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An important mediator of both tumorigenesis and resistance to treatment involves inhibition of apoptosis [7].
Fractalkine (CX3CL1) is a potential mediator of both atherosclerosis and metabolic disease.
Recently, we identified granulocyte-macrophage colony-stimulating factor (GM-CSF) as a critical mediator of both tumor necrosis factor-α– (TNF; modeling inflammation) and thrombin-induced (modeling abruption) weakening of the fetal membranes.
Therefore, a model has evolved whereby TIEG1 serves as an important mediator of both Runx2 expression levels and Runx2 transcriptional activity in osteoblasts (Figure 10).
TSC2 is a critical mediator of both MAPK and PI3K pathways [35], [36], [37], [38], hence we tested whether the interaction between 14-3-3γ 14-3-3γ 14-3-3γfected by the presence of PD98059/LY294002 inhibitors.
Smurf1 has been defined as a new recognized mediator of both viral autophagy and mitophagy.
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NADPH oxidases (Nox enzymes) are critical mediators of both physiologic and pathophysiologic processes.
They are mediators of both adaptive and innate immune regulation supporting the theory that a close interplay of adaptive and innate immune regulation is critical in asthma.
These multimeric enzymes are mediators of both intra- and extracellular vectorial proton transport in all eukaryotic cells.
Cytokines are ultimate mediators of both responses.
Segmental duplications have been recognized as important mediators of both gene and genome evolution [ 1- 9].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com