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Although residual complexity can solve this problem in certain situations, relative modification of the parameter can generate dramatically different results.
The first strategy can be applied with minimal a-priori information on the masses (i.e. using a parameter that quantifies an eventual relative modification of the total mass of the structure before and after damage).
The measure of behavioral adaptation was well transcribed by the relative modification of RTs and error rates in post-success and post-error trials.
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Kinetic analysis successfully quantified the variation in the catalytic activity by using the relative modification coefficient to consider the degree of carbon deposition.
Specifically, based on a simulation study, our investigation had limited power to detect a relative effect modification of 2 but reasonable power to detect a relative effect modification of 3.
However, for a relative effect modification of 3, we had 81% power even with a gene prevalence of 20%.
Our simulation study showed that, for a relative effect modification of 2, we had 47% power for a gene prevalence of 20% rising to 67% power for a gene prevalence of 50%.
For some genotypes, including GSTM1, GSTT1, and GSTP1, we found a relative effect modification of approximately 2 in this analysis, so our lack of significance may be a result of power limitations.
Finally, we repeated this analysis 1,000 times for relative effect modification of 2 and 3 and took the power to be the fraction of time a significant interaction was found.
Such an enhancement of the (A/P+AP/DV) class in the relative absence of modification of the D/V class indicates that the direction of rotation is genetically separable from fate choice.
As shown in Figure 2A, modifications at the 3'-end of PD-ODN2006 enhanced NF-κB activity relative to no modification of PD-ODN2006.
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