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In the present study, we evaluated their expression and localization in gestational tissues (placenta, decidua, fetal membranes), and their effect on placental adrenocorticotropic hormone secretion.
We also annotated transcripts that may have glycosylation-related functions, and evaluated their expression abundance to generate the global view of glycogenes in High Five and Sf21 cell lines.
Therefore, we evaluated their expression in placentae from pregnancies complicated by early- and late-onset preeclampsia.
To identify transcripts derived from gene ID 11313 potentially coding for GAP-43 acyl-protein thioesterases, we evaluated their expression both in CHO-K1 and HeLa cells by RT-PCR using specific primers for each transcript (Fig. 4B).
To determine the best RT-qPCR reference genes from the gene panel with 20 candidates, we evaluated their expression stability across 15 aging- or neurodegeneration-related samples (Table S3).
To better address an association between TB progression and inflammatory reaction in the lungs, we selected several factors (IL-1β, IL-11, TNF-α, CCL3, CXCL2, MMP-8 and iNOS) and evaluated their expression in an additional 27 mice.
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The objectives of this study were to generate a collection of expressed sequence tags (ESTs) from C. zeae-maydis and evaluate their expression during vegetative, infectious, and reproductive growth.
In acute aerobic exercise studies, 40% revealed a decline in the expression of the receptors, 7% reported no significant difference, 40% showed an increase, and 13% did not evaluate their expression.
Therefore, to investigate the presence of NPY, AGRP, POMC, CART and Orexin-A in hypothalamic neurospheres and evaluate their expression during culture in proliferative conditions, we evaluated the immunoreactivity and mRNA content of these neuropeptides by immunostaining and qRT-PCR, respectively (Figure 3).
Thus, we chose to evaluate their expression levels in plasma using an additional set of 30 patients (Table 1).
Thus, we explored their potential role in OSCC by evaluating their expression levels in several OSCC cell lines compared with normal human oral keratinocytes.
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