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We also explored evidence for a dose related effect on outcomes.
We explored evidence for different rates of evolution using whole genome sequence divergence.
We studied their predicted structures and putative functions, and explored evidence for selection acting on their diversification.
We explored evidence for interaction by repeating logistic and linear models (adjusted for age and current smoking) for Cd, Pb, and Mo while stratifying on potentially protective metals.
We also explored evidence for age and sex differences, although the magnitude and direction of age and sex inequalities in the stage of cancer diagnosis varies by cancer type (Lyratzopoulos et al, 2013).
First, we explored evidence for non-constant diversification rate in Lepisorus using the Constant Rate (CR) birth death model test [ 54] as implemented in several programs including Gammastatistics V.10 (http://www.oekologie.biologie.uni-mainz.de/people/evi/home/html) and in R applications (http://www.R-project.org): APE [ 77], GEIGER [ 78] and LASER [ 55].
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We can now conclude that at least chronic pain conditions lack clear evidence for the efficacy of the explored surgical interventions (eg, classic surgery and endoscopic procedures.
These orthologs, where explored, are known to have considerable overlap in function, but evidence for functional specialization continues to mount.
The evidence for that?
Evidence for mental turmoil?
Our data provide no evidence for an association between 11 diabetes-related risk alleles and different indicators of socioeconomic status in a population-based cohort, suggesting that the explored genetic variants do not contribute to health inequalities in diabetes.
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