ライフサイエンスコーパス: live imaging

1 r aggregates and monitor sorting outcomes by live imaging.

2 o lysolecithin exposure could be captured by live imaging.

3 grations with unprecedented resolution using live imaging.

4 termined by single-molecule FISH (smFISH) or live imaging.

5 scale data from two approaches: genomics and live imaging.

6 during zebrafish optic cup morphogenesis by live imaging.

7 ion of native PER2 protein (PER2::VENUS) for live imaging.

8 calization of AIS Kv7.2/7.3 heteromers using live imaging.

9 pulations in the chicken embryo, and ex vivo live imaging.

10 hin the intestine using larval zebrafish and live imaging.

11 somes requires a variety of tools, including live imaging.

12 ve bone resorption, which can be assessed by live imaging.

13 ated with versus without free fatty acids by live imaging.

14 recording cell shape and trajectory through live imaging.

15 exploiting its suitability for quantitative live-imaging.

16 We demonstrate the 3D live imaging ability of TLS-SPIM by imaging cellular and

17 Live imaging after treatment with transgene-encoded or c

18 Although advances in live imaging allow us to directly visualize this process

19 Single-cell tracking by live imaging allowed us to gain mechanistic insight into

20 Quantitative live imaging analyses show that the amnion initiates EE

21 Live imaging analysis revealed a strong correlation betw

22 Here, we use a combination of live imaging and biochemical methods to show that the in

23 Using live imaging and computational approaches, we found that

24 Using super resolution live imaging and correlative light and electron microsco

25 ng transgenic zebrafish lines, cell tracing, live imaging and different markers, we investigated if p

26 hod would allow functional studies involving live imaging and electrophysiology from juvenile and adu

27 ish model as it offers unique attributes for live imaging and facile genetics.

28 High-resolution live imaging and functional analyses revealed that endod

29 e caveats of traditional media when used for live imaging and functional assays on neuronal cultures

30 Extensive live imaging and genetic analyses show that abscission f

31 Here, we use live imaging and genetic manipulations to determine how

32 Through live imaging and genetic mosaics to dissect interactions

33 This method, combined with time-lapse live imaging and glutamate uncaging, could detect plasti

34 Using three-dimensional live imaging and in vivo clonal analysis, we reveal the

35 Thus, live imaging and lineage tracing enabled us to clarify p

36 In toto live imaging and lineage tracing of drl-based reporters

37 ted viable muscle identity mutants, allowing live imaging and locomotion assays.

38 Quantitative live imaging and mathematical modeling allow us to corre

39 in insights into these processes, we perform live imaging and molecular perturbation of migrating chi

40 Here we have used quantitative live imaging and mutant analysis to determine whether si

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 By combining live imaging and quantitative image analysis, we track t

45 been made, in part, thanks to innovations in live imaging and reporter animals.

46 Utilizing non-invasive live imaging and selectively induced apoptosis, we repor

47 Importantly, live imaging and sequence analysis of repair products re

48 in mammalian tissues, but opportunities for live imaging and the genetic tractability of Drosophila

49 Using live imaging and tomographic reconstructions of spermato

50 Live imaging and transfection assays for Arc overexpress

51 Using live imaging and transplantation in zebrafish embryos, w

52 ed a combination of root phenotyping assays, live-imaging and auxin quantification, and analysed the

53 Combination of live-imaging and live-manipulation of developing embryos

54 Here we utilize quantitative live-imaging and mathematical modelling to outline the r

55 Using live-imaging and perturbation experiments we show that l

56 ysis using Wnt-coated microbeads (12-18 h of live imaging) and to create a Wnt platform on a glass su

57 From a series of biochemical studies, live imaging, and analyses of mutant proteins, we propos

58 chniques in situ, such as patch-clamping and live imaging, and cell-specific transcriptomic analyses.

59 models are a powerful system for discovery, live imaging, and functional investigation of cell state

60 In this study, we combine proteomics, live imaging, and genetics in the fly to identify a nove

61 Optogenetic perturbations, live imaging, and time-resolved ChIP-seq assays in Droso

62 ate regulatory consequence, we established a live imaging approach that enabled visualization of step

63 Using electrophysiological and live imaging approaches, we find that GSK3alpha, but not

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 al model and use genetic, thermogenetic, and live-imaging approaches to uncover the contributions of

67 When combined with longitudinal live-imaging approaches, this technology facilitated the

68 Using live-imaging approaches, we investigate the birth, migra

69 Using genetic and live-imaging approaches, we revealed that the torsion ph

70 ce of tendon progenitors by fate mapping and live imaging, as well as underlying molecular stimuli li

71 In vitro and live-imaging assays to investigate the underlying mechan

72 Live imaging at stage 9 reveals that bicoid mRNA particl

73 scriptional studies and slow-scan two-photon live imaging capable of identifying the number of motile

74 nhibits homing of germ cells in vivo Using a live-imaging chemotaxis assay in a 3D matrix, we show th

75 ng scanning electron microscopy and confocal live imaging combined with quantification of cellular gr

76 d micromere, using high-resolution long-term live imaging complemented with a live-cell cycle reporte

77 This is in agreement with bioluminescence live imaging, confocal microscopy, and histology.

78 Intra-lymphatic immune cell transfer and live imaging data further show that activated T cells co

79 Using quantitatively measured 4D live-imaging data, features of V2 cell-shape at each tim

80 Rapidly accumulating live imaging datasets make it increasingly important to

81 llus fumigatus zebrafish in vivo infections, live imaging demonstrated conidia initially phagocytosed

82 Live imaging demonstrated direct presentation to T cells

83 Live imaging demonstrated that concomitant cellular inte

84 Live imaging demonstrated that microridge morphogenesis

85 Two-photon live imaging demonstrates that the history of visual exp

86 synaptic homeostatic potentiation (PHP), and live imaging during acute expression of PHP reveals prop

87 Live imaging during compression provides accurate inform

88 Live imaging during reproduction revealed distinct and s

89 fusing region-specific organoids followed by live imaging enabled analysis of human interneuron migra

90 Through live imaging experiments during the adaptation to acute

91 Live-imaging experiments combined with pharmacological a

92 Live-imaging experiments show that FGF controls the inte

93 n--largely emerging from superresolution and live-imaging experiments--and place this new information

94 lusion was validated by long-term time-lapse live-imaging experiments.

95 Here we use novel reporter mouse lines and live imaging for continuous single-cell long-term quanti

96 We employ live imaging for continuous visualization of intercellul

97 expressed in extra-embryonic mesoderm, while live imaging for F-actin showed abundance of actin filam

98 ysis, mitochondrial stress testing, confocal live imaging for mitochondrial inner membrane polarity,

99 ing algorithm, which allows extension of the live imaging for more than an hour.

100 Using a combination of live imaging, genetic and pharmacological tools, we show

101 Live imaging, genetics, and computational modeling revea

102 Using immunofluorescence, live imaging, genetics, cell-cycle analyses, in utero le

103 chemical cues were thought to be sufficient, live imaging, genetics, modeling, and simulations show t

104 Here, combining live imaging, genome engineering, and acute chemical and

105 bundle orientation in embryonic utricles by live-imaging GFP-labeled centrioles in HCs.

106 Live imaging greatly aids these efforts, but the horizon

107 We have used a combination of live imaging, growth analyses, and computational modelin

108 ous potential as a model system, longer-term live imaging has been technically challenging because of

109 Live imaging has revealed lysosome subpopulations with d

110 s genetic tractability and opportunities for live imaging, has recently established Drosophila as a p

111 is compatible with high-throughput studies, live imaging, immunofluorescence staining, fluorescent i

112 Using in vivo live imaging in fission yeast and in vitro MT dynamics a

113 Live imaging in human endothelial cells in vitro reveale

114 Using live imaging in mice, we found that juxtavascular microg

115 By combining single-molecule assays and live imaging in rat hippocampal neurons, we have identif

116 describe the latest advances in the field of live imaging in the lymph nodes, grouping the different

117 We investigated this by live imaging in wounded zebrafish larvae, where damage o

118 Live imaging in zebrafish revealed that macrophages are

119 New biosensors and live imaging in zebrafish revealed that neutrophil chemo

120 Here we show, using quantitative live imaging in zebrafish, that differential ligand-indu

121 Using live imaging in zebrafish, we demonstrate that neural cr

122 ect observation of embryogenesis via in vivo live imaging is vital to understanding embryogenesis; ye

123 Here, we show the usefulness of live-imaging laser scanning confocal microscopy to inves

124 Here, by using live imaging, lineage tracing, single-cell transcriptomi

125 nd presents newly established techniques for live imaging marine embryos.

126 Here, using advanced live imaging methods, we systematically analyze the dyna

127 Using live-imaging methods and quantitative analysis, we exami

128 Here, we employ live-imaging methods to visualize the Snail repressor, w

129 Here, we use live-imaging methods to visualize the temporal dynamics

130 nsient actin reset (CaAR) measurable through live imaging microscopy using lifeact-mCherry as an acti

131 luidic platform in combination with advanced live-imaging microscopy to study the effects of Cl NPs o

132 coral micropropagates are ideally suited for live-imaging microscopy, while the microfluidic platform

133 ransport and accumulation were visualized by live-imaging microscopy.

134 We use live imaging, modeling, and genetics to deconstruct thes

135 Here, using a combination of live imaging, modeling, and microsurgical perturbations,

136 In this study, we have combined live imaging, mutant backgrounds in which fertilization

137 lasmic reticulum Ca release, by simultaneous live imaging of 500 to 1000 individual mitochondria.

138 oral activity profiles of these proteases by live imaging of a transgenic reporter substrate in wild-

139 Recent development of innovative tools for live imaging of actin filaments (F-actin) enabled the de

140 Here, we use single cell live imaging of an endogenous HES5 reporter and absolute

141 Ca(2+) signalling triggered by nitrate with live imaging of an ultrasensitive biosensor in Arabidops

142 Here, using live imaging of apical polarity proteins in Nematostella

143 Quantitative live imaging of asymmetric cell-fate decision-making and

144 d particles, such as adipocytes, as shown by live imaging of AT, 45-um bead uptake ex vivo, and highe

145 The 'NMJ chip' enables real-time, live imaging of axonal outgrowth, NMJ formation and musc

146 hus allowed us for the first time to perform live imaging of Ca(2+) fluxes in genetically unmodified

147 Through live imaging of calcium transients from cultured pupal n

148 scopy reconstructions and is compatible with live imaging of cargo transport and MT dynamics.

149 By using live imaging of cell-cycle dynamics, we show that leader

150 e believe these FRs will be useful tools for live imaging of cellular RNAs.

151 Live imaging of chromosome dynamics in zebrafish neurons

152 first to enable time-lapsed, high-throughput live imaging of cnidarian larvae and their algal symbion

153 unolocalization against endogenous proteins, live imaging of dendritic endosomes, and interference ap

154 escribe a procedure that allows simultaneous live imaging of development in 80-100 embryos and provid

155 s limited by the paucity of mouse models for live imaging of distal pre-metastatic niches.

156 The LiveFISH approach enables real-time live imaging of DNA and RNA during genome editing, trans

157 Here live imaging of Drosophila and hippocampal neuron dense-

158 20) investigate control of nuclear growth by live imaging of early embryogenesis, perturbations of bl

159 We performed live imaging of early flower development and showed that

160 Here we use live imaging of embryonic brain tissue to visualize, for

161 of beta-catenin, as measured by single-cell live imaging of endogenous beta-catenin, and subsequent

162 tic cancer xenografts to provide noninvasive live imaging of events associated with cancer-induced ca

163 ivo neural circuits, neuronal culturing, and live imaging of fluorescent fusion proteins have enabled

164 re thought to be widespread, and single-cell live imaging of gene expression has lead to a surge of d

165 Live imaging of genome has offered important insights in

166 nterest, as demonstrated by our simultaneous live imaging of genomic loci together with a cell cycle

167 Live imaging of GFP-tagged tau aggregates showed that ta

168 ese vessels contain immune cells and perform live imaging of immune cell trafficking and transmigrati

169 In this study, we use quantitative live imaging of ingressing neuroblasts (NBs) in Drosophi

170 Finally, using live imaging of ingrowing pupal photoreceptor axons, we

171 oscopy approaches, which are well suited for live imaging of large systems with high spatiotemporal r

172 Here, we establish continuous live imaging of leg regeneration at single-cell resoluti

173 zebrafish larval model is highly amenable to live imaging of leukocyte behavior, and we report that i

174 rating transgenic zebrafish lines that allow live imaging of MCs and by lineage tracing in vivo To co

175 Live imaging of meiotic divisions in condensin-depleted

176 Using a mouse model for live imaging of microglial activation crossed with SOD1(

177 Using high-resolution live imaging of mouse embryos, we observed randomly dist

178 luorescent RNA-protein complexes that enable live imaging of mRNA in living cells.

179 illumination microscopy, high-resolution 3D live imaging of multicellular specimens remains challeng

180 This approach first performs one-color live imaging of multiple genomic loci and then uses sequ

181 Live imaging of Myo5b KO-derived enteroids confirmed the

182 Live imaging of outgrowths from kanadi1 kanadi2 Arabidop

183 cell sorting and a microfluidics system for live imaging of oxidation dynamics.

184 Live imaging of PMNs showed that MRS2578 represses neutr

185 Live imaging of progenitors from a neurogenesis mutant,

186 Live imaging of roots indicates that SCM:GFP is localize

187 d straightforward method for the whole-plant live imaging of ROS in mature plants grown in soil.

188 4D-live imaging of rotating MCF10A mammary acini further su

189 euchromatic loci in Drosophila melanogaster Live imaging of single DSBs in larval imaginal discs rec

190 We confirm this acceleration both by live imaging of single Th2 cells and in an ex vivo Th1 m

191 asy access for experimental manipulation and live imaging of specific molecules; however, technical l

192 Here, using live imaging of the developmental migration program of D

193 l as for rag2, and used them for noninvasive live imaging of the entire thymus in medaka (Oryzias lat

194 itation, we have developed a methodology for live imaging of the germ cell lineage within floral orga

195 oral dynamics of this translocation, we used live imaging of the mTORC1 component RAPTOR and a cell p

196 In conclusion, longitudinal live imaging of the retina in the PDGF-alpha-syn::GFP mi

197 We here dissect this process using live imaging of the TSM1 axon of the developing Drosophi

198 Live imaging of the TSM1 axon of the developing Drosophi

199 defined size are amenable to high resolution live imaging of their dynamics and space-filling propert

200 Confocal live imaging of tissue explants revealed that although t

201 Live imaging of transcription revealed that genome activ

202 and molecular targets were identified using live imaging of transgenic fish and RNA sequencing.

203 Live imaging of transgenic zebrafish crestin reporters s

204 Live imaging of Tuba1a-mutant neurons revealed slowed mi

205 Live-imaging of CSF-treated neurons, using a fluorescent

206 Live-imaging of single cilia shows that V2R activation i

207 CARS and SHG microscopy and demonstrate the live-imaging of the same developing neo-tissue over time

208 By live-imaging oligodendrocyte Ca(2+) activity in vivo, we

209 Here we use genetics, Airyscan microscopy, live imaging, optogenetics, and Forster resonance energy

210 Using live imaging over multiple cell cycles, we demonstrate t

211 olving complex structures and optimizes SPIM live imaging performance by using a real-time adjustable

212 Fluorescence live imaging, photothermal, and photoacoustic analysis w

213 Using live imaging, quantitative image analyses and modeling,

214 tudies utilizing biochemical, metabolic, and live imaging readouts showed that, relative to controls,

215 erturbation analysis in vivo, which combines live imaging, real-time image analysis, and automated op

216 Finally, live imaging revealed an early and sustained host metabo

217 Live imaging revealed Rac-dependent F-actin enrichment a

218 Live imaging revealed that antibiotic treatment promoted

219 Live imaging revealed that Centrosomin localized to the

220 Live imaging revealed that DSAs were sequestrated in the

221 Live imaging revealed that Dstyk regulates fusion of mem

222 Live imaging revealed that juxtavascular microglia withi

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 Live imaging revealed that tracheal sprouts invade IFMs

227 Live imaging revealed that upon Rankl induction, Cxcr3.2

228 Live imaging revealed unstimulated or purine-induced mic

229 Live imaging revealed unsynchronized initiation of react

230 dynamics of developmental BBB leakage using live imaging, revealing a combination of steady accumula

231 Live imaging reveals that endogenous Eggless gradually a

232 Live imaging reveals that spindle angles vary widely dur

233 Further, live imaging reveals that the spatiotemporal dynamics of

234 Live imaging showed that an ESCRT-related protein (PDCD6

235 ining, lineage tracing, clonal analysis, and live imaging showed that NEB progenitors, initially dist

236 (CRB2) and delaminate in a stepwise manner; live imaging shows that as one cell delaminates, the nex

237 Live imaging shows that microspikes containing E-cadheri

238 Correlative electron microscopy after live imaging shows tubulovesicular membranes present at

239 Live-imaging shows that the staggered muscle pattern inv

240 tential targets for meningioma therapy using live imaging, single cell RNA sequencing, CRISPR interfe

241 Using ex vivo live imaging, small interfering RNA knockdown of calpain

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 Co-expression and live imaging studies indicate that the expansion does no

245 Live imaging studies of OPC migration in ex vivo cerebel

246 Live imaging studies reveal Abeta activates NgRs on the

247 neurons showed no morphological changes, but live imaging studies revealed that the dynamics of the a

248 Although live-imaging studies have been performed previously, con

249 Live imaging suggests that precise terminal branching pa

250 Live imaging suggests that this occurs through Dispatche

251 Using a combination of live imaging, superresolution microscopy, and modeling,

252 Here we present a live imaging system for targeted detection of genomic re

253 Here, we utilized the MS2 live imaging system to evaluate the expression of the Dl

254 ance microscopy (SICM) is a super-resolution live imaging technique that uses a glass nanopipette as

255 Here, we use advanced live imaging techniques of organotypic slice cultures, c

256 ment in electron microscopy and quantitative live imaging techniques.

257 Live-imaging techniques are at the forefront of biology

258 highlight studies in zebrafish that utilized live-imaging techniques to analyze macrophage activities

259 A perspective on the future use of live imaging technologies and overcoming their current l

260 New methodologies such as high-resolution live imaging, tension sensors, and force-mapping techniq

261 f cisternae, we show using three-dimensional live imaging that cis-Golgi and trans-Golgi remain stabl

262 We demonstrate through live imaging that LRC are leaving the primary tumor mass

263 neage-tracing assays with short-term in vivo live imaging, the cellular basis of this stochastic stem

264 oviral-based multicolor clonal analysis with live imaging, the results show that single chondrocyte p

265 Here, we use live imaging to demonstrate that NuMA plays a spindle-in

266 We used live imaging to discover that all stages of chamber/shel

267 , we combined microfluidics with single-cell live imaging to monitor Saccharomyces cerevisiae galacto

268 We use live imaging to probe the effects of Wnd and Ttk69 on R7

269 system to visualize nascent transcripts and live imaging to record dynamics, we analyze bursting as

270 First, we used live imaging to show a novel arrangement of the microtub

271 We use live imaging to study the dynamics of this process and t

272 mental cues of native brain-derived ECMs and live imaging to systematically evaluate patient-derived

273 ecent Science paper, Rompolas et al. utilize live imaging to track epidermal stem cells over their li

274 We used live imaging to visualize the transcriptional dynamics o

275 This live imaging tool opens a new window into the dynamics o

276 our results establish the utility of the new live-imaging tools for the study of molecular-neural int

277 Live imaging using a probe for F-actin reveals that at l

278 SU crystals was evaluated by high-throughput live imaging using confocal microscopy.

279 iors of epicardial cells can be monitored by live imaging using stereofluorescence microscopy.

280 the production of the microfluidic chip and live imaging using the calcium sensor GCaMP, expressed i

281 lve ultrastructure similar to mammals, while live imaging using transgenic lines identified the devel

282 Furthermore, using 3D and live imaging we observed reduced OF hyaloid vascularizat

283 Counterintuitively, through live imaging we observed that variability of neighboring

284 By combining ChIP-seq and single molecule live imaging we report that CTCF positions cohesin, but

285 g between computational modeling and in vivo live imaging, we demonstrate that the rate of tip-cell s

286 With live imaging, we directly observe the intercellular move

287 Using live imaging, we discover that Magoh deficiency delays p

288 Using high-resolution live imaging, we examined the spatiotemporal dynamics of

289 Using live imaging, we found that Abelson (Abl) tyrosine kinas

290 ctrical cell substrate impedance sensing and live imaging, we found that, in the absence of Podxl, hu

291 Using electrophysiology and live imaging, we identified defects in spontaneous neuro

292 Using live imaging, we investigated reactivation of mitochondr

293 of KIF20B in a human cell line and fixed and live imaging, we show that KIF20B has a cell-autonomous

294 Using live imaging, we show that the somitogenesis clock is ac

295 Using live imaging, we show, however, that R8 growth cones rea

296 aches, microindentation, laser ablation, and live imaging, we showed that XyGs are important for meri

297 Using live imaging, we tracked high Rad51 cells from different

298 to monitor the behavior of single cells via live imaging when confronted with bifurcating microchann

299 preted in the Drosophila embryo by combining live imaging with computational modeling to infer transc

300 e myotome, we combine single-cell resolution live imaging with quantitative image analysis and theore