Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
Hereditary haemochromatosis is an inherited disorder of iron absorption that leads to excessive iron storage in the liver and other organs. A candidate disease gene HFE has been identified that encodes a novel MHC class I like protein. We report the development of a monoclonal antibody (HFE-JB1) spe...
Үндсэн зохиолчид: | Bastin, J, Jones, M, O'Callaghan, C, Schimanski, L, Mason, D, Townsend, A |
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Формат: | Journal article |
Хэл сонгох: | English |
Хэвлэсэн: |
1998
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Ижил төстэй зүйлс
Ижил төстэй зүйлс
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Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload
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