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To investigate the influence of miRNAs on gene expressions, Lim et al. transfected exogenous miRNAs into the HeLa cells and measured gene expression changes of genes in the transfected cells versus non-transfected cells using two-channel Agilent microarrays [23].
To capture both acute and chronic responses to hypertonicity, we measured gene expression changes after 15 minutes, 1 hour, 6 hours, and 1 full generation of growth (∼96 hours) on 200 mM NaCl NGM plates.
To elucidate the immune response to Bd and evaluate the physiological effects of chytridiomycosis, we measured gene expression changes in several tissues (liver, skin, spleen) following exposure to Bd.
In agreement with the above premise, these simulation results suggest that the measured gene expression changes allowed S. cerevisiae to tolerate higher WOA uptake rates.
To determine the effect that immunotherapy has on the inflammatory state, we measured gene expression changes in the hippocampus for classical inflammation, alternative inflammation and acquired deactivation.
We used an ex vivo culture model and measured gene expression changes in human lung fibroblasts after stimulation with BMPs and their antagonists using HEEBO microarrays.
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Microarrays are able to measure gene expression changes, but are limited by the availability of Expressed Sequence Tags (ESTs).
We apply this method to microarray data measuring gene expression changes in cell lines transfected with certain miRNAs or anti-miRNAs (miRNA-specific inhibitors).
The PCR and Northern-blotting assays have been widely used for measuring gene expression changes in humans and animals for years; however, they are only capable of monitoring a limited number of genes at a time.
Agilent oligonucleotide technology was used to measure gene expression changes in the samples of interest.
Buchholz et al. [ 35] employed cDNA microarray to measure gene expression changes during chemotherapy in 5 patients with breast cancer.
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