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Multistage functionality was evaluated by cellular uptake and tissue distribution behaviors of the multilayer NPs.
Biological functionality was evaluated using a rat mesenchymal stem cell (RMSCs) culture.
The microstructure was characterized and functionality was evaluated via hardness mapping.
In vitro islet functionality was evaluated by glucose-stimulated insulin release of islets in static incubation with human serum.
In vivo islet functionality was evaluated by monitoring non-fasting blood glucose level in streptozotocin-induced diabetic (SCID) immunocompromized mice after intraportal transplantation of porcine islets.
In vivo functionality was evaluated after transplantation into diabetic nonobese diabetic severe combined immunodeficiency mice.Compared with unmodified and singly-modified Ad5 vectors, Ad5RGDpK7 demonstrated the highest infectivity.
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In addition, the effects of modeling resolution on the calculated fragilities, the estimated direct losses, and the associated functionality are evaluated.
Based on the framework, a proof-of-concept platform is developed and its performance and functionality are evaluated by employing two usage scenarios.
After every cycle hepatic, renal, bone marrow and cardiac functionality were evaluated.
The effects of the mutations on protein structure and functionality were evaluated by a bioinformatic approach.
SERT expression and functionality were evaluated through the measurement of [H]paroxetine binding and the [H]serotonin uptake itself.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com