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Correspondingly, we observed an augmentation of MHC class II-expressing cells following WNV infection.
Moreover, we observed an augmentation of TAA-LP-specific T helper type 1 cell responses and tumor antigen-spreading in HNSCC patients vaccinated with TAA-SPs.
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We did not, however, perform a complete dose-response study to determine which dose(s) of the 5-HT4 agonist permit(s) to observe an optimal augmentation.
We observed a tendency of augmentation of Mxi-1 in severe hypoxia (0.5% O2) and a significant decrease in c-Myc expression (Figs. 6A and B, respectively).
However, as we found no differences in resting potential and AP accommodation, and observed a speeding and augmentation rather than a slowing and reduction of APs in Ts65Dn GCs, it is unlikely that the voltage-dependent increase in input resistance in Ts65Dn GCs is explained by a decreased contribution of TASK-3 channels.
In discussing augmentation of the fbEs, we should recall that we observed a sudden appearance of the Esc layer in replacement of the normally observed Esq layers (identified with black arrows in Fig. 3).
This might result from an increased mineral density, as usually observed after augmentation, and the concomitant higher bone-to-implant contact [20].
Measures of arterial stiffness did not change from baseline after either walnut supplementation or control, and there were no differences observed in augmentation index (−6.6±6.5 % versus −8.4±6.3 %), or augmented pressure (−2.2±2.1 mmHg versus −2.7±2.4 mmHg) or at the end of each 4 week period.
In addition, we observed the augmentation of inhibitory action against MMP-9 enzymatic activity by 4′-demethylated nobiletin, which is a major metabolite of nobiletin.
Importantly, we also observed similar augmentation of TGF β1-induced EMT in these TAK1-knockdown cells.
When CskAS OTI CD8+ T cells were stimulated by APCs preloaded with peptides of different agonist potency during strong CskAS inhibition (5 μM), we observed marked augmentation of CD69 expression in responses to weak (T4, Q4H7, G4) agonists, contrasting with only slight enhancement of the responses to strong (OVA, Q4R7) agonists.
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