Finally, we demonstrate that system dynamics dictate which type of engineered control is optimal.
Finally, we demonstrate that cells tagged with nanodisks can migrate within spatially confined environments.
Finally, we demonstrate that the optimal contract can be closely approximated by the "first loss piece".
Finally, we demonstrate that surface expression of CD19 requires CD81, even in non-B cells.
Finally, we demonstrate that both Acr families from S. thermophilus phages inhibit Cas9-mediated genome editing of human cells.
Finally, we demonstrate that the π-plasmon energy depends on the charge carrier concentration.
Finally, we demonstrate that our tool enables social scientists to gain novel insights into three active research questions.
Finally, we demonstrate that NF110b associates with the dsRBM-containing transcriptional co-activator, RNA helicase A, independently of RNA binding.
Finally, we demonstrate that CrvA promotes motility in hydrogels and confers an advantage in host colonization and pathogenesis.
Finally, we demonstrate that codon usage regulates protein function by affecting co-translational protein folding.
Finally, we demonstrate that auxin-induced cytosolic Ca2+ changes are required for rapid growth inhibition.
