet systems.

95 Two-photon time-lapse imaging indicated that microglia depletion reduced

96 Furthermore, long-term time-lapse imaging indicates that aggregates of mutant PKCgam

97 Time-lapse imaging is a fundamental tool for studying cellula

98 rther provides a novel tool for in vivo time-lapse imaging of adult fish for non-cardiac studies, as

99 cence microscopy have made snapshot and time-lapse imaging of bacterial cells commonplace, yet fundam

100 Furthermore, using time-lapse imaging of beating hearts in conjunction with a Cd

101 Cell tracking and time-lapse imaging of chimeric drMM cultures indicated that t

102 Combined with time lapse imaging of development in culture, we demonstrate

103 Time-lapse imaging of dissociated hippocampal neuronal cultur

104 With time-lapse imaging of ECM micro-fiber morphology, the local a

105 um; its lumenal space is rich in Ca(2+) Time-lapse imaging of isolated hPSCs reveals that the apicoso

106 Time-lapse imaging of lac-operator-tagged chromosome regions

107 Using time-lapse imaging of Lifeact-GFP-transfected chromaffin cell

108 SP enables unmixing of seven signals in time-lapse imaging of living zebrafish embryos.

109 aging that permits prolonged label-free time-lapse imaging of microglia in the presence of neurons an

110 , high-contrast, and high-dynamic-range time-lapse imaging of migrating cells in complex three-dimens

111 Time-lapse imaging of multiple labels is challenging for biol

112 icroscopy to perform three-dimensional, time-lapse imaging of neutrophil-like HL-60 cells crawling th

113 ivo two-photon microscopy, we performed time-lapse imaging of radial glial cells and measured filopod

114 Using two-photon glutamate uncaging and time-lapse imaging of rat hippocampal CA1 neurons, we show th

115 Here, using quantitative single-cell time-lapse imaging of Saccharomyces cerevisiae, we show that

116 ) and long-term operations ("large T"), time-lapse imaging of shear-wave velocity (V S ) structures i

117 Time-lapse imaging of static liquid cultures demonstrates tha

118 Using in vivo time-lapse imaging of tectal neuron structure and visually ev

119 We developed a novel method for time-lapse imaging of the rapid dynamics of miRNA activity in

120 We performed time-lapse imaging of thousands of neurons over weeks in the

121 ipulation, gene expression analysis and time-lapse imaging of zebrafish embryos.

122 fferent topographies, using fluorescent time-lapse imaging over 21 days.

123 Traction force microscopy and time-lapse imaging reveal that closure of gaps begins with co

124 Time-lapse imaging revealed dynamic changes in the metabolic

125 Time-lapse imaging revealed that knockdown of miR-219 functio

126 Time-lapse imaging revealed that MSCs recruited MRL.Fas(lpr)

127 Time-lapse imaging reveals rapid pulsatile level changes in G

128 Time-lapse imaging reveals that alpha-actinin-1 puncta within

129 Time-lapse imaging reveals that branching events are synchron

130 Time-lapse imaging reveals that SAC proteins are in distinct

131 Time-lapse imaging showed that hepatic-specified endoderm iPS

132 Time-lapse imaging shows that iNSCs are tumouritropic, homing

133 Here, we use non-invasive time-lapse imaging to continuously examine hPSC maintenance a

134 Using time-lapse imaging to correlate mitotic behavior with cell fa

135 opy, optogenetic activation and in vivo time-lapse imaging to show that newly generated OSNs form hig

136 e use two-photon glutamate uncaging and time-lapse imaging to show that non-ionotropic NMDAR signalin

137 combined single-cell laser axotomy with time-lapse imaging to study the dynamics of phosphatidylserin

138 rse genetics and multivariate long-term time-lapse imaging to test current cell shape control models.

139 essments of cellular rearrangements and time-lapse imaging to visualize cochlear remodeling in mouse.

140 Time-lapse imaging using a Forster resonance energy transfer

141 Using long-term time-lapse imaging with intact Drosophila larvae, we found th

142 Extended time-lapse imaging with less than one virion per cell allows

143 ed pluripotent stem cells (iPSCs) using time-lapse imaging, immunostaining, and single-cell RNA seque

144 Using time lapse imaging, it is possible to observe these events at

145 tion with single-axon laser axotomy and time-lapse imaging, monitoring the initial changes in transec

146 (MADM), combined with organ culture and time-lapse imaging, to trace the movements and divisions of i

147 cterized cell-cycle delay identified by time-lapse imaging, was used to clarify the relationship betw

148 Using simultaneous time-lapse imaging, we find that early endosome-associated Px

149 Using time-lapse imaging, we find that mesenchymal cell condensatio

150 Using sparse-labeling and time-lapse imaging, we visualized for the first time the beha

151 of the invading cords were revealed by time-lapse imaging, which showed cells actively extending and

152 lity of the method in vivo in mice with time-lapse imaging.

153 NCC migration was studied using time-lapse imaging.

154 dy their mobility characteristics using time-lapse imaging.

155 ing and transcriptomics approaches with time-lapse imaging.

156 n an intact microvascular network using time-lapse imaging.

157 Time-lapsed imaging of GFP-laced rodlets in human cells revea

158 A control analysis ruled out a general lapse in attention or mind wandering as being predictive

159 horter than Hb, this could indicate a recent lapse in glycemic control for that patient.

160 n annual PCSK9i drug price of $14300, with a lapse in US patent protection that would reduce the pric

161 Using a combination of time-lapse in vivo single-cell analysis and Caenorhabditis el

162 e, and reaction time variability-an index of lapses in attention.

163 main understudied and could possibly signify lapses in care and missed opportunities for intervention

164 youths are experiencing clinically important lapses in care or other negative health effects due to t

165 pose that dystonia-like symptoms result from lapses in descending inhibition, exposing excess activit

166 Lapses in essential device reprocessing steps such as cl

167 neous disease severity may be the outcome of lapses in immunoregulatory mechanisms; because as much,

168 P = .03) and less likely to report frequent lapses in interpreter use (2 of 117 [1.7%] vs. 7 of 91 [

169 ion and interpretation quality, frequency of lapses in interpreter use, and ability to name the child

170 tly name the child's diagnosis and had fewer lapses in interpreter use.

171 ions of the fusion protein.IMPORTANCE Due to lapses in vaccination worldwide that have caused localiz

172 ntional control we observed is distinct from lapses in vigilant attention, as corroborated by the spe

173 ous impact of SD is frequently attributed to lapses in vigilant attention, but this account fails to

174 performance that is not readily explained by lapses in vigilant attention.

175 lon4 group, 1 recovered from dementia, but 3 lapsed into dementia.

176 Using 3D, time-lapse intravital imaging for direct visualization of the

177 In this study, using time-lapse intravital imaging of the spleen, we identify a tr

178 Our results show that cognitive lapses involve local state-dependent changes in neuronal

179 Furthermore, during cognitive lapses, LFPs exhibit a relative local increase in slow/t

180 Time-lapse live cell imaging revealed active migration of hPG

181 ning and confocal microscopy as well as time lapse live imaging after injection of mRNA encoding fusi

182 In this study, we utilize 3D time-lapse live-cell imaging to monitor the role of NuSAP in

183 , that assemble in situ and enable long time-lapse, live-cell nanoscopy of discrete cellular structur

184 Time lapse measurements revealed that the electric currents a

185 ed stage of a microscope for conducting time-lapse microphotography of multiple observations in 20 ch

186 icrofluidic device enabled quantitative time-lapse microphotography reported here should be suitable

187 was further verified experimentally by time-lapse microscopic examinations of the snf1Delta strain.

188 y temporal variance analysis of a short time-lapse microscopic image series to capture the motion dyn

189 Time-lapse microscopic-photography allows in-depth phenotypin

190 ing for cell perturbation, quantitative time-lapse microscopy and computational analysis of time-laps

191 Time-lapse microscopy and electron microscopy confirmed the v

192 he mobilities of labeled glycolipids by time-lapse microscopy and fluorescence recovery after photobl

193 Here, we used time-lapse microscopy and fluorescent reporters of DNA replic

194 We used time-lapse microscopy and fluorescently labelled SeqA to dete

195 We use time-lapse microscopy and genetic assays to show that recombi

196 orhabditis elegans embryos by combining time-lapse microscopy and image analysis.

197 at cellular and whole tissue levels via time-lapse microscopy and quantitative PCR.

198 In this study, we use time-lapse microscopy coupled with quantitative single-cell t

199 eover, it can correct temporal drift in time-lapse microscopy data and thus improve continuous single

200 In live-cell time-lapse microscopy experiments, we could not detect any si

201 Using in vitro time-lapse microscopy in a mouse transplant model, we investi

202 Here, we used electron, confocal and time-lapse microscopy in combination with pharmacological inh

203 Time-lapse microscopy of cell-population behavior in response

204 Here we use single-cell time-lapse microscopy of Cyclin-Dependent Kinase 2 (CDK2) act

205 ext, from single-cell, single-RNA level time-lapse microscopy of independent lineages of Escherichia

206 Using high-resolution time-lapse microscopy of living Caenorhabditis elegans embryo

207 on process is monitored by using either time-lapse microscopy or fluorescence-activated cell sorting

208 Lineage tracing and time-lapse microscopy reveal that Lgr5+ cells transdifferenti

209 Time-lapse microscopy revealed that PIK3C2A was required for

210 O-1 or occludin, but longer term (12 h) time-lapse microscopy reveals strikingly decreased tight junc

211 Time-lapse microscopy reveals that Dll4 is induced in leader

212 Time lapse microscopy showed that isogenic cells express hete

213 We used time-lapse microscopy to analyze the dynamic effects of four

214 We used high-precision time-lapse microscopy to characterize the maturation kinetics

215 Here, we use two-photon time-lapse microscopy to demonstrate that CCR4 promotes medul

216 nvestigated this topic using two-photon time-lapse microscopy to directly visualize thymocyte migrati

217 Here we use single cell analysis and time-lapse microscopy to identify a subpopulation of host cel

218 is method is based on automated digital time-lapse microscopy to observe the growth and morphological

219 improved image analysis algorithms for time-lapse microscopy to reveal a defense against stationary

220 We later utilised time-lapse microscopy to show that internalised mitochondria

221 we employed long-term, high-resolution, time-lapse microscopy to track the fate of unambiguously iden

222 in Caulobacter crescentus and then used time-lapse microscopy to visualize the ensuing chromosome dyn

223 followed at the single-cell level using time-lapse microscopy, and showed two distinct, albeit dynami

224 enesis is now possible with advances in time-lapse microscopy, but a true understanding of their comp

225 content screening, super-resolution and time-lapse microscopy, digital pathology, public genetic or c

226 Time-lapse microscopy, immunostaining, and particle image vel

227 city in chronic settings, sophisticated time-lapse microscopy, or bulky/expensive chemo-stat instrume

228 iological lumenal expansion detected by time-lapse microscopy, recapitulating one of the hallmarks of

229 rving monocytes undergoing apoptosis by time-lapse microscopy, we discovered a new type of membrane p

230 Using in vivo time-lapse microscopy, we found that only 25% of oligodendroc

231 among single Pseudomonas cells by using time-lapse microscopy.

232 bing fibres (CFs) in mice using in vivo time-lapse microscopy.

233 fluorescence loss after photoconversion time-lapse microscopy.

234 hip in combination with high-resolution time-lapse microscopy.

235 owells), and imaged using multi-channel time-lapse microscopy.

236 cent images are acquired with automated time-lapse microscopy.

237 els in pure culture (e.g., for 'virtual time-lapse' microscopy) or in situ labeling of complex enviro

238 The time-lapse morphological changes along with the flow cytometr

239 apid and accurate stitching of large 2D time-lapse mosaics.

240 colour-separated microscope image in a time-lapse movie and using only simple means, we simultaneous

241 ticularly when dealing with hundreds of time-lapse movies collected in a high-throughput manner.

242 Finally, we generate time-lapse movies of complex neural arborization through auto

243 icroscopy and computational analysis of time-lapse movies.

244 sources, which can process terabytes of time-lapse multi-channel mosaics 15 to 100 times faster than

245 n this issue of Cell, Langen et al. use time-lapse multiphoton microscopy to show how Drosophila phot

246 ell cycle synchronization and live-cell time-lapse observation are widely used to analyze these proce

247 Lapses of attention can have negative consequences, incl

248 Lapses of attention were reliably preceded by progressiv

249 a ubiquitous cognitive process resulting in lapses of attention.

250 at lapses of entrainment would correspond to lapses of attention.

251 s for preparatory attentional control beyond lapses of attentional engagement.

252 of nonhuman primates, and hypothesized that lapses of entrainment would correspond to lapses of atte

253 , such as the loss of mental flexibility and lapses of responsiveness.

254 condition and smoking outcome (lapse vs non-lapse) on whole-brain connectivity with ventral and dors

255 Results indicated a significant condition by lapse outcome interaction for both right and left ventra

256 We used in vivo time-lapse quantitative microscopy to show that clathrin, dyn

257 sensitive dependence of climate velocity on lapse rate and derive biotic velocity as a rigid elevati

258 orcing in warmer climates, suggest that the "lapse rate feedback" in simulations of anthropogenic cli

259 1 order of magnitude, were correlated to the lapse rate under nocturnal inversions.

260 f convective entrainment on the tropospheric lapse rate, and we demonstrate the importance of this in

261 ave cloud feedback) and with a less negative lapse-rate feedback, as expected from a decrease in stab

262 ely the app will incorporate a detailed time lapse record of cell shape, beginning with neurons.

263 Furthermore, using confocal imaging and time-lapse recordings, we demonstrated "intracellular crawlin

264 neural circuitry structure and function and lapse/relapse vulnerability in 2 independent studies of

265 aving and drug taking, and set the stage for lapse/relapse.

266 mediated IC, gray-matter volume, and smoking lapse/relapse.

267 well constrained by the data, we obtain time-lapse repeatability of about 2% in the model domain-a th

268 Here, time-lapse scanning tunneling microscopy (STM) and density fu

269 We used time-lapsed scanning tunneling microscopy between 43 and 50 K

270 Here, using time-lapsed scanning tunnelling microscopy and density functi

271 Time-lapse SECM imaging revealed a suitable window of 30 min

272 by tracking single CPR molecules using time-lapse single-molecule fluorescence imaging and subsequen

273 Using live time-lapse, single-cell microscopy measurements, we show that

274 Time-lapse SPECT imaging results illustrated both local and g

275 tiview, multichannel, multiillumination time-lapse SPIM data on a single workstation or in parallel o

276 It also enables time-lapse studies of entire cell cultures in multiple imagin

277 Time-lapse studies show how convective tissue displacement pa

278 uctively over time through '4D' in situ time-lapse studies.

279 ventional computed tomography (CT) in a time-lapse study.

280 This approach is well suited for time-lapsed study of the mechanobiology of differentiating st

281 and organelles in living cells by long time-lapse super-resolution microscopy is challenging, as it

282 Using time-lapse superresolution microscopy in brain slices, we rep

283 A novel time-lapse synchrotron deep-UV microscopy methodology was dev

284 Specifically, time-lapsed TEM image series acquired of the material during

285 We find that, just before cognitive lapses, the selective spiking responses of individual ne

286 the follow-up by digital dermoscopy during a lapse time of a few months.

287 Time-lapse total internal reflection fluorescence (TIRF) micr

288 l changes in axonal boutons imaged with time-lapse two-photon laser scanning microscopy (2PLSM).

289 vian embryonic organ culture, we employ time-lapse two-photon laser scanning microscopy to observe pr

290 By using time-lapse two-photon microendoscopy in the CA1 hippocampal a

291 Time-lapse two-photon microscopy in adult slices was used to

292 ts in slow behavioral performance (cognitive lapses) typically attributed to attentional thalamic and

293 we report the first end-to-end study of time-lapse V S imaging that uses traffic noise continuously r

294 Time-lapse video imaging compiled from the optical screening

295 Time-lapse video microscopy revealed that deposition of LC3 o

296 of abstinence condition and smoking outcome (lapse vs non-lapse) on whole-brain connectivity with ven

297 When indicators of an attentional lapse were detected in the brain, we gave human particip

298 entrainment by external stimuli, attentional lapses were also characterized by high-amplitude alpha o

299 Here we report time-lapse X-ray crystallography snapshots of catalytic event

300 Here the authors use time-lapse X-ray crystallography to capture the states of pol