An extension of this method to arbitrary shapes is possible and requires capturing the geometry by laser scaling and laser heating from more directions.
Timely intervention is possible, and requires explicit formulation.
Clearance of cryptococcal cells within the central nervous system is possible, and requires Th1 cytokines, in addition to chemokines to attract cells required for degradation (Buchanan and Doyle, 2000; Hill and Aguirre, 1994; Huffnagle and McNeil, 1999).
Alternative explanations of the data, including, for instance, adaptation of the different alleles to different kinds of hosts are possible and require further epidemiological and functional studies.
It follows that any model hoping to capture and replicate all observed behaviour is necessarily going to require a level of complexity and parameterization which, even if it were possible and the required knowledge and understanding were available, would negate the need for such models in the first place.
However, for analysis and feature extraction purposes, translation, into other domains, is possible and often required.
Thus, the simplest explanation of these findings is that the factor VII is unlikely to cause an alteration in apoB or fibrinogen, but a causal effect on CRP is possible and would require a larger sample to confirm or refute reliably.
This is possible and it does not require inventing new technology, but rather scaling proven solutions that we have seen work on the ground.
The MEA recording method utilized here is non-invasive, thus long term chronic measurements are possible and it does not require precise positioning of electrodes, thus it is ideal for functional screens.
Canopy trees have long generation times, and thus may invade habitats slowly relative to other organisms [13] — nevertheless, projecting how fast the S. macrophylla population is growing is possible, and recommended, but will require building a formal demographic model (e.g., [61]).
