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Cell morphology changes were quantified as ratio of long axis to short axis for each cell.
Morphological changes were quantified by measuring capillary cross-sectional areas.
Overexpression and knockdown fold changes were quantified using the geNORM ΔΔCt equations.
Cell morphological changes were quantified as a ratio of long axis to short axis for each cell.
Under the optimized conditions, the dual signal changes were quantified using square wave voltammetry (SWV).
Under the optimized conditions, the signal changes were quantified using square wave voltammetry (SWV).
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The ecosystem sensitivity to temperature changes was quantified using the Q10 index.
The effect of temperature and reaction time on the changes was quantified by measuring 152Eu through gamma spectrometry.
Possible changes are discussed, and potential implications of those changes are quantified using a model of a typical HS2 node in Railsys.
The parenchymal dimensional changes are quantified via the o/e LHR or MRI.
The severity of histopathological changes was quantified according to an arbitrary scale as described before, with some modifications.
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