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A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans.
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Cell
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8.18
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Cell
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7.22
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2003
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4.96
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Nat Genet
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Coexpression of normally incompatible developmental pathways in retinoblastoma genesis.
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Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos.
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Mol Cell Biol
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Increased sensitivity to UV radiation in mice with a p53 point mutation at Ser389.
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RING protein Trim32 associated with skin carcinogenesis has anti-apoptotic and E3-ubiquitin ligase properties.
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Distinct roles of Mdm2 and Mdm4 in red cell production.
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Regulation of the p53-MDM2 pathway by 14-3-3 sigma and other proteins.
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Molecular pathways: targeting Mdm2 and Mdm4 in cancer therapy.
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The E3 ubiquitin ligase GRAIL regulates T cell tolerance and regulatory T cell function by mediating T cell receptor-CD3 degradation.
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p53 prevents progression of nevi to melanoma predominantly through cell cycle regulation.
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Mdm2 is required for survival of hematopoietic stem cells/progenitors via dampening of ROS-induced p53 activity.
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EWS-FLI1 induces developmental abnormalities and accelerates sarcoma formation in a transgenic mouse model.
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High levels of the p53 inhibitor MDM4 in head and neck squamous carcinomas.
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Targeted mutation of p53 and Rb in mesenchymal cells of the limb bud produces sarcomas in mice.
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p53 status in stromal fibroblasts modulates tumor growth in an SDF1-dependent manner.
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Differential gene expression profiling of aggressive and nonaggressive follicular carcinomas.
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Loss of the novel tumour suppressor and polarity gene Trim62 (Dear1) synergizes with oncogenic Ras in invasive lung cancer.
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