| P50 | author | Guenter Weiss | Q42254473 |
| | Manfred Nairz | Q56816089 |
| P2093 | author name string | Egon Demetz | |
| | David Haschka | |
| P2860 | cites work | Tumour necrosis factor alpha regulates iron transport and transporter expression in human intestinal epithelial cells | Q80489412 |
| | Time-course analysis of hepcidin, serum iron, and plasma cytokine levels in humans injected with LPS | Q81734651 |
| | Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization | Q24310115 |
| | IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin | Q24568204 |
| | Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens | Q24630289 |
| | ER stress controls iron metabolism through induction of hepcidin | Q24630714 |
| | Siderophore biosynthesis but not reductive iron assimilation is essential for Aspergillus fumigatus virulence | Q24647631 |
| | Natural resistance to infection with intracellular pathogens: the Nramp1 protein is recruited to the membrane of the phagosome | Q24670206 |
| | Mechanisms of mammalian iron homeostasis | Q27010510 |
| | Iron overload favors the elimination of Leishmania infantum from mouse tissues through interaction with reactive oxygen and nitrogen species | Q27305261 |
| | Iron traffics in circulation bound to a siderocalin (Ngal)–catechol complex | Q27662810 |
| | Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein | Q28214986 |
| | Ferritin, iron homeostasis, and oxidative damage | Q28216801 |
| | Two to tango: regulation of Mammalian iron metabolism | Q28287034 |
| | Transcriptional Adaptation of Mycobacterium tuberculosis within Macrophages: Insights into the Phagosomal Environment | Q28487339 |
| | Nramp transfection transfers Ity/Lsh/Bcg-related pleiotropic effects on macrophage activation: influence on oxidative burst and nitric oxide pathways | Q28511331 |
| | A mammalian siderophore synthesized by an enzyme with a bacterial homolog involved in enterobactin production | Q28511945 |
| | Lipocalin 2-deficient mice exhibit increased sensitivity to Escherichia coli infection but not to ischemia-reperfusion injury | Q28591880 |
| | Nramp1 promotes efficient macrophage recycling of iron following erythrophagocytosis in vivo | Q28593895 |
| | Ferritin, iron homeostasis, and oxidative damage1,2 1Guest Editor: Mario Comporti 2This article is part of a series of reviews on “Iron and Cellular Redox Status.” The full list of papers may be found on the homepage of the journal. | Q29399399 |
| | Nitric oxide and the immune response | Q29617591 |
| | Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron | Q29619561 |
| | Iron and its relation to immunity and infectious disease | Q30978515 |
| | Iron transport into mycobacterium avium-containing phagosomes from an Nramp1(Gly169)-transfected RAW264.7 macrophage cell line. | Q31996280 |
| | Quercetin interferes with iron metabolism in Leishmania donovani and targets ribonucleotide reductase to exert leishmanicidal activity | Q33320399 |
| | Increased serum hepcidin and alterations in blood iron parameters associated with asymptomatic P. falciparum and P. vivax malaria | Q33529583 |
| | Iron chelation therapy for malaria: a review | Q33537442 |
| | Salmonella enterica serovar Typhi impairs CD4 T cell responses by reducing antigen availability | Q33603033 |
| | Regulation of mammalian siderophore 2,5-DHBA in the innate immune response to infection | Q33702939 |
| | Combinatorial effects of malaria season, iron deficiency, and inflammation determine plasma hepcidin concentration in African children | Q33714721 |
| | Nramp1: a link between intracellular iron transport and innate resistance to intracellular pathogens. | Q33782048 |
| | Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin | Q33818360 |
| | Taming the elephant: Salmonella biology, pathogenesis, and prevention | Q33877264 |
| | Rescuing iron-overloaded macrophages by conservative relocation of the accumulated metal | Q38649814 |
| | Effect of iron chelation therapy on recovery from deep coma in children with cerebral malaria | Q39029074 |
| | Iron acquisition by Mycobacterium tuberculosis residing within myeloid dendritic cells | Q39344560 |
| | Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. | Q39968051 |
| | The anemia of chronic disorders | Q40052338 |
| | Effect of provision of daily zinc and iron with several micronutrients on growth and morbidity among young children in Pakistan: a cluster-randomised trial | Q40106335 |
| | The iron efflux protein ferroportin regulates the intracellular growth of Salmonella enterica | Q40290550 |
| | Iron ERRs with Salmonella | Q40443127 |
| | Serum neopterin, interleukin-4, and interleukin-6 concentrations in cerebral malaria patients and the effect of iron chelation therapy. | Q40672934 |
| | Regulatory interactions between iron and nitric oxide metabolism for immune defense against Plasmodium falciparum infection. | Q40813924 |
| | Regulation of iron metabolism in murine J774 macrophages: role of nitric oxide-dependent and -independent pathways following activation with gamma interferon and lipopolysaccharide | Q40926865 |
| | Central role of transcription factor NF-IL6 for cytokine and iron-mediated regulation of murine inducible nitric oxide synthase expression. | Q40956310 |
| | Functional requirement of the hypoxia-responsive element in the activation of the inducible nitric oxide synthase promoter by the iron chelator desferrioxamine | Q41110961 |
| | Pathways for the regulation of macrophage iron metabolism by the anti-inflammatory cytokines IL-4 and IL-13. | Q41143770 |
| | Iron regulates nitric oxide synthase activity by controlling nuclear transcription | Q41447238 |
| | Modulation of iron metabolism in monocyte cell line U937 by inflammatory cytokines: changes in transferrin uptake, iron handling and ferritin mRNA. | Q41513908 |
| | Iron modulates interferon-gamma effects in the human myelomonocytic cell line THP-1 | Q41621241 |
| | Nitric oxide and salmonella pathogenesis | Q42100653 |
| | Effects of routine prophylactic supplementation with iron and folic acid on admission to hospital and mortality in preschool children in a high malaria transmission setting: community-based, randomised, placebo-controlled trial | Q42170063 |
| | Inverse agonist of estrogen-related receptor γ controls Salmonella typhimurium infection by modulating host iron homeostasis | Q42222690 |
| | Iron supplementation in HIV-infected Malawian children with anemia: a double-blind, randomized, controlled trial. | Q42275870 |
| | TLR4-dependent hepcidin expression by myeloid cells in response to bacterial pathogens | Q42741793 |
| | Role of iron homeostasis in trypanosomiasis-associated anemia | Q43410557 |
| | Nramp1 functionality increases inducible nitric oxide synthase transcription via stimulation of IFN regulatory factor 1 expression | Q43664582 |
| | Iron overload alters innate and T helper cell responses to Candida albicans in mice. | Q43705216 |
| | Decreased susceptibility to Plasmodium falciparum infection in pregnant women with iron deficiency | Q43944520 |
| | Role of IL-10 for induction of anemia during inflammation | Q44092330 |
| | Labile plasma iron in iron overload: redox activity and susceptibility to chelation | Q44477026 |
| | Pathways for the regulation of interferon-gamma-inducible genes by iron in human monocytic cells. | Q44529298 |
| | Scrutinizing the mechanisms underlying the induction of anemia of inflammation through GPI-mediated modulation of macrophage activation in a model of African trypanosomiasis. | Q46352622 |
| | Tuberculosis and iron overload in Africa: a review. | Q46697838 |
| | Biosynthesis and IroC-dependent export of the siderophore salmochelin are essential for virulence of Salmonella enterica serovar Typhimurium | Q46808987 |
| | Dysregulated monocyte iron homeostasis and erythropoietin formation in patients with anemia of chronic disease | Q46909992 |
| | Iron fortification and malaria risk in children | Q47835970 |
| | Metabolic adaptation to tissue iron overload confers tolerance to malaria | Q48025726 |
| | Modulatory potential of iron chelation therapy on nitric oxide formation in cerebral malaria | Q48035061 |
| | Regulation of reticuloendothelial iron transporter MTP1 (Slc11a3) by inflammation | Q48853976 |
| | Nramp1-functionality increases iNOS expression via repression of IL-10 formation | Q50058295 |
| | The co-ordinated regulation of iron homeostasis in murine macrophages limits the availability of iron for intracellular Salmonella typhimurium | Q50072262 |
| | A physiological model to study iron recycling in macrophages. | Q50758548 |
| | Regulation of iron homeostasis in anemia of chronic disease and iron deficiency anemia: diagnostic and therapeutic implications. | Q51764368 |
| | Role of iron in T cell activation: Th1 clones differ from TH2 clones in their sensitivity to inhibition of DNA synthesis caused by IGG mabs against the transferrin receptor and the iron chelator deferoxamine | Q54298211 |
| | Iron trafficking and metabolism in macrophages: contribution to the polarized phenotype | Q56942373 |
| | Ferroportin-encapsulated nanoparticles reduce infection and improve immunity in mice infected with Leishmania major | Q58836346 |
| | Autocrine formation of hepcidin induces iron retention in human monocytes | Q58876413 |
| | Hepcidin regulation by innate immune and infectious stimuli | Q59401841 |
| | Metallobiology of host–pathogen interactions: an intoxicating new insight | Q62801421 |
| | Association of pulmonary tuberculosis with increased dietary iron | Q74442113 |
| | Hereditary hemochromatosis results in decreased iron acquisition and growth by Mycobacterium tuberculosis within human macrophages | Q79234100 |
| | Understanding the multiple functions of Nramp1. | Q33887474 |
| | Regulation of transferrin receptor expression and ferritin content in human mononuclear phagocytes. Coordinate upregulation by iron transferrin and downregulation by interferon gamma | Q33893144 |
| | Salmonella typhimurium IroN and FepA proteins mediate uptake of enterobactin but differ in their specificity for other siderophores | Q33992252 |
| | Role of iron in Nramp1-mediated inhibition of mycobacterial growth. | Q34000686 |
| | Biosynthesis of nitric oxide activates iron regulatory factor in macrophages | Q34059787 |
| | Iron status predicts treatment failure and mortality in tuberculosis patients: a prospective cohort study from Dar es Salaam, Tanzania | Q34273983 |
| | Nutritional immunity: transition metals at the pathogen-host interface | Q34288184 |
| | Hereditary hemochromatosis--a new look at an old disease | Q34324340 |
| | Divalent-metal transport by NRAMP proteins at the interface of host-pathogen interactions | Q34341978 |
| | Host-mediated regulation of superinfection in malaria | Q34356504 |
| | Anemia of chronic disease. | Q34401570 |
| | Microbial siderophore-mediated transport | Q34526524 |
| | Erythropoietin contrastingly affects bacterial infection and experimental colitis by inhibiting nuclear factor-κB-inducible immune pathways | Q34544348 |
| | Iron and immunity: a double-edged sword. | Q34557043 |
| | Host iron redistribution as a risk factor for incident tuberculosis in HIV infection: an 11-year retrospective cohort study | Q34566723 |
| | Iron and microbial infection | Q34650077 |
| | Iron availability and infection | Q34803576 |
| | Iron and the anemia of chronic disease. | Q34966625 |
| | Low hepcidin levels in severely anemic malawian children with high incidence of infectious diseases and bone marrow iron deficiency | Q35067289 |
| | Nifedipine affects the course of Salmonella enterica serovar Typhimurium infection by modulating macrophage iron homeostasis | Q35164461 |
| | Iron deficiency and anemia predict mortality in patients with tuberculosis | Q35677249 |
| | Hepcidin antimicrobial peptide transgenic mice exhibit features of the anemia of inflammation | Q35804433 |
| | Iron deficiency protects against severe Plasmodium falciparum malaria and death in young children | Q35845332 |
| | Hepcidin is the major predictor of erythrocyte iron incorporation in anemic African children | Q35955702 |
| | The iron chelator deferasirox protects mice from mucormycosis through iron starvation | Q35960985 |
| | The multifaceted roles of neutrophil gelatinase associated lipocalin (NGAL) in inflammation and cancer | Q35996059 |
| | Iron metabolism and toxicity | Q35998155 |
| | The Deferasirox-AmBisome Therapy for Mucormycosis (DEFEAT Mucor) study: a randomized, double-blinded, placebo-controlled trial | Q36058200 |
| | Oxidative stress fuels Trypanosoma cruzi infection in mice | Q36068270 |
| | Anemia of chronic disease: pathophysiology and laboratory diagnosis | Q36080048 |
| | Slc11a1 (Nramp1) impairs growth of Salmonella enterica serovar typhimurium in macrophages via stimulation of lipocalin-2 expression | Q36091290 |
| | Lipocalin 2 deficiency dysregulates iron homeostasis and exacerbates endotoxin-induced sepsis. | Q36140013 |
| | Slc11a1 limits intracellular growth of Salmonella enterica sv. Typhimurium by promoting macrophage immune effector functions and impairing bacterial iron acquisition. | Q36305784 |
| | Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. II. Effects on microbial proliferation and host survival in vivo | Q36368755 |
| | Repression of SPI2 transcription by nitric oxide-producing, IFNgamma-activated macrophages promotes maturation of Salmonella phagosomes | Q36402842 |
| | Nitric oxide and oxidative stress (H2O2) control mammalian iron metabolism by different pathways | Q36560913 |
| | Iron uptake controls the generation of Leishmania infective forms through regulation of ROS levels | Q36603547 |
| | Iron depletion limits intracellular bacterial growth in macrophages | Q36787471 |
| | Nitric oxide-mediated regulation of ferroportin-1 controls macrophage iron homeostasis and immune function in Salmonella infection | Q36822684 |
| | The iron export protein ferroportin 1 is differentially expressed in mouse macrophage populations and is present in the mycobacterial-containing phagosome. | Q36838527 |
| | Neutrophil gelatinase-associated lipocalin and interleukin-10 regulate intramacrophage Chlamydia pneumoniae replication by modulating intracellular iron homeostasis | Q36852751 |
| | On risks and benefits of iron supplementation recommendations for iron intake revisited | Q36909917 |
| | Iron in infection and immunity | Q36913895 |
| | Iron overload and immunity | Q36923159 |
| | Iron and citrate export by a major facilitator superfamily pump regulates metabolism and stress resistance in Salmonella Typhimurium | Q37031868 |
| | Lipocalin 2 deactivates macrophages and worsens pneumococcal pneumonia outcomes | Q37052936 |
| | Probiotic bacteria reduce salmonella typhimurium intestinal colonization by competing for iron | Q37118020 |
| | Iron in innate immunity: starve the invaders | Q37157743 |
| | Lipocalin 2 is required for pulmonary host defense against Klebsiella infection | Q37257477 |
| | Bone morphogenetic protein signaling is impaired in an HFE knockout mouse model of hemochromatosis | Q37376502 |
| | Absence of functional Hfe protects mice from invasive Salmonella enterica serovar Typhimurium infection via induction of lipocalin-2. | Q37398323 |
| | Lipocalin-2 resistance confers an advantage to Salmonella enterica serotype Typhimurium for growth and survival in the inflamed intestine | Q37401782 |
| | Selective modulation of TLR4-activated inflammatory responses by altered iron homeostasis in mice | Q37403137 |
| | Leishmania donovani depletes labile iron pool to exploit iron uptake capacity of macrophage for its intracellular growth | Q37414550 |
| | Transition metal ions at the crossroads of mucosal immunity and microbial pathogenesis | Q37511583 |
| | Leishmania-mediated inhibition of iron export promotes parasite replication in macrophages. | Q37534221 |
| | Iron metabolism in trypanosomatids, and its crucial role in infection | Q37691483 |
| | Neutrophils are a source of gamma interferon during acute Salmonella enterica serovar Typhimurium colitis | Q37713277 |
| | The struggle for iron - a metal at the host-pathogen interface. | Q37801985 |
| | Divergent modulation of Chlamydia pneumoniae infection cycle in human monocytic and endothelial cells by iron, tryptophan availability and interferon gamma | Q37852650 |
| | The receptor that tames the innate immune response | Q37970027 |
| | Hepcidin and the iron-infection axis | Q38058767 |
| | Anaemia in inflammatory rheumatic diseases | Q38059457 |
| | The complex interplay of iron metabolism, reactive oxygen species, and reactive nitrogen species: insights into the potential of various iron therapies to induce oxidative and nitrosative stress. | Q38137617 |
| | Translational regulation via iron-responsive elements by the nitric oxide/NO-synthase pathway | Q38316713 |
| | Cytokine-mediated regulation of iron transport in human monocytic cells | Q38358858 |
| | Effect of iron fortification on malaria incidence in infants and young children in Ghana: a randomized trial | Q38445196 |
| P304 | page(s) | 152 | |
| P577 | publication date | 2014-07-16 | |
| P1433 | published in | Frontiers in Pharmacology | Q2681208 |
| P1476 | title | Iron at the interface of immunity and infection | |
| P478 | volume | 5 | |