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Varady et al 8 suggest that a minimum weight loss of 5% is required to have an effect on levels of key adipokines (adiponectin, leptin, and resistin), but this differs from other studies which report the need for a 10% weight loss for modification in levels of some adipokines (eg, adiponectin) and that this varies with the degree of obesity.
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The mechanism for this is not established but evidence supports direct action of KBs together with modifications in levels of hormones, which influence appetite, such as ghrelin and leptin.
Popa et al. [ 23] and Tam et al. [ 24] reported significant modifications in levels of total cholesterol and triglycerides in patients with RA receiving infliximab, but Bosello et al. [ 25] and Peters et al. [ 26] did not find significant changes in lipid levels after treatment with infliximab.
PFP has been identified to result in modification in activity levels, however it is unknown the extent of activity levels in individuals with and without PFP.
Treatment for 7 days with 17β-HSD3 inhibitoRM-532-10505 by s.c. injection or oral gavage exerted no effect on the testis, prostate and seminal vesicle weight and no modification in the levels of plasma steroids.
This interaction might induce modification in calcium levels in the neighborhood of the cells.
Altogether, our MSAP analysis suggests modification in the level of cytosine methylation and alterations in DNA methylation patterns, particularly de-methylation, during in vitro culture.
Two mechanisms of resistance to Bt toxins have been described in insects: (1) altered protoxin activation by gut proteases, and (2) modification in transcription level and/or protein sequence of Cry receptors resulting in lower of failure in toxin binding [ 39- 41].
Two main mechanisms of resistance to Cry toxins have been described in insects so far: altered protoxin activation by gut proteases, and modification in transcription level and/or protein sequence of Cry receptors resulting in lower or failure in toxin binding [ 19– 219.
This independency is further extended to the cell activities inferred from the ontological analysis of transcriptome and translatome differentially expressed genes, with a clear tendency of translation-related genes to be controlled purely at the translational level without modifications in the levels of their transcripts.
The present study was aimed at investigating by a microarray approach whether HdIV injection induces modifications in the levels of S. frugiperda gene transcript levels, resulting either directly from viral gene products or from upstream regulations or feed-back mechanisms.
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