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[3] In humans, defects in GSS are inherited in an autosomal recessive way and are the cause of severe metabolic acidosis, 5-oxoprolinuria, increased rate of haemolysis, and defective function of the central nervous system

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Hum Reprod 28:13391347 Ryu S, Bazer FW, Lim W, Song G (2019) Chrysin leads to cell death in endometriosis by regulation of endoplasmic reticulum stress and cytosolic calcium level

PI3 kinase/Akt/HIF-1 pathway is associated with hypoxia-induced epithelialmesenchymal transition in fibroblast-like synoviocytes of rheumatoid arthritis