review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1022544655 |
P356 | DOI | 10.1007/S12026-010-8199-1 |
P932 | PMC publication ID | 3085559 |
P698 | PubMed publication ID | 21161695 |
P5875 | ResearchGate publication ID | 49686708 |
P2093 | author name string | Bobby J Cherayil | |
P2860 | cites work | Current findings, challenges and novel approaches in human genetic susceptibility to tuberculosis | Q22251435 |
Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples | Q24289511 | ||
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization | Q24310115 | ||
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis | Q24310146 | ||
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin | Q24568204 | ||
Hepcidin mediates transcriptional changes that modulate acute cytokine-induced inflammatory responses in mice | Q24617847 | ||
Siderophore-based iron acquisition and pathogen control | Q24681774 | ||
Modulation of bone morphogenetic protein signaling in vivo regulates systemic iron balance | Q24682390 | ||
The neutrophil lipocalin NGAL is a bacteriostatic agent that interferes with siderophore-mediated iron acquisition | Q27640027 | ||
Iron traffics in circulation bound to a siderocalin (Ngal)–catechol complex | Q27662810 | ||
The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors | Q27860900 | ||
Experimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolism | Q28137777 | ||
The C282Y mutation causing hereditary hemochromatosis does not produce a null allele | Q28138010 | ||
Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene | Q28187006 | ||
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans | Q28187047 | ||
An iron delivery pathway mediated by a lipocalin | Q28216116 | ||
HFE gene knockout produces mouse model of hereditary hemochromatosis | Q28263309 | ||
Hepcidin expression and iron transport in alveolar macrophages | Q83221889 | ||
Bioinorganic chemistry: Getting a grip on iron | Q84580166 | ||
Systemic iron homeostasis and the iron-responsive element/iron-regulatory protein (IRE/IRP) regulatory network | Q28280607 | ||
Ferroportin (Q248H) mutations in African families with dietary iron overload | Q28285601 | ||
Two to tango: regulation of Mammalian iron metabolism | Q28287034 | ||
Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases | Q28388335 | ||
TRAM couples endocytosis of Toll-like receptor 4 to the induction of interferon-beta | Q28506630 | ||
Lack of the bone morphogenetic protein BMP6 induces massive iron overload | Q28510138 | ||
Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing | Q28510853 | ||
A mammalian siderophore synthesized by an enzyme with a bacterial homolog involved in enterobactin production | Q28511945 | ||
Nramp1 equips macrophages for efficient iron recycling | Q28513176 | ||
A cell-surface receptor for lipocalin 24p3 selectively mediates apoptosis and iron uptake | Q28587213 | ||
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 | ||
Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism | Q29617479 | ||
Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron | Q29619561 | ||
Rapid development of colitis in NSAID-treated IL-10-deficient mice. | Q33184999 | ||
Siderocalin inhibits the intracellular replication of Mycobacterium tuberculosis in macrophages | Q33658322 | ||
Regulation of hepcidin transcription by interleukin-1 and interleukin-6. | Q33836338 | ||
Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment | Q34120394 | ||
Iron biology in immune function, muscle metabolism and neuronal functioning | Q34131878 | ||
Diagnosis and management of iron deficiency anemia in patients with IBD. | Q34141999 | ||
Multiple hepatic abscesses due to Yersinia enterocolitica infection secondary to primary haemochromatosis. | Q34331002 | ||
Divalent-metal transport by NRAMP proteins at the interface of host-pathogen interactions | Q34341978 | ||
Siderocalin (Lcn 2) also binds carboxymycobactins, potentially defending against mycobacterial infections through iron sequestration | Q34383190 | ||
Cross-talk between iron homeostasis and intestinal inflammation | Q34558183 | ||
Host-pathogen interactions: the role of iron | Q34621342 | ||
Iron and microbial infection | Q34650077 | ||
Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression | Q34658174 | ||
Hemochromatosis, iron and septicemia caused by Vibrio vulnificus | Q34813463 | ||
Siderocalins: siderophore-binding proteins of the innate immune system | Q34934297 | ||
Mechanisms of cellular iron acquisition: another iron in the fire | Q35015885 | ||
Iron homeostasis and the inflammatory response | Q35024676 | ||
The pathogen-associated iroA gene cluster mediates bacterial evasion of lipocalin 2. | Q35133896 | ||
The IL-6- and lipopolysaccharide-induced transcription of hepcidin in HFE-, transferrin receptor 2-, and beta 2-microglobulin-deficient hepatocytes | Q35316703 | ||
Neutrophil-mediated innate immune resistance to mycobacteria | Q35865371 | ||
The molecular mechanism of hepcidin-mediated ferroportin down-regulation | Q35901835 | ||
24p3 and its receptor: dawn of a new iron age? | Q36353482 | ||
How pathogenic bacteria evade mammalian sabotage in the battle for iron | Q36399419 | ||
Role of iron in the pathogenesis of Vibrio vulnificus infections | Q36430563 | ||
Stimulus-dependent impairment of the neutrophil oxidative burst response in lactoferrin-deficient mice | Q36512248 | ||
The transferrin receptor modulates Hfe-dependent regulation of hepcidin expression | Q36539421 | ||
Forging a field: the golden age of iron biology | Q36742479 | ||
Iron depletion limits intracellular bacterial growth in macrophages | Q36787471 | ||
The Troll in Toll: Mal and Tram as bridges for TLR2 and TLR4 signaling. | Q36798080 | ||
Intracellular labile iron. | Q36798824 | ||
The effect of the host's iron status on tuberculosis | Q36816940 | ||
Nramp1 phagocyte intracellular metal withdrawal defense | Q37006940 | ||
Hepcidin-induced internalization of ferroportin requires binding and cooperative interaction with Jak2. | Q37129387 | ||
Lipocalin 2 is required for pulmonary host defense against Klebsiella infection | Q37257477 | ||
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 | ||
Impaired intestinal iron absorption in Crohn's disease correlates with disease activity and markers of inflammation | Q37458338 | ||
Iron sequestration and anemia of inflammation | Q37604592 | ||
Anemia and inflammatory bowel diseases | Q37605066 | ||
A critical review of the roles of host lactoferrin in immunity | Q37689610 | ||
Ironing out the wrinkles in host defense: interactions between iron homeostasis and innate immunity | Q37726751 | ||
Hepcidin and disorders of iron metabolism | Q37795819 | ||
Role of Ferroportin in Macrophage-Mediated Immunity | Q39656348 | ||
Lipocalin 2-dependent inhibition of mycobacterial growth in alveolar epithelium | Q39909785 | ||
Attenuated inflammatory responses in hemochromatosis reveal a role for iron in the regulation of macrophage cytokine translation | Q39953240 | ||
Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. | Q39968051 | ||
The iron efflux protein ferroportin regulates the intracellular growth of Salmonella enterica | Q40290550 | ||
Nramp1 modulates iron homoeostasis in vivo and in vitro: evidence for a role in cellular iron release involving de-acidification of intracellular vesicles | Q40793044 | ||
BMP6 is a key endogenous regulator of hepcidin expression and iron metabolism | Q41871982 | ||
TLR4-dependent hepcidin expression by myeloid cells in response to bacterial pathogens | Q42741793 | ||
Increased susceptibility to Mycobacterium avium in hemochromatosis protein HFE-deficient mice. | Q42754682 | ||
Decreased serum lipocalin-2 levels in human immunodeficiency virus-infected patients: increase during highly active anti-retroviral therapy | Q45397427 | ||
GERD: GERD and insomnia-first degree relatives or distant cousins? | Q48375787 | ||
The co-ordinated regulation of iron homeostasis in murine macrophages limits the availability of iron for intracellular Salmonella typhimurium | Q50072262 | ||
Autocrine formation of hepcidin induces iron retention in human monocytes | Q58876413 | ||
Decreased concentrations of tumor necrosis factor-alpha in supernatants of monocytes from homozygotes for hereditary hemochromatosis | Q68090198 | ||
Hereditary hemochromatosis results in decreased iron acquisition and growth by Mycobacterium tuberculosis within human macrophages | Q79234100 | ||
P433 | issue | 1 | |
P304 | page(s) | 1-9 | |
P577 | publication date | 2011-05-01 | |
P1433 | published in | Immunologic Research | Q15754981 |
P1476 | title | The role of iron in the immune response to bacterial infection | |
P478 | volume | 50 |
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Q43887764 | Blood parameters as biomarkers in a Salmonella spp. disease model of weaning piglets. |
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Q47731915 | Determination of the Molecular Structures of Ferric Enterobactin and Ferric Enantioenterobactin Using Racemic Crystallography |
Q33781475 | Differences in responses of grass carp to different types of grass carp reovirus (GCRV) and the mechanism of hemorrhage revealed by transcriptome sequencing |
Q94582059 | Distinct iron homeostasis in C57BL/6 and Balb/c mouse strains |
Q92659581 | Dual RNA-Seq of Mtb-Infected Macrophages In Vivo Reveals Ontologically Distinct Host-Pathogen Interactions |
Q52872929 | Effect of tiron on remote organ injury in rats with severe acute pancreatitis induced by L-arginine. |
Q55279879 | Ferritin H Deficiency in Myeloid Compartments Dysregulates Host Energy Metabolism and Increases Susceptibility to Mycobacterium tuberculosis Infection. |
Q36958146 | Fungal Innate Immunity Induced by Bacterial Microbe-Associated Molecular Patterns (MAMPs). |
Q34591625 | Hepcidin expression in psoriasis patients |
Q37551280 | Human Metabolome-derived Cofactors Are Required for the Antibacterial Activity of Siderocalin in Urine |
Q92932269 | Increased intestinal permeability exacerbates sepsis through reduced hepatic SCD-1 activity and dysregulated iron recycling |
Q56602775 | Insect cold hardiness: metabolic, gene, and protein adaptation1This review is part of a virtual symposium on recent advances in understanding a variety of complex regulatory processes in insect physiology and endocrinology, including development, met |
Q28082191 | Iron and zinc exploitation during bacterial pathogenesis |
Q39371536 | Iron deficiency across chronic inflammatory conditions: International expert opinion on definition, diagnosis, and management |
Q56968591 | Iron deficiency in chronic heart failure: case-based practical guidance |
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Q36140013 | Lipocalin 2 deficiency dysregulates iron homeostasis and exacerbates endotoxin-induced sepsis. |
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Q40228124 | Proteomic profiling of the influence of iron availability on Cryptococcus gattii. |
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