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The comparison of two different training groups displayed a difference of mean values of 3.1 ± 2.1 (p < 0.001).
Species which have two Putative SOS1-like proteins similar in length (∆ < 110 amino acid residues) showed a difference in dN/dS values less than 0.1, while species that retain two putative SOS1-like proteins with very different length (∆ > 400 amino acid residues) displayed a difference in dN/dS values always greater than 0.2.
The absolute value of the slope for such a response displayed a difference just about 1% from that for the response of absorbance at 420 nm to ethanolamine quantities.
At 6, 24, and 48 h p.i., 125I-Fab displayed a difference in tumour uptake between the high- and moderate-CD44v6-expressing tumours, although not as pronounced as for 111In-Fab, ranging between 1.3 and 1.4 times higher for the high-CD44v6-expressing A431 tumours compared to the medium-CD44v6-expressing H314 tumours.
Based on this analysis, a total of 289 gene products (36% of analyzed mRNA-protein pairs) displayed a difference of two or more between the values of PC-1 in mRNA and protein domains (|PC-1mRNA−PC-1protein|≥2).
They displayed a difference of 1.9 °C.
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However, in their study, only one marker displays a difference in frequency up to 71%.
Other EBC ions either did not display a difference between groups and/or the difference was not significant.
Data shown are signature genes that display a difference in expression level (P<0.01) relative to mock-transfected cells.
The process of normalizing the edge weights will highlight edges that display a difference in correlation over response labels.
However, we could not display a difference between these drug classes when we examined deaths attributable to fungal infections.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com