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Because of the published data from P.falciparum puf2 parasites we did not investigate sexual development and differentiation of Pbpuf2 parasites in great detail other than to confirm the previous findings, i.e. an increase in gametocytogenesis in puf2 parasites, partly due to increased male gametocyte differentiation.
Because of the published success rate of Procera after 10 years in clinical service [ 13], our in vitro results suggest that Denzir copings, sandblasted or not, and cemented with zinc phosphate cement are likely to perform equally well as Procera crowns, at least regarding retention.
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Nevertheless, it is very difficult to compare directly with our samples because most of the published electrical transport properties data either do not define the chirality of the measured SWNTs or it is about SWNTs with larger diameters than ours.
Because most of the published epidemiologic literature reports measures of total mercury rather than MeHg, we focused principally on studies with mercury exposure measures in blood or hair as matrices most reflective of MeHg.
Because some of the published reports gave SRT and CRT data only as means ± SDs, all regression lines were fitted to means, even for CCI, where individual-subject data were available.
Largely because most of the published clinical evaluations did not report resource use/cost data, they are heterogeneous in nature and it was unclear whether any were commercially available (and therefore had an associated user fee).
There are limitations of this study because of characteristics of the published literature identified.
Because the majority of the published gene expression signatures had less than 100 genes, the top 100 genes from the Cox regression were used as a signature to predict tumor recurrence for the remaining patients.
This selection was made, because the majority of the published exonic sequence variants for the selected genes were either synonymous or frame shift or nonsense mutations, suggesting that they were pathogenic mutations.
Because of the dependency of the published methods on boiling sample pre-treatment with SDS and unavailability of a commercial assay, we developed an enzyme-linked immunosorbent assay (ELISA) for direct determination of total inhibin.
There are numerous reactions known to be present in various pathways but without any official EC numbers, most of which have no hope to be given ones because of the lack of the published articles on enzyme assays.
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