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3 of channel block and found that our results were best fitted assuming that only one Ag+ ion need bin
4 eptide concentrations, the FA titration data are best fit by a model in which the D2R peptide binds t
6 ibrium sedimentation data on crm45 at pH 5.0 are best fit by a single species with a mass of 1000 +/-
8 Our tree topology and divergence times also are best fit by diversification models in which Northern
14 be approximated by a power law, but the data are best fitted by a Waring distribution for all time de
16 3 </= N </= 5, peregrine attack trajectories are best fitted by lower navigation constants (median N
17 urality of modern vertebrate clades examined are best fitted by pulsed processes over models of incre
18 s from 14 continuous sites across the region are best-fit by interseismic strain accumulation on the
20 f A and V were seen to co-vary with the data being best fit by the equation V=0.86+2.65A (linear regr
21 orescence increase for each of these mutants is best fit by a double-exponential function indicating
22 f E-imine product, monitored simultaneously, is best fit by a process involving wall-associated water
23 azepam, and the other has a decay phase that is best fit by a sum of two exponential functions (tau(f
24 ynchronously rotating triaxial ellipsoid but is best fit by such a body orbiting closer to Saturn tha
25 coefficient as a function of polymer weight is best fitted by a "compressed exponential" with the co
34 in response due to desensitization ('onset') was best fitted by the sum of two exponentials with the
37 rbamate (HDTX) metabolite biliary excretion, were best fit by a two compartment model, with both line
39 and autosomal recessive models, and the data were best fit by either a dominant or codominant model.
40 ng small-angle scattering intensity profiles were best fit by models of the heavy meromyosin head-tai
42 easurements on the peptide Ac-WAAAH(+)-NH(2) were best fit by two relaxation modes on the approximate
46 bility of containing only one active channel were best fitted by five exponential functions; the appa
48 uency distribution histograms of open events were best fitted by the sum of two exponential component
51 ide polymorphism data, we show that the data are best fitted if the mutation bias is assumed to be co
54 pathways, since the k(obs) vs [olefin] plots are best fitted to k(obs) = k(D).k(4)/k(-D).[olefin]/(1
55 d with increasing concentration of inhibitor is best fit to a function that suggests three SNARE comp
56 the time-dependent ORD signal at 230 nm that is best fit to a single-exponential decay with a time co
57 the nitroxide diradicals at low temperature is best fit to the model of one-dimensional S = 1 Heisen
58 SsuD and FMNH2 mixed with oxygenated buffer was best fit to a double exponential with no observed fo
59 ellar membranes with imidazobenzodiazepine 9 was best fitted to a single population of sites with an
60 rption data collected from these experiments were best fit to a 1:1 Pb2+ -CF model and a 2:1 Pb2+ -DF
61 folding and refolding of WT betaA3 with urea were best fit to a three-state model with transition mid
62 um unfolding transitions of the tsf variants were best fit to a three-state model, N if I if U, where
63 ta across different substrate concentrations were best fit to the sigmoidal Hill equation, with a K(0
66 CH, dihydroxy-TBECH, and monohydroxy-TriBECH were best fitted to a Michaelis-Menten enzyme kinetic mo
69 ical imaging, they find that LFP selectivity is best fit using signals within 250 microm of the recor
71 X-ray absorption fine structure (EXAFS) data are best fit with oxygen/nitrogen ligands and reveal a C
72 xtended x-ray absorption fine structure data are best fit with oxygennitrogen ligands and a 2.57-A Cu
74 Longitudinal SEQ in the mild/no ROP group was best fit with a linear model, with a rate of -0.004
75 or "not toy." Activation in the hippocampus was best fit with a power function, consistent with pred
76 The Ca(2+) dependence of hIK1 activation was best fit with a stimulatory constant (K(s)) of 350 n
77 tion for neurons isolated from immature rats was best fitted with a Gaussian distribution with a mean
78 .2 which is expressed independently of SUR1) was best fitted with a single, low-affinity site (Ki = 1
79 bution for neurons isolated from mature rats was best fitted with the sum of two Gaussian distributio
81 ein B, the kinetics of Hdinitrosyl formation were best fit with a biphasic A --> B --> C model, indic
84 ivity generated shut-time distributions that were best fitted with a mixture of five and six exponent
85 th, distributions of super-cluster durations were best fitted with a mixture of six exponential compo
88 or the descending phases of the contractions were best fitted with linear functions for both control
89 h stimulation, however, firing rate profiles were best fitted with linear functions or with less stee
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