Overexpression of HFE in HepG2 cells reveals differences in intracellular distribution and co-localization of wt- and mutated forms
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference45 articles.
1. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis;Feder;Nat. Genet.,1996
2. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding;Feder;Proc. Natl. Acad. Sci. U. S. A.,1998
3. Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces and iron-deficient phenotype;Corsi;FEBS Lett.,1999
4. Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis;Salter-Cid;Proc. Natl. Acad. Sci. U. S. A.,1999
5. Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis;Waheed;Proc. Natl. Acad. Sci. U. S. A.,2002
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Intracellular iron uptake is favored in Hfe ‐KO mouse primary chondrocytes mimicking an osteoarthritis‐related phenotype;BioFactors;2019-05-27
2. ERAD defects and the HFE-H63D variant are associated with increased risk of liver damages in Alpha 1-Antitrypsin Deficiency;PLOS ONE;2017-06-15
3. The functional significance of E277K and V295A HFE mutations;British Journal of Haematology;2012-05-25
4. ER Stress and Iron Homeostasis: A New Frontier for the UPR;Biochemistry Research International;2011
5. Iron metabolism in macrophages from HFE hemochromatosis patients;Molecular Genetics and Metabolism;2010-10
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3