In addition, we extended our test to one human glial cell and three human glioma cell lines.
This lead us to extend our test lab with wireless link emulation capabilities.
It would thus be useful to extend our test to detect selection in pathway submodules, which should be the object of future work.
Here, we extended our study to test the therapeutic effect of DHMEQ on CIA, and to test the efficacy on the inhibition of the inflammatory pathway in human RA FLS.
Therefore, we extended our analyses to test the impact of mixed carbon sources.
We extended our study by testing the effect of muraglitazar on carrageenan-induced paw inflammation in the mouse.
Next, we extended our study and tested if the effects of locally reduced or enhanced auxin levels in general could influence stem cell proliferation in the shoot apex as they do affect morphogenesis of the gynoecium.
Further, to analyze the possible effect of in vivo exposure to PAH (Benzopyrene) on IL-4, IFN-γ and ACSL3 mRNA expression, we extended our study and tested the effect of chronic exposure to PAH in Wistar albino rats.
Here, we extended our previous investigations by testing the antigenic/immunogenic properties of Nefmut-based VLPs incorporating much larger heterologous products, i.e., human hepatitis C virus (HCV) NS3 and influenza virus NP proteins, which are composed of 630 and 498 amino acids, respectively.
When we extended our NDGA assay to test for the transport of other mitotic checkpoint proteins off kinetochores, we found that hMad1, hMps1, hSpindly, hCdc27 and cyclin-B were also transported by dynein/dynactin to the spindle poles (Figure 6B, S4).
