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While activation measures in the inhibitory networks of both delay variants were highly comparable, the neural responses to fixed delay trials were more variable across participants.
Proline-substituted FR-15 variants were highly selective toward bacteria and fungi over hRBCs and murine 3T3 cells and also retained their antibacterial activities at high salt, serum and elevated temperatures.
Probe sets that detected potentially alternatively splice variants were highly correlated with over 80% with correlation coefficients over 0.5.
Due to the use of Monte-Carlo sampling in the gene design, all of these variants were highly divergent in sequence identity from each other.
In contrast to A-type RIFINs, the expression patterns observed for B-type RIFIN variants were highly consistent between all three experiments and indicated strict regulation during sexual differentiation (Table 3, Fig. 6).
Patterns of gains and losses shown by the different MCF-7 variants were highly diverse (Table 1 and Figure 1).
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This residue defines the classical allele four-digit allele HLA-A*0201 HLA-A*0201 identifiedanalysin and the two variants are highly correlated (r2=0.94).
A new study in Nature demonstrates that structural variants are highly prevalent in human gut microbiomes and that some associate with host disease risk factors.
A recent epigenetic annotation study has demonstrated that MS risk variants are highly enriched in immune enhancers active in T and B cells3, suggesting that risk variant-mediated MS susceptibility is driven by changes in gene regulation in lymphocytes.
Although the fluorescent response of the aptamer variants was highly dependent on experimental temperature, we have found one of the variants showing suitable fluorescent response by titration with adenosine.
Comparison of ankyrin-B protein primary sequence from different species (Figure 1B) shows that the identified variants are highly conserved in vertebrates.
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