scholarly article | Q13442814 |
P2093 | author name string | Altuvia S | |
Rosenshine I | |||
Kohen R | |||
Elgrably-Weiss M | |||
Schlosser-Silverman E | |||
P2860 | cites work | Mutation Caused by Human Phagocytes | Q50216797 |
H2O2-driven reduction of the Fe3+-quin2 chelate and the subsequent formation of oxidizing species | Q73695202 | ||
The crystal structure of Dps, a ferritin homolog that binds and protects DNA | Q27749085 | ||
FACS-optimized mutants of the green fluorescent protein (GFP) | Q29547322 | ||
The ability of Salmonella to enter mammalian cells is affected by bacterial growth state | Q33616743 | ||
Linkage map of Salmonella typhimurium, Edition VI | Q33628173 | ||
Oxidative stress | Q33632507 | ||
Periplasmic superoxide dismutase protects Salmonella from products of phagocyte NADPH-oxidase and nitric oxide synthase. | Q33740986 | ||
The Salmonella typhimurium AhpC polypeptide is not essential for virulence in BALB/c mice but is recognized as an antigen during infection | Q33756294 | ||
DNA damage and oxygen radical toxicity | Q34172435 | ||
A set of lacZ mutations in Escherichia coli that allow rapid detection of each of the six base substitutions | Q34290231 | ||
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 | ||
Role of Salmonella typhimurium Mn-superoxide dismutase (SodA) in protection against early killing by J774 macrophages. | Q35408581 | ||
DNA repair is more important than catalase for Salmonella virulence in mice | Q35552688 | ||
The transcriptional regulator SoxS is required for resistance of Salmonella typhimurium to paraquat but not for virulence in mice | Q35561401 | ||
Nitric oxide potentiates hydrogen peroxide-induced killing of Escherichia coli. | Q36365394 | ||
Virulent Salmonella typhimurium has two periplasmic Cu, Zn-superoxide dismutases | Q36398159 | ||
Regulation of ribosomal RNA promoters with a synthetic lac operator | Q37576600 | ||
Relapsing Salmonella enteritidis infection in a young adult male with chronic granulomatous disease | Q38650890 | ||
Aromatic-dependent Salmonella typhimurium are non-virulent and effective as live vaccines | Q39513114 | ||
Protection of DNA during oxidative stress by the nonspecific DNA-binding protein Dps. | Q39846834 | ||
Comparison of the sensitivities of Salmonella typhimurium oxyR and katG mutants to killing by human neutrophils | Q40374459 | ||
Multiple beta 1 chain integrins are receptors for invasin, a protein that promotes bacterial penetration into mammalian cells | Q41511934 | ||
Phenotype of mice and macrophages deficient in both phagocyte oxidase and inducible nitric oxide synthase. | Q45274479 | ||
A small, stable RNA induced by oxidative stress: role as a pleiotropic regulator and antimutator | Q48047346 | ||
High mutation frequencies among Escherichia coli and Salmonella pathogens | Q48057867 | ||
Salmonella pathogenicity island 2-dependent evasion of the phagocyte NADPH oxidase | Q50122203 | ||
Incidence, severity, and prevention of infections in chronic granulomatous disease | Q50195575 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | macrophage | Q184204 |
Escherichia coli | Q25419 | ||
P1104 | number of pages | 6 | |
P304 | page(s) | 5225-5230 | |
P577 | publication date | 2000-09-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Characterization of Escherichia coli DNA lesions generated within J774 macrophages | |
P478 | volume | 182 |
Q34315068 | A Salmonella enterica serovar typhimurium hemA mutant is highly susceptible to oxidative DNA damage |
Q37629621 | A long-term epigenetic memory switch controls bacterial virulence bimodality |
Q40282609 | A novel category of enteropathogenic Escherichia coli simultaneously utilizes the Nck and TccP pathways to induce actin remodelling. |
Q34585540 | A novel family of regulated helicases/nucleases from Gram-positive bacteria: insights into the initiation of DNA recombination. |
Q54213943 | A requirement for septins and the autophagy receptor p62 in the proliferation of intracellular Shigella. |
Q33826314 | An antimicrobial peptide that targets DNA repair intermediates in vitro inhibits Salmonella growth within murine macrophages |
Q36588950 | Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans |
Q37901961 | Base excision and nucleotide excision repair pathways in mycobacteria |
Q36710744 | Beta-hydroxybutyrate abrogates formation of bovine neutrophil extracellular traps and bactericidal activity against mammary pathogenic Escherichia coli |
Q34462401 | Binding to Na(+) /H(+) exchanger regulatory factor 2 (NHERF2) affects trafficking and function of the enteropathogenic Escherichia coli type III secretion system effectors Map, EspI and NleH. |
Q34045574 | Carbonic anhydrase is essential for Streptococcus pneumoniae growth in environmental ambient air. |
Q40241367 | Characterization of TccP-mediated N-WASP activation during enterohaemorrhagic Escherichia coli infection |
Q40326388 | Characterization of enteropathogenic Escherichia coli mutants that fail to disrupt host cell spreading and attachment to substratum |
Q30157618 | Cortactin recruitment by enterohemorrhagic Escherichia coli O157:H7 during infection in vitro and ex vivo |
Q34295655 | Cycling of Etk and Etp phosphorylation states is involved in formation of group 4 capsule by Escherichia coli |
Q33775617 | Direct injection of functional single-domain antibodies from E. coli into human cells |
Q37474918 | Direct observation of single stationary-phase bacteria reveals a surprisingly long period of constant protein production activity |
Q33621525 | Dissecting the role of the Tir:Nck and Tir:IRTKS/IRSp53 signalling pathways in vivo |
Q34191816 | DnaE2 polymerase contributes to in vivo survival and the emergence of drug resistance in Mycobacterium tuberculosis |
Q35020400 | Drug targets in mycobacterial sulfur metabolism |
Q42796756 | Dynamics of expression and maturation of the type III secretion system of enteropathogenic Escherichia coli |
Q36422086 | Enteropathogenic Escherichia coli O125:H6 triggers attaching and effacing lesions on human intestinal biopsy specimens independently of Nck and TccP/TccP2. |
Q41862570 | Enteropathogenic Escherichia coli type III effectors EspG and EspG2 disrupt the microtubule network of intestinal epithelial cells |
Q34739814 | Enteropathogenic and enterohemorrhagic Escherichia coli type III secretion effector EspV induces radical morphological changes in eukaryotic cells |
Q42085878 | EspJ of enteropathogenic and enterohaemorrhagic Escherichia coli inhibits opsono-phagocytosis |
Q39915122 | EspT triggers formation of lamellipodia and membrane ruffles through activation of Rac-1 and Cdc42. |
Q42103443 | EspZ of enteropathogenic and enterohemorrhagic Escherichia coli regulates type III secretion system protein translocation |
Q40142217 | FNR Regulates the Expression of Important Virulence Factors Contributing to the Pathogenicity of Avian Pathogenic Escherichia coli |
Q39110732 | Helicobacter pylori genes involved in avoidance of mutations induced by 8-oxoguanine |
Q40328880 | Host cell attachment elicits posttranscriptional regulation in infecting enteropathogenic bacteria. |
Q40507118 | Identification of Salmonella typhimurium genes responsible for interference with peptide presentation on MHC class I molecules: Deltayej Salmonella mutants induce superior CD8+ T-cell responses |
Q40705484 | Identification of a novel Citrobacter rodentium type III secreted protein, EspI, and roles of this and other secreted proteins in infection |
Q41850747 | Identification of amino acid residues within the N-terminal domain of EspA that play a role in EspA filament biogenesis and function |
Q42875394 | Identification of an Escherichia coli operon required for formation of the O-antigen capsule |
Q39254914 | Increased survival of antibiotic-resistant Escherichia coli inside macrophages |
Q92030122 | Intraepithelial neutrophils in mammary, urinary and gall bladder infections |
Q40731104 | Ler is a negative autoregulator of the LEE1 operon in enteropathogenic Escherichia coli |
Q38766756 | Mitochondria mediate septin cage assembly to promote autophagy of Shigella |
Q41845486 | Mutational analysis of the locus of enterocyte effacement-encoded regulator (Ler) of enteropathogenic Escherichia coli |
Q42713418 | N-terminal type III secretion signal of enteropathogenic Escherichia coli translocator proteins |
Q35095367 | New targets and inhibitors of mycobacterial sulfur metabolism. |
Q30479103 | Noise in timing and precision of gene activities in a genetic cascade |
Q34298692 | PafR, a novel transcription regulator, is important for pathogenesis in uropathogenic Escherichia coli. |
Q24554222 | Pathogen DNA as target for host-generated oxidative stress: role for repair of bacterial DNA damage in Helicobacter pylori colonization |
Q33420369 | Phagocytic superoxide specifically damages an extracytoplasmic target to inhibit or kill Salmonella |
Q40439695 | Polarity of enteropathogenic Escherichia coli EspA filament assembly and protein secretion |
Q33340911 | Quantitative kinetic analysis of the bacteriophage lambda genetic network |
Q34976514 | RecA and RadA proteins of Brucella abortus do not perform overlapping protective DNA repair functions following oxidative burst. |
Q34105911 | Role of the RecBCD recombination pathway in Salmonella virulence. |
Q50043378 | Salmonella detoxifying enzymes are sufficient to cope with the host oxidative burst |
Q42375349 | SepL resembles an aberrant effector in binding to a class 1 type III secretion chaperone and carrying an N-terminal secretion signal |
Q60302896 | Septins Recognize and Entrap Dividing Bacterial Cells for Delivery to Lysosomes |
Q24641915 | Small RNAs encoded within genetic islands of Salmonella typhimurium show host-induced expression and role in virulence |
Q42815784 | Subversion of actin dynamics by EspM effectors of attaching and effacing bacterial pathogens |
Q40103041 | T3SS-dependent microvascular thrombosis and ischemic enteritis in human gut xenografts infected with enteropathogenic Escherichia coli. |
Q40495870 | TccP is an enterohaemorrhagic Escherichia coli O157:H7 type III effector protein that couples Tir to the actin-cytoskeleton |
Q35689242 | TccP2 of O157:H7 and non-O157 enterohemorrhagic Escherichia coli (EHEC): challenging the dogma of EHEC-induced actin polymerization |
Q33910276 | TccP2-mediated subversion of actin dynamics by EPEC 2 - a distinct evolutionary lineage of enteropathogenic Escherichia coli |
Q54259627 | The Bacteriophage Lambda CII Phenotypes for Complementation, Cellular Toxicity and Replication Inhibition Are Suppressed in cII-oop Constructs Expressing the Small RNA OOP. |
Q33455516 | The Base Excision Repair system of Salmonella enterica serovar typhimurium counteracts DNA damage by host nitric oxide |
Q38718455 | The Enterohemorrhagic Escherichia coli Effector EspW Triggers Actin Remodeling in a Rac1-Dependent Manner |
Q33518483 | The T3SS effector EspT defines a new category of invasive enteropathogenic E. coli (EPEC) which form intracellular actin pedestals |
Q90474195 | The Third Transmembrane Domain of EscR Is Critical for Function of the Enteropathogenic Escherichia coli Type III Secretion System |
Q42373973 | The WxxxE effector EspT triggers expression of immune mediators in an Erk/JNK and NF-κB-dependent manner |
Q42708074 | The enteropathogenic Escherichia coli effector NleH inhibits apoptosis induced by Clostridium difficile toxin B. |
Q34506955 | The enteropathogenic Escherichia coli type III secretion system effector Map binds EBP50/NHERF1: implication for cell signalling and diarrhoea |
Q39910582 | The mechanisms used by enteropathogenic Escherichia coli to control filopodia dynamics |
Q34596147 | The type III secretion effector NleF of enteropathogenic Escherichia coli activates NF-κB early during infection |
Q24563309 | Transcriptional response of Candida albicans upon internalization by macrophages |
Q34164992 | Vimentin is secreted by activated macrophages |
Q24597091 | sRNAs and the virulence of Salmonella enterica serovar Typhimurium |
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