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E. coli AW1.7 and its Δcfa mutant were more resistant to pressure and heat but less resistant to acid stress than E. coli MG1655.
Similarly, fibrils from ΔK14 mutant were more abundant, slightly thinner (8 13 nm) and more tangled than AChE586-599 (Figure 9A).
We also observed that the expression of XacPNP is induced upon infection and that lesions produced in leaves infected with a XacPNP deletion mutant were more necrotic than those observed with the wild type and the highly necrotic tissue led to earlier bacterial cell death in the mutant.
Double peaks for the Q3 mutant were more likely to show a shielded behavior, where the second peak was lower in force than the first peak by ~10%.
However, data from the aprataxin K38A mutant were more illuminating and showed a three-fold decrease in binding to both monophosphorylated XRCC1 and XRCC4 peptides (Fig. 5B).
Endosperm starch granules from the sbe1a mutant were more resistant to digestion by pancreatic α-amylase, and the sbe1a mutant starch had an altered branching pattern for amylopectin and amylose.
Similar(51)
USP15 mutantD967H mutant is more sensitive to PARP1 inhibitor (Fig. 7f).
In contrast, both DesHDAP3 and its proline mutant translocate poorly, though the DesHDAP3 proline mutant is more potent.
The simulation analysis revealed that V27T mutant is more stable than WT and mutant simulation was successful completely.
Similarly, the phosphomimetic Apaf-1 mutant is more susceptible to 14-3-3ε-dependent 14-3-3ε-dependent 14-3-3ε-dependent 14-3-3ε-dependent to the presence of Cc.
Differential scanning calorimetric study shows that the mutant is more stable than the wild type complex as indicated by a 4.3 °C increase in the thermo-denaturation temperature.
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