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While, the lowest cell elongation and highest cell number were achieved on the TiO2 nanotube arrays with 470 nm diameter.
The sample containing the highest cell number (i.e. 1014 cells/ml) was diluted to various degrees using PBS as a diluent.
The response of ACL cells was found to be dependent on polymer composition, with the highest cell number measured on PLLA-Fn scaffolds.
The highest cell number obtained was under control condition (9.9 × 106/ml culture) with 0.77 optical density, 0.61 g L−1 dry weight and 0.228 g L−1 day−1 lipid productivity.
The highest cell elongation (nearly 10 1), the lowest cell number, and the peak of ALP activity were observed on TiO2 nanotubes with 470-nm diameter, and the lowest cell elongation and highest cell number were achieved on TiO2 nanotubes with 150-nm diameter [26, 27].
During dormancy, when no cells have formed newly, the number of cells in the cambial zone (Fig. 1A) varied between four and nine (Table 2) showing significant differences among sites (ANOVA, F = 38.19, P < 0.001) with highest cell number at O1 (7.7 ± 1 cells; Tukey Test, P < 0.001).
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The highest nitrogen concentration displays the highest cell numbers.
Highest cell numbers were observed on uncoated β-TCP in the presence of MesenCult medium).
Woywodt et al. demonstrated that patients with acute vascular rejection had the highest cell numbers compared with other patients [ 61].
Simulations with genome G2 displayed highest cell numbers and more cells reached stage five from stages three and four while no cells of these stages reached stage five in simulations with genome G1.
Highest cell numbers were found on Day 3 showing a 9-fold increase within the PF of TM-treated mice compared with PBS-treated controls (11.6 ± 5.3 × 10 versus 1.3 ± 0.5 × 10; P < 0.01; Fig. 1a).
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