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doi: 10.1177/0394632016659494
Normalization was carried out to account for technical variation, and keratins identified in blank Schirmer strip controls were removed, as previously published 30
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Rossmeier, A
Grijalvo S, Mayr J, Eritja R, Daz DD
Before nanocarrier cell entry experiments, the non-toxic concentrations of endocytosis and metabolic inhibitors on the cARLA treated hEC were determined by cell viability assays, namely impedance measurement and MTT tests (Fig
