review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Weinberg ED | |
P2860 | cites work | Factors affecting the susceptibility of staphylococci to killing by the cationic proteins from rabbit polymorphonuclear leucocytes: the effects of alteration of cellular energetics and of various iron compounds | Q28335409 |
Attachment of gonococci to sperm. Influence of physical and chemical factors | Q33655071 | ||
Recurrent genital candidosis and iron metabolism | Q33655491 | ||
Fever and survival | Q33930286 | ||
Ferritin in serum. Clinical and biochemical implications | Q33977973 | ||
Nutritional factors in anaemia | Q34007225 | ||
An other look at iron: Role in host pathogen interaction | Q34065042 | ||
Fate of human lactoferrin and myeloperoxidase in phagocytizing human neutrophils: effects of immunoglobulin G subclasses and immune complexes coated on latex beads | Q34128545 | ||
Pathogenesis and immunology of experimental gonococcal infection: role of iron in virulence | Q34132295 | ||
Changes in lactoferrin, immunoglobulin G, bovine serum albumin, and alpha-lactalbumin during acute experimental and natural coliform mastitis in cows | Q34388335 | ||
Detection and differentiation of iron-responsive avirulent mutants on Congo red agar | Q34416025 | ||
Bacteriostatic effect of human milk and bovine colostrum on Escherichia coli: importance of bicarbonate | Q34424548 | ||
Virulence and the role of iron in Pseudomonas aeruginosa infection | Q34500029 | ||
Mycobactins: iron-chelating growth factors from mycobacteria | Q34661736 | ||
Intramuscular iron-dextran and susceptibility of neonates to bacterial infections. In vitro studies | Q34985931 | ||
Letter: Administration of parenteral iron to newborn infants | Q34988978 | ||
Haemoglobin Levels in Normal Infants Aged 3 to 24 Months, and the Effect of Iron | Q35149588 | ||
Reduced bactericidal capacity of polymorphs in iron deficiency | Q35150873 | ||
Iron status of preterm low birthweight infants and their response to oral iron | Q35151340 | ||
Necrotizing enterocolitis in low-birth-weight infants fed an elemental formula | Q47346262 | ||
Elevated serum iron, low unbound transferrin and candidiasis in acute leukemia | Q47680302 | ||
Inhibition of bacteria by lactoferrin and other iron-chelating agents | Q47689750 | ||
Factors influencing host resistance to Salmonella infections: the effects of hemolysis and erythrophagocytosis | Q47723423 | ||
Shock in Bantu Siderosis | Q47756318 | ||
Suppression of infection by famine and its activation by refeeding--a paradox? | Q47843257 | ||
Lactoferrin-an iron binding protein in synovial fluid | Q47964895 | ||
Altered absorption and regulation of iron in chicks with acute Salmonella gallinarum infection | Q50225549 | ||
Enhancement of survival in acute experimental fowl typhoid in chicks by the administration of iron dextran | Q50225797 | ||
Enterobacterial chelators of iron: their occurrence, detection, and relation to pathogenicity | Q50228508 | ||
Stimulation of antimicrobial activity in the rat with leukocytic endogenous mediator | Q50229451 | ||
Nutritional Iron Deficiency as a Determinant of Host Resistance in the Rat | Q50232696 | ||
Symptoms, septicemia and death in salmonellosis | Q50242896 | ||
Salmonellosis complicating neoplastic diseases | Q50243091 | ||
HODGKIN'S DISEASE AND SALMONELLA TYPHIMURIUM INFECTION | Q50267406 | ||
Salmonellosis complication in human bartonellosis. | Q50508442 | ||
A conspectus of research on iron requirements of man | Q50930394 | ||
Blue-green algae: their excretion of iron-selective chelators enables them to dominate other algae | Q50957168 | ||
Lactoferrin and transferrin: a comparative study. | Q53754828 | ||
Serum transferrin, serum iron and total iron binding capacity: the role of transferrin in nonspecific immune defence. | Q53758092 | ||
The incidence of urinary infection in 5000 pregnant women. | Q53765096 | ||
Defect of cell-mediated immunity in patients with iron-deficiency anaemia. | Q54029447 | ||
Upper respiratory tract infections in relation to iron medication in healthy students. | Q54515307 | ||
Inhibition of Escherichia coli by bovine colostrum and post-colostral milk. II. The bacteriostatic effect of lactoferrin on a serum susceptible and serum resistant strain of E. coli | Q54631361 | ||
The role of iron in nonspecific resistance to infection induced by endotoxin. | Q54641660 | ||
Cell-mediated immunity in iron- and vitamin-deficient children | Q55423460 | ||
Iron-deficiency anaemia and immunological responses | Q66706075 | ||
Mouth Lesions in Iron-Deficient Anemia: Relationship to Candida albicans in Saliva and to Impairment of Lymphocyte Transformation | Q66891660 | ||
In vitro competition between ferrichrome and phage for the outer membrane T5 receptor complex of Escherichia coli | Q66897646 | ||
Increased incidence of gram-negative neonatal sepsis with intramuscula iron administration | Q67055768 | ||
Sensitivity of the immunological response to the nutritional status of rats | Q67293507 | ||
THE ANEMIA OF INFECTION. I. HYPOFERREMIA, HYPERCUPREMIA, AND ALTERATIONS IN PORPHYRIN METABOLISM IN PATIENTS. | Q35164674 | ||
THE COPPER AND NON-HEMOGLOBINOUS IRON CONTENTS OF THE BLOOD SERUM IN DISEASE | Q35173171 | ||
Stimulatory effect of dihydroxyphenyl compounds on the aerotolerance of Spirillum volutans and Campylobacter fetus subspecies jejuni | Q35219360 | ||
Iron: metabolism, biochemistry, and clinical pathological physiology; review of recent literature | Q35265040 | ||
VIRULENCE OF PASTEURELLA PESTIS AND IMMUNITY TO PLAGUE. | Q35522212 | ||
The mutual effects of antimicrobial compounds and metallic cations | Q35660463 | ||
INTAKES AND EXCRETIONS OF IRON, COPPER, AND ZINC IN THE NEONATAL PERIOD | Q36060688 | ||
The action of iron on local Klebsiella infection of the skin of the guinea-pig and its relation to the decisive period in primary infective lesions | Q36090573 | ||
The effect of parenteral iron preparations on experimental pyelonephritis | Q36129584 | ||
Inactivation of bacterial exotoxins and endotoxin by iron. In vitro studies | Q36264753 | ||
Coordinate regulation by iron of the synthesis of phenolate compounds and three outer membrane proteins in Escherichia coli | Q36602843 | ||
Relationship between the tonB locus and iron transport in Escherichia coli | Q36608372 | ||
The effect of passage and iron on the virulence of Pseudomonas aeruginosa | Q36633922 | ||
Iron and Immunocompetence | Q36930040 | ||
Roles of metallic ions in host-parasite interactions | Q37195362 | ||
Mechanisms of Pathogenesis in Listeria monocytogenes Infection I. Influence of Iron | Q37389375 | ||
UTILIZATION OF EXTERNAL GROWTH FACTORS BY INTRACELLULAR MICROBES: MYCOBACTERIUM PARATUBERCULOSIS AND WOOD PIGEON MYCOBACTERIA. | Q37417100 | ||
Infections in iron deficiency and other types of anaemia in the tropics | Q39221750 | ||
Refeeding-malaria and hyperferraemia | Q39283311 | ||
Sequential changes in the concentration of specific serum proteins during typhoid fever infection in man. | Q39381113 | ||
Anaemia and immune response | Q39382761 | ||
Starvation suppression and refeeding activation of infection. An ecological necessity? | Q39418696 | ||
Somali food shelters in the Ogaden famine and their impact on health | Q39467190 | ||
Lactoferrin as a factor of resistance to infection of the bovine mammary gland | Q39624657 | ||
Human Milk and Colostrum Proteins: A Review | Q39640910 | ||
Fuctional organization of the outer membrane of escherichia coli: Phage and colicin receptors as components of iron uptake systems | Q39792782 | ||
Uptake of ferrienterochelin by Escherichia coli: energy dependent stage of uptake | Q39811779 | ||
Virulence-Associated Acquisition of Iron in Mammalian Serum by Escherichia coli | Q39811965 | ||
Sexuality and physical disabilities. The physician's role | Q39818975 | ||
Immunology of malarial infection and its possible consequences | Q39868052 | ||
The role of iron in bacterial infections, with special consideration of host-tubercle bacillus interaction | Q39879284 | ||
Salmonellosis in patients with neoplastic disease. A review of 100 episodes at Memorial Cancer Center over a 13-year period | Q39894190 | ||
Iron absorption | Q39928450 | ||
Iron and susceptibility to infectious disease | Q39940354 | ||
Haemorrhagic manifestations of influenza A infection in children | Q39944047 | ||
Structure and function of transferrins. II. Transferrin and iron metabolism | Q39945248 | ||
The effect of iron and haematin on the killing of staphylococci by rabbit polymorphs | Q39948153 | ||
Demographic and prognostic characteristics of bacteriuria in pregnancy | Q39966781 | ||
The Microbiology of the Hen's Egg | Q39991294 | ||
Bacterial infection and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literature | Q40004574 | ||
Roles of Iron in Host-Parasite Interactions | Q40006180 | ||
Neutrophilic granulocytes in acute bacterial infection. Sequential studies on lysozyme, myeloperoxidase and lactoferrin | Q40038441 | ||
Influence of metal ions on the formation of mycobactin and salicylic acid in Mycobacterium smegmatis grown in static culture | Q40096861 | ||
Influence of Temperature on the Biosynthesis of Iron Transport Compounds by Salmonella typhimurium | Q40098585 | ||
Influence of Temperature on the Iron Metabolism of a Fluorescent Pseudomonad | Q40104517 | ||
The virulence-enhancing effect of iron on nonpigmented mutants of virulent strains of Pasteurella pestis. | Q40294207 | ||
Trace element in infectious processes | Q40526642 | ||
Effects of iron chelators and iron overload on Salmonella infection | Q40767634 | ||
Increased resistance of iron-deficient mice to salmonella infection | Q40810275 | ||
Control of salmonellosis pacifarin biosynthesis by iron | Q40880084 | ||
Detection of a leukocytic endogenous mediator-like mediator of serum amino acid and zinc depression during various infectious illnesses | Q40880560 | ||
Effect of iron on leukocyte function: inactivation of H2O2 BY IRON | Q40881234 | ||
In vitro growth inhibition of mastitis-causing coliform bacteria by bovine apo-lactoferrin and reversal of inhibition by citrate and high concentrations of apo-lactoferin | Q40882062 | ||
Survival value of fever in fish | Q40882694 | ||
Iron absorption and pyrexia | Q40926872 | ||
The Effects of Francisella Tularensis Infection on Iron Metabolism in Man | Q40939237 | ||
INFECTIOUS HEPATITIS COMPLICATED BY SECONDARY INVASION WITH SALMONELLA. | Q40975752 | ||
THE ANEMIA OF INFECTION. V. FATE OF INJECTED RADIOACTIVE IRON IN THE PRESENCE OF INFLAMMATION. | Q40976371 | ||
Generalized Yersinia enterocolitica Infection | Q41550309 | ||
Isolation of Yersinia Pseudotuberculosis Serotype V from The Blood of a Patient with Sickle-Cell Anaemia | Q41551586 | ||
Double effects of an iron drug in induction of mouse plague caused by an attenuated strain | Q41551597 | ||
Pasteurella pestis: Role of Pesticin I and Iron in Experimental Plague | Q41562748 | ||
Citrate in milk: a harbinger of lactogenesis | Q42019067 | ||
The involvement of lactoferrin in the hyposideremia of acute inflammation | Q42091283 | ||
Effect of gestational age and intrauterine nutrition on plasma transferrin and iron in the newborn | Q42130501 | ||
Impaired immunocompetence associated with iron deficiency | Q44020881 | ||
Bacteriuria and Hemoglobin Levels in Pregnancy | Q44221456 | ||
Chelate mediated transfer of iron from transferrin to desferrioxamine | Q44413994 | ||
Transferrin, iron, and dermatophytes. I. Serum dematophyte inhibitory component definitively identified as unsaturated transferrin | Q44525334 | ||
Incidence of anemia in full-term infants seen in private practice | Q44562065 | ||
Iron absorption from human milk, simulated human milk, and proprietary formulas | Q44690112 | ||
Structure and function of transferrins. I. Physical, chemical, and iron-binding properties | Q44764967 | ||
Antimicrobial factors in human milk | Q44796093 | ||
Salmonella osteomyelitis and abnormal hemoglobin disease | Q44942653 | ||
Comparison of leukocytic pyrogen and leukocytic endogenous mediator | Q45030676 | ||
INFECTIOUS SYNDROMES OF LEUKEMIAS AND LYMPHOMAS. | Q45228284 | ||
Effect of Acute Infection and Endotoxemia on Zinc Absorption in the Rat | Q45260154 | ||
Depressed cell-mediated immunity in megaloblastic anemia due to folic acid deficiency | Q46140895 | ||
Hematologic Changes in Chronic Arthritis of Mice Induced by Mycoplasma arthritidis | Q67359788 | ||
Tuberculosis After Jejunoileal Bypass for Obesity | Q67430292 | ||
Lactoferrin Concentration During Involution of the Bovine Mammary Gland | Q67435678 | ||
Ferric iron and the antibacterial effects of horse 7S antibodies to Escherichia coli O111 | Q67518242 | ||
Iron as a replacement for mucin in the establishment of meningococcal infection in mice | Q67522324 | ||
Copper, iron, and zinc contents of mature human milk | Q67766856 | ||
Effect of leukocytic endogenous mediator (LEM) on zinc absorption in the rat | Q67819579 | ||
Depressed phagocytic function exhibited by polymorphonuclear leucocytes from chronically iron deficient rabbits | Q67829848 | ||
The abolition of the protective effect of Clostridium welchii type A antiserum by ferric iron | Q68564632 | ||
Storage iron kinetics. VI. The effect of inflammation on iron exchange in the rat | Q68795891 | ||
The Relationship of Bottle Feeding to Malnutrition and Gastroenteritis in a Pre-Industrial Setting | Q68977467 | ||
Iron-binding Proteins in Milk and Resistance to Escherichia coli Infection in Infants | Q69154757 | ||
The effect of Escherichia coli endotoxin on the plasma iron concentration in the domestic fowl | Q69360454 | ||
Amounts of Lactoferrin in Human Colostrum and Milk | Q69380371 | ||
Growth of Bacteriain Vitroin Blood from Patients with Severe Iron Deficiency Anemia and from Patients with Sickle Cell Anemia | Q69515469 | ||
Nutrition and infection | Q69939722 | ||
The anaemia of chronic disorders | Q69940495 | ||
Listeriosis complicating malignant disease. A new association | Q69995421 | ||
Cell-mediated immunity and phagocytosis and killing function in children with severe iron-deficiency anaemia | Q70032567 | ||
Serum protein alterations induced by Listeria monocytogenes infections | Q70067088 | ||
Iron metabolism by reticuloendothelial cells in vitro. Physical and chemical conditions, lipotrope deficiency, and acute inflammation | Q70118520 | ||
Infection and iron overload in thalassemia | Q70121275 | ||
Immunoglobulins, transferrin, caeruloplasmin and heterophile antibodies in kwashiorkor | Q70131676 | ||
Transferrin andStaphylococcus aureusin Kwashiorkor | Q70372121 | ||
Normal incorporation of oral iron into intestinal ferritin in inflammation | Q70448960 | ||
Pasteurella pseudotuberculosis. Acute sepsis with survival | Q70580219 | ||
Serum iron as a differential diagnostic aid in acute leukemia in children | Q70988847 | ||
Septicemia With Pasteurella pseudotuberculosis and Liver Disease | Q71797632 | ||
Plasma Hemoglobin and Hemoglobin Fractions in Sickle Cell Crisis | Q71816848 | ||
Hazard of Overwhelming Infection after Splenectomy in Childhood | Q72218645 | ||
Effect of endotoxin on iron absorption | Q72227381 | ||
Utilization of dietary iron by term infants. A study of 1,048 infants from a low socioeconomic population | Q72751685 | ||
On serum iron levels in different blood diseases; their importance for differential diagnosis | Q73172346 | ||
The serum iron in experimental hepatocellular necrosis | Q73498597 | ||
The behavior of serum iron in acute hepatitis | Q78513364 | ||
[The A2 influenza pandemia of 1957. Its characteristics and its development in France.] | Q78810816 | ||
Albumin and transferrin metabolism in infectious and toxic diseases | Q78936505 | ||
Irreversible shock in haemochromatosis | Q78939635 | ||
Relation of transferrin to serum bacteriostatic activity in agammaglobulinemic and other patients | Q79004228 | ||
Salmonellosis--a review of some unusual aspects | Q79162645 | ||
Urinary infection and anaemia in pregnancy | Q79396401 | ||
Hematologic manifestations of malignant disease | Q79452918 | ||
RAW HEN EGG WHITE AND THE ROLE OF IRON IN GROWTH INHIBITION OF SHIGELLA DYSENTERIAE, STAPHYLOCOCCUS AUREUS, ESCHERICHIA COLI AND SACCHAROMYCES CEREVISIAE | Q81034347 | ||
Immunity, transferrin, and survival in kwashiorkor | Q93670501 | ||
Effect of Iron on the Bactericidal Proteins from Rabbit Polymorphonuclear Leucocytes | Q93804792 | ||
P433 | issue | 1 | |
P921 | main subject | iron | Q677 |
P304 | page(s) | 45-66 | |
P577 | publication date | 1978-03-01 | |
P1433 | published in | Microbiological Reviews | Q26842868 |
P1476 | title | Iron and infection | |
P478 | volume | 42 |
Q40167769 | A cluster of five genes specifying the aerobactin iron uptake system of plasmid ColV-K30 |
Q35546248 | A mutant form of the Neisseria gonorrhoeae pilus secretin protein PilQ allows increased entry of heme and antimicrobial compounds |
Q41875120 | A new model for studying nutrition in peritonitis. The adverse effect of overfeeding |
Q36996292 | A pleiotropic iron-uptake mutant of Neisseria meningitidis lacks a 70-kilodalton iron-regulated protein |
Q40267636 | A siderophore production mutant of Bordetella bronchiseptica cannot use lactoferrin as an iron source |
Q71193322 | A simple and inexpensive method for the identification of Staphylococcus epidermidis and Staphylococcus hominis |
Q36437515 | Ability of Neisseria gonorrhoeae, Neisseria meningitidis, and commensal Neisseria species to obtain iron from lactoferrin |
Q34524626 | Ability of Pseudomonas pseudomallei malleobactin to acquire transferrin-bound, lactoferrin-bound, and cell-derived iron |
Q39975593 | Absence of siderophore activity in Legionella species grown in iron-deficient media |
Q36338685 | Accumulation of iron by yersiniae |
Q36332989 | Acquisition of iron by Aeromonas salmonicida |
Q39514424 | Actinobacillus pleuropneumoniae iron transport: a set of exbBD genes is transcriptionally linked to the tbpB gene and required for utilization of transferrin-bound iron |
Q36955039 | Activity and specificity of a mouse monoclonal antibody to ferric aerobactin |
Q40600057 | Acute iron overload in mice: pathogenesis of Salmonella typhimurium infection |
Q37038245 | Aerobactin iron transport genes commonly encoded by certain ColV plasmids occur in the chromosome of a human invasive strain of Escherichia coli K1 |
Q33603028 | Aerobactin mediates virulence and accounts for increased siderophore production under iron-limiting conditions by hypervirulent (hypermucoviscous) Klebsiella pneumoniae |
Q35833755 | Aerobactin, but not yersiniabactin, salmochelin, or enterobactin, enables the growth/survival of hypervirulent (hypermucoviscous) Klebsiella pneumoniae ex vivo and in vivo |
Q40598806 | Amelioration by muramyl dipeptide of the effect of induced hyperferremia upon Klebsiella infection in mice |
Q37908016 | Anaemia in rheumatoid arthritis: pathogenesis, diagnosis and treatment |
Q33700341 | Analysis of a DtxR-regulated iron transport and siderophore biosynthesis gene cluster in Corynebacterium diphtheriae |
Q33736702 | Analysis of the exochelin locus in Mycobacterium smegmatis: biosynthesis genes have homology with genes of the peptide synthetase family |
Q37063033 | Analysis of theCorynebacterium diphtheriaeDtxR Regulon: Identification of a Putative Siderophore Synthesis and Transport System That Is Similar to theYersiniaHigh-Pathogenicity Island-Encoded Yersiniabactin Synthesis and Uptake System |
Q33215950 | Anemia as a risk factor for infectious diseases in infants and toddlers: results from a prospective study |
Q35695655 | Antibacterial effect of bovine lactoferrin against udder pathogens |
Q33731080 | Antibacterial effect of scandium and indium complexes of enterochelin on Klebsiella pneumoniae |
Q33973443 | Antifungal effects of lysozyme and lactoferrin against genetically similar, sequential Candida albicans isolates from a human immunodeficiency virus-infected southern Chinese cohort |
Q34007901 | Antigenic and sequence diversity in gonococcal transferrin-binding protein A. |
Q36446919 | Assmilation of iron by pathogenic Neisseria spp. |
Q40168770 | Association of hydroxamate siderophore (aerobactin) with Escherichia coli isolated from patients with bacteremia. |
Q35182319 | Bacterial transferrin receptors ? structure, function and contribution to virulence |
Q39832623 | Bactericidal activity of M14659 enhanced in low-iron environments |
Q36437142 | Bactericidal activity of human lactoferrin: differentiation from the stasis of iron deprivation. |
Q36447191 | Bactericidal activity of human lactoferrin: influence of physical conditions and metabolic state of the target microorganism. |
Q33904131 | Bactericidal activity of human lactoferrin: sensitivity of a variety of microorganisms |
Q36361714 | Bacteriocin-resistant mutants of Erwinia chrysanthemi: possible involvement of iron acquisition in phytopathogenicity |
Q35767237 | Bacteriostatic and fungostatic action of catecholamide iron chelators |
Q33898871 | Bacteriostatic effect of serum: role of antibody to lipopolysaccharide. |
Q33899127 | Bacteriostatic enterochelin-specific immunoglobulin from normal human serum. |
Q34132423 | BhuR, a virulence-associated outer membrane protein of Bordetella avium, is required for the acquisition of iron from heme and hemoproteins |
Q35060371 | Bifidobacteria strains isolated from stools of iron deficient infants can efficiently sequester iron |
Q35603469 | Binding and surface exposure characteristics of the gonococcal transferrin receptor are dependent on both transferrin-binding proteins |
Q42845552 | Biosynthetic analysis of the petrobactin siderophore pathway from Bacillus anthracis. |
Q30317484 | Biotrophy-specific downregulation of siderophore biosynthesis in Colletotrichum graminicola is required for modulation of immune responses of maize |
Q27648724 | Bis-methionyl Coordination in the Crystal Structure of the Heme-binding Domain of the Streptococcal Cell Surface Protein Shp |
Q35577089 | Bordetella pertussis fur gene restores iron repressibility of siderophore and protein expression to deregulated Bordetella bronchiseptica mutants |
Q36264826 | Buried Treasure: Evolutionary Perspectives on Microbial Iron Piracy. |
Q34188778 | Candida albicans heme oxygenase and its product CO contribute to pathogenesis of candidemia and alter systemic chemokine and cytokine expression |
Q39465835 | Candida species exhibit differential in vitro hemolytic activities. |
Q34009982 | Cell wall and secreted proteins of Candida albicans: identification, function, and expression |
Q40176923 | Ceruloplasmin and regulation of transferrin iron during Neisseria meningitidis infection in mice |
Q41510502 | Characterization of a hemin-storage locus of Yersinia pestis |
Q35627475 | Characterization of a periplasmic protein involved in iron utilization of Actinobacillus actinomycetemcomitans |
Q35428005 | Characterization of lbpA, the structural gene for a lactoferrin receptor in Neisseria gonorrhoeae. |
Q39930060 | Characterization of the Vibrio anguillarum fur gene: role in regulation of expression of the FatA outer membrane protein and catechols. |
Q90228042 | Characterization of the hemolytic activity of Riemerella anatipestifer |
Q35416535 | Characterization of the hgbA locus encoding a hemoglobin receptor from Haemophilus ducreyi |
Q35441392 | Characterization of transferrin binding proteins 1 and 2 in invasive type b and nontypeable strains of Haemophilus influenzae. |
Q31116093 | Cloning and expression of a transferrin-binding protein from Actinobacillus pleuropneumoniae |
Q30991914 | Cloning and expression of two novel hemin binding protein genes from Treponema denticola |
Q36412569 | Cloning of the aerobactin-mediated iron assimilation system of plasmid ColV |
Q35582900 | Cloning, sequencing, and characterization of the gene encoding FrpB, a major iron-regulated, outer membrane protein of Neisseria gonorrhoeae |
Q36426029 | ColV plasmid-specific aerobactin synthesis by invasive strains of Escherichia coli |
Q58549317 | Cold plasma effect on the proteome of Pseudomonas aeruginosa - Role for bacterioferritin |
Q35276257 | Comparative Study of Esterase and Hemolytic Activities in Clinically Important Candida Species, Isolated From Oral Cavity of Diabetic and Non-diabetic Individuals. |
Q40109707 | Comparative genomic analysis and characterization of incompatibility group FIB plasmid encoded virulence factors of Salmonella enterica isolated from food sources |
Q35100342 | Comparison of the abilities of different protein sources of iron to enhance Neisseria meningitidis infection in mice |
Q39512685 | Construction and characterization of Moraxella catarrhalis mutants defective in expression of transferrin receptors |
Q39502627 | Construction and consequences of directed mutations affecting the hemin receptor in pathogenic Corynebacterium species |
Q28492457 | Cooperation between LepA and PlcH contributes to the in vivo virulence and growth of Pseudomonas aeruginosa in mice |
Q40146378 | Degradation of native human hemoglobin following hemolysis by Prevotella loescheii |
Q49229396 | Determination of heme in microorganisms using HPLC-MS/MS and cobalt(III) protoporphyrin IX inhibition of heme acquisition in Escherichia coli |
Q93167136 | Development and Validation of a Bordetella pertussis Whole-Genome Screening Strategy |
Q47343822 | Dietary and prophylactic iron supplements : Helpful or harmful? |
Q60906250 | Differential inhibition of the MLR by iron: Association with HLA phenotype |
Q34100157 | Disseminated Gonococcal Infection in Mice |
Q39919241 | Effect of Iron Limitation on "Pseudomonas plantarii" Growth and Tropolone and Protein Production |
Q68885753 | Effect of elevated temperatures and low levels of trace metals on the growth and phenotypic development of Candida albicans |
Q36298900 | Effect of growth temperature on the acquisition of iron by Salmonella typhimurium and Escherichia coli |
Q37051835 | Effect of inclusion of key foods on in vitro iron bioaccessibility in composite meals |
Q79277693 | Effect of infusing lactoferrin hydrolysate into bovine mammary glands with subclinical mastitis |
Q54620568 | Effect of iron and phagocytosis on murine macrophage activation in vitro. |
Q36384898 | Effect of iron limitation on growth, siderophore production, and expression of outer membrane proteins of Vibrio cholerae |
Q37098687 | Effect of iron on antibacterial immunity in vaccinated mice |
Q73952651 | Effect of iron on fluconazole activity against Candida albicans in presence of human serum or monocyte-derived macrophages |
Q54796798 | Effect of iron on neonatal gut flora during the first three months of life. |
Q53727157 | Effect of iron on neonatal gut flora during the first week of life. |
Q39305261 | Effect of iron on surface charge and hydrophobicity of Neisseria gonorrhoeae |
Q36438691 | Effect of pyochelin on the virulence of Pseudomonas aeruginosa |
Q36446999 | Effect of siderophores on virulence of Neisseria gonorrhoeae |
Q39833796 | Effect of subinhibitory concentrations of cephalosporins on surface properties and siderophore production in iron-depleted Klebsiella pneumoniae |
Q49011103 | Effects of iron and desferrioxamine on Rhizopus infection |
Q37037046 | Effects of iron and desferrioxamine on infections with Yersinia enterocolitica |
Q46827516 | Effects of repetitive immunogen injections and fasting versus feeding on iron, zinc, and copper metabolism in chicks |
Q37022650 | Effects of serum carrier proteins on the growth of pathogenic neisseriae with heme-bound iron |
Q30451232 | Elimination of the vitamin B12 uptake or synthesis pathway does not diminish the virulence of Escherichia coli K1 or Salmonella typhimurium in three model systems |
Q40614078 | Energy-independent uptake of iron from citrate by isolated outer membranes of Neisseria meningitidis |
Q39816719 | Enhanced activity of combination of tobramycin and piperacillin for eradication of sessile biofilm cells of Pseudomonas aeruginosa |
Q36428801 | Enhancement of Neisseria meningitidis infection in mice by addition of iron bound to transferrin |
Q37038138 | Enhancement of Vibrio parahaemolyticus virulence by lysed erythrocyte factor and iron. |
Q35760208 | Enhancement of copper toxicity by siderophores in Bacillus megaterium |
Q34718907 | Enhancement of in vitro growth of pathogenic bacteria by norepinephrine: importance of inoculum density and role of transferrin |
Q34082056 | Enterochelin (enterobactin): virulence factor for Salmonella typhimurium |
Q36137987 | Erythrocytic Iron Deficiency Enhances Susceptibility to Plasmodium chabaudi Infection in Mice Carrying a Missense Mutation in Transferrin Receptor 1 |
Q35754096 | Establishment of aging biofilms: possible mechanism of bacterial resistance to antimicrobial therapy |
Q34033214 | Evaluation of recombinant lipidated P2086 protein as a vaccine candidate for group B Neisseria meningitidis in a murine nasal challenge model |
Q70077279 | Experimental candidiasis in iron overload |
Q34009866 | Expression analysis of the yersiniabactin receptor gene fyuA and the heme receptor hemR of Yersinia enterocolitica in vitro and in vivo using the reporter genes for green fluorescent protein and luciferase |
Q35103809 | Expression of Neisseria meningitidis iron-regulated outer membrane proteins, including a 70-kilodalton transferrin receptor, and their potential for use as vaccines |
Q40613402 | Expression of a high-affinity mechanism for acquisition of transferrin iron by Neisseria meningitidis. |
Q36637747 | Factors promoting acute and chronic diseases caused by yersiniae |
Q39698276 | Failure of iron to promote attachment of gonococci to human spermatozoa under physiological conditions |
Q89820544 | FeGenie: A Comprehensive Tool for the Identification of Iron Genes and Iron Gene Neighborhoods in Genome and Metagenome Assemblies |
Q35534700 | Ferric iron reduction by Cryptococcus neoformans |
Q33761365 | Ferrous iron uptake in Cryptococcus neoformans |
Q33645325 | Frequency evaluation of genes encoding siderophores and the effects of different concentrations of Fe ions on growth rate of uropathogenic Escherichia coli |
Q37106105 | Fungistatic mechanism of human transferrin for Rhizopus oryzae and Trichophyton mentagrophytes: alternative to simple iron deprivation |
Q33900474 | Fur activates the expression of Salmonella enterica pathogenicity island 1 by directly interacting with the hilD operator in vivo and in vitro |
Q36200981 | Genetic analysis of the iron uptake region of the Vibrio anguillarum plasmid pJM1: molecular cloning of genetic determinants encoding a novel trans activator of siderophore biosynthesis |
Q70499185 | Genetic and biochemical characterization of the aerobactin synthesis operon on pColV |
Q37077411 | Genetic and biochemical evidence for a siderophore-dependent iron transport system in Corynebacterium diphtheriae. |
Q39511031 | Genetic characterization of wild-type and mutant fur genes of Bordetella avium |
Q36253781 | Genetic evidence that Neisseria gonorrhoeae produces specific receptors for transferrin and lactoferrin |
Q36240778 | Genetic organization of multiple fep genes encoding ferric enterobactin transport functions in Escherichia coli |
Q33648650 | Genome-wide characterization of the SloR metalloregulome in Streptococcus mutans |
Q36107908 | Gonococcal transferrin-binding protein 2 facilitates but is not essential for transferrin utilization |
Q40376065 | Growth of Moraxella catarrhalis with human transferrin and lactoferrin: expression of iron-repressible proteins without siderophore production. |
Q43588881 | Haematologic consequences of viral infections including serum iron status |
Q36723003 | Haemochromatosis and aldosterone deficiency presenting with Yersinia pseudotuberculosis septicaemia |
Q37048551 | Haemophilus influenzae can use human transferrin as a sole source for required iron |
Q38990107 | Heavy metals monitoring using bivalves from Mediterranean Sea and Red Sea. |
Q32084487 | Helicobacter pylori ribBA-mediated riboflavin production is involved in iron acquisition. |
Q28398038 | Hemolysis, toxicity, and randomly amplified polymorphic DNA analysis of Stachybotrys chartarum strains |
Q36964550 | Hemolytic activity in the periodontopathogen Porphyromonas gingivalis: kinetics of enzyme release and localization. |
Q37034157 | Hereditary Hemochromatosis Predisposes Mice to Yersinia pseudotuberculosis Infection Even in the Absence of the Type III Secretion System |
Q37075634 | Highly toxinogenic but avirulent Park-Williams 8 strain of Corynebacterium diphtheriae does not produce siderophore |
Q37013906 | Human immune response to iron-repressible outer membrane proteins of Neisseria meningitidis |
Q40151109 | Human immunoglobulin G antibody response to iron-repressible and other membrane proteins of Porphyromonas (Bacteroides) gingivalis |
Q37009287 | Human immunoglobulin G antibody response to the major gonococcal iron-regulated protein |
Q41015660 | Hydrogen bond donation to the heme distal ligand of Staphylococcus aureus IsdG tunes the electronic structure. |
Q36348829 | Hydroxamate siderophore production by opportunistic and systemic fungal pathogens |
Q40335572 | Hydroxamate-mediated transport of iron controlled by ColV plasmids |
Q33724556 | Identification and characterization of alcR, a gene encoding an AraC-like regulator of alcaligin siderophore biosynthesis and transport in Bordetella pertussis and Bordetella bronchiseptica |
Q35398076 | Identification and characterization of genes encoding the human transferrin-binding proteins from Haemophilus influenzae |
Q35069776 | Identification and characterization of the heme-binding proteins SeShp and SeHtsA of Streptococcus equi subspecies equi |
Q40159723 | Identification and characterization of the human lactoferrin-binding protein from Neisseria meningitidis |
Q33613524 | Identification and cloning of a fur homolog from Neisseria gonorrhoeae |
Q36132555 | Identification and molecular analysis of a 63-kilodalton stress protein from Neisseria gonorrhoeae |
Q39571817 | Identification and molecular analysis of lbpBA, which encodes the two-component meningococcal lactoferrin receptor |
Q35531161 | Identification and purification of a hemoglobin-binding outer membrane protein from Neisseria gonorrhoeae |
Q40155876 | Identification and purification of transferrin- and lactoferrin-binding proteins of Bordetella pertussis and Bordetella bronchiseptica |
Q30760681 | Identification of a two-component signal transduction system from Corynebacterium diphtheriae that activates gene expression in response to the presence of heme and hemoglobin |
Q37076208 | Identification of an iron-regulated 37,000-dalton protein in the cell envelope of Neisseria gonorrhoeae. |
Q35580416 | Identification of an iron-regulated outer membrane protein of Neisseria meningitidis involved in the utilization of hemoglobin complexed to haptoglobin |
Q36437711 | Identification of coprogen B and its breakdown products from Histoplasma capsulatum. |
Q34507120 | Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach. |
Q33885702 | Identification of the iron-responsive genes of Neisseria gonorrhoeae by microarray analysis in defined medium |
Q39833169 | Identification, characterization, and immunogenicity of the lactoferrin-binding protein from Helicobacter pylori |
Q40147293 | Immunogenicity and antigenic heterogeneity of a human transferrin-binding protein in Neisseria meningitidis |
Q36313837 | Impact of alcaligin siderophore utilization on in vivo growth of Bordetella pertussis |
Q40157284 | Impact of proteases on iron uptake of Pseudomonas aeruginosa pyoverdin from transferrin and lactoferrin |
Q43253233 | Impaired phagocytic activity of neutrophils in patients receiving haemodialysis: the critical role of iron overload. |
Q35939266 | Impaired polymorphonuclear leukocyte function in chronically hemodialyzed patients with iron overload |
Q46505284 | In vitro evaluation of putative virulence attributes of oral isolates of Candida spp. obtained from elderly healthy individuals |
Q38712186 | In vitro simulation of in vivo conditions: physical state of the culture medium |
Q37097219 | In vivo comparison of avirulent Vwa- and Pgm- or Pstr phenotypes of yersiniae |
Q37047968 | In vivo evidence that bacteria in urinary tract infection grow under iron-restricted conditions. |
Q37104056 | In vivo function of hemolysin in the nephropathogenicity of Escherichia coli |
Q54741379 | Incidence of aerobactin-positive Escherichia coli strains in patients with symptomatic urinary tract infection. |
Q36423735 | Increased virulence of Neisseria meningitidis after in vitro iron-limited growth at low pH |
Q72132621 | Induction of an antimicrobial biotin-binding egg white protein (avidin) in chick tissues in septic Escherichia coli infection |
Q40168472 | Inflammation triggers hypoferremia and de novo synthesis of serum transferrin and ceruloplasmin in mice |
Q39964722 | Influence of growth rate and iron limitation on the expression of outer membrane proteins and enterobactin by Klebsiella pneumoniae grown in continuous culture |
Q39823331 | Influence of iron-limited continuous culture on physiology and virulence of Legionella pneumophila |
Q50210557 | Inhibition of bacterial multiplication by the iron chelator deferoxamine: potentiating effect of ascorbic acid |
Q39694155 | Inhibition of the growth of Neisseria meningitidis by reduced ferritin and other iron-binding agents |
Q39820188 | Interaction of biofilm bacteria with antibiotics in a novel in vitro chemostat system |
Q40147361 | Interaction of ruminant transferrins with transferrin receptors in bovine isolates of Pasteurella haemolytica and Haemophilus somnus |
Q36281382 | Interspecies variations in Bordetella catecholamine receptor gene regulation and function |
Q35903368 | Involvement of multiple distinct Bordetella receptor proteins in the utilization of iron liberated from transferrin by host catecholamine stress hormones |
Q41814448 | IroT/mavN, a new iron-regulated gene involved in Legionella pneumophila virulence against amoebae and macrophages |
Q37834538 | Iron acquisition and the pathogenesis of meningococcal and gonococcal disease |
Q33601247 | Iron acquisition by Helicobacter pylori: importance of human lactoferrin |
Q33898946 | Iron acquisition by Neisseria meningitidis in vitro. |
Q35819666 | Iron acquisition from heme and hemoglobin by a Serratia marcescens extracellular protein |
Q40154866 | Iron acquisition in Pasteurella haemolytica: expression and identification of a bovine-specific transferrin receptor |
Q71705555 | Iron and host defence |
Q70383726 | Iron and infection |
Q86836903 | Iron and neoplasia |
Q28388335 | Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases |
Q28369399 | Iron chelators as therapeutic agents against Pneumocystis carinii |
Q36491518 | Iron homeostasis and oxidative stress in idiopathic pulmonary alveolar proteinosis: a case-control study |
Q36345057 | Iron in Neisseria meningitidis: minimum requirements, effects of limitation, and characteristics of uptake |
Q39658142 | Iron metabolism during infection and neoplasia |
Q32051592 | Iron starvation of Bordetella avium stimulates expression of five outer membrane proteins and regulates a gene involved in acquiring iron from serum |
Q39972520 | Iron transport in Mycobacterium smegmatis: Uptake of iron from ferric citrate. |
Q70212406 | Iron uptake and iron limited growth of Escherichia coli K-12 |
Q36057876 | Iron uptake by Pasteurella piscicida and its role in pathogenicity for fish |
Q36995624 | Iron uptake from lactoferrin and transferrin by Neisseria gonorrhoeae |
Q36333093 | Iron uptake system medicated by Vibrio anguillarum plasmid pJM1 |
Q28360169 | Iron, siderophores, and the pursuit of virulence: independence of the aerobactin and enterochelin iron uptake systems in Escherichia coli |
Q42980120 | Iron-containing lipoprotein SiaA in SiaABC, the primary heme transporter of Streptococcus pyogenes |
Q41180727 | Iron-controlled infection with Neisseria meningitidis in mice |
Q40159195 | Iron-regulated hemolysin production and utilization of heme and hemoglobin by Vibrio cholerae. |
Q36290821 | Iron-regulated outer membrane protein OM2 of Vibrio anguillarum is encoded by virulence plasmid pJM1 |
Q39832949 | Iron-regulated outer membrane proteins of Escherichia coli K-12 and mechanism of action of catechol-substituted cephalosporins |
Q41190696 | Iron-suppressible production of hydroxamate by Escherichia coli isolates. |
Q37074819 | Iron-vibriobactin transport system is not required for virulence of Vibrio cholerae |
Q40810202 | Is fever beneficial? |
Q39923074 | Isolation and Characterization of an Fe(III)-Chelating Compound Produced by Pseudomonas syringae |
Q35620938 | Isolation and characterization of a hemin-regulated gene, hemR, from Porphyromonas gingivalis |
Q72362649 | Isolation and structure elucidation of acinetobactin, a novel siderophore from Acinetobacter baumannii |
Q33902305 | Isolation of enterochelin from the peritoneal washings of guinea pigs lethally infected with Escherichia coli. |
Q40158931 | Killing of Actinobacillus actinomycetemcomitans by human lactoferrin |
Q37099610 | Lack of homology between the iron transport regions of two virulence-linked bacterial plasmids |
Q73272472 | Lactoferrin concentration in milk of bovine clinical mastitis |
Q35114451 | Lactoferrin in human milk: its role in iron absorption and protection against enteric infection in the newborn infant |
Q36946970 | Lactoferrin-binding proteins in Shigella flexneri |
Q41210478 | Listeria monocytogenes meningitis and decreased phagocytosis associated with iron overload. |
Q38614097 | Liver abscess due to Yersinia enterocolitica: case report and review of the literature |
Q36439263 | Localization in Yersinia pestis of peptides associated with virulence |
Q36126720 | Localization of a Porphyromonas gingivalis 26-kilodalton heat-modifiable, hemin-regulated surface protein which translocates across the outer membrane |
Q37001974 | Loss of transferrin receptor activity in Neisseria meningitidis correlates with inability to use transferrin as an iron source |
Q45183433 | Low protein diets improve survival from peritonitis in guinea pigs |
Q40178040 | Mechanism of impaired iron release by the reticuloendothelial system during the hypoferremic phase of experimental Neisseria meningitidis infection in mice. |
Q28472648 | Mechanistic insights into a novel exporter-importer system of Mycobacterium tuberculosis unravel its role in trafficking of iron |
Q40190530 | Media for study of growth kinetics and envelope properties of iron-deprived bacteria |
Q42038140 | Metal regulation of siderophore synthesis in Pseudomonas aeruginosa and functional effects of siderophore-metal complexes |
Q40232360 | Metal requirements of Legionella pneumophila. |
Q39816827 | Mode of action of GR69153, a novel catechol-substituted cephalosporin, and its interaction with the tonB-dependent iron transport system |
Q36757768 | Modes of action and inhibitory activities of new siderophore-beta-lactam conjugates that use specific iron uptake pathways for entry into bacteria |
Q36435367 | Modulatory effect of iron on the pathogenesis of Pseudomonas aeruginosa mouse corneal infections. |
Q40770905 | Molecular characterization of diphtheria toxin repressor (dtxR) genes present in nontoxigenic Corynebacterium diphtheriae strains isolated in the United Kingdom |
Q36304218 | Molecular cloning and expression of genetic determinants for the iron uptake system mediated by the Vibrio anguillarum plasmid pJM1. |
Q34123132 | Molecular cloning of the fur gene from Actinobacillus actinomycetemcomitans |
Q36346320 | Molecular factors associated with virulence of marine vibrios isolated from striped bass in Chesapeake Bay |
Q37254091 | Molecular mechanisms of Staphylococcus aureus iron acquisition. |
Q34188433 | Molecular-level tradeoffs and metabolic adaptation to simultaneous stressors |
Q35104508 | Monoclonal antibodies against the 70-kilodalton iron-regulated protein of Neisseria meningitidis are bactericidal and strain specific |
Q24803309 | Monoclonal antibodies against the iron regulated outer membrane Proteins of Acinetobacter baumannii are bactericidal |
Q33899202 | Mucin model for group B type III streptococcal infection in mice |
Q33801072 | Neutrophil elastase increases airway epithelial nonheme iron levels |
Q35596266 | Nfu facilitates the maturation of iron-sulfur proteins and participates in virulence in Staphylococcus aureus. |
Q53698735 | No effects without causes: the Iron Dysregulation and Dormant Microbes hypothesis for chronic, inflammatory diseases. |
Q39907007 | Novel iron uptake system specified by ColV plasmids: an important component in the virulence of invasive strains of Escherichia coli |
Q37054086 | Occurrence of chromosome- or plasmid-mediated aerobactin iron transport systems and hemolysin production among clonal groups of human invasive strains of Escherichia coli K1 |
Q24680333 | Oral lactoferrin treatment of experimental oral candidiasis in mice |
Q39826077 | Outer membrane protein B1, an iron-repressible protein conserved in the outer membrane of Moraxella (Branhamella) catarrhalis, binds human transferrin |
Q39956903 | Outer membrane protein mediating iron uptake via pyoverdinpss, the fluorescent siderophore produced by Pseudomonas syringae pv. syringae |
Q36277341 | OxyR activation in Porphyromonas gingivalis in response to a hemin-limited environment |
Q29615096 | Oxygen toxicity, oxygen radicals, transition metals and disease |
Q33586582 | Parenteral trace element provision: recent clinical research and practical conclusions |
Q34247203 | Pathogenesis of Campylobacter fetus infections. Role of surface array proteins in virulence in a mouse model |
Q37242801 | Pathogenic properties of Edwardsiella species |
Q39570284 | Phase variation of hemoglobin utilization in Neisseria gonorrhoeae. |
Q40791618 | Present status and future prospects of oral iron chelation therapy in thalassaemia and other diseases |
Q40376252 | Production of a hemolytic factor by Candida albicans. |
Q36637917 | Proteases from Entamoeba spp. and Pathogenic Free-Living Amoebae as Virulence Factors. |
Q37427039 | Proteus mirabilis genes that contribute to pathogenesis of urinary tract infection: identification of 25 signature-tagged mutants attenuated at least 100-fold |
Q41806886 | Purification and characterization of the major iron-regulated protein expressed by pathogenic Neisseriae |
Q34423007 | Purification of Pyoverdines of Pseudomonas fluorescens 2-79 by Copper-Chelate Chromatography |
Q71358023 | Purification, spectroscopic analysis and biological activity of the macrocyclic dihydroxamate siderophore alcaligin produced by Bordetella pertussis and Bordetella bronchiseptica |
Q42070145 | Purified meningococcal transferrin-binding protein B interacts with a secondary, strain-specific, binding site in the N-terminal lobe of human transferrin. |
Q43187867 | QSAR study of antimicrobial 3-hydroxypyridine-4-one and 3-hydroxypyran-4-one derivatives using different chemometric tools. |
Q28383660 | Quantification of siderophore and hemolysin from Stachybotrys chartarum strains, including a strain isolated from the lung of a child with pulmonary hemorrhage and hemosiderosis |
Q33932861 | Regulation of petrobactin and bacillibactin biosynthesis in Bacillus anthracis under iron and oxygen variation |
Q37188572 | Regulation of plasmid-mediated iron transport and virulence inVibrio anguillarum |
Q33856152 | Regulation of the iron uptake system in Vibrio anguillarum: evidence for a cooperative effect between two transcriptional activators |
Q36307542 | Relationship of siderophore-mediated iron assimilation to virulence in crown gall disease |
Q35093476 | Resistance to infection in murine beta-thalassemia |
Q37017062 | Resistance to pesticin, storage of iron, and invasion of HeLa cells by Yersiniae |
Q37074913 | Response of Neisseria gonorrhoeae to iron limitation: alterations in expression of membrane proteins without apparent siderophore production |
Q36947590 | Role of aerobactin in systemic spread of an opportunistic strain of Escherichia coli from the intestinal tract of gnotobiotic lambs |
Q37111457 | Role of antibody and enterobactin in controlling growth of Escherichia coli in human milk and acquisition of lactoferrin- and transferrin-bound iron by Escherichia coli |
Q54324435 | Role of bacterial and host factors in the pathogenesis of Shigella septicemia. |
Q34603205 | Role of iron in Trypanosoma cruzi infection of mice |
Q40177263 | Role of iron in intracellular growth of Trypanosoma cruzi. |
Q41767557 | Role of iron in the enhancement by Agrobacterium tumefaciens infection in mice |
Q36430563 | Role of iron in the pathogenesis of Vibrio vulnificus infections |
Q39946429 | Roles of porphyrins and host iron transport proteins in regulation of growth of Porphyromonas gingivalis W50 |
Q36331557 | Selection of nonmucoid derivatives of mucoid Pseudomonas aeruginosa is strongly influenced by the level of iron in the culture medium |
Q34762364 | Septicaemia due to Yersinia enterocolitica after oral overdoses of iron |
Q35699588 | Shotgun Metagenomic Sequencing Reveals Functional Genes and Microbiome Associated with Bovine Digital Dermatitis |
Q40148529 | Siderophore production and membrane alterations by Bordetella pertussis in response to iron starvation |
Q40152710 | Siderophore production by Pseudomonas pseudomallei |
Q37107637 | Siderophore production by Vibrio vulnificus |
Q72799636 | Siderophores as antimicrobial agents |
Q40146703 | Significant role of an exocellular protease in utilization of heme by Vibrio vulnificus |
Q35682345 | Sociality in Escherichia coli: Enterochelin Is a Private Good at Low Cell Density and Can Be Shared at High Cell Density. |
Q34007214 | Specific antibodies to Porphyromonas gingivalis Lys-gingipain by DNA vaccination inhibit bacterial binding to hemoglobin and protect mice from infection |
Q35509207 | Specific induction of fibronectin binding activity by hemoglobin in Candida albicans grown in defined media |
Q34117720 | Specific ligand binding attributable to individual epitopes of gonococcal transferrin binding protein A. |
Q26991866 | Staphylococcal response to oxidative stress |
Q93051919 | Structural Basis for Evasion of Nutritional Immunity by the Pathogenic Neisseriae |
Q72341963 | Structure of acinetoferrin, a new citrate-based dihydroxamate siderophore from Acinetobacter haemolyticus |
Q72341948 | Structure of vulnibactin, a new polyamine-containing siderophore from Vibrio vulnificus |
Q36535770 | Study of streptococcal hemoprotein receptor (Shr) in iron acquisition and virulence of M1T1 group A streptococcus |
Q45070397 | Subversion of Nutritional Immunity by the Pathogenic Neisseriae |
Q35758043 | Susceptibilities of bacterial and fungal urinary tract isolates to desferrioxamine |
Q50210662 | Synergy between the iron chelator deferoxamine and the antimicrobial agents gentamicin, chloramphenicol, cefalothin, cefotiam and cefsulodin |
Q33623678 | Temperature and host defense |
Q26767235 | The Basics of Bacteriuria: Strategies of Microbes for Persistence in Urine |
Q24619875 | The Cryptococcus neoformans capsule: a sword and a shield |
Q38311832 | The SloR/Dlg metalloregulator modulates Streptococcus mutans virulence gene expression |
Q37048925 | The ability of Salmonella typhimurium to produce the siderophore enterobactin is not a virulence factor in mouse typhoid |
Q91617393 | The affinity of MhuD for heme is consistent with a heme degrading function in vivo |
Q70037720 | The effect of experimental iron-overload on splenic T cell function: analysis using cloning techniques |
Q52136810 | The effect of iron (Fe3+) on the cloning efficiency of human memory T4+ lymphocytes. |
Q70042537 | The effect of non-transferrin-bound iron on murine T lymphocyte subsets: analysis by clonal techniques |
Q71524773 | The effects of iron and temperature on the growth of Listeria monocytogenes in cell-free media |
Q35131521 | The gene coding for the 190,000-dalton iron-regulated protein of Yersinia species is present only in the highly pathogenic strains |
Q50216483 | The growth-promoting effect of bacterial iron for serum-exposed bacteria. |
Q37724633 | The haem-uptake gene cluster in Vibrio fischeri is regulated by Fur and contributes to symbiotic colonization |
Q39285519 | The hemochromatosis protein HFE 20 years later: An emerging role in antigen presentation and in the immune system |
Q50218117 | The in vivo division and death rates of Salmonella typhimurium in the spleens of naturally resistant and susceptible mice measured by the superinfecting phage technique of Meynell |
Q36035341 | The influence of iron availability on human salivary microbial community composition |
Q33626434 | The meningococcus and mechanisms of pathogenicity |
Q35600334 | The ornithine decarboxylase gene odc is required for alcaligin siderophore biosynthesis in Bordetella spp.: putrescine is a precursor of alcaligin |
Q39570597 | The protective effects of lactoferrin feeding against endotoxin lethal shock in germfree piglets |
Q36164265 | The virulence-associated chrysobactin iron uptake system of Erwinia chrysanthemi 3937 involves an operon encoding transport and biosynthetic functions |
Q37256551 | This is not your mother's repressor: the complex role of fur in pathogenesis |
Q44990827 | Trace element metabolism in the chemically diabetic rat. |
Q36961078 | Transcript analysis of nrrF, a Fur repressed sRNA of Neisseria gonorrhoeae |
Q39831444 | Transcription of the Corynebacterium diphtheriae hmuO gene is regulated by iron and heme |
Q40599596 | Turnover in the transferrin iron pool during the hypoferremic phase of experimental Neisseria meningitidis infection in mice |
Q70484333 | Urinary excretion and blood concentrations of trace elements and electrolytes during total parenteral nutrition in Crohn's disease |
Q40205437 | Utilization of exogenous siderophores by Campylobacter species |
Q39800270 | Utilization of hemin and hemoglobin by Vibrio vulnificus biotype 2. |
Q36843552 | Utilization of host iron sources by Corynebacterium diphtheriae: identification of a gene whose product is homologous to eukaryotic heme oxygenases and is required for acquisition of iron from heme and hemoglobin |
Q44143282 | Utilization of siderophores by Candida albicans |
Q37100429 | Vibrio cholerae expresses iron-regulated outer membrane proteins in vivo. |
Q24631649 | Vibrio cholerae iron transport systems: roles of heme and siderophore iron transport in virulence and identification of a gene associated with multiple iron transport systems |
Q37405123 | Vibrio vulnificus: disease and pathogenesis |
Q28468751 | Virulence factors in Escherichia coli urinary tract infection |
Q40162677 | Virulence of iron transport mutants of Shigella flexneri and utilization of host iron compounds. |
Q35597231 | bvg Repression of alcaligin synthesis in Bordetella bronchiseptica is associated with phylogenetic lineage |
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