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The XTEN sequence has been demonstrated to controllably increase the serum half-life of peptides and proteins [18].
For example, in mice the transgenerational epigenetic inheritance of the agouti viable yellow (A vy) allele and the axin-fused (Axin Fu) allele, which both include a IAP retrotransposon in their sequence, has been demonstrated [35], [36].
The triad of findings included micrognathia, glossoptosis and respiratory obstruction; however, considerable confusion in the medical literature delineating Robin sequence has been demonstrated [ 2, 3].
The positioning of the nucleosomes reconstituted with yeast histones and the 601 sequence or the significantly weaker 5S sequence has been demonstrated by several groups through nuclease digestion assays.
For example, the poor applicability of process theories of motivation in cultures where the linkages among actions, outcomes, and reinforcements are less likely to follow in sequence has been demonstrated (13).
Other groups have already suggested an important role for the HNF1 binding site [ 22- 24], and in vitro HNF1 binding to this sequence has been demonstrated by gelshift assays [ 24].
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It should, however, be noted that recently some proteins with a pseudokinase-like sequence have been demonstrated to bind ATP and display an active conformation [47], or even possess catalytic activity [48], [49], [50].
Synthetic peptides containing the RGD sequence have been demonstrated to be able to disrupt the cell-cell and cell-matrix interaction mediated by integrins, as well as to inhibit the cellular activity stimulated by integrin engagement.
An involvement of the hippocampus in memory of temporal sequences has been demonstrated in animals and humans [1], [2].
The utility of this technique in GAG oligosaccharide sequencing has been demonstrated [ 78– 80].
Whole genome sequencing and re-sequencing has been demonstrated in this study to be a powerful approached to select diagnostic markers from genetic maps.
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