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To avoid the occlusion of the coronary or brachiocephalic artery (BCA) due to stent graft migration, we used right ventricular rapid pacing and BCA ballooning.
To uncover the mechanisms by which multicellular tissues align their surrounding ECM before migration, we used an engineered three-dimensional culture model to investigate the dynamics of ECM alignment around tissues of defined geometry.
To examine monocyte migration we used a transwell in vitro migration assay (figure 3).
To further analyze the role of FAK in androgen-induced cell migration, we used FAK+/+ and FAK-/ fibroblasts.
To investigate the in vivo activity of SFA on DC migration we used the FITC-skin-painting model [28].
To evaluate the effective of HSPG binding peptide in endothelial cell migration, we used rhVEGF165 to induce HUVECs migration in a transwell assay (Materials and Methods).
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To determine the direction of migration, we use the difference in the potentials between the two rooms as in the following.
To capture the short-term migration, we use the second definition in which a person is defined as a short-term migrant if she/he has no registration books and has lived in Hanoi and HCMC since 2008, i.e., have lived in the cities for less than 2 years.
To assess the role of syndecan-1 in cell migration directly, we used a phagokinetic colloid gold migration assay [33] to measure the movement of individual cells over 24 h (Figure 4A).
To investigate net migration rates we used data from the United Nations World Population Prospects United Nations Population Divisionn, 2010) [33].
For the Migration assay, we used the Transwell chambers with inserts that contained the same type of membrane but without the matrigel coating.
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