Article
FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development.
The Journal of pathology - 1 Jun 2011
Davis Hayley, Lewis Annabelle, Spencer-Dene Bradley, Tateossian Hilda, Stamp Gordon, Behrens Axel, Tomlinson Ian
Abstract excerpt
FBXW7 is the substrate recognition component of a SCF-type E3 ubiquitin ligase. It has multiple targets such as Notch1, c-Jun, and cyclin E that function in critical developmental and signalling pathways. Mutations in FBXW7 are often found in many types of cancer. In most cases, these mutations do not inactivate the protein, but are mono-allelic missense changes at specific arginine resides involved in substrate...
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