Associated Papers
Hdm2 disrupts HdmX-mediated nuclear export of p53 by sequestering it in nucleus.
Ni Y et al.
Experimental Cell Research, 2024
MDM2 Integrates Cellular Respiration and Apoptotic Signaling through NDUFS1 and the Mitochondrial Network.
Elkholi R et al.
Molecular Cell, 2019
TBP-like Protein (TLP) Disrupts the p53-MDM2 Interaction and Induces Long-lasting p53 Activation.
Maeda R et al.
The Journal of Biological Chemistry, 2017
Genome and network visualization facilitates the analyses of the effects of drugs and mutations on protein-protein and drug-protein networks.
Céol A et al.
Bmc Bioinformatics, 2016
26961139 (PubMed )
Supplement: 12859_2016_908_MOESM2_ESM.pdf
Mutual dependence of MDM2 and MDMX in their functional inactivation of p53.
Gu J et al.
The Journal of Biological Chemistry, 2002
Hdmx recruitment into the nucleus by Hdm2 is essential for its ability to regulate p53 stability and transactivation.
Migliorini D et al.
The Journal of Biological Chemistry, 2002
The contribution of the RING finger domain of MDM2 to cell cycle progression.
Argentini M et al.
Oncogene, 2000
Cytoplasmically "sequestered" wild type p53 protein is resistant to Mdm2-mediated degradation.
Zaika A et al.
The Journal of Biological Chemistry, 1999
A genetic approach to mapping the p53 binding site in the MDM2 protein.
Freedman DA et al.
Molecular Medicine (cambridge, Mass.), 1997
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