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Finally, from the comparison of various nuclear MED desalination systems we confirmed the potential of the KAIST HTGR + MED system that may be one of the best desalination options in mass production of desalted water.
Using two different cellular systems, we confirmed that TGFβ treatment strongly decreased Myc levels and demonstrated that this suppression was accompanied by transcriptional and translational responses reversed to the ones observed upon Myc activation, including TE modulation of ribosomal protein genes and of ECM and adhesion protein genes.
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Furthermore, via the simulations under the settings of practical systems, we confirm our intuition for the general scenarios.
Using the prototype system, we confirmed that the task context-aware platform executed the required services on the basis of the task context model.
After derivatization with folate on the phospholipid-capped FMSNs (denoted fa-Lipo-FMSNs/PpIX, the so-called nanoPDT system), we confirmed the nanoPDT systems' selective targeting of and entry into the folic acid receptor-overexpressed HeLa cells by means of cell viability assessment and confocal microscopic analysis.
By using luciferase reporter vector system, we confirmed that miR-20b directly targeted the 3'UTR of Hif1a and Vegfa.
Using this system, we confirmed that induction of vGPCR expression in endothelial cells leads to the potent upregulation of VEGF, as previously reported (Fig. 1C) [18], [18].
Indeed, using a self-quenched DQ-ovalbumin particle system, we confirmed that the decreased acidification of lysosomes of CHM patients significantly affected proteolytic abilities of the monocytes [25], [26].
Using this system we confirmed sumoylation of PCNA, the processivity factor for DNA polymerase δ, and RFC2 (Figure 1C), a subunit of the factor that loads PCNA onto DNA.
Also in this experimental system, we confirmed physical association between WWOX and ΔNp63 α.
We generated transgenic flies expressing full-length Trap1, and using UAS-GAL4 system we confirmed the expression of the transgene by western blot analysis.
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