| P50 | author | Moshe Oren | Q6988150 |
| | Pier Paolo Pandolfi | Q7191735 |
| | Silvia Di Agostino | Q42724855 |
| | Claudio Sette | Q47421898 |
| | Pamela Bielli | Q57028358 |
| P2093 | author name string | M Sudol | |
| | G Blandino | |
| | M Cioce | |
| | S Strano | |
| | F Fausti | |
| P2860 | cites work | PML regulates p53 acetylation and premature senescence induced by oncogenic Ras | Q22254666 |
| | Physical interaction with Yes-associated protein enhances p73 transcriptional activity | Q24291023 |
| | PML regulates p53 stability by sequestering Mdm2 to the nucleolus | Q24296743 |
| | The Hippo transducer TAZ confers cancer stem cell-related traits on breast cancer cells | Q24296824 |
| | Chromatin immunoprecipitation to analyze DNA binding sites of HMGA2 | Q24300947 |
| | Activation of the ATM kinase by ionizing radiation and phosphorylation of p53 | Q24311891 |
| | TEAD mediates YAP-dependent gene induction and growth control | Q24336045 |
| | A biomarker that identifies senescent human cells in culture and in aging skin in vivo | Q24562644 |
| | Identification and validation of oncogenes in liver cancer using an integrative oncogenomic approach | Q24633776 |
| | Sam68 regulates translation of target mRNAs in male germ cells, necessary for mouse spermatogenesis | Q24641891 |
| | IL-6 triggers malignant features in mammospheres from human ductal breast carcinoma and normal mammary gland | Q24669531 |
| | Atmospheric carbon dioxide concentrations over the past 60 million years | Q28144787 |
| | The Hippo-YAP pathway in organ size control and tumorigenesis: an updated version | Q28281214 |
| | Excess of rare cancers in Werner syndrome (adult progeria) | Q28285360 |
| | Mst2 and Lats kinases regulate apoptotic function of Yes kinase-associated protein (YAP) | Q28287783 |
| | Characterization of the mammalian YAP (Yes-associated protein) gene and its role in defining a novel protein module, the WW domain | Q28303362 |
| | Both TEAD-binding and WW domains are required for the growth stimulation and oncogenic transformation activity of yes-associated protein | Q28306685 |
| | Role of the beta catenin destruction complex in mediating chemotherapy-induced senescence-associated secretory phenotype | Q28484422 |
| | Enhanced phosphorylation of p53 by ATM in response to DNA damage | Q28609838 |
| | A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen | Q29615061 |
| | Senescence-associated secretory phenotypes reveal cell-nonautonomous functions of oncogenic RAS and the p53 tumor suppressor | Q29615559 |
| | RecQ helicases: caretakers of the genome | Q29618390 |
| | Positional cloning of the Werner's syndrome gene | Q29618393 |
| | The senescence-associated secretory phenotype: the dark side of tumor suppression | Q29620106 |
| | Unwinding the 'Gordian knot' of helicase action. | Q31879197 |
| | RecQ helicases: guardian angels of the DNA replication fork | Q33314341 |
| | The transcriptional coactivator Yes-associated protein drives p73 gene-target specificity in response to DNA Damage. | Q34418866 |
| | Werner protein protects nonproliferating cells from oxidative DNA damage | Q34467601 |
| | Molecular genetics of RecQ helicase disorders | Q34637883 |
| | The roles of tumor-derived exosomes in cancer pathogenesis | Q35606520 |
| | The transcriptional coactivator TAZ regulates mesenchymal differentiation in malignant glioma | Q35642059 |
| | Cell detachment activates the Hippo pathway via cytoskeleton reorganization to induce anoikis | Q35674584 |
| | Restriction of intestinal stem cell expansion and the regenerative response by YAP. | Q36508081 |
| | Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability | Q36573932 |
| | PML Surfs into HIPPO Tumor Suppressor Pathway. | Q36647912 |
| | Telomere ResQue and preservation--roles for the Werner syndrome protein and other RecQ helicases. | Q37022414 |
| | YAP: at the crossroad between transformation and tumor suppression | Q37357685 |
| | PML, YAP, and p73 are components of a proapoptotic autoregulatory feedback loop. | Q38357857 |
| | An indirect role for ASPP1 in limiting p53-dependent p21 expression and cellular senescence | Q39446297 |
| | SASP mediates chemoresistance and tumor-initiating-activity of mesothelioma cells | Q39454272 |
| | The Werner syndrome protein affects the expression of genes involved in adipogenesis and inflammation in addition to cell cycle and DNA damage responses. | Q39841661 |
| | Yes-associated protein (YAP) functions as a tumor suppressor in breast. | Q39962753 |
| | ERKs and p38 kinase phosphorylate p53 protein at serine 15 in response to UV radiation | Q40883900 |
| | Recombinant ATM protein complements the cellular A-T phenotype | Q41099853 |
| | Evidence for a Growth-Stabilizing Regulatory Feedback Mechanism between Myc and Yorkie, the Drosophila Homolog of Yap | Q42023045 |
| | MYC-driven tumorigenesis is inhibited by WRN syndrome gene deficiency | Q43097729 |
| | DNA damage is able to induce senescence in tumor cells in vitro and in vivo. | Q43931306 |
| | Inhibition of ATM and ATR kinase activities by the radiosensitizing agent, caffeine. | Q52536369 |
| | Physical and Functional Interaction between p53 Mutants and Different Isoforms of p73 | Q58073315 |
| | Induction of senescence with doxorubicin leads to increased genomic instability of HCT116 cells | Q81419187 |
| | PGC1α confers specificity-metabolic stress and p53-dependent transcription | Q82588762 |
| P433 | issue | 11 | |
| P304 | page(s) | 1498-1509 | |
| P577 | publication date | 2013-08-09 | |
| P1433 | published in | Cell Death & Differentiation | Q2943974 |
| P1476 | title | ATM kinase enables the functional axis of YAP, PML and p53 to ameliorate loss of Werner protein-mediated oncogenic senescence | |
| P478 | volume | 20 | |