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1 scale data from two approaches: genomics and live imaging.
2  during zebrafish optic cup morphogenesis by live imaging.
3 ion of native PER2 protein (PER2::VENUS) for live imaging.
4 calization of AIS Kv7.2/7.3 heteromers using live imaging.
5 ological assessment and for ICC-SC homing by live imaging.
6 s and whole cell in keratinocytes studied by live imaging.
7 ts and a decrease in fusions, as revealed by live imaging.
8 erstanding of cytoskeletal dynamics requires live imaging.
9 actin (F-actin) structures by both fixed and live imaging.
10 lop in utero, have presented a challenge for live imaging.
11 termined by single-molecule FISH (smFISH) or live imaging.
12                        We demonstrate the 3D live imaging ability of TLS-SPIM by imaging cellular and
13 nd confocal microscopy as well as time lapse live imaging after injection of mRNA encoding fusion pro
14                                              Live imaging after treatment with transgene-encoded or c
15                         Although advances in live imaging allow us to directly visualize this process
16              The combination of genetics and live imaging allows us to describe and understand the ti
17                                              Live imaging also reveals that intrinsic asymmetry in EG
18                                 Quantitative live imaging analyses show that the amnion initiates EE
19                      Immunoprecipitation and live imaging analysis demonstrated that AP2 and PICALM c
20 associated with NE disassembly, we performed live-imaging analysis of control and VRK1-depleted cells
21                                        Using live-imaging analysis, we show that growth is dynamicall
22   The accessibility of this system to direct live imaging and biochemical analysis makes it ideal for
23                                        Using live imaging and biochemical approaches we show that TTC
24                                 Quantitative live imaging and biophysical approaches reveal that both
25  available to the Drosophila geneticist with live imaging and biophysical techniques.
26                                              Live imaging and clonal analyses revealed a temporal bia
27                                     In vitro live imaging and colocalization experiments revealed tha
28 et model of H1N1pdm virus infection, we used live imaging and comprehensive histological analyses to
29 hod would allow functional studies involving live imaging and electrophysiology from juvenile and adu
30                                  Here we use live imaging and ex vivo culture to report a dual role o
31                              High-resolution live imaging and functional analyses revealed that endod
32                                 Here, we use live imaging and genetic manipulations to determine how
33                                      Through live imaging and genetic mosaics to dissect interactions
34                       Using a combination of live imaging and gradients of activators/inhibitors in t
35 1(+) mesothelial cell entry into the lung by live imaging and identified their progenies in subpopula
36             Here, we prove this concept with live imaging and immunolocalization of two dual, N- and
37                      Using three-dimensional live imaging and in vivo clonal analysis, we reveal the
38                                        Thus, live imaging and lineage tracing enabled us to clarify p
39                                 Quantitative live imaging and mathematical modeling allow us to corre
40                               In this study, live imaging and paired patch clamp recording at the zeb
41 iated endocytosis was visualized using a new live imaging and particle tracking method.
42 well as the fine ER distribution in rhd3 Our live imaging and pharmacologic modification of root hair
43                                        Using live imaging and pharmacological modulation of the MT cy
44 (2014) combine loss-of-function experiments, live imaging and proteomics to unveil the physiological
45                                       We use live imaging and pulse labeling to quantitatively determ
46                                 By combining live imaging and quantitative image analysis, we track t
47                                Here, we used live imaging and quantitative, 4D image analysis to meas
48                       Utilizing non-invasive live imaging and selectively induced apoptosis, we repor
49                                           By live imaging and semiquantitative fluorescent in situ hy
50                                 Importantly, live imaging and sequence analysis of repair products re
51  in mammalian tissues, but opportunities for live imaging and the genetic tractability of Drosophila
52                                        Using live imaging and three-dimensional image reconstruction,
53                                              Live imaging and transcriptome analysis of lung-branchin
54                                              Live imaging and transfection assays for Arc overexpress
55                  Using immunohistochemistry, live imaging and transmission electron microscopy, we de
56                                        Using live imaging and transplantation in zebrafish embryos, w
57                               Combination of live-imaging and live-manipulation of developing embryos
58                 Here we utilize quantitative live-imaging and mathematical modelling to outline the r
59                                        Using live-imaging and perturbation experiments we show that l
60 abnormal polarization toward endothelium via live-imaging and wound-healing studies, we screened PAH
61 ysis using Wnt-coated microbeads (12-18 h of live imaging) and to create a Wnt platform on a glass su
62        From a series of biochemical studies, live imaging, and analyses of mutant proteins, we propos
63 ate regulatory consequence, we established a live imaging approach that enabled visualization of step
64 s, embryos, pupae or adults by stainings and live imaging approaches.
65   Recent data from genetic, biochemical, and live-imaging approaches have greatly enhanced our unders
66              When combined with longitudinal live-imaging approaches, this technology facilitated the
67                            Using genetic and live-imaging approaches, we revealed that the torsion ph
68 s, whereas studies in zebrafish have allowed live imaging as well as genetic and transgenic approache
69                                 In vitro and live-imaging assays to investigate the underlying mechan
70                                              Live imaging at stage 9 reveals that bicoid mRNA particl
71 ll (ESC)-derived hematopoiesis incorporating live imaging at the single-cell level to track hematopoi
72  how to construct environmental chambers for live imaging by digital scanned light-sheet microscopy (
73 e integration of data from fixed embryos and live imaging, can be extended to other developmental sys
74                         Here, we exploit the live imaging capabilities of Xenopus to chart the progre
75 scriptional studies and slow-scan two-photon live imaging capable of identifying the number of motile
76 ng scanning electron microscopy and confocal live imaging combined with quantification of cellular gr
77                                              Live-imaging, combined with modeling of cell mechanics,
78 d micromere, using high-resolution long-term live imaging complemented with a live-cell cycle reporte
79    This is in agreement with bioluminescence live imaging, confocal microscopy, and histology.
80                        Using high-resolution live-imaging data on tagged +TIPs, we show that TACC3 lo
81                                              Live-imaging data show that autophagosome traffic and au
82             Using quantitatively measured 4D live-imaging data, features of V2 cell-shape at each tim
83 models of cell fate differentiation based on live-imaging data.
84                      Electron microscopy and live imaging demonstrate movement of the ER to the WRAMP
85                 Ultrastructural analyses and live imaging demonstrate that alpha-syn accumulations do
86                                              Live imaging demonstrated direct presentation to T cells
87                                              Live imaging demonstrated that both neutrophils and macr
88                                              Live imaging demonstrated that concomitant cellular inte
89                                              Live imaging during compression provides accurate inform
90                                              Live imaging during reproduction revealed distinct and s
91                                              Live-imaging EGFP-beta-actin or dendra2-beta-actin revea
92             Using an integrative approach of live imaging, electron microscopy, and genetics, we show
93 fusing region-specific organoids followed by live imaging enabled analysis of human interneuron migra
94                                      Through live imaging experiments and analysis of mutants that af
95                                              Live-imaging experiments combined with pharmacological a
96 ecular components, we performed quantitative live-imaging experiments in primary hippocampal neurons.
97                                              Live-imaging experiments show that FGF controls the inte
98 n--largely emerging from superresolution and live-imaging experiments--and place this new information
99                                        Using live-imaging fluorescent microscopy coupled to stochasti
100   Here we use novel reporter mouse lines and live imaging for continuous single-cell long-term quanti
101                  We developed a quantitative live imaging framework to characterize INM dynamics with
102                                              Live imaging, gene targeting, and cell-cycle inhibitors
103                    Using immunofluorescence, live imaging, genetics, cell-cycle analyses, in utero le
104                                              Live imaging greatly aids these efforts, but the horizon
105                We have used a combination of live imaging, growth analyses, and computational modelin
106 s genetic tractability and opportunities for live imaging, has recently established Drosophila as a p
107                                     Previous live imaging in Drosophila dendritic arborization neuron
108                                              Live imaging in human endothelial cells in vitro reveale
109      By combining single-molecule assays and live imaging in rat hippocampal neurons, we have identif
110 describe the latest advances in the field of live imaging in the lymph nodes, grouping the different
111 sgene product was visualized by fluorescence live imaging in the scAAV2/8-mG1hp4-treated retinas.
112                      We investigated this by live imaging in wounded zebrafish larvae, where damage o
113                                              Live imaging in zebrafish revealed that macrophages are
114                               We show, using live imaging in zebrafish, that oligodendrocytes make ne
115       In the field of developmental biology, live imaging is a powerful tool for studying, in real ti
116                                           3D live imaging is important for a better understanding of
117 he original Brainbow for Drosophila in which live imaging is practical during much of its development
118 ect observation of embryogenesis via in vivo live imaging is vital to understanding embryogenesis; ye
119              Here, we show the usefulness of live-imaging laser scanning confocal microscopy to inves
120 can be found in thin tissue sections or upon live imaging, making it difficult to comprehensively loc
121 nd presents newly established techniques for live imaging marine embryos.
122 ng whole-genome transcriptome analyses with (live) imaging mass spectrometry (IMS), we observed multi
123 ting the utility of combining new probes and live imaging methods for investigating chemical signalin
124        In this study, we employ quantitative live imaging methods to assess the function of pairs of
125     We present the use of recently developed live imaging methods to examine the dynamic regulation o
126                                        Using live-imaging methods and quantitative analysis, we exami
127                              Here, we employ live-imaging methods to visualize the Snail repressor, w
128                                 Here, we use live-imaging methods to visualize the temporal dynamics
129 coral micropropagates are ideally suited for live-imaging microscopy, while the microfluidic platform
130 lasmic reticulum Ca release, by simultaneous live imaging of 500 to 1000 individual mitochondria.
131 oral activity profiles of these proteases by live imaging of a transgenic reporter substrate in wild-
132                                              Live imaging of acetylcholine receptors (AChRs) in cultu
133                       Numerous tools for the live imaging of actin have been generated by fusing the
134  Ca(2+) signalling triggered by nitrate with live imaging of an ultrasensitive biosensor in Arabidops
135                                  Here, using live imaging of apical polarity proteins in Nematostella
136                                 Quantitative live imaging of asymmetric cell-fate decision-making and
137                                              Live imaging of B. burgdorferi caught in the act of bein
138 hus allowed us for the first time to perform live imaging of Ca(2+) fluxes in genetically unmodified
139                                      Through live imaging of calcium transients from cultured pupal n
140 scopy reconstructions and is compatible with live imaging of cargo transport and MT dynamics.
141                                     By using live imaging of cell-cycle dynamics, we show that leader
142 unolocalization against endogenous proteins, live imaging of dendritic endosomes, and interference ap
143                      In vivo high-resolution live imaging of developing brains as well as loss and ga
144                                              Live imaging of developmental gene expression in Drosoph
145 s limited by the paucity of mouse models for live imaging of distal pre-metastatic niches.
146                                         Here live imaging of Drosophila and hippocampal neuron dense-
147 inach riboswitch in Escherichia coli enables live imaging of dynamic changes in intracellular TPP con
148                                 We performed live imaging of early flower development and showed that
149                                  Here we use live imaging of embryonic brain tissue to visualize, for
150 the site of inflammation, new findings using live imaging of embryonic zebrafish and other modalities
151 ection of fluorescent markers with dsRNA for live imaging of embryos with disrupted caudal gene funct
152                                      We used live imaging of endosomal trafficking in vivo to show th
153                                              Live imaging of endothelial to hematopoietic conversion
154 tic cancer xenografts to provide noninvasive live imaging of events associated with cancer-induced ca
155                                      We used live imaging of ferrets to monitor host responses within
156 ivo neural circuits, neuronal culturing, and live imaging of fluorescent fusion proteins have enabled
157 lity in class IV da neuron dendrites through live imaging of fluorescently labeled nos mRNA.
158 re thought to be widespread, and single-cell live imaging of gene expression has lead to a surge of d
159                                              Live imaging of genome has offered important insights in
160 nterest, as demonstrated by our simultaneous live imaging of genomic loci together with a cell cycle
161                                              Live imaging of GFP-tagged tau aggregates showed that ta
162 issue of Cell, Tamplin et al. (2015) perform live imaging of hematopoietic stem and progenitor cells
163                                              Live imaging of HSV-1-expressed luciferase showed infect
164                                              Live imaging of Hyal1, sucrose gradient centrifugation,
165           In this study, we use quantitative live imaging of ingressing neuroblasts (NBs) in Drosophi
166 oscopy approaches, which are well suited for live imaging of large systems with high spatiotemporal r
167                Here, we establish continuous live imaging of leg regeneration at single-cell resoluti
168 zebrafish larval model is highly amenable to live imaging of leukocyte behavior, and we report that i
169 rating transgenic zebrafish lines that allow live imaging of MCs and by lineage tracing in vivo To co
170                                              Live imaging of meiotic divisions in condensin-depleted
171 l Cell, Iyengar and colleagues (2015) employ live imaging of melanocyte regeneration in adult zebrafi
172 B in pancreata of mice, this was observed by live imaging of mice given infusions of adeno-associated
173                      Using a mouse model for live imaging of microglial activation crossed with SOD1(
174                        Using high-resolution live imaging of mouse embryos, we observed randomly dist
175                                 In addition, live imaging of MTs in P1c(-/-), as well as in plectin-n
176  illumination microscopy, high-resolution 3D live imaging of multicellular specimens remains challeng
177       This approach first performs one-color live imaging of multiple genomic loci and then uses sequ
178                                              Live imaging of multiple RGCs revealed that axons target
179                                       We use live imaging of NCC behavior in vivo to show that Cdh6 p
180 ave an intermediate nuclear migration defect-live imaging of nuclei or LMN-1::GFP shows that many nuc
181                                              Live imaging of outgrowths from kanadi1 kanadi2 Arabidop
182                                              Live imaging of PMNs showed that MRS2578 represses neutr
183                                   High-speed live imaging of polarized adult primary RPE cells and da
184                                              Live imaging of progenitors from a neurogenesis mutant,
185                                              Live imaging of roots indicates that SCM:GFP is localize
186                                           4D-live imaging of rotating MCF10A mammary acini further su
187  Multi-isotope imaging mass spectrometry and live imaging of single differentiating hair cells captur
188  euchromatic loci in Drosophila melanogaster Live imaging of single DSBs in larval imaginal discs rec
189         We confirm this acceleration both by live imaging of single Th2 cells and in an ex vivo Th1 m
190 asy access for experimental manipulation and live imaging of specific molecules; however, technical l
191                                              Live imaging of spinal MNs from the adult disease mice d
192                                        Using live imaging of synaptic growth, we characterized this d
193                                              Live imaging of the differentiation process reveals that
194 l as for rag2, and used them for noninvasive live imaging of the entire thymus in medaka (Oryzias lat
195 oral dynamics of this translocation, we used live imaging of the mTORC1 component RAPTOR and a cell p
196                                              Live imaging of the presynaptic F-actin cytoskeleton rev
197               Multiphoton microscopy enables live imaging of the renal glomerulus.
198                  In conclusion, longitudinal live imaging of the retina in the PDGF-alpha-syn::GFP mi
199                                              Live imaging of these transgenic lines showed that Cftr
200                                     Confocal live imaging of tissue explants revealed that although t
201                                              Live imaging of transcription and RNA dynamics has been
202 e, we performed single-particle tracking and live imaging of transfected, epitope-tagged Nrxn variant
203                                              Live imaging of transgenic zebrafish crestin reporters s
204                                              Live imaging of Tuba1a-mutant neurons revealed slowed mi
205 gression of viral spread in mouse lungs, for live imaging of virus-infected cells, and for differenti
206                                              Live imaging of wound-induced syncytium formation in the
207                                              Live imaging of zebrafish embryos shows defective calciu
208                                        Using live imaging of zebrafish embryos, in combination with p
209                                           By live-imaging oligodendrocyte Ca(2+) activity in vivo, we
210   This allowed us to perform high-resolution live imaging on endogenous HSPCs not currently possible
211 olving complex structures and optimizes SPIM live imaging performance by using a real-time adjustable
212                                        Using live imaging, quantitative image analyses and modeling,
213 erturbation analysis in vivo, which combines live imaging, real-time image analysis, and automated op
214                                     Finally, live imaging revealed an early and sustained host metabo
215                                              Live imaging revealed multiple cytoplasmic nodules surro
216                                              Live imaging revealed Rac-dependent F-actin enrichment a
217                                              Live imaging revealed robust calcium activity during axo
218                                              Live imaging revealed that Centrosomin localized to the
219                                              Live imaging revealed that Dlg1 is required for directed
220                                              Live imaging revealed that DSAs were sequestrated in the
221                                              Live imaging revealed that epidermal cells rapidly inter
222                                     In vitro live imaging revealed that spatially confined expression
223                                              Live imaging revealed that the reduced levels of SCG10 i
224                                              Live imaging revealed that the spindle undergoes a cycle
225                              High-throughput live imaging revealed that this DPP/Brk branch is dispen
226 lective AVE migration, while high-resolution live imaging revealed that this is associated with rando
227 ransport vesicles for dendrite delivery, and live imaging reveals cotransport of both proteins.
228                                              Live imaging reveals that autophagosomes merge with tubu
229                                              Live imaging reveals that CMT2B proteins are inefficient
230                                              Live imaging reveals that NEEP21-positive, EEA1-negative
231                                              Live imaging reveals that spindle angles vary widely dur
232                                              Live imaging showed that an ESCRT-related protein (PDCD6
233                                              Live imaging showed that CD45 ligation specifically redu
234                                              Live imaging showed that mesenchymal stromal cells ancho
235 ining, lineage tracing, clonal analysis, and live imaging showed that NEB progenitors, initially dist
236                                     Instead, live imaging shows that the duration of prometaphase is
237        Correlative electron microscopy after live imaging shows tubulovesicular membranes present at
238                                              Live imaging shows unidirectional and actin-dependent mo
239                   Here, using a high-content live-imaging small interfering RNA screen, we identify M
240                                Using ex vivo live imaging, small interfering RNA knockdown of calpain
241                                              Live imaging studies by Nile red staining suggested that
242                                              Live imaging studies give unparalleled insight into dyna
243 ally required for Notch-mediated EHT In vivo live imaging studies indicate that evi1 suppression impa
244                                              Live imaging studies of OPC migration in ex vivo cerebel
245                                              Live imaging studies reveal Abeta activates NgRs on the
246                                              Live imaging studies reveal that Sema4D elicits a rapid
247 neurons showed no morphological changes, but live imaging studies revealed that the dynamics of the a
248                                              Live imaging studies show that sterols function in traff
249 nd will help advance influenza virus-related live-imaging studies in vitro and in vivo.
250                                Additionally, live-imaging studies of coronavirus replicase proteins h
251                                      Dynamic live-imaging studies of murine cutaneous wounds demonstr
252  have recently been recanted, based on novel live-imaging studies.
253                                              Live imaging suggests that this occurs through Dispatche
254                            Here we present a live imaging system for targeted detection of genomic re
255 Here, we offer a novel, prolonged and robust live imaging system for visualizing the development of a
256       We describe LOLLIbow, a Brainbow-based live imaging system with applications in developmental b
257          We further developed a quantitative live imaging technique for Xenopus left-right organizer
258 ance microscopy (SICM) is a super-resolution live imaging technique that uses a glass nanopipette as
259                           Furthermore, using live imaging techniques in a three-dimensional flow cham
260                               More recently, live-imaging techniques have been used to reveal ODCs.
261                                        Using live-imaging techniques, we have found that SynGAP is ra
262                                        Using live imaging technologies, we demonstrate that enterocyt
263                                              Live-imaging technology has markedly advanced in the fie
264    New methodologies such as high-resolution live imaging, tension sensors, and force-mapping techniq
265 f cisternae, we show using three-dimensional live imaging that cis-Golgi and trans-Golgi remain stabl
266                       We demonstrate through live imaging that LRC are leaving the primary tumor mass
267 neage-tracing assays with short-term in vivo live imaging, the cellular basis of this stochastic stem
268 oviral-based multicolor clonal analysis with live imaging, the results show that single chondrocyte p
269            A new study applies sophisticated live imaging to assess mitotic progression and cell cycl
270 FN-beta gene required the use of single-cell live imaging to define the efficacy of the inhibitors du
271 ystematic histological analysis coupled with live imaging to gain access to these relationships in fe
272                                       We use live imaging to probe the effects of Wnd and Ttk69 on R7
273 ecent Science paper, Rompolas et al. utilize live imaging to track epidermal stem cells over their li
274 our results establish the utility of the new live-imaging tools for the study of molecular-neural int
275 ver, not all plant tissues are accessible to live imaging using confocal microscopy, necessitating al
276 SU crystals was evaluated by high-throughput live imaging using confocal microscopy.
277 iors of epicardial cells can be monitored by live imaging using stereofluorescence microscopy.
278  the production of the microfluidic chip and live imaging using the calcium sensor GCaMP, expressed i
279                            Strikingly, using live imaging we also observe the inappropriate movement
280                                        Using live imaging we found that KV morphogenesis is disrupted
281                  Counterintuitively, through live imaging we observed that variability of neighboring
282 per, using genetic mouse model combined with live imaging, we demonstrate that syntaphilin (SNPH) med
283 g between computational modeling and in vivo live imaging, we demonstrate that the rate of tip-cell s
284                               Using confocal live imaging, we directly observed the cellular processe
285                        Using high-resolution live imaging, we examined the spatiotemporal dynamics of
286 efore, using super-resolution microscopy and live imaging, we focused on the subjunctional distributi
287                                        Using live imaging, we found that Abelson (Abl) tyrosine kinas
288 tracing, genetic cell ablation, and confocal live imaging, we identified a migratory population of Fg
289                                        Using live imaging, we investigated reactivation of mitochondr
290                             From single cell live imaging, we investigated the spatial kinetics and h
291                            Using single-cell live imaging, we observed that Tregs rapidly reduce Ca(2
292                                        Using live imaging, we show for the first time that transient
293                                      Through live imaging, we show that a secondary F-actin ring is f
294                                        Using live imaging, we show that activation of beta-catenin sp
295                   Using genetic analysis and live imaging, we show that exc-6 regulates MT and F-acti
296 of KIF20B in a human cell line and fixed and live imaging, we show that KIF20B has a cell-autonomous
297                                        Using live imaging, we show, however, that R8 growth cones rea
298                                        Using live-imaging, we determine a revised cell lineage of the
299 co-transport of BRP and RBP using intravital live imaging, with both proteins co-accumulating in axon
300 desirable in biology and medicine to perform live imaging without affecting cell function and to obta

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