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AOD9604 A modified fragment of human growth hormone (residues 176-191) investigated for its lipolytic properties, cartilage regeneration potential, and favorable safety profile without effects on blood glucose or IGF-1 levels

Furthermore, the impaired sequestration of mitochondria into autophagosomes in Nix mutant erythroid cells prevents mitochondrial clearance, revealing a crucial function for NIX-mediated mitophagy in the maturation of erythrocytes [150, 151]

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(2000) Evidence for the role of megalin in renal uptake of transthyretin

Abstract Tyrosinemia type II (RichnerHanhart syndrome) is a rare disorder caused by mutations in the TAT gene, leading to elevated blood tyrosine and impaired metabolism