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With respect to phase II metabolism, expression of in total 89 enzymes was analyzed (see additional file 2).
24 Even though B1KO and B1B2KO mice show similarities in some aspects of metabolism, expression of CART seems to be different in the two strains.
With respect to lipid metabolism, expression of genes encoding acyl-coenzyme-A-synthetase and acyl-coenzyme-A-dehydrogenase related to fatty acid metabolism was significantly upregulated by the microbiota presumably to increase cellular energy supply.
To further analyze the link between iron and copper metabolism, expression of components of the two high-affinity iron uptake systems was analyzed at the transcriptional level in wt, Δ freB, Δ sidA, and Δ freBΔ sidA (Fig. 2B).
In terms of lipid metabolism, expression of LC-PUFA and lipid biosynthesis genes, as well as of key regulator transcriptional factors, was differentially affected by diet depending on the genetic background of the fish.
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To further elucidate the respective physiological functions of CmADH1 and CmADH2A during sugar metabolism, expression profiles of CmADH isozymes were analyzed (Figure 6).
Various biological explanations, including differences in [18F]FLT metabolism, expression and activity of thymidine kinase and adenosine triphosphate levels (this is a cofactor for tyrosine kinase activity), have been proposed to explain these conflicting findings [16, 17].
Mammary, liver and adipose tissue metabolism and expression of genes that regulate lipid metabolism were altered by HG exposure.
MacroH2A1.1 over-expressing cells display ameliorated glucose metabolism, reduced expression of lipidogenic genes and fatty acids content.
Bacterial pathogens need to integrate their nutritional metabolism with expression of virulence genes but little is known of how this is done in E. coli O157 H7.
In addition to these nitrogen metabolism genes, expression of different regulatory genes also induced by nitrate.
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