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The aim of this study was to perform a comparative profiling of NVP biotransformation in rat intestine and liver and evaluate whether or not it is organ- and sex-dependent.
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In this study we performed a comparative profiling of miRNA expression during in vitro osteogenic differentiation of BM-MSCs isolated from OA and Control subjects.
Finally, we perform a comparative analysis of the energy efficiency of these models.
Applying a stochastic immune response model, we perform a comparative study of IgG substitution therapies.
In the present study, we performed a comparative miRNA profiling of susceptible (Arka Lohit-AL) and resistant (Punjab Lal-PL) chilli cultivars to identify 35 differentially expressed miRNAs that could be classified as positive, negative or basal regulators of defense against C. truncatum, the most potent anthracnose pathogen.
Here we used a human ex vivo lung cancer model involving culture of fresh tumor fragments in a hypoxic atmosphere to mimic in vivo tumor hypoxia and performed a comparative expression profiling study.
We performed a comparative gene expression profiling of the opposing responses of immature and mature primary B cells to BCR cross-linking, which led us to identify 24 genes that could discriminate the early responses of the two cell types.
Using next generation sequencing, we performed a comparative xylem transcriptome profiling analysis between limiting and luxuriant N fertilization treatments that highlighted classes of genes differentially expressed upon nitrogen availability.
We have performed a comparative proteomic analysis to profile differentially expressed proteins in the transformation process.
We performed a comparative analysis of transcriptional profiles between TM-1 and the im mutant during fiber SCW development using cDNA microarrays, identified and analyzed differentially expressed genes (DEGs) and their potential functional roles during fiber development.
First, we performed a comparative analysis of the expression profile of head and neck paragangliomas and medullary thyroid carcinoma, obtained after complementary DNA array analysis of 2 series of fresh-frozen samples of paragangliomas and medullary thyroid carcinoma, respectively.
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