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Pharmacokinetic studies performed herein demonstrate that excellent drug exposure can be accomplished with twice-daily administration.
We herein demonstrate that, during targeting, most mature domains maintain loosely packed folding intermediates.
The wettability studies described herein demonstrate that RAB is a reliable method to achieve strong, gas-tight bonding between the dissimilar materials.
We herein demonstrate that G. lucidum polysaccharides (GLPS) activated BALB/c mouse B cells and macrophages, but not T cells, in vitro.
We herein demonstrate that sialic acid-mimic heptapeptides are identified through a selection from a primary library against influenza virus HA.
We herein demonstrate that the accumulation of hScrib protein might therefore be involved in colon carcinogenesis while also providing a possible link between hScrib and β-catenin.
The results presented herein demonstrate that a conical geometry can be successfully introduced by oxygen plasma treatment to a hollow cylindrical CNT pillar.
The results presented herein demonstrate that there are some limitations to the current Hybrid III ATD under the loading conditions evaluated in the current study.
We herein demonstrate that IL-23-treated monocyte/macrophages selectively produce IL-17A, IL-22 and IFN-γ, and display a distinct lineage gene expression profile in sharply contrast to M1 and M2 subsets.
Collectively, the data presented herein demonstrate that IRF3 is activated upon infection with WT HSV-1.
We herein demonstrate that DNA vaccination protects from proinflammatory Th17 cell responses during induction of EAE.
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