| scholarly article | Q13442814 |
| P50 | author | Guy Tran Van Nhieu | Q33275946 |
| P2093 | author name string | Julie Guignot | |
| P2860 | cites work | Annexin A8 displays unique phospholipid and F-actin binding properties | Q24320766 |
| Small-Molecule Inhibitors of the Type III Secretion System | Q26781403 | ||
| Bacterial serine proteases secreted by the autotransporter pathway: classification, specificity, and role in virulence | Q26828625 | ||
| Damage control: cellular mechanisms of plasma membrane repair | Q27022016 | ||
| More than a pore: the cellular response to cholesterol-dependent cytolysins | Q27023593 | ||
| The IpaC carboxyterminal effector domain mediates Src-dependent actin polymerization during Shigella invasion of epithelial cells | Q27318175 | ||
| Structure of a bacterial type III secretion system in contact with a host membrane in situ | Q27340227 | ||
| The Structures of Coiled-Coil Domains from Type III Secretion System Translocators Reveal Homology to Pore-Forming Toxins | Q27677178 | ||
| A bacterial type III secretion system inhibits actin polymerization to prevent pore formation in host cell membranes | Q28360416 | ||
| The type III secretion injectisome | Q29617944 | ||
| K⁺ efflux is the common trigger of NLRP3 inflammasome activation by bacterial toxins and particulate matter | Q29620146 | ||
| Port of entry--the type III secretion translocon | Q30320840 | ||
| The role of potassium in inflammasome activation by bacteria | Q30494136 | ||
| Spontaneous formation of IpaB ion channels in host cell membranes reveals how Shigella induces pyroptosis in macrophages | Q30525355 | ||
| S100A11 is required for efficient plasma membrane repair and survival of invasive cancer cells | Q30578437 | ||
| Injection of Pseudomonas aeruginosa Exo toxins into host cells can be modulated by host factors at the level of translocon assembly and/or activity | Q31047709 | ||
| Proinflammatory interactions of pneumolysin with human neutrophils. | Q31918190 | ||
| Cytoskeleton-modulating effectors of enteropathogenic and enterohemorrhagic Escherichia coli: role of EspL2 in adherence and an alternative pathway for modulating cytoskeleton through Annexin A2 function | Q33389611 | ||
| Innate immune detection of the type III secretion apparatus through the NLRC4 inflammasome | Q33733606 | ||
| Nlrc4/Ipaf/CLAN/CARD12: more than a flagellin sensor | Q33823658 | ||
| Enterohaemorrhagic Escherichia coli haemolysin is cleaved and inactivated by serine protease EspPα | Q33830049 | ||
| The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes | Q33878820 | ||
| A Yersinia effector protein promotes virulence by preventing inflammasome recognition of the type III secretion system | Q33906693 | ||
| The type III secretion system tip complex and translocon. | Q34011259 | ||
| Translocators YopB and YopD from Yersinia enterocolitica form a multimeric integral membrane complex in eukaryotic cell membranes | Q34048607 | ||
| Structure, biological functions and applications of the AB5 toxins | Q34102115 | ||
| Type III secretion in Yersinia: injectisome or not? | Q34270387 | ||
| Distinct contributions of interleukin-1α (IL-1α) and IL-1β to innate immune recognition of Pseudomonas aeruginosa in the lung. | Q34298681 | ||
| Annexin 2 is a phosphatidylinositol (4,5)-bisphosphate binding protein recruited to actin assembly sites at cellular membranes | Q34330170 | ||
| Analysis of the function of enteropathogenic Escherichia coli EspB by random mutagenesis | Q34334195 | ||
| Role of pore-forming toxins in bacterial infectious diseases | Q34346202 | ||
| Influence of oligomerization state on the structural properties of invasion plasmid antigen B from Shigella flexneri in the presence and absence of phospholipid membranes. | Q34389407 | ||
| Caspase-1 activation of lipid metabolic pathways in response to bacterial pore-forming toxins promotes cell survival | Q34567790 | ||
| Bacterial pore-forming toxins: the (w)hole story? | Q34711740 | ||
| Caspase-11 activation in response to bacterial secretion systems that access the host cytosol. | Q34769269 | ||
| Visualization of the type III secretion sorting platform of Shigella flexneri | Q35037858 | ||
| Identification of mammalian proteins that collaborate with type III secretion system function: involvement of a chemokine receptor in supporting translocon activity | Q35111099 | ||
| Inflammasome activation in response to the Yersinia type III secretion system requires hyperinjection of translocon proteins YopB and YopD. | Q35111107 | ||
| AB toxins: a paradigm switch from deadly to desirable | Q35155875 | ||
| Escherichia coli α-hemolysin counteracts the anti-virulence innate immune response triggered by the Rho GTPase activating toxin CNF1 during bacteremia | Q35187869 | ||
| Functional analysis of the Shigella flexneri IpaC invasin by insertional mutagenesis. | Q35546085 | ||
| The Serine Protease EspC from Enteropathogenic Escherichia coli Regulates Pore Formation and Cytotoxicity Mediated by the Type III Secretion System. | Q35680038 | ||
| An emergency response team for membrane repair | Q36146942 | ||
| Immune recognition of Pseudomonas aeruginosa mediated by the IPAF/NLRC4 inflammasome. | Q36294419 | ||
| Phospholipases C and A2 control lysosome-mediated IL-1 beta secretion: Implications for inflammatory processes | Q36448740 | ||
| Repair of injured plasma membrane by rapid Ca2+-dependent endocytosis | Q36491740 | ||
| Activation of cytosolic phospholipase A2alpha in resident peritoneal macrophages by Listeria monocytogenes involves listeriolysin O and TLR2. | Q36543744 | ||
| General aspects and recent advances on bacterial protein toxins | Q36554621 | ||
| Salmonella Promotes ASC Oligomerization-dependent Caspase-1 Activation. | Q36592793 | ||
| Current fluctuation analysis of the PopB and PopD translocon components of the Pseudomonas aeruginosa type III secretion system. | Q36742777 | ||
| The role of the inflammasome in cellular responses to toxins and bacterial effectors | Q36931668 | ||
| Two-way traffic on the road to plasma membrane repair | Q36995027 | ||
| The Annexin A2/p11 complex is required for efficient invasion of Salmonella Typhimurium in epithelial cells | Q37578058 | ||
| Membrane targeting and pore formation by the type III secretion system translocon | Q37823656 | ||
| Plasma membrane repair and cellular damage control: the annexin survival kit. | Q37827208 | ||
| Serine protease autotransporters of enterobacteriaceae (SPATEs): biogenesis and function | Q37954294 | ||
| The RTX pore-forming toxin α-hemolysin of uropathogenic Escherichia coli: progress and perspectives. | Q38068485 | ||
| Regulation of the Yersinia type III secretion system: traffic control | Q38079815 | ||
| Modulation of innate immune responses by Yersinia type III secretion system translocators and effectors | Q38120033 | ||
| Cell targeting by the Staphylococcus aureus pore-forming toxins: it's not just about lipids | Q38162658 | ||
| Targeting the type III secretion system to treat bacterial infections. | Q38167861 | ||
| Dealing with damage: plasma membrane repair mechanisms | Q38245685 | ||
| The cell death response to enteropathogenic Escherichia coli infection | Q38255302 | ||
| Review: Annexin-A5 and cell membrane repair. | Q38363318 | ||
| Caspase-11: arming the guards against bacterial infection | Q38423373 | ||
| Potassium efflux fires the canon: Potassium efflux as a common trigger for canonical and noncanonical NLRP3 pathways | Q38579052 | ||
| Defying death: Cellular survival strategies following plasmalemmal injury by bacterial toxins | Q38611295 | ||
| Oligomerization and pore formation by equinatoxin II inhibit endocytosis and lead to plasma membrane reorganization | Q38796009 | ||
| Impact of host membrane pore formation by the Yersinia pseudotuberculosis type III secretion system on the macrophage innate immune response | Q39214573 | ||
| Recruitment and membrane interactions of host cell proteins during attachment of enteropathogenic and enterohaemorrhagic Escherichia coli | Q39348067 | ||
| SipB-SipC complex is essential for translocon formation | Q39356519 | ||
| Autophagy is induced by the type III secretion system of Vibrio alginolyticus in several mammalian cell lines | Q39636412 | ||
| The extreme C terminus of Shigella flexneri IpaB is required for regulation of type III secretion, needle tip composition, and binding. | Q39896038 | ||
| Oligomerization of type III secretion proteins PopB and PopD precedes pore formation in Pseudomonas | Q39927824 | ||
| Type III secretion translocation pores of Yersinia enterocolitica trigger maturation and release of pro-inflammatory IL-1beta | Q40054680 | ||
| IpaD of Shigella flexneri is independently required for regulation of Ipa protein secretion and efficient insertion of IpaB and IpaC into host membranes. | Q40454544 | ||
| Oligomeric states of the Shigella translocator protein IpaB provide structural insights into formation of the type III secretion translocon. | Q40564027 | ||
| Bordetella type III secretion induces caspase 1-independent necrosis | Q40671375 | ||
| The YopD translocator of Yersinia pseudotuberculosis is a multifunctional protein comprised of discrete domains. | Q40909327 | ||
| A process for controlling intracellular bacterial infections induced by membrane injury | Q41462474 | ||
| Proinflammatory signalling stimulated by the type III translocation factor YopB is counteracted by multiple effectors in epithelial cells infected with Yersinia pseudotuberculosis | Q41468714 | ||
| EspZ of enteropathogenic and enterohemorrhagic Escherichia coli regulates type III secretion system protein translocation | Q42103443 | ||
| Pore-forming Activity of the Escherichia coli Type III Secretion System Protein EspD. | Q42622184 | ||
| PLA2 activity is required for nuclear shrinkage in caspase-independent cell death | Q42917986 | ||
| Cell-surface attachment of pedestal-forming enteropathogenic E. coli induces a clustering of raft components and a recruitment of annexin 2. | Q43860812 | ||
| Caspase-11: the noncanonical guardian of cytosolic sanctity | Q46538540 | ||
| Type III secretion system | Q46841371 | ||
| The type III secretion system needle tip complex mediates host cell sensing and translocon insertion. | Q53575352 | ||
| Pore Formation by T3SS Translocators: Liposome Leakage Assay | Q61975683 | ||
| Potassium regulates IL-1 beta processing via calcium-independent phospholipase A2 | Q73755857 | ||
| Characterization of translocation pores inserted into plasma membranes by type III-secreted Esp proteins of enteropathogenic Escherichia coli | Q74581423 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 84 | |
| P577 | publication date | 2016-01-01 | |
| P1433 | published in | Frontiers in Immunology | Q27723748 |
| P1476 | title | Bacterial Control of Pores Induced by the Type III Secretion System: Mind the Gap | |
| P478 | volume | 7 |
| Q28068755 | Behind the lines-actions of bacterial type III effector proteins in plant cells |
| Q38764395 | Characterization of V. cholerae T3SS-dependent cytotoxicity in cultured intestinal epithelial cells. |
| Q92700449 | Plant Aquaporins in Infection by and Immunity Against Pathogens - A Critical Review |
| Q92676267 | Rice aquaporin PIP1;3 and harpin Hpa1 of bacterial blight pathogen cooperate in a type III effector translocation |
| Q98465479 | Three Proteins (Hpa2, HrpF and XopN) Are Concomitant Type III Translocators in Bacterial Blight Pathogen of Rice |
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