Sandra C. Viegas

This study investigates the structural and mechanistic role of Dis3L2 in RNA degradation, identifying a critical residue involved in double-stranded RNA processing.

This study identifies Dis3L2 as a regulator of cell proliferation through a PI3-Kinase dependent pathway in both Drosophila and human cells.

This paper presents a synthetic small RNA-based system for modulating gene expression in P. putida to redesign its metabolism for industrial biocatalysis.

This study identifies DIS3L2 as a key player in human nonsense-mediated mRNA decay, showing it degrades full-length transcripts and depends on uridylation.