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. Author manuscript; available in PMC: 2021 Feb 1.
Published in final edited form as: Neuropathol Appl Neurobiol. 2020 Jan 7;46(1):73–85. doi: 10.1111/nan.12591

Figure 2. The H3K27M mutation impacts multiple aspects of tumourigenesis in pHGG models, including decreased animal survival time, increased progenitor self-renewal capacity and altered differentiation, and propensity for hindbrain tumour location.

Figure 2.

Red dots on mouse brains indicate the approximate location and frequency (size of dot) of tumours with the different genetic driver combinations shown.