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Although the averaged equations for low frequencies are not valid and we cannot interpret the results presented in Fig. 5b e in terms of a stabilization of the fixed point of the averaged neuron dynamics, the pronounced jump of the oscillation amplitude is still present in these figures.
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However, they cannot interpret the results of classification to users.
Consequently, we cannot interpret the magnetic behavior based on the above simple argument.
Therefore, we cannot interpret the observed SSE as a direct response to an external stress change.
However, we cannot interpret this result as adherence to the use of the program since in our unit the syringe pumps are also used for other infusions (saline solution or platelet transfusions) that are not included in the program's drug library.
All of these results indicate that the RESS mechanism might be compromised in Δ Ncap3m, even though we still cannot interpret the detailed mechanism at present.
At this reviewer's request a multivariate analysis has been added here (next page) and as you can see the confidence intervals of the AOR are very large, which means the level of uncertainty are so high that we cannot confidently interpret the result.
Until they exclude sequencing artifacts, including those resulting from strand bias, they cannot interpret the data as actual biological strand bias.
Without knowing the optimal way to monitor adherence, one cannot accurately interpret the results of clinical trials or properly treat patients [ 1, 7].
How can we interpret the results?
How do we interpret the results of our second simulation?
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