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It is generally assumed that more cells evaluated signifies more reliable results as attested to by narrower confidence intervals.
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Polysomy of chromosome 17 was defined as the presence of three or more CEP17 signals in more than 6% of the tumor cells evaluated.
The tumor was considered as CISH amplification positive if the copy number was ≥4 signals per nucleus in more than 40% of tumor cells evaluated [ 16].
More cell lines must be evaluated to characterize fully the antitumor actions of celecoxib, including identification of its primary targets, the precise molecular mechanism of cell damage, and the basis for its preferential effect on tumor cells.
And more cells.
No more cells.
Enter data in 2 or more cells.
Tumour-related methylated forms of three genes (RAR β2, RASSF1A and HIC-1) were much more frequently evaluated in the cell-surface-bound cirDNA compared with cell-free cirDNA in tumour-bearing patients (Table 2).
More than 400 cells were evaluated for each of these cases.
Furthermore, in our study, in order to characterize the cells more accurately, we evaluated the association between the number of circulating non-HSCs and the expression of the markers analysed at the mRNA level.
To investigate whether ST3Gal III overexpressing clones might lead to the acquisition of a more migratory cell phenotype, we evaluated cell migration on collagen Type-I using a transwell migration assay (results shown in Figure 5).
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