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Furthermore, the root mean square error (RMSE) for estimating the ΔG hyd values of SAMPL4 molecules appears to decrease substantially from 2.56 to 1.66 kcal/mol due to the additional parameterization for IHBs.
Homology modeling of the NTNHA structure implied that a consensus K-C-L-I-K-X35-D sequence common among all NTNHA serotype molecules appears to coordinate a single zinc atom.
The relative flexibility of dipeptide sequences found in the flexible regions is about a factor of five higher than that found for the flexibility of the rigid regions, and the flexibility of types II and III collagen molecules appears to be higher than that found for the type I collagen molecule.
In mixed monolayers with cadmium stearate (CdSt), the folding of PMDI molecules appears to be substantially changed compared to the monolayer of the pure polymer, leading to a surface potential that is higher than observed for monolayers of pure PMDI and of pure CdSt.
Thus the only viable mechanism for the uptake of molecules appears to be transport through connexin hemichannels.
These same molecules are the target of corticosteroids, and depletion of these adhesion molecules appears to protect against pilocarpine or clinical seizures.
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The BB molecules appear to form polymers on enzymatic oxidation and form a precipitate.
These molecules appear to be valuable markers of severity and effects of CAI.
The different amount of coordinated water molecules appear to affect the solid state networks.
Interestingly, the molecules appear to act as agonists for the receptor in certain surrogate cellular assays.
Planar molecules appear to access and pack in slit-shape pores more efficiently as compared to nonplanar molecules.
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