Mary A. Farwell

TL;DR: qRT‐PCR evaluation and analysis demonstrated that traditionally used reference genes, such as 18s RNA, β‐actin, and GAPDH, are not reliable reference genes for pharmacogenomics and toxicogenomics studies, and hTBCA and small RNAs are more stable during drug treatment, and they are better reference genes in pharmacogenetics and toxicgenomics studies.

TL;DR: Early detection of cancers and delivery miRNAs and/or anti‐miRNAs for miRNA gene therapy and the potential toxicity effect of mi RNA gene therapy are discussed.

TL;DR: It is shown that 5‐FU significantly alters the global expression profile of miRNAs in vitro, and target prediction and GO analysis suggest that these differentially expressed mi RNAs potentially target many oncogenes, tumor suppressor genes and genes related to programmed cell death, activation of immune response, and cellular catabolic processes.

TL;DR: The method of diffraction imaging flow cytometry has the capacity as a platform for high-throughput and label-free classification of biological cells and demonstrates the potential for rapid classification among six types of cultured cells.