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In our microarray experiment, several genes downstream of the WNT canonical pathway were identified.
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This method requires data from many microarray experiments (several hundreds).
To overcome the limitations of microarray experiments, several computational methods have been proposed as compensatory methods to find cell cycle regulated genes in yeast.
From the manufacturing process up until the reading of probe spots intensities, the microarray experiment has several complex steps.
These studies have helped illuminate some aspects of the microarray experiment; however, several fundamental observations of microarray behavior remain poorly understood.
Despite a lack of clear signal when analyzed across pathways or higher level biological processes, analysis of gene expression across the EST libraries and microarray experiment revealed several candidate genes that may play an important role in eye-stalk evolution.
Although BR and ABA display an antagonistic relationship in some physiological responses, we observed in a microarray experiment that several ABA-responsive genes and one ABA biosynthesis gene were upregulated by EBR and HS [P. Krishna and coworkers, unpublished results].
The microarray experiments revealed several putative target genes of IpsA.
Consequently we divide the genes from the microarray experiments into several classes, depending on whether they are detected as periodically expressed or not.
We did not identify changes in expression of CHST11 or any other sulfotransferase in bovine articular chondrocytes in response to TGF-β in our microarray experiments, although several are spotted on the array and are annotated in the bovine genome.
The top gene ontologies represented in current association studies fit within the major biological processes underlying ALI development on the basis of different microarray experiments among several studies using diverse animal models of the disease and cellular models of stretch-induced injury [ 51].
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