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Microarray assay identified the early response of Arabidopsis to As stress and possible differences in the mechanisms to achieve tolerance in the accessions.
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In addition to Ance, the microarray assay identifies multiple genes that vary in expression level between infected and uninfected cells.
Therefore, we utilized an in vivo nickel enrichment DNA microarray assay to identify DNA binding based on methods such as nickel agarose-based chromatin enrichment [54].
These results suggest that Solexa sequencing is a more specific and efficient tool than the miRNA microarray assay for identifying mature miRNAs.
To further illustrate how Smad3 contributes to ESC stability, we performed microarray assay to identify genes that show an obvious change after Smad3 depletion.
In the present study, we transiently overexpressed and silenced ZNF191 gene in the human embryo kidney (HEK293) cells and then applied microarray assay to identify possible ZNF191 target genes.
Based on our microarray assays, we identified 63 genes that were differentially regulated between 3937 and WPP96.
Combining computational predictions with microarray assays, we identified 46 B. mori miRNAs, 13 of which were miRNA*s.
In conclusion, combining computational predictions with microarray assays, we identified 46 B. mori miRNAs, 13 of which were miRNA*s.
Using three datasets based on physical interaction assays, genome-wide RNA interference (RNAi) screens and microarray assays, we identified 714 putative DENV-associated mosquito proteins.
In this report, we describe the development of a new NP-based genomic microarray assay that specifically identifies H5N1 viral nucleic acid and simultaneously provides subtype identification of influenza A virus in the absence of target amplification procedures such as RT-PCR.
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