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The recovery as well as selectivity can be further improved by selecting sorbents resistant to swelling.
This difference in cross-species subunit selectivity can be exploited for design of proteasome inhibitors with selective parasite killing effects.
Selectivity can be high while the rate of transfer of the selective component can also be large.
General strategies for selectivity can be inferred by analyzing the statistics of the nodes involved in selective perturbations.
The selectivity can be simply controlled by the irradiation wavelength.
RIS methods coupled with isotopic selectivity can be extremely useful in nuclear physics.
Selectivity can be achieved through control of dosage, timing, and method of application.
We show that the H2/N2 selectivity can be tuned by varying the composition of this distribution of molecules.
Some of this selectivity can be imposed by raising hurdle rates and tightening assumptions around terminal values.
Selectivity can be enhanced by chemical modification (grafting, for example, sulfur compounds).
Finally, the selectivity can be optimized by controlling the reactant distribution in the liquid phase.
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