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1 he underlying activity distribution remained lognormal.
8 tral-limit theorem then explains the central lognormal, and a number of possible mechanisms could exp
10 -induced IPIs during the unloading phase was lognormal, bimodal, and independent of previously inject
12 cr-1 E. coli by small gull flocks followed a lognormal curve and gulls shed one strain >10(1) log10 C
13 dilution curve is closely approximated by a lognormal curve and that loss of lithium in the lungs fo
15 oi polyhedra distribution that is defined by lognormal curve having a constant standard deviation tha
17 M fail to fit empirical data better than the lognormal distribution 95% of the time, it also fails to
18 ss the neuronal population as reflected in a lognormal distribution and demonstrate that half of the
19 is based on a flexible multivariate Poisson-lognormal distribution and is seen to be a natural gener
20 iates considerably from the commonly assumed lognormal distribution and predicts considerably more ra
25 ion of rates such as a gamma distribution or lognormal distribution has deservedly been popular, but
27 CD34(+) cells and blood vessels exhibited a lognormal distribution indicating a shared spatial niche
28 d that the fit does not suffer when a common lognormal distribution is assumed for all 18 genes compa
29 mal and plant communities, while the Poisson lognormal distribution is the best model for microbes, t
31 of a realistic heterogeneous lung, namely a lognormal distribution of spatial ventilation and perfus
32 to increasing T cell search efficiency: 1) a lognormal distribution of step lengths, 2) motion that i
33 theoretical model successfully explained the lognormal distribution of the temporal parameters and th
34 e movement patterns can be approximated by a lognormal distribution rather than a power-law distribut
35 Connection weights exhibit a heavy-tailed lognormal distribution spanning five orders of magnitude
39 other diffusion and nondiffusion models; the lognormal distribution which has heavier tails (lower se
40 croplastic counts are modeled by the Poisson-lognormal distribution with inputs estimated from duplic
41 le wild populations were best described by a lognormal distribution with power-law scaled tails, the
44 N-gons, in a type-I network are fitted by a lognormal distribution, whereas those in type-II display
45 levels of CA1 neurons showed a right-skewed lognormal distribution, with a small portion of highly a
46 me enhancements and inferred fluxes follow a lognormal distribution, with the top 10% emitters contri
56 s, directed Erdos-Renyi graphs with a broad (lognormal) distribution of synaptic weights best capture
57 ater concentration by randomly sampling from lognormal distributions for random error in the yearly p
58 ultiplicative cell growth, and the mixing of lognormal distributions having different variances, may
59 ng regimes of species-area relationships and lognormal distributions of species abundance with an exc
61 iles parametric quantile regression assuming lognormal distributions was used to estimate the average
63 n incubation period using gamma, Weibull and lognormal distributions, with respective means of 8.52 (
70 ckouts in S. cerevisiae fits a double Pareto-lognormal (DPLN) distribution better than any of the alt
75 I, 3.6-5.9), or a delay of 33.3 minutes; the lognormal estimate for ED LOS was 0.1 (95% CI, 0.0-0.1),
76 inutes, and for antihypertensive orders, the lognormal estimate was 4.8 (95% CI, 3.6-5.9), or a delay
79 monstrate that the mixture of the decomposed lognormal flight distributions associated with each moda
80 ifurcating point gives rise to an asymptotic lognormal flow distribution with a positive skewness.
84 th 210Po was shown to be well described by a lognormal (LN) distribution function with the aid of aut
85 s with a number of distributions: power law, lognormal, loglogistic, loggamma, right Pareto-lognormal
86 , right Pareto-lognormal (RPLN), left Pareto-lognormal (LPLN), normal, lognormal, exponential, and Pa
96 ral generalization of the univariate Poisson-lognormal models used in the ecological studies of biodi
99 am network forms spatial response fields and lognormal number codes that resemble those observed in t
105 s over time, and overdispersion using latent lognormal Poisson dynamic generalized linear models.
106 alyses indicate an age of 110.9 (exponential/lognormal priors)/118.7 (uniform priors) million years (
109 ds applied to the log-transformed GFR (i.e., lognormal) quantify only rigid shifts in a given outcome
111 robability distributions: DPLN, right Pareto-lognormal (RPLN), left Pareto-lognormal (LPLN), normal,
113 tions observed at glacial calving fronts and lognormal size-frequency distributions observed globally
116 species abundance distribution resembling a lognormal with higher rarity, together with the observat
117 n of ~1.0 MJ/m, and that the distribution is lognormal with respect to energy per length and frequenc