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8388 A completed Phase I/IIA multicenter dose-ranging clinical trial that sought to assess the safety and efficacy of TLK286 found that the compound was highly efficacious
"An Activator of Mutant and Wildtype Aldehyde Dehydrogenase Reduces Ischemic Damage to the Heart"
& Pfau, J
FSP1 knockout cell lines were significantly more sensitive to ferroptosis inducers and were rescued by overexpression of FSP1
Also of note, the serum VitB12 level exhibited significant moderate value in predicting insomnia risk (AUC = 0.61)
Transplantation (2013) 95:9605
