Ontology highlight
ABSTRACT:
INSTRUMENT(S):
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Neuronal Stem Cell
DISEASE(S): Brain Glioma
SUBMITTER:
Jimi Wills
LAB HEAD: Steven M Pollard
PROVIDER: PXD021270 | Pride | 2021-09-09
REPOSITORIES: Pride
| Action | DRS | |||
|---|---|---|---|---|
| 02_CTL-1.raw | Raw | |||
| 03_CTL-2.raw | Raw | |||
| 04_CTL-3.raw | Raw | |||
| 05_P2D3-G34R-1.raw | Raw | |||
| 06_P2D3-G34R-2.raw | Raw |
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Bressan Raul Bardini RB Southgate Benjamin B Ferguson Kirsty M KM Blin Carla C Grant Vivien V Alfazema Neza N Wills Jimi C JC Marques-Torrejon Maria Angeles MA Morrison Gillian M GM Ashmore James J Robertson Faye F Williams Charles A C CAC Bradley Leanne L von Kriegsheim Alex A Anderson Richard A RA Tomlinson Simon R SR Pollard Steven M SM
Cell stem cell 20210224 5
Point mutations within the histone H3.3 are frequent in aggressive childhood brain tumors known as pediatric high-grade gliomas (pHGGs). Intriguingly, distinct mutations arise in discrete anatomical regions: H3.3-G34R within the forebrain and H3.3-K27M preferentially within the hindbrain. The reasons for this contrasting etiology are unknown. By engineering human fetal neural stem cell cultures from distinct brain regions, we demonstrate here that cell-intrinsic regional identity provides differ ...[more]