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Repeat-sequence analysis revealed that the abundance of LINEs might be due to a GC bias of the restriction sites and that the GC content of silkworm LINEs was higher than that of mammalian LINEs.
The activity of pp60c-src from six of nine carcinoma cell lines was higher (on average, fivefold as measured by enolase phosphorylation, or eightfold as measured by autophosphorylation) than that of pp60c-src from normal colonic mucosal cells, or human or rodent fibroblasts.
The membership probability of 212 lines was higher than 0.6 for one of the four subpopulations.
Under Fe-sufficient conditions, the NA concentration in 35S-HvNAS1 lines was higher than that in lines harboring the HvNAS1 genomic fragment (Higuchi et al. 2001a).
In addition, the biomass of OX lines was higher than that of WT (Fig. 3d-e), which might mainly be attributed to the increased tiller number at vegetative stage.
The rate of NO3− influx into roots of OX lines was higher than that of WT (Fig. 4a), indicating that elevated expression of OsNPF7.2 enhanced nitrate uptake by roots.
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Viability of both cell lines was high according to the MTT assay after incubation with various SA-FSNP concentrations (Fig. 6a), suggesting that SA-FSNP showed minimal cytotoxicity.
The amount and extent of radiolucent lines was high in both groups.
Furthermore, the range of body weights in B lines was high compared with that in T and L lines (Table 1).
Despite minimal cytopathic effect, virus propagation in cell lines was highest in Vero cells (50% tissue culture infectious dose, 107.9/mL), most likely because this cell line lacks interferon.
Since the variation of GUS activity between different transgenic lines was high, we used northern blot analysis to investigate the regulation of ProDH2 expression.
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