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She was involved in the study of biological molecule interaction with low doses of ionizing and microwave irradiation, ligands, anti-cancer drugs, metal and carbon nanostructures.
The site-specificity of the CO probe molecule interaction with the Cu+/MFI system is investigated by a combination of experimental and theoretical techniques.
Additional interactions not observed in previous hDAAO ligand structures included a hydrogen bond between the coumarin hydroxyl and the carbonyl backbone of Gln and a water molecule interaction with the cyclic oxygen and carbonyl of compound 2's coumarin ring.
The unique facet-dependent variations in surface electrostatic potential observed in nanodiamonds also promotes water molecule interaction with nanodiamond surfaces, a property that results in nanodiamond gadolinium contrast agents producing among the highest per-gadolinium relaxivity increases ever reported.
ROS produced by immune cells has the ability to cause direct damage to muscle tissue or may act indirectly through the activation of catabolic signaling through immune molecule interaction with muscle receptors [ 126].
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Two assays are presented to exemplify the detection of small molecule interactions with the biosensor.
Evaluation of spatial orientation of the designed molecule interactions with the hERG protein recognizes the cardiotoxicity level of molecules [20].
Currently, the most commonly used purification strategies for recombinant BChE enzymes involve using affinity resins based on small molecule interactions with the enzyme's substrate binding site.
These results offer further insight into pharmacological activation of Kv7 channels, add to the understanding of small molecule interactions with the channels and may contribute to the design of subtype selective modulators.
Our method is broadly applicable for the prediction of protein-small molecule interactions with several novel applications to biological research and drug development.
As the TLR4 activity of natural TLR4 ligands (lipopolysaccharide, LPS and its biologically active part, the lipid A) depends on both the structure of endotoxin aggregates in solution and on single-molecule interaction with MD-2 and CD14 receptors, the rational design of TLR4 modulators should in principle take into account both these factors.
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