戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1              NCC migration was studied using time-lapse imaging.
2  question using single-molecule tracking and time-lapse imaging.
3 n capacity was assessed by scratch assays in time-lapse imaging.
4 nd then monitored spine survival rates using time-lapse imaging.
5  slice culture using two-photon and confocal time-lapse imaging.
6 lants in heterogeneous environments using 3D time-lapse imaging.
7 to low- and high-efficiency transfection and time-lapse imaging.
8 on and wound closure were investigated using time-lapse imaging.
9 matrix (ECM) protein surfaces was studied by time-lapse imaging.
10 with KIF5B along axons revealed by two-color time-lapse imaging.
11                Dye uptake was measured using time-lapse imaging.
12 calcium signaling throughout RV infection by time-lapse imaging.
13  spots, turning on and off, are confirmed by time-lapse imaging.
14 e utility of the method in vivo in mice with time-lapse imaging.
15 e study their mobility characteristics using time-lapse imaging.
16 -tracing and transcriptomics approaches with time-lapse imaging.
17 within an intact microvascular network using time-lapse imaging.
18                                        Using time-lapse imaging accompanied by immunostaining and mol
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                                              Time-lapse imaging and analysis of reporter transgenics
22 ring controls axon remodeling, using in vivo time-lapse imaging and electrophysiological analysis of
23                                              Time-lapse imaging and fate mapping demonstrate that the
24 and in response to DNA damage using confocal time-lapse imaging and fluorescence cross-correlation sp
25                                              Time-lapse imaging and genetic cell-lineage tracing were
26                         Here, we use in vivo time-lapse imaging and genetic manipulation in Drosophil
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 successful application of reporter lines for time-lapse imaging and mouse transplantation experiments
32                                              Time-lapse imaging and mutagenesis studies further estab
33                                              Time-lapse imaging and quantitative analysis of axon dyn
34                                              Time-lapse imaging and scanning electron microscopy reve
35                                 Here, we use time-lapse imaging and single cell RNA-seq to measure ac
36 ng the archaeal cells to enable quantitative time-lapse imaging and single-cell analysis, which would
37                         The software enabled time-lapse imaging and the use of temporally varying cha
38  both isovariants was observed directly with time-lapse imaging and total internal reflection fluores
39 gle dimension, facilitating high-resolution, time-lapse imaging and tracking of individual cells.
40                                 Here, we use time-lapse imaging and transgenesis in zebrafish to visu
41 lted in cleavage-stage arrest as assessed by time-lapse imaging and was associated with aneuploidy ge
42                                        Using time-lapsed imaging and statistical tools, we show that
43                     Through a combination of time-lapse imaging, and chemical and mechanical perturba
44 we present a high-content framework in which time-lapse imaging, and single-particle-tracking algorit
45                     Using a microchip-based, time-lapse imaging approach allowing the entire contact
46 ich timescales are most accessible using the time-lapse imaging approach and explore uncertainties in
47           This study used a novel, prolonged time-lapse imaging approach to continuously track the be
48                                      Using a time-lapse imaging assay, we found that developing amacr
49                                              Time-lapse imaging assays also revealed the essential ro
50            Subsequent FRET-based single cell time-lapse imaging at conditions where transcription dep
51                                              Time-lapse imaging at subcellular resolution shows that
52 er time, and we combined it with deep-tissue time-lapse imaging based on fast two-photon microscopy t
53 nship between synthesis and hydrolysis using time-lapse imaging, biophysical measurements of cell-wal
54                                           In time-lapse imaging, blocking the tPA function promotes e
55         Using a complementary combination of time-lapse imaging by fluorescence confocal microscopy a
56      Results indicate that use of continuous time-lapse imaging can distinguish cellular heterogeneit
57 ddress this problem through a combination of time-lapse imaging, clonal analysis, and computational m
58  single-cell resolution from high-throughput time-lapse imaging data, especially, the interactions be
59             Here we introduce cellular-level time-lapse imaging deep within the live mammalian brain
60                                      In vivo time-lapse imaging demonstrated that local TH first incr
61                                              Time-lapse imaging demonstrated that SEC3a and SEC8 were
62                                              Time-lapse imaging depicts a dynamic picture in which ex
63                                              Time-lapse imaging ends within 12 h, with subsequent tra
64                                              Time-lapse imaging experiments of TCs exhibited pause an
65                               In single cell time-lapse imaging experiments, VHA(B) -eGFP localizatio
66                                Using in vivo time-lapse imaging, fluorescence recovery after photoble
67                                              Time-lapse imaging further reveals that Fgf8a acts as a
68 tion of approaches, including FACS analysis, time-lapse imaging, immunofluorescence microscopy, and c
69            Using a rat primary neuron model, time-lapse imaging, immunohistochemistry, and confocal m
70 induced pluripotent stem cells (iPSCs) using time-lapse imaging, immunostaining, and single-cell RNA
71                  Despite the introduction of time-lapse imaging improvements in IVF success rates hav
72 n vivo after transplantation and 3D confocal time-lapse imaging in a living chick embryo.
73 itu genotyping of a library of strains after time-lapse imaging in a microfluidic device overcomes th
74 lly delivered fluorescent probes and in vivo time-lapse imaging in a mouse model of demyelination to
75                                   Through 3D time-lapse imaging in a secreting organ, we show that F-
76                                     Confocal time-lapse imaging in acute slices reveals that groups o
77                                        Using time-lapse imaging in an obstetrical brachial plexus inj
78          Here we address this question using time-lapse imaging in hippocampal neurons.
79 -photon and two-photon microscopy, including time-lapse imaging in light-sheet systems.
80 cal and cell biological assays combined with time-lapse imaging in live snph wild-type and mutant neu
81                                        Using time-lapse imaging in primary mouse neurons, we found th
82 e tested here this hypothesis using confocal time-lapse imaging in rat hippocampal organotypic slices
83                                              Time-lapse imaging in the intact zebrafish embryo with t
84                                              Time-lapse imaging in vivo revealed that exercise partia
85 eneration dynamics in these animals requires time-lapse imaging in vivo, which has been difficult to
86                                              Time-lapse imaging in zebrafish shows that EphB-Pak2a si
87 al contributions, we use lineage tracing and time-lapse imaging in zebrafish to identify an endoderma
88  we use laser nerve transection and in vivo, time-lapse imaging in zebrafish to investigate the role
89                                Using in vivo time-lapse imaging in zebrafish we found that, in the ab
90                                Using in vivo time-lapse imaging in zebrafish, we observed that prior
91  into the dorsal root entry zone (DREZ) with time-lapse imaging in zebrafish.
92                                   Two-photon time-lapse imaging indicated that microglia depletion re
93                                              Time-lapse imaging indicated that neither tail region is
94                                              Time-lapse imaging indicated that peripheral axon guidan
95                       Furthermore, long-term time-lapse imaging indicates that aggregates of mutant P
96                                              Time-lapse imaging is a fundamental tool for studying ce
97                                        Using time lapse imaging, it is possible to observe these even
98  cell-cell interactions from high-throughput time-lapse imaging microscopy data of cells in nanowell
99                                        Using time-lapse imaging microscopy in nanowell grids (TIMING)
100 Asp/Ala330Leu/Ile332Glu (DLE), and developed Time-lapse Imaging Microscopy in Nanowell Grids to analy
101 eneration with single-axon laser axotomy and time-lapse imaging, monitoring the initial changes in tr
102                                Combined with time lapse imaging of development in culture, we demonst
103 rons using dissociated cultures coupled with time lapse imaging of fluorophore-fused HCN channels.
104 llumination Microscopy (SPIM) revolutionized time lapse imaging of live cells and organisms due to it
105                                              Time lapse imaging of rod formation shows abundant small
106 trate that 1) rapid, quantitative 3D and 4D (time lapse) imaging of cellular and subcellular processe
107                                      In vivo time-lapse imaging of abGCs revealed that dendritic spin
108 It further provides a novel tool for in vivo time-lapse imaging of adult fish for non-cardiac studies
109              This allows P-IID to be used in time-lapse imaging of apoptosis using confocal laser sca
110                                              Time-lapse imaging of autophagosomes and ATP/ADP levels
111 uorescence microscopy have made snapshot and time-lapse imaging of bacterial cells commonplace, yet f
112                                              Time-lapse imaging of BAX recruitment and mitochondrial
113                           Furthermore, using time-lapse imaging of beating hearts in conjunction with
114                                     Using 3D time-lapse imaging of beating zebrafish hearts, we obser
115 rylatable (S39A) fascin variants followed by time-lapse imaging of brain slices demonstrates that the
116                                       During time-lapse imaging of C. elegans meiosis, the contractil
117 e performed long-term, non-invasive, in vivo time-lapse imaging of c1vpda embryonic and larval morpho
118 tern blots, confocal immunofluorescence, and time-lapse imaging of Ca(2+) signals and of secretion of
119  strategy for in vivo longitudinal and rapid time-lapse imaging of CC presynaptic terminal developmen
120                                              Time-lapse imaging of cells expressing FAK tagged with g
121                                              Time-lapse imaging of cells expressing the K1646R mutant
122                                      In vivo time-lapse imaging of CF elimination revealed that (1) C
123                            Cell tracking and time-lapse imaging of chimeric drMM cultures indicated t
124 esolution microscopy, photostable cQDs allow time-lapse imaging of chromatin and nucleoli during cell
125                    Cell labeling and in vivo time-lapse imaging of CI cells reveal waves of migration
126                                              Time-lapse imaging of dark-grown Arabidopsis (Arabidopsi
127                     We used high-resolution, time-lapse imaging of dark-grown Arabidopsis seedlings t
128 g of pSIVA as well as for its application in time-lapse imaging of degenerating neurons in culture; t
129                            Recently, in vivo time-lapse imaging of dendritic spines in the cerebral c
130 s based on data from fixed tissues, by using time-lapse imaging of denervated dentate granule cells i
131                                              Time-lapse imaging of dissociated hippocampal neuronal c
132                       We carried out in vivo time-lapse imaging of Drosophila adult sensory neuron di
133 blish a robust strategy for long-term (24 h) time-lapse imaging of E6.5-8.5 mouse embryos with light-
134                                         With time-lapse imaging of ECM micro-fiber morphology, the lo
135                                              Time-lapse imaging of ENCCs within the embryonic gut dem
136                                        Using time-lapse imaging of fluorescence recovery after photob
137  nascent synapses, we performed simultaneous time-lapse imaging of fluorescently-tagged ribbons in re
138                We used confocal fluorescence time-lapse imaging of FOXO1-GFP in adult isolated living
139                                              Time-lapse imaging of germ-line transformed Tie1-YFP rep
140                                 Furthermore, time-lapse imaging of herpes simplex virus 1 infected ep
141             In line with these observations, time-lapse imaging of identified spines formed after the
142 e fission yeast Schizosaccharomyces pombe by time-lapse imaging of individual endocytic sites.
143                                 We performed time-lapse imaging of individual ipsilaterally projectin
144                                              Time-lapse imaging of intact eggs argues that trigger wa
145  cilium; its lumenal space is rich in Ca(2+) Time-lapse imaging of isolated hPSCs reveals that the ap
146                       Immunofluorescence and time-lapse imaging of Kupffer's vesicle morphogenesis in
147                                              Time-lapse imaging of lac-operator-tagged chromosome reg
148                                              Time-lapse imaging of late-stage ERMS revealed that myf5
149                                        Using time-lapse imaging of Lifeact-GFP-transfected chromaffin
150  spin-down, and turbidity assays, as well as time-lapse imaging of liquid droplet formation.
151       Measurement of filopodium formation by time-lapse imaging of live cells also revealed that depl
152     Using genetic mouse models combined with time-lapse imaging of live neurons, we previously discov
153           Here we show, with high-resolution time-lapse imaging of living mouse embryos, that mesoder
154 tudy their migration via immunohistology and time-lapse imaging of living slice cultures.
155 at HySP enables unmixing of seven signals in time-lapse imaging of living zebrafish embryos.
156 se imaging that permits prolonged label-free time-lapse imaging of microglia in the presence of neuro
157 color, high-contrast, and high-dynamic-range time-lapse imaging of migrating cells in complex three-d
158                                              Time-lapse imaging of multiple labels is challenging for
159                                              Time-lapse imaging of multipolar cells in the subventric
160 eet microscopy to perform three-dimensional, time-lapse imaging of neutrophil-like HL-60 cells crawli
161 ate the performance of the PIC by performing time-lapse imaging of planarian wound closure and sequen
162 tes the potential of SIM for superresolution time-lapse imaging of plant cells, showing unprecedented
163 e show live alveologenesis, using long-term, time-lapse imaging of precision-cut lung slices.
164                                   Using live time-lapse imaging of primary resected tumors, we discov
165  in vivo two-photon microscopy, we performed time-lapse imaging of radial glial cells and measured fi
166      Using two-photon glutamate uncaging and time-lapse imaging of rat hippocampal CA1 neurons, we sh
167         Here, using quantitative single-cell time-lapse imaging of Saccharomyces cerevisiae, we show
168 ge N") and long-term operations ("large T"), time-lapse imaging of shear-wave velocity (V S ) structu
169                       Indeed, using 2-photon time-lapse imaging of SP-transgenic granule cells in mou
170                                              Time-lapse imaging of static liquid cultures demonstrate
171                                Using in vivo time-lapse imaging of tectal neuron structure and visual
172                                              Time-lapse imaging of the axonal transport of chimeric f
173               Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely cha
174 d human corneal epithelial cell sheets using time-lapse imaging of the cell culture process every 20
175                                 Here, we use time-lapse imaging of the developing zebrafish to show t
176                                 We performed time-lapse imaging of the mitochondrial inner membrane o
177              We developed a novel method for time-lapse imaging of the rapid dynamics of miRNA activi
178                                           3D time-lapse imaging of this biosensor in embryos revealed
179                                 We performed time-lapse imaging of thousands of neurons over weeks in
180                                              Time-lapse imaging of transgenic embryos demonstrated th
181 vitro neurite outgrowth assays together with time-lapse imaging of whole embryonic cochleae.
182 As a case study, we present super-resolution time-lapse imaging of wild-type Bacillus subtilis spores
183             These findings were supported by time-lapse imaging of WT and syntaphilin-deficient axons
184                                        Using time-lapse imaging of WT melanocyte/keratinocyte cocultu
185                         By combining in vivo time-lapse imaging of Xenopus tectal neurons with electr
186 l manipulation, gene expression analysis and time-lapse imaging of zebrafish embryos.
187                                              Time-lapse imaging of zebrafish larvae at 5-7 days after
188                                Using in vivo time-lapse imaging of zebrafish retinas, we show that RI
189                                              Time-lapsed imaging of GFP-laced rodlets in human cells
190                         Here, we used 3D and time lapse imaging on young leaves at different stages o
191                                      Through time-lapse imaging, optical highlighting, and combined g
192 d and the consequences followed with in vivo time-lapse imaging or immunostaining assays.
193 he different topographies, using fluorescent time-lapse imaging over 21 days.
194                                              Time-lapse imaging over 4 weeks revealed a pronounced, c
195  applications, including cellular isolation, time-lapse imaging, protocol optimization, and lineage-t
196                                              Time-lapse imaging provides new details and important in
197                                          Our time-lapse imaging quantifies membrane fluctuations at t
198                Traction force microscopy and time-lapse imaging reveal that closure of gaps begins wi
199                                              Time-lapse imaging revealed disruption of the initial st
200                                              Time-lapse imaging revealed dynamic changes in the metab
201                                      In vivo time-lapse imaging revealed that a typical migrating NC
202                                    Live-cell time-lapse imaging revealed that BI2536-treated giant LN
203                                              Time-lapse imaging revealed that branching is highly dyn
204                                              Time-lapse imaging revealed that calcium transients in a
205                                    Long term time-lapse imaging revealed that cofilin rods block intr
206                                              Time-lapse imaging revealed that cranial NCCs were attra
207                                              Time-lapse imaging revealed that early exposure to eleva
208                                              Time-lapse imaging revealed that JNK-inhibited cortical
209                                      Indeed, time-lapse imaging revealed that JosD1 enhances membrane
210                                              Time-lapse imaging revealed that knockdown of miR-219 fu
211                                      In vivo time-lapse imaging revealed that LT-HSCs at steady-state
212                                 For example, time-lapse imaging revealed that MEC-3 (LIM homeodomain)
213                                              Time-lapse imaging revealed that MSCs recruited MRL.Fas(
214                                              Time-lapse imaging revealed that NG2(+) cells in the cor
215                                              Time-lapse imaging revealed that NL dendrites respond to
216                            Moreover, in vivo time-lapse imaging revealed that thiabendazole reversibl
217                                              Time-lapse imaging revealed that this was caused by a re
218                                   Two-photon time-lapse imaging revealed that thymocyte death and pha
219                                              Time-lapse imaging revealed the direct differentiation o
220                                              Time-lapse imaging reveals a nuanced role for p21 in can
221                                              Time-lapse imaging reveals how only orbiting mode cells
222                                              Time-lapse imaging reveals rapid pulsatile level changes
223                                              Time-lapse imaging reveals that alpha-actinin-1 puncta w
224                                              Time-lapse imaging reveals that branching events are syn
225                                              Time-lapse imaging reveals that mitochondria are anchore
226                                              Time-lapse imaging reveals that SAC proteins are in dist
227                                              Time-lapse imaging reveals that the distinct myelinating
228                              High-resolution time-lapse imaging reveals the dynamic phases of precurs
229                                              Time-lapse imaging reveals two sequential waves of migra
230 lysis of cellular dynamics from high-content time-lapse imaging screens with little prior knowledge a
231 cells appeared to be partially inhibited and time-lapse imaging showed a possible role for host macro
232                                              Time-lapse imaging showed that hepatic-specified endoder
233                                              Time-lapse imaging shows dynamic formation and eliminati
234                                              Time-lapse imaging shows that iNSCs are tumouritropic, h
235                                              Time-lapse imaging shows that non-motile bacteria 'hitch
236  ET receptor activation, whereas multiphoton time-lapse imaging shows that selective ET receptor anta
237                         Furthermore, in vivo time-lapse imaging shows that Sox2-expressing neural pro
238                                              Time-lapse imaging shows that the mutations act by facil
239                        In this paper, we use time-lapse imaging, single-cell analysis, and embryo sta
240                                              Time lapse imaging studies indicated that spirohexenolid
241 ens up exciting new opportunities for direct time-lapse imaging studies over a 24-hour time course, t
242 uorescence recovery after photobleaching and time-lapse imaging studies provide evidence for a direct
243                                              Time-lapse imaging studies show that both Sema3d and Sem
244                                              Time-lapse imaging studies show that the neural crest an
245                                     Instead, time-lapse imaging studies suggest a prominent role for
246                                 Furthermore, time-lapse imaging suggests that cytokinesis acts as an
247 l microscopic assessment or more recently by time-lapse imaging systems.
248 -clamp recordings, immunohistochemistry, and time-lapse imaging techniques revealed that rMS induces
249 wth cone on low laminin plus aggrecan during time-lapse imaging than did cortical neurons.
250                    Here, we use non-invasive time-lapse imaging to continuously examine hPSC maintena
251                                        Using time-lapse imaging to correlate mitotic behavior with ce
252         Here we combined neurite-tracing and time-lapse imaging to define the events that lead to the
253                                       We use time-lapse imaging to demonstrate that Laminin acting di
254 e use structured illumination microscopy and time-lapse imaging to dissect the behavior of ESCRTs dur
255                                        Using time-lapse imaging to follow divisions and fates of basa
256            We show that DeSOS can be used in time-lapse imaging to generate super-resolution movies i
257                       In this study, we used time-lapse imaging to investigate the relationship betwe
258           We use quantitative microscopy and time-lapse imaging to observe pulses in the activity of
259 e of Cell, Fisher et al. use high-resolution time-lapse imaging to peer into bacterial genome (nucleo
260                           We used two-photon time-lapse imaging to reveal a high level of filopodia f
261 beled cells of different Carm1 levels, using time-lapse imaging to reveal dynamics of their behavior,
262  murine lung-on-chip infection model and use time-lapse imaging to reveal the dynamics of host-Mycoba
263 ial killing, and performed low magnification time-lapse imaging to reveal time-dependent statistics o
264                                      We used time-lapse imaging to show that dendrites fail to withdr
265 croscopy, optogenetic activation and in vivo time-lapse imaging to show that newly generated OSNs for
266 re, we use two-photon glutamate uncaging and time-lapse imaging to show that non-ionotropic NMDAR sig
267   We combined single-cell laser axotomy with time-lapse imaging to study the dynamics of phosphatidyl
268  reverse genetics and multivariate long-term time-lapse imaging to test current cell shape control mo
269                Here we used high-resolution, time-lapse imaging to trace the reprogramming process ov
270                                 Here, we use time-lapse imaging to track radial glia progenitor behav
271 l assessments of cellular rearrangements and time-lapse imaging to visualize cochlear remodeling in m
272 roduce SIFT, single-cell isolation following time-lapse imaging, to address these limitations.
273 kers (MADM), combined with organ culture and time-lapse imaging, to trace the movements and divisions
274                                              Time-lapse imaging using a Forster resonance energy tran
275                                              Time-lapse imaging using a probe to measure neuronal cel
276 ere counted and measured in fixed cells, and time-lapse imaging was used to assess cell motility and
277                                              Time-lapse imaging was used to assess T-cell motility.
278                                              Time-lapse imaging was used to evaluate mechanisms of ce
279 characterized cell-cycle delay identified by time-lapse imaging, was used to clarify the relationship
280                                 By utilizing time-lapse imaging we show that cranial vessels originat
281 assays (Boyden chambers, explants, and video time-lapse imaging), we demonstrate that CNTF controls t
282                                        Using time-lapse imaging, we demonstrated that rapsyn is remar
283                                        Using time-lapse imaging, we examined the dynamic behaviors of
284                           Using simultaneous time-lapse imaging, we find that early endosome-associat
285                                        Using time-lapse imaging, we find that mesenchymal cell conden
286 ng a combination of focal dye injections and time-lapse imaging, we find that neural crest and dorsal
287                                        Using time-lapse imaging, we found that sensory dendrites form
288                 Using three-dimensional (3D) time-lapse imaging, we found that stomatal pore formatio
289                                        Using time-lapse imaging, we found that, as motor neurons diff
290 emporal matrix maps with in vitro functional time-lapse imaging, we show that key components of this
291  genetics, interspecific gene transfers, and time-lapse imaging, we show that leaflet development req
292                    Using sparse-labeling and time-lapse imaging, we visualized for the first time the
293  tips of the invading cords were revealed by time-lapse imaging, which showed cells actively extendin
294  over 28 days and processed for quantitative time-lapse imaging with dynamic histomorphometry.
295                                 By combining time-lapse imaging with genetics, we here identify the l
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                                 By combining time-lapse imaging with scDNA-seq, we determined that mu
300                              We used in vivo time-lapse imaging with two-photon microscopy through cr

 
Page Top