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This conformational heterogeneity in both RNAs in the Rev-monomer-bound species suggests similar binding patterns for both the RNAs.
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Concerted mathematical and experimental analysis of global binding patterns for 10 key haematopoietic TFs in both cell types suggests that cell type-specific binding is not opportunistic, but instead makes meaningful contributions to cell type-specific transcriptional control.
In one of the two cases analysed with both antibodies (case 1; Figure 7), we observed similar binding patterns for TS1 and anti-SSTR2.
In the above context, the OGC WS-Phase 5 interoperability programme [23] developed and demonstrated SOAP/WSDL binding patterns for WMS, WCS-T, WFS-T and WPS.
Comparison of peak sets identified using ChIP-chip and ChIP-seq for H3K9me3, SETDB1, and KAP1 and a comparison of the binding patterns for H3K9me3, SETDB1, and KAP1 using the different platforms is shown in Supplementary Figure S6.
However, this cellular transformation mechanism has not been identified because an investigation of the primary interaction of adaptor proteins following kinase activation induced by growth hormones results in relatively small differences in protein binding patterns for cells expressing either single- or multiple-species of ErbB receptors [8] [10].
Analysis of binding within bidirectional promoters revealed interesting binding patterns for CREB.
Of these, a majority of them (80.7%) were classified into "Only" or "Shift" binding patterns for AKT1-tranfected MCF10A cells.
It is also shown [ 24] that binding patterns for some TFs are dynamic and change under different environmental conditions.
We show significantly different (p<0.01) ChIP-Chip binding patterns for factors at the two groups of genes.
We observed similar binding patterns for the mammalian influenza (H1N1) viruses, with the exception that the pandemic strains had reduced binding to chicken erythrocytes.
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