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We hypothesized that assessing the gene expression of the chemotherapy response modifiers multidrug resistance gene 1 (MDR1) and excision repair crosscomplementing 1 (ERCC1) may help identify the group of patients benefiting from cisplatin-based adjuvant chemotherapy.
Thus, the experimental dataset was obtained by assessing the gene expression levels of the 20 genes by real time PCR in a cohort of 104 subjects, composed by healthy controls and patients with MS (see Table 1 for details of the clinical characteristics and Table S1 for statistically summary of gene expression levels).
Generally, the parameters, transcriptional read amounts and reads per kilobase of coding sequence per million reads (RPKM) are used for assessing the gene expression levels when analyzing RNA-seq data.
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To gain insight into the mechanism underlying the increase in RFT1 in 45OX transgenic rice, we assessed the gene expression levels of OsMADS14 and OsMADS18.
Therefore, in this study, we assessed the gene expression of identified lung lineage genes to study their role in distinguishing lung adenocarcinoma diversities.
In addition, we also assessed the gene expression levels of sod, cat, apx and gr and found that 25% HRW treatment induced the expression of these genes (Fig. 6), which was consistent with the changes in the activities of these antioxidants.
Discs with an AF defect and challenged with IFNα2β were used in a bovine IVD organ culture model to test the effect of HA on the IFNα2β pathway, as well as the matrix proteins aggrecan and collagen I. qRT-PCR was used to assess the gene expression of IFNα2β signaling molecules.
DNA microarrays were used to assess the gene expression for surgically derived pancreatic adenocarcinomas, islet cell tumors, and mesenchymal tumors.
In order to better understand periparasitic events characterizing the host response to infection, we assessed the gene expression profile in the periparasitic liver tissue during early chronic AE.
To assess the gene expression patterns during embryogenesis, we turned to mouse, where expression data are abundant from all developmental stages.
In order to identify both direct and indirect transcriptional targets of c-Myb in breast cells, Agilent microarrays were used to assess the gene expression differences between shMYB cells (n = 5) versus shGFP cells (n = 6).
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