1. Using molecular biology and biochemical approaches to find out why proximal polyadenylation signals are being ignored in normal cells but being recognized and used in stem cells and cancer cells.
  2. Using genomic approaches to learn about the consequences of APA.
  3. To identify regulatory elements other than miRNAs in 3’UTRs.
  4. To identify cancer subtypes, conditions and signaling pathways that influence 3’ end formation of mRNAs using cell culture and cell biology methods.
  5. To learn if shorter 3’UTRs are a cause or a consequence of oncogenic transformation applying mouse genetics.