scholarly article | Q13442814 |
P2093 | author name string | Finlay BB | |
DeVinney R | |||
Goosney D | |||
Gauthier A | |||
Puente JL | |||
P2860 | cites work | Genome sequence of enterohaemorrhagic Escherichia coli O157:H7 | Q22122385 |
Neural Wiskott-Aldrich syndrome protein is implicated in the actin-based motility of Shigella flexneri | Q24533240 | ||
Wiskott-Aldrich syndrome protein physically associates with Nck through Src homology 3 domains | Q24651136 | ||
Crystal structure of enteropathogenic Escherichia coli intimin-receptor complex | Q27625285 | ||
SH2 domains recognize specific phosphopeptide sequences | Q27860748 | ||
A complex of N-WASP and WIP integrates signalling cascades that lead to actin polymerization | Q28139787 | ||
GRB2 links signaling to actin assembly by enhancing interaction of neural Wiskott-Aldrich syndrome protein (N-WASp) with actin-related protein (ARP2/3) complex | Q28142883 | ||
Iha: a novel Escherichia coli O157:H7 adherence-conferring molecule encoded on a recently acquired chromosomal island of conserved structure | Q30839913 | ||
Two enteropathogenic Escherichia coli type III secreted proteins, EspA and EspB, are virulence factors | Q31975587 | ||
Enteropathogenic E. coli Tir binds Nck to initiate actin pedestal formation in host cells | Q33292526 | ||
The Epidemiology of Infections Caused by Escherichia coli O157: H7, Other Enterohemorrhagic E. coli, and the Associated Hemolytic Uremic Syndrome | Q33375970 | ||
Illnesses associated with Escherichia coli O157:H7 infections. A broad clinical spectrum | Q33445897 | ||
How WASP-family proteins and the Arp2/3 complex convert intracellular signals into cytoskeletal structures | Q33840324 | ||
Role of the eaeA gene in experimental enteropathogenic Escherichia coli infection | Q33902441 | ||
Role of tir and intimin in the virulence of rabbit enteropathogenic Escherichia coli serotype O103:H2. | Q34003963 | ||
Role of EspB in experimental human enteropathogenic Escherichia coli infection | Q34004849 | ||
Enteropathogenic E. coli acts through WASP and Arp2/3 complex to form actin pedestals | Q39254264 | ||
Interaction of enteropathogenic or enterohemorrhagic Escherichia coli with HeLa cells results in translocation of cortactin to the bacterial adherence site | Q39513832 | ||
Recruitment of cytoskeletal and signaling proteins to enteropathogenic and enterohemorrhagic Escherichia coli pedestals | Q39520034 | ||
Mechanical fractionation reveals structural requirements for enteropathogenic Escherichia coli Tir insertion into host membranes | Q39538062 | ||
The complete DNA sequence and analysis of the large virulence plasmid of Escherichia coli O157:H7. | Q39724981 | ||
Diarrhea Due to Escherichia coli in the Rabbit: A Novel Mechanism | Q40758321 | ||
-Actinin Accumulation in Epithelial Cells Infected with Attaching and Effacing Gastrointestinal Pathogens | Q41277263 | ||
Insertion of EspD into epithelial target cell membranes by infecting enteropathogenic Escherichia coli | Q41483133 | ||
A plasmid-encoded type IV fimbrial gene of enteropathogenic Escherichia coli associated with localized adherence | Q42601818 | ||
Identification of a novel genetic locus that is required for in vitro adhesion of a clinical isolate of enterohaemorrhagic Escherichia coli to epithelial cells. | Q42617902 | ||
The complete sequence of the locus of enterocyte effacement (LEE) from enteropathogenic Escherichia coli E2348/69. | Q42677853 | ||
Enterohaemorrhagic Escherichia coli O157:H7 target Peyer's patches in humans and cause attaching/effacing lesions in both human and bovine intestine | Q43086295 | ||
Actin-based motility of vaccinia virus mimics receptor tyrosine kinase signalling. | Q45746416 | ||
Complete nucleotide sequences of 93-kb and 3.3-kb plasmids of an enterohemorrhagic Escherichia coli O157:H7 derived from Sakai outbreak | Q47969070 | ||
Enteropathogenic E. coli (EPEC) transfers its receptor for intimate adherence into mammalian cells | Q48042079 | ||
Parallel evolution of virulence in pathogenic Escherichia coli | Q50120324 | ||
A cloned pathogenicity island from enteropathogenic Escherichia coli confers the attaching and effacing phenotype on E. coli K-12. | Q54574143 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
Enteropathogenic Escherichia coli | Q13419512 | ||
enteropathogen | Q63500873 | ||
P304 | page(s) | 1445-1458 | |
P577 | publication date | 2001-09-01 | |
P1433 | published in | Molecular Microbiology | Q6895967 |
P1476 | title | Enterohaemorrhagic and enteropathogenic Escherichia coli use a different Tir-based mechanism for pedestal formation | |
P478 | volume | 41 |
Q43936783 | A tyrosine-phosphorylated 12-amino-acid sequence of enteropathogenic Escherichia coli Tir binds the host adaptor protein Nck and is required for Nck localization to actin pedestals |
Q45207808 | Actin and alpha-actinin dynamics in the adhesion and motility of EPEC and EHEC on host cells |
Q28292054 | Actin-dependent movement of bacterial pathogens |
Q35142691 | Adhesion of enteropathogenic Escherichia coli to host cells. |
Q33380835 | All blood, no stool: enterohemorrhagic Escherichia coli O157:H7 infection |
Q40953710 | Amino acid residues within enterohemorrhagic Escherichia coli O157:H7 Tir involved in phosphorylation, alpha-actinin recruitment, and Nck-independent pedestal formation |
Q24805862 | Analysis of host response to bacterial infection using error model based gene expression microarray experiments. |
Q37021415 | Attaching effacing Escherichia coli and paradigms of Tir-triggered actin polymerization: getting off the pedestal |
Q33872252 | Bacterial and host determinants of MAL activation upon EPEC infection: the roles of Tir, ABRA, and FLRT3 |
Q34713695 | Change is good: variations in common biological mechanisms in the epsilonproteobacterial genera Campylobacter and Helicobacter |
Q43254870 | Conditioned medium from enterohemorrhagic Escherichia coli-infected T84 cells inhibits signal transducer and activator of transcription 1 activation by gamma interferon |
Q30159835 | Cortactin is essential for F-actin assembly in enteropathogenic Escherichia coli (EPEC)- and enterohaemorrhagic E. coli (EHEC)-induced pedestals and the alpha-helical region is involved in the localization of cortactin to bacterial attachment sites |
Q35193511 | Current progress in enteropathogenic and enterohemorrhagic Escherichia coli vaccines |
Q37755414 | Cytoskeleton-modulating effectors of enteropathogenic and enterohaemorrhagic Escherichia coli: Tir, EspFU and actin pedestal assembly |
Q39741576 | Differential modulation by Ca2+ of type III secretion of diffusely adhering enteropathogenic Escherichia coli |
Q54457370 | Enterohaemorrhagic Escherichia coli Tir requires a C-terminal 12-residue peptide to initiate EspF-mediated actin assembly and harbours N-terminal sequences that influence pedestal length. |
Q40592357 | Enterohaemorrhagic and enteropathogenic Escherichia coli use different mechanisms for actin pedestal formation that converge on N-WASP. |
Q39730042 | Enterohemorrhagic Escherichia coli O157:H7 disrupts Stat1-mediated gamma interferon signal transduction in epithelial cells |
Q64096526 | Enteropathogenic Escherichia coli Stimulates Effector-Driven Rapid Caspase-4 Activation in Human Macrophages |
Q52569420 | Enteropathogenic Escherichia coli Tir translocation and pedestal formation requires membrane cholesterol in the absence of bundle-forming pili. |
Q28590623 | Enteropathogenic Escherichia coli and vaccinia virus do not require the family of WASP-interacting proteins for pathogen-induced actin assembly |
Q36104202 | Enteropathogenic and enterohemorrhagic Escherichia coli infections: translocation, translocation, translocation |
Q42973812 | Environmental cues and symbiont microbe-associated molecular patterns function in concert to drive the daily remodelling of the crypt-cell brush border of the Euprymna scolopes light organ |
Q41753440 | EspFU, a type III-translocated effector of actin assembly, fosters epithelial association and late-stage intestinal colonization by E. coli O157:H7. |
Q36438769 | Exploiting pathogenic Escherichia coli to model transmembrane receptor signalling |
Q40719063 | Host focal adhesion protein domains that bind to the translocated intimin receptor (Tir) of enteropathogenic Escherichia coli (EPEC). |
Q38631456 | Identification of regions within the Legionella pneumophila VipA effector protein involved in actin binding and polymerization and in interference with eukaryotic organelle trafficking. |
Q33999847 | Interactions with M cells and macrophages as key steps in the pathogenesis of enterohemorrhagic Escherichia coli infections |
Q38127457 | Intimate host attachment: enteropathogenic and enterohaemorrhagic Escherichia coli |
Q30492670 | Invasive and adherent bacterial pathogens co-Opt host clathrin for infection |
Q30009263 | Nck adaptors, besides promoting N-WASP mediated actin-nucleation activity at pedestals, influence the cellular levels of enteropathogenic Escherichia coli Tir effector |
Q39387553 | Nexilin is a dynamic component of Listeria monocytogenes and enteropathogenic Escherichia coli actin-rich structures |
Q35923564 | Pathogen-induced actin filament rearrangement in infectious diseases. |
Q41845103 | Phosphorylated YDXV motifs and Nck SH2/SH3 adaptors act cooperatively to induce actin reorganization |
Q41820150 | Role for CD2AP and other endocytosis-associated proteins in enteropathogenic Escherichia coli pedestal formation |
Q46809881 | Role of EHEC O157:H7 virulence factors in the activation of intestinal epithelial cell NF-kappaB and MAP kinase pathways and the upregulated expression of interleukin 8. |
Q34975645 | Role of Escherichia coli O157:H7 virulence factors in colonization at the bovine terminal rectal mucosa |
Q88737469 | SM22 is required for the maintenance of actin-rich structures generated during bacterial infections |
Q33883322 | SepZ/EspZ is secreted and translocated into HeLa cells by the enteropathogenic Escherichia coli type III secretion system |
Q30418173 | Serine protease EspP from enterohemorrhagic Escherichia coli is sufficient to induce shiga toxin macropinocytosis in intestinal epithelium |
Q30360953 | Shiga toxin 2a and Enteroaggregative Escherichia coli--a deadly combination |
Q37816402 | Sticky situation: localized adherence of enteropathogenic Escherichia coli to the small intestine epithelium |
Q30362055 | The presence of the pAA plasmid in the German O104:H4 Shiga toxin type 2a (Stx2a)-producing enteroaggregative Escherichia coli strain promotes the translocation of Stx2a across an epithelial cell monolayer |
Q33908381 | The spectrin cytoskeleton is crucial for adherent and invasive bacterial pathogenesis. |
Q40138256 | Tir phosphorylation and Nck/N-WASP recruitment by enteropathogenic and enterohaemorrhagic Escherichia coli during ex vivo colonization of human intestinal mucosa is different to cell culture models |
Q33883293 | Tyrosine phosphorylation of the chlamydial effector protein Tarp is species specific and not required for recruitment of actin |
Q35176257 | Virulence of enteropathogenic Escherichia coli, a global pathogen |
Q27323111 | Visualizing the Translocation and Localization of Bacterial Type III Effector Proteins by Using a Genetically Encoded Reporter System |
Q33769710 | tir- and stx-positive Escherichia coli in stream waters in a metropolitan area |
Search more.