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Yet, HINT predicts better interaction of most activators, except for -catechin sulfate, with the activated form of antithrombin than with the native form supporting the observation in solution that these molecules function as activators of the inhibitor.
The interaction of most ligands with their binding sites can be characterized in terms of binding free energy or binding energy (BE).
Although MPP8 and CBX7 have been shown to negatively influence transcription of specific genes [ 71, 80], the functional and biological significance of the interaction of most of these H3K9me3 readers with H3K9me3 remains poorly understood.
In 9-day RBCs, the level of mutual interaction of most of the regulatory elements of the β-globin gene domain increases compared to the levels in 3-day RBCs.
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The daily interactions of most people are confined to members of their own community, whether in urban neighbourhoods or country villages.
These sequences confirm what other studies have previously stipulated that the primer-primer interactions of most concern contain stable complements at the 3′ ends (Fig. 1A), allowing for polymerase binding and elongation1,9,10.
In addition, the effects and interactions of most influenced parameters were evaluated and optimized by using a central composite design model and a response surface methodology.
Docking analysis indicated that besides the typical interactions of most selective c-Met inhibitors, the intramolecular halogen bond and additional hydrogen bond interactions with kinase are beneficial to the binding.
Its importance derives from the principles of equality and fairness it seeks to promote, the redress it promises to victims of harassment, and, not least, from the loose but omnipresent regulatory structure it imposes on the daily interactions of most American workers.
There were no temporal interactions of most HF quality measures with diabetes status.Approximately 44% of hospitalized HF patients have diabetes, and this proportion has been increasing over the past 10years, particularly among those patients with new-onset HFpEF.
In order to predict the exact binding mode and to know the interactions of most active compounds (8h and 8l) within NNIBP of HIV-1 RT, docking studies were carried out on X-ray coordinates of HIV-1 RT enzyme (PDB ID: 3MEE).
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