NMDA receptor activation mediates copper homeostasis in hippocampal neurons.

Comparison of "B" readers' interpretations of chest radiographs for asbestos related changes.

Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.

A fungal multicopper oxidase restores iron homeostasis in aceruloplasminemia.

Role of copper in the proteosome-mediated degradation of the multicopper oxidase hephaestin.

Clinical, molecular, and PET study of a case of aceruloplasminaemia presenting with focal cranial dyskinesia.

Wilson disease.

The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein.

Complications of small intestinal submucosa for corporal body grafting for proximal hypospadias.

Mechanisms of biosynthesis of mammalian copper/zinc superoxide dismutase.

Endothelium-dependent relaxation and endothelial hyperpolarization by P2Y receptor agonists in rat-isolated mesenteric artery.

Hepatic copper metabolism: insights from genetic disease.

Intravesical phallus in cloacal exstrophy.

Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes ATPase.

Mechanisms of copper incorporation into human ceruloplasmin.