Quantitative analyses reveal the importance of regulated Hdmx degradation for P53 activation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 30, 2007, Pages 12365-12370

  Wang, Yunyuan V ^a   Wade, Mark ^a   Wong, EeTsin ^b   Li, Yao Cheng ^a   Rodewald, Luo Wei ^a   Wahl, Geoffrey M ^a  

^a SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^b INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

Author keywords

HDM2; HDMX; Mdmx; Quantitation; Stoichiometry

Indexed keywords

PROTEIN HDMX; PROTEIN MDM2; PROTEIN P53; REGULATOR PROTEIN; UBIQUITIN PROTEIN LIGASE; UNCLASSIFIED DRUG;

APOPTOSIS; ARTICLE; CELL AGING; CELL CYCLE ARREST; CELL GROWTH; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; HUMAN; HUMAN CELL; PLANT STRESS; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; QUANTITATIVE ANALYSIS; TRANSACTIVATION;

CELL LINE; DNA; DNA DAMAGE; GENE EXPRESSION REGULATION; HUMANS; KINETICS; NUCLEAR PROTEINS; PROTEIN BINDING; PROTO-ONCOGENE PROTEINS; TRANS-ACTIVATION (GENETICS); TUMOR SUPPRESSOR PROTEIN P53;

EID: 34547615407     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0701497104     Document Type: Article

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