Exact(1)
Regression analysis of the data was carried out to develop equations for the composites in which the wear volumes of the specimens were expressed in terms of simultaneous contribution from the influence of load, abrading particle size, sliding speed and their mutual interactions.
Similar(7)
Thus VDRs and VDRl mRNA abundance in all studied tissue specimens was expressed as mRNA copy number per 1 μg of total RNA.
Bacterial concentration in specimens was expressed in: i) Aa cells/ml paper point suspension for subgingival plaque and ii) Aa cells/ml saliva in saliva samples.
It has been demonstrated that PDGFC in PTC specimens is expressed mainly in the cell membrane, the cytosol and in the perinuclear area of the tumour cells, and that the ~43 kDa non-SUMO1 modified form is the predominant [ 19].
A standard curve was constructed for standards of ACTB (TaqMan DNA Template Reagents Kit, Applied Biosystems) and mRNA abundance in all tissue specimens was expressed as mRNA copy number per 1 μg of total RNA.
For quantification of protein levels, the relative amount of pAkt (Ser-473), pAkt (Thr-308), and pS6 in tumor tissue specimens was expressed as a ratio of the optical density for the tumor specimen to that for the corresponding non-neoplastic specimen (set at 1.0) by densitometric analysis, as described previously [ 16, 17].
Viral loads in each specimen were expressed as the number of HPV copies per 10 cells.
About 3% of dry salt in the specimen was expressed by way of immersing the specimen (50*50*20 mm) in 10% (wt%) NaCl solution for 24 h.
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