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An in vitro study showed that HQH extractum protects against podocyte injuries by regulating the p-ERK/CHOP signaling pathway to promote podocyte proliferation and suppress podocyte apoptosis21.
In vitro study showed significant enhancement with 6 MV radiation and titania NPs.
In vitro study showed that eGFP2A protein, as expected, was expressed and processed properly from the nascent viral polyprotein.
In vitro study showed that high glucose stimulation increased oxidative stress and cell apoptosis in mesangial cells.
Data from an in vitro study showed that compound 12A inhibited microtubule polymerization in a similar fashion to nocodazole.
In vitro study showed that cells re-collected from the construct maintained good viability and osteogenic potentials.
In vitro study showed that E7 peptide modified P MTMC-LA) films suP MTMC-LAMSCs adhesion and prolifilmsion compared to unmodified P(MTMC-LA) film.
The in vitro study showed the transfection efficiency to be in the following descending order: TMCO-60% > C(43 45 KDa, 87%) > C(230 KDa, 90%).
The in vitro study showed markedly enhanced endocytosis of WGA NP compared to NP in Calu-3 cells and significant inhibition of uptake in the presence of chitin.
The in vitro study showed that scaffolds with a lower permeability gave rise to a significantly higher number of cells attached to the scaffolds after seeding.
In vitro study showed that the PNIPAAm/SWCNTs hydrogel demonstrated significantly higher bioactivities to encapsulated BASCs compared with onefold PNIPAAm hydrogel, including promoting cell adhesion and proliferation.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com