ライフサイエンスコーパス: fluorescence imaging

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

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

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

4 conjugated with MIP-NANA was demonstrated by fluorescence imaging.

5 nters in diamond for correlated magnetic and fluorescence imaging.

6 ogen processes based on medium-throughput 3D fluorescence imaging.

7 gel pad array is achieved with single filter fluorescence imaging.

8 d by 4D live-cell and snapshot deconvolution fluorescence imaging.

9 on, trafficking, and signaling processes via fluorescence imaging.

10 ting tissue autofluorescence associated with fluorescence imaging.

11 light to all-trans-retinol using single cell fluorescence imaging.

12 , which was validated by immunohistochemical fluorescence imaging.

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

14 and tested in vivo by PET and near-infrared fluorescence imaging.

15 n tumors under chemotherapy in near-infrared fluorescence imaging.

16 protein, thereby permitting radionuclide and fluorescence imaging.

17 for three-dimensional (3D) super-resolution fluorescence imaging.

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

19 t probes with molecular-scale dimensions for fluorescence imaging.

20 + Fe(3+)} has been shown to label cells with fluorescence imaging.

21 n optical devices, analysis, biosensing, and fluorescence imaging.

22 le of streptavidin in 10 muL of sample using fluorescence imaging.

23 st polymer microfluidic chip with concurrent fluorescence imaging.

24 y of solution conditions using oblique angle fluorescence imaging.

25 lor, and histology readouts toward precision fluorescence imaging.

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

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

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

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

30 rowding membrane environment using live-cell fluorescence imaging.

31 idine orange in activated sludge by confocal fluorescence imaging.

32 red state transitions in vivo by chlorophyll fluorescence imaging.

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

34 enabling cellular force mapping directly by fluorescence imaging.

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

36 escence from environment severely interferes fluorescence imaging.

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

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

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

40 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 d

41 to determine the optimal time for SPECT and fluorescence imaging after injection of dual-labeled MN-

42 the main advantages of QDs compared to other fluorescence imaging agents.

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

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

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

46 For the first time, the fluorescence imaging analysis of DAT was combined with t

47 ells: a chemical probe for dynamic live-cell fluorescence imaging and a combination of scanning trans

48 luorescently labeled lectins was assessed by fluorescence imaging and an excellent selectivity to spe

49 Fluorescence imaging and biodistribution studies showed

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

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

52 After fluorescence imaging and data storage, the fluorophores

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

54 al activity in vitro by simultaneous calcium fluorescence imaging and diffusion MR acquisition.

55 s such as array tomography, super-resolution fluorescence imaging and electron microscopy.

56 We employed fluorescence imaging and GCaMP6 reporter mice to generat

57 We show by quantitative fluorescence imaging and gene reporter assays that drug

58 mples, enabling correlative super-resolution fluorescence imaging and high-quality electron microscop

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

60 ZW800-1-labeled Bs-F(ab)2 for near-infrared fluorescence imaging and image-guided surgical resection

61 Cell fractionation, fluorescence imaging and immunoelectron microscopy demon

62 Whole-body fluorescence imaging and immunohistochemical staining we

63 Confocal fluorescence imaging and live cell microscopy showed tha

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

65 These models have largely relied on fluorescence imaging and microscopy to quantify cells in

66 uspended and adherent cells according to the fluorescence imaging and morphological features.

67 Using fluorescence imaging and positron emission tomography, w

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

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

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

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

72 I fluorescence compared with traditional NIR fluorescence imaging and thus much deeper penetration de

73 Single-molecule-fluorescence imaging and tracking has been used to measu

74 ic dyes are fundamental for super-resolution fluorescence imaging and tracking methods.

75 sing electrochemical impedance spectroscopy, fluorescence imaging and X-ray photoelectron spectroscop

76 escence molecular tomography, intraoperative fluorescence imaging, and (68)Ga-NODAGA-RGD PET for alph

77 , all-atom MD, analytical modeling, confocal fluorescence imaging, and electron microscopic imaging.

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

79 electrophysiology, confocal and conventional fluorescence imaging, and immunoblotting.

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

81 FP)-tagged chimeric proteins was examined by fluorescence imaging, and the association of the protein

82 ion of the mixed FliG ring was estimated via fluorescence imaging, and the probability of CW rotation

83 Drug delivery was assessed by using fluorescence imaging, and tumor necrosis was quantified

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

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

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

87 Pull-down assays and fluorescence imaging approaches revealed that TSPO physi

88 Confocal Raman microspectroscopy and fluorescence imaging are two well-established methods pr

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

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

91 with a compact, low cost platform for direct fluorescence imaging based on surface plasmon enhanced f

92 evelop a high-resolution and high-throughput fluorescence imaging-based approach for the unbiased map

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

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

95 Using a fluorescence-imaging-based genetic screen, we found that

96 e and accessible method for super-resolution fluorescence imaging, but generating high-quality data i

97 Super-resolution fluorescence imaging by photoactivation or photoswitchin

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

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

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

101 Using two-photon fluorescence imaging combined with patch-clamp in acute

102 Live-cell fluorescence imaging combined with single-particle level

103 ed localization precision in high-resolution fluorescence imaging compared to single organic dyes.

104 Fluorescence imaging confirmed targeting of tumors and l

105 Optical bioluminescence and fluorescence imaging confirmed tumor-specific probe accu

106 An application in single-molecule fluorescence imaging demonstrates the algorithm when app

107 Whole-body fluorescence imaging detected fluorescent signals in the

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

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

110 NIR2, 950-1,400 nm) is promising for in vivo fluorescence imaging due to deep tissue penetration and

111 New developments in super-resolution fluorescence imaging, electron microscopy, and quantitat

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

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

114 uction in surface expression was verified by fluorescence imaging experiments.

115 y pursued by using gamma tracing followed by fluorescence imaging (FI) and, when applicable, blue-dye

116 Fluorescence Imaging (FI) is a powerful technique in bio

117 im of this study was to evaluate the role of fluorescence imaging (FI) using an intraoperative inject

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

119 imaging (BLI) and the respective multicolor fluorescence imaging (FLI) of the iRFPs.

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

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

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

123 sis and highlight the utility of chlorophyll fluorescence imaging for revealing transient stress-indu

124 opathy (LHON) into the mouse germ line using fluorescence imaging for tissue-specific enrichment in t

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

126 al tissue with 3D precision, high-resolution fluorescence imaging has revolutionized biological resea

127 As revealed by near-infrared fluorescence imaging, hyperfibrinolytic mice presented a

128 Fluorescence imaging identified four genomic regions lin

129 Live in vivo fluorescence imaging identified robust, quantifiable and

130 ing is combined with sensitive and versatile fluorescence imaging in a polymeric material for in vivo

131 Fluorescence imaging in deep tissue with high spatial re

132 hown responsible for providing intracellular fluorescence imaging in HepG2 cells.

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

134 ng down a foundation for translating in vivo fluorescence imaging in preclinical noninvasive kidney f

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

136 Fluorescence imaging in synaptopHluorin (spH) mice revea

137 s with large diameters were used for in vivo fluorescence imaging in the long-wavelength NIR region (

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

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

140 Fluorescence imaging in the second near-infrared window

141 Fluorescence imaging in the second near-infrared window

142 In vivo fluorescence imaging in the second near-infrared window

143 of a mouse, which has not been observed with fluorescence imaging in this window before.

144 ombined magnetic resonance and near-infrared fluorescence imaging in vivo.

145 Total internal reflection fluorescence imaging indicated that LFA-1 and both chemo

146 Notably, the post-STEM fluorescence imaging indicated that the bacterial cell w

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

148 Single-molecule fluorescence imaging is a good read-out scheme for compe

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

150 Indocyanine green fluorescence imaging is a surgical tool with increasing

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

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

153 Intraoperative fluorescence imaging is emerging as a highly effective m

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

155 Due to the confocal pinhole, deep tissue fluorescence imaging is not practical.

156 of reporter fluorophores in single-molecule fluorescence imaging is of paramount importance, as it d

157 Calcium indicator fluorescence imaging is one of the main techniques for i

158 Although fluorescence imaging is regularly used for laboratory st

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

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

161 strategy resulted in far less background in fluorescence imaging, it better preserved epitope recogn

162 ipulation, a newly developed single-molecule fluorescence imaging magnetic tweezers nanoscopic approa

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

164 Both radionuclide detection and fluorescence imaging may provide useful information to i

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

166 In the last two decades, fluorescence imaging methods have been developed that re

167 However, traditional fluorescence imaging methods have only limited detection

168 By integrating fluorescence imaging methods we observed evidence for di

169 Using single-molecule fluorescence imaging methods, we have quantified the nat

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

171 ovel near-infrared (NIR), two-photon induced fluorescence imaging modality, which significantly enhan

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

173 ngle photon emission computed tomography and fluorescence imaging/MRI were identified, and targeting

174 e multimodality nanoprobes for near-infrared fluorescence imaging (NIRFI), magnetic resonance imaging

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

176 mouse Y-type ganglion cells with two-photon fluorescence imaging of a glutamate sensor (iGluSnFR) ex

177 Fluorescence imaging of a red fluorescent protein (mStra

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

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

180 Fluorescence imaging of brain slices found that IN admin

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

182 les on the use of nanoparticles in (a) plain fluorescence imaging of cells, (b) targeted imaging, (c)

183 tform for high-resolution, three-dimensional fluorescence imaging of complete tissue volumes that ena

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

185 lytical system was developed that integrates fluorescence imaging of intracellular probes with high-s

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

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

188 ination microscopy allows high-speed 3D live fluorescence imaging of living cellular and multicellula

189 Fluorescence imaging of microfluidic droplets showed the

190 e, we report through-scalp and through-skull fluorescence imaging of mouse cerebral vasculature witho

191 Fluorescence imaging of mouse eyes and fluorescence micr

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

193 tion limit imposed by diffraction and allows fluorescence imaging of nanoscale features.

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

195 on nanotubes (SWNTs) as bacterial probes for fluorescence imaging of pathogenic infections.

196 c phagolysosomes, we herein report "turn-on" fluorescence imaging of phagocytosis with viable bacteri

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

198 oltage-sensitive microelectrodes or confocal fluorescence imaging of plasma membrane PIP2 to characte

199 Using single-molecule fluorescence imaging of quantum dot-labeled TRF1 and TRF

200 Here, we use fluorescence imaging of single cells during hyperosmotic

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

202 Using in vivo two-photon fluorescence imaging of the barrel cortex in fully awake

203 then demonstrate non-invasive through-skull fluorescence imaging of the brain vasculature of murine

204 onstrate nanometre-precision single-molecule fluorescence imaging of the individual motor domains (he

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

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

207 were similar to those obtained from ex vivo fluorescence imaging of transport gradients across the p

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

209 Single-motor total internal reflection fluorescence imaging of YFP-MotB (part of a stator force

210 llowed us to directly compare the ability of fluorescence imaging (of the fluorescent proteins) and q

211 Fluorescence imaging offers expanding capabilities for r

212 by implementing high-sensitivity, wide-field fluorescence imaging on a confocal Raman microscope.

213 n wavelengths: 550 nm for high quantum-yield fluorescence imaging on the one hand and 808 nm for phot

214 ry and Src were formed as observed by direct fluorescence imaging or imaging of an Src kinase sensor

215 In conjunction with fluorescence imaging, our results suggest that even thou

216 Ca(2+) indicator Fluo-4, and imaged using a Fluorescence Imaging Plate Reader Tetra.

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

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

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

220 Nevertheless, fluorescence imaging provides the surgeon with previousl

221 on scattering in this spectral region allows fluorescence imaging reaching a depth of >2 mm in mouse

222 to variable-molecular-weight tags exhibiting fluorescence imaging, reporter, and electrophoresis appl

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

224 or radionuclide detection and intraoperative fluorescence imaging, respectively.

225 Confocal fluorescence imaging revealed facile uptake of functiona

226 Fluorescence imaging reveals polymerases remaining bound

227 Single-cell fluorescence imaging reveals that individual damaged cel

228 oes not require any major change in existing fluorescence imaging setups, only the addition of an app

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

230 Live-cell fluorescence imaging shows dramatic relocalisation of Vi

231 in the absence of syringe pumps and portable fluorescence imaging solutions makes this technology pro

232 oparticle-enhanced MRI and quantum-dot-based fluorescence imaging, sound technologies for intraoperat

233 Recent single-molecule fluorescence imaging studies mostly argue against the ex

234 Fluorescence imaging studies suggest an increase in PLCb

235 g mitochondria, as demonstrated by live cell fluorescence imaging studies.

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

237 Here we describe the Fluorescence Imaging System (FluorIS), based on a consum

238 A point-of-care fluorescence imaging system was used to image ICG fluore

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

240 Here, we present a new fluorescence imaging technique by which single fluoresce

241 on or detection to any environment-sensitive fluorescence imaging technique, the conformational analy

242 Unfortunately, current fluorescence imaging techniques are limited either in pe

243 Unlike conventional fluorescence imaging techniques that usually have a uniq

244 ll interactions can be answered by combining fluorescence imaging techniques with fluorescent protein

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

246 sed a combination of noninvasive chlorophyll fluorescence imaging technology and RNA sequencing to de

247 ment and experimental demonstration of a new fluorescence-imaging technology with a detection range o

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

249 ography, an automated method for whole-organ fluorescence imaging that integrates two-photon microsco

250 These technologies include macroscopic fluorescence imaging that provides contrast enhancement

251 ment of single-molecule and super-resolution fluorescence imaging, the subject of the 2014 Nobel Priz

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

253 al transfection system to the final stage of fluorescence imaging to assay for successful expression

254 Here we studied the potential of fluorescence imaging to detect ccRCC tumors in nude mice

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

256 c example, we demonstrate the feasibility of fluorescence imaging to differentiate this proliferative

257 Here we use single-molecule fluorescence imaging to directly monitor the movement of

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

259 of Raman spectral measurements and confocal fluorescence imaging to interrogate the pharmacological

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

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

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

263 Here, we use single-molecule fluorescence imaging to provide a comprehensive characte

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

265 -proteins, we used total internal reflection fluorescence imaging to study a transmembrane protease,

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

267 and built synthetic nanoprobe combined with fluorescence imaging to study protein-DNA interactions a

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

269 luid cell with STEM, followed by correlative fluorescence imaging to verify their membrane integrity.

270 ical method, named near-infrared II (NIR-II) fluorescence imaging, to image murine hindlimb vasculatu

271 was applied, in conjunction with two-photon fluorescence imaging, to probe the disposition of nanopa

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

273 Electrochemistry and fluorescence imaging tools have been developed to fill t

274 Coral fluorescence imaging tools have the potential to improve

275 bitors, through a combination of single-cell fluorescence imaging, transcriptomics, proteomics, and i

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

277 Live-cell fluorescence imaging validated the selectivity of the an

278 ical properties of FDNs resulted in enhanced fluorescence imaging via improved brightness and/or phot

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

280 Open-field fluorescence imaging was performed preoperatively and du

281 In vivo, ex vivo and microscopic fluorescence imaging was performed.

282 Fluorescence imaging was used to analyze the effectivene

283 Confocal X-ray fluorescence imaging was used to compare Se distribution

284 Fluorescence imaging was used to determine the height an

285 ed physical force measurement with sensitive fluorescence imaging we investigate the complex formed b

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

287 chromatin biochemistry, and single-molecule fluorescence imaging, we developed a novel and sensitive

288 Here, using single-molecule fluorescence imaging, we discover that SA1 displays two-

289 Here, using two-photon calcium fluorescence imaging, we observed the simultaneous dynam

290 ime in vivo imaging and subsequent composite fluorescence imaging, we show a widespread distribution

291 Here using multi-wavelength single-molecule fluorescence imaging, we show that mammalian Cor1B, Cof1

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

293 itro data along with optical bioluminescence/fluorescence imaging were used to validate acquired MSOT

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

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

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

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

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

299 ium oxyanions were characterized using X-ray fluorescence imaging (XFI) and scanning transmission X-r

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