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The expression levels of the reporter genes were enhanced, corresponding to the increase of transgene copy number.
When treated with stresses including salinity, heavy metal toxicity, drought, heat, cold and hormone, the expression of many GPX genes were enhanced dramatically (Holland et al. 1993; Avsian-Kretchmer et al. 2004; Ramos et al. 2009; Chang et al. 2009; Faltin et al. 2010).
Following serum addition (day 14), K18 gene expression was reduced while transcription of K5 and K14 genes were enhanced (Fig. 1-C, panel a).
Furthermore, islet mRNA levels of some stress/AOD genes were enhanced by supraphysiological glucose levels in vitro [18] or in vivo in pancreatectomized rats, but were reversed after glycemia normalization [19], [20].
Similarly, we found that 1906 genes were enhanced in female palps, 3037 genes were enhanced in male antennae, and 2284 genes were enhanced in male palps.
Expression levels of all six genes were enhanced in MtCBF4 transgenic plants under normal growth conditions.
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Transfection in the presence of activators of upregulated genes was enhanced, demonstrating the principle of altering endogenous gene expression profiles to enhance transfection.
Expression of sigB and σB-dependent genes was enhanced following entry into stationary phase of cells grown in complex medium (LB medium).
Furthermore, osteogenic differentiation of MSCs, indicated by ALP activity and expression of Runx2 and osteocalcin genes, was enhanced on the RGD-conjugated surface compared with the unmodified surfaces.
Expression of the three NAC genes was enhanced under salt and drought stress conditions.
In EMT the expression of epithelial proteins is suppressed and expression of mesenchymal genes is enhanced [12] [14].
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