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The most straightforward scenario explaining the evolution of the doubled karyomastigont is that diplomonads arose from enteromonads in a single evolutionary event.
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Second, a finite element model was utilized to simulate the damage evolution of the double lap joints.
The diversity of GS quaternary structures revealed here suggests a nonallosteric role for the evolution of the double-ringed architecture seen in all GS enzymes.
Computations are presented that were designed to model the conditions existing in two specific cases of large Leonid meteors for which we had photographs showing the evolution of the double trails.
In the absence of sexual selection pressure, is it possible that natural selection has driven the evolution of the double pulse call?
Thus, it appears that neither sexual selection nor natural selection provide convincing explanations for the evolution of the double pulse pattern.
The absence of a preference for the derived call pattern supports the hypothesis that female choice did not drive the evolution of the double pulse pattern in N. retusus and N. maxillosus.
More data on the molecular and cellular biology of diplomonads in addition to Giardia will be necessary for understanding the enigmatic evolution of the double karyomastigont of diplomonads.
The presence of Class I SMase D in different clades, however, seems to be the result of convergent evolution of the double disulphide bond in the molecule.
The biological relevance of the effects of overexpressing a DUX homologue in an organism of a species lineage that split from the common ancestor of mammals long before the evolution of the double-homeobox gene family is unclear.
This study reports the first structure of the trans-AT PKS EI domain, revealing how divergent evolution of the double-hotdog fold has rendered an additional PKS domain capable of distinct chemistry.
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