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A recent microarray analysis explored tissue-specific cassette exons and the exon correlation across more than 20 tissues and cell lines in mouse [ 24].
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Using microarray analysis, we explored the differences in gene expression in skin and oral mucosal wound healing in a murine model of paired equivalent sized wounds.
In this research, we performed microarray analysis to explore the possibility that BB regulates miRNA expression.
This study confirms that a population based cohort study such as NOWAC provides the opportunity to use high throughput technology (e.g., microarray analysis) to explore biologic variation in gene expression related to both endogenous and exogenous sex hormones.
Here we have used data from a genome microarray analysis to explore insertion-deletion (InDel) polymorphism among a diverse strain collection of Mycobacterium ulcerans, the causative agent of the devastating skin disease, Buruli ulcer.
We chose MCF-7 and MDA-MB-231 as representatives for luminal-like and mesenchymal-like subtypes, respectively, and used these cell lines for comparative analysis by MMSDK, array comparative genomic hybridization (aCGH) and gene expression microarray analysis to explore the correlation between DNA methylation, genomic stability and gene expression.
In the present study we used genome wide microarray analysis to further explore this phenomenon and to elucidate the underlying cellular mechanisms.
Complementary DNA (cDNA) microarray analysis was performed to explore the genes affected by BRG1.
Genome wide microarray analysis was undertaken to explore novel biological pathways associated with marbling in Hanwoo (Korean cattle).
In the present study, microarray analysis was used to explore potential gene transcription/regulatory consequences of hybridisation between wild and domesticated salmon.
Since ArcA is a transcription factor, we performed a microarray analysis in order to explore its effect on stationary phase gene expression in the ubiG strain.
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