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The hTau mouse model of tauopathy was utilized to assess gene expression changes in vulnerable hippocampal CA1 neurons.
Oligonucleotide microarray analysis following laser capture microdissection (LCM) and RNA amplification was used to assess gene expression changes associated with imatinib mesylate therapy.
Another study [69] adopted microarray to assess gene expression changes in the brains of male fetus and pups after the pregnant ICR mice were exposed to TiO2 NPs.
The overall trend of gene expression was confirmed by qRT-PCR experiments by Pearson correlation, indicating that the microarray for B. cenocepacia is reliable to assess gene expression changes in this strain as has been shown in previous studies [21], [44].
We used an Affymetrix gene chip approach to assess gene expression changes brought about as a consequence of constitutive loss of the chrna9 gene, encoding the α9 nAChR subunit, in an attempt to better define the role of this gene and nAChR activity in cochlear processing.
This study applied SAGE technology to assess gene expression changes that occur in Arabidopsis leaf tissue exposed to low temperature over a period of one week.
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Using microarray analysis, we assessed gene expression changes 24 h after MCAO in FVB and β2KO mice.
We systematically assessed gene expression changes induced by clorgyline in E-CA cells using high-density oligonucleotide microarrays.
Here, we assessed gene expression changes induced by DHA and EPA in the wildtype C57BL/6J murine small intestine using whole genome microarrays and functionally characterized the most prominent biological process.
We systematically assessed gene expression changes induced by the MAO-A – specific inhibitor, clorgyline, in primary cultures of prostatic epithelial cells from high grade cancer.
After re-assessing gene expression changes to account for leukocyte infiltration, we observed that ISGs remained highly over-expressed in muscle biopsies particularly from DM patients.
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