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The number shown 0.683E-09 can be seen in cell AU18.
For period 0, the number 0.05235 which can be seen in cell AV6 is the square root of the variance of revision error (V_{r}=0.00274) in cell AT6 already mentioned in cell AJ36.
However, some vGluT-immunolabeling can be seen in cell bodies of large monopolar neurons (Fig. 5C) and we could not rule out low levels of vGluT immunolabeling in dendrites of monopolar cells that also express OK371-Gal4 (see Fig. 7A3,B3).
Therefore, in short-term MTT experiments a difference can be seen in cell survival, yet the cells that survive in the short-term are unable to proliferate in long-term experiments.
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The paper notes that 12 of the 17 participants in this study (aged one to 14 years) had shortened telomeres, similar to what would be seen in cells from a healthy 69-year-old.
Interestingly, such induction was particularly apparent in cells expressing rTFs with 3ZfFLO11/F2, although the induction could also be seen in cells expressing rTFs with 6ZfFLO11/F2-F1.
Thus, accelerated ROS production can be seen in cells upon contact with other SE-expressing cells or with cell-free SE ligands.
Also, after 24 h incubation, a slight decrease was seen in cell viability and only concentrations of 100 and 200 µg/mL were significant (p < 0.05).
Significant improvements compared to lopinavir were seen in cell culture activity versus wild-type virus (pNL4-3) and the lopinavir-resistant mutant virus A17 (generated by in vitro serial passage of HIV-1 (pNL4-3) in MT-4 cells).
The same effect was seen in cell lines expressing recessive G309D or kinase dead PINK1 (data not shown).
A similar rescue of the mobile fraction deficit was seen in cell lines expressing the second PINK1 shRNA sequence (data not shown).
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