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Roughly speaking, the modification enables the dynamic anti-windup compensator to act more like a static anti-windup compensator in certain circumstances.
In particular, the modification enables the output of the compensator to decay more quickly than if it were absent, thereby effecting a swifter recovery of linear behaviour.
This modification enables the formation of a cleaved form of spike, and facilitates the activation of membrane fusion by subsequent intracellular protease treatment.
Additionally, genetic modification enables the tailoring of hPSC lines for specific purposes.
Such a genetic modification enables the secretion of IL-12 by the cells following specific antigen recognition via T-cell receptor.
The versatility of polymer synthesis and modification enables the production of synthetic polymers in different molecular structures, including star and branched polymers and multiple networks.
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This modification enabled the obtention of submicron-sized lipid particles.
This modification enabled the generation and sequencing of libraries from input phage gDNA quantities ranging from 1 ng to 500 ng (Table 3).
This PEST modification enabled the visualization of slight differences in FLO11 expression when selecting for His+ transformants.
The molecular and cellular interactions between these proteins and their modification enable the cells to sense micro environmental variations and activate various mechanisms, including signaling pathways and transcriptional regulation of specific genes.
Posttranslational acetylation of lysine residues is a highly conserved and important modification enabling the cellular calibration of protein function and/or stability resulting in effects ranging from cytoskeletal reorganization to changes in gene expression.
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