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Primary ESCs, obtained from non-pregnant endometrium and decidualized in vitro, are considered a model for cells that decidualize during the non-pregnant menstrual cycle.
Thus, our receptor desensitization model accounts for the hypothesized multi-step chemotactic navigation model for cells to reach the distant target [12], [13], and argues the importance of the multiple different chemoattractants based guiding mechanism.
10.7554/eLife.01916.016 Figure 3. Wild-type behavior matches the veto model for cells with a lower effective number of flagella.
Figure 12a shows the results of simulations with this model for cells with different optimal saccade amplitudes, ranging from R0 = 2 to 50 deg.
2) While the authors' data support the proposed model for cells dividing slightly away from the plane of the neuroepithelium, it is less clear how the data could explain cells dividing with their spindle oriented completely perpendicular to the neuroepithelium.
The purpose of this paper, therefore, is twofold: to present a new nonlinear constitutive model for cells that accounts for their inherent material non-uniformity as well as potential material and geometric nonlinearities, and to extend a prior solution from the finite elasticity literature for use in a sub-class of AFM studies of cell mechanics.
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Ariafar et al. (2011) purposed the model for cell layout in the shop and machines in the machine cells.
Ghezavati et al. (2011) proposed a robust model for cell formation and group scheduling with supply chain approach.
This model may be regarded as a simplification of a recently developed physically meaningful model for cell motility.
A recently developed nonlinear mathematical model for cell dynamics is used to design the controller (medication dosage).
Furthermore, a model for cell metabolism is incorporated representing the basic enzymic reactions of glycolysis and the Krebs cycle.
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