ATM and MET kinases are synthetic lethal with nongenotoxic activation of p53
Journal Article
Overview
publication date
- July 1, 2012
has subject area
- Apoptosis
- Carrier Proteins - Ataxia Telangiectasia Mutated Proteins
- Cell Cycle
- Cell Cycle Proteins
- Cell Line
- DNA-Binding Proteins
- Genes - Genes, p53
- Genes, Lethal
- Genes, Neoplasm - Genes, p53
- Genes, Synthetic
- Humans
- Imidazoles
- Nuclear Proteins - Ataxia Telangiectasia Mutated Proteins
- Piperazines
- Protein-Serine-Threonine Kinases
- Protein-Serine-Threonine Kinases - Ataxia Telangiectasia Mutated Proteins
- Protein-Tyrosine Kinases - Proto-Oncogene Proteins c-met
- Proto-Oncogene Proteins - Proto-Oncogene Proteins c-met
- Receptors, Cell Surface - Proto-Oncogene Proteins c-met
- Receptors, Growth Factor - Proto-Oncogene Proteins c-met
- Tumor Suppressor Proteins
has restriction
- bronze
Date in CU Experts
- September 9, 2013 9:30 AM
Full Author List
- Sullivan KD; Padilla-Just N; Henry RE; Porter CC; Kim J; Tentler JJ; Eckhardt SG; Tan AC; DeGregori J; Espinosa JM
author count
- 10
citation count
- 54
published in
- Nature Chemical Biology Journal
Other Profiles
International Standard Serial Number (ISSN)
- 1552-4450
Digital Object Identifier (DOI)
Additional Document Info
start page
- 646
end page
- 654
volume
- 8
issue
- 7