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1 cular proton-proton relaxation rate constant is interpreted in terms of 25 +/- 4 water molecules that
2 pic and redox properties of NEM-modified FTR are interpreted in terms of a [4Fe-4S]2+ cluster covalen
6 rom the double-jump stopped-flow experiments are interpreted in terms of a folding/unfolding model.
9 dent backbone proton lability of the F helix are interpreted in terms of a holoprotein which is less
11 context-dependent effects of a -2 nucleotide are interpreted in terms of a mechanism in which the bin
16 of the interfacial kinetic paradigm, results are interpreted in terms of a model in which several amp
25 nical calculations, the experimental results are interpreted in terms of a novel subfemtosecond contr
43 e electronic structure of Au(40)(SR)(24) can be interpreted in terms of a dimer of two 8-electron sup
44 uspended between optically trapped beads can be interpreted in terms of a generalized cross-bridge mo
48 lation reaction is biphasic, a fact that has been interpreted in terms of a mechanism for sequesterin
49 molecular simulation studies, however, have been interpreted in terms of a model where there are two
50 for a reevaluation of evidence that has long been interpreted in terms of a more conventional nucleos
52 stal diffraction; the fiber-like pattern has been interpreted in terms of a repeating unit with four
54 rium unfolding data for the heterodimer have been interpreted in terms of a three-state mechanism.
55 d phase of increasing fluorescence intensity is interpreted in terms of a combination of probe repart
58 s for the regulatory effects of component B, is interpreted in terms of a model involving carboxylate
59 p85 alpha phosphopeptide binding specificity is interpreted in terms of a model of the p85 alpha/PDGF
60 ffects on cell-wall binding and biosynthesis is interpreted in terms of a recent proposal that oritav
62 tion-selective (14,15)N and (17)O ENDOR data is interpreted in terms of a structural model of the ACC
63 ft with respect to pH, and the pH dependence is interpreted in terms of a two pK(a) model for proton
71 sence of interknuckle NOE cross-peaks, which were interpreted in terms of a more compact structure in
73 mer generated under H/D quenching conditions were interpreted in terms of a significant loss of struc
74 librating these reporters such that they can be interpreted in terms of absolute molecular counts, we
81 e observed with a factor of ~1.8 in D2O, and are interpreted in terms of an excited-state proton tran
83 nomalously low E value, which had previously been interpreted in terms of an axially symmetric (D(inf
85 he lifetime difference between binding modes is interpreted in terms of an anomeric effect on the exc
86 proceeds through a syn S(E)' mechanism which is interpreted in terms of an intramolecular delivery of
92 ific differences in apparent order parameter are interpreted in terms of backbone dynamics modes with
95 ce from allozyme and microsatellite data and is interpreted in terms of both extensive gene flow and
98 nct energy groupings, and Cl K-edge XAS data are interpreted in terms of Cl 1s transitions into both
99 ion rate nor its dependence on SA can simply be interpreted in terms of cluster evaporation or the mo
100 s of the 1-(E)-propenyl-2-methylcyclobutanes are interpreted in terms of competitive processes involv
103 n all five variants, the midpoint potentials are interpreted in terms of Cys11 and Cys17 ligating the
105 lizes data from Phi-value analysis that have been interpreted in terms of delocalized or polarized tr
107 s of these two types of [Fe(3)S(4)] clusters are interpreted in terms of different locations of the m
108 he systems investigated this observation can be interpreted in terms of different proportions of the
109 between the two enzymes with this substrate were interpreted in terms of different acyl-enzyme confo
110 the N-terminal domains; rather the data can be interpreted in terms of differential allosteric activ
111 on heavy metals for activity has invariably been interpreted in terms of direct metal binding to the
112 lobin in which the iron was replaced by Mg2+ are interpreted in terms of effects produced by electric
113 xplicitly related to film properties and can be interpreted in terms of elastic energy storage and vi
118 e translational control mechanism identified is interpreted in terms of flux adjustments needed in re
120 led clear spatiotemporal patterns, which can be interpreted in terms of gradients in concentrations o
121 unish defectors, this behavior has typically been interpreted in terms of group-level rather than ind
124 dies of plasticity in the visual cortex have been interpreted in terms of heterosynaptic competition
125 These calorimetrically determined values are interpreted in terms of high-resolution X-ray crysta
132 selectivity of the [2]rotaxane for chloride is interpreted in terms of its unique interlocked bindin
135 esponding N(epsilon)-H(epsilon) bond vectors were interpreted in terms of Lipari-Szabo model-free par
139 ces in the side chain of the cmF residue can be interpreted in terms of maintaining similar interacti
141 fficient; on the other hand, the high q data were interpreted in terms of mean square displacements.
142 for most of the aromatic spins in CTSYM that are interpreted in terms of microsecond to millisecond t
143 of DIC contrast of gold/silver nanoparticles is interpreted in terms of Mie's theory and DIC working
144 an be applied to hundreds of genomes and can be interpreted in terms of minimal histories of mutation
145 ure in the C-N coupling cyclization reaction is interpreted in terms of minimization of allylic strai
146 UV-vis-NIR spectra of the iodine-doped films are interpreted in terms of molecular-like transitions i
147 nd lumi intermediates in the mutant pigments are interpreted in terms of movement of the Schiff base
148 s in patterns of structural changes that can be interpreted in terms of movements of helices that ext
149 amino- and 2,4-bis(acylamino)pyrimidines can be interpreted in terms of multiple intra-/intermolecula
151 ng of coiled coil peptides has traditionally been interpreted in terms of native dimer and unfolded m
155 ne fibrin clots first reported by Ferry have been interpreted in terms of nonspecific ionic strength
157 al repertoire of nerve fibres, and here they are interpreted in terms of osmotic changes that may ill
161 ity of the force applied to a ssDNA template is interpreted in terms of preferential stabilization of
162 ically, allostery in structured proteins has been interpreted in terms of propagated structural chang
165 allow the measured cross-relaxation rates to be interpreted in terms of relative interaction strength
169 dielectric-semiconductor interface has long been interpreted in terms of Schottky's theory with modi
174 requires thermodynamic measurements that can be interpreted in terms of specific chemical interaction
175 mulation allowed the H/D exchange results to be interpreted in terms of specific interactions between
177 buffer in membrane-reconstituted alamethicin is interpreted in terms of stabilization by helical hydr
179 E with increasing degree of unsaturation can be interpreted in terms of structural changes associated
194 se in thermodynamic potentials, and the data are interpreted in terms of the model of two-state confo
197 differences in the mass spectra of mixtures are interpreted in terms of the more significant effects
199 Y356F and double mutant Y356F and Y122F R2, are interpreted in terms of the possible role of Y356 in
201 netic sensitivity of Drosophila cryptochrome are interpreted in terms of the radical pair mechanism a
202 rom oriented fibers of the EtBr:DNA complex, are interpreted in terms of the relative orientations of
204 associated with inorganic phosphate binding are interpreted in terms of the specific interactions of
208 ctive positions in each conformer, which may be interpreted in terms of the accessibility of the site
209 by ion mobility spectrometry (IMS) can often be interpreted in terms of the coexistence of different
210 It is suggested that these phenomena can be interpreted in terms of the combined effects of parti
211 des mentioned above allows the IR spectra to be interpreted in terms of the conformation and solvatio
212 olecule information, the latter of which can be interpreted in terms of the cooperativity of unfoldin
215 fibers in the thin lamellipodial region can be interpreted in terms of the number of filaments in th
217 -directed spin-labeling experiments that can be interpreted in terms of the protein tertiary fold, it
220 high affinity of IgE for FcepsilonRI can now be interpreted in terms of the recently determined cryst
221 how the information in these sequences might be interpreted in terms of the structure, function, and
223 r the first time, spin-label orientation has been interpreted in terms of the orientation of a labele
224 For decades, rates of protein evolution have been interpreted in terms of the vague concept of functi
226 exhibit a reversal in solvatochromism, which is interpreted in terms of the ability of the media to s
227 The fast and efficient N-arylation reaction is interpreted in terms of the bifunctionality of the su
228 The significance of these dynamic results is interpreted in terms of the catalytic cycle of the en
229 BSA binding event from whole serum, and this is interpreted in terms of the difference in RI contrast
231 ference between the NMR and X-ray structures is interpreted in terms of the existence of two conforma
233 olarity of the environment of the nitroxide, is interpreted in terms of the nitroxide moiety being cl
236 mple of the missing mode effect; the spacing is interpreted in terms of the time-dependent overlaps i
245 erences between the two nanosheet assemblies were interpreted in terms of the relative stereoelectron
246 between the PF6(-) and NTf2(-) ionic liquids were interpreted in terms of the tight versus loose ion
247 uld processes of gene expression and control be interpreted in terms of their capacity to allow futur
248 3) in the Protein Data Bank and the Q-scores were interpreted in terms of their structural underpinni
249 carboxylic acids and halides, a result that was interpreted in terms of these former species binding
251 t the end of such sorting out phenomena have been interpreted in terms of tissue surface tensions ari
253 st, right hemisphere activation changes have been interpreted in terms of transcallosal disinhibition
254 rogen exchange results for cytochrome c have been interpreted in terms of transient hydrogen bond-bre
256 s in the nematode Caenorhabditis elegans has been interpreted in terms of two metabolic theories of a
258 ntary carbonate and total organic carbon can be interpreted in terms of variations in the global carb
259 ure dependence of internal side-chain motion is interpreted in terms of volume fluctuations on the na
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