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cerevisiae (Sigma-Aldrich), 0.8 mM HED (0.15 mM Cys-SG) and 1.6 M protein
Thus, drugs avoid the hepatic first-pass effect and/or degradation in the bloodstream, which is a crucial issue in the case of peptide drugs [20,21]
In addition to above mentioned mechanism, GCs exert also non-genomic actions involving membrane-bound GRs [57]
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