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Previous microarray analyses had suggested that transcription occurs before the MZT in the zebrafish (Mathavan et al., 2005) and RNA-seq experiments have also described changes in mRNA levels prior to the MZT, suggesting that such changes were due to the post-transcriptional regulation of mRNAs (Aanes et al., 2011).
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Gene microarray analyses have suggested that EGFR signaling via phospholipase C-γ (PLCγ) induces uPAR transcription.
DNA microarray analyses have led to the identification of novel genes in the BvgA/S regulon, some of which are activated by BvgA/S and others are repressed by BvgA/S.
In different studies, microarray analyses have been performed on root, leaf and panicle under drought stress (Smita et al. 2013) and on two contrasting genotypes under drought stress (Lenka et al. 2011), rice samples subjected to heat and/or oxidative stresses (Mittal et al. 2012a, 2012b) and heat stress followed by recovery (Sarkar et al. 2014).
The raw data from our microarray analyses have been submitted to GenBank GEO.
Previous microarray analyses have suggested that PtdIns5P negatively influences ATX1 activity [12].
Developing a universal framework for microarray analyses has proved to be more problematic than may have been expected.
In the last year microarray analyses, have contributed to shed light in understanding the molecular basis of MM development and progression.
Here detailed microarray analyses have been used to study the transcriptome of root nodules induced by either wild type or mutant strains of Sinorhizobium meliloti.
Recent microarray analyses have uncovered novel transcriptional programs that coordinate the regeneration and repair of damaged muscle following eccentric exercise [10], [34], [35].
Conventional microarray analyses have contributed to the mechanistic understanding of complex disorders by attempting to determine conserved individual gene level changes.
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