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In an exploratory analyses, we also assessed the relationship of telomere length to the duration of the current major depressive episode.
In secondary analyses, we also assessed associations with lung function.
For these analyses, we also assessed correlations between scales across regions.
For these analyses, we also assessed the change from baseline to each of the post-baseline visits.
In independent analyses, we also assessed possible topological discordance using the approximately unbiased (AU) test (Shimodaira 2002).
In exploratory analyses, we also assessed whether hCAP18 levels on ICU day 1 differed by sepsis severity, primary type of infection, or primary organism.
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As a control, we also assessed whether the analyses performed using both cross-validation and jackknife procedures yielded the same values of correct classifications; because no differences were found, we only show the results of the jackknife matrix.
We also assessed glomerular morphology by analysing wt1a expression, a gene encoding a podocyte transcription factor (39, 40) and by electron microscopy.
In all multivariate logistic regression analyses, we also sought to assess the role of multicollinearity.
In addition to using tree cores for isotope analyses, we also used them to assess growth responses to drought.
For explorative purposes, in the subsequent regression analyses we also considered visual learning as assessed by means of the Rey Visual Design Learning Test (Table 2).
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