scholarly article | Q13442814 |
P356 | DOI | 10.1038/SJ.ONC.1202528 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/sj.onc.1202528 |
P698 | PubMed publication ID | 10208414 |
P5875 | ResearchGate publication ID | 13090688 |
P2093 | author name string | B Wasylyk | |
J Abecassis | |||
R Salvi | |||
C Dureuil | |||
L Debussche | |||
M Argentini | |||
C Wasylyk | |||
I Delumeau | |||
P2860 | cites work | p53 and ATM: cell cycle, cell death, and cancer. | Q41438652 |
Regulation of mdm2 expression by p53: alternative promoters produce transcripts with nonidentical translation potential | Q41451986 | ||
Tumor suppressors: a developing role for p53? | Q41480402 | ||
Mdm2: keeping p53 under control | Q41585894 | ||
Involvement of p53 in cell differentiation and development | Q41592444 | ||
MDM2--arbiter of p53's destruction | Q41633106 | ||
p53 tumor-suppressor gene: clues to molecular carcinogenesis | Q41640484 | ||
E2F: a nodal point in cell cycle regulation | Q41679355 | ||
Role of E2F in cell cycle control and cancer | Q41747104 | ||
Induction of Mdm2 and enhancement of cell survival by bFGF. | Q42833951 | ||
A reversible, p53-dependent G0/G1 cell cycle arrest induced by ribonucleotide depletion in the absence of detectable DNA damage. | Q45985375 | ||
MDM2 expression during mouse embryogenesis and the requirement of p53. | Q47890601 | ||
Targeted expression of MDM2 uncouples S phase from mitosis and inhibits mammary gland development independent of p53. | Q52195712 | ||
A teratologic suppressor role for p53 in benzo[a]pyrene-treated transgenic p53-deficient mice. | Q52207983 | ||
The retro-inverso form of a homeobox-derived short peptide is rapidly internalised by cultured neurones: a new basis for an efficient intracellular delivery system. | Q54162483 | ||
High prognostic significance of Mdm2/p53 co-overexpression in soft tissue sarcomas of the extremities | Q56566036 | ||
Teratogen-induced eye defects mediated by p53-dependent apoptosis | Q71526996 | ||
MDM2 gene amplification and transcript levels in human sarcomas: relationship to TP53 gene status | Q72138136 | ||
Conserved mechanisms of Ras regulation of evolutionary related transcription factors, Ets1 and Pointed P2 | Q73111451 | ||
Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain | Q24314763 | ||
ARF promotes MDM2 degradation and stabilizes p53: ARF-INK4a locus deletion impairs both the Rb and p53 tumor suppression pathways | Q24321528 | ||
Mdm2 promotes the rapid degradation of p53 | Q24322597 | ||
Interaction between the retinoblastoma protein and the oncoprotein MDM2 | Q24323385 | ||
Net (ERP/SAP2) one of the Ras-inducible TCFs, has a novel inhibitory domain with resemblance to the helix-loop-helix motif | Q24561871 | ||
The ribosomal L5 protein is associated with mdm-2 and mdm-2-p53 complexes | Q24608783 | ||
Functional interaction between DP-1 and p53 | Q24648034 | ||
Regulation of p53 stability by Mdm2 | Q27860744 | ||
p53, the cellular gatekeeper for growth and division | Q27860990 | ||
WAF1, a potential mediator of p53 tumor suppression | Q27861121 | ||
DNA damage-induced phosphorylation of p53 alleviates inhibition by MDM2 | Q28254119 | ||
The MDM2 C-terminal region binds to TAFII250 and is required for MDM2 regulation of the cyclin A promoter | Q28255693 | ||
Inhibition of cell proliferation by p107, a relative of the retinoblastoma protein | Q28260016 | ||
The Ink4a tumor suppressor gene product, p19Arf, interacts with MDM2 and neutralizes MDM2's inhibition of p53 | Q28266637 | ||
Stabilization of wild-type p53 by hypoxia-inducible factor 1alpha | Q28267232 | ||
Amplification of a gene encoding a p53-associated protein in human sarcomas | Q28270924 | ||
The mdm-2 oncogene product forms a complex with the p53 protein and inhibits p53-mediated transactivation | Q28280958 | ||
The p53-mdm-2 autoregulatory feedback loop | Q28609811 | ||
Rescue of embryonic lethality in Mdm2-deficient mice by absence of p53 | Q29614430 | ||
Myc signaling via the ARF tumor suppressor regulates p53-dependent apoptosis and immortalization | Q29614701 | ||
Oncoprotein MDM2 conceals the activation domain of tumour suppressor p53 | Q29615851 | ||
Rescue of early embryonic lethality in mdm2-deficient mice by deletion of p53 | Q29617850 | ||
Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours | Q29618396 | ||
p53 protein stability in tumour cells is not determined by mutation but is dependent on Mdm2 binding. | Q30428424 | ||
Nucleo-cytoplasmic shuttling of the hdm2 oncoprotein regulates the levels of the p53 protein via a pathway used by the human immunodeficiency virus rev protein. | Q33888123 | ||
The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2. | Q33889383 | ||
Stimulation of E2F1/DP1 transcriptional activity by MDM2 oncoprotein | Q34313966 | ||
A functional p53-responsive intronic promoter is contained within the human mdm2 gene | Q34761984 | ||
p53 and E2F-1 cooperate to mediate apoptosis | Q35185411 | ||
E1A signaling to p53 involves the p19(ARF) tumor suppressor | Q35206764 | ||
Synergistic activation of p53 by inhibition of MDM2 expression and DNA damage | Q35671727 | ||
E2F1 overexpression in quiescent fibroblasts leads to induction of cellular DNA synthesis and apoptosis. | Q35837977 | ||
Deregulated transcription factor E2F-1 expression leads to S-phase entry and p53-mediated apoptosis | Q35885582 | ||
Functional and physical interactions of the ARF tumor suppressor with p53 and Mdm2 | Q36174385 | ||
The MDM2 oncoprotein binds specifically to RNA through its RING finger domain | Q36437940 | ||
Transcription abnormalities potentiate apoptosis of normal human fibroblasts. | Q36438161 | ||
The mdm-2 oncogene can overcome wild-type p53 suppression of transformed cell growth | Q36659029 | ||
Molecular characterization of the hdm2-p53 interaction | Q36871109 | ||
Immunological evidence for the association of p53 with a heat shock protein, hsc70, in p53-plus-ras-transformed cell lines | Q36919740 | ||
The state of the p53 and retinoblastoma genes in human cervical carcinoma cell lines | Q37537138 | ||
Alternatively spliced mdm2 transcripts with loss of p53 binding domain sequences: transforming ability and frequent detection in human cancer. | Q38354926 | ||
CTS1: a p53-derived chimeric tumor suppressor gene with enhanced in vitro apoptotic properties | Q39796556 | ||
mdm-2 inhibits the G1 arrest and apoptosis functions of the p53 tumor suppressor protein | Q40018842 | ||
Amplification of MDM2 inhibits MyoD-mediated myogenesis | Q40019821 | ||
A transcriptionally active DNA-binding site for human p53 protein complexes | Q40655196 | ||
Physical and functional interactions between p53 and cell cycle co-operating transcription factors, E2F1 and DP1. | Q40790222 | ||
The p53-MDM2 interaction in a cancer-prone family, and the identification of a novel therapeutic target | Q41024588 | ||
Induction of DNA synthesis and apoptosis are separable functions of E2F-1. | Q41099375 | ||
E2F1-induced apoptosis requires DNA binding but not transactivation and is inhibited by the retinoblastoma protein through direct interaction | Q41099382 | ||
The mdm2 proto-oncogene | Q41100486 | ||
Tolerance of high levels of wild-type p53 in transformed epithelial cells dependent on auto-regulation by mdm-2. | Q41115527 | ||
Expression of Bcl-xL and loss of p53 can cooperate to overcome a cell cycle checkpoint induced by mitotic spindle damage | Q41158289 | ||
P53 gene alterations in human tumors: perspectives for cancer control. | Q41205883 | ||
p53; from inductive signal to cellular effect | Q41345451 | ||
Mdm-2: "big brother" of p53. | Q41370313 | ||
Deregulated expression of E2F-1 induces S-phase entry and leads to apoptosis | Q41415956 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | overexpression | Q61643320 |
P304 | page(s) | 1921-1934 | |
P577 | publication date | 1999-03-01 | |
P1433 | published in | Oncogene | Q1568657 |
P1476 | title | p53 mediated death of cells overexpressing MDM2 by an inhibitor of MDM2 interaction with p53. | |
P478 | volume | 18 |
Q23912432 | Anticancer peptide PNC-27 adopts an HDM-2-binding conformation and kills cancer cells by binding to HDM-2 in their membranes |
Q57890248 | Bioactive Natural Peptides |
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Q58738105 | Chemical Instability and Promiscuity of Arylmethylidenepyrazolinone-Based MDMX Inhibitors |
Q47717539 | Co-operative intra-protein structural response due to protein-protein complexation revealed through thermodynamic quantification: study of MDM2-p53 binding. |
Q40842578 | Controlled access of p53 to the nucleus regulates its proteasomal degradation by MDM2. |
Q35010309 | Cytotoxic effect of a non-peptidic small molecular inhibitor of the p53-HDM2 interaction on tumor cells |
Q33964769 | Defect in the p53-Mdm2 autoregulatory loop resulting from inactivation of TAF(II)250 in cell cycle mutant tsBN462 cells |
Q34379259 | Differentiation of Hdm2-mediated p53 ubiquitination and Hdm2 autoubiquitination activity by small molecular weight inhibitors |
Q42055434 | Docking Analysis and Multidimensional Hybrid QSAR Model of 1,4-Benzodiazepine-2,5-Diones as HDM2 Antagonists |
Q36558129 | Drugs targeting protein-protein interactions |
Q35082710 | E3 ubiquitin ligases as cancer targets and biomarkers |
Q28550874 | Energetic Landscape of MDM2-p53 Interactions by Computational Mutagenesis of the MDM2-p53 Interaction |
Q29048586 | Evaluation of the use of therapeutic peptides for cancer treatment |
Q35058579 | Inhibiting the p53-MDM2 interaction: an important target for cancer therapy |
Q34400571 | Inhibition of Siah ubiquitin ligase function. |
Q38796979 | Inhibition of cell proliferation, migration and invasion by a glioma-targeted fusion protein combining the p53 C terminus and MDM2-binding domain |
Q34594105 | Intrinsic disorder in scaffold proteins: getting more from less |
Q38007557 | Intrinsically disordered proteins and novel strategies for drug discovery |
Q39989774 | Isoquinolin-1-one inhibitors of the MDM2-p53 interaction |
Q35081240 | Ligand-dependent interaction of the glucocorticoid receptor with p53 enhances their degradation by Hdm2 |
Q28138926 | MDM2--master regulator of the p53 tumor suppressor protein |
Q35572466 | Mdm2: A regulator of cell growth and death |
Q28210052 | MdmX is a RING finger ubiquitin ligase capable of synergistically enhancing Mdm2 ubiquitination |
Q40200606 | Mouse double minute antagonist Nutlin-3a enhances chemotherapy-induced apoptosis in cancer cells with mutant p53 by activating E2F1. |
Q34677800 | Negative cross-talk between p53 and the glucocorticoid receptor and its role in neuroblastoma cells |
Q35011473 | Novel targeted therapeutics: inhibitors of MDM2, ALK and PARP. |
Q37709228 | On the industrial applications of MCRs: molecular diversity in drug discovery and generic drug synthesis |
Q23915398 | PNC-28, a p53-derived peptide that is cytotoxic to cancer cells, blocks pancreatic cancer cell growth in vivo |
Q23918117 | Peptides from the amino terminal mdm-2-binding domain of p53, designed from conformational analysis, are selectively cytotoxic to transformed cells |
Q40476066 | Progesterone inhibition of MDM2 p90 protein in MCF-7 human breast cancer cell line is dependent on p53 levels. |
Q46409564 | Proneness to UV-induced apoptosis in human fibroblasts defective in transcription coupled repair is associated with the lack of Mdm2 transactivation |
Q35397776 | Protein-protein interaction modulator drug discovery: past efforts and future opportunities using a rich source of low- and high-throughput screening assays |
Q33265016 | Protoporphyrin IX interacts with wild-type p53 protein in vitro and induces cell death of human colon cancer cells in a p53-dependent and -independent manner |
Q38223668 | QTc prolongation induced by targeted biotherapies used in clinical practice and under investigation: a comprehensive review. |
Q79733375 | Reactivation of the p53 tumor suppressor pathway by a stapled p53 peptide |
Q37524156 | Recent advances in validating MDM2 as a cancer target. |
Q54703151 | Sequence-specific 1H, 15N, and 13C assignment of the N-terminal domain of the human oncoprotein MDM2 that binds to p53. |
Q27027835 | Small molecule compounds targeting the p53 pathway: are we finally making progress? |
Q24292513 | Sp100 interacts with ETS-1 and stimulates its transcriptional activity |
Q35295410 | Structural basis for inhibition of the MDM2:p53 interaction by an optimized MDM2-binding peptide selected with mRNA display |
Q36020398 | Targeting intrinsically disordered proteins in neurodegenerative and protein dysfunction diseases: another illustration of the D(2) concept |
Q33655329 | Targeting p53 for Novel Anticancer Therapy |
Q35903526 | Targeting the p53-MDM2 interaction to treat cancer |
Q74200562 | The contribution of the RING finger domain of MDM2 to cell cycle progression |
Q73787111 | The contribution of the acidic domain of MDM2 to p53 and MDM2 stability |
Q74244104 | The initial evaluation of non-peptidic small-molecule HDM2 inhibitors based on p53-HDM2 complex structure |
Q23923633 | The penetratin sequence in the anticancer PNC-28 peptide causes tumor cell necrosis rather than apoptosis of human pancreatic cancer cells |
Q37564522 | Therapeutic peptides for cancer therapy. Part I - peptide inhibitors of signal transduction cascades. |
Q45878720 | Trans-membrane peptide therapy for malignant glioma by use of a peptide derived from the MDM2 binding site of p53. |
Q24791038 | Transcriptional Targeting in Cancer Gene Therapy |
Q45864999 | Tumour regression in a ligand inducible manner mediated by a chimeric tumour suppressor derived from p53. |
Q30385084 | Understanding protein non-folding. |
Q28386936 | mRNA Display Selection of an Optimized MDM2-Binding Peptide That Potently Inhibits MDM2-p53 Interaction |
Q37982458 | p53-Mdm2 inhibitors: patent review (2009 - 2010). |
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