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The cytotoxicity of high molecular weight PEI reduced the cell viability leading to the reduced function of expressed transgene.
Pretreatment with orlistat reduced the cell killing activity of PPD.
HA coating reduced the cell attachment and proliferation on PHA although the materials had increased hydrophilicity.
Blocking with haloperidol to compete with [99mTc]5 significantly reduced the cell uptake.
Of these 7, 10 and 14 significantly reduced the cell growth.
Nanosilicas reduced the cell viabilities of CHKs in a dose-dependent manner.
In ancillary tests, they observed reduction in gene expression and increases in mitotic spindle dysfunction only for the AM-EMF exposure that reduced the cell growth rate.
50 μg/mL of SLE markedly reduced the cell invasiveness by 32.9% for A375 cells and 55.4% for B16F10 cells (Fig. 4C and D).
Reduced Akt phosphorylation resulted in lowered expression of EGR-1 and hence, reduced the cell proliferation rate.
Eicosapentaenoic acid (EPA) had no impact on gene transcription in this study, but reduced the cell secretion of PGE2.
ES-PCL successfully prevented the occurrence of vasodilation and aneurysm formation after transplantation and reduced the cell inflammatory infiltration.
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CEO of Professional Science Editing for Scientists @ prosciediting.com