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The cytotoxicity of bare PF127-Chol and FA-PF127-Chol micelles was also evaluated on mouse fibroblast L292 cells.
When the effect of both acarbose and GO2KA1 were evaluated on mouse intestinal SI complex, on mRNA level, we observed that acarbose resulted in reduced expression in all three parts of the intestine, while GO2KA1 administration resulted to reduced expression only in the middle and lower parts.
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Here, we investigated a straightforward approach to produce a biocompatible, radiopaque, and stable polymer-based nanoparticle contrast agent, which was evaluated on mice.
In an attempt to improve the therapeutic effect of mitoxantrone (MTO) against breast cancer and its lymph node metastases, solid lipid nanoparticles (SLN) of MTO were prepared, characterized and evaluated on mice.
The preliminary anti-inflammatory activity of T. stocksianum was evaluated on mice of either sex 25-300 g).
Furthermore, PDI effect of TOPFNs was evaluated on the mice in vivo condition in order to check the possibility of practical medical application.
The antitumor efficacy of all gene nanoparticles (groups FNP, GNP, and HNP) was further evaluated on SCID mice of an average body weight of approximately 17.8 g and an average initial tumor volume of approximately 103 mm3.
In vivo, the anticancer activity of mTOR inhibitors was evaluated on nude mice bearing colon cancer xenografts.
The compounds were evaluated on human and mouse enzymes.
The optical correlates of CSD have been evaluated on both a mouse and a rat model by Ayata et al. [88].
Mt-I, Mt-II, Ntx and Ctx activities were evaluated on isolated peritoneal mouse macrophages.
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CEO of Professional Science Editing for Scientists @ prosciediting.com