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In conclusion, integrated gene expression and copy number microarray analysis highlighted genes that may be critically important for gastric carcinogenesis.
Microarray analysis highlighted activation of pathways involved in apoptosis induction, autophagy, RNA/protein metabolism, starvation responses, and solute transport.
Our microarray analysis highlighted a set of stress responsive genes whose transcription was early affected by As III).
Our microarray analysis highlighted marked changes in several molecular pathways in CM-S compared to CM-R mice, particularly at early stages of infection.
With respect to the underlying mechanism of BiP-mediated increases in water deficit tolerance that provided the foundation for pursuing these studies, the results of the microarray analysis highlighted relevant insights.
Unsupervised clustering performed by using processed data from miRNA microarray analysis highlighted differential expression profiles of 48 miRNAs, interestingly clustering the samples into 2 groups, OA versus normal chondrocyte micropellets.
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A significant perturbation in the angiogenesis and inflammation gene pathways was also observed by microarray analysis, highlighting that gene expression analysis is a crucial issue for the study of common diseases.
Candidate genes identified through microarray analysis highlight those that are highly differentially or chronically expressed, whereas those identified through network analysis instead feature genes that are highly connected.
This microarray analysis highlights clear differences in the expression of apoptotic genes in infected cells compared to uninfected cells, and interestingly, STS does not affect this pattern of apoptotic gene expression in infected cells.
In all, the combined microarray and transcript analysis highlighted several interesting genes as potential target genes for gastric cancer.
Microarray analysis also highlighted the differential expression of many stromal extracellular matrix proteins that may act as paracrine signals between the stroma and the epithelium, but which have not been pursued here.
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