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In FE models, the structures of interest, such as the brain, meninges and skull, are built by separating three-dimensional models of the structures using tens of thousands or millions of discrete elements.
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In network models, the structure provides features that influence the transmission of an infectious disease.
Nonlinear time-history analysis and modeling the structures are carried out using the OpenSees software.
First we modeled the structures of 10 proteins and then provided models for 40 additional interactions.
In the model, the structures are assumed to be generated by random walks.
Modeling the structures of individual PCSK enzymes has offered little insights into the specificity determinants.
We used UCSF Chimera (http://www.cgl.ucsf.edu/chimera/) to model the structures seen by TEM.
The structural equation model includes the measurement model and the structure model.
One way forward is to model the structure of these proteins using similarity modelling methods.
It occurred to him that he could use them to make models of the structures associated with Mr. Fuller.
We built models for the structures of the remaining proteins.
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