| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Gottfried Wilharm | Q41465371 |
| P2093 | author name string | Christine Heider | |
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| Factors influencing the loss of virulence in Pasteurella pestis. | Q40314816 | ||
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| Studies on the nutrition and physiology of Pasteurella pestis. II. A defined medium for the growth of Pasteurella pestis | Q40433530 | ||
| ppGpp-dependent stationary phase induction of genes on Salmonella pathogenicity island 1. | Q40552048 | ||
| Intestinal short-chain fatty acids alter Salmonella typhimurium invasion gene expression and virulence through BarA/SirA. | Q40687509 | ||
| Pore-forming activity of type III system-secreted proteins leads to oncosis of Pseudomonas aeruginosa-infected macrophages | Q40813368 | ||
| Yersinia Ysc-Yop type III secretion feedback inhibition is relieved through YscV-dependent recognition and secretion of LcrQ. | Q41390830 | ||
| Attenuated enzootic (pestoides) isolates of Yersinia pestis express active aspartase | Q41440629 | ||
| Gene expression profiling of Yersinia pestis with deletion of lcrG, a known negative regulator for Yop secretion of type III secretion system | Q41440817 | ||
| A missense mutation causes aspartase deficiency in Yersinia pestis | Q41443948 | ||
| Microarray analysis of temperature-induced transcriptome of Yersinia pestis | Q41460599 | ||
| LcrQ/YscM1, regulators of the Yersinia yop virulon, are injected into host cells by a chaperone-dependent mechanism. | Q41478672 | ||
| YscM1 and YscM2, two Yersinia enterocolitica proteins causing downregulation of yop transcription. | Q41487121 | ||
| Modulation of virulence factor expression by pathogen target cell contact | Q41490662 | ||
| Aeromonas hydrophila AH-3 type III secretion system expression and regulatory network. | Q42570485 | ||
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| The bacterial signal molecule, ppGpp, regulates Salmonella virulence gene expression | Q44928503 | ||
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| Dynamics of adaptive microevolution of hypermutable Pseudomonas aeruginosa during chronic pulmonary infection in patients with cystic fibrosis. | Q46002328 | ||
| High-cell-density regulation of the Pseudomonas aeruginosa type III secretion system: implications for tryptophan catabolites | Q46454749 | ||
| The genetic basis of tetrathionate respiration in Salmonella typhimurium | Q50126588 | ||
| A Salmonella typhimurium mutant unable to utilize fatty acids and citrate is avirulent and immunogenic in mice | Q50130275 | ||
| Type iii protein secretion in yersinia species | Q34762503 | ||
| LcrQ blocks the role of LcrF in regulating the Ysc-Yop type III secretion genes in Yersinia pseudotuberculosis | Q35128329 | ||
| Nutritional and metabolic requirements for the infection of HeLa cells by Salmonella enterica serovar Typhimurium | Q35163250 | ||
| Intestinal inflammation allows Salmonella to use ethanolamine to compete with the microbiota | Q35409022 | ||
| METABOLISM OF MICROORGANISMS AS RELATED TO THEIR PATHOGENICITY. | Q35439983 | ||
| Plasmid virulence gene expression induced by short-chain fatty acids in Salmonella dublin: identification of rpoS-dependent and rpo-S-independent mechanisms | Q35620234 | ||
| The yersiniae--a model genus to study the rapid evolution of bacterial pathogens | Q35709112 | ||
| Phage-mediated acquisition of a type III secreted effector protein boosts growth of salmonella by nitrate respiration | Q36029218 | ||
| The PEP-pyruvate-oxaloacetate node as the switch point for carbon flux distribution in bacteria | Q36231163 | ||
| A major surface protein on group A streptococci is a glyceraldehyde-3-phosphate-dehydrogenase with multiple binding activity | Q36231622 | ||
| Temperature-controlled plasmid regulon associated with low calcium response in Yersinia pestis | Q36281599 | ||
| Consequences of aspartase deficiency in Yersinia pestis | Q36344235 | ||
| Carbon metabolism of intracellular bacteria | Q36347854 | ||
| Glyceraldehyde-3-phosphate dehydrogenase on the surface of group A streptococci is also an ADP-ribosylating enzyme | Q36513821 | ||
| NleB, a bacterial effector with glycosyltransferase activity, targets GAPDH function to inhibit NF-κB activation | Q36557738 | ||
| Effect of metabolic imbalance on expression of type III secretion genes in Pseudomonas aeruginosa | Q36575720 | ||
| On the role of specific chaperones, the specific ATPase, and the proton motive force in type III secretion. | Q36663477 | ||
| How phosphotransferase system-related protein phosphorylation regulates carbohydrate metabolism in bacteria | Q36678721 | ||
| The cyclic AMP receptor protein, CRP, is required for both virulence and expression of the minimal CRP regulon in Yersinia pestis biovar microtus. | Q36950057 | ||
| Regulation of whole bacterial pathogen transcription within infected hosts | Q37081655 | ||
| Metabolic regulation of type III secretion gene expression in Pseudomonas aeruginosa. | Q37124570 | ||
| Cross-talk between type three secretion system and metabolism in Yersinia | Q37169480 | ||
| Temporal global changes in gene expression during temperature transition in Yersinia pestis | Q37494579 | ||
| Correlations between carbon metabolism and virulence in bacteria | Q37507126 | ||
| Carbon metabolism of intracellular bacterial pathogens and possible links to virulence | Q37746934 | ||
| The Csr/Rsm system of Yersinia and related pathogens: a post-transcriptional strategy for managing virulence | Q37984185 | ||
| A global role for Fis in the transcriptional control of metabolism and type III secretion in Salmonella enterica serovar Typhimurium. | Q38338833 | ||
| Deletions in the pyruvate pathway of Salmonella Typhimurium alter SPI1-mediated gene expression and infectivity | Q39296439 | ||
| Expression of ExsA in trans confers type III secretion system-dependent cytotoxicity on noncytotoxic Pseudomonas aeruginosa cystic fibrosis isolates | Q39517996 | ||
| Activation of the Pseudomonas aeruginosa type III secretion system requires an intact pyruvate dehydrogenase aceAB operon | Q39655427 | ||
| Salmonella typhimurium loci involved in survival within macrophages | Q39860005 | ||
| Constitutive uptake and degradation of fatty acids by Yersinia pestis | Q39975155 | ||
| Genetically manipulated virulence of Yersinia enterocolitica. | Q40167837 | ||
| The central metabolism regulator EIIAGlc switches Salmonella from growth arrest to acute virulence through activation of virulence factor secretion. | Q40206932 | ||
| EFFECTS OF BICARBONATE ON GROWTH OF PASTEURELLA PESTIS. II. CARBON DIOXIDE FIXATION INTO OXALACETATE BY CELL-FREE EXTRACTS | Q40249622 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bacteria | Q10876 |
| host microbial interaction | Q68260314 | ||
| macromolecular substance | Q75174158 | ||
| P304 | page(s) | 150 | |
| P577 | publication date | 2014-10-27 | |
| P1433 | published in | Frontiers in Cellular and Infection Microbiology | Q27724376 |
| P1476 | title | Interrelationship between type three secretion system and metabolism in pathogenic bacteria | |
| P478 | volume | 4 |
| Q37838071 | A small-molecule compound belonging to a class of 2,4-disubstituted 1,3,4-thiadiazine-5-ones suppresses Salmonella infection in vivo. |
| Q26765871 | Environmental Regulation of Yersinia Pathophysiology |
| Q90400965 | Life After Secretion-Yersinia enterocolitica Rapidly Toggles Effector Secretion and Can Resume Cell Division in Response to Changing External Conditions |
| Q40480159 | Metabolic flux analyses of Pseudomonas aeruginosa cystic fibrosis isolates. |
| Q33582467 | Plasma metabolomics for the diagnosis and prognosis of H1N1 influenza pneumonia |
| Q96302537 | Pseudomonas aeruginosa core metabolism exerts a widespread growth-independent control on virulence |
| Q42290753 | The NAG Sensor NagC Regulates LEE Gene Expression and Contributes to Gut Colonization by Escherichia coli O157:H7. |
| Q93173167 | ptsI gene in the phosphotransfer system is a potential target for developing a live attenuated Salmonella vaccine |
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