The ferroportin disease.
作者信息
Pietrangelo Antonello
机构信息
Division of Internal Medicine 2 and Center for Hemochromatosis University Hospital of Modena Modena Italy.
出版信息
Clin Liver Dis (Hoboken). 2014 May 27;3(5):98-100. doi: 10.1002/cld.340. eCollection 2014 May.
Abstract
摘要
相似文献
1
The ferroportin disease.铁转运蛋白病
Clin Liver Dis (Hoboken). 2014 May 27;3(5):98-100. doi: 10.1002/cld.340. eCollection 2014 May.
2
A male patient with ferroportin disease B and a female patient with iron overload similar to ferroportin disease B.一名患有B型铁转运蛋白病的男性患者和一名患有与B型铁转运蛋白病相似的铁过载的女性患者。
Clin J Gastroenterol. 2014 Jun;7(3):260-4. doi: 10.1007/s12328-014-0487-1. Epub 2014 Apr 19.
3
Identification of Antibody and Small Molecule Antagonists of Ferroportin-Hepcidin Interaction.铁转运蛋白-铁调素相互作用的抗体和小分子拮抗剂的鉴定
Front Pharmacol. 2017 Nov 21;8:838. doi: 10.3389/fphar.2017.00838. eCollection 2017.
4
The dynamics of hepcidin-ferroportin internalization and consequences of a novel ferroportin disease mutation.亚铁转运蛋白内吞作用的动态变化和新型亚铁转运蛋白疾病突变的后果。
Am J Hematol. 2017 Oct;92(10):1052-1061. doi: 10.1002/ajh.24844. Epub 2017 Jul 29.
5
Impact of D181V and A69T on the function of ferroportin as an iron export pump and hepcidin receptor.D181V和A69T对作为铁输出泵和铁调素受体的铁转运蛋白功能的影响。
Biochim Biophys Acta. 2014 Sep;1842(9):1406-12. doi: 10.1016/j.bbadis.2014.05.011. Epub 2014 May 21.
6
Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation.常染色体显性遗传性血色病新型铁蛋白基因突变所致的临床表现和分子病理生理学
Hepatology. 2010 Mar;51(3):788-95. doi: 10.1002/hep.23377.
7
Structure-function analysis of the human ferroportin iron exporter (SLC40A1): effect of hemochromatosis type 4 disease mutations and identification of critical residues.人亚铁转运蛋白（SLC40A1）的结构-功能分析：血色病 4 型疾病突变的影响及关键残基的鉴定。
Hum Mutat. 2013 Oct;34(10):1371-80. doi: 10.1002/humu.22369. Epub 2013 Sep 10.
8
The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis.铁输出蛋白铁转运蛋白/溶质载体家族40成员1（Ferroportin/Slc40a1）对铁稳态至关重要。
Cell Metab. 2005 Mar;1(3):191-200. doi: 10.1016/j.cmet.2005.01.003.
9
Association of iron metabolic enzyme hepcidin expression levels with the prognosis of patients with pancreatic cancer.铁代谢酶铁调素表达水平与胰腺癌患者预后的关联
Oncol Lett. 2018 May;15(5):8125-8133. doi: 10.3892/ol.2018.8357. Epub 2018 Mar 26.
10
Bone marrow iron distribution, hepcidin, and ferroportin expression in renal anemia.肾性贫血中的骨髓铁分布、铁调素及铁转运蛋白表达
Hematology. 2015 Oct;20(9):543-52. doi: 10.1179/1607845415Y.0000000004. Epub 2015 Mar 8.
引用本文的文献
1
A small molecule redistributes iron in ferroportin-deficient mice and patient-derived primary macrophages.一种小分子可在铁蛋白缺乏的小鼠和患者来源的原代巨噬细胞中重新分配铁。
Proc Natl Acad Sci U S A. 2022 Jun 28;119(26):e2121400119. doi: 10.1073/pnas.2121400119. Epub 2022 Jun 22.
2
Decreased ferroportin in hepatocytes promotes macrophages polarize towards an M2-like phenotype and liver fibrosis.肝细胞中铁蛋白减少促进巨噬细胞向 M2 样表型极化和肝纤维化。
Sci Rep. 2021 Jun 28;11(1):13386. doi: 10.1038/s41598-021-92839-z.
3
Therapeutic phlebotomy.治疗性放血术
Clin Liver Dis (Hoboken). 2014 Dec 9;4(5):102-106. doi: 10.1002/cld.408. eCollection 2014 Nov.
本文引用的文献
1
Non-HFE hepatic iron overload.非 HFE 相关性肝铁过载。
Semin Liver Dis. 2011 Aug;31(3):302-18. doi: 10.1055/s-0031-1286061. Epub 2011 Sep 7.
2
Disease progression and liver cancer in the ferroportin disease.铁转运蛋白病中的疾病进展与肝癌
Gut. 2007 Jul;56(7):1030-2. doi: 10.1136/gut.2007.122549.
3
Magnetic resonance imaging to identify classic and nonclassic forms of ferroportin disease.磁共振成像用于识别铁转运蛋白病的经典和非经典形式。
Blood Cells Mol Dis. 2006 Nov-Dec;37(3):192-6. doi: 10.1016/j.bcmd.2006.08.007. Epub 2006 Oct 18.
4
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization.铁调素通过与铁转运蛋白结合并诱导其内化来调节细胞铁外流。
Science. 2004 Dec 17;306(5704):2090-3. doi: 10.1126/science.1104742. Epub 2004 Oct 28.
5
The ferroportin disease.铁转运蛋白病
Blood Cells Mol Dis. 2004 Jan-Feb;32(1):131-8. doi: 10.1016/j.bcmd.2003.08.003.
6
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene.常染色体显性遗传性血色素沉着症与铁转运蛋白（SLC11A3）基因突变有关。
J Clin Invest. 2001 Aug;108(4):619-23. doi: 10.1172/JCI13468.
7
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.溶质载体家族11成员3（SLC11A3）中的一种突变与常染色体显性遗传性血色素沉着症相关。
Nat Genet. 2001 Jul;28(3):213-4. doi: 10.1038/90038.
8
Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene.成人遗传性血色素沉着症，血色素沉着症基因无致病突变
N Engl J Med. 1999 Sep 2;341(10):725-32. doi: 10.1056/NEJM199909023411003.
Zotero 插件