| scholarly article | Q13442814 |
| review article | Q7318358 |
| P6179 | Dimensions Publication ID | 1007436683 |
| P356 | DOI | 10.1038/35042073 |
| P698 | PubMed publication ID | 11252750 |
| P50 | author | Nancy Andrews | Q4793337 |
| P2093 | author name string | N C Andrews | |
| P2860 | cites work | Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family | Q22010394 |
| Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor | Q22011090 | ||
| A novel mammalian iron-regulated protein involved in intracellular iron metabolism | Q22253435 | ||
| Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family | Q42485956 | ||
| Iron metabolism and absorption studies in the X-linked anaemia of mice | Q45170543 | ||
| Early embryonic lethality of H ferritin gene deletion in mice. | Q52171353 | ||
| Microcytic anemia with iron malabsorption: an inherited disorder of iron metabolism | Q56383988 | ||
| Commentary on | Q59513017 | ||
| Ferrokinetics in the syndrome of familial hypoferremic microcytic anemia with iron malabsorption | Q64225641 | ||
| Iron deficiency anaemia in newborn sla mice: a genetic defect of placental iron transport | Q67402379 | ||
| Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors | Q68352478 | ||
| Defect of Intestinal Mucosal Iron Uptake in Mice with Hereditary Microcytic Anemia | Q70504811 | ||
| Malabsorption and defective utilization of iron in three siblings | Q70766915 | ||
| A thalassemia-like disorder in Belgrade laboratory rats | Q70989960 | ||
| X-linked pyridoxine-responsive sideroblastic anemia due to a Thr388-to-Ser substitution in erythroid 5-aminolevulinate synthase | Q72240979 | ||
| Tissue iron loading and histopathological changes in hypotransferrinaemic mice | Q72696255 | ||
| Neonatal hemochromatosis | Q73803202 | ||
| The molecular defect in hypotransferrinemic mice | Q74055142 | ||
| Iron overload in patients with sideroblastic anaemia is not related to the presence of the haemochromatosis Cys282Tyr and His63Asp mutations | Q74459497 | ||
| Waiting for frataxin | Q93899465 | ||
| A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis | Q24310146 | ||
| Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor | Q24336313 | ||
| Juvenile hemochromatosis locus maps to chromosome 1q. | Q24540265 | ||
| Aceruloplasminemia: molecular characterization of this disorder of iron metabolism | Q24564471 | ||
| The iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomes | Q24676869 | ||
| A yeast manganese transporter related to the macrophage protein involved in conferring resistance to mycobacteria | Q27939911 | ||
| Transferrin receptor is necessary for development of erythrocytes and the nervous system | Q28118509 | ||
| Experimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolism | Q28137777 | ||
| A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation | Q28140006 | ||
| Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter | Q28145559 | ||
| Cloning and characterization of a mammalian proton-coupled metal-ion transporter | Q28245045 | ||
| Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis | Q28254820 | ||
| HFE gene knockout produces mouse model of hereditary hemochromatosis | Q28263309 | ||
| Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis | Q28270814 | ||
| Iron overload in Africa. Interaction between a gene and dietary iron content | Q28286305 | ||
| Congenital Atransferrinemia A Case Report and Review of the Literature | Q28287207 | ||
| A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans | Q28287958 | ||
| Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse | Q28297185 | ||
| Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation | Q28510128 | ||
| The ferritins: molecular properties, iron storage function and cellular regulation | Q28609366 | ||
| Molecular pathogenesis of Friedreich ataxia | Q33751669 | ||
| A population-based study of the clinical expression of the hemochromatosis gene | Q33872904 | ||
| The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. | Q33901224 | ||
| Iron metabolism in copper-deficient swine | Q34278455 | ||
| Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis | Q34472009 | ||
| An Iron-binding Component in Human Blood Plasma | Q34654929 | ||
| Genes that modify the hemochromatosis phenotype in mice | Q35159180 | ||
| Hereditary defect of intestinal iron transport in mice with sex-linked anemia | Q35580667 | ||
| Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux | Q35632453 | ||
| Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport. | Q35796864 | ||
| malvolio, the Drosophila homologue of mouse NRAMP-1 (Bcg), is expressed in macrophages and in the nervous system and is required for normal taste behaviour. | Q37619472 | ||
| Regulation of the distribution of tissue iron. Lessons learned from the hypotransferrinemic mouse | Q39650091 | ||
| Characterization and partial purification of a ferrireductase from human duodenal microvillus membranes | Q41772474 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 208-217 | |
| P577 | publication date | 2000-12-01 | |
| P1433 | published in | Nature Reviews Genetics | Q1071824 |
| P1476 | title | Iron homeostasis: insights from genetics and animal models | |
| P478 | volume | 1 |
| Q44321547 | 2002 E. Mead Johnson Award for Research in Pediatrics Lecture: the molecular biology of the anemia of chronic disease: a hypothesis |
| Q91948030 | A Golgi-targeting fluorescent probe for labile Fe(ii) to reveal an abnormal cellular iron distribution induced by dysfunction of VPS35 |
| Q28117449 | A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency |
| Q46755743 | A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice |
| Q24602264 | A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice |
| Q36267869 | A precious metal: Iron, an essential nutrient for all cells |
| Q24800118 | A spontaneous, recurrent mutation in divalent metal transporter-1 exposes a calcium entry pathway |
| Q47664327 | Activity-based sensing fluorescent probes for iron in biological systems |
| Q24329079 | Alternative splicing regulates the subcellular localization of divalent metal transporter 1 isoforms |
| Q46548909 | An in vitro examination of intestinal iron absorption in a freshwater teleost, rainbow trout (Oncorhynchus mykiss). |
| Q36947503 | Anaemia, prenatal iron use, and risk of adverse pregnancy outcomes: systematic review and meta-analysis |
| Q43434757 | Assessment and interpretation of micronutrient status during pregnancy |
| Q36058819 | Associations between Common Variants in Iron-Related Genes with Haematological Traits in Populations of African Ancestry. |
| Q24671532 | Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene |
| Q33943025 | Beta-thalassaemia intermedia: evaluation of endocrine and bone complications |
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| Q37227305 | Busulfan produces efficient human cell engraftment in NOD/LtSz-Scid IL2Rgamma(null) mice |
| Q35053949 | Caco-2 cell acquisition of dietary iron(III) invokes a nanoparticulate endocytic pathway |
| Q26851312 | Cancer cells with irons in the fire |
| Q35954736 | Cellular and mitochondrial iron homeostasis in vertebrates |
| Q35783963 | Chlamydial Hsp60-2 is iron responsive in Chlamydia trachomatis serovar E-infected human endometrial epithelial cells in vitro |
| Q24300212 | Co-localization of the mammalian hemochromatosis gene product (HFE) and a newly identified transferrin receptor (TfR2) in intestinal tissue and cells |
| Q44428883 | Comparative analysis of mouse hepcidin 1 and 2 genes: evidence for different patterns of expression and co‐inducibility during iron overload1 |
| Q55472145 | Comparative transcriptomic and proteomic analyses reveal upregulated expression of virulence and iron transport factors of Aeromonas hydrophila under iron limitation. |
| Q89759530 | Comprehensive analysis of iron utilization by Mycobacterium tuberculosis |
| Q31171958 | Computational modeling and analysis of iron release from macrophages |
| Q28510378 | Coordination of PGC-1beta and iron uptake in mitochondrial biogenesis and osteoclast activation |
| Q56761893 | Decreased activity of the antioxidant heme oxygenase enzyme: implications in ischemia and in Alzheimer’s disease1,2 1Guest Editors: Mark A. Smith and George Perry 2This article is part of a series of reviews on “Causes and Consequences of Oxidati |
| Q24321894 | Definition of the residues required for the interaction between glycine-extended gastrin and transferrin in vitro |
| Q88561649 | Deletion of ferroportin in murine myeloid cells increases iron accumulation and stimulates osteoclastogenesis in vitro and in vivo |
| Q34296810 | Development of artemisinin compounds for cancer treatment |
| Q33707674 | Disrupted iron regulation in the brain and periphery in cocaine addiction |
| Q34341978 | Divalent-metal transport by NRAMP proteins at the interface of host-pathogen interactions |
| Q40187775 | Effect of hypoxia on the binding and subcellular distribution of iron regulatory proteins |
| Q38322649 | Effects of elevated dietary iron on the gastrointestinal expression of Nramp genes and iron homeostasis in rainbow trout (Oncorhynchus mykiss). |
| Q88197797 | Evaluation of iron loading in four types of hepatopancreatic cells of the mangrove crab Ucides cordatus using ferrocene derivatives and iron supplements |
| Q36153980 | Examination of an inducible expression system for limiting iron availability during Chlamydia trachomatis infection |
| Q48399766 | Expression of a membrane-bound form of the ferroxidase ceruloplasmin by leptomeningeal cells |
| Q37253121 | FeoA and FeoC are essential components of the Vibrio cholerae ferrous iron uptake system, and FeoC interacts with FeoB. |
| Q34722798 | Fine-mapping and genetic analysis of the loci affecting hepatic iron overload in mice. |
| Q36742479 | Forging a field: the golden age of iron biology |
| Q92374095 | Functions and regulation of lipocalin-2 in gut-origin sepsis: a narrative review |
| Q35110839 | Gastrin-deficient mice have disturbed hematopoiesis in response to iron deficiency |
| Q35114084 | Genetic control of susceptibility to bacterial infections in mouse models |
| Q35626388 | Genetic insights into the clinical diversity of beta thalassaemia |
| Q58561424 | Genetic predisposition for inflammation exacerbates effects of striatal iron content on cognitive switching ability in healthy aging |
| Q28586520 | Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice |
| Q38077447 | HCV and oxidative stress in the liver. |
| Q24312763 | HFE association with transferrin receptor 2 increases cellular uptake of transferrin-bound iron |
| Q35121442 | Hemochromatosis gene modifies course of hepatitis C viral infection. |
| Q24651444 | Hepcidin revisited, disulfide connectivity, dynamics, and structure |
| Q93007291 | Hydrogen Peroxide Mediates Artemisinin-Derived C-16 Carba-Dimer-Induced Toxicity of Human Cancer Cells |
| Q84643654 | Hypoxia regulates the ferrous iron uptake and reactive oxygen species level via divalent metal transporter 1 (DMT1) Exon1B by hypoxia‐inducible factor‐1 |
| Q33699479 | Identification of Chlamydia trachomatis genomic sequences recognized by chlamydial divalent cation-dependent regulator A (DcrA). |
| Q37575558 | Impaired renal function and development in Belgrade rats |
| Q46249324 | In vivo bioluminescence imaging of labile iron accumulation in a murine model of Acinetobacter baumannii infection. |
| Q64136859 | Inhalation of iron-abundant gas metal arc welding-mild steel fume promotes lung tumors in mice |
| Q59512928 | Iron Metabolism: Disorders |
| Q33349194 | Iron and porphyrin trafficking in heme biogenesis |
| Q37667481 | Iron and reactive oxygen species: friends or foes of cancer cells? |
| Q35893730 | Iron incorporation into MnSOD A (bacterial Mn-dependent superoxide dismutase) leads to the formation of a peroxidase/catalase implicated in oxidative damage to bacteria |
| Q38548605 | Iron metabolic disorder in chronic hepatitis C: insights from recent evidence |
| Q37064842 | Iron metabolism genes, low-level lead exposure, and QT interval |
| Q81484247 | Iron metabolism mutant hbd mice have a deletion in Sec15l1, which has homology to a yeast gene for vesicle docking |
| Q35172307 | Iron misregulation in the brain: a primary cause of neurodegenerative disorders |
| Q33828414 | Iron overload in Plasmodium berghei-infected placenta as a pathogenesis mechanism of fetal death |
| Q33861129 | Iron overload in sickle cell disease. |
| Q34462620 | Iron status in mice carrying a targeted disruption of lactoferrin |
| Q55434525 | Iron supplementation in pregnant sicklers: an opinion. |
| Q37603508 | Iron transport machinery of human cells: players and their interactions |
| Q29615656 | Iron, brain ageing and neurodegenerative disorders |
| Q51837219 | Iron, manganese, and cobalt transport by Nramp1 (Slc11a1) and Nramp2 (Slc11a2) expressed at the plasma membrane |
| Q41688540 | Ironing Out the Unconventional Mechanisms of Iron Acquisition and Gene Regulation in Chlamydia |
| Q28586797 | Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice |
| Q29619561 | Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron |
| Q44620754 | Localization of iron metabolism–related mRNAs in rat liver indicate that HFE is expressed predominantly in hepatocytes |
| Q57791191 | Magnetite nanoparticles coated with oleic acid: accumulation in hepatopancreatic cells of the mangrove crab Ucides cordatus |
| Q34440506 | Manganese homeostasis in Saccharomyces cerevisiae |
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| Q64078616 | Measuring Dynamic Changes in the Labile Iron Pool in Vivo with a Reactivity-Based Probe for Positron Emission Tomography |
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| Q34740822 | Mycobacterium tuberculosis can utilize heme as an iron source |
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| Q38127242 | Oxidative stress and hepatitis C virus |
| Q36259242 | PPE Surface Proteins Are Required for Heme Utilization by Mycobacterium tuberculosis |
| Q37725581 | Pathophysiology of the Belgrade rat. |
| Q38130388 | Pathways of iron acquisition and utilization in Leishmania. |
| Q34205528 | Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias. |
| Q24306074 | Previously uncharacterized isoforms of divalent metal transporter (DMT)-1: implications for regulation and cellular function |
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| Q28509001 | Slc11a2 is required for intestinal iron absorption and erythropoiesis but dispensable in placenta and liver |
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