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In agreement with this, a group of activating or pro-inflammatory genes were down-regulated in decidual macrophages compared to their blood counterparts.
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Overall, every patient had his own group of activated genes and activation of heterochromatic genes was not restricted to chromosome 21, but occurred in several chromosomes (Table 3).
Although DNA hypomethylation was generalized to all the heterochromatic genes and to all ICF patients, gene expression was restricted to some genes and every patient had his own group of activated genes.
Although DNA hypomethylation occurred in all the analyzed heterochromatic genes and in all the ICF patients, gene expression was restricted to some genes, every patient having his own group of activated genes.
A large group of activated genes encode TF, many of which control differentiation of diverse cell types (e.g. ppar2b, cebpa, sox3, junbb, hes1, klf4).
In this case, the common group of activated downstream genes might be encoded by the response of common immune cells which have a full repertoire of Tlr receptors whereas the specific response might be the result of a distinct transcriptional response of specialized cells that do not encode all Tlr receptors.
In contrast, groups of activating mutation sites, such as those in the vicinity of the FRB and FAT domains, are located outside of the catalytic domain in mTOR.
In bifunctional catalysis, two functional groups capable of activating substrates are mounted on one scaffold.[ 17] It was hypothesized that if such a scaffold incorporated a reversible bond as shown in Figure 1 a, a dynamic combinatorial system of potential bifunctional catalysts could be generated.
The choice of activating group, leaving group, and protecting group(s) must be considered during synthetic design in order to facilitate conversion of the initial radiofluorinated intermediate into the final product.
Recent advances in the arena of polyene cyclizations are presented, with critical coverage on efforts to render such transformations diastereo- and enantioselective with a range of activating groups and functional group arrays.
Borderline patients presented a higher frequency of inhibitory pairs when compared to the control group, and a higher frequency of activating pairs as compared to the LL group.
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