Sentence examples for most potent inducer from inspiring English sources

The most potent inducer of GSH identified in this study, congener 6a, was minimally toxic to cells and was able to provide neuroprotection in the 6-OHDA model of neurotoxicity, suggesting GSH induction as a neuroprotective strategy.

Among the diversified carbon sources tested, starch was found to be the most potent inducer of amylase activity (2293.34 ± 30.3 U/g) from strain ALA4, while relatively lower amylase yield ranging from 612.12 ± 18.3 to 1834.23 ± 23.2 U/g was observed with other carbon sources used such as lactose, mannose, xylose, glucose, maltose, and sucrose (Fig. 2f).

The most potent inducer of VEGF gene expression is hypoxia [23].

IL-1β is the most potent inducer of KGF in fibroblasts.

Among these mediators, IL-1β appears to be the most potent inducer of KGF expression in fibroblasts derived from multiple tissues [65], [66].

Even though C18 2 was not the most potent inducer of gene expression, one could speculate that it likely represents the quantitatively most important dietary activator of PPARα, as the average intake of C18 2 is much higher than that of C18 3, C20 5 and C22 6.

Other carbon substrates, such as xylose, arabinose and sophorose (one of the most potent inducers of T. reesei cellulases), do not induce β-glucosidase (BGL1) and, in high concentrations, even repress its formation [ 10, 34].

UFPs were shown to be the most potent inducers of oxidative stress in macrophages and epithelial cells by inducing heme oxygenase-1 and depleting intracellular glutathione.

Furthermore, the elevated levels of IL-6 may also be contributing to increasing the systemic levels of the inflammatory marker CRP in the trained obese animals, since IL-6 is one of the most potent inducers of CRP release from the liver [ 7] and it can also induce the release of CRP from adipose tissue in MS [ 57].

Vascular Endothelial Growth Factor (VEGF) is one of the most potent inducers of angiogenesis and is up-regulated in carcinoma of the cervix.

Several 4,6-dimethoxy and 5-hydroxyaurones induced NQO1 activity of Hepa1c1c7 cells by 2-fold at submicromolar concentrations, making these the most potent inducers to be identified from this class.