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Despite the obvious involvement of several of the globular heads in binding to CS-A, sufficient binding sites were present to bind HAGG in the microtiter plate assay.
One or more EBNA-1 binding sites were present in the promoters of 4 out of 11 TRs (36.4%) that were regulated early affected by EBNA-1 induction (Table S4).
A greater proportion of evolutionarily conserved predicted Lhx1 consensus binding sites were present within proximal regulatory regions of SCN-enriched genes relative to randomly selected genes.
We found that miR156/miR529 binding sites were present in subgroup II-2 SBP-box genes, but were not present in group I or subgroup II-1 genes (Additional file 1 and 4).
NOVA binding sites were present in both the 3′ UTR and introns, and in both locations these sites harbored NOVA binding elements (clusters of the sequence YCAY; (Zhang et al., 2010)).
Although Su(H) binding sites were present in only a minority of NB and PNS enhancers, the conservation of core bases, as well as the complexity of their flanking conserved sequences points to a diversity of Su(H) function and interaction with other factors.
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It has been shown that, both in vitro and in vivo, 5-HT1B binding sites are present in very low concentration in trigeminal nucleus caudalis and cervical dorsal horn, below 12% of total specific sumatriptan binding.
Enhanced display of Bt toxin libraries using Phaberge and SRP translocation sequence are likely to select binders with moderate affinity due to the selection of binders by avidity since several binding sites are present in one phage particle.
Multiple E-box binding sites are present within the −2 kb promoter regions.
Two binding sites are present, flanking each the P2 and the P1 promoters, overlapping the transcription start sites.
Similarly, miRNA binding sites are present at increased frequency in the LARK targets identified in experiment two (Figure 1E).
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