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The finding of clear differences in the proliferation inhibition of slowly proliferating normal and neoplastic targets suggested that proliferation per se may not fully mirror the consequences of the macrophage/target cell interaction.
There were no significant (P > 0.05) differences in the proliferation of splenocytes harvested from the mice in the different treatment groups.
Furthermore, the absence of any observable differences in the proliferation and differentiation rates of dt and wild-type cells was not due to an overexpression of plectin, another crosslinker protein, in dt cells.
There were no significant differences in the proliferation of both HL-7702 cells and NIH3T3 cells between the Corning microplate and two kinds of zein films, except that the zein film composed of smaller particles at the lowest concentration exhibited a very good ability for proliferation of both the cells, while PLA was a poor matrix in the latter period of the cell proliferation.
Interesting differences in the proliferation of epithelial keratinocytes were noted in the presence or absence of SDF-1.
Therefore, the differences in the proliferation were likely due to the expansion of Tregs during the progression of disease.
Similar(28)
In the study of Stomper and colleagues [ 8], comparison was made between single biopsies of either fat or dense areas in different women; they found no difference in the proliferation rates in the dense and fat areas.
No significant difference in the proliferation rate was detected in anti-miR-200c treated and corresponding control groups in both mouse and human keratinocytes (Fig. 2c).
On the other hand, there was no significant difference in the proliferation and glycosaminoglycan synthesis of chondrocytes between EO gas-treated and HPG-treated PLGA scaffolds.
The cell viability assay (CCK-8) indicated no significant difference in the proliferation of parental DCs and DC/NF cells (Fig. 3a).
In the current study, we tested the hypothesis that there is no difference in the proliferation and differentiation capacities of osteoblastic cells when cultured on titanium disks mimicking the surface of 3M™ESPE™ MDIs or standard (Ankylos®) implants.
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