1 n capacity was assessed by scratch assays in
time-lapse imaging.
2 nd then monitored spine survival rates using
time-lapse imaging.
3 slice culture using two-photon and confocal
time-lapse imaging.
4 lants in heterogeneous environments using 3D
time-lapse imaging.
5 to low- and high-efficiency transfection and
time-lapse imaging.
6 e study their mobility characteristics using
time-lapse imaging.
7 on and wound closure were investigated using
time-lapse imaging.
8 with KIF5B along axons revealed by two-color
time-lapse imaging.
9 Dye uptake was measured using
time-lapse imaging.
10 -tracing and transcriptomics approaches with
time-lapse imaging.
11 llagen gels was analyzed using computational
time-lapse imaging.
12 within an intact microvascular network using
time-lapse imaging.
13 gittal slice explant culture and 3D confocal
time-lapse imaging.
14 e utility of the method in vivo in mice with
time-lapse imaging.
15 NCC migration was studied using
time-lapse imaging.
16 question using single-molecule tracking and
time-lapse imaging.
17 Using
time-lapse imaging,
a recent study described visualizing
18 Time-lapse imaging allows quantification of primordial v
19 Our cell fate and
time-lapse imaging analyses reveal that the sorting of P
20 Localization and
time-lapse imaging analysis reveals that MAP7 is enriche
21 Using
time lapse imaging and fluorescence recovery after photo
22 Time-lapse imaging and analysis of reporter transgenics
23 uring C. elegans embryogenesis, based on 3D,
time-lapse imaging and automated image analysis.
24 ring controls axon remodeling, using in vivo
time-lapse imaging and electrophysiological analysis of
25 Time-lapse imaging and fate mapping demonstrate that the
26 and in response to DNA damage using confocal
time-lapse imaging and fluorescence cross-correlation sp
27 This type of system enables high-resolution
time-lapse imaging and is suitable for a wide range of c
28 Here, we performed atomic force microscopy
time-lapse imaging and mechanical mapping of actin in th
29 Time-lapse imaging and molecular analyses indicate that
30 Time-lapse imaging and motion analysis using epicardial
31 Time-lapse imaging and mutagenesis studies further estab
32 Time-lapse imaging and quantitative analysis of axon dyn
33 Time-lapse imaging and scanning electron microscopy reve
34 ng the archaeal cells to enable quantitative
time-lapse imaging and single-cell analysis, which would
35 The software enabled
time-lapse imaging and the use of temporally varying cha
36 both isovariants was observed directly with
time-lapse imaging and total internal reflection fluores
37 gle dimension, facilitating high-resolution,
time-lapse imaging and tracking of individual cells.
38 lted in cleavage-stage arrest as assessed by
time-lapse imaging and was associated with aneuploidy ge
39 EPSPs) simultaneously with combined 2-photon
time-lapse imaging and whole-cell recordings from hippoc
40 Using
time-lapsed imaging and statistical tools, we show that
41 we present a high-content framework in which
time-lapse imaging,
and single-particle-tracking algorit
42 Using a microchip-based,
time-lapse imaging approach allowing the entire contact
43 This study used a novel, prolonged
time-lapse imaging approach to continuously track the be
44 Using a
time-lapse imaging assay, we found that developing amacr
45 Time-lapse imaging assays also revealed the essential ro
46 Subsequent FRET-based single cell
time-lapse imaging at conditions where transcription dep
47 Time-lapse imaging at subcellular resolution shows that
48 er time, and we combined it with deep-tissue
time-lapse imaging based on fast two-photon microscopy t
49 Neuronal
time-lapse imaging,
behavioral analyses, and electrophys
50 nship between synthesis and hydrolysis using
time-lapse imaging,
biophysical measurements of cell-wal
51 In
time-lapse imaging,
blocking the tPA function promotes e
52 Using a complementary combination of
time-lapse imaging by fluorescence confocal microscopy a
53 Results indicate that use of continuous
time-lapse imaging can distinguish cellular heterogeneit
54 The information in
time-lapse imaging can provide valuable mechanistic insi
55 ddress this problem through a combination of
time-lapse imaging,
clonal analysis, and computational m
56 single-cell resolution from high-throughput
time-lapse imaging data, especially, the interactions be
57 Here we introduce cellular-level
time-lapse imaging deep within the live mammalian brain
58 In vivo
time-lapse imaging demonstrated that local TH first incr
59 Time-lapse imaging demonstrated that SEC3a and SEC8 were
60 Time-lapse imaging depicts a dynamic picture in which ex
61 Time-lapse imaging ends within 12 h, with subsequent tra
62 Time-lapse imaging experiments of TCs exhibited pause an
63 To test these predictions, we use
time-lapse imaging experiments to show that damage often
64 Using in vivo
time-lapse imaging,
fluorescence recovery after photoble
65 Time-lapse imaging further reveals that Fgf8a acts as a
66 These techniques can be used for
time-lapse imaging,
gain- and loss-of-function experimen
67 induced pluripotent stem cells (iPSCs) using
time-lapse imaging,
immunostaining, and single-cell RNA
68 n vivo after transplantation and 3D confocal
time-lapse imaging in a living chick embryo.
69 lly delivered fluorescent probes and in vivo
time-lapse imaging in a mouse model of demyelination to
70 Through 3D
time-lapse imaging in a secreting organ, we show that F-
71 Clonal analysis and
time-lapse imaging in aurora-A mutants show single neuro
72 Using
time-lapse imaging in both SVZ cells and organotypic bra
73 mmunocytochemistry, confocal microscopy, and
time-lapse imaging in dissociated cultures of cortical n
74 Here we address this question using
time-lapse imaging in hippocampal neurons.
75 -photon and two-photon microscopy, including
time-lapse imaging in light-sheet systems.
76 cal and cell biological assays combined with
time-lapse imaging in live snph wild-type and mutant neu
77 e tested here this hypothesis using confocal
time-lapse imaging in rat hippocampal organotypic slices
78 ht- and electron-microscopic (EM) levels and
time-lapse imaging in slice cultures to analyze migratio
79 Time-lapse imaging in the intact zebrafish embryo with t
80 ombined patch-clamp recording and two-photon
time-lapse imaging in the same CA1 pyramidal neurons in
81 Time-lapse imaging in vivo revealed that exercise partia
82 eneration dynamics in these animals requires
time-lapse imaging in vivo, which has been difficult to
83 Time-lapse imaging in zebrafish shows that EphB-Pak2a si
84 we use laser nerve transection and in vivo,
time-lapse imaging in zebrafish to investigate the role
85 Using in vivo
time-lapse imaging in zebrafish we found that, in the ab
86 Using in vivo
time-lapse imaging in zebrafish, we observed that prior
87 Using
time-lapse imaging in zebrafish, we show that perineuria
88 Using
time-lapse imaging in zebrafish, we show that various pa
89 Two-photon
time-lapse imaging indicated that microglia depletion re
90 Time-lapse imaging indicated that neither tail region is
91 Time-lapse imaging indicated that peripheral axon guidan
92 Furthermore, long-term
time-lapse imaging indicates that aggregates of mutant P
93 Time-lapse imaging is a fundamental tool for studying ce
94 Using
time lapse imaging,
it is possible to observe these even
95 More recently, in vivo
time-lapse imaging methods have been used to monitor acu
96 Using in vivo
time-lapse imaging methods, we discovered that in the la
97 Using
time-lapse imaging microscopy in nanowell grids (TIMING)
98 Asp/Ala330Leu/Ile332Glu (DLE), and developed
Time-lapse Imaging Microscopy in Nanowell Grids to analy
99 eneration with single-axon laser axotomy and
time-lapse imaging,
monitoring the initial changes in tr
100 Combined with
time lapse imaging of development in culture, we demonst
101 rons using dissociated cultures coupled with
time lapse imaging of fluorophore-fused HCN channels.
102 Time lapse imaging of rod formation shows abundant small
103 In vivo
time-lapse imaging of abGCs revealed that dendritic spin
104 We used
time-lapse imaging of adult dorsal root ganglion neurons
105 It further provides a novel tool for in vivo
time-lapse imaging of adult fish for non-cardiac studies
106 uorescence microscopy have made snapshot and
time-lapse imaging of bacterial cells commonplace, yet f
107 Furthermore, using
time-lapse imaging of beating hearts in conjunction with
108 Using 3D
time-lapse imaging of beating zebrafish hearts, we obser
109 rylatable (S39A) fascin variants followed by
time-lapse imaging of brain slices demonstrates that the
110 During
time-lapse imaging of C. elegans meiosis, the contractil
111 tern blots, confocal immunofluorescence, and
time-lapse imaging of Ca(2+) signals and of secretion of
112 Here, we show by
time-lapse imaging of cells expressing either green fluo
113 Time-lapse imaging of cells expressing FAK tagged with g
114 In vivo
time-lapse imaging of CF elimination revealed that (1) C
115 Cell tracking and
time-lapse imaging of chimeric drMM cultures indicated t
116 Cell labeling and in vivo
time-lapse imaging of CI cells reveal waves of migration
117 Time-lapse imaging of dark-grown Arabidopsis (Arabidopsi
118 We used high-resolution,
time-lapse imaging of dark-grown Arabidopsis seedlings t
119 g of pSIVA as well as for its application in
time-lapse imaging of degenerating neurons in culture; t
120 Recently, in vivo
time-lapse imaging of dendritic spines in the cerebral c
121 s based on data from fixed tissues, by using
time-lapse imaging of denervated dentate granule cells i
122 Time-lapse imaging of dissociated hippocampal neuronal c
123 blish a robust strategy for long-term (24 h)
time-lapse imaging of E6.5-8.5 mouse embryos with light-
124 Time-lapse imaging of EB1-GFP in polarized MDCK cells sh
125 With
time-lapse imaging of ECM micro-fiber morphology, the lo
126 Time-lapse imaging of ENCCs within the embryonic gut dem
127 Time-lapse imaging of fibroblasts from CMT4J patients de
128 Using
time-lapse imaging of fluorescence recovery after photob
129 Time-lapse imaging of fluorescent fusion proteins reveal
130 Time-lapse imaging of germ-line transformed Tie1-YFP rep
131 Time-lapse imaging of green fluorescent protein-tagged d
132 assemble in vivo, comparing our results with
time-lapse imaging of human endothelial-cell tube format
133 In line with these observations,
time-lapse imaging of identified spines formed after the
134 e fission yeast Schizosaccharomyces pombe by
time-lapse imaging of individual endocytic sites.
135 Time-lapse imaging of intact eggs argues that trigger wa
136 cilium; its lumenal space is rich in Ca(2+)
Time-lapse imaging of isolated hPSCs reveals that the ap
137 ion were examined in vivo and in vitro using
time-lapse imaging of isolated OPCs and acute brain slic
138 Immunofluorescence and
time-lapse imaging of Kupffer's vesicle morphogenesis in
139 Time-lapse imaging of labeled blastomeres shows that the
140 Time-lapse imaging of lac-operator-tagged chromosome reg
141 Time-lapse imaging of late-stage ERMS revealed that myf5
142 Using
time-lapse imaging of Lifeact-GFP-transfected chromaffin
143 Measurement of filopodium formation by
time-lapse imaging of live cells also revealed that depl
144 Time-lapse imaging of live cells shows that small aggreg
145 Using genetic mouse models combined with
time-lapse imaging of live neurons, we previously discov
146 Here we show, with high-resolution
time-lapse imaging of living mouse embryos, that mesoder
147 tudy their migration via immunohistology and
time-lapse imaging of living slice cultures.
148 at HySP enables unmixing of seven signals in
time-lapse imaging of living zebrafish embryos.
149 to biochemical compounds and high-resolution
time-lapse imaging of many animals on a single chip with
150 se imaging that permits prolonged label-free
time-lapse imaging of microglia in the presence of neuro
151 color, high-contrast, and high-dynamic-range
time-lapse imaging of migrating cells in complex three-d
152 Time-lapse imaging of multiple labels is challenging for
153 Time-lapse imaging of multipolar cells in the subventric
154 We used
time-lapse imaging of NCCs in the zebrafish hindbrain to
155 eet microscopy to perform three-dimensional,
time-lapse imaging of neutrophil-like HL-60 cells crawli
156 ate the performance of the PIC by performing
time-lapse imaging of planarian wound closure and sequen
157 tes the potential of SIM for superresolution
time-lapse imaging of plant cells, showing unprecedented
158 in vivo two-photon microscopy, we performed
time-lapse imaging of radial glial cells and measured fi
159 Using two-photon glutamate uncaging and
time-lapse imaging of rat hippocampal CA1 neurons, we sh
160 Here, using quantitative single-cell
time-lapse imaging of Saccharomyces cerevisiae, we show
161 ge N") and long-term operations ("large T"),
time-lapse imaging of shear-wave velocity (V S ) structu
162 We performed
time-lapse imaging of single QDs bound to AMPA receptors
163 Time-lapse imaging of static liquid cultures demonstrate
164 Time-lapse imaging of synaptic vesicle protein transport
165 Using in vivo
time-lapse imaging of tectal neuron structure and visual
166 Time-lapse imaging of the axonal transport of chimeric f
167 Time-lapse imaging of the beta2 adrenergic receptor expr
168 Here, we use
time-lapse imaging of the developing zebrafish to show t
169 We developed a novel method for
time-lapse imaging of the rapid dynamics of miRNA activi
170 Ultrasensitive three-dimensional confocal
time-lapse imaging of the temperature-sensitive membrane
171 We performed
time-lapse imaging of thousands of neurons over weeks in
172 Using
time-lapse imaging of tissue explants in culture, fluore
173 Time-lapse imaging of transgenic embryos demonstrated th
174 Using two-photon
time-lapse imaging of transgenic zebrafish, we trace the
175 vitro neurite outgrowth assays together with
time-lapse imaging of whole embryonic cochleae.
176 These findings were supported by
time-lapse imaging of WT and syntaphilin-deficient axons
177 Using
time-lapse imaging of WT melanocyte/keratinocyte cocultu
178 By combining in vivo
time-lapse imaging of Xenopus tectal neurons with electr
179 Time-lapse imaging of yellow fluorescent protein:ATK5 re
180 l manipulation, gene expression analysis and
time-lapse imaging of zebrafish embryos.
181 Time-lapse imaging of zebrafish larvae at 5-7 days after
182 Using in vivo
time-lapse imaging of zebrafish retinas, we show that RI
183 Time-lapsed imaging of GFP-laced rodlets in human cells
184 d and the consequences followed with in vivo
time-lapse imaging or immunostaining assays.
185 he different topographies, using fluorescent
time-lapse imaging over 21 days.
186 The ability to perform extended
time-lapse imaging over 3D volumes in living retina usin
187 Time-lapse imaging over 4 weeks revealed a pronounced, c
188 Time-lapse imaging over hours or days revealed that asce
189 With
time-lapse imaging,
polymerized MreB [filamentous MreB (
190 Time-lapse imaging provides new details and important in
191 Our
time-lapse imaging quantifies membrane fluctuations at t
192 Traction force microscopy and
time-lapse imaging reveal that closure of gaps begins wi
193 Time-lapse imaging revealed dynamic changes in the metab
194 Time-lapse imaging revealed mitotic failure before chrom
195 In vivo
time-lapse imaging revealed that a typical migrating NC
196 Time-lapse imaging revealed that ast and slit1a morphant
197 Live-cell
time-lapse imaging revealed that BI2536-treated giant LN
198 Time-lapse imaging revealed that branching is highly dyn
199 Time-lapse imaging revealed that calcium transients in a
200 Long term
time-lapse imaging revealed that cofilin rods block intr
201 Time-lapse imaging revealed that cranial NCCs were attra
202 Live,
time-lapse imaging revealed that CRH reduced spine densi
203 Time-lapse imaging revealed that early exposure to eleva
204 Live-cell
time-lapse imaging revealed that exogenous fluorescently
205 Time-lapse imaging revealed that JNK-inhibited cortical
206 Indeed,
time-lapse imaging revealed that JosD1 enhances membrane
207 Time-lapse imaging revealed that knockdown of miR-219 fu
208 For example,
time-lapse imaging revealed that MEC-3 (LIM homeodomain)
209 Time-lapse imaging revealed that MSCs recruited MRL.Fas(
210 Time-lapse imaging revealed that NG2(+) cells in the cor
211 Time-lapse imaging revealed that NL dendrites respond to
212 Time-lapse imaging revealed that pre-existing clusters o
213 Moreover, in vivo
time-lapse imaging revealed that thiabendazole reversibl
214 Time-lapse imaging revealed that this was caused by a re
215 Two-photon
time-lapse imaging revealed that thymocyte death and pha
216 Time-lapse imaging revealed the direct differentiation o
217 Finally,
time lapse imaging reveals that synaptic AChEs and AChRs
218 Time-lapse imaging reveals a gradient of conformational
219 Time-lapse imaging reveals how only orbiting mode cells
220 Time-lapse imaging reveals rapid pulsatile level changes
221 Time-lapse imaging reveals that alpha-actinin-1 puncta w
222 Time-lapse imaging reveals that branching events are syn
223 Time-lapse imaging reveals that mitochondria are anchore
224 Time-lapse imaging reveals that SAC proteins are in dist
225 In vivo
time-lapse imaging reveals that Sema3D or L1 knockdown c
226 High-resolution
time-lapse imaging reveals the dynamic phases of precurs
227 Time-lapse imaging reveals two sequential waves of migra
228 Time-lapse imaging showed dramatic and controlled moveme
229 Time-lapse imaging showed IH scanning plant cell walls b
230 Time-lapse imaging showed that hepatic-specified endoder
231 different colors of streptavidin followed by
time-lapse imaging showed that synaptic AChEs are nearly
232 Time-lapse imaging shows dynamic formation and eliminati
233 Time-lapse imaging shows that iNSCs are tumouritropic, h
234 Time-lapse imaging shows that neuropilin-1 siRNA transfe
235 ET receptor activation, whereas multiphoton
time-lapse imaging shows that selective ET receptor anta
236 Furthermore, in vivo
time-lapse imaging shows that Sox2-expressing neural pro
237 Time-lapse imaging shows that the mutations act by facil
238 In this paper, we use
time-lapse imaging,
single-cell analysis, and embryo sta
239 Time lapse imaging studies indicated that spirohexenolid
240 uorescence recovery after photobleaching and
time-lapse imaging studies provide evidence for a direct
241 Time-lapse imaging studies show that both Sema3d and Sem
242 Time-lapse imaging studies show that the neural crest an
243 Instead,
time-lapse imaging studies suggest a prominent role for
244 Furthermore,
time-lapse imaging suggests that cytokinesis acts as an
245 Time-lapse imaging suggests that tension on cell-cell ju
246 -clamp recordings, immunohistochemistry, and
time-lapse imaging techniques revealed that rMS induces
247 wth cone on low laminin plus aggrecan during
time-lapse imaging than did cortical neurons.
248 We discovered by in vivo
time-lapse imaging that retinal ganglion cell (RGC) dend
249 Confocal laser
time-lapse imaging through a cranial window showed that
250 tissue transplantation and in vivo confocal
time-lapse imaging to analyze changes in chick cranial n
251 ncy and used fluorescent protein fusions and
time-lapse imaging to assess the roles of P41 and P24 in
252 Here, we use non-invasive
time-lapse imaging to continuously examine hPSC maintena
253 Using
time-lapse imaging to correlate mitotic behavior with ce
254 Here we combined neurite-tracing and
time-lapse imaging to define the events that lead to the
255 We use
time-lapse imaging to demonstrate that Laminin acting di
256 l crest EMT, we performed live cell confocal
time-lapse imaging to determine the sequence of cellular
257 e use structured illumination microscopy and
time-lapse imaging to dissect the behavior of ESCRTs dur
258 In this study, we used high-resolution,
time-lapse imaging to examine the long-term effects of e
259 n of single-cell gene expression mapping and
time-lapse imaging to identify individual MPs, their loc
260 In this study, we used
time-lapse imaging to investigate the relationship betwe
261 e of Cell, Fisher et al. use high-resolution
time-lapse imaging to peer into bacterial genome (nucleo
262 We used two-photon
time-lapse imaging to reveal a high level of filopodia f
263 beled cells of different Carm1 levels, using
time-lapse imaging to reveal dynamics of their behavior,
264 ial killing, and performed low magnification
time-lapse imaging to reveal time-dependent statistics o
265 We used
time-lapse imaging to show that dendrites fail to withdr
266 croscopy, optogenetic activation and in vivo
time-lapse imaging to show that newly generated OSNs for
267 re, we use two-photon glutamate uncaging and
time-lapse imaging to show that non-ionotropic NMDAR sig
268 We use chromosomal inversions and in vivo
time-lapse imaging to show that parS is the Caulobacter
269 erial reconstruction electron microscopy and
time-lapse imaging to show that plasma membrane for such
270 We combined single-cell laser axotomy with
time-lapse imaging to study the dynamics of phosphatidyl
271 reverse genetics and multivariate long-term
time-lapse imaging to test current cell shape control mo
272 Here we used high-resolution,
time-lapse imaging to trace the reprogramming process ov
273 Here, we use
time-lapse imaging to track radial glia progenitor behav
274 l assessments of cellular rearrangements and
time-lapse imaging to visualize cochlear remodeling in m
275 kers (MADM), combined with organ culture and
time-lapse imaging,
to trace the movements and divisions
276 Time-lapse imaging using a Forster resonance energy tran
277 Time-lapse imaging using a probe to measure neuronal cel
278 ere counted and measured in fixed cells, and
time-lapse imaging was used to assess cell motility and
279 Time-lapse imaging was used to assess T-cell motility.
280 characterized cell-cycle delay identified by
time-lapse imaging,
was used to clarify the relationship
281 By utilizing
time-lapse imaging we show that cranial vessels originat
282 assays (Boyden chambers, explants, and video
time-lapse imaging),
we demonstrate that CNTF controls t
283 Using
time-lapse imaging,
we demonstrated that rapsyn is remar
284 Using
time-lapse imaging,
we examined the dynamic behaviors of
285 Using simultaneous
time-lapse imaging,
we find that early endosome-associat
286 Using
time-lapse imaging,
we find that mesenchymal cell conden
287 ng a combination of focal dye injections and
time-lapse imaging,
we find that neural crest and dorsal
288 Using
time-lapse imaging,
we found that sensory dendrites form
289 Using
time-lapse imaging,
we found that, as motor neurons diff
290 nduced activation of single EYFP fusions and
time-lapse imaging,
we obtained sub-40 nm resolution ima
291 Using
time-lapse imaging,
we show that cell-cell contact trigg
292 emporal matrix maps with in vitro functional
time-lapse imaging,
we show that key components of this
293 genetics, interspecific gene transfers, and
time-lapse imaging,
we show that leaflet development req
294 Using sparse-labeling and
time-lapse imaging,
we visualized for the first time the
295 tips of the invading cords were revealed by
time-lapse imaging,
which showed cells actively extendin
296 Using long-term
time-lapse imaging with intact Drosophila larvae, we fou
297 Here we combine non-invasive
time-lapse imaging with karyotypic reconstruction of all
298 Extended
time-lapse imaging with less than one virion per cell al
299 ses simultaneously using combined two photon
time-lapse imaging with patch-clamp recording in acute h
300 We used in vivo
time-lapse imaging with two-photon microscopy through cr