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Evidence for the interaction of the hereditary haemochromatosis protein, HFE, with the transferrin receptor in endocytic compartments.

HFE, the protein mutated in hereditary haemochromatosis type 1, is known to interact with the transferrin receptor (TfR) on the cell surface and during endocytosis [Gross, Irrinki, Feder and Enns (1998) J. Biol. Chem. 273, 22068-22074; Roy, Penny, Feder and Enns (1999) J. Biol. Chem. 274, 9022-9028]...

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Detalhes bibliográficos
Main Authors: Davies, Paige S, Zhang, An-Sheng, Anderson, Emily L, Roy, Cindy N, Lampson, Michael A, McGraw, Timothy E, Enns, Caroline A
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1223471/
https://ncbi.nlm.nih.gov/pubmed/12667138
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20030202
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