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