| scholarly article | Q13442814 |
| P2093 | author name string | Y Xu | |
| D G Guiney | |||
| F C Fang | |||
| S J Libby | |||
| N A Buchmeier | |||
| J Switala | |||
| P C Loewen | |||
| P2860 | cites work | Oxidative stress responses in Escherichia coli and Salmonella typhimurium | Q24634713 |
| Genetic mapping of katG, a locus that affects synthesis of the bifunctional catalase-peroxidase hydroperoxidase I in Escherichia coli | Q24682447 | ||
| Multicellular oxidant defense in unicellular organisms | Q27469185 | ||
| Catalase, superoxide dismutase, and virulence of Staphylococcus aureus. In vitro and in vivo studies with emphasis on staphylococcal--leukocyte interaction | Q30449755 | ||
| Diminished neutrophil oxidative metabolism after phagocytosis of virulent Salmonella typhi. | Q30450525 | ||
| Exonuclease III and the catalase hydroperoxidase II in Escherichia coli are both regulated by the katF gene product | Q33853850 | ||
| A novel DNA-binding protein with regulatory and protective roles in starved Escherichia coli | Q33969406 | ||
| Recombination-deficient mutants of Salmonella typhimurium are avirulent and sensitive to the oxidative burst of macrophages | Q34355873 | ||
| Intracellular survival of wild-type Salmonella typhimurium and macrophage-sensitive mutants in diverse populations of macrophages | Q35088169 | ||
| Loss of catalase activity in Tn1545-induced mutants does not reduce growth of Listeria monocytogenes in vivo | Q35100963 | ||
| Mutants of Salmonella typhimurium that cannot survive within the macrophage are avirulent | Q35617117 | ||
| The effect of oxygen-dependent antimicrobial systems on strains of Legionella pneumophila of different virulence | Q36153191 | ||
| Cloning, genetic characterization, and nucleotide sequence of the hemA-prfA operon of Salmonella typhimurium | Q36179946 | ||
| Bimodal pattern of killing of DNA-repair-defective or anoxically grown Escherichia coli by hydrogen peroxide | Q36284865 | ||
| In vivo administration of recombinant growth hormone or gamma interferon activities macrophages: enhanced resistance to experimental Salmonella typhimurium infection is correlated with generation of reactive oxygen intermediates | Q36946482 | ||
| Contribution of superoxide dismutase and catalase activities to Shigella flexneri pathogenesis. | Q36977326 | ||
| The alternative sigma factor katF (rpoS) regulates Salmonella virulence | Q37346357 | ||
| Bacterial defenses against oxidative stress | Q37570468 | ||
| Genetic characterization of the stabilizing functions of a region of broad-host-range plasmid RK2. | Q37608295 | ||
| Bacterial adaptation to oxidative stress: implications for pathogenesis and interaction with phagocytic cells | Q38308873 | ||
| Salmonella as an intracellular parasite | Q38766399 | ||
| Virulence and Resistance to Superoxide, Low pH and Hydrogen Peroxide among Strains of Mycobacterium tuberculosis | Q39182715 | ||
| Plasmid vectors for the genetic analysis and manipulation of rhizobia and other gram-negative bacteria | Q39499786 | ||
| Genetic mapping of katF, a locus that with katE affects the synthesis of a second catalase species in Escherichia coli | Q39966075 | ||
| Isolation of catalase-deficient Escherichia coli mutants and genetic mapping of katE, a locus that affects catalase activity | Q39967804 | ||
| The respiratory burst of phagocytes | Q40141105 | ||
| The role of oxygen and its derivatives in microbial pathogenesis and host defense | Q40191358 | ||
| The recA+ gene product is more important than catalase and superoxide dismutase in protecting Escherichia coli against hydrogen peroxide toxicity | Q40334564 | ||
| Light emission from a Mudlux transcriptional fusion in Salmonella typhimurium is stimulated by hydrogen peroxide and by interaction with the mouse macrophage cell line J774.2. | Q40374003 | ||
| Comparison of the sensitivities of Salmonella typhimurium oxyR and katG mutants to killing by human neutrophils | Q40374459 | ||
| Positive control of a regulon for defenses against oxidative stress and some heat-shock proteins in Salmonella typhimurium | Q41771946 | ||
| Transformation with katG restores isoniazid-sensitivity in Mycobacterium tuberculosis isolates resistant to a range of drug concentrations | Q42288948 | ||
| Nucleotide sequence of katG of Salmonella typhimurium LT2 and characterization of its product, hydroperoxidase I. | Q42635405 | ||
| The correlation of biochemical virulence factors and enterotoxin production with LD50 of Salmonella typhimurium in mice | Q50188465 | ||
| Incidence, severity, and prevention of infections in chronic granulomatous disease | Q50195575 | ||
| Susceptibility of Salmonella typhimurium and Salmonella typhi to oxygen metabolites. | Q50195680 | ||
| Visualization of catalase on acrylamide gels. | Q53798813 | ||
| Catalase and superoxide dismutase in Escherichia coli | Q54497214 | ||
| Catalases HPI and HPII in Escherichia coli are induced independently. | Q54790507 | ||
| Microassays for superoxide and hydrogen peroxide production and nitroblue tetrazolium reduction using an enzyme immunoassay microplate reader | Q70167373 | ||
| A phage P22 gene controlling integration of prophage | Q72211666 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1047-1053 | |
| P577 | publication date | 1995-03-01 | |
| P1433 | published in | Journal of Clinical Investigation | Q3186904 |
| P1476 | title | DNA repair is more important than catalase for Salmonella virulence in mice | |
| P478 | volume | 95 |
| Q30669898 | A functional genomic analysis of type 3 Streptococcus pneumoniae virulence |
| Q34585540 | A novel family of regulated helicases/nucleases from Gram-positive bacteria: insights into the initiation of DNA recombination. |
| Q35139132 | Acinetobacter baumannii RecA protein in repair of DNA damage, antimicrobial resistance, general stress response, and virulence |
| Q33826314 | An antimicrobial peptide that targets DNA repair intermediates in vitro inhibits Salmonella growth within murine macrophages |
| Q35210323 | Antimicrobial actions of reactive oxygen species |
| Q28283086 | Antimicrobial reactive oxygen and nitrogen species: concepts and controversies |
| Q38924600 | Bacterial Stress Responses during Host Infection |
| Q35966527 | Bacterial infection as assessed by in vivo gene expression |
| Q34742721 | Brucella: a pathogen without classic virulence genes. |
| Q28486907 | CarD is an essential regulator of rRNA transcription required for Mycobacterium tuberculosis persistence |
| Q33971121 | Catalytic and non-catalytic roles for the mono-ADP-ribosyltransferase Arr in the mycobacterial DNA damage response. |
| Q39500741 | Characterization of Escherichia coli DNA lesions generated within J774 macrophages |
| Q47244865 | Characterization of Invasive Salmonella Serogroup C1 Infections in Mali |
| Q35210751 | Characterization of the RpoS status of clinical isolates of Salmonella enterica |
| Q33594007 | Characterization of the mycobacterial AdnAB DNA motor provides insights into the evolution of bacterial motor-nuclease machines |
| Q35598618 | Cloning and characterization of the katB gene of Pseudomonas aeruginosa encoding a hydrogen peroxide-inducible catalase: purification of KatB, cellular localization, and demonstration that it is essential for optimal resistance to hydrogen peroxide |
| Q24649162 | Constraint-based analysis of metabolic capacity of Salmonella typhimurium during host-pathogen interaction |
| Q53704376 | Conversion of RpoS- Attenuated Salmonella enterica Serovar Typhi Vaccine Strains to RpoS+ Improves Their Resistance to Host Defense Barriers. |
| Q33838288 | DNA damage and reactive nitrogen species are barriers to Vibrio cholerae colonization of the infant mouse intestine |
| Q38821378 | Distinct innate responses are induced by attenuated Salmonella enterica serovar Typhimurium mutants. |
| Q41140854 | Dynamics of growth and death within a Salmonella typhimurium population during infection of macrophages |
| Q39760069 | Effect of growth temperature on Crl-dependent regulation of sigmaS activity in Salmonella enterica serovar Typhimurium |
| Q34002586 | Effect of mutS and recD mutations on Salmonella virulence |
| Q50025600 | Effects of hydrogen peroxide on the motility, catalase and superoxide dismutase of dam and/or seqA mutant of Salmonella typhimurium |
| Q24643457 | Efficient translation of the RpoS sigma factor in Salmonella typhimurium requires host factor I, an RNA-binding protein encoded by the hfq gene |
| Q42799573 | Enterococcus faecalis mutations affecting virulence in the Caenorhabditis elegans model host |
| Q34231035 | Fusidic acid-resistant mutants of Salmonella enterica serovar Typhimurium with low fitness in vivo are defective in RpoS induction. |
| Q34123367 | Genetic and redox determinants of nitric oxide cytotoxicity in a Salmonella typhimurium model |
| Q30884913 | Genome wide evolutionary analyses reveal serotype specific patterns of positive selection in selected Salmonella serotypes |
| Q38037547 | Haemophilus influenzae and oxidative stress |
| Q33997234 | Hydrogen peroxide fluxes and compartmentalization inside growing Escherichia coli |
| Q25255677 | Hydrogen peroxide scavenging is not a virulence determinant in the pathogenesis of Haemophilus influenzae type b strain Eagan |
| Q42645499 | Identification of a non-haem catalase in Salmonella and its regulation by RpoS (sigmaS). |
| Q42159933 | Importance of catalase in the adaptive response to hydrogen peroxide: analysis of acatalasaemic Saccharomyces cerevisiae |
| Q34008406 | In vitro and in vivo assessment of Salmonella enterica serovar Typhimurium DT104 virulence |
| Q35168489 | Inhibition of bacterial DNA replication by zinc mobilization during nitrosative stress |
| Q33921859 | Live recombinant Salmonella Typhi vaccines constructed to investigate the role of rpoS in eliciting immunity to a heterologous antigen |
| Q36736283 | Loss of Multicellular Behavior in Epidemic African Nontyphoidal Salmonella enterica Serovar Typhimurium ST313 Strain D23580. |
| Q28501841 | Mechanism of nonhomologous end-joining in mycobacteria: a low-fidelity repair system driven by Ku, ligase D and ligase C |
| Q34007536 | Mycobacterium bovis BCG recA deletion mutant shows increased susceptibility to DNA-damaging agents but wild-type survival in a mouse infection model. |
| Q34560917 | Neisseria gonorrhoeae DNA recombination and repair enzymes protect against oxidative damage caused by hydrogen peroxide |
| Q40054491 | Neutrophils to the ROScue: Mechanisms of NADPH Oxidase Activation and Bacterial Resistance |
| Q35894834 | Non-heme manganese catalase--the 'other' catalase |
| Q33963146 | Overexpression of the recA gene decreases oral but not intraperitoneal fitness of Salmonella enterica |
| Q35910961 | Oxidative stress enzymes are required for DAF-16-mediated immunity due to generation of reactive oxygen species by Caenorhabditis elegans |
| Q33740986 | Periplasmic superoxide dismutase protects Salmonella from products of phagocyte NADPH-oxidase and nitric oxide synthase. |
| Q35598786 | Peroxide stimulon and role of PerR in group A Streptococcus |
| Q33420369 | Phagocytic superoxide specifically damages an extracytoplasmic target to inhibit or kill Salmonella |
| Q30833778 | Phylogenomic analysis of natural selection pressure in Streptococcus genomes |
| Q35759680 | Physiological effects of Crl in Salmonella are modulated by sigmaS level and promoter specificity |
| Q33840580 | Reactive nitrogen intermediates and the pathogenesis of Salmonella and mycobacteria |
| Q41010019 | RecA versus catalase: who's on first? |
| Q36198016 | Redox active thiol sensors of oxidative and nitrosative stress |
| Q58790706 | Reduce, Induce, Thrive: Bacterial Redox Sensing during Pathogenesis |
| Q36970833 | Redundant catalases detoxify phagocyte reactive oxygen and facilitate Histoplasma capsulatum pathogenesis |
| Q37247851 | Redundant hydrogen peroxide scavengers contribute to Salmonella virulence and oxidative stress resistance. |
| Q33595947 | Regulation of Brucella abortus catalase |
| Q37363200 | Regulation of bacterial virulence gene expression by the host environment |
| Q35132152 | Responses to reactive oxygen intermediates and virulence of Salmonella typhimurium |
| Q31082848 | Rhodococcus equi's extreme resistance to hydrogen peroxide is mainly conferred by one of its four catalase genes |
| Q41235661 | Role of Escherichia coli rpoS and associated genes in defense against oxidative damage |
| Q29346764 | Role of Pseudomonas aeruginosa dinB-encoded DNA polymerase IV in mutagenesis |
| Q35689430 | Role of RpoS in fine-tuning the synthesis of Vi capsular polysaccharide in Salmonella enterica serotype Typhi |
| Q39516878 | Role of catalase in Campylobacter jejuni intracellular survival |
| Q34161257 | Salmonella acquires ferrous iron from haemophagocytic macrophages |
| Q92823213 | Salmonella and Reactive Oxygen Species: A Love-Hate Relationship |
| Q39656301 | Salmonella enterica serovar Typhimurium periplasmic superoxide dismutases SodCI and SodCII are required for protection against the phagocyte oxidative burst |
| Q37099435 | Salmonella enterica serovar typhimurium strains with regulated delayed attenuation in vivo |
| Q34469840 | Salmonella evasion of the NADPH phagocyte oxidase |
| Q40826516 | Salmonella typhimurium mutants that downregulate phagocyte nitric oxide production |
| Q40020029 | Selection against the dihydrofolate reductase-thymidylate synthase (DHFR-TS) locus as a probe of genetic alterations in Leishmania major. |
| Q35973388 | Small-molecule inhibitors of bacterial AddAB and RecBCD helicase-nuclease DNA repair enzymes |
| Q89548709 | Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway |
| Q34353973 | The Brucella abortus xthA-1 gene product participates in base excision repair and resistance to oxidative killing but is not required for wild-type virulence in the mouse model |
| Q33756294 | The Salmonella typhimurium AhpC polypeptide is not essential for virulence in BALB/c mice but is recognized as an antigen during infection |
| Q47115917 | The Sit-and-Wait Hypothesis in Bacterial Pathogens: A Theoretical Study of Durability and Virulence |
| Q34000770 | The alternative sigma factor, sigmaE, is critically important for the virulence of Salmonella typhimurium |
| Q35549402 | The ferritin-like Dps protein is required for Salmonella enterica serovar Typhimurium oxidative stress resistance and virulence |
| Q35044792 | The interplay between Salmonella typhimurium and its macrophage host--what can it teach us about innate immunity? |
| Q33728733 | The periplasmic, group III catalase of Vibrio fischeri is required for normal symbiotic competence and is induced both by oxidative stress and by approach to stationary phase |
| Q35546681 | The spv genes on the Salmonella dublin virulence plasmid are required for severe enteritis and systemic infection in the natural host. |
| Q33876934 | Thiol peroxidase protects Salmonella enterica from hydrogen peroxide stress in vitro and facilitates intracellular growth |
| Q33717130 | Toxic effects of modified fenton reactions on xanthobacter flavus FB71 |
| Q57632263 | Virulence of Pasteurella multocida recA mutants |
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