ライフサイエンスコーパス: fluorescence imaging

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

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

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

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

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

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

7 ncentration dynamics using simple wide-field fluorescence imaging.

8 cation of these subfields using flavoprotein fluorescence imaging.

9 ectroscopy with the versatility and speed of fluorescence imaging.

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

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

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

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

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

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

16 lor, and histology readouts toward precision fluorescence imaging.

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

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

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

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

21 rowding membrane environment using live-cell fluorescence imaging.

22 idine orange in activated sludge by confocal fluorescence imaging.

23 red state transitions in vivo by chlorophyll fluorescence imaging.

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

25 enabling cellular force mapping directly by fluorescence imaging.

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

27 escence from environment severely interferes fluorescence imaging.

28 mors and metastases in mice were detected by fluorescence imaging.

29 t complex assessed by pull down and confocal fluorescence imaging.

30 essed by measuring the FAD+/NADH ratio using fluorescence imaging.

31 Fe and Zn enrichment was visualized by X-ray fluorescence imaging.

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

33 or cancer cell capture and direct smartphone fluorescence imaging.

34 nfocal laser scanning microscopy and in vivo fluorescence imaging.

35 toplasmic protein kinases), via quantitative fluorescence imaging.

36 xenografts were visualized using in vivo NIR fluorescence imaging.

37 their distribution in mammalian cells using fluorescence imaging.

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

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

40 lation of micrometer-sized objects for X-ray 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 Ex vivo fluorescence imaging after overnight cold exposure and f

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

45 These techniques include fluorescence imaging along with computational image proc

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

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

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

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

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

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

52 After fluorescence imaging and data storage, the fluorophores

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

54 Using live and fixed fluorescence imaging and electrophysiological techniques

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

56 Using a combination of fluorescence imaging and electrophysiology in neocortica

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

58 Using fluorescence imaging and fluorescence correlation spectr

59 We employed fluorescence imaging and GCaMP6 reporter mice to generat

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

61 Cell fractionation, fluorescence imaging and immunoelectron microscopy demon

62 Confocal fluorescence imaging and live cell microscopy showed tha

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

64 Here, we use single-molecule fluorescence imaging and quantitative cell biology appro

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

66 ations normally required for single-molecule fluorescence imaging and should be broadly applicable to

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

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

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

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

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

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

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

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

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

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

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

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

79 activity in behaving mice, we have developed fluorescence imaging approaches based on two- and miniat

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

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

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

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

84 To enable fluorescence imaging at cellular scale in freely moving

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

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

87 t technological advances including live-cell fluorescence imaging-based approaches and microfluidic d

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

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

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

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

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

93 Super-resolution fluorescence imaging by photoactivation or photoswitchin

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

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

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

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

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

99 ing bio-imaging modality in situations where fluorescence imaging cannot be applied.

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

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

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

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

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

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

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

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

108 lex calcium and neurotransmitter activity in fluorescence imaging datasets.

109 Indocyanine green fluorescence imaging demonstrated complete coverage of t

110 Whole-body fluorescence imaging detected fluorescent signals in the

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

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

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

114 We review and compare two critical fluorescence imaging directions: one that uses nonspecif

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

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

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

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

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

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

121 Fluorescence imaging experiments demonstrate motor clust

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

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

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

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

126 ression using immunostaining and light-sheet fluorescence imaging, followed by automated mapping and

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

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

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

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

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

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

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

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

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

136 Laser-Stimulated Fluorescence imaging furthermore reveals different inten

137 Fluorescence imaging gave similar results.

138 Furthermore, fluorescence-imaging-guided phototherapy demonstrates th

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

140 The conventional fluorescence imaging has limited spatial resolution in c

141 Fluorescence imaging has seen enduring use in blood flow

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

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

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

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

146 Fluorescence imaging in centimeter-deep tissues with hig

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

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

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

150 demonstrate the use of DSIMe during in vivo fluorescence imaging in patients undergoing surgery for

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

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

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

154 Fluorescence imaging in the second near-infrared window

155 Fluorescence imaging in the second near-infrared window

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

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

158 Indocyanine green fluorescence imaging is a surgical tool with increasing

159 Fluorescence imaging is an indispensable tool in biology

160 In this work, single-molecule fluorescence imaging is applied to measuring rates of hy

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

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

163 Intraoperative fluorescence imaging is emerging as a highly effective m

164 Hyperspectral fluorescence imaging is gaining popularity for it enable

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

166 Fluorescence imaging is often used to monitor dynamic ce

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

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

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

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

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

172 Second harmonic generation 2-photon fluorescence imaging is widely applicable to the study o

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

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

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

176 By integrating fluorescence imaging methods we observed evidence for di

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

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

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

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

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

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

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

184 DCO2 inside RBCs was determined by fluorescence imaging of [H(+)] dynamics in cells under s

185 Fluorescence imaging of a red fluorescent protein (mStra

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

187 -3/7 in vitro and was successfully tested by fluorescence imaging of apoptotic cells.

188 The use of 6 in the fluorescence imaging of BALB/c mice bearing a 4T1-luc2 t

189 Fluorescence imaging of brain slices found that IN admin

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

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

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

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

194 Fluorescence imaging of ex vivo mouse brain slices was u

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

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

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

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

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

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

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

202 ctivity-based probe that enables ratiometric fluorescence imaging of labile iron pools in living syst

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

204 he trafficking process using single molecule fluorescence imaging of live cells and have quantified o

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

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

207 Fluorescence imaging of microfluidic droplets showed the

208 Fluorescence imaging of mouse eyes and fluorescence micr

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

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

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

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

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

214 Typically, the approximate time frame for fluorescence imaging of SoNar is 30 min for living cells

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

216 In vivo, fluorescence imaging of the pancreatic surface allows, f

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

218 Furthermore, fluorescence imaging of tissue cryosections allowed high

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

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

221 white-light imaging of burrow formation with fluorescence imaging of tracer particle redistribution b

222 plate-reader-based assay, along with in vivo fluorescence imaging of tumor xenografts expressing SoNa

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

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

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

226 NIR-II fluorescence imaging overcomes the penetration/contrast

227 Single-molecule fluorescence imaging permits the measurement of reaction

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

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

230 y, we developed and characterized HYPOX-4, a fluorescence-imaging probe capable of detecting retinal-

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

232 mbined optical trapping with single-molecule fluorescence imaging provides a powerful methodology to

233 Nevertheless, fluorescence imaging provides the surgeon with previousl

234 n detection and simultaneous single molecule fluorescence imaging represent a unique platform for nov

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

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

237 Fluorescence imaging revealed localization of EHD2 to ca

238 In vivo fluorescence imaging revealed that PEG30 kDa-conjugated

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

240 While fluorescence imaging seems promising to non-intrusively

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

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

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

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

245 Fluorescence imaging studies suggest an increase in PLCb

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

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

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

249 The X-ray fluorescence imaging technique allows not only the imagi

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

251 in the near-infrared are highly desirable in fluorescence imaging techniques.

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

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

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

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

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

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

258 fluorescence tagging and live-cell confocal fluorescence imaging to explore the biosynthesis and sub

259 Here we use DNA curtains and single-molecule fluorescence imaging to investigate how Msh2-Msh3, a euk

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

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

262 ne fixed-point laser excitation and scanning fluorescence imaging to locally alter the concentration

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

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

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

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

267 used 64Cu-PET-CT, MRI, autoradiography, and fluorescence imaging to track the kinetics of long-circu

268 ultiple technological formats from real-time fluorescence imaging, to solar energy materials, to opto

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

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

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

272 Real-time fluorescence imaging using giant unilamellar vesicles re

273 Results: Fluorescence imaging was able to improve surgical decisi

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

275 Open-field fluorescence imaging was performed preoperatively and du

276 Open-field fluorescence imaging was performed throughout the surgic

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

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

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

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

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

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

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

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

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

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

287 Flow cytometry and fluorescence imaging were applied to approve quantitativ

288 referenced hyperspectral and high-resolution fluorescence imaging were coupled to microspatially mapp

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

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

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

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

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

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

295 Fluorescence imaging with photodetectors (PDs) toward ne

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

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

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

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

300 hus have developed chemically specific X-ray fluorescence imaging (XFI) at the sulfur K-edge to image