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Histone H3.3G34-mutant interneuron progenitors co-opt PDGFRA for gliomagenesis
Histone H3.3 glycine 34 to arginine/valine (G34R/V) mutations drive deadly gliomas and show exquisite regional and temporal specificity, suggesting a developmental context permissive to their effects. Here, we show that 50% of G34R/V-tumours (n=95) bear activating PDGFRA mutations that display stron...
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| Udgivet i: | Cell |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7791404/ https://ncbi.nlm.nih.gov/pubmed/33259802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2020.11.012 |
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