Moreover, predictions are suggested that may be addressed by selection experiments.
Three areas of research are suggested that may repay intensive investigation.
New treatment delivery and trial design strategies are suggested that could accelerate agent initiation in neuroprotective treatment trials.
Several sources of error are suggested that could cause the small differences between the simulated results and the measured data for the constructed generator.
New approaches are suggested that may either refute or support competing dynamic models of EEG and can have major impacts on the experimental design of new cognitive studies.
Particle synthesis parameters are suggested that could be controlled to enable micrometer-scale Al particles to achieve the performance of nanoscale Al particles.
Solutions are suggested that might help merge these records together in order to generate more robust physical risk scenarios for communities potentially at risk from these events and from which detection of human-induced changes to the frequency and magnitude of events can be discerned.
A few mutations are suggested that might have an effect on differential binding/regulation.
