Disease-associated mutations at copper ligand histidine residues of superoxide dismutase 1 diminish the binding of copper and compromise dimer stability.

Chemical genetics suggests a critical role for lysyl oxidase in zebrafish notochord morphogenesis.

Copper and iron disorders of the brain.

Genetic deficiency of cyclooxygenase-2 attenuates abdominal aortic aneurysm formation in mice.

Plant science. Distributing nutrition.

Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity.

Copper and nitric oxide meet in the plasma.

Atp7a determines a hierarchy of copper metabolism essential for notochord development.

Plasma proteins in health and disease: a scientific symposium to celebrate the career and accomplishments of Harvey R. Colten, M.D.

GLUT1 deficiency links nutrient availability and apoptosis during embryonic development.

Mechanisms of the copper-dependent turnover of the copper chaperone for superoxide dismutase.

Selective cyclooxygenase-2 inhibition with celecoxib decreases angiotensin II-induced abdominal aortic aneurysm formation in mice.

Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus.

Management of perinatal torsion: today, tomorrow or never?

History of infection before the onset of juvenile dermatomyositis: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Research Registry.