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The results indicated that the CPTES modification allowed the PDMS surface to have better hydrophilicity than the APTMS modification.
This modification allowed the identification of new bioisosteric ligands with fairly good activity on PPARα and fine-tuned moderate activity on PPARγ.
In addition, the modification allowed the adsorption of CO2 reversible, and the saturated adsorbent was regenerated at the ambient temperature either by purging it with the purified gas or by vacuuming.
This modification allowed the lifting of both outer bowls while the reward was still covered underneath the inner bowl.
This modification allowed the total χ score to be decreased slightly, but the mean values for each mode were essentially unperturbed.
Indeed, we observed significant brain targeting only when the sulphamidase was additionally modified with the ApoB-BD, indicating that this modification allowed the sulphamidase to effectively cross the BBB.
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This modification allows the user to solve the 3D Richards' equation only in selected parts of the model domain.
This modification allows the porosity evolution of the membrane to be predicted under a variety of EPD processes.
This modification allows the model to represent removal of fines in marl-rich catchments, without the need to introduce a fully explicit travel distance formulation.
This critical modification allows the enzymes to bind to specific receptors on the membrane of the Golgi, which then directs them into vesicles leading to a lysosome rather than a secretory vesicle.
These type of modification allow the reversible targeting of a protein to a membrane.
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