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Collagen I-containing substrates cause Erk1/2 phosphorylation to reach maximal levels at 30 min and remain near maximal levels until 90 min.
Following amputation, mRNA transcripts of these molecules began to increase within 1 2 dpa, reaching maximal levels at 4 7 dpa and declined thereafter (Figs. 5A, 6A, 7A).
A2.01 cells were resistant to HIV-1 infection even at the highest MOI and viral productions from A3.01 and H9 cells reached the maximal levels at MOI 500 on day 8.
This was in contrast with the frequencies of viral genome-positive GC B cells in mice infected with wild type virus and vM2Y-R, which reached maximal levels at day 14 post-infection (Table 1).
In contrast and consistent with data shown in Figure 1B, activation of Cdk1 was delayed in cells expressing fl-hCdc14B, reaching maximal levels at 15 h, which declined more slowly than in parental cells (Fig. 5A, middle).
Phosphorylated JNK was detectable at 5 min and reached maximal levels at 60 120 min.
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The expression of LycRab5A was reached to the maximal level at 24 h after infection.
However, enzyme activity decreased greatly at pH 8.0 and decreased to 56.0% of its maximal level at pH 9.0.
Transcriptional level of ctfAB reached the maximal level at 79 h when using corn-based substrate, which was approximately sevenfold higher than that in cassava-based fermentation.
We found that the surfactant activity was detected at the early log-phase and soon reached maximal level at the onset of stationary phase (Fig. 4b).
The result showed that protofibrils caused an increase in the intracellular Ca2+ from about 30 min after addition, reaching a maximal level at around 2 h, after which the Ca2+ level decreased again (Fig. 9).
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