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Exact(6)
Translations (migration) were measured at the gravitational center of the markers inserted into the fixture.
Therefore, in our study, the effects of I seed and X-ray irradiation on GBM cell migration were measured.
In addition, both cell proliferation and migration were measured in a concentration-response curve in presence of NECA.
Cell invasion and migration were measured using the BD BioCoat Matrigel Invasion Chambers (BD Biosciences, San Jose, CA, USA).
One hundred and sixty-seven different mRNA species involved in stemness, inflammation, immunity, self-renewal, differentiation and migration were measured (see Supplementary information).
To illustrate the mechanism of this beneficial effect in ELCs, the gene expressions related to angiogenesis and migration were measured by RT-PCR for ANG1, NRP1, VEGFR1, VEGFR2, CD31, and vWF under normoxia or under hypoxia in DFO treatment).
Similar(54)
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.
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