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(c e) Lung appearances at the end of the experiment are shown as representative photographs of whole lungs with median LGV for (c) non-treated control animals (LGV: 0.7 ml kg-1) and animals treated with (d) 2%rSP-C33LeurSP-C33LeuPOPG (68 31) (LGV: 18.6 ml kg-1) or (e) Curosurf (LGV: 18.9 ml kg-1).
Here, NS3and SBS3gels have been shown as representative systems.
Among all the plots that were obtained, only a few are shown as representative in Figs. 5, 6, 7, 8, 9, 10, 11, and 12.
The results were expressed as means ± SD or shown as representative data.
When absolute cell numbers were examined (shown as representative data in Figure 5), protected mice had a higher absolute number of CD4+ T lymphocytes (Figure 5A) in lung tissues on days 3, 7, and 14 post-secondary challenge compared to non-protected mice.
However, when we examined the absolute total number of pulmonary leukocytes (shown as representative data in Figure 3), we found increased CD45+ cells at days 3 and 7 post-secondary challenge in protected mice compared to non-protected mice (Figure 3A).
Data are shown as representative experiments or as mean ± SEM.
T1D and type 2 diabetes (T2D) are shown as representative autoimmune and metabolic diseases.
The results with LNT are shown as representative of the entire effort.
All experiments were performed in triplicate, and data are shown as representative results.
Such a dataset was shown as representative of PubMed activity in our analysis.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com