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Motivated by the phenomenon of wall-induced migration, we apply the lubricated immersed boundary method to simulate an elastic vesicle near a wall in shear flow.
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To check whether our cells induce myofibroblast proliferation or migration, we applied conditioned medium (CM) to 10T1/2 cells, and found that proliferation and migration rates were significantly increased when the cells were stimulated with U87-C CM compared to Mock or U87si CM (Figure 1D).
In order to evaluate the effect of E2 on single and collective cell migration, we applied 2 typical assays: boyden chamber and wound healing, respectively.
To address whether miR-101 expression can suppress lung cancer cell migration, we applied wound-healing assays to the above transfected cells.
To do this we apply again the Migration rate computing algorithm defined previously by replacing the Equations (3), (4), and (5) by these analogous (7), (10), and (9), respectively.
Then, we apply the F-K migration algorithm in aiming to get a better focused image.
Using these tomographic models as migration velocity models, we applied the traveltime mapping method to obtain the reflector distribution along each profile (Fig. 3(g) and 3(h)).
To assess the role of CSF-1R in migration of cancer cells we applied a wound-healing test.
To test the relationship between migration stage and path formation, we applied a previously employed mathematical technique that distinguishes between multipolar and bipolar neurons by path formation in-vitro [ 25].
We applied Isolation-Migration models, assignment analyses and estimated the genetic differentiation and diversity between species and between populations within species.
We applied prestack depth migration by using the results of the high-density velocity analysis and further analyzed this region.
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