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Computer modeling of genetic processes may be considered as an advanced branch of cellular automata, named by Wolfram (2002) as "A new kind of science".
They found that the autonomic nervous system, platelet receptors and function, coagulation factors (e.g. fibrinogen, PAI-1), pro-inflammatory cytokines, endothelial function as well as hormonal and genetic processes may be involved [ 1, 4, 12].
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Genetic and non-genetic processes may be responsible for trait deterioration in laboratory-cultured biological control agents.
Genetic and non-genetic processes may be responsible for trait deterioration in laboratory-cultured bio-control agents and their symbionts.
In allopatry, however, isolation by distance and geography are known to cause differentiation between populations within species and can confound interpretations of species diversity because genetic clusters arising from these processes may be mistaken as separate species.
The involvement of TF in pathological processes may be modulated by genetic factors influencing TF expression and activity.
These processes may be influenced by both genetic and environmental factors [ 6- 8, 23].
Sociological processes may be driving these changes.
Genetic processes may, of course, be implicated in the generation of chromosomal change.
Therefore, the end result of this process may be relatively high levels of genetic variation in endemic island species.
This process may be repeated several times.
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