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1  the two folding transitions gives a complex titration curve.
2 te to +/- 0.1 pH unit at the midpoint of the titration curve.
3  near 7.5 and has a well-defined, single-pKa titration curve.
4 lmer (MSV) equation for fitting fluorescence titration curves.
5  in calculating and interpreting complicated titration curves.
6 ammerhead RNA give very different isothermal titration curves.
7 ins the observed complex and varied spectral titration curves.
8  approximately described the observed (1) pH titration curve, (2) Ca, Mg, and Mn concentration by cat
9 -4) M), two peaks were observed in the force titration curve (adhesion force versus pH) at pH 4.5 and
10                         We predict that such titration curves, along with accurate mass measurements,
11                                          The titration curves also indicate that the binding is anti-
12 cide with the midpoint of the far-UV CD acid titration curve and suggest that the protonation of one
13 d from the midpoint and slope of the calcium titration curve and the concentration of membrane bindin
14 te-Seq, that is capable of measuring binding titration curves and corresponding affinities for thousa
15  of biomolecules such as isoelectric points, titration curves and energies of protonation microstates
16                               Simulations of titration curves and line shapes show that a primary dis
17                              Calculations of titration curves and pH-stability profiles are presented
18 m electrostatic techniques, we calculate the titration curves and the stability of dimer and tetramer
19 nd some residues will have anomalous thermal titration curves and unusual baseline behaviour monitore
20                               Potentiometric titration curves are analyzed using the NICA equations a
21                                          The titration curves are demonstrated to be pH-independent a
22 resis as unfolding and refolding equilibrium titration curves are non-coincident even after equilibra
23     For all three cases, the experimental pH titration curves are notably more consistent with the X-
24                            Chemical shift-pH titration curves are obtained from cross-peaks for repor
25 )(2) [d(pGpG)] adduct exhibit pH-independent titration curves, attributable to the added effect of th
26              A significant difference in the titration curves between the holo and apo forms of the W
27   The values, when plotted against pH, fit a titration curve corresponding to a pKa of 8.4 +/- 0.1.
28  be defined as the point of singularity in a titration curve, corresponding to the solution pH value
29     Second, by numerical integration of H(+) titration curves (Delta) measured potentiometrically und
30                           The measurement of titration curves eliminates the confounding effects of a
31 tead, proton transport activity followed the titration curve for Asp-97, with an apparent pK(a) of 7.
32                                            A titration curve for the LCC was generated that showed th
33      Analysis of the theoretical microscopic titration curves for all of the ionizable residues of th
34 f CD, Trp fluorescence, and Soret absorbance titration curves for all the variants requires a six-sta
35                                              Titration curves for His 55 and the two other histidines
36                                    While the titration curves for most of the side-chain carboxyl res
37                                              Titration curves for two biological warfare agents, Baci
38 e measured potentials were used to produce a titration curve from which the end point of a reaction w
39                                          The titration curves gave dissociation binding constants for
40                                              Titration curves in the presence of BSA and micelles are
41 hibition, as measured by the slope of linear titration curves in this system, was observed with PA, G
42                                      Peptide titration curves indicated that this effect was not due
43  the biggest contributor to the shape of the titration curve, indicating that the formation of this s
44  side chains give rise to two- or three-step titration curves, indicative of the influence of multipl
45 per, a general expression for solute-protein titration curves is predicted, using an indirect mechani
46 h increasing pH in the manner expected for a titration curve model in which deprotonation of the hist
47                                The resultant titration curve (normalized fluorescence intensity vs. l
48                       However, the triphasic titration curve obtained from the ITC study suggests tha
49                                          The titration curves obtained by differential excitation usi
50  the 1:1 binding model, separate analyses of titration curves obtained while varying either P450 or C
51                                              Titration curves, obtained by fitting the donor's emissi
52                      We demonstrate that the titration curve of a site in a group of interacting site
53                                          The titration curve of an individual site in the molecule is
54               As follows from the fit of the titration curve of Asp-85, deprotonation of X' increases
55 ependent and correlated with the theoretical titration curve of the imidazole group.
56                                 The acoustic titration curves of 160 bp DNA revealed three stages of
57 stified by the observation that the biphasic titration curves of D85E and Y185F are converted to mono
58 ively low Mg2+ concentration, the normalized titration curves of DNA mobility were well fit by Mannin
59                                          The titration curves of lambda(max) for mutants on the EF lo
60 ent pKa values were also determined from the titration curves of phase angles and modulations versus
61                                              Titration curves of sera from rabbits immunized with P.
62                                          The titration curves of several known HIV-RT inhibitors have
63                                              Titration curves of the Fe-His frequency against pH are
64 ng sites can be accurately reconstructed, if titration curves of the other sites are known.
65 ed by integrating the difference between the titration curves of the two species.
66                            Comparison of the titration curves of the unliganded enzyme with that obta
67  a pK value (defined as the mid-point of the titration curve) of 7.1 and a slope of 0.6.
68 o have a pH dependence, which was fit with a titration curve (pKa = 7.7), suggesting the protonation
69                              The form of the titration curve predicted from this lateral pressure mec
70                                              Titration curves predicted significant differences in ch
71 ad to relatively broad histograms and broad "titration" curves, providing clear evidence for kinetic
72  amino acid position 623 (E623Q) displayed a titration curve shifted to the left relative to wild typ
73                             Propidium iodide titration curves showed that rewinding of DNA supercoils
74            The FT Raman spectra and the acid titration curves suggest that the 391 nm form of the chr
75 he presence of urea show curved or sigmoidal titration curves suggestive of direct urea binding.
76 ve CD band near 200 nm, and biphasic thermal titration curves that reflect varied stability of these
77 rs, percentages probabilities, and slopes of titration curves, that can be more accurately quantified
78         The shape of the equilibrium binding titration curve, the effects on the 2Fe-2S EPR spectrum,
79 as a function of the midpoint of the calcium titration curve, the Hill coefficient, and the concentra
80         We show that theoretical microscopic titration curves (THEMATICS) can be used to identify act
81         The power of theoretical microscopic titration curves (THEMATICS), when coupled with a statis
82 labeled peptide for binding to NCS-1 shifted titration curves to higher NCS-1 concentrations, suggest
83 fitting of the resultant equilibrium binding titration curves to the Adair-Pauling equations, and mod
84             Nonlinear curve fitting of metal titration curves using the multiple independent binding
85                      A biphasic fluorescence titration curve was observed, confirming the previous ob
86                               Parallelism in titration curves was observed in the III-HSA but not in
87 f the effects of ionic strength on the force titration curves, we discuss the applicability of JKR th
88                            Chemical shift-pH titration curves were obtained for the lysine side-chain
89                                Resulting EPR titration curves were simulated assuming different redox
90 cases, up to three steps in the fluorescence titration curves were visible, which were fit to apparen
91 epentaacetate (DTPA) exhibiting nonmonotonic titration curves, where it gives an excellent fit to exp
92 rin was strikingly pH-sensitive, producing a titration curve with a midpoint at pH 6.8.
93 llowing conclusions: 1) Asp-85 has a complex titration curve with two values of pKa; in addition to a
94 ss than 100 fg DNA or 10(2) CFU/ml in serial titration curves with pure bacteria.
95 owever, block was not complete; the best-fit titration curves yielded an acid pH asymptote of 10-15%,
96                    Fitting of the normalized titration curves yields an apparent pKa = 7.16(+/-0.02)

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