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Exact(31)
(d) SiHa cell migration was assayed with the indicated supplementations to upper and lower wells.
Cell migration was assayed in Boyden chambers [8.0-μm-pore-size polyethylene terephthalate membrane with a Falcon cell-culture insert (Becton Dickinson)].
Cell migration was assayed in the presence of glucose in both wells, with and without NAC in the upper well where indicated (ns, not significant, *P<0.05, ***P<0.005 compared to migration of control cells without NAC in the upper wells; n=4-11).
(e) SiHa (left, n=6) and HeLa (right, n=4) cell migration was assayed with glucose or without glucose in the lower well and with N-acetyl-L-cysteine (NAC) in the upper well where indicated (ns, not significant, **P<0.01 compared to basal migration; #P<0.01, ###P<0.005 compared to migration from the glucose-starved to the glucose-containing wells).
Tumor cell migration was assayed in transwell chambers (Millipore) (Hung et al. 2009).
Spheroid migration was assayed as described previously [56] with some modifications.
Similar(29)
Cell invasion and migration were assayed following the methods described by Yang et al. [ 27].
Cell migration and invasion were assayed using cell migration and invasion assays.
In addition, cell migration was tested using scratch assays.
Corneal endothelial cells migration was evaluated by scratch assay and analyzed with Axiovision software.
Macrophage migration was assessed by Transwell assays.
More suggestions(15)
migration was investigated
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transfer was assayed
migration was ascertained
migration was appraised
migrate was assayed
migration was measured
migration was estimated
migration was enhanced
migration was tinged
migration was allowed
migration was considered
migration was conducted
migration was performed
migration was inhibited
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