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Mao found that treating cancer cells with GPX4 inhibitors resulted in acute depletion of N-carbamyl-L-aspartate (C-ASP, a pyrimidine biosynthesis intermediate), accompanied by accumulation of uridine, which could be inhibited by fer-1, a ferroptosis inhibitor [18]

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They also meet requirements for DNA analysis support in molecular diagnostics, immunodiagnostics, next-generation sequencing, and Sanger sequencing