The molecular mechanisms of copper metabolism and its roles in human diseases.
Chen J, Jiang Y, Shi H, Peng Y, Fan X, Li C.
Pflugers Arch. 2020 Oct;472(10):1415-1429. doi: 10.1007/s00424-020-02412-2. Epub 2020 Jun 7.
PMID:32506322
Copper deficiency myelopathy.
Jaiser SR, Winston GP.
J Neurol. 2010 Jun;257(6):869-81. doi: 10.1007/s00415-010-5511-x. Epub 2010 Mar 16.
PMID:20232210
Diagnosis and therapy of Menkes syndrome, a genetic form of copper deficiency.
Kaler SG.
Am J Clin Nutr. 1998 May;67(5 Suppl):1029S-1034S. doi: 10.1093/ajcn/67.5.1029S.
PMID:9587147
Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice.
Guthrie LM, Soma S, Yuan S, Silva A, Zulkifli M, Snavely TC, Greene HF, Nunez E, Lynch B, De Ville C, Shanbhag V, Lopez FR, Acharya A, Petris MJ, Kim BE, Gohil VM, Sacchettini JC.
Science. 2020 May 8;368(6491):620-625. doi: 10.1126/science.aaz8899.
PMID:32381719
The contemporaneous epidemic of chronic, copper deficiency.
Klevay LM.
J Nutr Sci. 2022 Oct 11;11:e89. doi: 10.1017/jns.2022.83. eCollection 2022.