Soma S, et al. (2018) Elesclomol restores mitochondrial function in genetic models of copper deficiency. Proc Natl Acad Sci U S A 115(32):8161-8166 PMID:30038027
McLoughlin DM, et al. (2001) The neuronal adaptor protein X11alpha interacts with the copper chaperone for SOD1 and regulates SOD1 activity. J Biol Chem 276(12):9303-7 PMID:11115513
Wong PC, et al. (2000) Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase. Proc Natl Acad Sci U S A 97(6):2886-91 PMID:10694572
Hung IH, et al. (1998) HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense. J Biol Chem 273(3):1749-54 PMID:9430722
Payne AS and Gitlin JD (1998) Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases. J Biol Chem 273(6):3765-70 PMID:9452509
Hung IH, et al. (1997) Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae. J Biol Chem 272(34):21461-6 PMID:9261163
Klomp LW, et al. (1997) Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis. J Biol Chem 272(14):9221-6 PMID:9083055