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The in vivo efficacy was demonstrated using noninvasive far-red in vivo imaging.
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The efficacy of our vaccine was demonstrated using in vivo challenge experiments with radioactive [3H]-nicotine, followed by an analysis of nicotine distribution in the lung, liver, blood and brain.
The efficacy of this approach was demonstrated using the dystrophin/utrophin knock-out mouse, where restoration of muscle function was demonstrated [6].
The efficacy of this method was demonstrated using two generalized mass action (GMA) models, where the method significantly outperformed single-step estimations.
Unparalleled clinical efficacy has been demonstrated using anti CD19-CAR-T cells to treat refractory B-cell malignancies.
Its efficacy and validity are demonstrated using a fed-batch structured/unstructured model of antibody-secreting hybridoma cultures.
Unparallelled clinical efficacy has recently been demonstrated using this approach to treat patients with refractory B-cell malignancy.
The efficacy of the method is demonstrated using numerical simulations.
The efficacy of the method is demonstrated using data from a rural watershed in Alberta, Canada.
The efficacy of the approach is demonstrated using data collected from children in grades 3 5, namely 34.6% of partial words with reasonable evidence in the speech signal are detected at a low false alarm rate of 0.5%.
The efficacy of our system is demonstrated using both simulations and real-world executions in the experimental section.
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