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Currently, research focuses on post mortem human brain tissue and animal models, and although considerable advances have been made using these resources, post mortem tissue can never provide the basis for dynamic functional studies and post mortem effect and suitable control matching will always be problematic [12].
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Finally, the spatial and temporal resolution will affect the result, especially for dynamic functional connectivity studies like ours.
Low gamma-band (30 Hz to 50 Hz) synchronization between neural groups coding the various features of objects currently populating experience has been proposed as a mechanism for such dynamic functional integration in the brain, and has been suggested to be the biological basis of perceptual experience and feature binding [6] [8].
Some evidence for a dynamic functional balance between heterochromatin and euchromatin has been already provided by Ebert et al. (2004).
Dynamic functional testing, for example the horizontal hop test, reproduces the functional movement, although its accuracy is somewhat questionable.
Here we have investigated the molecular basis for such functional plasticity involved in this model.
This structure may serve as a basis for further functional studies of nsp4.
They form the basis for future functional dissection of innate immune signaling.
The basis for this functional diversification is not clear.
It also serves as basis for further functional genes studies.
And, the sRNA target lists could serve as the basis for further functional investigations.
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