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To independently test the validity of the differential expression signatures determined by microarray analysis, we measured the expression patterns of some of the putative biomarkers.
To verify this hypothesis, we measured the expression patterns of DR1709 and DR2263 in MOxyR_sdC, which contained a reduced OxyR protein due to its C210 mutation.
To independently test the validity of the differential expression patterns determined by microarray, we measured the expression patterns of 3 representative genes in 4 tissue samples using quantitative real-time polymerase chain reaction (qRT-PCR).
In addition to small RNA sequencing and identification, Illumina sequencing technology as performed in previous reports [ 5, 36], also measured the expression patterns of each identified miRNA in response to LPS.
AB215 and tamoxifen both appeared to reduce the size of tumor xenografts following 3 months of treatment in the presence of an E2 release pellet.To further compare the effects of AB215 and tamoxifen on tumor progression, we measured the expression patterns and levels of the nuclear proliferation marker Ki67.
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The apoptotic and necrotic status of the INS-1E cells at different glucose levels and after zinc chelation was tested by measuring the expression patterns of the anti-apoptotic gene, B-cell leukemia/lymphoma 2 (Bcl-2), and the pro-apoptotic gene, Bcl-2-associated X protein (Bax) and by measuring DNA fragmentation.
Quantitative RT-PCR (qRT-PCR) was used to measure the expression patterns of selected genes in mammary tissue samples taken from each animal 16 h after the S. aureus infusion (Fig. 1).
Measuring the expression pattern of LOV1 protein using HA-tagged LOV1 protein, we found that the expression level of the LOV1-HA fusion protein also oscillated under continuous light conditions, with a broader peak around dusk and lower expression levels around dawn.
Three indices i.e. expression level, expression breadth and maximum expression level were used to measure the expression pattern of a given gene.
Combining recently developed genomic resources for Phaseolus vulgaris, including predicted gene calls, with RNA-Seq technology, we measured the gene expression patterns from 24 samples collected from seven tissues at developmentally important stages and from three nitrogen treatments.
To quantify expression divergence, we used Euclidean distance to measure the dissimilarity between the expression patterns across multiple tissues [ 23, 35].
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