Site of principal metabolic defect in idiopathic haemochromatosis: insights from transplantation of an affected organ.
作者信息
Dabkowski P L, Angus P W, Smallwood R A, Ireton J, Jones R M
机构信息
Victorian Liver Transplant Unit, Austin Hospital, Heidelberg, Australia.
出版信息
BMJ. 1993 Jun 26;306(6894):1726. doi: 10.1136/bmj.306.6894.1726.
Abstract
摘要
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Site of principal metabolic defect in idiopathic haemochromatosis: insights from transplantation of an affected organ.特发性血色素沉着症主要代谢缺陷的部位：来自受累器官移植的见解
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Heterozygous recipient and donor HFE mutations associated with a hereditary haemochromatosis phenotype after liver transplantation.肝移植后与遗传性血色素沉着症表型相关的杂合受体和供体HFE突变。
Gut. 2003 Mar;52(3):433-5. doi: 10.1136/gut.52.3.433.
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Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man.β2微球蛋白基因敲除小鼠的铁稳态缺陷重现了人类遗传性血色素沉着症。
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本文引用的文献
1
Intestinal mucosal uptake of iron and iron retention in idiopathic haemochromatosis as evidence for a mucosal abnormality.特发性血色素沉着症中肠道黏膜对铁的摄取及铁潴留：黏膜异常的证据
Gut. 1970 Sep;11(9):727-31. doi: 10.1136/gut.11.9.727.
2
Hepatic iron in the control of iron absorption in a rat liver transplantation model.
Transplantation. 1989 Jul;48(1):19-21. doi: 10.1097/00007890-198907000-00005.
3
Differential expression of transferrin receptor in duodenal mucosa in iron overload. Evidence for a site-specific defect in genetic hemochromatosis.铁过载时十二指肠黏膜中转铁蛋白受体的差异表达。遗传性血色素沉着症中位点特异性缺陷的证据。
Gastroenterology. 1990 Apr;98(4):976-84. doi: 10.1016/0016-5085(90)90022-s.
4
Hepatic iron clearance from serum in treated hemochromatosis.治疗性血色素沉着症中血清铁的肝脏清除率。
Gastroenterology. 1978 Nov;75(5):856-9.
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