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The variety and strength of the mechanisms of Rg1 establish it as the perfect candidate for additional research as a PD therapy

In addition to the general lack of UPR activation during ferroptosis, inhibition of key UPR transcription factors XBP1, ATF4, or ATF6 expression did not alter the cellular sensitivity to erastin in MDA-MB-231 cells (Fig

We found that an absence of Gclc in FoB prevented this FCCP-mediated uncoupling (Fig

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In men, it mimics luteinising hormone (LH), acting on Leydig cells in the testes to stimulate testosterone and sperm production