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Metabolism of CPF (and CPFO) in the Timchalk et al. (2002) models was assigned to occur in the blood and liver, with the excreted metabolite, TCPY, lumped into a single compartment.
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After that, these material models are assigned to fiber elements.
Tree species without valid height-diameter models were assigned to corresponding species with available models.
At the model development stage, all models are assigned version 0. Once the model is built, relevant model quality parameters are shown.
Interdependent cross-disciplinary design parameters are separated in accordance with their uncertainty levels, and different fidelity analysis models are assigned to each set of parameters accordingly.
The methods are applied in a real case, where the input parameters of the models are assigned based on the key issues involved in a spherical tank construction.
The regression models are assigned binary regression weights which map metagenes to probabilities of radiation exposure.
Different substitution models were assigned to the partitions as described in the phylogenetic partitioned BI analysis.
Using a quasi-experimental study design, three different referral models were assigned to four detoxification centers.
Furthermore, even at 100% sequence identity, some gene models were assigned to other chromosomes.
Predictive studies with no regression model or only univariate models were assigned a level five ranking, the lowest quality ranking.
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