The copper-iron connection: hereditary aceruloplasminemia.

Copper chaperones for cytochrome c oxidase and human disease.

Congenital mid ureteral stricture presenting as prenatal hydronephrosis.

Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.

Biochemical analysis of a missense mutation in aceruloplasminemia.

Interpretation accuracy of a CCD film digitizer.

Ceruloplasmin metabolism and function.

How to make a metalloprotein.

Antiproliferative B cell translocation gene 2 protein is down-regulated post-transcriptionally as an early event in prostate carcinogenesis.

Identification of two distinct vasodilator pathways activated by ATP in the mesenteric bed of the rat.

The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis.

The neuronal adaptor protein X11alpha interacts with the copper chaperone for SOD1 and regulates SOD1 activity.

Hepatic iron overload in aceruloplasminaemia.

Interpretation of Emergency Department radiographs: a comparison of emergency medicine physicians with radiologists, residents with faculty, and film with digital display.

Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase.