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