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A full-scale 'theoretical' pressure vessel was used and the described methodologies were applied in its design to see if there were any similarities between the methods.
This includes also descriptions for how to integrate the various logistical components in modeling logistical tools that are currently available to implement the described methodologies.
The described methodologies may be extended to preserve power under other disease models.
Small interfering RNAs (siRNAs) can also be detected using the described methodologies (both endogenous-siRNAs and exogenous therapeutic siRNA oligonucleotides).
The described methodologies to label GPCRs provide the possibility to monitor the expression and cellular localization of these biomolecules.
In future, the described methodologies will be complemented with additional methods and platforms to address gaps in metabolome coverage identified by the pathway mapping procedures.
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A case example is analyzed based on the described methodology.
Three different control schemes are designed using the described methodology.
The usefulness of the described methodology was exemplified by two practical use cases.
To this aim, a kind of calibration step has been added to the described methodology.
In this section, we present results which have been achieved using the described methodology.
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