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1 , are stable in aqueous solution with strong visible absorption.
2 m peroxidase-mediated oxidation based on its visible absorption.
3 to explore other metal clusters with broader visible absorption.
4 gas chromatography-mass spectrometry, and UV-visible absorption.
5 no-naphthalene-1-sulfonic acid fluorescence, visible absorption, activity, and differential scanning
6 l and spectroscopic techniques, including UV-visible absorption and 57Fe Mossbauer spectroscopies, ha
7 ers can be produced at 20 degrees C and have visible absorption and CD spectra identical to the dimer
11 center in azurin has been investigated by UV-visible absorption and electron paramagnetic resonance s
12 a characteristic bathochromic shift of their visible absorption and emission bands by ca. 200 nm comp
13 ay absorption spectroscopy, together with UV-visible absorption and emission spectroscopy, indicates
15 e electrochemical scan cycles as shown by UV-visible absorption and energy dispersive X-ray spectrosc
17 dialysate and retentate were analyzed by UV-visible absorption and high-resolution Orbitrap mass spe
18 fraction, cyclic voltammetry and NMR, and UV-visible absorption and low-temperature luminescence spec
19 litting parameters, respectively) and the UV-visible absorption and magnetic CD spectra are dominated
22 d II) or Compound ES] is characterized by UV-visible absorption and magnetic circular dichroism spect
24 smission Electron Microscopy (TEM), FTIR, UV-Visible absorption and Photoluminiscence (PL) techniques
27 d a [Fe(4)S(4)](2+,+) cluster as shown by UV-visible absorption and resonance Raman studies of the ox
28 atic polycyclic compounds resulted in strong visible absorption and sharp fluorescence with efficient
30 -reduced samples using the combination of UV-visible absorption and variable-temperature magnetic cir
31 -modified forms, using the combination of UV-visible absorption and variable-temperature magnetic cir
34 03 mm/s, DeltaE(Q) = 0.58 +/- 0.03 mm/s), UV-visible absorption, and circular dichroism studies of th
35 g high-performance liquid chromatography, UV-visible absorption, and electron spin resonance spectros
36 ctron microscopy (HRTEM), zeta potential, UV-visible absorption, and photoluminescence spectroscopy.
37 R, resonance Raman, Fourier transform IR, UV-visible absorption, and variable-temperature variable-fi
38 nsitions and accompanying blue-shifts of the visible absorptions, as the ligand pi-systems are extend
39 21G azurin resulted in a species with strong visible absorptions at 350 and 452 nm and a relatively l
40 and we show this species to have a distinct visible absorption band and a transition moment that we
42 ads to a decrease in the magnitude of the UV-visible absorption band at approximately 400 nm that we
44 eaction is observed upon excitation into the visible absorption band of ethidium, higher-energy irrad
47 and others lead to a model in which the two visible absorption bands correspond to GFP in two ground
49 ts bathochromic shifts in both the Soret and visible absorption bands in the presence of Cc and an ab
50 e effect of nonplanar deformations on the UV-visible absorption bands is then probed experimentally w
51 contrast, time-resolved perturbations of the visible absorption bands of L29F and V68L deoxyMb genera
52 iew that the large red shifts seen in the UV-visible absorption bands of peripherally crowded nonplan
53 d or Co 3d --> corrin pi* transitions and by visible absorption bands similar to the corrin pi-->pi*
55 t a qualitative picture of the origin of the visible absorption based on molecular orbital perturbati
56 he switched state as indicated by an intense visible absorption (ca. 530 nm) and near-infrared (ca. 1
58 uestions, in vitro spectroscopic studies (UV-visible absorption/CD, resonance Raman and Mossbauer) ha
59 6-N2 dihedral angle could be consistent with visible absorption changes and the chemical shift differ
64 sfolding of the opsins as observed by the UV/visible absorption characteristics and by separation of
65 catechuate 3,4-dioxygenase (3,4-PCD) with UV/visible absorption, circular dichroism (CD), magnetic CD
68 d forms have been characterized using the UV-visible absorption, circular dichroism, and variable-tem
70 -anilinonaphthalene-1-sulfonic acid binding, visible absorption, copper content, and oxidase activity
71 ing a five points regression graph of the UV-visible absorption data collected at the wavelength of m
72 iquid chromatography (HPLC) with ultraviolet-visible absorption detection and tandem mass spectrometr
77 esults, in combination with complementary UV-visible absorption, EPR, and resonance Raman spectroscop
80 transition of the solvent and the absence of visible absorption features associated with the Mn(II)2
81 and subunit size, amino-acid composition, UV-visible absorption, heme content, pH optimum, inhibitor
82 esonance, mass spectrometry, and ultraviolet-visible absorption identify the enhancer as lumichrome,
83 ow these results may relate to the origin of visible absorption in (Ga(1-x)Zn(x))(N(1-x)O(x)) and its
88 he self-assembly of these molecules using UV/visible absorption, luminescence, and circular dichroism
90 mparison with that of wild-type nNOS with UV-visible absorption, magnetic circular dichroism, and ele
91 BPR, respectively), on the basis of both the visible absorption maxima (530 versus 490 nm) and photoc
92 varying degrees of blue-shift in the flavin visible absorption maxima while visible CD spectra of th
93 rameters obtained from the wavelengths of UV/Visible absorption maxima with solute H-bond parameters
94 S oxygenase domain thus prepared exhibits UV-visible absorption (maxima at 419 and 553 nm, shoulder a
95 a slow light inactivation and a red-shifted visible absorption maximum as compared with the more ext
97 ich are in excellent agreement with previous visible absorption measurements, showing the molecular m
99 scaffold protein has been demonstrated by UV-visible absorption, Mossbauer, and resonance Raman spect
100 tical and spectroscopic methods including UV-visible absorption, Mossbauer, EPR, and HYSCORE spectros
101 ereof were shown to effectively modulate the visible absorption of anthocyanins from strawberry (Frag
102 ipates in proton transfers and regulates the visible absorption of bacteriorhodopsin and its photoint
106 by direct observation of the characteristic visible absorption of the oxidized and inhibited states.
107 imately 1 micros) excited-state lifetime and visible absorption of the sensor simplifies measurements
108 tride (InN) nanocrystals that exhibit both a visible absorption onset ( approximately 1.8 eV) and a s
109 DNA precipitated is accurately determined by visible absorption or fluorescence spectroscopic analyse
110 in reduction was measured either directly by visible absorption or indirectly by coupling ferredoxin
113 The two [4Fe-4S]2+ clusters have similar UV-visible absorption, resonance Raman, and Mossbauer prope
114 een investigated using the combination of UV-visible absorption, resonance Raman, and Mossbauer spect
120 ctroelectrochemical measurements afforded UV-visible absorption spectra for both the radical cations
123 ces, core volumes, (57)Fe isomer shifts, and visible absorption spectra make evident the high degree
126 room temperature was determined from the UV/visible absorption spectra of several pH indicators.
128 ation that is clearly evident in the EPR and visible absorption spectra of the protein and suggests t
129 ured electrochemical redox potentials and UV-visible absorption spectra reveal little or no ground-st
133 Mn(III)SOD from Thermus thermophilus and by visible absorption spectra showing that azide binding to
135 d Schiff base, and the pH-independence of UV-visible absorption spectra suggests that the protonated
137 to contain [2Fe-2S] clusters of which the UV-visible absorption spectra were identical to that of the
138 homolog purified as a homodimer, and the UV-visible absorption spectra were nearly identical to that
140 PP, however, TCPP aggregates below pH 1 have visible absorption spectra which depend on the counterio
141 rhodopsin by the following criteria: (i) UV-visible absorption spectra, (ii) the formation of metarh
142 ncreased rhombicity evident from its EPR and visible absorption spectra, and an increase in distance
149 n both crystal and solution using EPR and UV-visible absorption spectrometry as a function of tempera
150 scopy, electron impact mass spectroscopy, UV visible absorption spectrometry, GC and high pressure li
151 nce liquid chromatography (HPLC)-ultraviolet/visible absorption spectrophotometry (UV/Vis)-mass spect
154 oteins also makes it possible to observe its visible absorption spectroscopic features more clearly.
157 onal theory, nuclear magnetic resonance, and visible absorption spectroscopies provide valuable insig
162 d from purified NirS and characterized by UV-visible absorption spectroscopy and finally identified b
163 ted with pH-dependent resonance Raman and UV-visible absorption spectroscopy and molecular mechanics
164 the acrylic double bond, as indicated by UV-visible absorption spectroscopy and resonance Raman spec
166 inic acid in n-dodecane have been studied by visible absorption spectroscopy and X-ray absorption fin
168 ymes with magnetic circular dichroism and UV-visible absorption spectroscopy in order to determine th
169 ) nanocrystal formation was studied using UV-visible absorption spectroscopy integrated with an autom
171 e photoproduct dynamics by using ultraviolet-visible absorption spectroscopy on the 10(-7)-10(-1) s t
173 extraction followed by HPLC analysis and UV-visible absorption spectroscopy support the above model
175 e exclusion chromatography, (1)H NMR, and UV/visible absorption spectroscopy with cobalt(II) as a spe
176 ingle-crystal x-ray diffraction, ultraviolet-visible absorption spectroscopy, and scanning electron m
179 orm IR difference spectroscopy combined with visible absorption spectroscopy, isotope labeling, and e
180 yl)porphyrins have been investigated with UV-visible absorption spectroscopy, resonance Raman spectro
182 The nanocrystals are characterized using UV-visible absorption spectroscopy, transmission electron m
183 fluorescence microscopy, fluorescence and UV-visible absorption spectroscopy, zeta potential analysis
192 gives rise to a shoulder at 391 nm in the UV/visible absorption spectrum and indicates that the hydro
193 of SRFA in the dialysate had a different UV-visible absorption spectrum and was enriched in low mole
194 litatively similar perturbations of the MTOX visible absorption spectrum are observed for complexes f
197 environmental sensitivity of quercetin's UV-visible absorption spectrum gave information about querc
201 n of the DHOase secondary structure, but the visible absorption spectrum of a Co(2+)-substituted DHOa
202 The PAS instrument is used to measure the UV-visible absorption spectrum of ambient aerosol demonstra
209 llamine (SNAP), indicate a rapid loss of the visible absorption spectrum of the [2Fe-2S] cluster.
212 This yields a significant change in the visible absorption spectrum of the film, with a decrease
213 alently attached to the polypeptide, and the visible absorption spectrum of the mutant protein is ide
217 mol of S (2-) per ApbC monomer and had a UV-visible absorption spectrum similar to known [4Fe-4S] cl
218 n of the C9-linked perylene wire) exhibits a visible absorption spectrum that is the sum of the spect
219 rified N-terminal domain has an identical UV/visible absorption spectrum to the wild-type protein and
222 chromatography (HPTLC) and a characteristic visible absorption spectrum with a peak near 450 nm.
223 ectrum of the chromophores was compared with visible absorption spectrum, and both were deconvoluted.
224 concentrations is in agreement with CPO-II's visible absorption spectrum, which shows no change over
225 ibit intense metal-to-ligand charge-transfer visible absorptions that are red-shifted and more intens
226 buted to the broad, high oscillator strength visible absorption, the ordered molecular packing, and a
227 Further, we investigate the nature of this visible absorption using electron attachment/detachment
228 were investigated using a combination of UV-visible absorption, variable temperature magnetic circul
229 results, taken together with the previous UV-visible absorption, variable temperature magnetic circul
230 ty of methods including electrochemistry, UV-visible absorption, variable temperature photoluminescen
231 e been investigated by the combination of UV/visible absorption, variable-temperature magnetic circul
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