Network Analysis for the Identification of Differentially Expressed Hub Genes Using Myogenin Knock-down Muscle Satellite Cells.

Differentially expressed genes - Midguts from sugar and blood fed female insects were dissected and total RNA purified.The cDNA obtained by RT- PCR was separated on

Relative gene expression for all six genes measured by RT-qPCR was compared with RNA-Seq data on days 2 and 5 for the July experiment.. In the first comparison relative expression

The expression of heat shock (HSP70) and cold shock genes (CIRBP and RBMγ) was quantified at the mRNA level by RT-PCR in WIβ6 cells cultured at β5°C for 1 and 5 days before warming

RNA isolated from EV preparations and corresponding source cells was analyzed by real-time quanitative RT-PCR for indicated backspliced circRNAs and the linear spliced mRNA

As a result of gene expression analysis based on whole blood RNA, the number of expressed genes was less in fetal stage and infancy period but increased with age, presenting a

Here we show that down-regulation of endogenous myogenin gene expression in terminally differentiated mouse muscle cells causes cleavage of myotubes into mononucleated cells and

In order to confirm enrichment of basal and luminal cells after fractionation based on Epcam/ CD44 expression, quantitative RT-PCR analysis was performed on total RNA isolated

TTR knock-down cells (TTR kd ) showed altered mRNA expression of myogenic genes. A) A decrease in mRNA expression was observed on day 6 of transfection in TTR and day 5 in MYOG