Up‐regulation of the E2F‐dependent transcriptional network has been identified in nearly every human malignancy and is an important driver of tumorigenesis. Two members of the E2F family, E2F7 and E2F8, are potent repressors of E2F‐dependent transcription. They are atypical in that they do not bind to dimerization partner proteins and are not controlled by retinoblastoma protein. The physiological relevance of E2F7 and E2F8 remains incompletely understood, largely because tools to manipulate their activity in vivo have been lacking.
E2F7 Is a Potent Inhibitor of Liver Tumor Growth in Adult Mice
Eva Moreno,M. Toussaint,S. V. van Essen,L. Bongiovanni,E. V. van Liere,M. Koster,Ruixue Yuan,J. V. van Deursen,B. Westendorp,A. de Bruin
Published 2020 in Hepatology
ABSTRACT
PUBLICATION RECORD
- Publication year
2020
- Venue
Hepatology
- Publication date
2020-04-07
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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