Intracellular pathways of copper trafficking in yeast and humans.

Identification of genes associated with stromal hyperplasia and glandular atrophy of the prostate by mRNA differential display.

CSF abnormalities in patients with aceruloplasminemia.

The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase.

Aceruloplasminemia.

Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.

Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis.

Race and survival after out-of-hospital cardiac arrest in a suburban community.

Functional expression of the menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases.

HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense.

Increased very long-chain fatty acids in erythrocyte membranes of patients with aceruloplasminemia.

The copper chaperone for superoxide dismutase.

Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae.

Experience with comparative picture archiving and communication system baseline data collection at four Veterans Affairs Medical Centers: methodology, lessons learned, and suggestions for improvement.

Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis.