In our analysis, outcome-locked activity in ventromedial PFC in response to gains only was the dependent variable, with (gain) outcome-locked activities in ventral striatum and dorsolateral PFC as covariates and group was a fixed factor.
However, this scenario appears to be unlikely to occur because our deletion analysis outcomes indicated that the first 16 amino acids (the Nα motif) are not essential for NaTrxh secretion, instead it was the inner domain, the Nβ motif, the one that directly led its secretion.
However, some limitations exist in our analysis regarding outcome ascertainment.
10, 16 These 8804 women gave birth to 9153 children, 9024 of whom were included in our analysis of outcome at discharge from hospital.
Our analysis of outcomes in relation to PLAB attainment levels was motivated by Kane's "direct, criterion-related approach" for standard setting, and it was used because no direct method of assessing entry equivalence is currently available in the UK.
For our next analysis, our outcome variables were the risk perception scores for the 13 substances.
The primary outcome for our analysis was the primary outcome investigated in the review.
Therefore, we ignored this mutation during our analysis of clinical outcome, along with other mutations that did not result in amino-acid changes.
We restricted our analysis to this outcome because it reflects the opportunities for hand hygiene.
Third, our analysis focused on outcome after the first regimen following bevacizumab study therapy.
We restrict our analysis to dichotomous outcome data measured using odds-ratio (OR) due to its mathematical properties [ 27– 29].
