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We also found that PLD1 and phospho-Akt are coexpressed in some breast tumours, a fact which could complicate the utility of rapamycin-based therapies, as patients expressing both proteins could differ in sensitivity to mTOR inhibitors.
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Therefore, both proteins could undergo a similar retrotranslocation processes.
Furthermore, the protein-modifying enzymes involved could differ between the two isoforms, even for sites that are identical in sequence.
Indeed, it is very likely that the protein-modifying enzymes involved could differ between isoforms, even for sites that are identical in sequence.
This mutation and resultant differences in physicochemical properties imply that IPT activity could differ between the protein products of the ZmIPT2- T and ZmIPT2- C alleles.
At high fiber content, both modulus and tensile strength could differ by as much as 40% along the flow and transverse to the flow.
The detailed analyses of certain precursor proteins showed that even when cells of two developmental states had equal abundances of a protein, the number of endogenous peptides could differ significantly (Additional files 18 and 19).
Using a candidate protein approach, we investigated proteins involved in TSC/mTORC1 pathway, which levels of expression could differ after over-expression of E2F1.
We believe that the H and L2 complexes which both bind the MYBb element of EgCAD2 could differ from each other by the addition of one or more protein(s) which can be subjected to phosphorylation.
The function of protein isoforms derived from the same TU could differ significantly.
One plausible explanation for the ability of a phage like PST to switch hosts between Yersinia and E. coli is that some of its HVSs recognize β-barrel porin epitopes that are common to the E. coli and Y. pseudotuberculosis versions of this protein (fig. 5), but other epitopes could differ more between the two versions of the porin.
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