コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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
11 lly transparent thin-film electrode chip for fluorescence and absorption spectroelectrochemistry has
17 xyphenyl)squaraine core with bright deep-red fluorescence and excellent photostability, (b) an N-meth
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
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.
29 col for simultaneous dual-channel two-photon fluorescence anisotropy microscopy acquisition to perfor
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,
38 condary ion mass spectrometry (nanoSIMS) and fluorescence-based biorthogonal non-canonical amino acid
41 infrared dye surface modified K(+) NS allows fluorescence-based potassium sensing in the range of 20
43 ng effect of the honey matrix on leptosperin fluorescence but otherwise leptosperin was chemically st
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
48 oscopy, 2) photoconvertible proteins, and 3) fluorescence correlation microscopy, to quantitatively m
50 fluorescence recovery after photobleaching, fluorescence correlation spectroscopy and electron micro
54 HarvestWatch, a system based on chlorophyll fluorescence DCA (DCA-CF), and static controlled atmosph
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
64 were identified by proteomic two-dimensional fluorescence difference gel electrophoresis and mass spe
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
75 nalyzed with conventional methods, including fluorescence, enzymatic assays (ELISA), and quantitative
77 othesis, molecular size distributions of the fluorescence fractions were broad and chromatographicall
79 kinetics, and feasibility for intraoperative fluorescence guidance were investigated in tumor-bearing
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
89 ed sections of the lungs were analyzed using fluorescence imaging, autoradiography, and immunohistoch
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
94 s of genome transcription and replication, a fluorescence in situ hybridization (FISH) protocol was e
96 sitive (HER2+) or -negative (HER2-) based on fluorescence in situ hybridization (FISH)-supplemented i
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
105 ctivity by luminescence, vascular leakage by fluorescence in vivo imaging, histopathological changes
110 with the alum/MNrgp120 vaccine (gp120 median fluorescence intensities [FIs] in infants = 7,118 and in
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
115 was shown that after reaching a maximum, the fluorescence intensity gradually decreased toward longer
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
121 lass I, a higher frequency and a higher mean fluorescence intensity value of C1q-dnDSA at all time-po
124 y to quantify the diffusion, photobleaching, fluorescence intermittency, and photoconversion dynamics
126 When TPE is entrapped in a nanocrystal, fluorescence is emitted when the nanocrystal is opticall
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
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
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
147 or can be used to image PI4KB in cells using fluorescence-lifetime imaging microscopy (FLIM) microsco
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
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
159 visualized at the single-molecule level in a fluorescence microscope upon isothermal amplification an
161 oteins by in vitro total internal reflection fluorescence microscopy (TIRFM) and kinetic and thermody
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
175 d during dielectrophoretic manipulation with fluorescence microscopy making use of their fluorescence
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
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
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
188 Using in vitro total internal reflection fluorescence microscopy, we show that bacterial mini mic
205 ed organs, including calcified bone, but the fluorescence of proteins and immunohistochemical labels
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
210 n demonstrated that the change in tryptophan fluorescence of the Y162W mutant is extremely rapid upon
214 or detecting small differences with standard fluorescence optics, particularly in situations where sa
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
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
226 in conjunction with the membrane-impermeable fluorescence quencher trypan blue to selectively image i
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
232 Cell-cell coupling was assessed by calcein fluorescence recovery after photobleach during intracell
234 number and brightness analysis combined with fluorescence recovery after photobleaching, fluorescence
240 f bacterial enzymes using a highly sensitive Fluorescence Resonance Energy Transfer (FRET) based assa
242 anophotonic zero-mode waveguides (ZMWs) with fluorescence resonance energy transfer (FRET) to resolve
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
250 ator results in a nonenantioselective off-on fluorescence response that is independent of the enantio
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
256 7 azide in vitro showed significantly higher fluorescence signal from (18)F-FDG-treated than untreate
259 ard to intraoperative navigation, a specific fluorescence signal was detected in PSMA-expressing tiss
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
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
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
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
285 PECT/CT and DPA-713-IRDye800CW near-infrared fluorescence to delineate pancreatic, liver, or intestin
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
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-
294 molecular counting results (single-molecule fluorescence voltammetry) indicated a surface-controlled
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
299 merization lies in their ability to minimize fluorescence while enhancing electron transfer rates bet
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。