Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: Implications for cellular iron homeostasis

Hereditary hemochromatosis is a common autosomal recessive disorder of iron metabolism. Recent demonstration of an association between transferrin receptor (TfR) and HFE, a major histocompatibility complex class I-like molecule that has been implicated to play a role in hereditary hemochromatosis, f...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Salter-Cid, Luisa, Brunmark, Anders, Li, Yuanhao, Leturcq, Didier, Peterson, Per A., Jackson, Michael R., Yang, Young
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1999
Assuntos:	Biological Sciences
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC21877/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10318901/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.10.5434
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