| scholarly article | Q13442814 |
| P2093 | author name string | Corrella S Detweiler | |
| Sarah M Moreland | |||
| Toni A Nagy | |||
| P2860 | cites work | Hemophagocytic syndromes and infection | Q24653852 |
| Hemophagocytic macrophages harbor Salmonella enterica during persistent infection | Q27319444 | ||
| One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
| Macrophage-dependent induction of the Salmonella pathogenicity island 2 type III secretion system and its role in intracellular survival | Q27976514 | ||
| Nramp transfection transfers Ity/Lsh/Bcg-related pleiotropic effects on macrophage activation: influence on oxidative burst and nitric oxide pathways | Q28511331 | ||
| A novel secretion pathway of Salmonella enterica acts as an antivirulence modulator during salmonellosis | Q30157714 | ||
| Iron transport into mycobacterium avium-containing phagosomes from an Nramp1(Gly169)-transfected RAW264.7 macrophage cell line. | Q31996280 | ||
| Phagocytic superoxide specifically damages an extracytoplasmic target to inhibit or kill Salmonella | Q33420369 | ||
| The Nramp1 protein and its role in resistance to infection and macrophage function. | Q33694066 | ||
| IroN, a novel outer membrane siderophore receptor characteristic of Salmonella enterica | Q33726945 | ||
| Salmonella pathogenicity island 2. | Q33938216 | ||
| Salmonella typhimurium IroN and FepA proteins mediate uptake of enterobactin but differ in their specificity for other siderophores | Q33992252 | ||
| Characterization of grvA, an antivirulence gene on the gifsy-2 phage in Salmonella enterica serovar typhimurium | Q33995341 | ||
| Salmonella typhimurium encodes a putative iron transport system within the centisome 63 pathogenicity island. | Q34000980 | ||
| Salmonella enterica replication in hemophagocytic macrophages requires two type three secretion systems | Q34045086 | ||
| Catecholate receptor proteins in Salmonella enterica: role in virulence and implications for vaccine development | Q46695998 | ||
| Biosynthesis and IroC-dependent export of the siderophore salmochelin are essential for virulence of Salmonella enterica serovar Typhimurium | Q46808987 | ||
| The NRAMP proteins of Salmonella typhimurium and Escherichia coli are selective manganese transporters involved in the response to reactive oxygen | Q47854702 | ||
| Dynamics of bacterial growth and distribution within the liver during Salmonella infection | Q50103038 | ||
| Biodistribution and genetic stability of the novel antitumor agent VNP20009, a genetically modified strain of Salmonella typhimurium | Q50120814 | ||
| Relationship of cutaneous delayed hypersensitivity to protection from challenge exposure with Salmonella typhimurium in calves. | Q50208336 | ||
| Identification of the receptor scavenging hemopexin-heme complexes | Q50337480 | ||
| Structural changes of Escherichia coli ferric uptake regulator during metal-dependent dimerization and activation explored by NMR and X-ray crystallography. | Q54465449 | ||
| Selection procedure for deregulated iron transport mutants (fur) in Escherichia coli K 12: fur not only affects iron metabolism | Q68221693 | ||
| Regulation of ferric iron transport in Escherichia coli K12: isolation of a constitutive mutant | Q70183756 | ||
| Oxygen-dependent anti-Salmonella activity of macrophages | Q34134518 | ||
| Recombination-deficient mutants of Salmonella typhimurium are avirulent and sensitive to the oxidative burst of macrophages | Q34355873 | ||
| Subcellular localization of iron and heme metabolism related proteins at early stages of erythrophagocytosis | Q34364627 | ||
| The proinflammatory response induced by wild-type Yersinia pseudotuberculosis infection inhibits survival of yop mutants in the gastrointestinal tract and Peyer's patches | Q34491834 | ||
| Role of receptor proteins for enterobactin and 2,3-dihydroxybenzoylserine in virulence of Salmonella enterica | Q34940802 | ||
| Hypervirulence and pathogen fitness | Q35089497 | ||
| Contribution of TonB- and Feo-mediated iron uptake to growth of Salmonella typhimurium in the mouse | Q35528349 | ||
| DNA repair is more important than catalase for Salmonella virulence in mice | Q35552688 | ||
| Fur regulon of Salmonella typhimurium: identification of new iron-regulated genes. | Q35592292 | ||
| A glycine betaine importer limits Salmonella stress resistance and tissue colonization by reducing trehalose production | Q35881567 | ||
| Slc11a1 (Nramp1) impairs growth of Salmonella enterica serovar typhimurium in macrophages via stimulation of lipocalin-2 expression | Q36091290 | ||
| 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. | Q36156332 | ||
| The macrophage scavenger receptor CD163. | Q36257860 | ||
| Hemophagocytic macrophages in murine typhoid fever have an anti-inflammatory phenotype | Q36277460 | ||
| Brucella abortus requires the heme transporter BhuA for maintenance of chronic infection in BALB/c mice | Q36313890 | ||
| Salmonella typhimurium persists within macrophages in the mesenteric lymph nodes of chronically infected Nramp1+/+ mice and can be reactivated by IFNgamma neutralization | Q36399044 | ||
| The iron export protein ferroportin 1 is differentially expressed in mouse macrophage populations and is present in the mycobacterial-containing phagosome. | Q36838527 | ||
| Yersinia outer proteins: Yops | Q37032798 | ||
| Gallbladder epithelium as a niche for chronic Salmonella carriage | Q37035982 | ||
| Leucine-responsive regulatory protein (Lrp) acts as a virulence repressor in Salmonella enterica serovar Typhimurium | Q37075381 | ||
| High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi | Q37119288 | ||
| Salmonella enterica causes more severe inflammatory disease in C57/BL6 Nramp1G169 mice than Sv129S6 mice | Q37161148 | ||
| Salmonella require the fatty acid regulator PPARδ for the establishment of a metabolic environment essential for long-term persistence | Q37202938 | ||
| Intracellular microbes and haemophagocytosis | Q37212318 | ||
| The ferric enterobactin transporter Fep is required for persistent Salmonella enterica serovar typhimurium infection | Q37264858 | ||
| From bench to bedside: stealth of enteroinvasive pathogens | Q37310216 | ||
| Identification of the Escherichia coli K-12 Nramp orthologue (MntH) as a selective divalent metal ion transporter | Q38314576 | ||
| Macrophage NRAMP1 and its role in resistance to microbial infections | Q38550457 | ||
| Regulation of divergent transcription from the iron-responsive fepB-entC promoter-operator regions in Escherichia coli | Q39517788 | ||
| Acquisition of Mn(II) in addition to Fe(II) is required for full virulence of Salmonella enterica serovar Typhimurium | Q39663606 | ||
| Characterization of the ferrous iron uptake system of Escherichia coli | Q39937148 | ||
| Interferon-gamma limits the availability of iron for intramacrophage Salmonella typhimurium. | Q39968051 | ||
| The role of DNA base excision repair in the pathogenesis of Salmonella enterica serovar Typhimurium | Q40562049 | ||
| The putative iron transport system SitABCD encoded on SPI1 is required for full virulence of Salmonella typhimurium. | Q40625112 | ||
| Macrophages inhibit Salmonella typhimurium replication through MEK/ERK kinase and phagocyte NADPH oxidase activities | Q40753427 | ||
| Restricted growth of ent(-) and tonB mutants of Salmonella enterica serovar Typhi in human Mono Mac 6 monocytic cells | Q40820022 | ||
| The ferrous iron transporter FtrABCD is required for the virulence of Brucella abortus 2308 in mice | Q45091061 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1314-1326 | |
| P577 | publication date | 2014-08-14 | |
| P1433 | published in | Molecular Microbiology | Q6895967 |
| P1476 | title | Salmonella acquires ferrous iron from haemophagocytic macrophages | |
| P478 | volume | 93 |
| Q90572987 | Autophagy Induction by a Small Molecule Inhibits Salmonella Survival in Macrophages and Mice |
| Q36410913 | Bacterial Stimulation of Toll-Like Receptor 4 Drives Macrophages To Hemophagocytose |
| Q90445090 | Hoodwinking the Big-Eater to Prosper: The Salmonella-Macrophage Paradigm |
| Q35609338 | Increased ferroportin-1 expression and rapid splenic iron loss occur with anemia caused by Salmonella enterica Serovar Typhimurium infection in mice |
| Q90375729 | Iron Acquisition by Bacterial Pathogens: Beyond tris-Catecholate Complexes |
| Q40497871 | Iron acquisition pathways and colonization of the inflamed intestine by Salmonella enterica serovar Typhimurium |
| Q89547519 | Iron trafficking in patients with Indian Post kala-azar dermal leishmaniasis |
| Q60938614 | Pathogenomics of Virulence Traits of That Were Deemed Inconclusive by Traditional Experimental Approaches |
| Q37287154 | Salmonella Infection Enhances Erythropoietin Production by the Kidney and Liver, Which Correlates with Elevated Bacterial Burdens |
| Q35072142 | Salmonella enterica infection stimulates macrophages to hemophagocytose |
| Q39442456 | Salmonella infection: Interplay between the bacteria and host immune system |
| Q35668833 | Strategies of Intracellular Pathogens for Obtaining Iron from the Environment |
| Q28493227 | Structural model of FeoB, the iron transporter from Pseudomonas aeruginosa, predicts a cysteine lined, GTP-gated pore |
| Q55267074 | The Ability to Acquire Iron Is Inversely Related to Virulence and the Protective Efficacy of Francisella tularensis Live Vaccine Strain. |
| Q89104000 | The Impact of Dietary Transition Metals on Host-Bacterial Interactions |
| Q89787491 | Xenosiderophore Utilization Promotes Bacteroides thetaiotaomicron Resilience during Colitis |
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