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These composite substrates appear to show a useful degree of alignment of the cells.
Therefore, both an adsorbed bioorganics and a surface topography of the substrates appear to influence cell adhesion and differentiation.
AlN nanowires (NWs) on Si substrates appear to be free of crystalline defects due to their free surfaces which relax the elastic strain introduced by lattice mismatch.
Besides their conserved Cys-Xxx-Xxx-Cys-His heme-binding motifs, the amino-terminal regions of apocytochrome c substrates appear to be important for CCHL function.
The experimental X-ray diffraction (XRD) spectra of films deposited on Si substrates appear to contain all of the strong peaks of α-C3N4 and β-C3N4, but there is considerable peak overlap, therefore the existence of these phases cannot, for certain, be claimed from this data.
The molecular interactions between lysine methyltransferases and their substrates appear to be regulated by posttranslational modifications surrounding the lysine methyl acceptor.
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The hybrid sample surfaces made in contact with air and substrates appeared to have different structures.
As shown in Figure 5a, b, c, d, film coverage on the ceramic and metallic substrates appears to be substrate-independent: the films are continuous with no observed porosity.
AFM observations showed that the surface structure of the film grown on (111) oriented substrates appears to be more ordered than that of films grown on (100) substrates.
An initial surplus of carbon in the SiC substrates appeared to be required as could be shown for boron doped polycarbosilane derived SiC.
All compounds that were BO substrates appeared to be oxidized in mycelial cultures to aldehydes, except for the two most polar compounds N′- 3-indolylmethyl -N′′-methylurea aN′- 3-indolylmethyl -N′′-methylureamate.
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