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For chemical structures of the tested compounds, see Supplemental Material, Figure S1.
The integration of the biological end points with the chemical structures of the tested substances enables computational mapping (interpolating) of untested chemical analogues into the toxicity data, thereby providing a prediction of their relative toxicological hazard potential.
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The structure of the tested materials allows osteoblasts to proliferate into the sample inner structure with the significant contribution of nanofiber content to cell proliferation.
This behavior is indicative of mesoporous structure of the tested sample [21 23].
This means that we are not interested in the internal behavior and structure of the tested function.
So s2m succeeds in calculating monomeric structures that cover totally or at least 3 / 4 of the atomic structure of the tested polymers.
Figure 1 shows the chemical structure of the tested compounds.
The impact of the genetic structure of the tested sheep populations could not be assessed here.
Furthermore, the small variations in the chemical structure of the tested compounds might provoke the difference in their intrinsic activity on the two cell lines.
Concerning the results of the spatial analysis, it was not possible to take into account the age structure of the tested population by aggregating the data per age group, given the relatively small number of L- and H-BSE cases.
The age structure of the tested population differed significantly from that of the national population in two adjacent départements: Haute-Vienne and Corrèze, which had a similar age structure.
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