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1 ng in terms of the divergence of the average time lapse.
2       In this paper, OPM is adapted to allow time-lapse 3-D imaging of 3-D biological cultures in com
3                                              Time-lapse 3-D imaging of multicellular spheroids expres
4                                      We used time-lapse 3D imaging and quantitative image analysis to
5                                              Time-lapse AFM imaging, in solution, show that over time
6             FN fibrillogenesis visualized by time-lapse AFM thus provides new structural and mechanis
7                     Here, we use single-cell time-lapse analyses to reveal that mycobacterial cell po
8 ach time point against the control (0 h) and time-lapse analysis by comparing each time point with th
9                                              Time-lapse analysis of cellular images is an important a
10                                              Time-lapse analysis revealed that OHCs isolated from WT
11                                              Time lapse and live cell images of human cells expressin
12 ell cycle of A. tumefaciens was monitored by time-lapse and superresolution microscopy to image the l
13                       Here we use wide-field time-lapse and three-dimensional structured illumination
14                                      Marker, time-lapse and ultrastructural studies indicated that ol
15 a combination of fluorescence microscopy and time-lapse atomic force microscopy (AFM) to visualize in
16 a combination of fluorescence microscopy and time-lapse atomic force microscopy (AFM) to visualize in
17                                        Using time-lapse atomic force microscopy, we analyzed the morp
18 e proposed cascade was addressed by means of time-lapse automated fluorescence microscopy, electron m
19                            Here, we report a time-lapse-based bright-field imaging analysis system th
20 cross lifetime, age at presentation, and the time lapse between surgery and the first AT episode vari
21 nd colloids- the probability distribution of time lapses between the passages of consecutive bodies e
22 ough most astrocytes appeared dormant during time-lapse calcium imaging, a subgroup displayed persist
23 ry method to traditional synchronization and time-lapse cell cycle analysis methods.
24                              Here we combine time-lapse, complete chromosomal assessment and single-c
25         This protocol describes multichannel time-lapse confocal imaging of anchor-cell invasion in l
26 y using a membrane-permeant PI3P derivative, time-lapse confocal imaging, electrophysiology, as well
27                                        Using time-lapse confocal imaging, parabiotic surgical pairing
28 of multicellular and molecular dynamics from time-lapse confocal microscopy data.
29               Ratiometric Ca(2+) imaging and time-lapse confocal microscopy demonstrated glutamate-in
30 insights generated by application of a novel time-lapse confocal microscopy method along with immunof
31                      We used multiphoton and time-lapse confocal microscopy to monitor intracellular
32           In this work, we exploit live-cell time-lapse confocal reflectance microscopy and image cor
33                      This is consistent with time-lapse crystallographic structures following inserti
34                                       Recent time-lapse crystallographic studies of DNA polymerases h
35                                  Here we use time-lapse crystallography to follow 8-oxo-dGTP insertio
36                           Using kinetics and time-lapse crystallography, we evaluated how a model DNA
37 ves unexpected features revealed recently in time-lapse crystallography.
38 to extract quantitative information from the time lapse data.
39 ur combination of computational modeling and time-lapse data analysis provides a general way to exami
40     PCI relies on quantitative phase imaging time-lapse data and, as such, functions in label-free mo
41                                          The time-lapse data indicate that the same cells are differe
42 segment and track neuronal morphodynamics in time-lapse datasets.
43                                              Time-lapse electrical resistivity imaging (ERI) was used
44                                  Here, using time-lapse embryonic imaging, genetics, protein-interact
45                                    Viewed by time-lapse epi-fluorescence microscopy, monocytes appear
46                                    Utilizing time-lapse epifluorescence microscopy, we observed that
47                                              Time-lapse ex vivo imaging revealed a drastic eliminatio
48 ter allowed us to study chitin deposition in time lapse experiments and by using it we have identifie
49 mentation and tracking of cells in long-term time-lapse experiments has emerged as a powerful method
50 alidated within the scientific community for time-lapse experiments, and combining them with simple g
51  tuning tracking parameters for high-content time-lapse experiments.
52 al time fluorescent imaging (zone adjustable time-lapse fluorescence image processor) and separation
53    Typically, the approximate time frame for time-lapse fluorescence imaging of mt-Keima is 20 h for
54                  Unexpectedly, we find using time-lapse fluorescence imaging that cdc-42 is not requi
55 ne order, and probed their expressions using time-lapse fluorescence microscopy and single-molecule f
56        Microfluidics coupled to quantitative time-lapse fluorescence microscopy is transforming our a
57                                  Here, using time-lapse fluorescence microscopy to examine PhoP-depen
58 ed a combination of microfluidic devices and time-lapse fluorescence microscopy to track oscillations
59                               In this study, time-lapse fluorescence microscopy was used to investiga
60                            We used live-cell time-lapse fluorescence microscopy, followed by 3D rende
61                                        Using time-lapse fluorescence microscopy, we carried out an in
62                                 Furthermore, time-lapse force measurements showed that these cells mi
63 astly, we use the microfluidic-incubator and time-lapsed FTIR imaging to determine the misfolding pat
64 enotypes, detect symmetry-breaking events in time-lapse image data, and quantify the time-dependent c
65 nalysis of microtubule dynamics from EB3-GFP time-lapse image sequences identified the products of th
66 experimental and modeling approach that uses time-lapse imagery to directly relate burrow formation t
67 d Lineage Mapper, an open-source tracker for time-lapse images of biological cells, colonies, and par
68 , as demonstrated by kymographs derived from time-lapse images of FtsZ ladder formation.
69 se fluorescence signals from single-molecule time-lapse images of individual Escherichia coli cells.
70 yed in vivo two-photon microscopy to produce time-lapse images of serotonin axons in the neocortex of
71                              The analysis of time-lapse images showing cells dividing to produce clon
72                                Combined with time lapse imaging of development in culture, we demonst
73                                        Using time lapse imaging, it is possible to observe these even
74                             Localization and time-lapse imaging analysis reveals that MAP7 is enriche
75                                              Time-lapse imaging and analysis of reporter transgenics
76 ring controls axon remodeling, using in vivo time-lapse imaging and electrophysiological analysis of
77                                              Time-lapse imaging and fate mapping demonstrate that the
78   Here, we performed atomic force microscopy time-lapse imaging and mechanical mapping of actin in th
79                                              Time-lapse imaging and mutagenesis studies further estab
80                                              Time-lapse imaging and quantitative analysis of axon dyn
81                                              Time-lapse imaging and scanning electron microscopy reve
82 ng the archaeal cells to enable quantitative time-lapse imaging and single-cell analysis, which would
83                         The software enabled time-lapse imaging and the use of temporally varying cha
84 gle dimension, facilitating high-resolution, time-lapse imaging and tracking of individual cells.
85           This study used a novel, prolonged time-lapse imaging approach to continuously track the be
86                                      Using a time-lapse imaging assay, we found that developing amacr
87                                              Time-lapse imaging assays also revealed the essential ro
88                                              Time-lapse imaging at subcellular resolution shows that
89         Using a complementary combination of time-lapse imaging by fluorescence confocal microscopy a
90      Results indicate that use of continuous time-lapse imaging can distinguish cellular heterogeneit
91  single-cell resolution from high-throughput time-lapse imaging data, especially, the interactions be
92                                      In vivo time-lapse imaging demonstrated that local TH first incr
93                                              Time-lapse imaging demonstrated that SEC3a and SEC8 were
94                                              Time-lapse imaging ends within 12 h, with subsequent tra
95                                              Time-lapse imaging further reveals that Fgf8a acts as a
96 lly delivered fluorescent probes and in vivo time-lapse imaging in a mouse model of demyelination to
97                                   Through 3D time-lapse imaging in a secreting organ, we show that F-
98          Here we address this question using time-lapse imaging in hippocampal neurons.
99 -photon and two-photon microscopy, including time-lapse imaging in light-sheet systems.
100                                              Time-lapse imaging in zebrafish shows that EphB-Pak2a si
101  we use laser nerve transection and in vivo, time-lapse imaging in zebrafish to investigate the role
102                                Using in vivo time-lapse imaging in zebrafish, we observed that prior
103                                   Two-photon time-lapse imaging indicated that microglia depletion re
104                       Furthermore, long-term time-lapse imaging indicates that aggregates of mutant P
105                                              Time-lapse imaging is a fundamental tool for studying ce
106                                        Using time-lapse imaging microscopy in nanowell grids (TIMING)
107 Asp/Ala330Leu/Ile332Glu (DLE), and developed Time-lapse Imaging Microscopy in Nanowell Grids to analy
108 It further provides a novel tool for in vivo time-lapse imaging of adult fish for non-cardiac studies
109 uorescence microscopy have made snapshot and time-lapse imaging of bacterial cells commonplace, yet f
110                           Furthermore, using time-lapse imaging of beating hearts in conjunction with
111                            Cell tracking and time-lapse imaging of chimeric drMM cultures indicated t
112                                              Time-lapse imaging of dissociated hippocampal neuronal c
113 blish a robust strategy for long-term (24 h) time-lapse imaging of E6.5-8.5 mouse embryos with light-
114                                         With time-lapse imaging of ECM micro-fiber morphology, the lo
115 e fission yeast Schizosaccharomyces pombe by time-lapse imaging of individual endocytic sites.
116  cilium; its lumenal space is rich in Ca(2+) Time-lapse imaging of isolated hPSCs reveals that the ap
117                                              Time-lapse imaging of lac-operator-tagged chromosome reg
118                                        Using time-lapse imaging of Lifeact-GFP-transfected chromaffin
119 at HySP enables unmixing of seven signals in time-lapse imaging of living zebrafish embryos.
120 se imaging that permits prolonged label-free time-lapse imaging of microglia in the presence of neuro
121 color, high-contrast, and high-dynamic-range time-lapse imaging of migrating cells in complex three-d
122                                              Time-lapse imaging of multiple labels is challenging for
123 eet microscopy to perform three-dimensional, time-lapse imaging of neutrophil-like HL-60 cells crawli
124 tes the potential of SIM for superresolution time-lapse imaging of plant cells, showing unprecedented
125  in vivo two-photon microscopy, we performed time-lapse imaging of radial glial cells and measured fi
126      Using two-photon glutamate uncaging and time-lapse imaging of rat hippocampal CA1 neurons, we sh
127         Here, using quantitative single-cell time-lapse imaging of Saccharomyces cerevisiae, we show
128 ge N") and long-term operations ("large T"), time-lapse imaging of shear-wave velocity (V S ) structu
129                                              Time-lapse imaging of static liquid cultures demonstrate
130                                Using in vivo time-lapse imaging of tectal neuron structure and visual
131              We developed a novel method for time-lapse imaging of the rapid dynamics of miRNA activi
132                                 We performed time-lapse imaging of thousands of neurons over weeks in
133             These findings were supported by time-lapse imaging of WT and syntaphilin-deficient axons
134 l manipulation, gene expression analysis and time-lapse imaging of zebrafish embryos.
135                                Using in vivo time-lapse imaging of zebrafish retinas, we show that RI
136 d and the consequences followed with in vivo time-lapse imaging or immunostaining assays.
137 he different topographies, using fluorescent time-lapse imaging over 21 days.
138                                              Time-lapse imaging over 4 weeks revealed a pronounced, c
139                                          Our time-lapse imaging quantifies membrane fluctuations at t
140                Traction force microscopy and time-lapse imaging reveal that closure of gaps begins wi
141                                              Time-lapse imaging revealed dynamic changes in the metab
142                                              Time-lapse imaging revealed that early exposure to eleva
143                                              Time-lapse imaging revealed that JNK-inhibited cortical
144                                              Time-lapse imaging revealed that knockdown of miR-219 fu
145                                              Time-lapse imaging revealed that MSCs recruited MRL.Fas(
146                                              Time-lapse imaging reveals rapid pulsatile level changes
147                                              Time-lapse imaging reveals that alpha-actinin-1 puncta w
148                                              Time-lapse imaging reveals that branching events are syn
149                                              Time-lapse imaging reveals that SAC proteins are in dist
150                                              Time-lapse imaging showed that hepatic-specified endoder
151                                              Time-lapse imaging shows that iNSCs are tumouritropic, h
152                                     Instead, time-lapse imaging studies suggest a prominent role for
153                    Here, we use non-invasive time-lapse imaging to continuously examine hPSC maintena
154                                        Using time-lapse imaging to correlate mitotic behavior with ce
155         Here we combined neurite-tracing and time-lapse imaging to define the events that lead to the
156 croscopy, optogenetic activation and in vivo time-lapse imaging to show that newly generated OSNs for
157 re, we use two-photon glutamate uncaging and time-lapse imaging to show that non-ionotropic NMDAR sig
158   We combined single-cell laser axotomy with time-lapse imaging to study the dynamics of phosphatidyl
159  reverse genetics and multivariate long-term time-lapse imaging to test current cell shape control mo
160 l assessments of cellular rearrangements and time-lapse imaging to visualize cochlear remodeling in m
161                                              Time-lapse imaging using a Forster resonance energy tran
162                              Using long-term time-lapse imaging with intact Drosophila larvae, we fou
163                                     Extended time-lapse imaging with less than one virion per cell al
164 induced pluripotent stem cells (iPSCs) using time-lapse imaging, immunostaining, and single-cell RNA
165 eneration with single-axon laser axotomy and time-lapse imaging, monitoring the initial changes in tr
166 kers (MADM), combined with organ culture and time-lapse imaging, to trace the movements and divisions
167 characterized cell-cycle delay identified by time-lapse imaging, was used to clarify the relationship
168                           Using simultaneous time-lapse imaging, we find that early endosome-associat
169                                        Using time-lapse imaging, we find that mesenchymal cell conden
170                                        Using time-lapse imaging, we found that, as motor neurons diff
171  genetics, interspecific gene transfers, and time-lapse imaging, we show that leaflet development req
172                    Using sparse-labeling and time-lapse imaging, we visualized for the first time the
173  tips of the invading cords were revealed by time-lapse imaging, which showed cells actively extendin
174 e utility of the method in vivo in mice with time-lapse imaging.
175              NCC migration was studied using time-lapse imaging.
176  question using single-molecule tracking and time-lapse imaging.
177 e study their mobility characteristics using time-lapse imaging.
178 -tracing and transcriptomics approaches with time-lapse imaging.
179 within an intact microvascular network using time-lapse imaging.
180                                              Time-lapsed imaging of GFP-laced rodlets in human cells
181                       Using a combination of time-lapse in vivo single-cell analysis and Caenorhabdit
182                    Histological analysis and time-lapse in vivo two-photon microscopy revealed that h
183                                    Using 3D, time-lapse intravital imaging for direct visualization o
184                         In this study, using time-lapse intravital imaging of the spleen, we identify
185 butyrate (PDBu) or a natural stimulant, UTP, time lapse live cell imaging movies indicated phosphoryl
186 ostaining and confocal microscopy as well as time lapse live imaging after injection of mRNA encoding
187                                              Time-lapse live cell imaging revealed active migration o
188                 In this study, we utilize 3D time-lapse live-cell imaging to monitor the role of NuSA
189 HMSiR, that assemble in situ and enable long time-lapse, live-cell nanoscopy of discrete cellular str
190                                 By combining time-lapse luminescence microscopy with a microfluidic d
191                                              Time lapse measurements revealed that the electric curre
192 torized stage of a microscope for conducting time-lapse microphotography of multiple observations in
193 The microfluidic device enabled quantitative time-lapse microphotography reported here should be suit
194 ction was further verified experimentally by time-lapse microscopic examinations of the snf1Delta str
195 employ temporal variance analysis of a short time-lapse microscopic image series to capture the motio
196                                              Time-lapse microscopic-photography allows in-depth pheno
197                                              Time lapse microscopy showed that isogenic cells express
198 handling for cell perturbation, quantitative time-lapse microscopy and computational analysis of time
199                                              Time-lapse microscopy and electron microscopy confirmed
200 ied the mobilities of labeled glycolipids by time-lapse microscopy and fluorescence recovery after ph
201                                Here, we used time-lapse microscopy and fluorescent reporters of DNA r
202                                      We used time-lapse microscopy and fluorescently labelled SeqA to
203                                       We use time-lapse microscopy and genetic assays to show that re
204  Caenorhabditis elegans embryos by combining time-lapse microscopy and image analysis.
205                     The advent of high-speed time-lapse microscopy and its use in monitoring the cell
206 dic devices in combination with fluorescence time-lapse microscopy and quantitative image analysis, w
207 fied at cellular and whole tissue levels via time-lapse microscopy and quantitative PCR.
208 t single-cell expression assays coupled with time-lapse microscopy can resolve the identity and the l
209                        In this study, we use time-lapse microscopy coupled with quantitative single-c
210   Moreover, it can correct temporal drift in time-lapse microscopy data and thus improve continuous s
211                                 In live-cell time-lapse microscopy experiments, we could not detect a
212 ysis of intracellular dynamic processes from time-lapse microscopy image data.
213                               Using in vitro time-lapse microscopy in a mouse transplant model, we in
214         Here, we used electron, confocal and time-lapse microscopy in combination with pharmacologica
215                                              Time-lapse microscopy of cell-population behavior in res
216                      Here we use single-cell time-lapse microscopy of Cyclin-Dependent Kinase 2 (CDK2
217     Next, from single-cell, single-RNA level time-lapse microscopy of independent lineages of Escheri
218                        Using high-resolution time-lapse microscopy of living Caenorhabditis elegans e
219 ulation process is monitored by using either time-lapse microscopy or fluorescence-activated cell sor
220                          Lineage tracing and time-lapse microscopy reveal that Lgr5+ cells transdiffe
221                                              Time-lapse microscopy revealed that PIK3C2A was required
222 GFP ZO-1 or occludin, but longer term (12 h) time-lapse microscopy reveals strikingly decreased tight
223                                              Time-lapse microscopy reveals that Dll4 is induced in le
224                                      We used time-lapse microscopy to analyze the dynamic effects of
225                       We used high-precision time-lapse microscopy to characterize the maturation kin
226                      Here, we use two-photon time-lapse microscopy to demonstrate that CCR4 promotes
227 has investigated this topic using two-photon time-lapse microscopy to directly visualize thymocyte mi
228         Here we use single cell analysis and time-lapse microscopy to identify a subpopulation of hos
229 is This method is based on automated digital time-lapse microscopy to observe the growth and morpholo
230 s and improved image analysis algorithms for time-lapse microscopy to reveal a defense against statio
231                            We later utilised time-lapse microscopy to show that internalised mitochon
232                    Here, we use quantitative time-lapse microscopy to show the spread of infectious c
233 ore, we employed long-term, high-resolution, time-lapse microscopy to track the fate of unambiguously
234 DSBs in Caulobacter crescentus and then used time-lapse microscopy to visualize the ensuing chromosom
235 were followed at the single-cell level using time-lapse microscopy, and showed two distinct, albeit d
236 rphogenesis is now possible with advances in time-lapse microscopy, but a true understanding of their
237 high-content screening, super-resolution and time-lapse microscopy, digital pathology, public genetic
238                                              Time-lapse microscopy, immunostaining, and particle imag
239 g a microfluidic gradient chamber system and time-lapse microscopy, in this paper, we uncover a new f
240  toxicity in chronic settings, sophisticated time-lapse microscopy, or bulky/expensive chemo-stat ins
241  physiological lumenal expansion detected by time-lapse microscopy, recapitulating one of the hallmar
242 ing integrated microfluidic cell culture and time-lapse microscopy, we demonstrate here that the spee
243  observing monocytes undergoing apoptosis by time-lapse microscopy, we discovered a new type of membr
244                                Using in vivo time-lapse microscopy, we found that only 25% of oligode
245 ism) among single Pseudomonas cells by using time-lapse microscopy.
246  climbing fibres (CFs) in mice using in vivo time-lapse microscopy.
247  and fluorescence loss after photoconversion time-lapse microscopy.
248 sis chip in combination with high-resolution time-lapse microscopy.
249  (nanowells), and imaged using multi-channel time-lapse microscopy.
250 e groups of cells growing on solid medium by time-lapse microscopy.
251 amics of damaged chromatin to be followed by time-lapse microscopy.
252 e long-lived and retained in mother cells by time-lapse microscopy.
253 uorescent images are acquired with automated time-lapse microscopy.
254 t labels in pure culture (e.g., for 'virtual time-lapse' microscopy) or in situ labeling of complex e
255                                          The time-lapse morphological changes along with the flow cyt
256 for rapid and accurate stitching of large 2D time-lapse mosaics.
257  each colour-separated microscope image in a time-lapse movie and using only simple means, we simulta
258 , particularly when dealing with hundreds of time-lapse movies collected in a high-throughput manner.
259                       In this study, we used time-lapse movies of C. neoformans-infected macrophages
260                         Finally, we generate time-lapse movies of complex neural arborization through
261 pse microscopy and computational analysis of time-lapse movies.
262 ng single-molecule RNA-FISH and quantitative time-lapse movies.
263 ng resources, which can process terabytes of time-lapse multi-channel mosaics 15 to 100 times faster
264     In this issue of Cell, Langen et al. use time-lapse multiphoton microscopy to show how Drosophila
265     Cell cycle synchronization and live-cell time-lapse observation are widely used to analyze these
266                              We used in vivo time-lapse quantitative microscopy to show that clathrin
267 timately the app will incorporate a detailed time lapse record of cell shape, beginning with neurons.
268      Furthermore, using confocal imaging and time-lapse recordings, we demonstrated "intracellular cr
269 t is well constrained by the data, we obtain time-lapse repeatability of about 2% in the model domain
270                                        Here, time-lapse scanning tunneling microscopy (STM) and densi
271                                      We used time-lapsed scanning tunneling microscopy between 43 and
272                                  Here, using time-lapsed scanning tunnelling microscopy and density f
273                                              Time-lapse SECM imaging revealed a suitable window of 30
274               Here, we report the first 24-h time-lapse sequences of post-implantation mouse embryo d
275                                              Time-lapse SIM imaging allowed the visualization of subd
276 in cultured neuronal network monitored using time-lapse single cell imaging increased in both amplitu
277 erved by tracking single CPR molecules using time-lapse single-molecule fluorescence imaging and subs
278                                   Using live time-lapse, single-cell microscopy measurements, we show
279                                              Time-lapse SPECT imaging results illustrated both local
280 e multiview, multichannel, multiillumination time-lapse SPIM data on a single workstation or in paral
281                              It also enables time-lapse studies of entire cell cultures in multiple i
282                                              Time-lapse studies show how convective tissue displaceme
283 destructively over time through '4D' in situ time-lapse studies.
284 h conventional computed tomography (CT) in a time-lapse study.
285             This approach is well suited for time-lapsed study of the mechanobiology of differentiati
286 tures and organelles in living cells by long time-lapse super-resolution microscopy is challenging, a
287                                        Using time-lapse superresolution microscopy in brain slices, w
288                                      A novel time-lapse synchrotron deep-UV microscopy methodology wa
289                                Specifically, time-lapsed TEM image series acquired of the material du
290                                              Time-lapse total internal reflection fluorescence (TIRF)
291 ctural changes in axonal boutons imaged with time-lapse two-photon laser scanning microscopy (2PLSM).
292 ust avian embryonic organ culture, we employ time-lapse two-photon laser scanning microscopy to obser
293                                     By using time-lapse two-photon microendoscopy in the CA1 hippocam
294                                              Time-lapse two-photon microscopy in adult slices was use
295 Here we report the first end-to-end study of time-lapse V S imaging that uses traffic noise continuou
296                                              Time-lapse video imaging compiled from the optical scree
297                                              Time-lapse video microscopy revealed that deposition of
298 e plane illumination microscope (diSPIM) for time-lapse volumetric (4D) imaging of living samples at
299                               Here we report time-lapse X-ray crystallography snapshots of catalytic
300                         Here the authors use time-lapse X-ray crystallography to capture the states o

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