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Blood 101(10):41894194 Krugliak M, Zhang J, Ginsburg H (2002) Intraerythrocytic Plasmodium falciparum utilizes only a fraction of the amino acids derived from the digestion of host cell cytosol for the biosynthesis of its proteins

DSIP carries a tryptophan residue at its N-terminus that gives a characteristic UV signature used in laboratory identification, and in the research literature it is studied in connection with sleep regulation and circadian rhythm

Wilson disease Wilson disease Wilson disease (hepatolenticular degeneration) is an autosomal recessive disorder caused by various mutations in the ATP7B gene, which regulates copper transport within hepatocytes

The percutaneous absorption of copper from copper chloride and copper sulfate were investigated in vitro on human skin by Pirot et al