Based on the pathway analysis, “response to oxidative stress” was identified as a highly significant pathway that is dysregulated in A2 RPE ( Figure 3 ), which may be a result of the increased levels of 7DHC (a highly oxygen-labile organic compound) observed in the sterol quantification studies.
← all excerpts
Morphological, biochemical, and transcriptomic characterization of iPSC-derived human RPE cells from normal and Smith-Lemli-Opitz syndrome patients.
1
—
—