review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1033565781 |
P356 | DOI | 10.1038/NRMICRO1046 |
P698 | PubMed publication ID | 15550940 |
P5875 | ResearchGate publication ID | 8176293 |
P50 | author | Stefan Kaufmann | Q2336447 |
Ulrich E Schaible | Q93269853 | ||
P2860 | cites work | Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor | Q22011090 |
A component of innate immunity prevents bacterial biofilm development | Q24298499 | ||
IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin | Q24568204 | ||
Recent advances in understanding haemochromatosis: a transition state | Q24676226 | ||
The iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomes | Q24676869 | ||
Lack of a role for iron in the Lyme disease pathogen | Q28145506 | ||
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter | Q28145559 | ||
Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation | Q28186993 | ||
Iron overload in Africa. Interaction between a gene and dietary iron content | Q28286305 | ||
Gallium disrupts iron metabolism of mycobacteria residing within human macrophages | Q28344777 | ||
The Mycobacterium tuberculosis IdeR is a dual functional regulator that controls transcription of genes involved in iron acquisition, iron storage and survival in macrophages | Q28487578 | ||
Nramp 2 (DCT1/DMT1) expressed at the plasma membrane transports iron and other divalent cations into a calcein-accessible cytoplasmic pool | Q28505462 | ||
Specific binding of the Listeria monocytogenes transcriptional regulator PrfA to target sequences requires additional factor(s) and is influenced by iron | Q48872375 | ||
MHC class Ia-restricted T cells partially account for beta2-microglobulin-dependent resistance to Mycobacterium tuberculosis. | Q52963484 | ||
The adverse effect of iron repletion on the course of certain infections | Q54956692 | ||
Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis | Q59512864 | ||
Reduction of exogenous ferric iron by a surface-associated ferric reductase of Listeria spp | Q71722983 | ||
The effects of iron deficiency and iron overload on cell-mediated immunity in the mouse | Q72422462 | ||
The IgM and IgG antibody responses in iron-deficient and iron-loaded mice | Q72625766 | ||
Systemic oxygen-free radical production in iron-loaded mice | Q73277440 | ||
The outcome of Leishmania major experimental infection in BALB/c mice can be modulated by exogenously delivered iron | Q73420724 | ||
Effect of transfusional iron overload on immune response | Q74177641 | ||
Association of pulmonary tuberculosis with increased dietary iron | Q74442113 | ||
African iron overload | Q78379536 | ||
Intraphagosomal Mycobacterium tuberculosis acquires iron from both extracellular transferrin and intracellular iron pools. Impact of interferon-gamma and hemochromatosis | Q78425267 | ||
Iron-source preference of Staphylococcus aureus infections | Q80551515 | ||
Adaptive Response of Iron Absorption to Anemia, Increased Erythropoiesis, Iron Deficiency, and Iron Loading in β2-Microglobulin Knockout Mice | Q100806660 | ||
Host resistance to intracellular infection: mutation of natural resistance-associated macrophage protein 1 (Nramp1) impairs phagosomal acidification | Q28513925 | ||
Bacterial iron homeostasis | Q29615095 | ||
Balancing acts: molecular control of mammalian iron metabolism | Q29620380 | ||
The Nramp1 protein and its role in resistance to infection and macrophage function. | Q33694066 | ||
Differential expression of iron-, carbon-, and oxygen-responsive mycobacterial genes in the lungs of chronically infected mice and tuberculosis patients | Q33716960 | ||
Regulation of transferrin receptor expression and ferritin content in human mononuclear phagocytes. Coordinate upregulation by iron transferrin and downregulation by interferon gamma | Q33893144 | ||
Iron metabolism in pathogenic bacteria. | Q33920195 | ||
Lactoferrin peptide increases the survival of Candida albicans-inoculated mice by upregulating neutrophil and macrophage functions, especially in combination with amphotericin B and granulocyte-macrophage colony-stimulating factor | Q34007871 | ||
Infections in E-beta thalassemia | Q34115650 | ||
Iron and Mycobacterium tuberculosis infection | Q34134803 | ||
Mechanisms of iron regulation in mycobacteria: role in physiology and virulence | Q34182066 | ||
Pumping iron: the strange partnership of the hemochromatosis protein, a class I MHC homolog, with the transferrin receptor | Q34190689 | ||
Lactoferrin inhibits or promotes Legionella pneumophila intracellular multiplication in nonactivated and interferon gamma-activated human monocytes depending upon its degree of iron saturation. Iron-lactoferrin and nonphysiologic iron chelates rever | Q34202817 | ||
Hereditary hemochromatosis--a new look at an old disease | Q34324340 | ||
Lactoferrin and host defense | Q34573857 | ||
Iron acquisition by Gram-positive bacterial pathogens | Q34935244 | ||
Mechanisms of cellular iron acquisition: another iron in the fire | Q35015885 | ||
Iron chelators modulate the fusogenic properties of Salmonella-containing phagosomes | Q35022961 | ||
Iron, mycobacteria and tuberculosis | Q35605944 | ||
Hemochromatosis and the enigma of misplaced iron: implications for infectious disease and survival | Q35747735 | ||
Iron, the HFE gene, and hepatitis C. | Q35909111 | ||
Role of transferrin, transferrin receptors, and iron in macrophage listericidal activity | Q36230297 | ||
Susceptibility of mice deficient in CD1D or TAP1 to infection with Mycobacterium tuberculosis | Q36367900 | ||
The relative importance of T cell subsets in immunity and immunopathology of airborne Mycobacterium tuberculosis infection in mice | Q36376221 | ||
Attenuation of virulence in Mycobacterium tuberculosis expressing a constitutively active iron repressor | Q36559920 | ||
Low iron availability modulates the course of Chlamydia pneumoniae infection | Q37873990 | ||
Antibacterial activity of lactoferrin and a pepsin-derived lactoferrin peptide fragment. | Q40374058 | ||
Neisseria meningitidis accelerates ferritin degradation in host epithelial cells to yield an essential iron source | Q40535223 | ||
The immunological system in hemochromatosis | Q41758965 | ||
Correction of the iron overload defect in beta-2-microglobulin knockout mice by lactoferrin abolishes their increased susceptibility to tuberculosis | Q42048353 | ||
Association between HLA class II alleles and protection from or susceptibility to chronic hepatitis C. | Q42987325 | ||
Iron loading and disease surveillance | Q43182725 | ||
Confrontation between intracellular bacteria and the immune system. | Q43459073 | ||
A novel bovine lactoferrin peptide, FKCRRWQWRM, suppresses Candida cell growth and activates neutrophils | Q43572569 | ||
Iron chelation via deferoxamine exacerbates experimental salmonellosis via inhibition of the nicotinamide adenine dinucleotide phosphate oxidase-dependent respiratory burst | Q43925973 | ||
Iron deficiency and in vitro iron chelation reduce the expression of cluster of differentiation molecule (CD)28 but not CD3 receptors on murine thymocytes and spleen cells | Q44502435 | ||
In vivo effects of bifidobacteria and lactoferrin on gut endotoxin concentration and mucosal immunity in Balb/c mice | Q44928090 | ||
Associations between cellular immune effector function, iron metabolism, and disease activity in patients with chronic hepatitis C virus infection | Q45746879 | ||
Iron-deficient mice fail to develop autoimmune encephalomyelitis | Q47726775 | ||
Metal ion homeostasis and intracellular parasitism | Q47956694 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | iron | Q677 |
P304 | page(s) | 946-953 | |
P577 | publication date | 2004-12-01 | |
P1433 | published in | Nature Reviews Microbiology | Q1071797 |
P1476 | title | Iron and microbial infection | |
P478 | volume | 2 |
Q33906314 | A 24-48 h fed Amblyomma americanum tick saliva immuno-proteome. |
Q33955520 | A Ferroxidase, Cfo1, Regulates Diverse Environmental Stress Responses of Cryptococcus neoformans through the HOG Pathway |
Q36227966 | A Leishmania amazonensis ZIP family iron transporter is essential for parasite replication within macrophage phagolysosomes. |
Q55450980 | A MFS-like plasma membrane transporter required for Leishmania virulence protects the parasites from iron toxicity. |
Q39235231 | A Novel Hybrid Iron Regulation Network Combines Features from Pathogenic and Nonpathogenic Yeasts |
Q37736387 | A Pseudomonas T6SS effector recruits PQS-containing outer membrane vesicles for iron acquisition. |
Q36254095 | A Superoxide Dismutase Capable of Functioning with Iron or Manganese Promotes the Resistance of Staphylococcus aureus to Calprotectin and Nutritional Immunity. |
Q36856126 | A copper hyperaccumulation phenotype correlates with pathogenesis in Cryptococcus neoformans |
Q28487138 | A genetic locus required for iron acquisition in Mycobacterium tuberculosis |
Q35325775 | A metaproteomics approach to elucidate host and pathogen protein expression during catheter-associated urinary tract infections (CAUTIs). |
Q35168885 | A novel antimycobacterial compound acts as an intracellular iron chelator |
Q36267869 | A precious metal: Iron, an essential nutrient for all cells |
Q27309201 | A putative P-type ATPase required for virulence and resistance to haem toxicity in Listeria monocytogenes |
Q24621536 | A small RNA promotes siderophore production through transcriptional and metabolic remodeling |
Q37398323 | Absence of functional Hfe protects mice from invasive Salmonella enterica serovar Typhimurium infection via induction of lipocalin-2. |
Q35739013 | Adaptation of Cryptococcus neoformans to mammalian hosts: integrated regulation of metabolism and virulence |
Q92563214 | Adjunctive transferrin to reduce the emergence of antibiotic resistance in Gram-negative bacteria |
Q52662918 | Airway surface liquid from smokers promotes bacterial growth and biofilm formation via iron-lactoferrin imbalance. |
Q36410933 | All Three TonB Systems Are Required for Vibrio vulnificus CMCP6 Tissue Invasiveness by Controlling Flagellum Expression |
Q36324280 | Aminopeptidase T of M29 Family Acts as A Novel Intracellular Virulence Factor for Listeria monocytogenes Infection. |
Q96222261 | An ECF-type transporter scavenges heme to overcome iron-limitation in Staphylococcus lugdunensis |
Q50225493 | An adequate Fe nutritional status of maize suppresses infection and biotrophic growth of Colletotrichum graminicola |
Q38914116 | An effective in vitro and in vivo antileishmanial activity and mechanism of action of 8-hydroxyquinoline against Leishmania species causing visceral and tegumentary leishmaniasis. |
Q28487486 | An extracellular siderophore is required to maintain the mutualistic interaction of Epichloë festucae with Lolium perenne |
Q38059457 | Anaemia in inflammatory rheumatic diseases |
Q92819129 | Anemia management in non-menopausal women in a primary care setting: a prospective evaluation of clinical practice |
Q28243702 | Annulling a dangerous liaison: vaccination strategies against AIDS and tuberculosis |
Q28388030 | Antifungal Susceptibility in Serum and Virulence Determinants of Candida Bloodstream Isolates from Hong Kong |
Q24457199 | Antiviral properties of lactoferrin--a natural immunity molecule |
Q35087604 | Are pathogenic bacteria just looking for food? Metabolism and microbial pathogenesis |
Q39953240 | Attenuated inflammatory responses in hemochromatosis reveal a role for iron in the regulation of macrophage cytokine translation |
Q39356682 | Bacterial cell wall constituents induce hepcidin expression in macrophages through MyD88 signaling |
Q37033033 | Beta2-microglobulin-dependent bacterial clearance and survival during murine Klebsiella pneumoniae bacteremia |
Q90701720 | Biomarkers of iron metabolism facilitate clinical diagnosis in M ycobacterium tuberculosis infection |
Q46808987 | Biosynthesis and IroC-dependent export of the siderophore salmochelin are essential for virulence of Salmonella enterica serovar Typhimurium |
Q38283363 | Biosynthesis of a complex yersiniabactin-like natural product via the mic locus in phytopathogen Ralstonia solanacearum |
Q91649393 | Blood serum acute phase proteins and iron dynamics during acute phase response of Salmonella enterica serotype Dublin experimentally infected buffalo calves |
Q26824358 | Body iron delocalization: the serious drawback in iron disorders in both developing and developed countries |
Q39545968 | Bovine lactoferrin (LTF) gene promoter haplotypes have different basal transcriptional activities. |
Q36313890 | Brucella abortus requires the heme transporter BhuA for maintenance of chronic infection in BALB/c mice |
Q48253005 | Burkholderia pseudomallei modulates host iron homeostasis to facilitate iron availability and intracellular survival |
Q60922209 | Burkholderia pseudomallei Δ Δ Live Attenuated Vaccine Strain Elicits Full Protective Immunity against Aerosolized Melioidosis Infection |
Q28477740 | Calcineurin signaling and membrane lipid homeostasis regulates iron mediated multidrug resistance mechanisms in Candida albicans |
Q36747010 | Candida albicans ferric reductases are differentially regulated in response to distinct forms of iron limitation by the Rim101 and CBF transcription factors |
Q42085794 | Cap2-HAP complex is a critical transcriptional regulator that has dual but contrasting roles in regulation of iron homeostasis in Candida albicans |
Q33565416 | Cell-Type Specific Determinants of NRAMP1 Expression in Professional Phagocytes |
Q34287676 | Cell-autonomous effector mechanisms against mycobacterium tuberculosis |
Q24634035 | Cell-cell contacts confine public goods diffusion inside Pseudomonas aeruginosa clonal microcolonies |
Q42599154 | Cellular iron distribution in Bacillus anthracis |
Q60299607 | Chapter 6 Rhizobacteria-Induced Systemic Resistance |
Q91763388 | Characterization of temperature-dependent hemin uptake receptors HupA and HvtA in Vibrio vulnificus |
Q129066712 | Chemical Synthesis of Cell Wall Constituents of Mycobacterium tuberculosis |
Q28542656 | Chemical interference with iron transport systems to suppress bacterial growth of Streptococcus pneumoniae |
Q49714985 | Clinical Relevance of Gastrointestinal Microbiota During Pregnancy: A Primer for Nurses |
Q49362091 | Clinical characteristics, therapy response, and outcome of 51 adult patients with hematological malignancy-associated hemophagocytic lymphohistiocytosis: a single institution experience. |
Q39179797 | Clinical quantitative susceptibility mapping (QSM): Biometal imaging and its emerging roles in patient care |
Q42641173 | Cloning, sequencing and expression analysis of the equine hepcidin gene by real-time PCR. |
Q36605345 | Comparative Analysis of Iron Homeostasis in Sub-Saharan African Children with Sickle Cell Disease and Their Unaffected Siblings |
Q41824709 | Comparative analysis of the complete genome of KPC-2-producing Klebsiella pneumoniae Kp13 reveals remarkable genome plasticity and a wide repertoire of virulence and resistance mechanisms |
Q40109707 | Comparative genomic analysis and characterization of incompatibility group FIB plasmid encoded virulence factors of Salmonella enterica isolated from food sources |
Q37339803 | Comparative virulence studies and transcriptome analysis of Staphylococcus aureus strains isolated from animals. |
Q41887439 | Comparison of the genome sequence of the poultry pathogen Bordetella avium with those of B. bronchiseptica, B. pertussis, and B. parapertussis reveals extensive diversity in surface structures associated with host interaction |
Q36116723 | Competing for Iron: Duplication and Amplification of the isd Locus in Staphylococcus lugdunensis HKU09-01 Provides a Competitive Advantage to Overcome Nutritional Limitation. |
Q35571421 | Complex interaction of deferasirox and Pythium insidiosum: iron-dependent attenuation of growth in vitro and immunotherapy-like enhancement of immune responses in vivo |
Q35217539 | Complex role of hemoglobin and hemoglobin-haptoglobin binding proteins in Haemophilus influenzae virulence in the infant rat model of invasive infection. |
Q53072956 | Conformationally Constrained Cinnolinone Nucleoside Analogues as Siderophore Biosynthesis Inhibitors for Tuberculosis. |
Q51827101 | Constitutive expression of Bcl-2 in the haematopoietic compartment alters the metabolism of iron and increases resistance to mycobacterial infection. |
Q35619514 | Contrasting host-pathogen interactions and genome evolution in two generalist and specialist microsporidian pathogens of mosquitoes |
Q36374709 | Coordination of hypoxia adaptation and iron homeostasis in human pathogenic fungi |
Q35773696 | Copper in microbial pathogenesis: meddling with the metal |
Q42720937 | Copper redistribution in murine macrophages in response to Salmonella infection |
Q91967958 | Correlation of Polymorphisms of Natural Resistance-Associated Macrophage Protein 1 (NRAMP1) Gene and Smoking with the Risk of Rheumatoid Arthritis in Chinese Han People |
Q34558183 | Cross-talk between iron homeostasis and intestinal inflammation |
Q28487128 | CtpV: a putative copper exporter required for full virulence of Mycobacterium tuberculosis |
Q34022066 | Dealing with oxidative stress and iron starvation in microorganisms: an overview |
Q44676853 | Delay of phagosome maturation by a mycobacterial lipid is reversed by nitric oxide |
Q52312160 | Desferrioxamine biosynthesis: diverse hydroxamate assembly by substrate-tolerant acyl transferase DesC. |
Q42718330 | Design, synthesis, and biological evaluation of α-hydroxyacyl-AMS inhibitors of amino acid adenylation enzymes. |
Q41951803 | Development of a serum-free liquid medium for Bartonella species |
Q38169805 | Dietary modulation of the inflammatory cascade |
Q43883502 | Differences in circulating non-transferrin-bound iron after oral administration of ferrous sulfate, sodium iron EDTA, or iron polymaltose in women with marginal iron stores |
Q37604815 | Direct ROS scavenging activity of CueP from Salmonella enterica serovar Typhimurium. |
Q41075973 | Discovery and Characterization of New Hydroxamate Siderophores, Baumannoferrin A and B, produced by Acinetobacter baumannii |
Q35826219 | Distinctive Genome Reduction Rates Revealed by Genomic Analyses of Two Coxiella-Like Endosymbionts in Ticks |
Q34982691 | Dynamic transcript profiling of Candida albicans infection in zebrafish: a pathogen-host interaction study |
Q92940378 | Early postnatal hypoferremia in low birthweight and preterm babies: A prospective cohort study in hospital-delivered Gambian neonates |
Q40219053 | Effect of storage period of red blood cell suspensions on helper T-cell subpopulations |
Q34111734 | Effects of Anaplasma phagocytophilum on host cell ferritin mRNA and protein levels |
Q55007714 | Environmental responsibilities of livestock feeding using trace mineral supplements. |
Q37139292 | Environmental stimuli shape biofilm formation and the virulence of periodontal pathogens |
Q43202040 | Erythrochelin--a hydroxamate-type siderophore predicted from the genome of Saccharopolyspora erythraea |
Q34544348 | Erythropoietin contrastingly affects bacterial infection and experimental colitis by inhibiting nuclear factor-κB-inducible immune pathways |
Q42374269 | Essential functional modules for pathogenic and defensive mechanisms in Candida albicans infections |
Q34014326 | Evaluation of iron deficiency as a nutritional adaptation to infectious disease: an evolutionary medicine perspective |
Q41409955 | Evolution of a novel lysine decarboxylase in siderophore biosynthesis |
Q43640329 | ExPEC-typical virulence-associated genes correlate with successful colonization by intestinal E. coli in a small piglet group |
Q44516881 | Experimental phasing using zinc and sulfur anomalous signals measured at the zinc absorption peak. |
Q33675978 | Expression of BfrH, a putative siderophore receptor of Bordetella bronchiseptica, is regulated by iron, Fur1, and the extracellular function sigma factor EcfI. |
Q40164975 | Expression of IroN, the salmochelin siderophore receptor, requires mRNA activation by RyhB small RNA homologues. |
Q51783832 | Factors Mediating Environmental Biofilm Formation by Legionella pneumophila. |
Q38108088 | Feeding the immune system. |
Q28662158 | FeoC from Klebsiella pneumoniae contains a [4Fe-4S] cluster |
Q55279879 | Ferritin H Deficiency in Myeloid Compartments Dysregulates Host Energy Metabolism and Increases Susceptibility to Mycobacterium tuberculosis Infection. |
Q46502857 | Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating serum hepcidin levels in Rwandese HIV-positive women |
Q36101152 | FmvB: A Francisella tularensis Magnesium-Responsive Outer Membrane Protein that Plays a Role in Virulence |
Q42957504 | FoxB of Pseudomonas aeruginosa functions in the utilization of the xenosiderophores ferrichrome, ferrioxamine B, and schizokinen: evidence for transport redundancy at the inner membrane |
Q33645325 | Frequency evaluation of genes encoding siderophores and the effects of different concentrations of Fe ions on growth rate of uropathogenic Escherichia coli |
Q37123826 | Functional features of TonB energy transduction systems of Acinetobacter baumannii |
Q51526729 | Functional genotypes are associated with commensal Escherichia coli strain abundance within-host individuals and populations. |
Q38562559 | Fungal dimorphism: the switch from hyphae to yeast is a specialized morphogenetic adaptation allowing colonization of a host |
Q33900474 | Fur activates the expression of Salmonella enterica pathogenicity island 1 by directly interacting with the hilD operator in vivo and in vitro |
Q29346523 | Fur controls iron homeostasis and oxidative stress defense in the oligotrophic alpha-proteobacterium Caulobacter crescentus |
Q22252427 | Future Vaccination Strategies against Tuberculosis: Thinking outside the Box |
Q54243572 | Gallium(iii) and iron(iii) complexes of quinolone antimicrobials. |
Q33288727 | Gene expression profiles of Chlamydophila pneumoniae during the developmental cycle and iron depletion-mediated persistence |
Q28084863 | Genes Involved in the Biosynthesis and Transport of Acinetobactin in Acinetobacter baumannii |
Q33295221 | Genome analysis of Minibacterium massiliensis highlights the convergent evolution of water-living bacteria |
Q33292673 | Genome sequence of Fusobacterium nucleatum subspecies polymorphum - a genetically tractable fusobacterium |
Q37062857 | Genome-sequence analysis of Acinetobacter johnsonii MB44 reveals potential nematode-virulent factors |
Q34335971 | Genome-wide analysis of copper, iron and zinc transporters in the arbuscular mycorrhizal fungus Rhizophagus irregularis |
Q29346524 | Global transcriptional response of Caulobacter crescentus to iron availability |
Q92726074 | Global transcriptomic analyses of Salmonella enterica in Iron-depleted and Iron-rich growth conditions |
Q39456663 | Gram-negative bacterial membrane vesicle release in response to the host-environment: different threats, same trick? |
Q33389543 | Growth of Yersinia pseudotuberculosis in human plasma: impacts on virulence and metabolic gene expression |
Q40383480 | Guanosine 5'-monophosphate-chelated calcium and iron feed additives maintains egg production and prevents Salmonella Gallinarum in experimentally infected layers |
Q26745893 | Hacker within! Ehrlichia chaffeensis Effector Driven Phagocyte Reprogramming Strategy |
Q33760802 | HapX positively and negatively regulates the transcriptional response to iron deprivation in Cryptococcus neoformans |
Q40004886 | Heme oxygenase 1 controls early innate immune response of macrophages to Salmonella Typhimurium infection. |
Q35130243 | Heme utilization in Campylobacter jejuni |
Q35805349 | Hemin binding protein C is found in outer membrane vesicles and protects Bartonella henselae against toxic concentrations of hemin |
Q33618005 | Hemoglobin uptake by Paracoccidioides spp. is receptor-mediated |
Q35955702 | Hepcidin is the major predictor of erythrocyte iron incorporation in anemic African children |
Q58608378 | Hepcidin mediated iron homeostasis as immune regulator in visceral leishmaniasis patients |
Q40157231 | Hepcidin-(In)dependent Mechanisms of Iron Metabolism Regulation during Infection by Listeria and Salmonella |
Q41543544 | Hepcidin-induced hypoferremia is a critical host defense mechanism against the siderophilic bacterium Vibrio vulnificus |
Q36314033 | High-affinity Zn2+ uptake system ZnuABC is required for bacterial zinc homeostasis in intracellular environments and contributes to the virulence of Salmonella enterica |
Q37852233 | Higher expression of ferritin protectsChlamydia trachomatisinfected HeLa 229 cells from reactive oxygen species mediated cell death |
Q28472490 | Histoplasma requires SID1, a member of an iron-regulated siderophore gene cluster, for host colonization |
Q90445090 | Hoodwinking the Big-Eater to Prosper: The Salmonella-Macrophage Paradigm |
Q28077266 | Host Matters: Medicinal Leech Digestive-Tract Symbionts and Their Pathogenic Potential |
Q34133040 | Human IRGM gene “to be or not to be” |
Q24620449 | Human nutrition, the gut microbiome and the immune system |
Q90439637 | HutZ is required for biofilm formation and contributes to the pathogenicity of Edwardsiella piscicida |
Q41959393 | Identification and characterization of a new ferric enterobactin receptor, CfrB, in Campylobacter |
Q47139186 | Identification and characterization of serovar-independent immunogens in Actinobacillus pleuropneumoniae. |
Q46343938 | Identification and occurrence of the hydroxamate siderophores aerobactin, putrebactin, avaroferrin and ochrobactin C as virulence factors from entomopathogenic bacteria |
Q35542366 | Immunology, genetics and microbiota in the COPD pathophysiology: potential scope for patient stratification |
Q54276501 | Increased hepcidin expression in multibacillary leprosy. |
Q85046237 | Increased iron in HCV infection: Collateral damage or antiviral defense? |
Q57811519 | Increased transferrin saturation is associated with subgingival microbiota dysbiosis and severe periodontitis in genetic haemochromatosis |
Q28267896 | Induction of the ferritin gene (ftnA) of Escherichia coli by Fe(2+)-Fur is mediated by reversal of H-NS silencing and is RyhB independent |
Q26859275 | Infections in myelodysplastic syndromes |
Q34388111 | Influence of iron regulation on the metabolome of Cryptococcus neoformans |
Q37620745 | Influences of pH and Iron Concentration on the Salivary Microbiome in Individual Humans with and without Caries |
Q51093978 | Inhibiting the BfrB:Bfd interaction in Pseudomonas aeruginosa causes irreversible iron accumulation in bacterioferritin and iron deficiency in the bacterial cytosol. |
Q56768198 | Insights into the pathophysiology of iron metabolism in Pythium insidiosum infections |
Q36536225 | Integrated Translatomics with Proteomics to Identify Novel Iron-Transporting Proteins in Streptococcus pneumoniae |
Q33767045 | Interaction of the heterotrimeric G protein alpha subunit SSG-1 of Sporothrix schenckii with proteins related to stress response and fungal pathogenicity using a yeast two-hybrid assay |
Q39968051 | Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. |
Q42432569 | Interleukin-8 secretion in response to aferric enterobactin is potentiated by siderocalin |
Q30494299 | Intracellular Mycobacterium avium intersect transferrin in the Rab11(+) recycling endocytic pathway and avoid lipocalin 2 trafficking to the lysosomal pathway |
Q92610921 | Intracellular iron availability modulates the requirement for Leishmania Iron Regulator 1 (LIR1) during macrophage infections |
Q36358981 | Investigation and conformational analysis of fluorinated nucleoside antibiotics targeting siderophore biosynthesis |
Q49497963 | Investigation of the Role of Genes Encoding Zinc Exporters zntA, zitB, and fieF during Salmonella Typhimurium Infection |
Q28481681 | Involvement of iron in biofilm formation by Staphylococcus aureus |
Q41814448 | IroT/mavN, a new iron-regulated gene involved in Legionella pneumophila virulence against amoebae and macrophages |
Q41971029 | Iron Availability Modulates the Persistence of Legionella pneumophila in Complex Biofilms. |
Q38872865 | Iron Efflux by PmtA Is Critical for Oxidative Stress Resistance and Contributes Significantly to Group A Streptococcus Virulence. |
Q37833858 | Iron Homeostasis in Tissues Is Affected during Persistent Chlamydia pneumoniae Infection in Mice. |
Q41914835 | Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation |
Q64935199 | Iron Toxicity and Hemopoietic Cell Transplantation: Time to Change the Paradigm. |
Q34033963 | Iron acquisition from transferrin by Candida albicans depends on the reductive pathway |
Q35097113 | Iron acquisition in Bacillus cereus: the roles of IlsA and bacillibactin in exogenous ferritin iron mobilization |
Q36631531 | Iron acquisition within host cells and the pathogenicity of Leishmania |
Q89473245 | Iron and Heme Metabolism at the Leishmania-Host Interface |
Q35214752 | Iron and Immunity: Immunological Consequences of Iron Deficiency and Overload |
Q37031868 | Iron and citrate export by a major facilitator superfamily pump regulates metabolism and stress resistance in Salmonella Typhimurium |
Q42837785 | Iron and malaria interactions: research needs from basic science to global policy |
Q40169383 | Iron and susceptibility to infections |
Q61796322 | Iron as a Central Player and Promising Target in Cancer Progression |
Q55167938 | Iron at the Centre of Candida albicans Interactions. |
Q33909430 | Iron at the interface of immunity and infection |
Q30250912 | Iron availability affects West Nile virus infection in its mosquito vector |
Q92205829 | Iron availability and oxygen tension regulate the Yersinia Ysc type III secretion system to enable disseminated infection |
Q40334668 | Iron availability influences aggregation, biofilm, adhesion and invasion of Pseudomonas aeruginosa and Burkholderia cenocepacia. |
Q28388335 | Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases |
Q37296446 | Iron biology, immunology, aging, and obesity: four fields connected by the small peptide hormone hepcidin |
Q33283091 | Iron deficiency and NRAMP1 polymorphisms (INT4, D543N and 3'UTR) do not contribute to severity of anaemia in tuberculosis in the Indonesian population |
Q37341829 | Iron deficiency or anemia of inflammation? : Differential diagnosis and mechanisms of anemia of inflammation |
Q36787471 | Iron depletion limits intracellular bacterial growth in macrophages |
Q37157743 | Iron in innate immunity: starve the invaders |
Q37376232 | Iron in intracellular infection: to provide or to deprive? |
Q59808741 | Iron in the Tumor Microenvironment-Connecting the Dots |
Q48121643 | Iron influences on the Gut-Brain axis and development of type 2 diabetes |
Q35435722 | Iron influences the abundance of the iron regulatory protein Cir1 in the fungal pathogen Cryptococcus neoformans |
Q39660185 | Iron inhibits replication of infectious hepatitis C virus in permissive Huh7.5.1 cells |
Q37093773 | Iron metabolism and infection |
Q26860448 | Iron metabolism and the innate immune response to infection |
Q37691483 | Iron metabolism in trypanosomatids, and its crucial role in infection |
Q46987213 | Iron overload is a major risk factor for severe infection after autologous stem cell transplantation: a study of 367 myeloma patients |
Q33264398 | Iron regulation of the major virulence factors in the AIDS-associated pathogen Cryptococcus neoformans |
Q53811265 | Iron replacement therapy and anemia associated with chronic infectious diseases in sub-Saharan Africa. |
Q90437919 | Iron sequestration by transferrin 1 mediates nutritional immunity in Drosophila melanogaster |
Q35091847 | Iron status is associated with asthma and lung function in US women |
Q89547519 | Iron trafficking in patients with Indian Post kala-azar dermal leishmaniasis |
Q37065752 | Iron- and Quorum-sensing Signals Converge on Small Quorum-regulatory RNAs for Coordinated Regulation of Virulence Factors in Vibrio vulnificus |
Q40287710 | Iron-related transcriptomic variations in CaCo-2 cells, an in vitro model of intestinal absorptive cells |
Q42142234 | Iron-responsive repression of urease expression in Helicobacter hepaticus is mediated by the transcriptional regulator Fur |
Q34634555 | Iron-saturated lactoferrin and pathogenic protozoa: could this protein be an iron source for their parasitic style of life? |
Q37726751 | Ironing out the wrinkles in host defense: interactions between iron homeostasis and innate immunity |
Q41019979 | Isoniazid@Fe2 O3 Nanocontainers and Their Antibacterial Effect on Tuberculosis Mycobacteria |
Q48117422 | KCa(H2 O)2 [FeIII (CN)6 ]⋅H2 O Nanoparticles as Antimicrobial Agent against Staphylococcus aureus. |
Q42927455 | Knocking out salicylate biosynthesis genes in Mycobacterium smegmatis induces hypersensitivity to p-aminosalicylate (PAS) |
Q41419781 | Label-free detection of a bacterial pathogen using an immobilized siderophore, deferoxamine |
Q37601346 | Lack of OxyR and KatG Results in Extreme Susceptibility of Francisella tularensis LVS to Oxidative Stress and Marked Attenuation In vivo |
Q37414550 | Leishmania donovani depletes labile iron pool to exploit iron uptake capacity of macrophage for its intracellular growth |
Q37534221 | Leishmania-mediated inhibition of iron export promotes parasite replication in macrophages. |
Q28545076 | Lipidomic analysis links mycobactin synthase K to iron uptake and virulence in M. tuberculosis |
Q35709328 | Lipidomic discovery of deoxysiderophores reveals a revised mycobactin biosynthesis pathway in Mycobacterium tuberculosis |
Q37335648 | Lipocalin 2 prevents intestinal inflammation by enhancing phagocytic bacterial clearance in macrophages |
Q36396704 | Lipocalin-2 ensures host defense against Salmonella Typhimurium by controlling macrophage iron homeostasis and immune response |
Q92650413 | Lipoprotein SPD_1609 of Streptococcus pneumoniae Promotes Adherence and Invasion to Epithelial Cells Contributing to Bacterial Virulence |
Q38363796 | Macrophage defense mechanisms against intracellular bacteria. |
Q34018936 | Macrophage replication screen identifies a novel Francisella hydroperoxide resistance protein involved in virulence. |
Q43253103 | Mapping of Char10, a novel malaria susceptibility locus on mouse chromosome 9. |
Q34750485 | Mechanisms for copper acquisition, distribution and regulation |
Q35574562 | Mechanisms of heme utilization by Francisella tularensis |
Q38052948 | Mechanisms of infection by the human fungal pathogen Cryptococcus neoformans |
Q38935352 | Mechanisms of inflammation-driven bacterial dysbiosis in the gut. |
Q28472648 | Mechanistic insights into a novel exporter-importer system of Mycobacterium tuberculosis unravel its role in trafficking of iron |
Q30658057 | Mechanistic insights into metal ion activation and operator recognition by the ferric uptake regulator |
Q58583965 | Melatonin Treatment Inhibits the Growth of pv. |
Q53064549 | Metabolic pathways related to oxidative stress in patients with hemoglobin h disease and iron overload. |
Q34580953 | Metabolic sensor governing bacterial virulence in Staphylococcus aureus |
Q33675274 | Metal uptake in host-pathogen interactions: role of iron in Porphyromonas gingivalis interactions with host organisms |
Q36662028 | Metalloreductase Steap3 coordinates the regulation of iron homeostasis and inflammatory responses |
Q44734655 | Microbial siderophores exert a subtle role in Arabidopsis during infection by manipulating the immune response and the iron status. |
Q39013089 | Microemulsions: Options To Expand the Synthesis of Inorganic Nanoparticles |
Q33534484 | Modulation of iron homeostasis in macrophages by bacterial intracellular pathogens |
Q24626906 | Molecular and cellular pathobiology of Ehrlichia infection: targets for new therapeutics and immunomodulation strategies |
Q27003237 | Molecular call and response: the physiology of bacterial small RNAs |
Q34314306 | Molecular strategies of microbial iron assimilation: from high-affinity complexes to cofactor assembly systems |
Q42497407 | Multiple polymorphic loci determine basal hepatic and splenic iron status in mice |
Q34435468 | Mycobacterium tuberculosis acquires iron by cell-surface sequestration and internalization of human holo-transferrin |
Q82241804 | Mycobactin-mediated iron acquisition within macrophages |
Q40066648 | NRAMP-1 expression modulates protein-tyrosine phosphatase activity in macrophages: impact on host cell signaling and functions |
Q35553554 | Native Wolbachia from Aedes albopictus Blocks Chikungunya Virus Infection In Cellulo |
Q36852751 | Neutrophil gelatinase-associated lipocalin and interleukin-10 regulate intramacrophage Chlamydia pneumoniae replication by modulating intracellular iron homeostasis |
Q33768879 | Neutrophil gelatinase-associated lipocalin expresses antimicrobial activity by interfering with L-norepinephrine-mediated bacterial iron acquisition |
Q92500593 | New Perspectives on Galleria mellonella Larvae as a Host Model Using Riemerella anatipestifer as a Proof of Concept |
Q36513326 | New challenges in studying nutrition-disease interactions in the developing world. |
Q28388477 | New insights into TB physiology suggest untapped therapeutic opportunities |
Q35164461 | Nifedipine affects the course of Salmonella enterica serovar Typhimurium infection by modulating macrophage iron homeostasis |
Q40231403 | Niobium uptake and release by bacterial ferric ion binding protein |
Q36822684 | Nitric oxide-mediated regulation of ferroportin-1 controls macrophage iron homeostasis and immune function in Salmonella infection |
Q51568362 | Nosocomial Trichosporon asahii fungemia in a patient with secondary hemochromatosis: a rare case report. |
Q38920767 | Nramp1 and NrampB Contribute to Resistance against Francisella in Dictyostelium |
Q50058295 | Nramp1-functionality increases iNOS expression via repression of IL-10 formation |
Q46295778 | Nutritional Requirements and Their Importance for Virulence of Pathogenic Cryptococcus Species. |
Q33761982 | Nutritional immunity beyond iron: a role for manganese and zinc. |
Q47070132 | Of two cytosolic aconitases expressed in Drosophila, only one functions as an iron-regulatory protein |
Q38916791 | Older red cell units are associated with an increased incidence of infection in chronically transfused adults with sickle cell disease |
Q89824505 | On a stake-out: Mycobacterial small RNA identification and regulation |
Q28538610 | Origin and evolution of the sodium -pumping NADH: ubiquinone oxidoreductase |
Q47356901 | Overcoming antibiotic resistance: Is siderophore Trojan horse conjugation an answer to evolving resistance in microbial pathogens? |
Q36277341 | OxyR activation in Porphyromonas gingivalis in response to a hemin-limited environment |
Q40233051 | Pathogenesis of urinary tract infections : An update |
Q34979350 | Pathogenic yeasts deploy cell surface receptors to acquire iron in vertebrate hosts |
Q34438667 | Phenylalanine hydroxylase from Legionella pneumophila is a thermostable enzyme with a major functional role in pyomelanin synthesis |
Q41363354 | Photorhabdus asymbiotica as an Insect and Human Pathogen. |
Q34056844 | Physiological and proteomic analysis of Escherichia coli iron-limited chemostat growth |
Q39422416 | Prevalence and risk factors of iron overload after hematopoietic stem cell transplantation for childhood acute leukemia: a LEA study |
Q36126290 | Protective and Pathogenic Roles of CD8+ T Lymphocytes in Murine Orientia tsutsugamushi Infection |
Q34766811 | Protein expressions and their immunogenicity from Riemerella anatipestifer cultured in iron restriction medium |
Q36094745 | Protein kinase A and fungal virulence: a sinister side to a conserved nutrient sensing pathway |
Q34042608 | Protein tyrosine phosphatases are regulated by mononuclear iron dicitrate |
Q35745541 | Proteomic Analyses of Intracellular Salmonella enterica Serovar Typhimurium Reveal Extensive Bacterial Adaptations to Infected Host Epithelial Cells |
Q91971657 | Proteomic Analysis Reveals a Predominant NFE2L2 (NRF2) Signature in Canonical Pathway and Upstream Regulator Analysis of Leishmania-Infected Macrophages |
Q58572049 | Proteomic Profiling of During Host Infection Using Bio-Orthogonal Noncanonical Amino Acid Tagging (BONCAT) |
Q33527554 | Proteomic analysis of iron acquisition, metabolic and regulatory responses of Yersinia pestis to iron starvation |
Q34113368 | Proteomic and transcriptomic characterization of a virulence-deficient phosphatidylcholine-negative Agrobacterium tumefaciens mutant |
Q37036107 | Pseudomonas aeruginosa uses multiple pathways to acquire iron during chronic infection in cystic fibrosis lungs |
Q41484183 | Pseudomonas fluorescens: iron-responsive proteins and their involvement in host infection |
Q37256486 | Purification of Legiobactin and importance of this siderophore in lung infection by Legionella pneumophila |
Q36229215 | Pyruvate kinase deficiency confers susceptibility to Salmonella typhimurium infection in mice |
Q26771978 | RNA-Binding Proteins in Trichomonas vaginalis: Atypical Multifunctional Proteins |
Q28485517 | Reactive oxygen species production and Brugia pahangi survivorship in Aedes polynesiensis with artificial Wolbachia infection types |
Q89966758 | Recent update in diagnosis and treatment of human pythiosis |
Q34747007 | Reduced synthesis of the Ybt siderophore or production of aberrant Ybt-like molecules activates transcription of yersiniabactin genes in Yersinia pestis |
Q48175634 | Regulation of Three Virulence Strategies of Mycobacterium tuberculosis: A Success Story |
Q36995110 | Regulation of iron acquisition and storage: consequences for iron-linked disorders |
Q33702939 | Regulation of mammalian siderophore 2,5-DHBA in the innate immune response to infection |
Q37099439 | Regulation of the Vibrio vulnificus hupA gene by temperature alteration and cyclic AMP receptor protein and evaluation of its role in virulence. |
Q39449979 | Replication of Crohn's disease-associated AIEC within macrophages is dependent on TNF-α secretion |
Q41910749 | Requirement of siderophore biosynthesis for plant colonization by Salmonella enterica |
Q38649814 | Rescuing iron-overloaded macrophages by conservative relocation of the accumulated metal |
Q33931556 | Restricted cytosolic growth of Francisella tularensis subsp. tularensis by IFN-gamma activation of macrophages |
Q36457765 | Role of CTR4 in the Virulence of Cryptococcus neoformans |
Q39656348 | Role of Ferroportin in Macrophage-Mediated Immunity |
Q34529950 | Role of Iron Uptake Systems in Pseudomonas aeruginosa Virulence and Airway Infection |
Q37374730 | Role of ferroxidases in iron uptake and virulence of Cryptococcus neoformans. |
Q57038543 | Rule-based modelling of iron homeostasis in tuberculosis |
Q40322355 | SRE1 regulates iron-dependent and -independent pathways in the fungal pathogen Histoplasma capsulatum |
Q35133715 | Salmonella adhesion, invasion and cellular immune responses are differentially affected by iron concentrations in a combined in vitro gut fermentation-cell model |
Q47151615 | Scientific Opinion on the welfare of cattle kept for beef production and the welfare in intensive calf farming systems |
Q34721071 | Search for Bacillus anthracis potential vaccine candidates by a functional genomic-serologic screen |
Q36964999 | Selected vitamins and trace elements support immune function by strengthening epithelial barriers and cellular and humoral immune responses |
Q55196635 | Selection and validation of reference genes for gene expression studies in Klebsiella pneumoniae using Reverse Transcription Quantitative real-time PCR. |
Q37403137 | Selective modulation of TLR4-activated inflammatory responses by altered iron homeostasis in mice |
Q37571317 | Self-poisoning of Mycobacterium tuberculosis by interrupting siderophore recycling |
Q33658322 | Siderocalin inhibits the intracellular replication of Mycobacterium tuberculosis in macrophages |
Q24681774 | Siderophore-based iron acquisition and pathogen control |
Q58112659 | Siderophore-mediated iron acquisition enhances the resistance to oxidative and aromatic compound stress in JMP134 |
Q52668328 | Significance and In Vivo Detection of Iron-Laden Microglia in White Matter Multiple Sclerosis Lesions. |
Q30524145 | Single-cell elemental analysis of bacteria: quantitative analysis of polyphosphates in Mycobacterium tuberculosis |
Q36305784 | Slc11a1 limits intracellular growth of Salmonella enterica sv. Typhimurium by promoting macrophage immune effector functions and impairing bacterial iron acquisition. |
Q55425615 | Small RNA profiling in Mycobacterium tuberculosis identifies MrsI as necessary for an anticipatory iron sparing response. |
Q30152755 | Staphylococcus aureus Pore-Forming Toxins. |
Q36081594 | Staphylococcus aureus Targets the Duffy Antigen Receptor for Chemokines (DARC) to Lyse Erythrocytes |
Q33769082 | Staphylococcus aureus fur regulates the expression of virulence factors that contribute to the pathogenesis of pneumonia |
Q46352053 | Still ironing out the best way to diagnose infection |
Q61818068 | Stress-Tolerant Yeasts: Opportunistic Pathogenicity Versus Biocontrol Potential |
Q28493227 | Structural model of FeoB, the iron transporter from Pseudomonas aeruginosa, predicts a cysteine lined, GTP-gated pore |
Q78232480 | Structure and Biosynthesis of Fimsbactins A-F, Siderophores fromAcinetobacter baumanniiandAcinetobacter baylyi |
Q36926801 | Structure elucidation and biosynthesis of fuscachelins, peptide siderophores from the moderate thermophile Thermobifida fusca |
Q28314915 | Structure of the bacterial plant-ferredoxin receptor FusA |
Q35632820 | Superinfection in malaria: Plasmodium shows its iron will |
Q28505375 | Suppression of hepcidin expression and iron overload mediate Salmonella susceptibility in ankyrin 1 ENU-induced mutant |
Q36630395 | Symbiotic conversations are revealed under genetic interrogation |
Q36341699 | Synthesis and Pharmacokinetic Evaluation of Siderophore Biosynthesis Inhibitors for Mycobacterium tuberculosis |
Q53590391 | TCA cycle activity in Staphylococcus aureus is essential for iron-regulated synthesis of staphyloferrin A, but not staphyloferrin B: the benefit of a second citrate synthase. |
Q33877264 | Taming the elephant: Salmonella biology, pathogenesis, and prevention |
Q35110055 | Targeting Staphylococcus aureus quorum sensing with nonpeptidic small molecule inhibitors |
Q41895920 | Tea polyphenols inhibit the growth and virulence properties of Fusobacterium nucleatum |
Q89426992 | Terpyridine-Micelles for Inhibiting Bacterial Biofilm Development |
Q90256883 | The 'Checkmate' for Iron Between Human Host and Invading Bacteria: Chess Game Analogy |
Q37355882 | The 58-kilodalton major virulence factor of Francisella tularensis is required for efficient utilization of iron |
Q27443131 | The Bacillus subtilis iron-sparing response is mediated by a Fur-regulated small RNA and three small, basic proteins |
Q48232558 | The Biochemistry of Sensing: Enteric Pathogens Regulate Type III Secretion in Response to Environmental and Host Cues. |
Q92430838 | The Ferric Uptake Regulator Represses Type VI Secretion System Function by Binding Directly to the clpV Promoter in Salmonella enterica Serovar Typhimurium |
Q40161225 | The Fungal Pathogen Candida glabrata Does Not Depend on Surface Ferric Reductases for Iron Acquisition |
Q92404565 | The Hap Complex in Yeasts: Structure, Assembly Mode, and Gene Regulation |
Q37675429 | The Influence of Host Stress on the Mechanism of Infection: Lost Microbiomes, Emergent Pathobiomes, and the Role of Interkingdom Signaling |
Q35956497 | The PRE-Derived NMR Model of the 38.8-kDa Tri-Domain IsdH Protein from Staphylococcus aureus Suggests That It Adaptively Recognizes Human Hemoglobin |
Q38530500 | The Physiological, Biochemical, and Molecular Roles of Zinc Transporters in Zinc Homeostasis and Metabolism. |
Q88427265 | The Role of Iron Competition in the Antagonistic Action of the Rice Endophyte Streptomyces sporocinereus OsiSh-2 Against the Pathogen Magnaporthe oryzae |
Q89660213 | The Secretion of Toxins and Other Exoproteins of Cronobacter: Role in Virulence, Adaption, and Persistence |
Q34044097 | The Yersinia pestis siderophore, yersiniabactin, and the ZnuABC system both contribute to zinc acquisition and the development of lethal septicaemic plague in mice. |
Q33705201 | The Zur-regulated ZinT protein is an auxiliary component of the high-affinity ZnuABC zinc transporter that facilitates metal recruitment during severe zinc shortage |
Q40230010 | The bacteriostatic protein lipocalin 2 is induced in the central nervous system of mice with west Nile virus encephalitis |
Q36156332 | The bhuQ gene encodes a heme oxygenase that contributes to the ability of Brucella abortus 2308 to use heme as an iron source and is regulated by Irr. |
Q46661263 | The effect of ferrous-chelating hairtail peptides on iron deficiency and intestinal flora in rats. |
Q36243198 | The extracellular proteome of two Bifidobacterium species reveals different adaptation strategies to low iron conditions |
Q37264858 | The ferric enterobactin transporter Fep is required for persistent Salmonella enterica serovar typhimurium infection |
Q33759901 | The heme sensing response regulator HssR in Staphylococcus aureus but not the homologous RR23 in Listeria monocytogenes modulates susceptibility to the antimicrobial peptide plectasin |
Q39718796 | The homeostasis of iron, copper, and zinc in paracoccidioides brasiliensis, cryptococcus neoformans var. Grubii, and cryptococcus gattii: a comparative analysis |
Q36861745 | The human microbiome and surgical disease |
Q30620192 | The immediate global responses of Aliivibrio salmonicida to iron limitations |
Q35915815 | The influence of human respiratory epithelia on Pseudomonas aeruginosa gene expression |
Q21184175 | The interferon-inducible p47 (IRG) GTPases in vertebrates: loss of the cell autonomous resistance mechanism in the human lineage |
Q35960985 | The iron chelator deferasirox protects mice from mucormycosis through iron starvation |
Q36540444 | The iron stimulon of Xylella fastidiosa includes genes for type IV pilus and colicin V-like bacteriocins |
Q38037549 | The iron-regulated staphylococcal lipoproteins. |
Q36380342 | The mouse Char10 locus regulates severity of pyruvate kinase deficiency and susceptibility to malaria |
Q29346567 | The novel transcriptional regulator SczA mediates protection against Zn2+ stress by activation of the Zn2+-resistance gene czcD in Streptococcus pneumoniae |
Q36954970 | The potential of desferrioxamine-gallium as an anti-Pseudomonas therapeutic agent. |
Q30413938 | The reduced genome of the Francisella tularensis live vaccine strain (LVS) encodes two iron acquisition systems essential for optimal growth and virulence |
Q38813702 | The risk of infections in patients with myelodysplastic syndromes in 2016. |
Q34134604 | The role of MglA for adaptation to oxidative stress of Francisella tularensis LVS. |
Q37342083 | The role of iron in patients after bone marrow transplantation |
Q34155194 | The role of iron in the immune response to bacterial infection |
Q33612952 | The role of iron uptake in pathogenicity and symbiosis in Photorhabdus luminescens TT01. |
Q34773337 | The role of the RNA chaperone Hfq in Haemophilus influenzae pathogenesis |
Q27664200 | The role of vicinal tyrosine residues in the function of Haemophilus influenzae ferric-binding protein A |
Q27003448 | The role of zinc in the interplay between pathogenic streptococci and their hosts |
Q28729993 | The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food |
Q52601066 | The siderophore biosynthetic gene SID1, but not the ferroxidase gene FET3, is required for full Fusarium graminearum virulence. |
Q28486666 | The structure of MbtI from Mycobacterium tuberculosis, the first enzyme in the biosynthesis of the siderophore mycobactin, reveals it to be a salicylate synthase |
Q40087615 | The timing of TNF and IFN-gamma signaling affects macrophage activation strategies during Mycobacterium tuberculosis infection |
Q26782915 | The trans-kingdom identification of negative regulators of pathogen hypervirulence |
Q33826085 | The yersiniabactin transport system is critical for the pathogenesis of bubonic and pneumonic plague |
Q33662164 | Toward a better understanding of the mechanisms of symbiosis: a comprehensive proteome map of a nascent insect symbiont |
Q41983453 | Transcriptional profile of Salmonella enterica subsp. enterica serovar Weltevreden during alfalfa sprout colonization |
Q92722885 | Transcriptome profile of Corynebacterium pseudotuberculosis in response to iron limitation |
Q33883214 | Transferrin iron starvation therapy for lethal bacterial and fungal infections |
Q46315141 | Transferrin polymorphism and opportunistic infections in HIV-infected women in Rwanda |
Q28084708 | Transferrin-mediated iron sequestration as a novel therapy for bacterial and fungal infections |
Q34171727 | Transfusion related morbidity in premature babies: Possible mechanisms and implications for practice |
Q45382997 | Transfusion-related biologic effects and free hemoglobin, heme, and iron |
Q36228684 | Trichomoniasis and lactoferrin: future prospects. |
Q57808855 | Tuning the Anti(myco)bacterial Activity of 3-Hydroxy-4-pyridinone Chelators through Fluorophores |
Q34136411 | Ubiquitination of lysine-331 by Kaposi's sarcoma-associated herpesvirus protein K5 targets HFE for lysosomal degradation |
Q34471871 | Undernutrition, the acute phase response to infection, and its effects on micronutrient status indicators |
Q36156270 | Unraveling the secret lives of bacteria: use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression |
Q64123510 | Uropathogenic employs both evasion and resistance to subvert innate immune-mediated zinc toxicity for dissemination |
Q38972894 | Vascular Pythiosis of the Lower Extremity in Northern Thailand: Ten Years' Experience |
Q37191011 | Viral infection and iron metabolism |
Q27348812 | Vitamin B2 as a virulence factor in Pseudogymnoascus destructans skin infection |
Q37852592 | War-Fe-re: iron at the core of fungal virulence and host immunity |
Q31156691 | Whole genome identification of Mycobacterium tuberculosis vaccine candidates by comprehensive data mining and bioinformatic analyses |
Q41920025 | Whole genome sequencing for the molecular characterization of carbapenem-resistant Klebsiella pneumoniae strains isolated at the Italian ASST Fatebenefratelli Sacco Hospital, 2012-2014. |
Q28611054 | Why Do We Feel Sick When Infected--Can Altruism Play a Role? |
Q50061386 | Withholding iron as a cellular defence mechanism--friend or foe? |
Q33511951 | Wolbachia interferes with ferritin expression and iron metabolism in insects |
Q59666097 | Xanthoferrin, the α -hydroxycarboxylate-type siderophore of Xanthomonas campestris pv. campestris , is required for optimum virulence and growth inside cabbage |
Q93102961 | You'd Better Zinc-Trace Element Homeostasis in Infection and Inflammation |
Q27972591 | ZIPCO, a putative metal ion transporter, is crucial for Plasmodium liver-stage development |
Q33386007 | the hyphal-associated adhesin and invasin Als3 of Candida albicans mediates iron acquisition from host ferritin |
Q39633551 | β 1-4 mannobiose enhances Salmonella-killing activity and activates innate immune responses in chicken macrophages |
Search more.