ApoE isoforms differentially alter baseline antioxidant levels critical to ferroptosis mitigation
Ontology highlight
ABSTRACT: U87 cells overexpressing ApoE isoforms were treated with sulforaphane for 18 hours for comparison with a DMSO control. ApoEChimp is on the ApoE4 backbone but contains R61T which is thought to be the isoform defining residue.
INSTRUMENT(S): Illumina NovaSeq 6000
ORGANISM(S): Homo sapiens
SUBMITTER: Max Thorwald
PROVIDER: E-MTAB-16242 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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