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Finally, we were able to identify the therapeutic potential of the Jagged1-Notch pathway in the animal model of MS, confirming its immunomodulatory effect.
Finally, we were able to identify common EN/GsbN binding sites corresponding to loci in which EN-regulated genes have been previously identified [18], [19], [21].
Finally, we were able to identify 220 non-redundant genes for the molecular classification of each of the 11 subcategories of follicular thyroid pathologies explored (Table 3).
Finally, we were able to identify associations only with classes of ADM, not with specific ADM.
Finally, we were able to identify workers primarily exposed to radium and those primarily exposed to uranium.
Finally, we were able to identify the polyadenylation sites (PASs) for a subset of NATs, demonstrating that at least some NATs are polyadenylated.
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Finally, given the common biomarkers, we were able to identify between 3 and 59 potentially unique biomarkers per cancer type.
Finally, by searching a dataset of novel exon-exon junction sequences, we were able to identify thousands of putative novel splicing events.
Finally, we were able to use genetics to identify pathways and molecules that affect these phenotypes.
Finally, we were able to screen NB TICs in parallel with non-transformed neural crest-like stem cells (SKPs) under identical in vitro conditions to identify NB TIC-selective compounds.
Authorities were able to identify both of the victims.
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finally we were able to determine
finally we were able to get
finally we were able to examine
finally we were able to convert
finally we were able to phenocopy
finally we were able to establish
finally we were able to celebrate
finally we were able to analyse
finally we were able to validate
finally we were able to replicate
finally we were able to present
finally we were able to reveal
finally we were able to purify
finally we were able to discharge
finally we were able to localize
finally we were able to arrange
finally we were able to adjust
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