Urinary Copper Elevation in a Mouse Model of Wilson's Disease Is a Regulated Process to Specifically Decrease the Hepatic Copper Load

Body copper homeostasis is regulated by the liver, which removes excess copper via bile. In Wilson's disease (WD), this function is disrupted due to inactivation of the copper transporter ATP7B resulting in hepatic copper overload. High urinary copper is a diagnostic feature of WD linked to liv...

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Detalhes bibliográficos
Main Authors: Gray, Lawrence W., Peng, Fangyu, Molloy, Shannon A., Pendyala, Venkata S., Muchenditsi, Abigael, Muzik, Otto, Lee, Jaekwon, Kaplan, Jack H., Lutsenko, Svetlana
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3390108/
https://ncbi.nlm.nih.gov/pubmed/22802922
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0038327
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