Thus, Step 1 in this model proceeds with the weakly nucleophilic C136 thiol initiating attack on the neutral C558′ Hg-C559′ complex, i.e., without activation of either the nucleophile or the electrophile.
Comparison of nested model proceeds with −2LL, the deviance statistic for significance testing.
Testing for interaction variables did not yield a significant effect, therefore the final model proceeds with the assumption that there is no difference in effect between the treatment settings.
We have demonstrated that tumourigenesis in the MMTV-c-ErbB2 model proceeds with reduced activation of ErbB2, ErbB3, Src, Gab2 and Shc when activated Akt1 is expressed by transgene.
In this paper, the Large-scale Atomic/Molecular Massively Parallel Simulator is used to build the MD model and proceed with MD simulations of the nano-cutting process.
Even though zero between-center variation in bias may have been observed in a simpler model, we proceeded with the more complex ones to check whether the variance estimates would change by including different terms into the model (e.g., inclusion of explanatory variables).
Because the RF predictor based on 11 masses, showed little improvement in diagnostic accuracy over PC-594 alone (the ROC-AUC based solely on PC-594 was 0.96 versus 0.98 for the RF model), we proceeded with further validation of PC-594 only.
We analyzed a number of metabolic parameters to confirm insulin resistance in our db/db murine model of diabetes before proceeding with microarrays.
As cancer risk modeling proceeds with geographic risk factors more precisely defined, the correlation among histotypes will eventually become attributable to specific geographic factors.
Before proceeding with models that explicitly test for the presence of selection on synonymous codons, we first tested for variability in synonymous substitution rates (the null condition being that all sites have comparable rates, with none more conserved or more diversified than others).
