scholarly article | Q13442814 |
P2093 | author name string | Roland K Strong | |
Colin Correnti | |||
P2860 | cites work | Characterization of human DHRS6, an orphan short chain dehydrogenase/reductase enzyme: a novel, cytosolic type 2 R-beta-hydroxybutyrate dehydrogenase | Q24299964 |
Anthrax pathogen evades the mammalian immune system through stealth siderophore production | Q24675112 | ||
Siderophore-based iron acquisition and pathogen control | Q24681774 | ||
Enterobactin: an archetype for microbial iron transport | Q24683689 | ||
The neutrophil lipocalin NGAL is a bacteriostatic agent that interferes with siderophore-mediated iron acquisition | Q27640027 | ||
Cell transformation by the v-myc oncogene abrogates c-Myc/Max-mediated suppression of a C/EBP beta-dependent lipocalin gene | Q27642238 | ||
Structure of the human transferrin receptor-transferrin complex | Q27643181 | ||
The Siderocalin/Enterobactin Interaction: A Link between Mammalian Immunity and Bacterial Iron Transport 1 | Q27651418 | ||
Iron traffics in circulation bound to a siderocalin (Ngal)–catechol complex | Q27662810 | ||
The v-myc-induced Q83 Lipocalin Is a Siderocalin | Q27664382 | ||
Transferrin receptor is necessary for development of erythrocytes and the nervous system | Q28118509 | ||
Lack of a role for iron in the Lyme disease pathogen | Q28145506 | ||
An iron delivery pathway mediated by a lipocalin | Q28216116 | ||
Systemic iron homeostasis and the iron-responsive element/iron-regulatory protein (IRE/IRP) regulatory network | Q28280607 | ||
Two to tango: regulation of Mammalian iron metabolism | Q28287034 | ||
A mammalian siderophore synthesized by an enzyme with a bacterial homolog involved in enterobactin production | Q28511945 | ||
The endocytic receptor megalin binds the iron transporting neutrophil-gelatinase-associated lipocalin with high affinity and mediates its cellular uptake | Q28577988 | ||
A cell-surface receptor for lipocalin 24p3 selectively mediates apoptosis and iron uptake | Q28587213 | ||
Lipocalin 2-deficient mice exhibit increased sensitivity to Escherichia coli infection but not to ischemia-reperfusion injury | Q28591880 | ||
Lipocalin 2 mediates an innate immune response to bacterial infection by sequestrating iron | Q29619561 | ||
Intracellular Mycobacterium avium intersect transferrin in the Rab11(+) recycling endocytic pathway and avoid lipocalin 2 trafficking to the lysosomal pathway | Q30494299 | ||
Molecular and biological analysis of eight genetic islands that distinguish Neisseria meningitidis from the closely related pathogen Neisseria gonorrhoeae | Q30847631 | ||
Mineralization in ferritin: an efficient means of iron storage | Q33707673 | ||
Biochemistry of iron uptake | Q33775784 | ||
The iron transporter DMT1. | Q33785097 | ||
The Yersinia high-pathogenicity island: an iron-uptake island | Q33952323 | ||
Microorganisms pumping iron: anaerobic microbial iron oxidation and reduction | Q33999612 | ||
Living with iron (and oxygen): questions and answers about iron homeostasis | Q34055551 | ||
Siderophores: Structure and Function of Microbial Iron Transport Compounds | Q34058117 | ||
Redox cycling in iron uptake, efflux, and trafficking | Q34094269 | ||
Stoichiometric and site characteristics of the binding of iron to human transferrin | Q34115007 | ||
The role of iron in the immune response to bacterial infection | Q34155194 | ||
The roles of iron in health and disease | Q34156115 | ||
Iron withholding: a defense against infection and neoplasia | Q34259767 | ||
Microbial iron compounds | Q34260986 | ||
Ironing out disease: inherited disorders of iron homeostasis | Q34289732 | ||
Siderocalin (Lcn 2) also binds carboxymycobactins, potentially defending against mycobacterial infections through iron sequestration | Q34383190 | ||
Microbial evasion of the immune system: structural modifications of enterobactin impair siderocalin recognition | Q34559548 | ||
Dual action of neutrophil gelatinase-associated lipocalin | Q34603152 | ||
The role of electrostatics in siderophore recognition by the immunoprotein Siderocalin | Q34893809 | ||
Siderocalins: siderophore-binding proteins of the innate immune system | Q34934297 | ||
The labile iron pool: characterization, measurement, and participation in cellular processes(1). | Q34956696 | ||
Chemistry for an essential biological process: the reduction of ferric iron | Q34983143 | ||
Multiple apoptotic defects in hematopoietic cells from mice lacking lipocalin 24p3 | Q35063479 | ||
Transferrin-iron uptake by Gram-negative bacteria | Q35109508 | ||
Trace Element Uptake and Distribution in Plants | Q35121120 | ||
The pathogen-associated iroA gene cluster mediates bacterial evasion of lipocalin 2. | Q35133896 | ||
Labile iron pool: the main determinant of cellular response to oxidative stress | Q35592855 | ||
Transferrins and heme-compounds as iron sources for pathogenic bacteria | Q35868925 | ||
Bacterial iron sources: from siderophores to hemophores | Q35919884 | ||
Amonabactin, a novel tryptophan- or phenylalanine-containing phenolate siderophore in Aeromonas hydrophila | Q36175468 | ||
ColV plasmid-specific aerobactin synthesis by invasive strains of Escherichia coli | Q36426029 | ||
Forging a field: the golden age of iron biology | Q36742479 | ||
Intracellular labile iron. | Q36798824 | ||
Lipocalin 2 promotes breast cancer progression | Q37129437 | ||
Iron transport & homeostasis mechanisms: their role in health & disease. | Q37357647 | ||
Lipocalin-2: pro- or anti-apoptotic? | Q37374543 | ||
Mammalian iron transport. | Q37502811 | ||
Mammalian iron metabolism | Q37658680 | ||
Iron regulatory proteins: from molecular mechanisms to drug development | Q37705384 | ||
Ironing out the wrinkles in host defense: interactions between iron homeostasis and innate immunity | Q37726751 | ||
Low molecular weight intracellular iron transport compounds | Q39634380 | ||
Human tear lipocalin exhibits antimicrobial activity by scavenging microbial siderophores | Q39954600 | ||
Lipocalin 2 is required for BCR-ABL-induced tumorigenesis | Q39956362 | ||
Isolation and characterization of a siderophore-like growth factor from mutants of SV40-transformed cells adapted to picolinic acid | Q40170600 | ||
Iron piracy: acquisition of transferrin-bound iron by bacterial pathogens | Q40506099 | ||
Induction of apoptosis by a secreted lipocalin that is transcriptionally regulated by IL-3 deprivation | Q40788252 | ||
Transferrin receptor of the rabbit reticulocyte | Q41052150 | ||
Iron, infections, and anemia of inflammation | Q41632665 | ||
Function and regulation of transferrin and ferritin. | Q41699844 | ||
Low molecular weight iron-binding factor from mammalian tissue that potentiates bacterial growth | Q42019610 | ||
Structure of schizokinen, an iron-transport compound from Bacillus megaterium | Q44537674 | ||
Catechol releases iron(III) from ferritin by direct chelation without iron(II) production. | Q45258496 | ||
Bcr-Abl-mediated suppression of normal hematopoiesis in leukemia | Q45286107 | ||
On mouse and man: neutrophil gelatinase associated lipocalin is not involved in apoptosis or acute response | Q46690537 | ||
The aerobactin iron transport system genes in Shigella flexneri are present within a pathogenicity island. | Q47945948 | ||
Acute phase lipocalin Ex-FABP is involved in heart development and cell survival. | Q52087233 | ||
Formation of Iron-binding Compounds by Micro-organisms | Q58934886 | ||
Mechanism of catalysis of Fe(II) oxidation by ferritin H chains | Q67518821 | ||
Domain preference in iron removal from human transferrin by the bacterial siderophores aerobactin and enterochelin | Q70067055 | ||
The occurrence of carboxymycobactin, the siderophore of pathogenic mycobacteria, as a second extracellular siderophore in Mycobacterium smegmatis | Q71519595 | ||
Inhibition of cell proliferation and induction of apoptosis by ExFABP gene targeting | Q73735851 | ||
A Preorganized Siderophore: Thermodynamic and Structural Characterization of Alcaligin and Bisucaberin, Microbial Macrocyclic Dihydroxamate Chelating Agents(1) | Q74832610 | ||
From a total synthesis of cepabactin and its 3:1 ferric complex to the isolation of a 1:1:1 mixed complex between iron (III), cepabactin and pyochelin | Q81474297 | ||
P433 | issue | 17 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 13524-13531 | |
P577 | publication date | 2012-03-02 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Mammalian siderophores, siderophore-binding lipocalins, and the labile iron pool | |
P478 | volume | 287 |
Q37716856 | "Pumping iron"-how macrophages handle iron at the systemic, microenvironmental, and cellular levels |
Q36708605 | A manganese-rich environment supports superoxide dismutase activity in a Lyme disease pathogen, Borrelia burgdorferi |
Q35804193 | A systematic analysis of human lipocalin family and its expression in esophageal carcinoma |
Q92575586 | ASP2397 Is a Novel Natural Compound That Exhibits Rapid and Potent Fungicidal Activity against Aspergillus Species through a Specific Transporter |
Q38955294 | An overview of the biological metal uptake pathways in Pseudomonas aeruginosa. |
Q38369809 | Bacterial siderophores promote plant growth: Screening of catechol and hydroxamate siderophores. |
Q34298407 | Bacterial siderophores that evade or overwhelm lipocalin 2 induce hypoxia inducible factor 1α and proinflammatory cytokine secretion in cultured respiratory epithelial cells. |
Q38368718 | Diverging roles of bacterial siderophores during infection. |
Q92190432 | Draft genomes and initial characteriaztion of siderophore producing pseudomonads isolated from mine dump and mine drainage |
Q37551280 | Human Metabolome-derived Cofactors Are Required for the Antibacterial Activity of Siderocalin in Urine |
Q35783053 | Human Urinary Composition Controls Antibacterial Activity of Siderocalin |
Q46249324 | In vivo bioluminescence imaging of labile iron accumulation in a murine model of Acinetobacter baumannii infection. |
Q28082191 | Iron and zinc exploitation during bacterial pathogenesis |
Q50892902 | Iron depletion strategy for targeted cancer therapy: utilizing the dual roles of neutrophil gelatinase-associated lipocalin protein. |
Q37376232 | Iron in intracellular infection: to provide or to deprive? |
Q38066761 | Iron speciation in the cytosol: an overview |
Q38187484 | Iron: the hard player in diabetes pathophysiology. |
Q36140013 | Lipocalin 2 deficiency dysregulates iron homeostasis and exacerbates endotoxin-induced sepsis. |
Q34735792 | Lipocalin-2 as mediator of chemokine expression and granulocyte infiltration during ischemia and reperfusion |
Q36655357 | Lipopolysaccharide-induced inflammation or unilateral ureteral obstruction yielded multiple types of glycosylated Lipocalin 2 |
Q34490463 | Metal limitation and toxicity at the interface between host and pathogen |
Q49958535 | Modulation of urinary siderophores by the diet, gut microbiota and inflammation in mice |
Q39014492 | Molecular basis of mycobacterial survival in macrophages |
Q28536426 | N-octanoyl dopamine inhibits the expression of a subset of κB regulated genes: potential role of p65 Ser276 phosphorylation |
Q97545704 | Parsing the functional specificity of Siderocalin/Lipocalin 2/NGAL for siderophores and related small-molecule ligands |
Q36333948 | Preparation of 3-benzyloxy-2-pyridinone functional linkers: Tools for the synthesis of 3,2-hydroxypyridinone (HOPO) and HOPO/hydroxamic acid chelators |
Q42253266 | Prospects for treating osteoarthritis: enzyme-protein interactions regulating matrix metalloproteinase activity. |
Q35924321 | Purification and Structural Characterization of "Simple Catechol", the NGAL-Siderocalin Siderophore in Human Urine |
Q26784135 | Roles of bacterial and mammalian siderophores in host-pathogen interactions |
Q21131297 | Shared and distinct mechanisms of iron acquisition by bacterial and fungal pathogens of humans |
Q57365954 | Siderophore-inspired nanoparticle-based biosensor for the selective detection of Fe3+ |
Q30243906 | Siderophores; iron scavengers: the novel & promising targets for pathogen specific antifungal therapy |
Q30796767 | Synthesis, spectroscopy, and binding constants of ketocatechol-containing iminodiacetic acid and its Fe(III), Cu(II), and Zn(II) complexes and reaction of Cu(II) complex with H₂O₂ in aqueous solution |
Q34819468 | Targeting iron acquisition blocks infection with the fungal pathogens Aspergillus fumigatus and Fusarium oxysporum |
Q37238644 | The Ligands of Neutrophil Gelatinase-Associated Lipocalin |
Q47098548 | The Metallophore Staphylopine Enables Staphylococcus aureus To Compete with the Host for Zinc and Overcome Nutritional Immunity. |
Q38704529 | The Yin and Yang of copper during infection |
Q51014926 | The fate of siderophores: antagonistic environmental interactions in exudate-mediated micronutrient uptake. |
Q88995043 | The iron hand of uropathogenic Escherichia coli: the role of transition metal control in virulence |
Q28109405 | The iron metallome in eukaryotic organisms |
Q58593664 | Tonicity inversely modulates lipocalin-2 (Lcn2/24p3/NGAL) receptor (SLC22A17) and Lcn2 expression via Wnt/β-catenin signaling in renal inner medullary collecting duct cells: implications for cell fate and bacterial infection |
Q37511583 | Transition metal ions at the crossroads of mucosal immunity and microbial pathogenesis |
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