| Literature DB >> 30525089 |
Eran Kotler1,2, Eran Segal1,2, Moshe Oren1.
Abstract
Phenotypic characterization of mutations in the tumor protein p53 (TP53) gene has so far focused on a handful of relatively frequent "hotspot" mutations, accounting for only ~ 30% of cases. We expanded the scope and quantitatively measured the impact of thousands of distinct TP53 mutations in vitro and in vivo, providing insights into the connections between structure, function, evolutionary conservation and clinical impact.Entities:
Keywords: deep mutational scan; gain of function (GOF); massively-parallel reporter assay (MPRA); mutant p53; phenotypic catalogue
Year: 2018 PMID: 30525089 PMCID: PMC6276857 DOI: 10.1080/23723556.2018.1511207
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556