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As new methods are being developed to incorporate descriptions of CS and IF effects in computer-assisted drug discovery, there are good prospects for the rational design of inhibitors targeting flexible proteins.
If effects are detectable, the mixture is fractionated according to the physico-chemical properties of the components.
If effects of electron inertia are added, reconnection of magnetic field lines is allowed, although the resulting model still possesses a noncanonical Hamiltonian structure.
If effects are found, for the risk assessment the NOAEL has to be determined by testing specific sensitive parameters as specified above.
If effects of other covariates (e.g. time or space) are suspected, we similarly recommend use of extreme value models which adequately capture sources of covariate variability for all design analysis.
If effects are constrained to private goods and services, then their prices should reflect an individual's willingness to pay and a producer's willingness to accept compensation for those goods and services.
If effects of repeated interactions (and, thereby, a "shadow of the future") shall be taken into account, this can be done by modifying the payoffs accordingly [3], [117].
If effects were significant, post-hoc tests were applied.
If effects are not significant, go to step 11.
If effects are random, then X = (1 − ι) Q has a central chi-square distribution.
If effects of multiple causal SNPs are allowed, the number of both the RR and the δ parameters increases substantially.
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