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These results indicate that rIDE enhances both infectivity and stability of cell-free VZV over a wide range of incubation times and incubation temperatures.
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We propose that the conformational change in gE elicited by IDE enhances infectivity and stability of the virus and leads to increased fusogenicity during VZV infection.
In addition, a VZV mutant virus lacking the IDE binding domain of gE was impaired for syncytia formation and membrane fusion, suggesting that IDE enhances infectivity and stability of the virus through eliciting a conformational change in gE and modulating fusogenicity during VZV infection.
Higher humidity levels affect the infectivity and stability of the virus in the ex vivo environment [ 33, 34].
The in vitro and in vivo infectivity and stability, including transmission through the natural tick vector of A. marginale, has been established for the mutant (hereafter referred to as AmTR) [ 10].
Higher levels of humidity may be indicative of moisture influencing the survival of rodent hosts but also is known to influence the infectivity and stability of the virus in the ex vivo environment (Hardestam et al. 2007; Vickery and Bider 1981; Zheng et al. 2008).
Thus, it appears that Rab7-positive late endosomes are used by Nef to block both infectivity and the CTL response.
However, this type of experiment is not suitable when interest is on improving both infectivity and susceptibility.
The propensity of these protozoans to cross species barriers results from the host nonspecificity of trophozoites of either genus, and the high infectivity and environmental stability of Giardia cyst and Cryptosporidium oocysts (Smith and Nichols, 2006).
Mutational analyses revealed that although mutations in both domains of the CA protein can alter or abolish capsid assembly, virus replication and infectivity, and protein stability, mutations in the CTD are more disruptive to capsid formation than mutations in the NTD.
One of the 15 non-vaccinated controls was enrolled as an extra volunteer to replace any infectivity control drop-outs, one was enrolled as a source of malaria-naïve peripheral blood mononuclear cells (PBMC) for cohort 4 (immunological control) and 13 were enrolled as infectivity controls or as both infectivity controls and immunological controls.
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