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Although texture and color feature subsets are likely to characterize corrosion individually, we demonstrated that when combining both of these subsets with a suboptimal sequential feature selection procedure the combination outperformed each one, that is, subset.
Both of these subsets are enriched by an IgM component, in addition to an IgG one.
In order to test the reproducibility of different test statistics (Fig. 6), two sets of three arrays were randomly selected from the 23 replicate arrays in Dataset 4. For both of these subsets, we calculated the several different test statistics described above.
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As CD4+CD25+ T cell subset consists largely of CD4+CD25high Treg (see Figure 2D), the expansion rate of both these subsets is comparable in the presence of RAPA.
This apparent discrepancy can be explained by the fact that IL-15 is needed for the survival of both memory and naïve CD8+ T cells and absence of this cytokine, can affect the survival of both these subsets [20].
As with MVA, adenovirus boosted both the CD4 and CD8 T cell activity, and priming of both these subsets was also observed when following immunization with adenovirus expressing mycobacterial antigens [18], [29], [33].
In the S. aureus patients, there was a significant expansion of both of these monocyte subsets.
Furthermore, we have shown that both of these DC subsets are present in synovial fluid (SF) from RA and psoriatic arthritis patients, although mDC significantly exceed pDC.
Each of these subsets has signature cytokines.
Clustering results of these subsets were examined.
In both these subsets of patients, the diagnosis of PBC was established histologically.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com