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Microarray data were confirmed for several genes using quantitative PCR analysis.
Data were confirmed for reasonable normality and homogeneity of variance.
The microarray data were confirmed for 5 out of 9 analyzed genes (Table 5).
These data were confirmed for one α-galactosidase encoding gene (aglC) and one β-galactosidase encoding gene (lacA) using Northern analysis.
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All data were confirmed, except for a few (3.8%) discrepancies.
These data were confirmed also for particular sensitive disease to chemotherapy, HER2-positive and triple negative, in which suboptimal chemotherapy with CMF-like or AC/EC for 4 cycles was prescribed in 24.2% and 22.2%, respectively.
These data were confirmed by PCR for expression of Crx, Nrl, arrestin, recoverin, Trβ2, rhodopsin and Pax6 (Figure 2B).
Gene expression data were confirmed by immunostaining for Sema3A protein on tissue sections, which showed a clear and progressive reduction in Sema3A abundance down to control levels in the areas of active angiogenesis by increasing VEGF doses (Fig 2B).
Staff then conducted confirmation interviews for any report of a breast cancer event or death for which medical records and death certificates were obtained, and data were confirmed at study end for >95% of participants.
However, although microarray data were confirmed by RT-PCR for PF14_001, PFL0260c, no differential expression was observed among the different groups of clinical isolates analyzed.
These data were confirmed by increased staining for cleaved caspase-3 in eosinophils, but not in mononuclear cells, in BAL from ova-challenged mice treated with H2O2 (Supplementary Figure 3).
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