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Figure 4 Diffraction efficiency of interference structures.
O-glycan synthesis was blocked by treating the cells with benzyl-α-GalNAc [20], an analogue of GalNAc that can not be used as substrate by subsequent glycosyltransferases. Efficiency of interference with glycosylation was confirmed using the high-mannose-specific lectin Con A and the GalNAc-specific lectin HPA.
Non-overlapping sequences of short hairpin RNA (shRNA) which have variable efficiency of interference can be exploited to generate "epi-allelic" cell lines with a range of protein silencing [ 13, 14].
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The efficiency of interference-tackling techniques of the present wireless technologies has been profoundly assessed in the literature.
This would improve the efficiency of crossover interference, since complete SC localization to chromosome axes is required for the execution of crossover interference (Hayashi et al. 2010; Hillers and Villeneuve 2003; Sym and Roeder 1994).
Figure 4 shows the diffraction efficiency of these interference structures recorded on annealed Ge25Se75 layers after exposure-annealing cycles that were repeated under the same conditions several times.
Contradictory reports in the literature have emphasised either the sequence of small interfering RNAs (siRNA) or the structure of their target molecules to be the major determinant of the efficiency of RNA interference (RNAi) approaches.
Disruption of P-bodies decreases the efficiency of RNA interference, suggesting that they are a critical site in the RNAi process.
The efficiency of RNA interference was assessed by qRT-PCR and immunofluorescence analysis (IF).
We first examined TLR3 mRNA expression in rats to evaluate the efficiency of RNA interference.
Due to the low basal Egr-1 mRNA and protein levels the silencing efficiency of RNA interference was analyzed in HOCl HDL-treated cells.
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