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But our scientists were undaunted
Inhibit or evade multidrug resistance P-glycoprotein in cancer treatment
As a result, the study authors developed a database called HERALD, which provides access to blood samples from patients in Region Stockholm
While it is less potent than natural ligands at the glucagon and GLP1 receptors (0.3 and 0.4 times as active, respectively), it is significantly more potent at the GIP receptor, with activity approximately 8.9 times higher than that of the endogenous ligand
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