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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 that both MPXV and HIV genomic cluster sizes are best fit by scale-free distributions, and that peopl
16 be approximated by a power law, but the data are best fitted by a Waring distribution for all time de
18 3 </= N </= 5, peregrine attack trajectories are best fitted by lower navigation constants (median N
19 urality of modern vertebrate clades examined are best fitted by pulsed processes over models of incre
20 s from 14 continuous sites across the region are best-fit by interseismic strain accumulation on the
23 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
24 orescence increase for each of these mutants is best fit by a double-exponential function indicating
25 f E-imine product, monitored simultaneously, is best fit by a process involving wall-associated water
26 azepam, and the other has a decay phase that is best fit by a sum of two exponential functions (tau(f
27 ynchronously rotating triaxial ellipsoid but is best fit by such a body orbiting closer to Saturn tha
28 coefficient as a function of polymer weight is best fitted by a "compressed exponential" with the co
40 in response due to desensitization ('onset') was best fitted by the sum of two exponentials with the
46 ppression and phase resetting action spectra were best fit by a single-opsin template with lambda(max
47 rbamate (HDTX) metabolite biliary excretion, were best fit by a two compartment model, with both line
49 and autosomal recessive models, and the data were best fit by either a dominant or codominant model.
50 ng small-angle scattering intensity profiles were best fit by models of the heavy meromyosin head-tai
52 easurements on the peptide Ac-WAAAH(+)-NH(2) were best fit by two relaxation modes on the approximate
56 bility of containing only one active channel were best fitted by five exponential functions; the appa
58 esults: (11)C-AS2471907 time-activity curves were best fitted by the 2-tissue-compartment (2TC) model
59 he adsorption isotherms and the kinetic data were best fitted by the Jovanovic and the Elovich models
60 uency distribution histograms of open events were best fitted by the sum of two exponential component
61 esults showed that the majority of observers were best-fit by either: 1) the Heuristic model, which u
64 ide polymorphism data, we show that the data are best fitted if the mutation bias is assumed to be co
67 pathways, since the k(obs) vs [olefin] plots are best fitted to k(obs) = k(D).k(4)/k(-D).[olefin]/(1
68 d with increasing concentration of inhibitor is best fit to a function that suggests three SNARE comp
69 the time-dependent ORD signal at 230 nm that is best fit to a single-exponential decay with a time co
70 the nitroxide diradicals at low temperature is best fit to the model of one-dimensional S = 1 Heisen
71 SsuD and FMNH2 mixed with oxygenated buffer was best fit to a double exponential with no observed fo
72 ellar membranes with imidazobenzodiazepine 9 was best fitted to a single population of sites with an
73 rption data collected from these experiments were best fit to a 1:1 Pb2+ -CF model and a 2:1 Pb2+ -DF
74 folding and refolding of WT betaA3 with urea were best fit to a three-state model with transition mid
75 um unfolding transitions of the tsf variants were best fit to a three-state model, N if I if U, where
76 ta across different substrate concentrations were best fit to the sigmoidal Hill equation, with a K(0
79 CH, dihydroxy-TBECH, and monohydroxy-TriBECH were best fitted to a Michaelis-Menten enzyme kinetic mo
82 ical imaging, they find that LFP selectivity is best fit using signals within 250 microm of the recor
84 X-ray absorption fine structure (EXAFS) data are best fit with oxygen/nitrogen ligands and reveal a C
85 xtended x-ray absorption fine structure data are best fit with oxygennitrogen ligands and a 2.57-A Cu
86 tral composite rotatable design was found to be best fitted with data having a higher R(2) (91 and 97
88 Longitudinal SEQ in the mild/no ROP group was best fit with a linear model, with a rate of -0.004
89 structure of the periplasmic binding protein was best fit with a molecular model containing a pyridox
90 or "not toy." Activation in the hippocampus was best fit with a power function, consistent with pred
91 The Ca(2+) dependence of hIK1 activation was best fit with a stimulatory constant (K(s)) of 350 n
92 tion for neurons isolated from immature rats was best fitted with a Gaussian distribution with a mean
93 .2 which is expressed independently of SUR1) was best fitted with a single, low-affinity site (Ki = 1
94 bution for neurons isolated from mature rats was best fitted with the sum of two Gaussian distributio
96 ein B, the kinetics of Hdinitrosyl formation were best fit with a biphasic A --> B --> C model, indic
97 ion whereas phenylacetaldehyde and o-quinone were best fit with a polynomial function containing quad
102 ivity generated shut-time distributions that were best fitted with a mixture of five and six exponent
103 th, distributions of super-cluster durations were best fitted with a mixture of six exponential compo
106 or the descending phases of the contractions were best fitted with linear functions for both control
107 h stimulation, however, firing rate profiles were best fitted with linear functions or with less stee
108 ow agonist concentrations (0.01-0.03 microM) were best fitted with three exponential components.
109 course extraction of lycopene-pectin complex were best fitted with two-site kinetic model, hinting th