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The activation energies for dislocation-based deformation as well as grain boundary sliding and migration were quantified by fitting simulation data to temperature using an Arrhenius relation.
Within these experiments, chemokine-independent baseline migration and CXCL12-dependent migration were quantified.
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Migration was quantified by counting the migrated cells in 10 random high-powered fields per filter.
Cell migration was quantified by counting all migrated cells in each membrane.
Cell migration was quantified by blind counting of the migrated cells on the lower surface of the membrane of 5 fields per chamber under microscope.
Migration was quantified by directly visualising and counting migrated cells under the microscope after cell staining.
Cell migration was quantified by the blind counting of migrated cells on the lower surface of the membrane, with three fields per chamber.
Cell migration was quantified by blind counting of the migrated cells on the lower surface of the membrane of five fields per chamber under microscope.
Migration was quantified using the ratio of the migrated cells over the total cells (migrated plus remaining cells) to determine the fraction of migrating cells in each individual experiment.
Efficiency of cell migration was quantified by counting the total number of migrating cells.
Cell migration was quantified by determining the number of cells that had migrated into the filters.
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