ライフサイエンスコーパス: live-cell imaging

1 to directly label transcription factors for live cell imaging.

2 h sufficiently fast implementations, permits live cell imaging.

3 , and contact dynamics using microchip-based live cell imaging.

4 er mammalian glycoside hydrolases for use in live cell imaging.

5 in skin keratinocytes analyzed by static and live cell imaging.

6 f spatial resolution or inability to perform live cell imaging.

7 r improvement of these important markers for live cell imaging.

8 hese dynamics occur render them invisible to live cell imaging.

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

10 cells morphology affected as demonstrated by live cell imaging.

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

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

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

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

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

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

17 of dynamic processes and are widely used in live-cell imaging.

18 builds cohesion revealed by TEV cleavage and live-cell imaging.

19 ome editing, transcriptional modulation, and live-cell imaging.

20 es, and we demonstrate their application for live-cell imaging.

21 te transporter, using microfluidics-assisted live-cell imaging.

22 ines, particularly as fluorogenic probes for live-cell imaging.

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

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

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

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

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

28 Live-cell imaging also shows similar single-focus recrui

29 Live-cell imaging analyses also reveal that PNPLA8 dynam

30 crucial role of these residues, and further live-cell imaging analysis shows a substantial reduction

31 Using live cell imaging and a genetically encoded Myosin activ

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

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

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

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

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

37 Here, we used a combination of live cell imaging and finite element computational model

38 matically characterized all eleven FgRabs by live cell imaging and genetic analysis.

39 Using live cell imaging and immuno-electron microscopy analyse

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

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 By combining high-resolution live cell imaging and quantitative morphometric analyses

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

45 By confocal live cell imaging and single cell analyses, we demonstra

46 Here, using a combination of live cell imaging and single-cell genome sequencing, we

47 not quantitative and often incompatible with live cell imaging and subsequent development.

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

49 extremity predominance and a combination of live-cell imaging and biochemical assays to show that th

50 Using live-cell imaging and computer simulations, we identify

51 ted in lipoplexes or lipid nanoparticles, by live-cell imaging and correlated it with knockdown of a

52 efects in vesicle scission, as shown by both live-cell imaging and electron microscopy of endocytic i

53 Using live-cell imaging and electron microscopy, we identify a

54 Using 4-dimensional live-cell imaging and electron microscopy, we show that

55 Complementary live-cell imaging and electron tomography show that beta

56 and macrophage cell populations in vitro, by live-cell imaging and flow cytometry, as well as in vivo

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

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

59 Using a combination of flow cytometry, live-cell imaging and image analysis we examined the eff

60 Live-cell imaging and immunoassay studies demonstrate th

61 Live-cell imaging and immunofluorescence studies demonst

62 Live-cell imaging and immunolocalization experiments rev

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

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

65 Using a combination of biochemical, live-cell imaging and mitochondrial respiration analysis

66 Results from live-cell imaging and molecular studies revealed that du

67 Live-cell imaging and morpholino depletion of axonemal P

68 Earlier analyses, based on classical optical live-cell imaging and mostly restricted by technical nec

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

70 Live-cell imaging and particle tracking provide rich inf

71 Live-cell imaging and pull-down results indicate that it

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

73 inetochores in budding yeast using real-time live-cell imaging and quantified recruitment in fixed ce

74 Live-cell imaging and reverse-genetic analyses of cp mut

75 We use live-cell imaging and RNAi in primary neurons from GFP-L

76 Zhang et al. use a new technique combining live-cell imaging and single-cell sequencing to demonstr

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

78 e labeling strategy is fully compatible with live cell imaging, and provides a valuable tool for trac

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

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

81 primary cortical and motor neuron cultures, live-cell imaging, and transgenic fly models and found t

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

83 ctions, have become increasingly popular for live-cell imaging applications.

84 ighlighting the practicality of probe use in live-cell imaging applications.

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

86 eNLs allow five-colour live-cell imaging, as well as detection of single protei

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

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

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

90 A live cell imaging-based approach is presented here to di

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

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

93 pecific membrane components, using real time live cell imaging, by delivering probes that enable acce

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

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

96 teraction was monitored and quantified using live cell imaging, confocal microscopy, flow cytometry,

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

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

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

100 Together, our in vitro and live-cell imaging data argue strongly that M18A coassemb

101 Our live-cell imaging data further demonstrate that gap junc

102 We integrated live-cell imaging data with statistical modelling for qu

103 microtubules on micropatterned surfaces and live cell imaging demonstrate that active integrins esta

104 Live-cell imaging demonstrates that at the initial stage

105 Live-cell imaging disclosed that both proteins are assoc

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

107 Live cell imaging enabled simultaneous visualization of

108 The multicolor live cell imaging experiments in HeLa cells showed high

109 Long-term fluorescence live-cell imaging experiments have long been limited by

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

111 Tissue fractionation and live-cell imaging experiments revealed that ABHD6 co-loc

112 Live-cell imaging experiments using fluorescence recover

113 Using live-cell imaging, flow cytometry, and kinetic modeling,

114 Live-cell imaging further reveals that PICK1-associated

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

116 Live cell imaging has improved our ability to measure ph

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

118 Live cell imaging illustrated that Zn(2+) entry from ext

119 re we have employed continuous monitoring by live cell imaging in a dual-reporter cell model to inves

120 Through cell cycle manipulation and live cell imaging in Caenorhabditis elegans, we show tha

121 Live cell imaging in concert with shRNA tau knockdown re

122 Using live cell imaging in zebrafish with labelled neutrophils

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

124 dogenous synaptic proteins for high-contrast live-cell imaging in brain tissue remains challenging.

125 ndary growth in fiber cells, was examined by live-cell imaging in cells expressing the fluorescently

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

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

128 Live-cell imaging in HEK293 cells revealed that delta op

129 Using quantitative live-cell imaging in mouse ES cells and tumor cells, we

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

131 Here we used live-cell imaging in parallel with genetics and biochemi

132 Using live-cell imaging in zebrafish we find that regenerating

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

134 Live-cell imaging, including fluorescence recovery after

135 To perform quantitative live cell imaging, investigators require fluorescent rep

136 f water insoluble fluorophore (perylene) for live cell imaging is explored.

137 When followed using ex vivo live cell imaging KSI rapidly accumulates in lumen forme

138 Here, we developed a quantitative live cell imaging method to analyze protein sorting and

139 Combining live-cell imaging methods and a pharmacological approach

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

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

142 ed over time, and migration was evaluated by Live Cell imaging microscopy.

143 DBu) or a natural stimulant, UTP, time lapse live cell imaging movies indicated phosphorylated Ser-36

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

145 Live cell imaging of green fluorescent protein-labeled a

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

147 Live cell imaging of lytic granules revealed their dynam

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

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

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

151 numerical simulations of a Rouse polymer and live cell imaging of the MAT-locus located on the yeast

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 Using live-cell imaging of a pH-sensitive AMPA receptor, we fo

155 Live-cell imaging of actin and tubulin revealed similar

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

157 loped an RNA-based fluorescent biosensor for live-cell imaging of cAG.

158 Live-cell imaging of cells expressing pairs of fluoresce

159 Live-cell imaging of EBOV-infected cells revealed actin-

160 Live-cell imaging of EBOV-infected cells revealed exit o

161 Live-cell imaging of EBOV-infected cells treated with di

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

163 rect observations demonstrate that real-time live-cell imaging of evolution at the molecular and indi

164 nucleocapsid mobility was also confirmed by live-cell imaging of fluorescent nucleocapsids of a viru

165 Live-cell imaging of fluorescently labeled cellulose syn

166 Structured illumination microscopy and live-cell imaging of Fus1, actin, and type V myosins rev

167 a ribonucleic acid (RNA) reporter system for live-cell imaging of gene expression to detect changes i

168 Live-cell imaging of infected zebrafish reveals that Shi

169 Live-cell imaging of macrophages expressing green fluore

170 We demonstrate the optical performance with live-cell imaging of microtubule and actin cytoskeletal

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

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

173 Live-cell imaging of OLs after genetic or pharmacologica

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

175 s of the RNA hairpin MS2-binding site (MBS), live-cell imaging of RNA dynamics at single RNA molecule

176 These tools provide a new avenue for live-cell imaging of RNA molecules in an intact vertebra

177 Live-cell imaging of single cells expressing recombinant

178 Live-cell imaging of the AMD mutant revealed that it is

179 of Arp2/3 by CK-666, coupled to quantitative live-cell imaging of the complex, showed that depletion

180 By performing live-cell imaging of the DCC orthologue UNC-40 during an

181 We develop an improved method for live-cell imaging of the division apparatus by orienting

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

183 otostable "vital dye" that enables prolonged live-cell imaging of the Golgi apparatus by 3D confocal

184 The live-cell imaging of the prepared bioconjugates brought

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

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

187 We demonstrate this by super-resolution live-cell imaging over timescales ranging from minutes t

188 activatable fluorophores are useful tools in live-cell imaging owing to their potential for precise s

189 nes a high-throughput toxicity screen with a live-cell imaging platform to measure mitotic fate.

190 t, a new photoactivatable organelle-specific live-cell imaging probe based on a 6pi electrocyclizatio

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

192 The fluorophore was successfully tested as a live-cell-imaging probe and efficiently stained MCF-7 br

193 Live-cell imaging provided direct evidence that followin

194 By live-cell imaging, recycling endosomal tubules of wild-t

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

196 Live cell imaging revealed Dsg3 order decreased more rap

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

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

199 Live cell imaging revealed that tight spatiotemporal con

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

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

202 Live-cell imaging revealed that the majority of Muller g

203 Live-cell imaging revealed that the protrusion is enrich

204 Live-cell imaging reveals minus end-directed dynein-dyna

205 Live-cell imaging reveals that exosome secretion directl

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

207 Live-cell imaging reveals that Rab8a is first recruited

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

209 Live cell imaging showed that annexin A6 orchestrates a

210 Remarkably, live cell imaging showed that depletion of SKP2, CUL1, o

211 Live cell imaging showed that MDMX depletion triggered t

212 Live cell imaging showed that NEK6 localizes to the micr

213 Microfluidic live cell imaging showed that Slit2 inhibited the abilit

214 Live cell imaging showed that TGFbeta blocked the format

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

216 Live-cell imaging showed that the phagosomes moved bidir

217 Live-cell imaging showed that, whereas most MIIA at the

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

219 Quantified live-cell imaging shows dynamic properties of localized

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

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

222 We used live-cell imaging, spatial image correlation spectroscop

223 otably, the late DDR protein, 53BP1 shows in live-cell imaging strikingly stronger recruitment to DSB

224 during SFTS virus replication, we conducted live cell imaging studies to gain further insight into t

225 Live-cell imaging studies indicate that the hourglass-to

226 Live-cell imaging studies revealed that the decreased mi

227 ction of optimal reagents and conditions for live-cell imaging studies.

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

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

230 ng fluorescence lifetime imaging microscopy, live-cell imaging suggests that the probe can be used to

231 type of a fully automated low-cost, portable live-cell imaging system for time-resolved label-free vi

232 ltiphoton fluorescence anisotropy microscopy live cell imaging technique to measure and map drug-targ

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

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

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

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

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

238 RNA translation requires specific and robust live-cell imaging technologies.

239 Here, we show, using high-resolution live cell imaging, that streptolysin S induces a dramati

240 Here we show, using live-cell imaging, that immobile alpha-syn inclusions ac

241 using fluorescence in situ hybridization and live-cell imaging, that persistent sister chromatid cohe

242 Using live cell imaging to correlate signaling histories with

243 sic motif, immunofluorescence microscopy and live cell imaging to investigate the interaction with th

244 Here we use live cell imaging to show that mammalian Lnp1 (mLnp1) af

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

246 o7 myosin were identified using quantitative live-cell imaging to characterize the ability of various

247 Here, we use live-cell imaging to demonstrate that OPTN, NDP52, and T

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

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

250 gation in the mammalian embryo and integrate live-cell imaging to examine the underlying cellular and

251 Here, we use dual-color live-cell imaging to investigate the neuron-specific mec

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

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

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

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

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

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

258 ved feature of vertebrate dendrites, we used live-cell imaging to systematically analyze microtubule

259 We use live-cell imaging to track the behavior of epithelial sh

260 is challenging given the paucity of suitable live-cell imaging tools.

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

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

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

264 orescence, scanning electron microscopy, and live-cell imaging using total internal reflectance micro

265 Live cell imaging was used to study effects of antibody

266 Live-cell imaging was used to systematically analyze mic

267 Using live cell imaging, we demonstrate the parkin-dependent r

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

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

270 Using quantitative live cell imaging, we found that Eqt-SM is enriched in a

271 Using live cell imaging, we identified mutations that enhance

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

273 Here, using live cell imaging, we obtained evidence that in contrast

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

275 Using live cell imaging, we show that degranulation is coupled

276 Using live cell imaging, we show that disruption of the DISC1-

277 dominant-negative approaches, combined with live cell imaging, we show that herpes simplex virus par

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

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

280 Here, using live-cell imaging, we characterize the dynamic interacti

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

282 sing a combination of biophysical assays and live-cell imaging, we find that oligomerization of the D

283 Using live-cell imaging, we identify a pathway for VAMP7 recyc

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

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

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

287 Using fixed and live-cell imaging, we show that mitochondrial and Gag po

288 Using genetics, biochemistry, and live-cell imaging, we show that the VAP-RELATED SUPPRESS

289 ntly labeled endosome/vesicle populations by live-cell imaging, we show that vesicle motility is redu

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

291 Using live-cell imaging, we uncover that autophagy promotes op

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 Here, we combine live-cell imaging with digital volume correlation to map

296 Analysis by live-cell imaging with fluorescence recovery after photo

297 Live-cell imaging with fluorescent activity-sensors infe

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

299 By combining live-cell imaging with laser microsurgery, fluorescence

300 ated and experimental data, and demonstrated live-cell imaging with temporal resolution of 2.5 second