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1 mostly depolarized over the majority of the emission spectrum.
2 th resulting color changes and shifts in the emission spectrum.
3 ompared to a bare organic material in a wide emission spectrum.
4 bsorption spectrum of the cell and the solar emission spectrum.
5 was recorded at 535 nm, the peak of the YFP emission spectrum.
6 at a single wavelength near the peak of the emission spectrum.
7 ncrease in the magnitude of the fluorescence emission spectrum.
8 also the dominant fluorophore of the native emission spectrum.
9 m red-shifted intrinsic protein fluorescence emission spectrum.
10 by a blue shift in the band position of the emission spectrum.
11 of ligand binding and return to the initial emission spectrum.
12 he solution, resulting also in change of its emission spectrum.
13 l molecular fingerprints in their long-lived emission spectrum.
14 ed iron K line and Compton hump in the X-ray emission spectrum.
15 otein pair and alteration of the fluorescent emission spectrum.
16 on in the Lamb-Dicke regime with sub-Doppler emission spectrum.
17 ing there a 'squeezed' narrowband near-field emission spectrum.
18 al (3D) imaging for four dyes 10 nm apart in emission spectrum.
19 aphene and substrate can be used to tune the emission spectrum.
20 ent, allowing for wavelength shifting of the emission spectrum.
21 the PpIX spectral signature in the collected emission spectrum (0.014-0.041 mug/ml in phantoms), and
22 random lasers often have a relatively broad emission spectrum, a random laser that utilizes vibratio
23 ed from hot objects is to tailor the thermal emission spectrum according to the desired application.
24 ganic light emitting diode (OLED), having an emission spectrum adapted to algal absorption spectrum a
25 anoparticles (UCNPs) were customized with an emission spectrum aligned to flavin absorption and conju
26 m with the blue most spectral feature of the emission spectrum allows an unambiguous assignment of th
29 n to be topotecan from the similarity of the emission spectrum and decay times observed for one-photo
30 thod enables on-demand, low-power control of emission spectrum and nanoscale localization of color ce
31 substitutions are commonly used to shift the emission spectrum and optimize luminescent properties, b
32 ding to characteristic Rabi splitting of the emission spectrum and providing the first example of an
33 bstrate binding leads to a blue shift in the emission spectrum and reduction in accessibility to pola
34 nt, Arg-144 --> Lys cause a red-shift in the emission spectrum and render the fluorophore more access
35 ngths near voltage-sensitive portions of the emission spectrum and shifts in the complete emission sp
36 nt of novel thermal sources that control the emission spectrum and the angular emission pattern is of
37 solar cells, the mismatch between the Sun's emission spectrum and the cells' absorption profile limi
40 t output versus drive current, with a narrow emission spectrum and the formation of a beam above the
41 c properties of nile red to extract both the emission spectrum and the position of each dye molecule
42 Receptor 2 exhibits a dual monomer-excimer emission spectrum and undergoes a remarked ratiometry in
43 e redox potential of the ferrocene unit, the emission spectrum, and a noticeable color change from ye
44 sensitivity limit (8.51 kBq/muL for (68)Ga), emission spectrum, and ex vivo and in vivo examples are
45 reened for relative light output, a shift in emission spectrum, and glow-type light emission kinetics
46 We simultaneously observe PL brightness, emission spectrum, and in-plane excitation dipole orient
48 py, quantum yield, and center of mass of the emission spectrum are consistent with the movement of th
49 nt and a 2 nm blue-shift in the fluorescence emission spectrum are consistent with tryptophan residue
50 orption spectrum emulating that of the solar emission spectrum are ideal, given that such combination
52 nergy distribution and the band shape of the emission spectrum are related to the nature of the 4f-5d
54 to use their characteristic, size-dependent emission spectrum as optical barcode but so far there is
55 aging has been hampered by its 481 nm peaked emission spectrum, as blue wavelengths are strongly atte
59 ation at 547 nm yields a glutamate-dependent emission spectrum between 550 and 700 nm that can be exp
60 g emission in the fluorescence line-narrowed emission spectrum can be accounted for, in part, by the
62 micontinuous films, and thus the fluorescent emission spectrum, can be controlled and significantly i
63 referencing, pH-sensitive dye SNAFL-1, whose emission spectrum changes at lambda = 550 in response to
67 d on assembly state-dependent changes in the emission spectrum demonstrated cell proliferation rate-d
69 ssion band fluorescent molecular rotor (FMR) emission spectrum displays a second peak at 620 nm, whic
70 device, suggested the AuI does not quell the emission spectrum for either the triple cation or the MA
71 ort ground-based observations of the dayside emission spectrum for HD 189733b between 2.0-2.4 microm
72 ctam ring in CCF2, changing its fluorescence emission spectrum from green (520 nm) to blue (447 nm) a
73 ed-E5, a fluorescent protein that shifts its emission spectrum from green to red over time, was expre
76 formed from above two reactions a bright CL emission spectrum having two peaks (518 nm for fluoresce
77 site, DC6C displayed a strongly blue-shifted emission spectrum, higher intrinsic fluorescence, and we
78 F80W:V21K also shows a shifted fluorescence emission spectrum in both di(C18:1)PC and di(C18:1)PA an
79 ction phenotype, and a shift in fluorescence emission spectrum in di(C18:1)PC not reversed in di(C18:
80 t in a significant shift in the fluorescence emission spectrum in dioleoylphosphatidylcholine [di(C18
82 units of AA Tauri possesses a rich molecular emission spectrum in the mid-infrared, indicating a high
83 the descriptors could be used to predict the emission spectrum in the NIR-II region only if DeltaE(gs
84 nifit displays a GABA-dependent fluorescence emission spectrum in the range of 500-700 nm that permit
86 ow for the control and tuning of the thermal emission spectrum in the wavelength regime from [Formula
88 max) = 499 nm) matches the photoluminescence emission spectrum, indicating that the emission is from
90 itio calculations, that the structure of the emission spectrum is attenuated by the presence of coher
96 ntally that the 1b(1) splitting in the x-ray emission spectrum is related to dynamics and is not evid
97 uorescent fatty acid analogue Laurdan, whose emission spectrum is sensitive to structural differences
98 laced by a dye molecule (coumarin 102) whose emission spectrum is sensitive to the local electric fie
99 ation of both TPrA and Al(HQS)3, and the ECL emission spectrum (lambda(max) = 499 nm) matches the pho
100 Our data show an anomalous dependence of emission spectrum, lifetimes, and quantum yield (QY) on
101 atively low quantum efficiencies and a broad emission spectrum, limiting potential applications.
103 d product displays blue fluorescence with an emission spectrum matching the bioluminescence spectrum
104 llows for resolution of subcomponents of the emission spectrum not previously possible at room temper
108 to unassembled tubulin was observed, but the emission spectrum of 2-AB-PT in the presence of the tubu
110 nt changes in the intensity and shape of the emission spectrum of [K(7)(NBD),Nle(12)] alpha-factor du
112 ploit this 'self-mixing' effect to infer the emission spectrum of a semiconductor laser using a laser
115 on of individual granules also resembles the emission spectrum of A2E, but the spectrum of individual
116 the very strong spectral overlap between the emission spectrum of benzimidazole (energy donor) and th
119 d characteristic changes in the fluorescence emission spectrum of dansyl-calmodulin, and had an appar
120 ed characteristic shifts in the fluorescence emission spectrum of dansyl-CaM, with apparent affinitie
123 Using intrinsic tryptophan fluorescence emission spectrum of ECD2 polypeptide and fluorescence a
124 or substitutions that alter the fluorescence emission spectrum of environmentally sensitive fluoresce
125 canning by exploiting the position-dependent emission spectrum of fluorophores above a simple biocomp
133 iloelectronvolts has long been sought in the emission spectrum of microquasars as evidence for the ex
137 rescence spectroscopy performance (i.e., the emission spectrum of rhodamine 6G can be acquired with g
138 e components (dark, shot, and flicker), (ii) emission spectrum of the analyte, (iii) emission spectru
139 ylation resulted in an 8-nm red-shift of the emission spectrum of the attached IAANS probe and a redu
141 ce of Mg(2+); in the presence of Mg(2+), the emission spectrum of the CheA(F455W):ATP complex was red
142 c)(4)](-) absorption spectrum and in the f-f emission spectrum of the Cm(III) mellitate upon pressuri
143 charge-coupled device detector monitors the emission spectrum of the coil, which includes the dark l
146 W subcomplex indicates that the fluorescence emission spectrum of the enzyme is maximally perturbed w
147 of the substrate overlapped the fluorescence emission spectrum of the enzyme, these abnormalities wer
151 een reported that shifts in the fluorescence emission spectrum of the introduced tryptophans in the b
153 the tubulin-colchicine complex resembled the emission spectrum of the ligand bound to microtubules.
154 e that ET is not dependent on overlap in the emission spectrum of the luminophore and the absorption
156 (ii) emission spectrum of the analyte, (iii) emission spectrum of the optical background, and (iv) tr
157 extractions, the nature of the fluorescence emission spectrum of the PEG phase after extraction was
159 and H(2)O absorption features in the thermal emission spectrum of the planet measured by the James We
163 - and far-UV CD spectra, in the fluorescence emission spectrum of the single tryptophan residue at po
164 intensity and blue-shift of the fluorescence emission spectrum of the single tryptophan residue of th
167 proach is the voltage-dependent shift in the emission spectrum of the voltage-sensitive dye di-8-buty
170 e (TL), OSL, radioluminescence (RL), and OSL emission spectrum of this new material and carried out a
174 a pronounced blue shift in the fluorescence emission spectrum of wild type MBP and a peak at about 2
175 ing produced a red shift in the fluorescence emission spectrum of wild type MBP and a sharp hypochrom
178 h ultraviolet B from lamps that have a broad emission spectrum or, more effectively, with lamps that
180 ties (including lifetime, quantum yield, and emission spectrum) over time or in different chemical en
181 luorescent molecules of the same type if the emission spectrum overlaps with the absorption spectrum.
182 iguing phenomena, such as the Mollow-triplet emission spectrum, photon antibunching and coherent phot
183 ters its intrinsic (tryptophan) fluorescence emission spectrum, providing a strong indication that li
186 large unilamellar lipid vesicles (LUVs), its emission spectrum shifts up to 30 nm to the blue with in
187 e, in the H117T mutant the 77-K fluorescence emission spectrum shows a much smaller amplitude at 695
188 this fluorophore is the observation that its emission spectrum shows near-zero overlap with the absor
189 metry of inhibition for thrombin and gave an emission spectrum that discriminated between native, cle
190 resence of 0.05 mol % CdS QDs, which have an emission spectrum that overlaps the absorption spectrum
191 l below the peak wavelength of the blackbody emission spectrum, the radiative heat flux increases by
192 m to long lifetime species with blue-shifted emission spectrum; the activation energy for nonradiativ
193 from short lifetime species with red-shifted emission spectrum to long lifetime species with blue-shi
194 orescence emission significantly, shifts the emission spectrum to shorter wavelengths, and also induc
197 vity of unstructured metals, resulting in an emission spectrum useful for solar thermophotovoltaics.
198 th recordings, or from opposite sides of the emission spectrum, varied linearly with the amplitude of
199 on of the polymer, leading to changes in the emission spectrum via Forster Resonance Energy Transfer
200 served, but the low-temperature fluorescence emission spectrum was drastically altered in the mutants
201 amatic spectral shifts in the absorption and emission spectrum wavelengths with added donor groups ar
202 emission spectrum and shifts in the complete emission spectrum were determined for emission from plas
203 apoA-I that exhibits a distinct fluorescence emission spectrum when in different states of lipid asso
204 ft manifests as a resonance splitting in the emission spectrum, which can be detected as a beat frequ
205 sing absorption profiles coinciding with the emission spectrum, which together fundamentally limit th