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- W202803896 abstract "AbstractRobust animal models have come to the forefront of understanding GBM biology and cancer biology in general. Specifically, genetically engineered murine models or GEMs have provided a great deal of understanding in investigating the role of p21-Ras in GBM. Elevation of Ras activity is a molecular hallmark of GBM and is under intense investigation. Several animal models have been engineered to express mutant forms of Ras or aberrantly express receptors, which modulate Ras activity. Embryonic stem cell transgenesis is a key methodology in engineering these mice models and so is tissue-specific targeting. We highlight several advantages of using ES-cell mediated transgenesis to generate mouse models expressing activated Ras. These animal models have been crucial in studying GBM formation, identifying novel GBM tumor suppressor genes using retroviral gene-trapping and how Ras synergizes with other signaling pathways to give rise to GBM. Lastly these models can be useful in identifying the potential cell of origin in GBM.KeywordsEmbryonic Stem CellGlial Fibrillary Acidic ProteinInner Cell MassGATA6 ExpressionMalignant AstrocytomaThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves." @default.
- W202803896 created "2016-06-24" @default.
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- W202803896 date "2009-01-01" @default.
- W202803896 modified "2023-09-26" @default.
- W202803896 title "Transgenic Mouse Models of CNS Tumors: Using Genetically Engineered Murine Models to Study the Role of p21-Ras in Glioblastoma Multiforme" @default.
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- W202803896 doi "https://doi.org/10.1007/978-1-60327-553-8_4" @default.
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