Ago-2-mediated slicer activity is essential for anti-flaviviral efficacy of RNAi.

Although the results of mecA gene detection in pDNA and RNA samples were negative, both probes presented ability to discriminate between complementary and non-complementary targets

Figure 5.1 - Heatmap of gene expression of all tested genes in all patients, including both cell. cultures (in both passages), and tissue

Using expression quantification, chromatin immunoprecipitation (ChIP), and reporter gene assays, we demonstrate that POU2F1 and RARA do bind upstream of the RPTOR gene to regulate

Observa-se, no entanto, que, relativamen- te ao estudo espanhol referenciado no ma- nual português, os nossos coeficientes são inferiores em comparação com os coeficien-

Third, gene reporter assays evaluating the COX2 promoter activity in response to gain- and loss-of-function experiments, including a constitutively active b - catenin protein

Sequences coding for proteins centrally involved in the miRNA pathway, namely DROSHA, DGCR8, XPO5, RAN, DICER, TARBP2, AGO and PIWI, have been methodically identified in the genomes

Figure 1. An RNAi screening system in Drosophila SL2 cells to identify regulators of MSL complex recruitment and function. A) Schematic of the MSL-dependent reporter system for

In order to investigate the dependence of NHEJ on DSB structure in normal and cancer cells, we used linearized plasmids with various, complementary or non-complementary,