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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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Davies, Paige S, Zhang, An-Sheng, Anderson, Emily L, Roy, Cindy N, Lampson, Michael A, McGraw, Timothy E, Enns, Caroline A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2003
Konular:
Research Article
Online Erişim: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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