Sentence examples for binding more efficiently to from inspiring English sources

In vitro studies confirmed that miR-659 can regulate PGRN expression, with miR-659 binding more efficiently to the high-risk T allele, thereby reducing PGRN levels.

We further demonstrate that miR-659 can regulate GRN expression in vitro, with miR-659 binding more efficiently to the high risk T-allele of rs5848 resulting in augmented translational inhibition of GRN.

We demonstrated a statistically significant difference between the cyto-adherence capacities of Mmm to BoLEC and CaLEC (p = 1.11 × 10-12), with Mmm binding more efficiently to BoLEC than CaLEC.

Compared to the bispecific/divalent diabody, the tetravalent di-diabody binds more efficiently to both of its target antigens and is more efficacious in blocking ligand binding to the receptors.

However, the rH1 appears to bind more efficiently to the templates, suggesting that a significant percentage of the endogenous H1 may be modified or in complex with other components in the reaction, and thus is unavailable for binding.

Thus, we speculated that binding of the phosphorylated ribosomal protein S6 to the human DPYSL2 5′-TOP tract is sensitive to the number of DNRs, with the 11 DNR transcript binding more efficiently than the 13 DNR transcript.

Indeed, co-expression of the BIR2-optimized SmacAVAV antagonized RIPK2 binding more efficiently than did Smac containing the normal AVPI N-terminus, whereas Smac lacking the essential N-terminal alanine (SmacLVPI) did not bind the BIR2 and was unable to antagonize RIPK2 binding (Fig 5F).

H3-P99 shighd high levels of binding to SAα2,6 and H5-Viet bound more efficiently to SAα2,3 than to SAα2,6, which is similar to observations with recombinant HAs in the solid-phase binding assay.

The LMα1 chain can thus be used more efficiently to distinguish between the roles of LM binding to dystroglycan and integrins in the neuromuscular system.

The peptides A7, C12, and C15 (see arrows in Figure  2B) bound on average 1000-times morefficientlyly to crystalline Ni3B as compared to the M13wt phage, which shows a binding affinity of 5 × 10 pfu/ml.

The combination of two computational techniques would helped to make a clear decision that compound 32 with well inhibitory activity bind more efficiently within the binding pocket even in case of mutant virus whereas compound 46 lost its interactions on mutation and marked as least active compound of the series.