ライフサイエンスコーパス: fluorescence image

1 intracellular 150 mM typical values (through fluorescence imaging).

2 tion recording tools (e.g. electrode arrays, fluorescence imaging).

3 performed after the acquisition of a single fluorescence image.

4 ultiple spectral components of hyperspectral fluorescence images.

5 nt and classify single bacterial cells in 3D fluorescence images.

6 data on a single-cell level from multi-cell fluorescence images.

7 rgery, the ILM flap may be visualized by ICG fluorescence imaging.

8 r imaging, positron-emission tomography, and fluorescence imaging.

9 lation of micrometer-sized objects for X-ray fluorescence imaging.

10 in (68)Ga-PSMA-I&F PET and in intraoperative fluorescence imaging.

11 ged to allow significant depth-extension for fluorescence imaging.

12 DNA nanostructures, and DNA ultra-resolution fluorescence imaging.

13 ncentration dynamics using simple wide-field fluorescence imaging.

14 cation of these subfields using flavoprotein fluorescence imaging.

15 ectroscopy with the versatility and speed of fluorescence imaging.

16 un to gain momentum in the field of advanced fluorescence imaging.

17 mplished within 4-6 h by those proficient in fluorescence imaging.

18 both genetically and for live assays such as fluorescence imaging.

19 rated the greatest virus binding as shown by fluorescence imaging.

20 FDG and exposed to Cy7 azide with subsequent fluorescence imaging.

21 or uptake in mice was imaged with PET/CT and fluorescence imaging.

22 lor, and histology readouts toward precision fluorescence imaging.

23 n that of ZD2-Cy5.5 (0.5 micromol kg(-1)) in fluorescence imaging.

24 e plethora of high-content data generated by fluorescence imaging.

25 ctively-coupled plasma-mass spectrometry and fluorescence imaging.

26 ophore (CyAm7) 24 hours before near-infrared fluorescence imaging.

27 rowding membrane environment using live-cell fluorescence imaging.

28 idine orange in activated sludge by confocal fluorescence imaging.

29 red state transitions in vivo by chlorophyll fluorescence imaging.

30 o 127-times higher than that obtained by NIR fluorescence imaging.

31 enabling cellular force mapping directly by fluorescence imaging.

32 CM) using three-dimensional super-resolution fluorescence imaging.

33 escence from environment severely interferes fluorescence imaging.

34 cking, as shown by total internal reflection fluorescence imaging.

35 or cancer cell capture and direct smartphone fluorescence imaging.

36 nfocal laser scanning microscopy and in vivo fluorescence imaging.

37 toplasmic protein kinases), via quantitative fluorescence imaging.

38 xenografts were visualized using in vivo NIR fluorescence imaging.

39 their distribution in mammalian cells using fluorescence imaging.

40 roteins (RSFPs) serve as markers in advanced fluorescence imaging.

41 p provides 3.6 x 4.2 x 6.5 mum resolution in fluorescence imaging, 7 x 7 x 3.5 mum in OCT in three di

42 allowed tumor identification with SPECT and fluorescence imaging, (99m)Tc-EuK-(SO(3))Cy5-mas(3) had

43 elegans worm in 3D using a time sequence of fluorescence images acquired at a single focal plane, di

44 es longer exposure time for microscopy-grade fluorescence image acquisition.

45 Ex vivo fluorescence imaging after overnight cold exposure and f

46 nance imaging (gadolinium) and near-infrared fluorescence imaging agents.

47 chine learning tools directly applied to the fluorescence images allow us to distinguish between the

48 These techniques include fluorescence imaging along with computational image proc

49 ts incorporation into peptides for live-cell fluorescence imaging-an approach that is applicable to m

50 Using biochemical and fluorescence imaging analyses, we show that Shh signalin

51 r image correlation spectroscopy (RICS) is a fluorescence image analysis method for extracting the mo

52 Scanning electron microscopy and fluorescence image analysis revealed cross-aligned and l

53 A combination of dye extraction and fluorescence image analysis was used to quantify the tot

54 cell identification for both brightfield and fluorescence images and can process large image sets.

55 quisite proteomic selectivity as revealed by fluorescence imaging and chemical proteomic activity-bas

56 We present a 3D-fluorescence imaging and classification tool for high th

57 ated using the novel technique near-infrared fluorescence imaging and compared with an age-, sex-, an

58 the correlation efficiency between live-cell fluorescence imaging and cryoEM/ET structural analysis,

59 After fluorescence imaging and data storage, the fluorophores

60 trics at single-cell resolution by combining fluorescence imaging and deep learning.

61 Using live and fixed fluorescence imaging and electrophysiological techniques

62 te controls as well as a combination of both fluorescence imaging and electrophysiological validation

63 Using a combination of fluorescence imaging and electrophysiology in neocortica

64 ormance when compared to annexin V, for both fluorescence imaging and flow cytometry.

65 Using fluorescence imaging and fluorescence correlation spectr

66 We employed fluorescence imaging and GCaMP6 reporter mice to generat

67 other techniques, including lower-resolution fluorescence imaging and higher-resolution atomic struct

68 Cell fractionation, fluorescence imaging and immunoelectron microscopy demon

69 Here we show by fluorescence imaging and microscopy that H202 and ROS ac

70 omogeneous spatial resolution for two-photon fluorescence imaging and required no modification of the

71 tumor cell death, using planar near-infrared fluorescence imaging and SPECT, respectively, was evalua

72 Here, we applied advanced fluorescence imaging and spectroscopy approaches on in v

73 vity and subcellular localization, live-cell fluorescence imaging and stimulated emission depletion s

74 R molecules using time-lapse single-molecule fluorescence imaging and subsequent analysis of tracks.

75 Single-molecule fluorescence imaging and time-dependent chemical trappin

76 rocontroller to control temperature, collect fluorescence images, and store the data in cloud storage

77 pon continuous cycles of target recognition, fluorescence imaging, and fluorophore cleavage, this app

78 ), chromatography, super resolution imaging, fluorescence imaging, and mass spectrometry.

79 g reduces protein adhesion as observed using fluorescence imaging, and platelet adhesion (81.7 +/- 2.

80 In addition, we cover fluorescence imaging- and MS-based approaches used to de

81 rk provides a strategy for advancing in vivo fluorescence imaging applications beyond the capabilitie

82 BPI improves the quality of a wide range of fluorescence imaging applications with live neurons in v

83 in the cell remains poorly characterized, as fluorescence imaging approaches are limited in the numbe

84 immunohistochemical, molecular-genetic, and fluorescence imaging approaches revealed that phosphatid

85 using molecular, biochemical, and live-cell fluorescence imaging approaches.

86 Multicolor fluorescence images are acquired and analyzed to determi

87 Wide-field fluorescence images are often corrupted by haze due to o

88 n water and identify testosterone in cell by fluorescence imaging as a visible biomarker.

89 latforms rely on time-consuming high-content fluorescence imaging as read-out, limiting assay through

90 To enable fluorescence imaging at cellular scale in freely moving

91 We use live-cell and in situ fluorescence imaging at the single-molecule level to exa

92 ed sections of the lungs were analyzed using fluorescence imaging, autoradiography, and immunohistoch

93 Detection rates for the fluorescence imaging-based detection were found to be 10

94 throughput cell microscopy (e.g., multicolor fluorescence imaging, bright-field imaging), cell focusi

95 "multi-color" imaging capability similar to fluorescence imaging but with high spatiotemporal resolu

96 lignant tissues are usually distinguished on fluorescence images by applying empirically determined f

97 acking of CTNFs using intraoperative optical fluorescence imaging by following the fate of NIR-labele

98 states are intramolecularly quenched, enable fluorescence imaging by increasing fluorophore brightnes

99 Super-resolution fluorescence imaging by photoactivation or photoswitchin

100 ess, then allows highly efficient 3D OCT and fluorescence imaging by using only one raster scan.

101 We hypothesize that real-time fluorescence imaging can enhance intraoperative decision

102 Time-lapse single-molecule fluorescence imaging can partially overcome the limits o

103 Single-molecule fluorescence imaging can profile individual markers in d

104 ICG-assisted NIR fluorescence imaging can serve as a useful tool for in v

105 ntrolled drug delivery systems with MB-based fluorescence imaging capability, apoptosis control, and

106 alibrated values of pixel intensities of the fluorescence images captured by a handhold fluorescence

107 roach for segmentation and classification of fluorescence images capturing cargo delivery within endo

108 ion were recorded using electrophysiology or fluorescence imaging: cardiomyocyte contraction and surv

109 cers and intravascular optical near-infrared fluorescence imaging catheters are emerging to assess ne

110 hysiology, cell volumetric measurements, and fluorescence imaging conducted in murine retinal cells a

111 Fluorescence imaging confirmed that MDT-28/PLIN-1 mediat

112 We evaluate the method on multiplexed fluorescence imaging data from both primary mouse neuron

113 rpretation and reproducibility of multicolor fluorescence imaging data, in particular under high (de)

114 ely segments nuclei across multiple types of fluorescence imaging data.

115 lex calcium and neurotransmitter activity in fluorescence imaging datasets.

116 Indocyanine green fluorescence imaging demonstrated complete coverage of t

117 Whole-body fluorescence imaging detected fluorescent signals in the

118 Intravascular 2-dimensional near-infrared fluorescence imaging detected nanoparticles in human cor

119 iltered array towards a miniaturized on-chip fluorescence imaging device, which may open up new oppor

120 On-chip fluorescence imaging devices are recognized for their mi

121 k examining astrocytic physiology centers on fluorescence imaging, due to development of sensitive fl

122 We demonstrated that differential fluorescence imaging enabled low limits of detection (31

123 Herein, we report that in vivo fluorescence imaging, enabled by renal-clearable near-in

124 Antibody-based dual-modality (PET/fluorescence) imaging enables both presurgery antigen-sp

125 HyP-1 is also compatible with NIR fluorescence imaging, establishing its versatility as a

126 The system is also capable of fluorescence imaging (excitation = 465 nm, emission = 51

127 Fluorescence imaging experiments demonstrate motor clust

128 This process seen in fluorescence imaging experiments has been called facilit

129 near-infrared window (NIR-II, 1000-1700 nm) fluorescence imaging (FI) and photoacoustic imaging (PAI

130 PNs with (177) Lu enables the integration of fluorescence imaging (FL) and photodynamic therapy (PDT)

131 tance spectroscopy (DRS) and high-resolution fluorescence imaging (FLI) into a smartphone platform.

132 similar labelling profiles were observed via fluorescence imaging for 2YnAd and 6YnAd, a previously r

133 e high sensitivity and spatial resolution of fluorescence imaging for improved surgical guidance, a P

134 to assess the clinical utility of real-time fluorescence imaging for intraoperative decision making.

135 RITERIA: fluorescence in situ hybridization, fluorescence imaging for lymph node mapping, nonmalignan

136 ope that allows quantitative reflectance and fluorescence imaging for monitoring of local Dox concent

137 ed nanoprobe for GRPR targeted near-infrared fluorescence imaging for OSCC.

138 sue mouse cancer models and enable real-time fluorescence imaging for tumor detection, resection, and

139 visualized with both small-animal SPECT and fluorescence imaging from the first week of tumor growth

140 atiotemporal resolutions superior to optical fluorescence imaging, functional OA neuroimaging bridges

141 Laser-Stimulated Fluorescence imaging furthermore reveals different inten

142 Fluorescence imaging gave similar results.

143 m)Tc-nanocolloid enables combined radio- and fluorescence image guidance during sentinel node (SN) bi

144 imaging with organ-level biodistribution and fluorescence image-guided identification of tumor margin

145 techniques implementing near-infrared (NIR) fluorescence image-guided navigation in the planning and

146 iew of clinicatrials.gov using search terms "fluorescence," "image-guided surgery," and "near-infrare

147 Furthermore, fluorescence-imaging-guided phototherapy demonstrates th

148 Since the 1970s fluorescence imaging has become a leading tool in the di

149 The conventional fluorescence imaging has limited spatial resolution in c

150 Fluorescence imaging has seen enduring use in blood flow

151 We used synchrotron X-ray fluorescence imaging, histology, and immunohistochemistr

152 Current fluorescence imaging, however, is limited to about four

153 for computationally efficient prediction of fluorescence images in three dimensions and over large f

154 ths in silico using a 3D COMSOL model of NIR fluorescence imaging in a human hand to examine imaging

155 recently proposed to realize high-resolution fluorescence imaging in centimeter-deep tissue.

156 Fluorescence imaging in centimeter-deep tissues with hig

157 iscussing surface coating, cell plating, and fluorescence imaging in detail.

158 allenges, we used high-speed single-molecule fluorescence imaging in live Escherichia coli cells.

159 rubicin prodrug activation and instantaneous fluorescence imaging in living cells.

160 ncerning cccDNA biology, we have developed a fluorescence imaging in situ hybridization (FISH)-based

161 In vivo fluorescence imaging in the near-infrared region between

162 re time of 20 ms for rare-earth based probes.Fluorescence imaging in the near-infrared window between

163 Fluorescence imaging in the second near-infrared window

164 However, the fluorescence imaging indicated that the increased NP ret

165 small studies have shown that intraoperative fluorescence imaging is a safe and feasible method to as

166 Indocyanine green fluorescence imaging is a surgical tool with increasing

167 Fluorescence imaging is an indispensable tool in biology

168 Although fluorescence imaging is being applied to a wide range of

169 chemical processes that can be studied using fluorescence imaging is considerably limited; the chemic

170 Hyperspectral fluorescence imaging is gaining popularity for it enable

171 s, however with a strong drawback: polarized fluorescence imaging is indeed spatially limited by opti

172 Fluorescence imaging is often used to monitor dynamic ce

173 co-localization analysis of super-resolution fluorescence imaging is prone to false positive signals

174 (CA) for safe magnetic resonance imaging and fluorescence imaging is reported.

175 Turn-on fluorescence imaging is routinely studied; however, turn

176 Live cell fluorescence imaging is the method of choice for studyin

177 For this type of problem, fluorescence imaging is usually the primary tool of choi

178 ctional probe, which is also detectable with fluorescence imaging, is composed of a heptamethine carb

179 Bimodal nuclear/fluorescence imaging may not only improve cancer detecti

180 We report a simple single-molecule fluorescence imaging method that increases the temporal

181 By integrating fluorescence imaging methods we observed evidence for di

182 Sub-diffraction-limited spatial resolution fluorescence imaging methods, which have been successful

183 oblasts, assayed by microfluidic studies and fluorescence imaged microdeformation, respectively, sign

184 imaging system by combining the traditional fluorescence imaging microscope with two imaging fiber b

185 for beta-cells and combines optoacoustic and fluorescence imaging modalities could prove to be import

186 We applied several fluorescence imaging modes, such as wide-field and confo

187 which further paired with a smartphone-based fluorescence imaging module and a self-developed smartph

188 Near-IR fluorescence imaging (NIRFI) is a highly promising techn

189 level data qualitatively captured the static fluorescence image of the cells and the intracellular Ca

190 e QLIPP with deep neural networks to predict fluorescence images of diverse cell and tissue structure

191 tubules and cisternae from multi-dimensional fluorescence images of plant ER.

192 fluorescence reader was designed to measure fluorescence images of the amplicons during a loop-media

193 Fluorescence images of the microbead column revealed cap

194 ives high contrast short-wavelength infrared fluorescence images of vasculature and lymphatic structu

195 y, fully automated serial cryosectioning and fluorescence imaging of 1 tumor-bearing animal as well a

196 Fluorescence imaging of a red fluorescent protein (mStra

197 Because of their high brightness, fluorescence imaging of a single carbon dot and CD aggre

198 -3/7 in vitro and was successfully tested by fluorescence imaging of apoptotic cells.

199 hat dual noninvasive bioluminescence and NIR fluorescence imaging of cancer xenograft models represen

200 In vivo NIR fluorescence imaging of CHL-GLP-1R xenografts was perfor

201 and sub-100 nm resolution deconvolved x-ray fluorescence imaging of diffusible and bound ions at nat

202 in vivo atomic force microscopy with upright fluorescence imaging of embryonic tissue, to show that d

203 Fluorescence imaging of ex vivo mouse brain slices was u

204 Live-cell single-molecule fluorescence imaging of G4s was carried out under condit

205 an observation supported by high-resolution fluorescence imaging of genetically marked cells in orga

206 vivo evidence of the feasibility of targeted fluorescence imaging of GLP-1R-positive lesions.

207 ovel method for targeted near-infrared (NIR) fluorescence imaging of glucagonlike peptide 1 receptor

208 which enabled noninvasive photoacoustic and fluorescence imaging of H(2)O(2).

209 cisternal maturation has been visualized by fluorescence imaging of individual cisternae in the yeas

210 ive Si photodiode array designed for on-chip fluorescence imaging of intracellular Ca(2+) dynamics.

211 ng diodes (OLEDs) are developed and used for fluorescence imaging of live cells and for mapping of ne

212 Time-lapse fluorescence imaging of live cells at super-resolution r

213 suit of this question, by high resolution 3D fluorescence imaging of living and fixed mammalian cells

214 Fluorescence imaging of microfluidic droplets showed the

215 Fluorescence imaging of mouse eyes and fluorescence micr

216 y, the approximate time frame for time-lapse fluorescence imaging of mt-Keima is 20 h for living cell

217 hoton microscopy has enabled high-resolution fluorescence imaging of neurons in deeper brain areas th

218 Studies that rely on fluorescence imaging of nonadherent cells that are cultu

219 X-ray fluorescence imaging of pinna cross-sections revealed pr

220 ha(IIb)beta(3) (GPIIb/IIIa) through confocal fluorescence imaging of primary rat megakaryocytes.

221 Earlier single-molecule fluorescence imaging of the archaeal model glutamate tra

222 dy supercoiled DNA using force spectroscopy, fluorescence imaging of the whole DNA, and rapid buffer

223 Furthermore, fluorescence imaging of tissue cryosections allowed high

224 ngth window (NIR-II, 1,000-1,700 nm) enables fluorescence imaging of tissue with enhanced contrast at

225 microscopy of proteins and synchrotron X-ray fluorescence imaging of trace metals, both performed wit

226 in vivo SPECT imaging, biodistribution, and fluorescence imaging on BALB/c nude mice with orthotopic

227 dy demonstrates the clinical applications of fluorescence imaging on intraoperative decision making.

228 ained to virtually refocus a two-dimensional fluorescence image onto user-defined three-dimensional (

229 ing a critical parameter for applications in fluorescence imaging or data storage with common two-pho

230 NIR-II fluorescence imaging overcomes the penetration/contrast

231 Single-molecule fluorescence imaging permits the measurement of reaction

232 Using live-cell fluorescence imaging, pharmacology, electrophysiology, a

233 rged, such as the recent excitation-emission fluorescence imaging platforms that provide 4D images, w

234 detection would save many lives, but current fluorescence imaging probes are limited in their detecti

235 orescent imaging (zone adjustable time-lapse fluorescence image processor) and separation controller.

236 The deconvolution of widefield fluorescence images provides only guesses of spatial fre

237 As such, this approach greatly improves the fluorescence image quality for examining live cell behav

238 trated on the fusion of real 3D Raman and 4D fluorescence images recorded on cross sections of rice l

239 Here, we employed synchronously amplified fluorescence image recovery (SAFIRe), which optically al

240 Subsequently, high-resolution fluorescence imaging results consolidated the potential

241 itted light microscopy and synchrotron X-ray fluorescence imaging revealed fluctuations in Ca concent

242 Fluorescence imaging revealed localization of EHD2 to ca

243 In vivo fluorescence imaging revealed that PEG30 kDa-conjugated

244 Importantly, X-ray fluorescence imaging revealed that the increased Zn was

245 While fluorescence imaging seems promising to non-intrusively

246 Synchotron Rapid Scanning X-ray Fluorescence imaging showed that the distributions of Zn

247 Variable-chlorophyll-fluorescence-imaging showed active photosynthesis with h

248 Microfocused X-ray fluorescence imaging shows that iron in immunopattern II

249 This paper explores the ability of molecular fluorescence imaging spectroscopy to identify and, more

250 levels as confirmed by quantitative in vitro fluorescence imaging studies.

251 (1), was successfully utilized for AIE-based fluorescence imaging study on methylmercury-contaminated

252 ncipal component analysis of high throughput fluorescence images suggests a dual-mechanism of action

253 esponses using a high-throughput chlorophyll fluorescence imaging system.

254 tion microscopy, a subdiffraction-resolution fluorescence imaging technique, to investigate the light

255 r three fluorophores simultaneously, we show fluorescence images that resolve the highly convoluted G

256 Unexpectedly, we find using time-lapse fluorescence imaging that cdc-42 is not required for epi

257 t a single molecule counting method based on fluorescence imaging that quantitatively maps endosomal

258 zation of ultrafast processes, time-resolved fluorescence imaging, three-dimensional depth imaging, a

259 The finding was verified using fluorescence imaging, tissue cross-sectioning, and histo

260 nabling 3D refocusing of a single wide-field fluorescence image to match confocal microscopy images a

261 It was also applied to epi-fluorescence images to quantify T cell localization with

262 itting methods borrowed from single-molecule fluorescence imaging to determine molecular positions be

263 Here we use 3D super-resolution fluorescence imaging to determine the directional outcom

264 In this work, we employ single-molecule fluorescence imaging to investigate the competitive kine

265 s study, we used high-resolution, wide-field fluorescence imaging to investigate the regulation of Ca

266 this probe system successfully used in cell fluorescence imaging to monitor levels of testosterone i

267 tal sulfide-utilizing powder diffraction and fluorescence imaging to resolve the former and absorptio

268 single-molecule atomic force microscopy and fluorescence imaging to study DNA binding dynamics of MB

269 co predictions, complemented with time-lapse fluorescence imaging to study live interactions of bacte

270 to broadband light sensing, highly sensitive fluorescence imaging, ultrasensitive biomedical diagnost

271 hrotron radiation based 3D confocal mu-X-ray fluorescence imaging upon a chemically fixed and air-dri

272 , and complemented by intraoperative far-red fluorescence imaging using a clinical laparoscope.

273 Real-time fluorescence imaging using giant unilamellar vesicles re

274 ies supporting collection of high-resolution fluorescence image volumes spanning hundreds of microns

275 Results: Fluorescence imaging was able to improve surgical decisi

276 ombining mass spectroscopy imaging (MSI) and fluorescence imaging was developed to localize in situ s

277 Open-field fluorescence imaging was performed preoperatively and du

278 Open-field fluorescence imaging was performed throughout the surgic

279 Before and directly after tumor excision, fluorescence imaging was performed to monitor the tracer

280 an epithelial cells and with high-resolution fluorescence imaging we show that dynamic lipid structur

281 Using single-cell fluorescence imaging, we characterized multiple cycles o

282 ements in planar lipid bilayers, and in vivo fluorescence imaging, we demonstrate here that ColN uses

283 Using single-molecule fluorescence imaging, we demonstrate these sacrificial n

284 o optimize a turn-on signal by using in vivo fluorescence imaging, we developed a new fluorogenic nea

285 ining and Tf-flux assays, FACS analysis, and fluorescence imaging, we report localization of Tf recep

286 polymerase (RNAP) in Escherichia coli Using fluorescence imaging, we show that RNAP quickly transiti

287 ing atomic absorption spectroscopy and X-ray fluorescence imaging, we show that Ru265 is transported

288 Using super-resolution fluorescence imaging, we show that under conditions typi

289 Flow cytometry and fluorescence imaging were applied to approve quantitativ

290 pectromicroscopy and synchrotron-based X-ray fluorescence imaging were first documented to be applied

291 ew optical imaging modalities alternative to fluorescence imaging, which expand greatly the range of

292 llenge could be overcome with intraoperative fluorescence imaging, which provides real-time lesion de

293 Near-infrared fluorescence imaging with DPA-713-IRDye800CW showed stro

294 Here, by combining fluorescence imaging with electrical field stimulation,

295 By combining single-molecule fluorescence imaging with high-pressure, rapidly switchi

296 Fluorescence imaging with photodetectors (PDs) toward ne

297 Here, we combined fluorescence imaging with scRNA-seq to measure cell cycl

298 into live bacteria, applied single-molecule fluorescence imaging with single-particle tracking and l

299 us assay by Western blotting using multiplex fluorescence imaging with specific antibodies against pa

300 process, in static or flow conditions using fluorescence imaging, within the traditional fields of L