scholarly article | Q13442814 |
P50 | author | Gonçalo Mesquita | Q90339061 |
Ana Rita Gomes | Q43185434 | ||
Maria Salomé Gomes | Q43185438 | ||
Ana C. Moreira | Q57539422 | ||
P2093 | author name string | Gonçalo Mesquita | |
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Erythrophagocytosis of desialylated red blood cells is responsible for anaemia during Trypanosoma vivax infection | Q43589316 | ||
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Rhodamine labeling of 3-hydroxy-4-pyridinone iron chelators is an important contribution to target Mycobacterium avium infection. | Q46630110 | ||
Serum ferritin is derived primarily from macrophages through a nonclassical secretory pathway. | Q46645329 | ||
Hepcidin deficiency and iron deficiency do not alter tuberculosis susceptibility in a murine M.tb infection model. | Q47554888 | ||
H-ferritin and proinflammatory cytokines are increased in the bone marrow of patients affected by macrophage activation syndrome. | Q47727637 | ||
Heme oxygenase-1 is an anti-inflammatory host factor that promotes murine plasmodium liver infection | Q47867896 | ||
Heme carrier protein 1 transports heme and is involved in heme-Fe metabolism | Q47914337 | ||
Metabolic adaptation to tissue iron overload confers tolerance to malaria | Q48025726 | ||
Antimycobacterial effect of IFNG (interferon gamma)-induced autophagy is dependent on the HMOX1 (heme oxygenase 1)-mediated increase in the intracellular calcium levels and modulation of PPP3/calcineurin-TFEB (transcription factor EB) axis. | Q49849006 | ||
The co-ordinated regulation of iron homeostasis in murine macrophages limits the availability of iron for intracellular Salmonella typhimurium | Q50072262 | ||
Increased erythrophagocytosis induces ferroptosis in red pulp macrophages in a mouse model of transfusion. | Q52582252 | ||
Ferritin heavy chain controls the HIF-driven hypoxic response by activating the asparaginyl hydroxylase FIH. | Q52629794 | ||
Differential regulation of iron homeostasis during human macrophage polarized activation. | Q53735318 | ||
Host heme oxygenase-1: Friend or foe in tackling pathogens? | Q54211658 | ||
The hepcidin-ferroportin axis controls the iron content of Salmonella-containing vacuoles in macrophages. | Q55001610 | ||
Ferritin H Deficiency in Myeloid Compartments Dysregulates Host Energy Metabolism and Increases Susceptibility to Mycobacterium tuberculosis Infection. | Q55279879 | ||
Cell iron status influences macrophage polarization. | Q55360082 | ||
Anti-band 3 and anti-spectrin antibodies are increased in Plasmodium vivax infection and are associated with anemia. | Q55426170 | ||
Malaria parasite-mediated alteration of macrophage function and increased iron availability predispose to disseminated non-typhoidal infection | Q56364525 | ||
Role of the hepcidin-ferroportin axis in pathogen-mediated intracellular iron sequestration in human phagocytic cells | Q56380046 | ||
HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis | Q24315610 | ||
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin | Q24568204 | ||
Serum ferritin: Past, present and future | Q24626621 | ||
Hemophagocytic syndromes and infection | Q24653852 | ||
Pharmacological Targeting of the Hepcidin/Ferroportin Axis | Q26738350 | ||
Hepcidin and Host Defense against Infectious Diseases | Q26796310 | ||
Hemopexin and haptoglobin: allies against heme toxicity from hemoglobin not contenders | Q26801681 | ||
A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload | Q28139987 | ||
Sequential regulation of ferroportin expression after erythrophagocytosis in murine macrophages: early mRNA induction by haem, followed by iron-dependent protein expression | Q28260693 | ||
Role of hepcidin in the setting of hypoferremia during acute inflammation | Q28507145 | ||
Iron uptake mediated by binding of H-ferritin to the TIM-2 receptor in mouse cells | Q28507904 | ||
Distinct roles for hepcidin and interleukin-6 in the recovery from anemia in mice injected with heat-killed Brucella abortus | Q28510247 | ||
Identification of an intestinal heme transporter | Q28513323 | ||
Scara5 is a ferritin receptor mediating non-transferrin iron delivery | Q28587430 | ||
A mouse model of anemia of inflammation: complex pathogenesis with partial dependence on hepcidin | Q28590264 | ||
Protective and pathogenic functions of macrophage subsets | Q29620351 | ||
The gene encoding the iron regulatory peptide hepcidin is regulated by anemia, hypoxia, and inflammation | Q29620394 | ||
Hepcidin-mediated iron sequestration protects against bacterial dissemination during pneumonia | Q30252780 | ||
Nutritional immunity. Escape from bacterial iron piracy through rapid evolution of transferrin | Q30653243 | ||
Iron chelation in the treatment of neurodegenerative diseases | Q31066051 | ||
Non-transferrin-bound iron (NTBI) uptake by T lymphocytes: evidence for the selective acquisition of oligomeric ferric citrate species | Q31144456 | ||
A novel animal model of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in humanized mice | Q33394809 | ||
Iron chelation therapy for malaria: a review | Q33537442 | ||
Heme-mediated SPI-C induction promotes monocyte differentiation into iron-recycling macrophages | Q33570011 | ||
Iron- and Hepcidin-Independent Downregulation of the Iron Exporter Ferroportin in Macrophages during Salmonella Infection | Q33619541 | ||
Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin | Q33818360 | ||
Host Iron Nutritional Immunity Induced by a Live Yersinia pestis Vaccine Strain Is Associated with Immediate Protection against Plague | Q33819353 | ||
Metabolic Adaptation Establishes Disease Tolerance to Sepsis | Q33824334 | ||
Chemistry and biology of siderophores | Q34109151 | ||
Quiescent haematopoietic stem cells are activated by IFN-gamma in response to chronic infection | Q34112414 | ||
Regulation of ferritin genes and protein | Q34126332 | ||
Sustained IL-4 exposure leads to a novel pathway for hemophagocytosis, inflammation, and tissue macrophage accumulation | Q34193528 | ||
HMOX1 gene promoter alleles and high HO-1 levels are associated with severe malaria in Gambian children | Q34205883 | ||
Iron status predicts treatment failure and mortality in tuberculosis patients: a prospective cohort study from Dar es Salaam, Tanzania | Q34273983 | ||
Host-mediated regulation of superinfection in malaria | Q34356504 | ||
A novel inflammatory pathway mediating rapid hepcidin-independent hypoferremia. | Q34461765 | ||
Dysfunction of the heme recycling system in heme oxygenase 1–deficient mice: effects on macrophage viability and tissue iron distribution | Q34541622 | ||
Host iron redistribution as a risk factor for incident tuberculosis in HIV infection: an 11-year retrospective cohort study | Q34566723 | ||
Heme oxygenase-1 and carbon monoxide suppress the pathogenesis of experimental cerebral malaria. | Q34627646 | ||
Leishmania donovani infection induces anemia in hamsters by differentially altering erythropoiesis in bone marrow and spleen | Q34637852 | ||
Heme oxygenase-1 affords protection against noncerebral forms of severe malaria | Q34659063 | ||
Plasma heme oxygenase-1 levels distinguish latent or successfully treated human tuberculosis from active disease | Q34720679 | ||
Targeting iron acquisition blocks infection with the fungal pathogens Aspergillus fumigatus and Fusarium oxysporum | Q34819468 | ||
Mycobacterium avium infection induces H-ferritin expression in mouse primary macrophages by activating Toll-like receptor 2 | Q35070608 | ||
Salmonella enterica infection stimulates macrophages to hemophagocytose | Q35072142 | ||
Hemophagocytic macrophages constitute a major compartment of heme oxygenase expression in sepsis | Q35103845 | ||
Hemophagocytosis causes a consumptive anemia of inflammation | Q35213574 | ||
The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE-, transferrin receptor 2-, and beta 2-microglobulin-deficient hepatocytes | Q35316703 | ||
Inflammation-induced hepcidin-25 is associated with the development of anemia in septic patients: an observational study | Q35567161 | ||
Hemopexin in severe inflammation and infection: mouse models and human diseases | Q35584877 | ||
Increased ferroportin-1 expression and rapid splenic iron loss occur with anemia caused by Salmonella enterica Serovar Typhimurium infection in mice | Q35609338 | ||
Superinfection in malaria: Plasmodium shows its iron will | Q35632820 | ||
Elevated Hepcidin Is Part of a Complex Relation That Links Mortality with Iron Homeostasis and Anemia in Men and Women with HIV Infection | Q35640004 | ||
NK-, NKT- and CD8-Derived IFNγ Drives Myeloid Cell Activation and Erythrophagocytosis, Resulting in Trypanosomosis-Associated Acute Anemia | Q35662327 | ||
Malaria impairs resistance to Salmonella through heme- and heme oxygenase-dependent dysfunctional granulocyte mobilization | Q35737998 | ||
A transient resistance to blood-stage malaria in interferon-γ-deficient mice through impaired production of the host cells preferred by malaria parasites. | Q35750275 | ||
Rapidly Escalating Hepcidin and Associated Serum Iron Starvation Are Features of the Acute Response to Typhoid Infection in Humans | Q35783676 | ||
Hemophagocytosis in Experimental Visceral Leishmaniasis by Leishmania donovani | Q35945848 | ||
Heme Oxygenase-1 Regulation of Matrix Metalloproteinase-1 Expression Underlies Distinct Disease Profiles in Tuberculosis | Q36031524 | ||
Stromal-derived IL-6 alters the balance of myeloerythroid progenitors during Toxoplasma gondii infection | Q36055984 | ||
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 | ||
Hemophagocytic macrophages in murine typhoid fever have an anti-inflammatory phenotype | Q36277460 | ||
The evolution of iron chelators for the treatment of iron overload disease and cancer. | Q36355224 | ||
Relationship Between Blood Concentrations of Hepcidin and Anemia Severity, Mycobacterial Burden, and Mortality Among Patients With HIV-Associated Tuberculosis | Q36365296 | ||
Late stage erythroid precursor production is impaired in mice with chronic inflammation | Q36366570 | ||
Hepcidin demonstrates a biphasic association with anemia in acute Plasmodium falciparum malaria | Q36366599 | ||
Minihepcidins prevent iron overload in a hepcidin-deficient mouse model of severe hemochromatosis | Q36370876 | ||
Dysregulation of the haem-haemopexin axis is associated with severe malaria in a case-control study of Ugandan children | Q36393876 | ||
Polymorphisms in the Fc gamma receptor IIIA and Toll-like receptor 9 are associated with protection against severe malarial anemia and changes in circulating gamma interferon levels | Q36396890 | ||
TIM-2 is expressed on B cells and in liver and kidney and is a receptor for H-ferritin endocytosis | Q36403570 | ||
Bacterial Stimulation of Toll-Like Receptor 4 Drives Macrophages To Hemophagocytose | Q36410913 | ||
Macrophage nutriprive antimicrobial mechanisms | Q36444224 | ||
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 | ||
Heme catabolism by heme oxygenase-1 confers host resistance to Mycobacterium infection | Q36970799 | ||
New functions for an iron storage protein: the role of ferritin in immunity and autoimmunity | Q37055701 | ||
On-demand erythrocyte disposal and iron recycling requires transient macrophages in the liver | Q37117562 | ||
Anti-erythrocyte antibodies may contribute to anaemia in Plasmodium vivax malaria by decreasing red blood cell deformability and increasing erythrophagocytosis | Q37150814 | ||
Reduced serum hepcidin levels in patients with chronic hepatitis C. | Q37387659 | ||
Siderophore vaccine conjugates protect against uropathogenic Escherichia coli urinary tract infection | Q37451220 | ||
IL-22 Controls Iron-Dependent Nutritional Immunity Against Systemic Bacterial Infections | Q37693697 | ||
Non-transferrin bound iron: a key role in iron overload and iron toxicity | Q37920197 | ||
Hepcidin and the iron-infection axis | Q38058767 | ||
Adult haemophagocytic syndrome | Q38167486 | ||
Impact of interferon-γ on hematopoiesis | Q38245847 | ||
Anaemia, iron deficiency and susceptibility to infections | Q38255136 | ||
Pathogenesis of macrophage activation syndrome and potential for cytokine- directed therapies | Q38267068 | ||
Ferritin: a versatile building block for bionanotechnology. | Q38356225 | ||
Heme Synthesis and Acquisition in Bacterial Pathogens. | Q38791019 | ||
A Red Carpet for Iron Metabolism. | Q39106718 | ||
Endogenous hepcidin and its agonist mediate resistance to selected infections by clearing non-transferrin-bound iron. | Q39488378 | ||
Cytoprotective function of heme oxygenase 1 induced by a nitrated cyclic nucleotide formed during murine salmonellosis | Q39876438 | ||
Heme-Oxygenase-1 Expression Contributes to the Immunoregulation Induced by Fasciola hepatica and Promotes Infection. | Q40097741 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | molecular medicine | Q3523816 |
P304 | page(s) | 84 | |
P577 | publication date | 2018-09-01 | |
P1433 | published in | Pharmaceuticals | Q15750667 |
P1476 | title | Modulation of Iron Metabolism in Response to Infection: Twists for All Tastes | |
P478 | volume | 11 |
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