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Our work sets the scene for using C. elegans as a model for studying animal domestication.
Our work sets the stage for studying the role of miRNAs in the key developmental transition from pluripotence to differentiation.
In this respect, our work sets the stage for further studies focused on unraveling the novel signaling mechanism mediating BRCA1 downregulation following UVC- or MMS-induced DNA damage.
Our work sets a quantitative basis to understand the diversification of Acinetobacter into emerging resistant and versatile pathogens.
In this regard, our work sets a good example for microarray-based discovery of prognostic gene sets.
Our work sets the foundation for future studies of evolution of innate behaviors at the molecular and neuronal level.
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On the bright side, I constantly hear from believers who say our work set them free from a lifetime of struggle.
Then, similarly to [29], we structure our working set by I^{imath }_{k}= bigl{ jin I^{imath }: g_{j} bigl(x^{k} bigr)+delta bigl(x^{k}, lambda^{k} bigr geq 0 bigr},qquad I_{k}= I^{ell } cup I^{imath }_{k}.
Our analysis suggests that our working set of insect-specific proteins had been shaped by strong natural selection, with environment as one of the selective influences.
As our working set was mostly composed of unphased genotype data, heterokaryotypes were excluded from the analysis to avoid inaccurate recombination rate estimates.
Note that the publication start year of each journal points out that not necessarily those journals reporting most disease-biomarker associations in our working set started their publication earlier than others (i.e., Plos ONE).
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com