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We have been using Legionella pneumophila and Coxiella burnetii as model pathogens to study this process.
The methods by which our galaxy eats and the telescopes used to study this process will be presented.
The inherent heterogeneity and asynchronous nature of the reprogramming process renders it difficult to study this process using bulk genomic techniques.
Here we study this process by combining a simple genetic circuit with quorum sensing to produce more complex computations in space.
To study this process, we used a tracheal allograft mouse model that recapitulates large airway changes observed in patients undergoing lung transplantation.
Although the misidentification effect was small in this study, this process is more important for analyses in which larger references are used, such as in RNA-Seq.6, because misidentification may occur more often in those cases.
In the mid-1980s, our ability to study this process received a boost, thanks to the discovery of a large family of genes that encode transcription factors containing a DNA-binding homeobox domain5.
However, little effort has been made to theoretically study this process with a full understanding of key phenomena.
In this study, this process is numerically analysed for the separation of polyethylene terephthalate (PET) from polypropylene (PP) particles.
However the application of one or two techniques to study this process means that the characterization is often only partial.
Numerical modelling is used to study this process and to arrive at predictions of current compaction-driven land subsidence rates.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com