Cell migration was measured by counting the number of migrated cells in five random non-overlapped fields at 100× magnification.
Aggregate measurements were taken at day 0, and migration was measured at 72 h (day 3) using a Zeiss Primo Vert microscope (Carl Zeiss Canada, Toronto, Ontario, Canada) with an ocular micrometer.
Cell migration was measured by counting the number of cells that migrated into the cleared area of the dish.
In vitro cellular migration was measured by determining the ability of cells to migrate through a transwell membrane using the Transwell permeable support system (Corning, Coring, NY, USA).
In 64 knees, migration was measured with radiostereometry.
Spontaneous migration was measured to be less than 3.5% in AT- and SN-cells (Fig. 3a).
Wound migration was measured in five selected fields and calculated based on the width of injury at 0 h.
The migration was measured at time 0 and 24 h post-wounding using a microscope Nikon Diaphod 300 INV (10 × ) and camera Canon Power shot A95.
The temperature and time dependence of the rate of migration was measured in the range 340 480 °C.
Migration was measured using a wound model (confluent monolayers ± 5-fluorouracil [5-FU] over 1-96 hours).
Proximal migration was measured as the distance between the tip of the lateral malleolus and the distal tibial articular surface in comparison with the opposite side [11].
