Exact(1)
Vectors based on currently used human vaccine viruses [i.e., poliovirus (the Sabin oral poliovirus vaccine (OPV)) and vaccinia (the smallpox vaccine)] are particularly appealing because of their well-characterized safety profiles in millions, if not billions, of vaccinees, as well as the extensively characterized ability of these vaccines to induce strong long-term immune responses in humans.
Similar(59)
The well-characterized ability of CaP minerals to bind and release plasmid DNA, coupled with the ability of biodegradable CaP coatings to form on the surface of common biomaterials, provides a potential mechanism for controlled release of plasmid DNA from various biomaterials.
We propose that this mechanism is involved in the well-characterized ability of the vascular endothelium to quickly adapt to sudden changes in the microenvironment.
To investigate possible contributions of the interferon (IFN) system to control HCV infection in HFLC, we exploited the well-characterized ability of paramyxovirus (PMV) V proteins to counteract both IFN induction and antiviral signaling.
To investigate the possible role of the innate immune system in controlling productive HCV infection in these cultures we exploited the well-characterized ability of paramyxovirus (PMV) V proteins to counteract both IFN induction 20 and antiviral signaling mediated by binding of the IFN receptor.
We then generated a rabbit polyclonal antibody against the N-terminal 500 amino acids (a.a). of USP9x and characterized the ability of this antibody to detect endogenous USP9x.
Using the panel of markers TNF-α, IFN-γ, MIP-1β, IL-2, and CD107a, we characterized the ability of CD8+ T-cells to simultaneously exert these 'functions' in response to both HCV and HIV peptides.
We characterized the ability of ChR2 to drive CIN activity in an acute brain slice using cell-attached recordings obtained from ChR2-positive CINs that were visually identified under epifluorescence (Fig. 1B).
Moreover, we characterized the ability of these TMEPAI antibodies in immunofluorescence staining.
Therefore, we characterized the ability of etoposide quinone to alter enzyme-mediated DNA cleavage and ligation.
Here, we characterized the ability of AS101 to enhance the expression and activity of the SIRT1 protein.
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