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The combined methodologies described here proved to be cost-effective and could be extended to other genes/proteins of interest.
The methodologies described here can be applied to other multi-parameter chemical systems, which should significantly improve the rate of parameter optimization.
The methodologies described here may benefit studies of other animal and human pathogens.
The methodologies described here can be applied to other less studied bacteria to gain functional insights into the transcriptional regulatory mechanisms that govern the spatio-temporal regulation of gene expression.
In conclusion, the methodologies described here could become a powerful tool to be used in a dermatological clinic for both early diagnosis and therapy follow-up purposes.
Further application of the methodologies described here may allow the elucidation of CIR sub-family A and B protein functions, including their contribution to antigenic variation and immune evasion.
Similar(54)
Furthermore, the methodology described here may be useful for the identification of new TRβ ligands.
The methodology described here can be readily transferred to other coastal systems.
The methodology described here adds great value to the overall Quality by Design approach to tablet development.
The methodology described here can be applied to any type of molecular material/wide band gap dielectric interfaces.
The methodology described here adds great value to the overall quality by design (QbD) approach to drug development.
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policies described here
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