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1 olecular weight, amino acid composition, and circular dichroism spectra.
2 ty, the complexes afford nearly mirror image circular dichroism spectra.
3 s judged by their similar near-UV and far-UV circular dichroism spectra.
4 termined by TD-DFT simulations of electronic circular dichroism spectra.
5 ut major structural changes, as evidenced by circular dichroism spectra.
6 n dependence for MALDI H/D exchange data and circular dichroism spectra.
7  in the 1D-IR (FTIR), 2D-IR, and vibrational circular dichroism spectra.
8 25 degrees C as indicated by near and far UV circular dichroism spectra.
9 t the same site but had little effect on the circular dichroism spectra.
10  absorption maxima, and (d) a sigmoid-shaped circular dichroism spectra.
11 scape reproduced the experimental electronic circular dichroism spectra.
12 Naturally Disordered Regions) prediction and circular dichroism spectra.
13 simulation of the electronic and vibrational circular dichroism spectra.
14 om a split-type Cotton effect in vibrational circular dichroism spectra.
15 yers as alpha-helices, as reflected in their circular dichroism spectra.
16 - or A-type structures on the basis of their circular dichroism spectra.
17 n of experimental and theoretical electronic circular dichroism spectra.
18 iparallel orientations, these showed similar circular dichroism spectra.
19 ed by thermal denaturation, mixing data, and circular dichroism spectra.
20 al data and their exciton UV-vis and induced circular dichroism spectra.
21 ical Rel transcription factors, as judged by circular dichroism spectra.
22   On the basis of the investigation of their circular dichroism spectra, all of the hairpins investig
23                                              Circular dichroism spectra also supported these evidence
24                                              Circular dichroism spectra analyses indicated only minor
25  and the variable region an extended "tail." Circular dichroism spectra analysis determined that the
26 esemble the wild type enzyme as indicated by circular dichroism spectra and are tetramers.
27                                              Circular dichroism spectra and biological assays of the
28  into the ternary complex as demonstrated by circular dichroism spectra and calorimetry.
29                                              Circular dichroism spectra and chemical cross-linking of
30                                              Circular dichroism spectra and chemical footprinting exp
31                                              Circular dichroism spectra and chromatographic informati
32                                              Circular dichroism spectra and chymotrypsin digestion ex
33     The experimental absorption, linear, and circular dichroism spectra and dephasing rates are recov
34 strated by a characteristic red shift in the circular dichroism spectra and dramatic NMR spectral cha
35                                  By in vitro circular dichroism spectra and fluorescence quenching, w
36                            Comparison of the circular dichroism spectra and kinetic properties of the
37                    Thermodynamic parameters, circular dichroism spectra and NMR data are presented fo
38  was proved by the comparison of the NMR and circular dichroism spectra and of the specific optical r
39                                          The circular dichroism spectra and other properties of these
40                                              Circular dichroism spectra and size-exclusion chromatogr
41                                              Circular dichroism spectra and thermal denaturation expe
42                                              Circular dichroism spectra and thermal stability analysi
43 ng or non-encysting cells, the change in its circular dichroism spectra and up to a 6-fold increase i
44                      Slight perturbations in circular dichroism spectra and weakened self-association
45                                     Oriented circular dichroism spectra and x-ray diffraction pattern
46       Examination of their melting behavior, circular dichroism spectra, and fluorescence properties
47  circular dichroism spectra, far-ultraviolet circular dichroism spectra, and infrared spectra in 1H2O
48 elative susceptibilities to proteolysis, UV, circular dichroism spectra, and temperature melting tran
49  evidenced by altered fluorescence emission, circular dichroism spectra, and ultracentrifugal analysi
50 ry structure content as determined by far-UV circular dichroism spectra, and urea-induced denaturatio
51 obtained optical rotation values, electronic circular dichroism spectra, and vibrational circular dic
52                                              Circular dichroism spectra are consistent with B-form DN
53                                              Circular dichroism spectra are consistent with the helic
54 intramonomer nuclear Overhauser effects, and circular dichroism spectra are consistent with transient
55                 Thermodynamic parameters and circular dichroism spectra are presented for RNA hairpin
56                                              Circular dichroism spectra are reported to show that, in
57                                        Since circular dichroism spectra are similar for wild type, H3
58 these proteins appear to be folded and their circular dichroism spectra are similar to those of their
59 in is supported by electronic absorption and circular dichroism spectra, as well as equilibrium analy
60 ady-state absorption, photoluminescence, and circular dichroism spectra, as well as transmission elec
61                                              Circular dichroism spectra at the two pH conditions show
62                                              Circular dichroism spectra at various temperatures indic
63 s end, we have measured the fluorescence and circular dichroism spectra at wavelengths of >300 nm for
64  spherical structures with silent electronic circular dichroism spectra but which fluoresce.
65 Lys42, Ile190, and Gly191 do not perturb the circular dichroism spectra, but have significant effects
66 ha-helix, as estimated by measurement of the circular dichroism spectra, but the region of the propep
67 fects of different end sequences on melting, circular dichroism spectra (CD), and enzyme binding prop
68 cts of different end sequences on stability, circular dichroism spectra (CD), and enzyme binding prop
69 de comprising Tyr-553 through Ile-563 showed circular dichroism spectra characteristic of alpha-helix
70                         These fragments show circular dichroism spectra characteristic of helical pro
71 ons of a strong denaturant nearly attain the circular dichroism spectra characteristic of random coil
72 ility relative to the unlabeled control, and circular dichroism spectra confirm B-form helical DNA st
73                                              Circular dichroism spectra confirm that the global confo
74                                              Circular dichroism spectra confirm that these molecules
75 rmed with a smaller entropic penalty feature circular dichroism spectra consistent with a non-compact
76 aggregates exhibit classical beta-sheet-rich circular dichroism spectra consistent with an amyloid-li
77 ch the optical response between two distinct circular dichroism spectra corresponding to either perpe
78                                              Circular dichroism spectra demonstrate that the intact p
79                              The mature GehD circular dichroism spectra differs from that of Cna but
80 ral changes revealed by studying solubility, circular-dichroism spectra, dimer formation, and aggrega
81  by SDS-PAGE, size exclusion chromatography, circular dichroism spectra, ELISA and basophil activatio
82                                       Far-UV circular dichroism spectra evidence an abrupt loss of 10
83  visible and near-ultraviolet absorption and circular dichroism spectra, far-ultraviolet circular dic
84                   Vibrational absorption and circular dichroism spectra for both enantiomers have bee
85                          The profiles of the circular dichroism spectra for CoFpg and ZnFpg are ident
86                                          The circular dichroism spectra for the two proteins were ess
87 ough taurocholate induced similar changes in circular dichroism spectra for wild type, R63A, and R423
88  The results obtained through UV-visible and circular dichroism spectra generated in the presence and
89       For each dione, specific rotations and circular dichroism spectra give identical absolute confi
90 cence intercalator displacement studies, and circular dichroism spectra, however, indicate that the c
91                                              Circular dichroism spectra in far UV and thermal denatur
92                                 The magnetic circular dichroism spectra in the near-infrared region e
93 anges for the Ser129Ser132 mutant; identical circular dichroism spectra in the ultraviolet region ind
94 r residues shown by the amplitude of near-UV circular dichroism spectra in the wavelength interval, 2
95 erization domain of the protein, and near-UV circular dichroism spectra indicate a concomitant change
96                                              Circular dichroism spectra indicate a distinctive struct
97                             Far- and near-UV circular dichroism spectra indicate modest changes in se
98                                              Circular dichroism spectra indicate that a native-like f
99                                              Circular dichroism spectra indicate that all peptides ar
100 ntial conformational heterogeneity, although circular dichroism spectra indicate that much of the alp
101 ifference spectrum absorption at 446 nm, and circular dichroism spectra indicate that the protein is
102                                          The circular dichroism spectra indicate that the self-assemb
103                                              Circular dichroism spectra indicate that these N-termina
104                                              Circular dichroism spectra indicated changes in the seco
105                                              Circular dichroism spectra indicated that the folded V a
106                             Fluorescence and circular dichroism spectra indicated that the recombinan
107                                          The circular dichroism spectra indicated the ellipticity of
108                                              Circular dichroism spectra indicated the presence of a h
109                           Analysis of far UV circular dichroism spectra indicates a predominantly bet
110 sitivity to limited proteolysis, and altered circular dichroism spectra indicative of perturbed domai
111 no-ol results in large Cotton effects in the circular dichroism spectra indicative of the handedness
112 ctured and highly mobile, as demonstrated by circular dichroism spectra indicative of unfolded protei
113 eric primers, as well as melting studies and circular dichroism spectra of 18-nt primer:PBS duplexes,
114 d into the enantiomeric gramicidin A-, gA-.) Circular dichroism spectra of [D-Ala10,12,14]gA, [D-Val1
115 and anisotropic Raman, FTIR, and vibrational circular dichroism spectra of a polypeptide.
116                                              Circular dichroism spectra of aged solutions of peptides
117                               The 300-500 nm circular dichroism spectra of ALAS and H282A diverged in
118 Singular value decomposition analysis of the circular dichroism spectra of AmB at different AmB/lipid
119                                      Near-UV circular dichroism spectra of apoLp-III showed well-defi
120                               At pH 4.0, the circular dichroism spectra of Bcl-XL and Bax were essent
121            Examination of the absorption and circular dichroism spectra of bilirubin bound to its hig
122                           The absorption and circular dichroism spectra of bilirubin bound to the abo
123                                              Circular dichroism spectra of bovine decorin extracted f
124                                          The circular dichroism spectra of cytochrome c (cytc) in 4.6
125                               Absorption and circular dichroism spectra of dimers and monomers are si
126      The UV--visible absorption and magnetic circular dichroism spectra of ferric AOS and of its cyan
127                                       Far UV circular dichroism spectra of full-length apoA-V and apo
128                          A comparison of the circular dichroism spectra of full-length Topo I and Top
129                                              Circular dichroism spectra of I1-64 indicate that bispho
130                                          The circular dichroism spectra of modified DNAs differ subst
131                                       Far-UV circular dichroism spectra of native decorin proteoglyca
132                                              Circular dichroism spectra of naturally occurring molecu
133                                          The circular dichroism spectra of poly(Gln) peptides with re
134                                          The circular dichroism spectra of purified wild-type and mut
135                                Comparison of circular dichroism spectra of recombinant proteins corre
136                                              Circular dichroism spectra of the 26 kDa recombinant pro
137         The H(alpha) chemical shifts and the circular dichroism spectra of the camstatins are consist
138                                    Comparing circular dichroism spectra of the chimera and the corres
139                               Absorption and circular dichroism spectra of the complex also support i
140                                              Circular dichroism spectra of the cyclo[D-Asp(i),Dap(i+3
141                          A comparison of the circular dichroism spectra of the free and DNA-bound pro
142 of the Cdk-inhibition domain from p27, since circular dichroism spectra of the full-length protein ar
143           The crystal structure and magnetic circular dichroism spectra of the H93G Mb beta-mercaptoe
144 etics, dimer-tetramer association constants, circular dichroism spectra of the heme region, and nucle
145                                          The circular dichroism spectra of the holo and the apo forms
146                           The absorption and circular dichroism spectra of the homogeneous enzyme wer
147                           The Cu(II) EPR and circular dichroism spectra of the initially formed compl
148                                              Circular dichroism spectra of the intact M2 protein in d
149         One-dimensional imino proton NMR and circular dichroism spectra of the modified RNAs reveal t
150                          Visible and near-UV circular dichroism spectra of the mofegiline-MAO-B adduc
151  correlated strongly with alterations in the circular dichroism spectra of the monomeric peptides.
152                                          The circular dichroism spectra of the mutants were the same
153                       Analysis of changes in circular dichroism spectra of the N-terminal segment of
154                            The R and T-state circular dichroism spectra of the position 49 mutants we
155         These conclusions were reinforced by circular dichroism spectra of the protein in all three e
156                                          The circular dichroism spectra of the purified mutant enzyme
157                            Calculations from circular dichroism spectra of the purified protein solub
158 ided by the respective 1H NMR and electronic circular dichroism spectra of the respective peptides, w
159                       We further showed that circular dichroism spectra of the Scl proteins contained
160                                          The circular dichroism spectra of the short helices are comp
161                                              Circular dichroism spectra of the synthesized peptides s
162                                          The circular dichroism spectra of the triplex having a 1-C-G
163                                 However, the circular dichroism spectra of the two circularly permute
164                           Differences in the circular dichroism spectra of the two forms of melittin
165                                              Circular dichroism spectra of the two mutants showed sig
166                                              Circular dichroism spectra of the unliganded enzyme and
167  We observed a "two-fold" odd-even effect in circular dichroism spectra of these derivatives, dependi
168                             Near- and far-UV circular dichroism spectra of these three forms of p21(H
169 lectron paramagnetic resonance, and magnetic circular dichroism spectra of these variants provide the
170 IIa RNA based upon observed decreases in the circular dichroism spectra of this RNA following binding
171    In the presence of 2 mM CaCl2, the far UV circular dichroism spectra of thrombospondin-2 and -4 co
172                   In 2 mM CaCl2, the near UV circular dichroism spectra of thrombospondin-2, but not
173                          A comparison of the circular dichroism spectra of wild-type enzyme and the v
174 pectral region specific rotations and of the circular dichroism spectra originating in n --> pi C=O g
175 haracteristics by several criteria including circular dichroism spectra, resistance to limited proteo
176 nantiomers have pronounced features in their circular dichroism spectra resulting solely from topolog
177                   Solid state structures and circular dichroism spectra reveal a change in configurat
178                                       Far-UV circular dichroism spectra revealed beta-sheet with some
179                                              Circular dichroism spectra revealed similar, highly alph
180  characterized by rheology measurements, and circular dichroism spectra revealed that hydrogel format
181 t low micromolar concentrations as judged by circular dichroism spectra, sediments as a dimeric speci
182                                              Circular dichroism spectra show conformational rearrange
183 etramers like the wild type enzyme; however, circular dichroism spectra show reductions in helix cont
184                Fluorescence, absorbance, and circular dichroism spectra show relatively small perturb
185                                       Far-UV circular dichroism spectra show Stt7 to be mostly alpha-
186                              Far-ultraviolet circular dichroism spectra show that [198-243]apoA-I is
187  1:1 stoichiometries for each duplex and the circular dichroism spectra show that both duplexes adopt
188                                              Circular dichroism spectra show that monomer 1 displays
189  similar absorption profiles, and the far UV circular dichroism spectra show that no global structura
190             Size-exclusion chromatograms and circular dichroism spectra show that the Ala --> Ser rep
191                                              Circular dichroism spectra show that the mutant protein
192 lectron paramagnetic resonance, and magnetic circular dichroism spectra showed a high spin ferric hem
193                                              Circular dichroism spectra showed secondary and tertiary
194                              Far-ultraviolet circular dichroism spectra showed that [1-44]apoA-I is u
195                                  Ultraviolet circular dichroism spectra showed that apo-ADP-hep 6-epi
196                                              Circular dichroism spectra showed that both types formed
197                                       Far UV circular dichroism spectra showed that each subdomain is
198                                       Far-UV circular dichroism spectra showed that LDL oxidation ind
199                                              Circular dichroism spectra showed that MIMOOX had mainly
200                                              Circular dichroism spectra showed that the amino acid re
201                                              Circular dichroism spectra showed that the ligation prod
202                                              Circular dichroism spectra showed that TLT35 folded into
203                                          The circular dichroism spectra, specific rotations, and fluo
204               On the other hand, the near UV circular dichroism spectra suggest differences in the lo
205                                              Circular dichroism spectra suggested that all three poly
206                                              Circular dichroism spectra suggested that although the m
207                                              Circular dichroism spectra suggested that each mutant wa
208                                              Circular dichroism spectra suggested that these lesions
209        Deamidation altered amine reactivity, circular dichroism spectra, surface hydrophobicity, and
210 usly reported state-dependent changes in the circular dichroism spectra that are associated with the
211 oulder at approximately 585 nm) and magnetic circular dichroism spectra that are nearly identical to
212                                   We present circular dichroism spectra that indicate the presence of
213 is of the fluorescence intensity pH profile, circular dichroism spectra, the effect of extrinsic quen
214 ally observed peaks in linear absorption and circular dichroism spectra to excited electronic states
215 rotocol covers methods to obtain and analyze circular dichroism spectra to measure changes in the fol
216  circular dichroism spectra, and vibrational circular dichroism spectra to their computationally simu
217 clusion was further supported by the near-UV circular dichroism spectra under two pH conditions.
218                         A dramatic change in circular dichroism spectra was observed during this proc
219                                              Circular dichroism spectra were also calculated from eac
220                                              Circular dichroism spectra were identical for phosphoryl
221                                              Circular dichroism spectra were recorded for purified si
222 two fluorescent ligands and cellotriose, and circular dichroism spectra were recorded.
223 intense excitonic couplets in the electronic circular dichroism spectra which are mirror imaged if th
224 e in the presence of calcium and DPPG yields circular dichroism spectra which suggest C-DNA but which
225                                          The circular dichroism spectra, which show greatest deviatio
226 6 in the H2 hydrophobic domain; (iv) near-UV circular dichroism spectra with a prominent ellipticity

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