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We next demonstrate that the bifurcation structure we have described can explain low-dimensional dynamics in example random networks.
Using a human tumor xenograft mouse model, we next demonstrate that AuNP-loaded T cells retain their capacity to migrate to tumor sites in vivo.
We next demonstrate how fast-slow analysis can beused to derive reduced equations for the evolution of solutions during both the silentand active phases.
To address this issue, we next demonstrate a feasible and effective strategy to suppress the relative interlayer sliding in the CNS, which can lead to a much more sustainable ultrafast CNS-based nano-oscillator.
Therefore, we next demonstrate the bare graphene transistors' sensitivity and the SLBs' seal performance.
We next demonstrate on our experimental data set that the empirical Bayes method removes batch effects that occur between experiments.
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We next demonstrated that TBH increased PPARγ reporter activity in SZ95 sebocytes.
We next demonstrated the rubrospinal tract and the CTT through the use of DiI.
We next demonstrated the utility of the pEnt-Emr marker cassette for BAC recombineering.
We next demonstrated that phagocytosis of muscle cell debris is a potent pro-inflammatory signal for macrophages in vitro.
We next demonstrated that the condition of whole-cell patch recording was stable and reliable when the PDMS was indented.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com