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1 se singular features of the data (e.g. whole fluorescence).
2 ividual virus particles exhibit brighter red fluorescence.
3 lls as an alternative to traditional optical fluorescence.
4  common classifications such as "humic-like" fluorescence.
5 egrated optical pH, oxygen sensors and algal fluorescence.
6 ith AuNPs leading to quenching effect on QDs fluorescence.
7 , protein interactions enhance the molecular fluorescence.
8 independently determined by monitoring the A fluorescence.
9 ally altering cell phenotypes, we employed a fluorescence activated cell sorting method to isolate ke
10 the intrinsic structures of both proteins by fluorescence analyses.
11 lly transparent thin-film electrode chip for fluorescence and absorption spectroelectrochemistry has
12          CO release is chaperoned by turn-on fluorescence and can be triggered by light (405 nm) as w
13 me conformational change was validated by 3D fluorescence and CD spectrum.
14 alysis of tyrosinase with BA was measured by fluorescence and circular dichroism spectroscopy.
15                                       Seeded fluorescence and co-sedimentation studies demonstrate MD
16                  Here, using single-molecule fluorescence and ensemble biophysical techniques, and a
17 xyphenyl)squaraine core with bright deep-red fluorescence and excellent photostability, (b) an N-meth
18 nducting polymer dots (Pdots), which possess fluorescence and mass signals.
19                   The potential of intrinsic fluorescence and principal component analysis (PCA) to c
20 ens in mouse models; and (d) use in affinity fluorescence and super-resolution microscopy.
21 lating column CO2, solar-induced chlorophyll fluorescence, and carbon monoxide observations from mult
22 phy-mass spectrometry, liquid chromatography-fluorescence, and mass spectrometry imaging approaches t
23  of live confocal, total internal reflection fluorescence, and superresolution microscopy, we now sho
24 ia a virtual screen followed by testing in a fluorescence anisotropy assay.
25 this work, we used protein semisynthesis and fluorescence anisotropy assays to explore the interactio
26 n of biomolecular interactions and establish fluorescence anisotropy imaging as a quantitative techni
27 bright internal label in microscopy, and for fluorescence anisotropy measurements of RNA dynamics.
28                                Time-resolved fluorescence anisotropy measurements were used to provid
29 col for simultaneous dual-channel two-photon fluorescence anisotropy microscopy acquisition to perfor
30                                  Here, using fluorescence anisotropy, we report that TRIP8b binding t
31               Applicability of phytoplankton fluorescence as a quick and effective ecological monitor
32 phocholine (DC18:1PC) lipid vesicles using a fluorescence assay for gA channel activity.
33       Using an in vitro optical trapping and fluorescence assay, we found that Kif15 slides anti-para
34  oxidized to resorufinat, with the resorufin fluorescence at 584nm being used to monitor the catalyti
35 ted by visible light irradiation and emitted fluorescence at the NIR region with large Stokes shift,
36                    Potency was assessed by a fluorescence-based assay measuring inhibition of UTP-ind
37 paralleled HOL1 expression, as assessed by a fluorescence-based bioreporter.
38 condary ion mass spectrometry (nanoSIMS) and fluorescence-based biorthogonal non-canonical amino acid
39                                        Using fluorescence-based Ca(2+) flux assays combined with phar
40 cities, is almost exclusively achieved using fluorescence-based detection schemes.
41 infrared dye surface modified K(+) NS allows fluorescence-based potassium sensing in the range of 20
42 2 and 80nM, respectively as calculated using fluorescence binding assays.
43 ng effect of the honey matrix on leptosperin fluorescence but otherwise leptosperin was chemically st
44                                              Fluorescence changes were detected with a high-speed, lo
45 nostructures with moieties for targeting and fluorescence, characterizing their biophysical propertie
46 port the development of an aptamer-initiated fluorescence complementation (AiFC) method for RNA imagi
47                          We used bimolecular fluorescence complementation to show that expression of
48 oscopy, 2) photoconvertible proteins, and 3) fluorescence correlation microscopy, to quantitatively m
49                                 We have used fluorescence correlation spectroscopy and cross-correlat
50  fluorescence recovery after photobleaching, fluorescence correlation spectroscopy and electron micro
51               Here a technique that combines fluorescence correlation spectroscopy and homo-FRET anal
52                                              Fluorescence correlation spectroscopy has been previousl
53 s using an optical trap, and diffusion using fluorescence correlation spectroscopy.
54  HarvestWatch, a system based on chlorophyll fluorescence DCA (DCA-CF), and static controlled atmosph
55      Salt resistance assays, acridine-orange fluorescence dequenching, solid supported membrane-based
56 rodimers of kainate and AMPA receptors using fluorescence-detected sedimentation velocity analytical
57 velocity analytical ultracentrifugation with fluorescence detection has emerged as a powerful method
58 igh-performance liquid chromatography (HPLC)-fluorescence detection of BaP-7,8,9,10-tetraols released
59 tion in living Drosophila embryos using dual-fluorescence detection of nascent transcripts containing
60 phenols in canned energy drinks by UPLC with fluorescence detection, after clean up on molecularly im
61 with coupled coulometric electrochemical and fluorescence detection, and PLP is analyzed by HPLC with
62  detection, and PLP is analyzed by HPLC with fluorescence detection.
63 lel to pH and oxygen sensors with integrated fluorescence detectors.
64 were identified by proteomic two-dimensional fluorescence difference gel electrophoresis and mass spe
65                                              Fluorescence dyes were used in order to characterize the
66                                          The fluorescence emission can be effectively quenched by gol
67                                              Fluorescence emission computed tomography detecting near
68                       In this study, tunable fluorescence emission CQDs originated from chlorophyll w
69  fluorescence microscopy making use of their fluorescence emission in the near IR.
70 persed GQDs that were 2-3nm in size with the fluorescence emission peak of GQDs located at 405nm.
71 based on either visual perception or the raw fluorescence emissions can be masked by background signa
72 ton lifetimes of thermally activated delayed-fluorescence-emitter molecules can be manipulated in the
73                                The augmented fluorescence enhancement by the GNR array can efficientl
74 able substrates with two orders of magnitude fluorescence enhancement.
75 nalyzed with conventional methods, including fluorescence, enzymatic assays (ELISA), and quantitative
76                 Here we describe an enhanced fluorescence fluctuation imaging analysis, which employs
77 othesis, molecular size distributions of the fluorescence fractions were broad and chromatographicall
78      Recent advances in the retrieval of Chl fluorescence from space using passive methods (solar-ind
79 kinetics, and feasibility for intraoperative fluorescence guidance were investigated in tumor-bearing
80                                        After fluorescence imaging and data storage, the fluorophores
81 trics at single-cell resolution by combining fluorescence imaging and deep learning.
82 other techniques, including lower-resolution fluorescence imaging and higher-resolution atomic struct
83 in the cell remains poorly characterized, as fluorescence imaging approaches are limited in the numbe
84    Intravascular 2-dimensional near-infrared fluorescence imaging detected nanoparticles in human cor
85 small studies have shown that intraoperative fluorescence imaging is a safe and feasible method to as
86 detection would save many lives, but current fluorescence imaging probes are limited in their detecti
87       Unexpectedly, we find using time-lapse fluorescence imaging that cdc-42 is not required for epi
88                                   Open-field fluorescence imaging was performed preoperatively and du
89 ed sections of the lungs were analyzed using fluorescence imaging, autoradiography, and immunohistoch
90                        Using single-molecule fluorescence imaging, we demonstrate these sacrificial n
91 gadolinium retention in the tibia with x-ray fluorescence in a laboratory at McMaster University.
92 ped a fluctuation test based on reversion to fluorescence in a set of virally encoded mutant green fl
93                          We observed intense fluorescence in distinct compartments of the protozoa, b
94 s of genome transcription and replication, a fluorescence in situ hybridization (FISH) protocol was e
95                           The development of fluorescence in situ hybridization (FISH) technologies e
96 sitive (HER2+) or -negative (HER2-) based on fluorescence in situ hybridization (FISH)-supplemented i
97                                              Fluorescence in situ hybridization analysis mapped the E
98                           Pyrosequencing and fluorescence in situ hybridization analysis revealed tha
99 fic repositioning events were then tested by fluorescence in situ hybridization during T-cell activat
100 , then barcodes those loci by DNA sequential fluorescence in situ hybridization in fixed cells and re
101   The Accelerate Pheno system uses automated fluorescence in situ hybridization technology with morph
102 ng cell numbers are already available (e.g., fluorescence in situ hybridization, 16-S rRNA gene ampli
103 rding to cytogenetic risk, as assessed using fluorescence in situ hybridization.
104  changes in the accumulation of ENA and VASP fluorescence in their tips over time.
105 ctivity by luminescence, vascular leakage by fluorescence in vivo imaging, histopathological changes
106            MAF amplification was assessed by fluorescence in-situ hybridisation of two cores of breas
107                               Changes of the fluorescence indexes related to tyrosine-like substances
108                               Changes of the fluorescence indexes that correspond to a group of humic
109                     For native BSA/curcumin, fluorescence indicated an enthalpic and entropic driven
110 with the alum/MNrgp120 vaccine (gp120 median fluorescence intensities [FIs] in infants = 7,118 and in
111 llaritis Banff score (P=0.002), and DSA mean fluorescence intensity (P<0.001) after treatment.
112 zation, and achieved 10-fold enhancement in fluorescence intensity compared to a bare glass substrat
113  In all three cases, it is observed that the fluorescence intensity consistently increases with resin
114  nanoparticles (NP-UCNPs) creates changes in fluorescence intensity during rotational motion.
115 was shown that after reaching a maximum, the fluorescence intensity gradually decreased toward longer
116 et molecules to be detected by measuring the fluorescence intensity of each droplet.
117 of the emission spectra of these PTMs to the fluorescence intensity of Trp, to determine semi-quantit
118 per and fluorophore emission spectra and the fluorescence intensity on an imaging system of interest
119                                              Fluorescence intensity profiles measured along the optic
120  emission spectra, thermal quenching ratios, fluorescence intensity ratios, and sensitivity.
121 lass I, a higher frequency and a higher mean fluorescence intensity value of C1q-dnDSA at all time-po
122 specific HLA antibodies (DSA) below 500 mean fluorescence intensity.
123                                              Fluorescence intermittency or blinking is observed in ne
124 y to quantify the diffusion, photobleaching, fluorescence intermittency, and photoconversion dynamics
125                 In addition, intrinsic algal fluorescence is detected to analyze the pesticide concen
126      When TPE is entrapped in a nanocrystal, fluorescence is emitted when the nanocrystal is opticall
127       Because this is a vertical transition, fluorescence is possible.
128 e to the dissolution of the nanocrystal, its fluorescence is quenched.
129                                    A drop in fluorescence is seen as N(tz)AD(+) is converted to N(tz)
130                                    Thus, GFP fluorescence is traced back to an intrinsic chromophore
131                Here using band shift assays, fluorescence Job plots, and yeast three-hybrid assays, w
132  we (i) show that the relative magnitudes of fluorescence (k(0)F), S1 --> S0 nonradiative decay (knr)
133 ight-stressed (NPQ) states, we find that the fluorescence kinetics of both PSI are nearly identical.
134 zed the capillary tufts by combining in vivo fluorescence labeling of endothelial cells, a novel tiss
135 microscope upon isothermal amplification and fluorescence labeling.
136                          The PE detection by fluorescence (lambdaex = 403 nm, lambdaem = 508 nm) occu
137                          Comparatively lower fluorescence levels were demonstrated for skin pretreate
138                                              Fluorescence lifetime analysis showed that mutations wit
139  monitoring kinase activity under two-photon fluorescence lifetime imaging microscopy (2pFLIM).
140           In this work, we employ two-photon fluorescence lifetime imaging microscopy (FLIM) to creat
141 rescent molecular rotors in combination with Fluorescence Lifetime Imaging Microscopy (FLIM) to image
142 raction with beta2 integrins, as revealed by fluorescence lifetime imaging microscopy, leading to int
143                          Spectrally resolved fluorescence lifetime imaging(1-3) and spatial multiplex
144 tly labeled drugs, using fluorophores with a fluorescence lifetime larger than the rotational correla
145  is the demonstration of how high-throughput fluorescence lifetime measurements correlate well to cha
146                                     The mean fluorescence lifetime, taum, was calculated from a 3-exp
147 or can be used to image PI4KB in cells using fluorescence-lifetime imaging microscopy (FLIM) microsco
148 ly correlated with concentrations of the MM1 fluorescence marker leptosperin in honeys.
149 ication of Leptospermum honeys using the MM1 fluorescence marker.
150                                  Chlorophyll fluorescence measurements from the leaves of polyprenol-
151                  By performing time-resolved fluorescence measurements on PSI isolated from Arabidops
152 we report a method involving single-molecule fluorescence measurements to determine the structural pr
153 nce of this PAni-based sensor is compared to fluorescence measurements, and it is shown that similar
154 unfolding of HdeA using NMR spectroscopy and fluorescence measurements, and obtained experimental evi
155 nd circulating tumor cells were detected via fluorescence measurements.
156  of the ER biomimetic was characterized with fluorescence micrographs and temperature-dependent fluor
157 g distance, and large field of view confocal fluorescence microscope (H(2)L(2)-CFM) with the capabili
158        We test this custom designed confocal fluorescence microscope for future use with brain clarif
159 visualized at the single-molecule level in a fluorescence microscope upon isothermal amplification an
160           Compatible with readily accessible fluorescence microscopes, these easy-to-use membrane DNA
161 oteins by in vitro total internal reflection fluorescence microscopy (TIRFM) and kinetic and thermody
162                                  Advances in fluorescence microscopy and calcium sensitive dyes has l
163                                        Using fluorescence microscopy and cryo-electron tomography, we
164                                        Using fluorescence microscopy and electron tomography, we find
165                                              Fluorescence microscopy and quantitative reverse transcr
166 his meshwork using live-cell superresolution fluorescence microscopy and spatio-temporal image correl
167 istent with similar measurements by confocal fluorescence microscopy and subcellular fractionation of
168                         Here the authors use fluorescence microscopy approaches to directly visualize
169                                 Steady state fluorescence microscopy cannot distinguish the drug from
170                                    Motorized fluorescence microscopy combined with high-throughput mi
171                                              Fluorescence microscopy demonstrated intense labelling o
172                                              Fluorescence microscopy experiments showed that I2 coloc
173                                For instance, fluorescence microscopy faces a 'colour barrier', owing
174                                     Confocal fluorescence microscopy images of the perpendicular and
175 d during dielectrophoretic manipulation with fluorescence microscopy making use of their fluorescence
176 a combination of atomic force microscopy and fluorescence microscopy of live cells.
177                                     Confocal fluorescence microscopy showed that a fraction of HCF222
178 rs to biological questions obtained via live fluorescence microscopy substantially affected by photot
179 roparticles, in both cases using light-sheet fluorescence microscopy to optically access the intestin
180         We combine Nomarski and multichannel fluorescence microscopy to study processes such as cell-
181 tions were observed in real time by confocal fluorescence microscopy using a Bodipy fluorogenic subst
182 rotome sectioning, differential staining and fluorescence microscopy were used to visualize patterns
183 al targeting, we used quantitative live-cell fluorescence microscopy, and compared the effects of the
184                As an extension of wide-field fluorescence microscopy, it is inherently capable of mul
185   Using dual-color total internal reflection fluorescence microscopy, we demonstrate complex formatio
186 By examining replisomes in live E. coli with fluorescence microscopy, we found that the Pol III* suba
187        Using multiwavelength single-molecule fluorescence microscopy, we observed the dynamics of Gre
188     Using in vitro total internal reflection fluorescence microscopy, we show that bacterial mini mic
189                                              Fluorescence microscopy-based in vitro reconstitution as
190 es that enable singe-molecule detection with fluorescence microscopy.
191 taken up by cells and could be visualized by fluorescence microscopy.
192  the resulting molecular self-assembly using fluorescence microscopy.
193 mputed tomography (CT), autoradiography, and fluorescence microscopy.
194 their subcellular location in the plastid by fluorescence microscopy.
195 n and oxidation is imaged by single-particle fluorescence microscopy.
196 l assay of (99m)Tc activity were detected by fluorescence mode imaging.
197                            The mechanism for fluorescence modulation in these sensors has been attrib
198         This further supports the claim that fluorescence modulation is not primarily a result of bin
199 s and improve the theranostic application of fluorescence molecular imaging.
200  in normal organs, as shown by near-infrared fluorescence (NIRF) imaging.
201                                    Intrinsic fluorescence of ApoL1 supported the presence of a signif
202 operates based on the signal response in the fluorescence of CdTe@CdS quantum dots (QDs).
203 rity is necessary to observe single-molecule fluorescence of GFP.
204 und-state complex by quenching the intrinsic fluorescence of PPO.
205 ed organs, including calcified bone, but the fluorescence of proteins and immunohistochemical labels
206 oped that made use of the natural tryptophan fluorescence of proteins.
207 ng, which included the decay kinetics of the fluorescence of the miRNA sensors, demonstrated that miR
208 get nucleic acid by digitizing the end-point fluorescence of the parallel micro-PCR reactions, using
209                                          The fluorescence of the QDs is inversely correlated to the C
210 n demonstrated that the change in tryptophan fluorescence of the Y162W mutant is extremely rapid upon
211                                              Fluorescence of Trp, its derivatives and argpyrimidine (
212 ine and spermidine, which results to restore fluorescence of Tyr on the surfaces of Au NPs.
213                                       In the fluorescence operation mode, the platform can attain the
214 or detecting small differences with standard fluorescence optics, particularly in situations where sa
215                    The time evolution of Hyp fluorescence originating from Hyp monomers dissolved in
216 ics associated with changes in the yields of fluorescence, photochemical (PhiPSII), and nonphotochemi
217 his approach, which is based on steady-state fluorescence polarization (FP) spectroscopy, kinetically
218 ed actin filament order in human cells using fluorescence polarization microscopy and found that clea
219 opy, leveraging molecular tension probes and fluorescence polarization microscopy to measure the magn
220  integrin head, and measure orientation with fluorescence polarization microscopy.
221 chlorins were prepared and their optical and fluorescence properties were determined in organic solve
222 ethod for RNA imaging by engineering a green fluorescence protein (GFP)-mimicking turn-on RNA aptamer
223 the duplex fluorescent output [green and red fluorescence proteins] allowed measurement of biosensor
224       High-resolution images of the stilbene fluorescence provided by macroscopy were supplemented by
225 d emission (706-707 nm), but also the lowest fluorescence quantum yields.
226 in conjunction with the membrane-impermeable fluorescence quencher trypan blue to selectively image i
227 nthophyll can efficiently induce chlorophyll fluorescence quenching in PSI.
228                                              Fluorescence quenching measurements revealed that the l-
229 results show that it is possible to overcome fluorescence quenching when functionalizing diamondoids
230   The phase transition is only observable by fluorescence quenching within a window of pH and in the
231                                              Fluorescence-RBT (FluoRBT) combines magnetic tweezers, i
232   Cell-cell coupling was assessed by calcein fluorescence recovery after photobleach during intracell
233                                        Using fluorescence recovery after photobleaching analysis, we
234 number and brightness analysis combined with fluorescence recovery after photobleaching, fluorescence
235 scence micrographs and temperature-dependent fluorescence recovery after photobleaching.
236  getting distance from AuNPs which result in fluorescence recovery.
237       Real-time imaging with reporter enzyme fluorescence (REF) that uses custom fluorogenic substrat
238 R700 fluorescent signal based on macroscopic fluorescence reflectance imagery.
239       However, in applications where a small fluorescence reporter is required or desirable, the choi
240 f bacterial enzymes using a highly sensitive Fluorescence Resonance Energy Transfer (FRET) based assa
241                                      Using a fluorescence resonance energy transfer (FRET) biosensor,
242 anophotonic zero-mode waveguides (ZMWs) with fluorescence resonance energy transfer (FRET) to resolve
243                                        While fluorescence resonance energy transfer (FRET)-based sens
244  quenched by gold nanoparticles (Au NPs) via fluorescence resonance energy transfer (FRET).
245 ed these mutants in cells with time-resolved fluorescence resonance energy transfer and death assays,
246  extensively used as donor-acceptor pairs in fluorescence resonance energy transfer experiments, espe
247                  Here, using single-molecule fluorescence resonance energy transfer imaging, we exami
248                              Using live-cell fluorescence resonance energy transfer studies, we demon
249 ion between the proteins was confirmed using fluorescence resonance energy transfer.
250 ator results in a nonenantioselective off-on fluorescence response that is independent of the enantio
251 t in which the sensor does not aggregate, no fluorescence response to fructose was observed.
252                                              Fluorescence sensors are useful tools for the non-destru
253 ynthesis platform for the development of new fluorescence sensors with high selectivity for chloride.
254 ace using passive methods (solar-induced Chl fluorescence, SIF) promise improved mapping of plant pho
255 ho-FF-Van results in a significant increased fluorescence signal at the MRSA infected site.
256 7 azide in vitro showed significantly higher fluorescence signal from (18)F-FDG-treated than untreate
257                                              Fluorescence signal from the reporter gene was detected
258  expression dynamics and effectively reduces fluorescence signal in growing cells.
259 ard to intraoperative navigation, a specific fluorescence signal was detected in PSMA-expressing tiss
260                     Quantitative analysis of fluorescence signals from cells reacted with fluorescent
261 illustrate a quantitative approach to relate fluorescence signals to malignant tissues and improve th
262 ing and ultrafast spectroscopic detection of fluorescence signals were developed for monitoring the r
263  algorithm utilizing chromaticity to analyze fluorescence signals, which improves the discrimination
264 er ablation plume and saturation behavior of fluorescence signals.
265 inserted into the dsDNA, generating enhanced fluorescence signals.
266                                          The fluorescence spectra indicate that the singlet excited s
267 verse centimetres) and featureless nature of fluorescence spectra that limits the number of resolvabl
268  by the patterned sensor can be converted to fluorescence spectra with high signal-to-noise ratio and
269 Grazing incidence and grazing emission X-ray fluorescence spectroscopy (GI/GE-XRF) are techniques tha
270 ce of dithiolthreitol is measured using both fluorescence spectroscopy and single droplet paper spray
271                  The potential of front-face fluorescence spectroscopy combined with second-order che
272                  These findings suggest that fluorescence spectroscopy could offer a rapid and high-t
273                    In this study, label-free fluorescence spectroscopy was used for the first time to
274 s different metal ions was investigated with fluorescence spectroscopy, amongst them Fe(3+) ions show
275 es in red wine were identified by Front-Face fluorescence spectroscopy, and the emission intensity tr
276 olding kinetics of a model OMP (tOmpA) using fluorescence spectroscopy, native mass spectrometry, and
277 uelva", were analyzed by excitation-emission fluorescence spectroscopy.
278 mass spectrometry (hydrophilic fraction) and fluorescence spectroscopy.
279  ADPH cycle can be monitored in real time by fluorescence spectroscopy.
280 teady-state and time-resolved absorption and fluorescence spectroscopy.
281 imple quantitative framework to select a low-fluorescence substrate that minimizes both the overlap o
282 are also proved to exhibit very clean on/off fluorescence switching properties for polar volatile org
283                                        As 3D fluorescence techniques are commonly applied to diverse
284                     The relative decrease in fluorescence through drug inhibition is characterized us
285 PECT/CT and DPA-713-IRDye800CW near-infrared fluorescence to delineate pancreatic, liver, or intestin
286  future research directions linking spectral fluorescence to photosynthesis, PhiPSII, and NPQ.
287  cross sections as characterized by confocal fluorescence tomography.
288 ly used as a dual probe for colorimetric and fluorescence turn-on assays of spermine and spermidine i
289 escribe an innovative method for a universal fluorescence turn-on enzyme assay, which relies on the t
290 art probes with tunable reaction rates, high fluorescence turn-on ratio, and easy access.
291 Cs has led to a focus on multiply-scattered, fluorescence, two-photon, and phase imaging techniques t
292  a low power benchtop total reflection X-ray fluorescence (TXRF) system has been developed for multi-
293 phore complex exhibits strong and consistent fluorescence under an excitation wavelength.
294  molecular counting results (single-molecule fluorescence voltammetry) indicated a surface-controlled
295                   Here, localized CL-induced fluorescence was detected in the tumors and remained sig
296 etween the electrochemical processes and the fluorescence was found during potentiostatic or multipul
297 anoFACS measurements of light scattering and fluorescence, we evaluated the sensitivity and specifici
298                 By following the loss of GFP fluorescence, we were able to observe the cells that had
299 merization lies in their ability to minimize fluorescence while enhancing electron transfer rates bet
300                                        X-ray fluorescence (XRF) microscopy, quantified with elemental

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