Evidence for the interaction of the hereditary haemochromatosis protein, HFE, with the transferrin receptor in endocytic compartments.
about
Molecular insights into the pathogenesis of hereditary haemochromatosisHereditary iron and copper deposition: diagnostics, pathogenesis and therapeutics.The regulation of cellular iron metabolism.The small-molecule iron transport inhibitor ferristatin/NSC306711 promotes degradation of the transferrin receptor.Processing of hemojuvelin requires retrograde trafficking to the Golgi in HepG2 cells.A general map of iron metabolism and tissue-specific subnetworks.Expression of the hereditary hemochromatosis protein HFE increases ferritin levels by inhibiting iron export in HT29 cells.Of mice and men: genetic determinants of iron status.HFE modulates transferrin receptor 2 levels in hepatoma cells via interactions that differ from transferrin receptor 1-HFE interactions.
P2860
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P2860
Evidence for the interaction of the hereditary haemochromatosis protein, HFE, with the transferrin receptor in endocytic compartments.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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name
Evidence for the interaction o ...... tor in endocytic compartments.
@en
type
label
Evidence for the interaction o ...... tor in endocytic compartments.
@en
prefLabel
Evidence for the interaction o ...... tor in endocytic compartments.
@en
P2093
P2860
P356
P1433
P1476
Evidence for the interaction o ...... tor in endocytic compartments.
@en
P2093
An-Sheng Zhang
Caroline A Enns
Cindy N Roy
Emily L Anderson
Michael A Lampson
Paige S Davies
Timothy E McGraw
P2860
P304
P356
10.1042/BJ20030202
P407
P577
2003-07-01T00:00:00Z