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Primary hyperoxaluria type 2 is caused by mutations in the GRHPR gene , which is also involved in glyoxylate metabolism

Angiogenesis support : Multiple studies describe upregulation of vascular endothelial growth factor (VEGF) and the promotion of new blood-vessel formation

Immune cell multiomics analysis reveals contribution of oxidative phosphorylation to B-cell functions and organ damage of lupus

Astragaloside IV alleviates neuronal ferroptosis in ischemic stroke by regulating fat mass and obesity-associated-N6-methyladenosine-acyl-CoA synthetase long-chain family member 4 axis

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At 5mg per week, a 10mg vial lasts 2 weeks