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1 or NAD+ (detected via changes in the protein intrinsic fluorescence).
2 ged), to study the possible changes of their intrinsic fluorescence.
3 was resolved by stopped-flow measurements of intrinsic fluorescence.
4 es being detected that cannot be resolved by intrinsic fluorescence.
5 s (K(d) = 11-12 microm) and changes in FV(a) intrinsic fluorescence.
6 s C by following a decrease in the protein's intrinsic fluorescence.
7 ide at this site would result in a change in intrinsic fluorescence.
8 nctional mutants was also investigated using intrinsic fluorescence.
9 dent denaturation and by iodide quenching of intrinsic fluorescence.
10 s were replaced by Phe residues, eliminating intrinsic fluorescence.
11 ha subunit conformational change detected by intrinsic fluorescence.
12 red mammalian-cell-expressed TIMP-(1-127) by intrinsic fluorescence.
13 uman plasma were characterized by changes in intrinsic fluorescence.
14 ent with the observed spectral properties of intrinsic fluorescence.
15 distinctive circular dichroism features, and intrinsic fluorescence.
16 ld be easily detected in gels based on their intrinsic fluorescence.
17 canning calorimetry, circular dichroism, and intrinsic fluorescence.
18 scanning calorimetry, circular dichroism, or intrinsic fluorescence.
19 by large changes in Stokes radius (11 A) and intrinsic fluorescence (2-fold).
20 y and cross-linking activity, but had little intrinsic fluorescence (370/440 nm).
21 po-forms of CP by far-UV circular dichroism, intrinsic fluorescence, 8-anilinonaphthalene-1-sulfonic
22                       R163K exhibited higher intrinsic fluorescence, a more negative molar ellipticit
23                    Measurement of changes in intrinsic fluorescence allowed determination of a K(d) f
24  this report, we show that extraction of the intrinsic fluorescence allows us: (a) to determine the f
25       Such studies can be complicated by the intrinsic fluorescence and absorbance properties of CheA
26 esponsible for the majority of the protein's intrinsic fluorescence and all of the quenching that acc
27 ange characterized by a 2-fold change in the intrinsic fluorescence and an 11 A change in the Stokes
28  indicated by the substantial enhancement in intrinsic fluorescence and blue shift of fluorescent max
29                       Temperature effects on intrinsic fluorescence and catalytic activity of hTS and
30 the stability of the R subunit was probed by intrinsic fluorescence and circular dichroism (CD) in th
31 major globular protein in kidney beans using intrinsic fluorescence and circular dichroism (CD).
32 ing and end-point structures as indicated by intrinsic fluorescence and circular dichroism, respectiv
33                Using measurements of protein intrinsic fluorescence and circular dichroism, we demons
34 mately 43 degrees C, monitored by changes in intrinsic fluorescence and circular dichroism.
35                                          The intrinsic fluorescence and difference absorption studies
36      Interestingly, spectral probes, such as intrinsic fluorescence and far-UV CD spectroscopy did no
37  oligomerization as determined by changes in intrinsic fluorescence and fluorescence resonance energy
38 nformational changes evidenced by changes in intrinsic fluorescence and in CD spectra and changes in
39                   Rapid decreases in protein intrinsic fluorescence and increases in TNP-ATP fluoresc
40                                              Intrinsic fluorescence and iodide quenching in the prese
41 studied by fluorescence quenching of protein intrinsic fluorescence and nephelometry.
42 ctured, having a similar circular dichroism, intrinsic fluorescence and NMR spectrum as the protein d
43 ce anisotropy of rhodamine-labeled profilin, intrinsic fluorescence and nucleotide exchange, give the
44 matic residues (near-UV circular dichroism), intrinsic fluorescence and peptide binding activity are
45                             The potential of intrinsic fluorescence and principal component analysis
46 mer formation, as demonstrated by changes in intrinsic fluorescence and quantitative native gel elect
47 t-index lens assembly for two-photon excited intrinsic fluorescence and second-harmonic generation im
48  vivo mouse tissue through the collection of intrinsic fluorescence and second-harmonic signal withou
49                                 Importantly, intrinsic fluorescence and sedimentation velocity analys
50  actin (W79) was generated that showed small intrinsic fluorescence and should be useful for studies
51 d by relative changes in iodide quenching of intrinsic fluorescence, and A-loop conformation was rank
52                          Circular dichroism, intrinsic fluorescence, and differential scanning calori
53 nitoring changes in its absorption spectrum, intrinsic fluorescence, and fluorescence of the Nile red
54  were observed by way of circular dichroism, intrinsic fluorescence, and Forster resonance energy tra
55 ion, we investigated plastic hydrophobicity, intrinsic fluorescence, and oligo attachment efficiency.
56 electrophoresis, nuclear magnetic resonance, intrinsic fluorescence, and proteolysis assays of wild-t
57 ere monitored by the changes in the receptor intrinsic fluorescence, and the data are consistent with
58                Return of enzymatic activity, intrinsic fluorescence, and the S1 pocket appeared to oc
59 th a 25% maximal glucose-related decrease in intrinsic fluorescence, and the saturation point was inc
60 ongly blue-shifted emission spectrum, higher intrinsic fluorescence, and weaker energy transfer from
61 ion experiments measuring lambda(max) of the intrinsic fluorescence as a function of guanidine hydroc
62                                           An intrinsic fluorescence assay shows that TH-2/3 also bind
63   Size exclusion chromatography and a simple intrinsic fluorescence assay were used to determine that
64                                 Furthermore, intrinsic fluorescence assays indicated that these metal
65 heme for mutant HIV-1 RT heterodimers, using intrinsic fluorescence assays.
66                        In this method we use intrinsic fluorescence biomarkers and the phasor approac
67 rescence anisotropy of dansyl-labeled GroES, intrinsic fluorescence, bis-ANS binding, sedimentation v
68  dysplastic and nondysplastic BE in terms of intrinsic fluorescence, bulk scattering properties, and
69 ing near-UV circular dichroism, quenching of intrinsic fluorescence by acrylamide and interactions wi
70                             Quenching of the intrinsic fluorescence by DNA and external dynamic quenc
71 ite-specific, ATP-dependent quenching of DNR intrinsic fluorescence by spin labels.
72 further elucidate the molecular basis of the intrinsic fluorescence change (and the source of the slo
73 , nucleotide analogue trapping kinetics, and intrinsic fluorescence changes accompanying nucleotide b
74           In this paper, we demonstrate that intrinsic fluorescence changes can be used to monitor th
75       To examine the structural basis of the intrinsic fluorescence changes that occur during the MgA
76                       GTP gamma S-stimulated intrinsic fluorescence changes were completely abolished
77                          Substrate-dependent intrinsic fluorescence changes were monitored in transpo
78 (2+) to apoFosA alters the UV absorption and intrinsic fluorescence characteristics of the protein su
79 on of HK97 in vitro by monitoring changes in intrinsic fluorescence, circular dichroism (CD), and SAX
80                                        Using intrinsic fluorescence, circular dichroism, and size exc
81  mutants were generated to permit the use of intrinsic fluorescence, circular dichroism, and ultravio
82 g tissue using two- and three-photon-excited intrinsic fluorescence combined with second harmonic gen
83                                              Intrinsic fluorescence combined with UV resonance Raman
84   An unprecedented class of macrocycles with intrinsic fluorescence consisting of phenolic trimers an
85 the assembly dependence of the site-specific intrinsic fluorescence data suggests that the CHC is par
86 ording to hydrogen exchange and stopped-flow intrinsic fluorescence data, unfolding of mAAT appears t
87     The association of activity loss with an intrinsic fluorescence decrease and loss of the S1-pocke
88                              Conversely, the intrinsic fluorescence decrease observed at higher LM pe
89 , induced a blue shift in the lambda(max) of intrinsic fluorescence derived from residues in the cent
90 gnals of aptamer binding to urea in terms of intrinsic fluorescence differences and color changes sim
91                                              Intrinsic fluorescence due to tryptophan of the mutant p
92                  Circular dichroism (CD) and intrinsic fluorescence emission (IFE) spectra of active
93 s dependently on the ionic strength, and the intrinsic fluorescence emission maxima of its single try
94                                          The intrinsic fluorescence emission of each single-Trp mutan
95                               Differences in intrinsic fluorescence emission spectra were observed du
96                                          The intrinsic fluorescence enhancement observed upon binding
97 n nucleotide binding, demonstrating that the intrinsic fluorescence enhancement of smooth muscle myos
98 k, we applied thioflavin T binding, tyrosine intrinsic fluorescence, fluorescence anisotropy measurem
99                                              Intrinsic fluorescence, FRET, and Fourier transform infr
100 ng using fluorescently labeled protein A and intrinsic fluorescence from fluorescein.
101                       We report the enhanced intrinsic fluorescence from several proteins in proximit
102 affinity and specificity) with those of GFP (intrinsic fluorescence, high stability, expression and s
103 reactivity concomitant with disappearance of intrinsic fluorescence (IC(50) approximately 20 microM).
104 ryptase were investigated by analysis of (i) intrinsic fluorescence, (ii) inhibitor binding, and (iii
105                                              Intrinsic fluorescence in proteins is dominated by the t
106 ntributor to nucleotide-dependent changes of intrinsic fluorescence in smooth muscle myosin.
107 beled actin fluorescence or by a decrease in intrinsic fluorescence in the absence of pyrene-labeled
108                                   With their intrinsic fluorescence in the NIR2 regime and lack of ph
109        Candidates for the observed quench of intrinsic fluorescence in W512 KO-MDE include W29 and W3
110 able free amino groups, decreased tryptophan intrinsic fluorescence, increased molecular mass and Ric
111 ndings are as follows: 1) differences in the intrinsic fluorescence indicate that the Trp microenviro
112 ifferent short-chain phospholipids on enzyme intrinsic fluorescence indicates that anionic phospholip
113 M on polyacrylamide gels, differences in the intrinsic fluorescence intensity and solvent accessibili
114                             In addition, the intrinsic fluorescence intensity of C403S is enhanced 3-
115 esterol/POPC large unilamellar vesicles, the intrinsic fluorescence intensity of sPLA2 shows an alter
116         Initial monitoring of changes in the intrinsic fluorescence intensity of vaults showed a 60%
117 ibrium unfolding transition was monitored by intrinsic fluorescence intensity, fluorescence anisotrop
118 unfolding can be monitored directly, because intrinsic fluorescence is quenched by denaturation.
119 nts with Trp at positions 15, 27 and 61, the intrinsic fluorescence is significantly quenched in the
120          Heparin affinity chromatography and intrinsic fluorescence kinetic analyses demonstrated tha
121               We have developed a label-free intrinsic fluorescence lifetime assay that uniquely can
122 red-shift in emission and an increase in the intrinsic fluorescence lifetime for the emitting state i
123                                              Intrinsic fluorescence, limited proteolysis, and molecul
124         This is the first demonstration that intrinsic fluorescence may be used to monitor calcium bi
125 (P = 1.9 x 10(-9)), was associated with skin intrinsic fluorescence measured by SCOUT DS (excitation
126 cellar or micellar state was investigated by intrinsic fluorescence measurement and dynamic light sca
127   Rather, confocal microscopy, SDS-PAGE, and intrinsic fluorescence measurements indicated tight bind
128                                              Intrinsic fluorescence measurements of binding by the pu
129                       Circular dichroism and intrinsic fluorescence measurements revealed significant
130                                              Intrinsic fluorescence measurements revealed that oligom
131                                Far UV CD and intrinsic fluorescence measurements show that this compa
132                                              Intrinsic fluorescence measurements showed that PT-(1-46
133                                              Intrinsic fluorescence measurements suggest the dissocia
134                                              Intrinsic fluorescence measurements suggested that Zn(2+
135                                              Intrinsic fluorescence measurements were performed to me
136 ecific GHS-R1a conformations, as assessed by intrinsic fluorescence measurements.
137     The importance of proton transfer on the intrinsic fluorescence observed in protein fibrils is si
138 ects of loop sequence and loop length on the intrinsic fluorescence of 13 DNA GQSs.
139                                          The intrinsic fluorescence of 3-OST-1 was increased in the p
140 est or, in selected instances, the change in intrinsic fluorescence of a DNA binding agent itself and
141                                          The intrinsic fluorescence of a single tryptophan (Trp-698)
142            In common fluorogenic probes, the intrinsic fluorescence of a small-molecule fluorophore i
143                                              Intrinsic fluorescence of a tryptophan at residue 698 (T
144                                 Here, we use intrinsic fluorescence of a tryptophan located at the di
145 sing two assays, including one that uses the intrinsic fluorescence of a tryptophan residue, we have
146                                    Using the intrinsic fluorescence of all-trans-retinyl esters, noni
147                                          The intrinsic fluorescence of alpha-tocopherol and its effec
148                                          The intrinsic fluorescence of alphaBF61N was marginally lowe
149                                    Using the intrinsic fluorescence of anthralin, rapid accumulation
150 rate that the increases and decreases in the intrinsic fluorescence of antithrombin during heparin bi
151                                              Intrinsic fluorescence of ApoL1 supported the presence o
152 er common peroxidases, (2) monitoring of the intrinsic fluorescence of dityrosine to determine optimu
153 y(G) stimulated proteolysis and quenched the intrinsic fluorescence of EF-3.
154                             Furthermore, the intrinsic fluorescence of fluorobodies correlates with b
155                 Glomerular imaging relied on intrinsic fluorescence of GFP or DsRed, or on whole-moun
156                                          The intrinsic fluorescence of GQSs may be useful for nucleic
157                                          The intrinsic fluorescence of hexokinase in solution (excita
158                   Specifically, by analyzing intrinsic fluorescence of human epithelial tissue as it
159 ine sensing which is based on monitoring the intrinsic fluorescence of in situ synthesized polydopami
160 l as for the determination of Kd's using the intrinsic fluorescence of LT.
161          Using two-photon microscopy and the intrinsic fluorescence of N-retinylamides, we showed tha
162 states by fluorescence quenching analysis of intrinsic fluorescence of native tryptophan (Trp) residu
163 etry and environment of its chromophore, the intrinsic fluorescence of OCP reveals changes in its ter
164 by the ligand urate, which also quenches the intrinsic fluorescence of PecS, indicating a direct inte
165   Two-photon excitation is used to probe the intrinsic fluorescence of peptide fragments through "dee
166 orms a ground-state complex by quenching the intrinsic fluorescence of PPO.
167 eagents, both the enzymatic activity and the intrinsic fluorescence of PR-DeltaPol are linearly depen
168                       We used changes in the intrinsic fluorescence of profilin, CD spectroscopy, and
169                                          The intrinsic fluorescence of smooth muscle myosin is sensit
170 L-1 was studied by monitoring changes in the intrinsic fluorescence of sP-selectin upon binding to sP
171 l biophysical analysis demonstrated that the intrinsic fluorescence of SP600125 changed markedly upon
172                                          The intrinsic fluorescence of Ssa1p's only tryptophan residu
173  altered nucleotide-dependent changes in the intrinsic fluorescence of Ssa1p.
174 ed video-rate imaging of tumors based on the intrinsic fluorescence of SWNTs in the second near-infra
175  sedimentation equilibrium and velocity, and intrinsic fluorescence of the 2 Trp residues.
176                               Basically, the intrinsic fluorescence of the amino acid tryptophan is e
177 sion difference is due to differences in the intrinsic fluorescence of the bound fluorophores rather
178                                          The intrinsic fluorescence of the catalytic portion of the c
179 is was carried out to ascertain the relative intrinsic fluorescence of the enzyme intermediates.
180                                          The intrinsic fluorescence of the intermediate suggested tha
181                  Upon binding of Ca(2+), the intrinsic fluorescence of the mutant decreases approxima
182 x formation is accompanied by an increase in intrinsic fluorescence of the primers, allowing simple a
183                                This used the intrinsic fluorescence of the protein to monitor the che
184 milar changes in the vibrational spectra and intrinsic fluorescence of the protein, which indicates t
185 te and is accompanied by a blue shift in the intrinsic fluorescence of the protein.
186                                          The intrinsic fluorescence of the six tyrosines located with
187                             By utilizing the intrinsic fluorescence of the tryptophan (Trp) and tyros
188                                          The intrinsic fluorescence of the tryptophans could be used
189 termined by titrations of the alterations in intrinsic fluorescence of the variant kringles with the
190 ound; and (c) Trp222 contributes most to the intrinsic fluorescence of the wt-RI-subunit, while Trp18
191                  Mg2+ altered the tryptophan intrinsic fluorescence of this polypeptide whereas Ba2+,
192 e formation in this part of the protein; the intrinsic fluorescence of this tryptophan was found to d
193                                          The intrinsic fluorescence of Tp38 was essentially unaltered
194                                     Thus the intrinsic fluorescence of Trp-11 provides a useful probe
195                      However, changes in the intrinsic fluorescence of truncated and Trp16 mutants up
196 n constant estimated from the changes in the intrinsic fluorescence of tubulin was found to be consis
197                   Spectroscopy examining the intrinsic fluorescence of tyrosine and tryptophan residu
198 o residues of tryptophan, which dominate the intrinsic fluorescence of unlabeled CF1.
199                                  Whereas the intrinsic fluorescence of W36-MDE is only slightly sensi
200                       In this study, we used intrinsic fluorescence of wild type Abeta-(1-40), fluore
201 ese tryptophans was found to account for the intrinsic fluorescence of wild-type actin, indicating th
202 lcium titrations monitored by changes in the intrinsic fluorescence of Y138 in site IV showed that th
203 s study, we investigated measurements of the intrinsic fluorescence of yeast hexokinase as an assay f
204  glutenins and gliadins was analyzed through intrinsic fluorescence parameters, phase diagram method,
205                             In addition, the intrinsic fluorescence polarization increases from 0.327
206 ptophan mutation at position 39 to create an intrinsic fluorescence probe and allow additional charac
207 on dynamics, using 2-aminopurine (Ap) as the intrinsic fluorescence probe and with femtosecond resolu
208 ng, we developed the ds-NIF (nucleoside with intrinsic fluorescence)-probe methodology for detection
209 turbation assay in which a change in the MAb intrinsic fluorescence produced by ligand binding was us
210                        The proteins' similar intrinsic fluorescence properties and corresponding quen
211 nvironment, we have studied the steady-state intrinsic fluorescence properties of the purine and pyri
212 predicted binding to complement C3d and with intrinsic fluorescence properties to enable detection.
213  nm, and after purification, the QDs exhibit intrinsic fluorescence quantum yield efficiencies of 15
214                            Immunological and intrinsic fluorescence quenching assays and the molecula
215 of 0.24 microM for the Efb-C3d binding using intrinsic fluorescence quenching assays.
216                   Isothermal calorimetry and intrinsic fluorescence quenching studies show that oxida
217 nderwent normal, two-stage calcium-dependent intrinsic fluorescence quenching, indicating that a fold
218 g SDS-polyacrylamide gel electrophoresis and intrinsic fluorescence quenching.
219                                              Intrinsic fluorescence, reflectance, and light-scatterin
220 tryptophans at various locations to serve as intrinsic fluorescence reporters, i.e. as topological pr
221                      Whereas the collective, intrinsic fluorescence response of E. coli CPS is largel
222                               Near UV CD and intrinsic fluorescence revealed that the tryptophan resi
223                                              Intrinsic fluorescence showed that wild-type rFV(a2)-C2
224  Previous work, in which the increase in the intrinsic fluorescence signal was used to monitor iron r
225 ignature that was readily separated from the intrinsic fluorescence signature of tumor cells.
226                                  Analysis of intrinsic fluorescence spectra demonstrates that uric ac
227                                              Intrinsic fluorescence spectra for both proteins were al
228 tion coefficient mapping has been applied to intrinsic fluorescence spectra of colonic tissue for the
229                         Then, we extract the intrinsic fluorescence spectra of sites from 35 patients
230 e emission peak, and causes quenching of the intrinsic fluorescence spectra of the proteins.
231                                              Intrinsic fluorescence spectra suggest that the associat
232 cularly, phospholipid/saposin C complexes by intrinsic fluorescence spectral shifts, fluorescence que
233 upon calcium binding, which was confirmed by intrinsic fluorescence spectroscopy and nondenaturing ge
234                                              Intrinsic fluorescence spectroscopy of purified proteins
235 ed from isothermal titration calorimetry and intrinsic fluorescence spectroscopy suggests that YKL-39
236 ptical cancer detection system that combines intrinsic fluorescence spectroscopy, diffuse reflectance
237               The highly sensitive method of intrinsic fluorescence spectroscopy, predicated on the m
238 was monitored by both circular dichroism and intrinsic fluorescence spectroscopy.
239                              Analysis of the intrinsic fluorescence, Stokes radius, thermal stability
240                                              Intrinsic fluorescence studies of the two mutants reveal
241                                              Intrinsic fluorescence studies were conducted to determi
242 d properties such as near- and far-UV CD and intrinsic fluorescence studies.
243 -UV circular dichroism spectrum and a higher intrinsic fluorescence than the heterodimer, demonstrati
244         We have characterized the changes in intrinsic fluorescence that the insulin receptor undergo
245 by monitoring the quenching of the protein's intrinsic fluorescence; the tartronate concentration dep
246 ith pyrene-labeled yeast actin, but not with intrinsic fluorescence, there is an overshoot in the flu
247     With the aid of two PNA analogues having intrinsic fluorescence, thiazole orange (TO)-PNA and [bi
248                                           An intrinsic fluorescence titration of various alpha-LA for
249  properties of rNK1/K1 were investigated via intrinsic fluorescence titration with kringle-specific o
250 spectroscopy, sedimentation equilibrium, and intrinsic fluorescence to monitor the reversible conform
251                       Using a combination of intrinsic fluorescence to report ATP-induced rearrangeme
252 sines to the C-terminal domain of TBP allows intrinsic fluorescence to separately report on the struc
253 rmeability, direct membrane association, and intrinsic fluorescence to study the activities of purifi
254                                 We have used intrinsic fluorescence to test the hypothesis that phosp
255 domain of p53 (p53C) using light scattering, intrinsic fluorescence, transmission electron microscopy
256 n HCT116 cells was measured using the drug's intrinsic fluorescence under conditions that alter pH(i)
257 al pH of 5.6, measurement of the increase in intrinsic fluorescence upon iron release from the recomb
258                                   Changes in intrinsic fluorescence upon nucleotide and inositide bin
259 phans except W512 (W512 KO-MDE) decreases in intrinsic fluorescence upon nucleotide binding, demonstr
260 and 700 MPa, where a significant decrease in intrinsic fluorescence was also observed.
261 ells for intracellular injection using their intrinsic fluorescence was developed.
262 e treatment whereas a noticeable decrease in intrinsic fluorescence was evidenced up to 600 MPa and t
263   A complex, time-dependent change in enzyme intrinsic fluorescence was observed upon exposure to glu
264 targeting and design of assembly inhibitors, intrinsic fluorescence was used to probe assembly-depend
265 g of wild-type RIalpha (wt-RI), monitored by intrinsic fluorescence, was described previously.
266 tains no tryptophan residues and exhibits no intrinsic fluorescence, was harvested from CHO cells cot
267                                 Activity and intrinsic fluorescence were used to measure the stabiliz
268 t protein structural changes, as measured by intrinsic fluorescence, were much slower (t1/2 = 16 min)
269 nding; (b) a temperature-induced increase in intrinsic fluorescence, which reflects formation of a tr
270 yll a molecules, which confer on them a high intrinsic fluorescence yield.

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