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1  in the 1D-IR (FTIR), 2D-IR, and vibrational circular dichroism spectra.
2 ical Rel transcription factors, as judged by circular dichroism spectra.
3 n of experimental and theoretical electronic circular dichroism spectra.
4 olecular weight, amino acid composition, and circular dichroism spectra.
5 ty, the complexes afford nearly mirror image circular dichroism spectra.
6 s judged by their similar near-UV and far-UV circular dichroism spectra.
7 ut major structural changes, as evidenced by circular dichroism spectra.
8 n dependence for MALDI H/D exchange data and circular dichroism spectra.
9 25 degrees C as indicated by near and far UV circular dichroism spectra.
10 t the same site but had little effect on the circular dichroism spectra.
11 termined by TD-DFT simulations of electronic circular dichroism spectra.
12  absorption maxima, and (d) a sigmoid-shaped circular dichroism spectra.
13 scape reproduced the experimental electronic circular dichroism spectra.
14 Naturally Disordered Regions) prediction and circular dichroism spectra.
15 simulation of the electronic and vibrational circular dichroism spectra.
16 om a split-type Cotton effect in vibrational circular dichroism spectra.
17 yers as alpha-helices, as reflected in their circular dichroism spectra.
18 - or A-type structures on the basis of their circular dichroism spectra.
19 iparallel orientations, these showed similar circular dichroism spectra.
20 ed by thermal denaturation, mixing data, and circular dichroism spectra.
21 al data and their exciton UV-vis and induced circular dichroism spectra.
22                                              Circular dichroism spectra, 2D-NMR spectroscopy, and the
23   On the basis of the investigation of their circular dichroism spectra, all of the hairpins investig
24                                              Circular dichroism spectra also indicated that AGE-IAPP
25                                              Circular dichroism spectra also supported these evidence
26                                              Circular dichroism spectra analyses indicated only minor
27  and the variable region an extended "tail." Circular dichroism spectra analysis determined that the
28 e could be overexpressed and had native-like circular dichroism spectra and 1D-NMR spectra typical of
29 esemble the wild type enzyme as indicated by circular dichroism spectra and are tetramers.
30                                              Circular dichroism spectra and biological assays of the
31  into the ternary complex as demonstrated by circular dichroism spectra and calorimetry.
32                                              Circular dichroism spectra and chemical cross-linking of
33                                              Circular dichroism spectra and chemical footprinting exp
34                                              Circular dichroism spectra and chromatographic informati
35                                              Circular dichroism spectra and chymotrypsin digestion ex
36     The experimental absorption, linear, and circular dichroism spectra and dephasing rates are recov
37 strated by a characteristic red shift in the circular dichroism spectra and dramatic NMR spectral cha
38                                  By in vitro circular dichroism spectra and fluorescence quenching, w
39                            Comparison of the circular dichroism spectra and kinetic properties of the
40                    Thermodynamic parameters, circular dichroism spectra and NMR data are presented fo
41  was proved by the comparison of the NMR and circular dichroism spectra and of the specific optical r
42                                          The circular dichroism spectra and other properties of these
43                                              Circular dichroism spectra and size-exclusion chromatogr
44         A comparison between the vibrational circular dichroism spectra and the scanning transmission
45                                              Circular dichroism spectra and thermal denaturation expe
46                                              Circular dichroism spectra and thermal stability analysi
47 ng or non-encysting cells, the change in its circular dichroism spectra and up to a 6-fold increase i
48                      Slight perturbations in circular dichroism spectra and weakened self-association
49                                     Oriented circular dichroism spectra and x-ray diffraction pattern
50       Examination of their melting behavior, circular dichroism spectra, and fluorescence properties
51  circular dichroism spectra, far-ultraviolet circular dichroism spectra, and infrared spectra in 1H2O
52 elative susceptibilities to proteolysis, UV, circular dichroism spectra, and temperature melting tran
53  evidenced by altered fluorescence emission, circular dichroism spectra, and ultracentrifugal analysi
54 ry structure content as determined by far-UV circular dichroism spectra, and urea-induced denaturatio
55 obtained optical rotation values, electronic circular dichroism spectra, and vibrational circular dic
56                                              Circular dichroism spectra are consistent with B-form DN
57                                              Circular dichroism spectra are consistent with the helic
58 intramonomer nuclear Overhauser effects, and circular dichroism spectra are consistent with transient
59                 Thermodynamic parameters and circular dichroism spectra are presented for RNA hairpin
60                                              Circular dichroism spectra are reported to show that, in
61                                        Since circular dichroism spectra are similar for wild type, H3
62 these proteins appear to be folded and their circular dichroism spectra are similar to those of their
63 in is supported by electronic absorption and circular dichroism spectra, as well as equilibrium analy
64 ady-state absorption, photoluminescence, and circular dichroism spectra, as well as transmission elec
65                                              Circular dichroism spectra at the two pH conditions show
66                                              Circular dichroism spectra at various temperatures indic
67 s end, we have measured the fluorescence and circular dichroism spectra at wavelengths of >300 nm for
68  spherical structures with silent electronic circular dichroism spectra but which fluoresce.
69 Lys42, Ile190, and Gly191 do not perturb the circular dichroism spectra, but have significant effects
70 ha-helix, as estimated by measurement of the circular dichroism spectra, but the region of the propep
71 fects of different end sequences on melting, circular dichroism spectra (CD), and enzyme binding prop
72 cts of different end sequences on stability, circular dichroism spectra (CD), and enzyme binding prop
73 de comprising Tyr-553 through Ile-563 showed circular dichroism spectra characteristic of alpha-helix
74                         These fragments show circular dichroism spectra characteristic of helical pro
75 ons of a strong denaturant nearly attain the circular dichroism spectra characteristic of random coil
76 led analysis of MCD together with electronic circular dichroism spectra combined to ab initio calcula
77 ility relative to the unlabeled control, and circular dichroism spectra confirm B-form helical DNA st
78                                              Circular dichroism spectra confirm that the global confo
79                                              Circular dichroism spectra confirm that these molecules
80 rmed with a smaller entropic penalty feature circular dichroism spectra consistent with a non-compact
81 aggregates exhibit classical beta-sheet-rich circular dichroism spectra consistent with an amyloid-li
82 e proteins yielded monodisperse species with circular dichroism spectra consistent with the hallucina
83 ch the optical response between two distinct circular dichroism spectra corresponding to either perpe
84                                              Circular dichroism spectra demonstrate that the intact p
85                              The mature GehD circular dichroism spectra differs from that of Cna but
86 ral changes revealed by studying solubility, circular-dichroism spectra, dimer formation, and aggrega
87  by SDS-PAGE, size exclusion chromatography, circular dichroism spectra, ELISA and basophil activatio
88 ly and computationally determined electronic circular dichroism spectra, enabling access to configura
89                                       Far-UV circular dichroism spectra evidence an abrupt loss of 10
90  visible and near-ultraviolet absorption and circular dichroism spectra, far-ultraviolet circular dic
91                   Vibrational absorption and circular dichroism spectra for both enantiomers have bee
92                          The profiles of the circular dichroism spectra for CoFpg and ZnFpg are ident
93                                          The circular dichroism spectra for the two proteins were ess
94 ough taurocholate induced similar changes in circular dichroism spectra for wild type, R63A, and R423
95  The results obtained through UV-visible and circular dichroism spectra generated in the presence and
96       For each dione, specific rotations and circular dichroism spectra give identical absolute confi
97 cence intercalator displacement studies, and circular dichroism spectra, however, indicate that the c
98                                              Circular dichroism spectra in far UV and thermal denatur
99                                 The magnetic circular dichroism spectra in the near-infrared region e
100 anges for the Ser129Ser132 mutant; identical circular dichroism spectra in the ultraviolet region ind
101 r residues shown by the amplitude of near-UV circular dichroism spectra in the wavelength interval, 2
102 erization domain of the protein, and near-UV circular dichroism spectra indicate a concomitant change
103                                              Circular dichroism spectra indicate a distinctive struct
104                             Far- and near-UV circular dichroism spectra indicate modest changes in se
105                                              Circular dichroism spectra indicate that a native-like f
106                                              Circular dichroism spectra indicate that all peptides ar
107 ntial conformational heterogeneity, although circular dichroism spectra indicate that much of the alp
108 ifference spectrum absorption at 446 nm, and circular dichroism spectra indicate that the protein is
109                                          The circular dichroism spectra indicate that the self-assemb
110                                              Circular dichroism spectra indicate that these N-termina
111                                              Circular dichroism spectra indicated changes in the seco
112                                              Circular dichroism spectra indicated that the folded V a
113                             Fluorescence and circular dichroism spectra indicated that the recombinan
114                                          The circular dichroism spectra indicated the ellipticity of
115                                              Circular dichroism spectra indicated the presence of a h
116                           Analysis of far UV circular dichroism spectra indicates a predominantly bet
117 sitivity to limited proteolysis, and altered circular dichroism spectra indicative of perturbed domai
118 no-ol results in large Cotton effects in the circular dichroism spectra indicative of the handedness
119 ctured and highly mobile, as demonstrated by circular dichroism spectra indicative of unfolded protei
120 eric primers, as well as melting studies and circular dichroism spectra of 18-nt primer:PBS duplexes,
121  the prediction of Kerr, Faraday and magneto-circular dichroism spectra of 2D heterostructures.
122  a simple theoretical model to calculate the circular dichroism spectra of 6-MI-substituted DNA const
123 d into the enantiomeric gramicidin A-, gA-.) Circular dichroism spectra of [D-Ala10,12,14]gA, [D-Val1
124 and anisotropic Raman, FTIR, and vibrational circular dichroism spectra of a polypeptide.
125                                              Circular dichroism spectra of aged solutions of peptides
126                               The 300-500 nm circular dichroism spectra of ALAS and H282A diverged in
127 Singular value decomposition analysis of the circular dichroism spectra of AmB at different AmB/lipid
128                                      Near-UV circular dichroism spectra of apoLp-III showed well-defi
129                               At pH 4.0, the circular dichroism spectra of Bcl-XL and Bax were essent
130            Examination of the absorption and circular dichroism spectra of bilirubin bound to its hig
131                           The absorption and circular dichroism spectra of bilirubin bound to the abo
132                                              Circular dichroism spectra of bovine decorin extracted f
133                                          The circular dichroism spectra of cytochrome c (cytc) in 4.6
134                               Absorption and circular dichroism spectra of dimers and monomers are si
135      The UV--visible absorption and magnetic circular dichroism spectra of ferric AOS and of its cyan
136                                       Far UV circular dichroism spectra of full-length apoA-V and apo
137                          A comparison of the circular dichroism spectra of full-length Topo I and Top
138                                              Circular dichroism spectra of I1-64 indicate that bispho
139                                          The circular dichroism spectra of modified DNAs differ subst
140                                       Far-UV circular dichroism spectra of native decorin proteoglyca
141                                              Circular dichroism spectra of naturally occurring molecu
142                                          The circular dichroism spectra of OmpA in NDs and SUVs were
143                                          The circular dichroism spectra of poly(Gln) peptides with re
144                                          The circular dichroism spectra of purified wild-type and mut
145                                Comparison of circular dichroism spectra of recombinant proteins corre
146                                              Circular dichroism spectra of recombinant Tp0126 also su
147                                              Circular dichroism spectra of the 26 kDa recombinant pro
148         The H(alpha) chemical shifts and the circular dichroism spectra of the camstatins are consist
149                                    Comparing circular dichroism spectra of the chimera and the corres
150                               Absorption and circular dichroism spectra of the complex also support i
151                                              Circular dichroism spectra of the cyclo[D-Asp(i),Dap(i+3
152                                 The electric circular dichroism spectra of the dimers show intense Co
153                          A comparison of the circular dichroism spectra of the free and DNA-bound pro
154 of the Cdk-inhibition domain from p27, since circular dichroism spectra of the full-length protein ar
155           The crystal structure and magnetic circular dichroism spectra of the H93G Mb beta-mercaptoe
156 etics, dimer-tetramer association constants, circular dichroism spectra of the heme region, and nucle
157                                          The circular dichroism spectra of the holo and the apo forms
158                           The absorption and circular dichroism spectra of the homogeneous enzyme wer
159                           The Cu(II) EPR and circular dichroism spectra of the initially formed compl
160                                              Circular dichroism spectra of the intact M2 protein in d
161         One-dimensional imino proton NMR and circular dichroism spectra of the modified RNAs reveal t
162                          Visible and near-UV circular dichroism spectra of the mofegiline-MAO-B adduc
163  correlated strongly with alterations in the circular dichroism spectra of the monomeric peptides.
164                                          The circular dichroism spectra of the mutants were the same
165                       Analysis of changes in circular dichroism spectra of the N-terminal segment of
166                            The R and T-state circular dichroism spectra of the position 49 mutants we
167         These conclusions were reinforced by circular dichroism spectra of the protein in all three e
168                                          The circular dichroism spectra of the purified mutant enzyme
169                            Calculations from circular dichroism spectra of the purified protein solub
170 ided by the respective 1H NMR and electronic circular dichroism spectra of the respective peptides, w
171                       We further showed that circular dichroism spectra of the Scl proteins contained
172                                          The circular dichroism spectra of the short helices are comp
173 ences in secondary structure were evident on circular dichroism spectra of the soluble extracts and d
174                                              Circular dichroism spectra of the synthesized peptides s
175                                          The circular dichroism spectra of the triplex having a 1-C-G
176                                 However, the circular dichroism spectra of the two circularly permute
177                           Differences in the circular dichroism spectra of the two forms of melittin
178                                              Circular dichroism spectra of the two mutants showed sig
179                                              Circular dichroism spectra of the unliganded enzyme and
180  We observed a "two-fold" odd-even effect in circular dichroism spectra of these derivatives, dependi
181                             Near- and far-UV circular dichroism spectra of these three forms of p21(H
182 lectron paramagnetic resonance, and magnetic circular dichroism spectra of these variants provide the
183 IIa RNA based upon observed decreases in the circular dichroism spectra of this RNA following binding
184    In the presence of 2 mM CaCl2, the far UV circular dichroism spectra of thrombospondin-2 and -4 co
185                   In 2 mM CaCl2, the near UV circular dichroism spectra of thrombospondin-2, but not
186                          A comparison of the circular dichroism spectra of wild-type enzyme and the v
187 pectral region specific rotations and of the circular dichroism spectra originating in n --> pi C=O g
188 haracteristics by several criteria including circular dichroism spectra, resistance to limited proteo
189                      Differences in C-domain circular dichroism spectra resulting from Tyr2561 sugges
190 nantiomers have pronounced features in their circular dichroism spectra resulting solely from topolog
191                   Solid state structures and circular dichroism spectra reveal a change in configurat
192                                       Far-UV circular dichroism spectra revealed beta-sheet with some
193                                              Circular dichroism spectra revealed similar, highly alph
194  characterized by rheology measurements, and circular dichroism spectra revealed that hydrogel format
195 t low micromolar concentrations as judged by circular dichroism spectra, sediments as a dimeric speci
196                                              Circular dichroism spectra show conformational rearrange
197 etramers like the wild type enzyme; however, circular dichroism spectra show reductions in helix cont
198                Fluorescence, absorbance, and circular dichroism spectra show relatively small perturb
199                                       Far-UV circular dichroism spectra show Stt7 to be mostly alpha-
200                              Far-ultraviolet circular dichroism spectra show that [198-243]apoA-I is
201  1:1 stoichiometries for each duplex and the circular dichroism spectra show that both duplexes adopt
202                                              Circular dichroism spectra show that d(GGGA)n sequences
203                                              Circular dichroism spectra show that monomer 1 displays
204  similar absorption profiles, and the far UV circular dichroism spectra show that no global structura
205             Size-exclusion chromatograms and circular dichroism spectra show that the Ala --> Ser rep
206                                              Circular dichroism spectra show that the mutant protein
207 lectron paramagnetic resonance, and magnetic circular dichroism spectra showed a high spin ferric hem
208                                              Circular dichroism spectra showed secondary and tertiary
209                              Far-ultraviolet circular dichroism spectra showed that [1-44]apoA-I is u
210                                  Ultraviolet circular dichroism spectra showed that apo-ADP-hep 6-epi
211                                              Circular dichroism spectra showed that both types formed
212                                       Far UV circular dichroism spectra showed that each subdomain is
213                                       Far-UV circular dichroism spectra showed that LDL oxidation ind
214                                              Circular dichroism spectra showed that MIMOOX had mainly
215                                              Circular dichroism spectra showed that the amino acid re
216                                              Circular dichroism spectra showed that the ligation prod
217                                              Circular dichroism spectra showed that TLT35 folded into
218                                          The circular dichroism spectra, specific rotations, and fluo
219               On the other hand, the near UV circular dichroism spectra suggest differences in the lo
220                                              Circular dichroism spectra suggested that all three poly
221                                              Circular dichroism spectra suggested that although the m
222                                              Circular dichroism spectra suggested that each mutant wa
223                                              Circular dichroism spectra suggested that these lesions
224        Deamidation altered amine reactivity, circular dichroism spectra, surface hydrophobicity, and
225 usly reported state-dependent changes in the circular dichroism spectra that are associated with the
226 oulder at approximately 585 nm) and magnetic circular dichroism spectra that are nearly identical to
227                                   We present circular dichroism spectra that indicate the presence of
228 is of the fluorescence intensity pH profile, circular dichroism spectra, the effect of extrinsic quen
229  at each ssDNA position; and (iii) employing circular dichroism spectra to characterize changes in ex
230 ally observed peaks in linear absorption and circular dichroism spectra to excited electronic states
231 rotocol covers methods to obtain and analyze circular dichroism spectra to measure changes in the fol
232  circular dichroism spectra, and vibrational circular dichroism spectra to their computationally simu
233 clusion was further supported by the near-UV circular dichroism spectra under two pH conditions.
234                    X-ray crystallography and circular dichroism spectra verified their enantiomeric n
235                         A dramatic change in circular dichroism spectra was observed during this proc
236                                              Circular dichroism spectra were also calculated from eac
237                                              Circular dichroism spectra were computed using the SESCA
238                                              Circular dichroism spectra were identical for phosphoryl
239                                              Circular dichroism spectra were recorded for purified si
240 two fluorescent ligands and cellotriose, and circular dichroism spectra were recorded.
241 intense excitonic couplets in the electronic circular dichroism spectra which are mirror imaged if th
242 e in the presence of calcium and DPPG yields circular dichroism spectra which suggest C-DNA but which
243                                          The circular dichroism spectra, which show greatest deviatio
244 6 in the H2 hydrophobic domain; (iv) near-UV circular dichroism spectra with a prominent ellipticity

 
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