Related references
Note: Only part of the references are listed.Hepcidin in human iron disorders: Therapeutic implications
Antonello Pietrangelo
JOURNAL OF HEPATOLOGY (2011)
Menkes disease
Zeynep Tumer et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment
Antonello Pietrangelo
GASTROENTEROLOGY (2010)
Niemann-Pick C1 protein transports copper to the secretory compartment from late endosomes where ATP7B resides
Chikatoshi Yanagimoto et al.
EXPERIMENTAL CELL RESEARCH (2009)
Ceruloplasmin in neurodegenerative diseases
Sarah J. Texel et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2008)
Diagnosis and treatment of Wilson disease: An update
Eve A. Roberts et al.
HEPATOLOGY (2008)
Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin
Ivana De Domenico et al.
EMBO JOURNAL (2007)
Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia
Satoshi Kono et al.
GASTROENTEROLOGY (2006)
Compound overload of copper and iron in patients with Wilson's disease
Hisao Hayashi et al.
MEDICAL MOLECULAR MORPHOLOGY (2006)
The Wilson disease protein ATP7B resides in the late endosomes with rab7 and the Niemann-Pick C1 protein
M Harada et al.
AMERICAN JOURNAL OF PATHOLOGY (2005)
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
E Nemeth et al.
SCIENCE (2004)
Aceruloplasminemia, an inherited disorder of iron metabolism
H Miyajima et al.
BIOMETALS (2003)
Role of ATP7B in biliary copper excretion in a human hepatoma cell line and normal rat hepatocytes
M Harada et al.
GASTROENTEROLOGY (2000)
Share Paper
