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In PF, the accuracy of the combination of both markers was higher than that of any individual marker, although the difference was only significant with respect to CEA (P<0.02).
RESULTS Expression of M2 polarization markers was higher in M2-polarized macrophages after IL4/IL13 treatment than in control (M0) or M1-polarized macrophages.
The averaged PIC of the nuclear markers was higher than the cytoplasmic, and the average of the mtDNA markers (0.29) was higher than the cpDNA (0.18) (Table 2).
Interestingly, the expression of these markers was higher in OT-induced cells than in cells stimulated by OT-GKR.
False negative for one marker was compensated for by a positive finding for one or both of the other markers, such that the sensitivity achieved by combination of two markers was higher than that achieved by either marker alone.
Since the circulating level of total cell death and apoptotic markers was higher in patients with severe fibrosis (F3) compared with patients with moderate fibrosis (F2) (data not shown), we investigated the pertinence of the levels of serum total cell death and apoptotic markers in predicting severe fibrosis.
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For the resistance gene BPH31, the initial genetic locus size was around 16 Mb and, hence, the chance of recombination between the genetic locus and the markers was high.
Expression of pluripotency markers was highest and most consistent at the edge of the colony, where most cells expressed between 3 5 of the pluripotency markers shown (Figure 2b c).
The correlation between HRV markers was highest for HF and rMSSD (ρ = 0.93).
Despite our small sample sizes, degree of differentiation for microsatellite markers was high and comparable to previous studies.
Comparatively, LD between markers was high in the SW, NAB, and WW datasets and much lower in the DTM dataset.
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