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Iron, melanin and dopamine interaction: relevance to Parkinsons disease

Shen Y, Jiang B, Luo B, Jiang X, Zhang Y, Wang Q

Because these patients symptoms skull asymmetry, infantile spasms, dwarfism, brain atrophy, sensory impairments, and glycosylation abnormalities resembled type II congenital disorder of glycosylation (CDG), this study established a link between Mn deficiency and hereditary CDG, showing that mutations in SLC39A8 can decrease the supply of Mn to the Golgi enzyme -1-galactosyltransferase, which is essential for glycoprotein biosynthesis

Erectile dysfunction in the community: a prevalence study

Once active GLP-1 is secreted, the enzyme DPP-4 quickly cleaves the majority of the hormone 10 and the remaining active GLP-1 enters circulation

2016 Hepatotoxicity: A Drug-Induced Cholestatic Pattern Laura Morales M