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STM3 in Fig. 6 with the corresponding system data was modeled with the PSS/E program.
The CTM as shown in Fig. 8 with the corresponding system data was modeled with the PSS/E program.
Data was modeled with the Multiplus AV software (Phoenix Flow Systems).
Individual animal data was modeled, with input for the dose of DCP or ECH administered to calculate the dose-normalized area under the curve in blood for DCP or ECH.
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The kinetics data was modelled with four kinetics models [pseudo-first-order (Lagergren 1898), pseudo-second-order (Ho and McKay 1999), Weber Morris intraparticle diffusion (1963a) and Boyd (1947) models].
At the individual participant level the data was modelled with the two conditions (emotion and neutral) each modelled by a boxcar function convolved with a synthetic haemodynamic response function.
In the first protocol all data are modeled with one GMM and in the second protocol two GMM models are designed for intermediate and positive data.
The sets of boundary data are modeled with reasonable geometric primitives and the parameters of the models are estimated in a manner that minimizes error.
Normal distributions were used to model muscle moment arms; electromyographic and muscle physiological cross-sectional area data were modeled with log-normal distributions.
Adsorption isotherms of fish muscle were measured at room temperature by the isopiestic method and data were modeled with BET and GAB equations.
In single-component experiments, experimental data were modeled with five isotherm equations (Langmuir, Freundlich, modified BET for liquid phase, Sips and Dubinin Radushkevich).
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