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Thus the (dis)assembly pathway would not be conserved upon fusion.
In the main text, we demonstrated both a strong tendency for (dis)assembly pathways to be conserved upon fusion, and a significant preference for fusions involving closer termini.
While not all steps in the full predicted (dis)assembly pathway have been observed, the observed subcomplexes are in full agreement with prediction and demonstrate that the (dis)assembly pathway of this complex would not be conserved upon fusion.
The (dis)assembly pathway for this complex therefore goes from 2 to αβ which is consistent with the interface-size prediction and shows that (dis)assembly would be conserved upon fusion.
(Dis Assembly Conservation Is Independent of the Tendency for Fusion between Closer Termini In the main text, we demonstrated both a strong tendency for (dis)assembly pathways to be conserved upon fusion, and a significant preference for fusions involving closer termini.
Although cell-free protein synthesis yielded an inferior TrEGI enzyme, we proceeded to use cell-free expression as a tool to rapidly screen mutants of TrEGI, with the assumption that the effect of mutations imparting thermostability will be conserved upon expression in fungal hosts such as T. reesei.
Similar(54)
Transient cell spreading conferred a memory of apoptosis inhibition which was conserved upon adoption of a conventional cell shape.
According to the results presented in Table 1, the thermal properties of RT21® are conserved upon microencapsulation in membranes with different pore sizes.
These results are consistent with a structural model in which water molecules bound to the antigen and the antibody are conserved upon complex formation and provide bonds which are important for the stability of the complex.
Collectively, our findings suggest that even though they are now located on different chromosomes, a large subset of ancestral PAR genes might share a common sequence or factor that was conserved upon translocation from the pseudoautosomal region on the X chromosome to their current autosomal locations in the mouse genome.
These findings indicate that whenever possible the original haematoma formed upon injury should be conserved during clinical fracture treatment to benefit from the inherent healing potential.
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