ライフサイエンスコーパス: live-cell imaging

1 a fluorescent ligand for VMAT2 suitable for live cell imaging.

2 ne bilayer has been ratified through in vivo live cell imaging.

3 of canonical WNT signals, using quantitative live cell imaging.

4 h sufficiently fast implementations, permits live cell imaging.

5 rowth and reduction kinetics monitored using live cell imaging.

6 cence, but this approach is not conducive to live cell imaging.

7 cells morphology affected as demonstrated by live cell imaging.

8 field strength, with particular benefits for live cell imaging.

9 , as well as the capacity for super-resolved live cell imaging.

10 approach has yet to be embraced as a tool in live cell imaging.

11 sed to anti-mitotic drugs and followed up by live cell imaging.

12 to directly label transcription factors for live cell imaging.

13 a separate fluorescent protein detectable by live cell imaging.

14 g fura-2, and contraction was observed using live cell imaging.

15 te (HDM) or IL-33 using RT-qPCR, Luminex and live cell imaging.

16 it impossible to resolve their values using live-cell imaging.

17 rganization revealed by super-resolution and live-cell imaging.

18 exocytic pathways can be next visualized via live-cell imaging.

19 uctures during extended cell migration using live-cell imaging.

20 m using molecular biology, biochemistry, and live-cell imaging.

21 se findings were functionally validated with live-cell imaging.

22 ood due to a lack of techniques suitable for live-cell imaging.

23 etwork at the cell periphery, as revealed by live-cell imaging.

24 transcription factors and complemented it by live-cell imaging.

25 Caenorhabditis elegans and zebrafish through live-cell imaging.

26 l biological fluorescent probes for in vitro live-cell imaging.

27 tissue culture conditions better adapted to live-cell imaging.

28 Here, we show by live-cell imaging a novel Cdc42 localization with ESCRT

29 Live-cell imaging after individual ASD-gene repression v

30 Live cell imaging allows direct observation and monitori

31 Using live cell imaging and a genetically encoded Myosin activ

32 Further, live cell imaging and analysis of 3D cell migration reve

33 field emission scanning electron microscopy, live cell imaging and biophysical measurements, we aimed

34 protein domain function in combination with live cell imaging and computational approaches.

35 Utilizing live cell imaging and computational modeling, we find th

36 By combining live cell imaging and computational modeling, we showed

37 chemical toolbox, AggFluor, that allows for live cell imaging and differentiation of complex aggrega

38 Here we use live cell imaging and electron cryo-tomography to descri

39 of the fungal retromer by genetic analysis, live cell imaging and immunological assay.

40 Using a combination of live cell imaging and in vitro single molecule binding m

41 ferent metabolic states has been advanced by live cell imaging and organelle specific analysis.

42 gical shear stress, using recently developed live cell imaging and particle-tracking methods for stud

43 athogenic mutations in VCP Using fluorescent live cell imaging and respiration analysis we demonstrat

44 DHA decreased cell necrosis demonstrated by live cell imaging and transmission electron microscopy.

45 We used a combination of quantitative live cell imaging and validation in primary patient cell

46 d two complementary, independent approaches: live-cell imaging and a predictive computational model.

47 ombine location-selective kinase inhibition, live-cell imaging and biochemical assays to probe the re

48 fic intracellular ANAP incorporation affords live-cell imaging and detection of Na(v)1.5 inactivation

49 We investigated this phenomenon using live-cell imaging and discovered that ectopic germ cells

50 ical model for closed mitosis(5)), genetics, live-cell imaging and electron tomography, we show that

51 trapping' in cells, we employed quantitative live-cell imaging and fluorescence recovery after photo-

52 d Myo5 during endocytosis using quantitative live-cell imaging and genetic perturbations.

53 Live-cell imaging and genetic tools reveal a new way in

54 -resolution microscopy, electron microscopy, live-cell imaging and genetics to show that C. elegans m

55 Live-cell imaging and high-resolution spectrofluorometer

56 tem that provides unparalleled advantages in live-cell imaging and high-throughput genetic analyses.

57 Live-cell imaging and immunofluorescence studies demonst

58 Live-cell imaging and immunolocalization experiments rev

59 Using live-cell imaging and laser microirradiation to induce D

60 Here, we used live-cell imaging and microfluidics to investigate the a

61 Live-cell imaging and microscopy were used to determine

62 Live-cell imaging and morpholino depletion of axonemal P

63 areas like the selective delivery of drugs, live-cell imaging and new theranostic approaches.

64 A combination of live-cell imaging and next-generation genomics revealed

65 ne-tuned to physiological sensing range, and live-cell imaging and quantification are demonstrated in

66 tiometric sensors can be broadly applied for live-cell imaging and quantification of metabolites, sig

67 ures of mouse hippocampal pyramidal cells by live-cell imaging and showed that they exhibit bi-direct

68 Here, we combine live-cell imaging and single-cell RNA sequencing to char

69 ated NF-kappaB RelA nuclear translocation by live-cell imaging and then quantified transcript number

70 Here we combine optogenetic control of RhoA, live-cell imaging and traction force microscopy to inves

71 genome organization and how low-throughput (live-cell imaging) and high-throughput (Hi-C and SPRITE)

72 use polarization-resolved microscopy, FRAP, live cell imaging, and a mutant of Adenomatous polyposis

73 roach combines serial affinity purification, live cell imaging, and cross-linking mass spectrometry t

74 using a combination of fixed cell analysis, live cell imaging, and mathematical modeling, we show th

75 We used structural modeling, immunoblotting, live cell imaging, and split green fluorescence protein

76 expression in the TJ-free cell line HEK 293, live-cell imaging, and Forster/FRET.

77 Herein, using immunofluorescence, live-cell imaging, and MS-based analyses, we demonstrate

78 with immunoprecipitation and immunoblotting, live-cell imaging, and protein-stability assays, we repo

79 Here, using super resolution microscopy, live-cell imaging, and tau knockdown, we show for the fi

80 cts in order to validate such conjugates for live cell imaging applications.

81 able for single-cell analysis and especially live-cell imaging applications.

82 ection of TNF cleavage in flow cytometry and live-cell imaging applications.

83 Using a live cell imaging assay, we further determined that KCC2

84 We first developed a novel in vitro live-cell imaging assay to demonstrate that while tether

85 We developed live-cell imaging assays which show that tetherin does n

86 M), we performed state-of-the-art dual-color live-cell imaging at physiological and lowered temperatu

87 We assessed cell migration and invasion with live-cell imaging-based migration assay and matrigel inv

88 RESOLFT nanoscopy is particularly suited for live cell imaging because it requires relatively low lig

89 Fluorescent peptides are valuable tools for live-cell imaging because of the high specificity of pep

90 Live-cell imaging can detect earlier roles of EAPs prece

91 from bacteria to mammalian cells, and expand live-cell imaging capabilities to include multi-cell typ

92 Live cell imaging, combined with domain-mapping analysis

93 ations of lipid peroxyl radicals produced in live cell imaging conditions.

94 Using live-cell imaging, confocal and electron microscopy, we

95 By combining live-cell imaging, correlative light electron microscopy

96 Live-cell imaging coupled with targeted gene knockouts a

97 m signaling in polar body formation, we used live-cell imaging coupled with temporally precise intrac

98 that such processes can explain experimental live-cell imaging data measuring distances between regul

99 Live-cell imaging demonstrates that at the initial stage

100 e as alkyne-state-dependent Raman probes for living cell imaging due to synergetic enhancement effect

101 Live cell imaging enabled simultaneous visualization of

102 Live cell imaging established that cytoprotection was as

103 he expression of RNAs in bacteria in no-wash live-cell imaging experiments and also report stimulated

104 for heterotrimeric G-proteins in a series of live-cell imaging experiments in primary human endotheli

105 Associated live-cell imaging experiments provide a mechanism for Ct

106 sensor of MAPK activity (SOMA) and performed live-cell imaging experiments using detached cotyledons.

107 Live-cell imaging experiments using fluorescence recover

108 ion of theoretical modeling and quantitative live-cell imaging experiments, we show that local deplet

109 Finally, live-cell imaging, fluorescence recovery after photoblea

110 xploits the power of C. elegans genetics and live-cell imaging for fundamental studies of dendritic s

111 We employed live-cell imaging, gene silencing and coimmunoprecipitat

112 A bottleneck to apply these approaches for live-cell imaging has become the availability of appropr

113 Live-cell imaging has opened an exciting window into the

114 Live-cell imaging has revolutionized our understanding o

115 f myosins, force measurement techniques, and live-cell imaging have advanced our understanding of how

116 cent technical advances in visualization and live-cell imaging have significantly altered our view of

117 Live cell imaging in concert with shRNA tau knockdown re

118 Here, using multiphoton live cell imaging in mouse kidney tissue, FIB-SEM, and o

119 xation or permeabilization, and thus, enable live cell imaging in various models.

120 Through live cell imaging in vitro, we observed rapid activation

121 Using live cell imaging in zebrafish with labelled neutrophils

122 Here we use superresolution live-cell imaging in a model fibroblast system to examin

123 Using acute inactivation approaches and live-cell imaging in Drosophila embryos, we dissect the

124 Finally, live-cell imaging in early postnatal brain slices reveal

125 Using fixed- and live-cell imaging in human microglia cells, we further s

126 Live-cell imaging in microfluidic devices now allows the

127 Using live-cell imaging in mouse hippocampal neurons, we estab

128 ing super-resolution microscopy (3D-SIM) and live-cell imaging including the use of FRET-based Rho GT

129 Live-cell imaging, including fluorescence recovery after

130 Combining live-cell imaging methods and a pharmacological approach

131 Here, live-cell imaging methods were developed for Giardia to

132 utrophils and monocytes and in studies using live cell imaging microscopy conducted under fluid shear

133 bation, correlative light and EM tomography, live-cell imaging, modeling, and high-resolution structu

134 LEM system encompasses a high-speed confocal live-cell imaging module to acquire an automated fLM gri

135 IncuCyte live cell imaging of 8 capillary proliferative capacity

136 quantitative 3D cell-cell adhesion assay and live cell imaging of cell-cell contact formation reveale

137 Live cell imaging of endocytosis has helped to decipher

138 Live cell imaging of green fluorescent protein-labeled a

139 Lastly, we successfully performed live cell imaging of HNO using NitroxylFluor.

140 gs, and demonstrate feasibility of long term live cell imaging of human cells in vitro.

141 Live cell imaging of lytic granules revealed their dynam

142 Live cell imaging of mammalian RNA polymerase II (Pol II

143 Finally, live cell imaging of mechano-insensitive formin mutant c

144 on with a cell-permeable organic dye enables live cell imaging of microproteins with minimal perturba

145 , prkdc-mutant zebrafish facilitated dynamic live cell imaging of muscle regeneration, repopulation o

146 r demonstrated, using biochemical assays and live cell imaging of nascent polypeptides in mammalian c

147 evidence for this statement through in-vitro live cell imaging of NF-kB in HUVECs exposed to differen

148 This strategy enables us to obtain real-time live cell imaging of redox states in TfR1-mediated endoc

149 and activates a conditional fluorophore for live cell imaging of RNA.

150 Live cell imaging of single viral particles revealed tha

151 microfilaments has become a gold standard in live cell imaging of the cytoskeleton.

152 , and total internal reflection fluorescence live cell imaging of transfected HEK293 cells, we demons

153 Live cell imaging of treated cells demonstrated that mit

154 aptamer-tagging provides a valuable tool for live cell imaging of viral RNA.

155 histological beta-cell mass measurements and live-cell imaging of beta-cell Ca(2+) oscillations.

156 Live-cell imaging of cells expressing pairs of fluoresce

157 Live-cell imaging of cultured striatal neuronal cell lin

158 toward the spinal cord in vivo Furthermore, live-cell imaging of end-binding protein 3 tagged with E

159 Through live-cell imaging of endogenous localization, conditiona

160 Using live-cell imaging of fission yeast, we provide evidence

161 Live-cell imaging of glioblastoma cells overexpressing a

162 Abs were used in flow-based adhesion assays, live-cell imaging of motility, and actin polymerization

163 pauses and occasional reversals observed in live-cell imaging of MT transport.

164 We used time-lapse live-cell imaging of Neurospora crassa in microfluidic e

165 Live-cell imaging of OLs after genetic or pharmacologica

166 Using quantitative live-cell imaging of primary human and mouse macrophages

167 Using simultaneous UVA exposure and live-cell imaging of primary human melanocytes, we found

168 hat support native pyroptosis and facilitate live-cell imaging of pyroptotic cell death.

169 Live-cell imaging of single cells expressing recombinant

170 Here, by using immunohistochemistry and live-cell imaging of specific mRNAs, we describe for the

171 alian cells and enables simple and versatile live-cell imaging of sub-cellular structures at the nano

172 act the genome during cell division by using live-cell imaging of the cytoskeleton, chromatin, and DN

173 We used live-cell imaging of the fluorescently labeled and bioac

174 inverted fluorescent microscope that enables live-cell imaging of thermophiles.

175 s the potential for developing new tools for live-cell imaging of tRNA with the unique advantage of b

176 electron microscopy, immunofluorescence, and live-cell imaging, our study shows that immediately afte

177 Using an MLF2-based live-cell imaging platform, we demonstrate that nuclear

178 pectral and biological characterization as a live-cell imaging probe for different fungal pathogens.

179 t time, be successfully applied as selective live cell imaging probes (at nanomolar concentrations) a

180 Results from flow cytometry, live-cell imaging, pulldown assays, and genetically-modi

181 Time-lapse live cell imaging revealed active migration of hPGCLCs o

182 Live cell imaging revealed Dsg3 order decreased more rap

183 Fluorescence live cell imaging revealed that extracellular Zn(2+) exe

184 Live cell imaging revealed that GFP-KIF5A and mCherry-Co

185 from 1.24 to 45.01 mum(2) (P < 0.0001), and live cell imaging revealed that the VFs were highly dyna

186 Force measurement and live cell imaging revealed that upon binding to CD80, fo

187 components, while repeating the screen with live-cell imaging revealed a role for Mediator complex s

188 Genetics and live-cell imaging revealed core CME spatiodynamic simila

189 Live-cell imaging revealed endocytosis of Ror2/caveolin1

190 In conclusion, live-cell imaging revealed multiple mechanisms involving

191 Live-cell imaging revealed that FLS2 and BRI1 form PM na

192 Spinning-disk live-cell imaging revealed that S. pneumoniae induces P2

193 Live-cell imaging revealed that the protrusion is enrich

194 -/-) cells show decreased WNT secretion, and live cell imaging reveals aberrant recycling of the WNT

195 Live-cell imaging reveals that HSPA1B nascent transcript

196 Rapid live-cell imaging reveals that microtubules are less abu

197 Live-cell imaging reveals that Rab8a is first recruited

198 xtensively used to study cells in real time (live cell imaging), separate cells using fluorescence ac

199 del plant Arabidopsis, we have established a live cell imaging setup to observe male meiocytes.

200 Quantitative live cell imaging showed dramatic differences in distrib

201 Live cell imaging showed that MDMX depletion triggered t

202 Live cell imaging showed that NEK6 localizes to the micr

203 Live cell imaging showed that TGFbeta blocked the format

204 C-Miro/Milton complexes at mitochondria, and live-cell imaging showed that loss of APC slowed the fre

205 Four-dimensional (4D) lattice light-sheet live-cell imaging showed that the majority of LELs in fr

206 Analysis of bioluminescent live-cell imaging shows a significantly greater number o

207 Quantified live-cell imaging shows dynamic properties of localized

208 Moreover, live-cell imaging shows that mitochondria arrested at th

209 Live-cell imaging shows that Rhes tunnels establish cont

210 he recent progress in structural biology and live-cell imaging shows the T6SS as a long contractile s

211 re we apply a straightforward combination of live cell imaging, single-particle tracking microscopy,

212 Moreover, live-cell imaging studies examining Vif-mediated degrada

213 Live-cell imaging studies revealed that the decreased mi

214 roteins via recording fluorescence bursts in live-cell imaging studies.

215 Lastly, live cell imaging suggests that MoVps17 can regulate ear

216 substrate affixed to a stretcher and the SHG live-cell imaging technique are unique tools for real-ti

217 Progress in live cell imaging techniques has recently revealed that

218 approach can be readily combined with other live cell imaging techniques, it will contribute to a be

219 Chemical-biology- and live cell-imaging techniques revealed that catalytically

220 In the current study, we used advanced live-cell imaging techniques and a fascin biosensor to d

221 cellular function, it is critical to develop live-cell imaging techniques that can probe the real-tim

222 Using live-cell imaging techniques, we reveal that, a fine ER

223 rrounding the brain, made possible by modern live-cell imaging technologies, have revived this discus

224 Here, we demonstrate by live cell imaging that the G4-ligand RHPS4 localizes pri

225 We used quantitative flow cytometry and live cell imaging to compare MCM loading during the long

226 Using live cell imaging to correlate signaling histories with

227 rid MD/worm-like chain polymer modeling, and live cell imaging to evaluate relative binding and signa

228 er (FRET)-based molecular tension sensor and live cell imaging to evaluate the effect of osteocytes,

229 We used live cell imaging to generate a quantitative inventory o

230 This work employs live cell imaging to probe how the multidomain scaffold

231 Here, we used live cell imaging to show that actin-based protrusions a

232 b proliferation and host cell death, we used live cell imaging to track Mtb infection outcomes in ind

233 o understand brush border formation, we used live cell imaging to visualize apical remodeling early i

234 Here, we use high-resolution live-cell imaging to analyze individual microtubule bund

235 We used live-cell imaging to characterize Ca(2+) pulse dynamics

236 gate cilium loss in mammalian cells, we used live-cell imaging to comprehensively characterize indivi

237 ulates transcription in human cells, we used live-cell imaging to detect and track nuclear RNAi trans

238 We used live-cell imaging to determine the intranuclear position

239 We used live-cell imaging to investigate the role of p53 dynamic

240 e developed a CRISPR/Cas9 assay with dynamic live-cell imaging to measure acute effects of knockout (

241 mically identified beta cells using 2-photon live-cell imaging to monitor FoxO1 localization.

242 In this study, we utilize 3D time-lapse live-cell imaging to monitor the role of NuSAP in chromo

243 transcriptomic and structural analyses with live-cell imaging to predict small molecule inhibitors o

244 Here we used genetics and quantitative live-cell imaging to probe the mechanisms that concentra

245 ic spindles in early C. elegans embryos with live-cell imaging to reconstruct all microtubules in 3D

246 0) employ unbiased proteomics approaches and live-cell imaging to reveal a key role for the histone c

247 Next, we used live-cell imaging to show that acute pharmacological dyn

248 In this issue, Hsu et al. use live-cell imaging to show that lytic granule convergence

249 Thus, we introduce a live-cell imaging tool to facilitate in vivo studies of

250 of the anomalous exponent, used to interpret live cell imaging trajectories.

251 Single-molecule live-cell imaging uncovered that two naive pluripotency

252 as observed throughout all mitotic phases in live cell imaging using GFP-labeled H2B as a fluorescent

253 Simultaneous live cell imaging using HeLa cells to investigate the in

254 ning CRISPR/Cas9-mediated genome editing and live cell imaging using lattice light sheet microscopy (

255 Live-cell imaging using macrophages isolated from mRFP-

256 Live cell imaging was used to analyze the interaction of

257 Live cell imaging was used to study effects of antibody

258 Live-cell imaging was used to systematically analyze mic

259 l genetics, super resolution microscopy, and live-cell imaging we discover that centrosomal delivery

260 Applying live cell imaging, we documented for the first time that

261 Using live cell imaging, we found that despite inclusions cont

262 Using high spatiotemporal resolution live cell imaging, we found that inhibiting the catalyti

263 By electron microscopy as well as live cell imaging, we have identified a population of pr

264 Using 4D live cell imaging, we observed that fluorescent structur

265 Here, using live cell imaging, we show that BET inhibition prolonged

266 eadouts and scaffolded activity reporters in live cell imaging, we show that PKCzeta has highly local

267 Using live cell imaging, we studied the effect of UV light on

268 Using live-cell imaging, we also find that MKlp2-dependent tar

269 s, pulldown and integrin-binding assays, and live-cell imaging, we demonstrate that full-length kindl

270 y, correlated light electron microscopy, and live-cell imaging, we demonstrate the existence of mobil

271 Using quantitative live-cell imaging, we demonstrated that mitotic entry re

272 Using live-cell imaging, we find that sequestration of misfold

273 Using live-cell imaging, we found that Calvarial-CM treatment

274 g analysis, biochemical assays, and advanced live-cell imaging, we identified that neferine, a natura

275 Using live-cell imaging, we investigate the role of the actin

276 To make procapsids accessible to live-cell imaging, we made a series of recombinant pseud

277 ruption of myosin activity with quantitative live-cell imaging, we observed decreased abundance of PM

278 Using superresolution nanoscopy and live-cell imaging, we observed that microtubules within

279 Using fluorescence live-cell imaging, we observed that the Polycomb repress

280 By quantitative live-cell imaging, we observed that the yeast nucleolus

281 olecule analysis, gene editing and zebrafish live-cell imaging, we report that mRNA polarisation acts

282 Using live-cell imaging, we show human primary T cells migrate

283 uctured illumination microscopy (3D-SIM) and live-cell imaging, we show in fly neural stem cells (neu

284 By light microscopy and live-cell imaging, we show that CD63 is enriched in micr

285 g, lineage tracing, whole-organ explant, and live-cell imaging, we show that homeostatic TM epidermis

286 Using live-cell imaging, we show that hyen D induces rapid mem

287 Employing live-cell imaging, we studied the time- and power-depend

288 Using microfluidics and live-cell imaging, we treat multiple E. coli populations

289 Its application is explored in live cell imaging, which exhibited cytoplasmic and mitoc

290 Using live cell imaging with a pH-sensitive Rosella biosensor

291 APD and calcium handling were assessed by live cell imaging with Arclight voltage and Fluo-4 calci

292 staged assembly intermediates by correlating live cell imaging with high-resolution electron tomograp

293 Coupling live-cell imaging with a computational approach to ident

294 and discuss the strengths and weaknesses of live-cell imaging with antibody-based probes.

295 SPARKL integrates high-content live-cell imaging with automated detection and analysis

296 Live-cell imaging with fluorescent activity-sensors infe

297 Here, we use live-cell imaging with fluorescent probes and Forster re

298 , such as those obtained in low-illumination live-cell imaging with GFP, we show that SRRF is general

299 In this work, we combined live-cell imaging with temporally controlled perturbatio

300 n was readily detected in infected cells via live-cell imaging, with intensity levels ~3-fold greater