| scholarly article | Q13442814 |
| P50 | author | Girija Ramakrishnan | Q91507385 |
| P2093 | author name string | Richard Johnson | |
| Bhaswati Sen | |||
| Natalie Pérez | |||
| P2860 | cites work | Genome characterisation of the genus Francisella reveals insight into similar evolutionary paths in pathogens of mammals and fish | Q21266704 |
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| A Hidden Markov Model method, capable of predicting and discriminating beta-barrel outer membrane proteins | Q24803433 | ||
| Subversion of host recognition and defense systems by Francisella spp | Q27025594 | ||
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| Evasion of IFN-γ signaling by Francisella novicida is dependent upon Francisella outer membrane protein C | Q28477609 | ||
| FeoB-mediated uptake of iron by Francisella tularensis | Q28675489 | ||
| Paralogous outer membrane proteins mediate uptake of different forms of iron and synergistically govern virulence in Francisella tularensis tularensis | Q30155300 | ||
| PRED-TMBB: a web server for predicting the topology of beta-barrel outer membrane proteins | Q30163988 | ||
| The FupA/B protein uniquely facilitates transport of ferrous iron and siderophore-associated ferric iron across the outer membrane of Francisella tularensis live vaccine strain | Q30408382 | ||
| The reduced genome of the Francisella tularensis live vaccine strain (LVS) encodes two iron acquisition systems essential for optimal growth and virulence | Q30413938 | ||
| The fslE homolog, FTL_0439 (fupA/B), mediates siderophore-dependent iron uptake in Francisella tularensis LVS. | Q30432826 | ||
| Characterization of the siderophore of Francisella tularensis and role of fslA in siderophore production | Q30440483 | ||
| fslE is necessary for siderophore-mediated iron acquisition in Francisella tularensis Schu S4 | Q30440726 | ||
| Construction and characterization of a highly efficient Francisella shuttle plasmid | Q40622839 | ||
| Characterization of fig operon mutants of Francisella novicida U112. | Q42600585 | ||
| Fast biological iron chelators: kinetics of iron removal from human diferric transferrin by multidentate hydroxypyridonates | Q43807548 | ||
| The interplay between siderophore secretion and coupled iron and copper transport in the heterocyst-forming cyanobacterium Anabaena sp. PCC 7120. | Q45763521 | ||
| The FeoA protein is necessary for the FeoB transporter to import ferrous iron | Q50026110 | ||
| Siderophore-mediated mechanism of gallium uptake demonstrated in the microorganism Ustilago sphaerogena | Q71334128 | ||
| Coordination Chemistry of the Carboxylate Type Siderophore Rhizoferrin: The Iron(III) Complex and Its Metal Analogs | Q74821931 | ||
| Comparative proteome analysis of cellular proteins extracted from highly virulent Francisella tularensis ssp. tularensis and less virulent F. tularensis ssp. holarctica and F. tularensis ssp. mediaasiatica. | Q31113818 | ||
| Iron transport in Francisella in the absence of a recognizable TonB protein still requires energy generated by the proton motive force | Q33346192 | ||
| Gallium disrupts iron uptake by intracellular and extracellular Francisella strains and exhibits therapeutic efficacy in a murine pulmonary infection model | Q33558904 | ||
| EVALUATION OF LIVE TULAREMIA VACCINE PREPARED IN A CHEMICALLY DEFINED MEDIUM. | Q33696706 | ||
| A mutant of Francisella tularensis strain SCHU S4 lacking the ability to express a 58-kilodalton protein is attenuated for virulence and is an effective live vaccine | Q34194818 | ||
| Whole-genome sequences of nine francisella isolates | Q34244266 | ||
| Low dose vaccination with attenuated Francisella tularensis strain SchuS4 mutants protects against tularemia independent of the route of vaccination | Q34291236 | ||
| Role of porins in iron uptake by Mycobacterium smegmatis | Q34433393 | ||
| Complete Genome Sequence of Francisella endociliophora Strain FSC1006, Isolated from a Laboratory Culture of the Marine Ciliate Euplotes raikovi | Q34580598 | ||
| Identification of Francisella tularensis genes affected by iron limitation | Q34721354 | ||
| Iron content differs between Francisella tularensis subspecies tularensis and subspecies holarctica strains and correlates to their susceptibility to H(2)O(2)-induced killing | Q34739719 | ||
| Contribution of the Shigella flexneri Sit, Iuc, and Feo iron acquisition systems to iron acquisition in vitro and in cultured cells | Q34853708 | ||
| Complete Genome Sequence of Francisella guangzhouensis Strain 08HL01032T, Isolated from Air-Conditioning Systems in China | Q35389199 | ||
| Growth of Francisella tularensis LVS in macrophages: the acidic intracellular compartment provides essential iron required for growth | Q35403392 | ||
| Mechanisms of heme utilization by Francisella tularensis | Q35574562 | ||
| In vivo negative selection screen identifies genes required for Francisella virulence | Q35699734 | ||
| Genome-wide identification of Francisella tularensis virulence determinants | Q35913441 | ||
| Copper homeostasis at the host-pathogen interface | Q35922366 | ||
| The major facilitator superfamily-type protein LbtC promotes the utilization of the legiobactin siderophore by Legionella pneumophila | Q35959585 | ||
| The Legionella pneumophila Siderophore Legiobactin Is a Polycarboxylate That Is Identical in Structure to Rhizoferrin | Q36053556 | ||
| Mechanisms of Francisella tularensis intracellular pathogenesis | Q36933178 | ||
| The iron-sulfur clusters of dehydratases are primary intracellular targets of copper toxicity | Q37208556 | ||
| FeoA and FeoC are essential components of the Vibrio cholerae ferrous iron uptake system, and FeoC interacts with FeoB. | Q37253121 | ||
| Porins increase copper susceptibility of Mycobacterium tuberculosis | Q37264105 | ||
| Reintroduction of two deleted virulence loci restores full virulence to the live vaccine strain of Francisella tularensis | Q37274784 | ||
| Intracellular biology and virulence determinants of Francisella tularensis revealed by transcriptional profiling inside macrophages | Q37353316 | ||
| The 58-kilodalton major virulence factor of Francisella tularensis is required for efficient utilization of iron | Q37355882 | ||
| Siderophore uptake in bacteria and the battle for iron with the host; a bird's eye view | Q37769428 | ||
| The struggle for iron - a metal at the host-pathogen interface. | Q37801985 | ||
| Highly reactive oxygen species: detection, formation, and possible functions. | Q37870856 | ||
| Iron speciation in the cytosol: an overview | Q38066761 | ||
| Microbial quest for food in vivo: 'nutritional virulence' as an emerging paradigm | Q38089379 | ||
| A 55 kDa hypothetical membrane protein is an iron-regulated virulence factor of Francisella tularensis subsp. novicida U112. | Q38297913 | ||
| Identification of differentially regulated francisella tularensis genes by use of a newly developed Tn5-based transposon delivery system. | Q38607194 | ||
| P433 | issue | 3 | |
| P921 | main subject | Francisella tularensis | Q1003460 |
| P304 | page(s) | 453-468 | |
| P577 | publication date | 2016-02-25 | |
| P1433 | published in | MicrobiologyOpen | Q27724394 |
| P1476 | title | Two parallel pathways for ferric and ferrous iron acquisition support growth and virulence of the intracellular pathogen Francisella tularensis Schu S4 | |
| P478 | volume | 5 |
| Q58709793 | Contribution of ATPase copper transporters in animal but not plant virulence of the crossover pathogen Aspergillus flavus |
| Q90375729 | Iron Acquisition by Bacterial Pathogens: Beyond tris-Catecholate Complexes |
| Q30353186 | Iron and Virulence in Francisella tularensis. |
| Q38920767 | Nramp1 and NrampB Contribute to Resistance against Francisella in Dictyostelium |
| Q55267074 | The Ability to Acquire Iron Is Inversely Related to Virulence and the Protective Efficacy of Francisella tularensis Live Vaccine Strain. |
| Q47417123 | The Multiple Localized Glyceraldehyde-3-Phosphate Dehydrogenase Contributes to the Attenuation of the Francisella tularensis dsbA Deletion Mutant. |
| Q57751873 | Toward a mechanistic understanding of Feo-mediated ferrous iron uptake |
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