scholarly article | Q13442814 |
P50 | author | Juliane Bubeck Wardenburg | Q96199264 |
P2093 | author name string | E Sachiko Seilie | |
P2860 | cites work | Assembly of Staphylococcus aureus leukocidin into a pore-forming ring-shaped oligomer on human polymorphonuclear leukocytes and rabbit erythrocytes | Q77918021 |
The staphylococcal saeRS system coordinates environmental signals with agr quorum sensing | Q79107840 | ||
LukM/LukF'-PV is the most active Staphylococcus aureus leukotoxin on bovine neutrophils | Q79747189 | ||
Human C5aR knock-in mice facilitate the production and assessment of anti-inflammatory monoclonal antibodies | Q80277959 | ||
Aromatic residues of Caveolin-1 binding motif of alpha-hemolysin are essential for membrane penetration | Q81239435 | ||
Expression of anaphylatoxin receptors on platelets in patients with coronary heart disease | Q86415018 | ||
Emergence of FY*A(null) in a Plasmodium vivax-endemic region of Papua New Guinea | Q22010821 | ||
The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts | Q24307875 | ||
Synthesis of staphylococcal virulence factors is controlled by a regulatory RNA molecule | Q24564360 | ||
Staphylococcus aureus α-hemolysin mediates virulence in a murine model of severe pneumonia through activation of the NLRP3 inflammasome | Q24594277 | ||
Community-acquired methicillin-resistant Staphylococcus aureus carrying Panton-Valentine leukocidin genes: worldwide emergence | Q24598936 | ||
Alpha-toxin of Staphylococcus aureus | Q24634703 | ||
Virulence of protein A-deficient and alpha-toxin-deficient mutants of Staphylococcus aureus isolated by allele replacement | Q24646910 | ||
Anti-alpha-hemolysin monoclonal antibodies mediate protection against Staphylococcus aureus pneumonia | Q24650729 | ||
[alpha]-Secretase ADAM10 as well as [alpha]APPs is reduced in platelets and CSF of Alzheimer disease patients | Q24676332 | ||
Staphylococcal manipulation of host immune responses | Q26798461 | ||
Staphylococcus aureus α-toxin: nearly a century of intrigue | Q26823686 | ||
The adherens junctions control susceptibility to Staphylococcus aureus α-toxin | Q27321037 | ||
Genome-wide CRISPR screen reveals novel host factors required for Staphylococcus aureus α-hemolysin-mediated toxicity. | Q27322587 | ||
Crystal structure of staphylococcal LukF delineates conformational changes accompanying formation of a transmembrane channel | Q27639846 | ||
Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore | Q27734044 | ||
Regulated cleavage of a contact-mediated axon repellent | Q28144522 | ||
Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia | Q28145964 | ||
Platelet-activating factor receptor and ADAM10 mediate responses to Staphylococcus aureus in epithelial cells | Q28215261 | ||
Poring over pores: alpha-hemolysin and Panton-Valentine leukocidin in Staphylococcus aureus pneumonia | Q28260215 | ||
Is Panton-Valentine leukocidin the major virulence determinant in community-associated methicillin-resistant Staphylococcus aureus disease? | Q28274375 | ||
The intersection of cell death and inflammasome activation | Q28274739 | ||
Kuzbanian controls proteolytic processing of Notch and mediates lateral inhibition during Drosophila and vertebrate neurogenesis | Q28646378 | ||
CC CKR5: a RANTES, MIP-1alpha, MIP-1beta receptor as a fusion cofactor for macrophage-tropic HIV-1 | Q28646859 | ||
Panton-Valentine leukocidin does play a role in the early stage of Staphylococcus aureus skin infections: a rabbit model | Q28741721 | ||
Molecular mechanisms of necroptosis: an ordered cellular explosion | Q29616004 | ||
Identification of a crucial residue required for Staphylococcus aureus LukAB cytotoxicity and receptor recognition. | Q30153456 | ||
Role of a disintegrin and metalloprotease 10 in Staphylococcus aureus alpha-hemolysin-mediated cellular injury | Q30156106 | ||
Functional form of Caveolin-1 is necessary for the assembly of alpha-hemolysin | Q30160830 | ||
Assembly of alpha-hemolysin on A431 cells leads to clustering of Caveolin-1. | Q30160831 | ||
Subunit composition of a bicomponent toxin: staphylococcal leukocidin forms an octameric transmembrane pore | Q30167424 | ||
Polymorphonuclear leukocytes mediate Staphylococcus aureus Panton-Valentine leukocidin-induced lung inflammation and injury. | Q30386697 | ||
Inhibition of S. aureus alpha-hemolysin and B. anthracis lethal toxin by beta-cyclodextrin derivatives | Q30441266 | ||
Stochastic assembly of two-component staphylococcal gamma-hemolysin into heteroheptameric transmembrane pores with alternate subunit arrangements in ratios of 3:4 and 4:3. | Q30712777 | ||
Bacterial survival amidst an immune onslaught: the contribution of the Staphylococcus aureus leukotoxins. | Q31111609 | ||
Evidence that clustered phosphocholine head groups serve as sites for binding and assembly of an oligomeric protein pore | Q33342899 | ||
Staphylococcus aureus leukotoxin GH promotes inflammation | Q36253043 | ||
Synergistic Action of Staphylococcus aureus α-Toxin on Platelets and Myeloid Lineage Cells Contributes to Lethal Sepsis | Q36274821 | ||
Staphylococcus aureus Panton-Valentine leukocidin induces an inflammatory response in human phagocytes via the NLRP3 inflammasome | Q36332700 | ||
Chemotaxis inhibitory protein of Staphylococcus aureus, a bacterial antiinflammatory agent. | Q36403878 | ||
CCR5 is a receptor for Staphylococcus aureus leukotoxin ED. | Q36508062 | ||
High resolution crystallographic studies of alpha-hemolysin-phospholipid complexes define heptamer-lipid head group interactions: implication for understanding protein-lipid interactions. | Q36519414 | ||
Tyrosine sulfation of chemokine receptor CCR2 enhances interactions with both monomeric and dimeric forms of the chemokine monocyte chemoattractant protein-1 (MCP-1) | Q36742094 | ||
TspanC8 tetraspanins differentially regulate the cleavage of ADAM10 substrates, Notch activation and ADAM10 membrane compartmentalization. | Q36762907 | ||
Staphylococcus aureus elaborates leukocidin AB to mediate escape from within human neutrophils | Q36826997 | ||
Interaction of staphylococcal alpha-toxin with artificial and natural membranes | Q36848080 | ||
Panton-Valentine leukocidin is not a virulence determinant in murine models of community-associated methicillin-resistant Staphylococcus aureus disease | Q36953300 | ||
Staphylococcus aureus LukAB cytotoxin kills human neutrophils by targeting the CD11b subunit of the integrin Mac-1. | Q36967664 | ||
Staphylococcus aureus Coordinates Leukocidin Expression and Pathogenesis by Sensing Metabolic Fluxes via RpiRc. | Q37027315 | ||
Identification and treatment of the Staphylococcus aureus reservoir in vivo | Q37047344 | ||
Staphylococcus aureus α-hemolysin promotes platelet-neutrophil aggregate formation | Q37070344 | ||
Regulation of exoprotein expression in Staphylococcus aureus by a locus (sar) distinct from agr | Q37111343 | ||
The Panton-Valentine leukocidin vaccine protects mice against lung and skin infections caused by Staphylococcus aureus USA300 | Q37132230 | ||
Necroptosis Promotes Staphylococcus aureus Clearance by Inhibiting Excessive Inflammatory Signaling. | Q37211555 | ||
Improved Protection in a Rabbit Model of Community-Associated Methicillin-Resistant Staphylococcus aureus Necrotizing Pneumonia upon Neutralization of Leukocidins in Addition to Alpha-Hemolysin | Q37287867 | ||
Yersinia pestis: mechanisms of entry into and resistance to the host cell | Q37412102 | ||
Listeria monocytogenes internalin and E-cadherin: from bench to bedside | Q37412630 | ||
Staphylococcus aureus leukotoxin ED targets the chemokine receptors CXCR1 and CXCR2 to kill leukocytes and promote infection. | Q37422943 | ||
Antimicrobial mechanisms of phagocytes and bacterial evasion strategies | Q37445493 | ||
Staphylococcus aureus leukotoxin GH promotes formation of neutrophil extracellular traps | Q37520251 | ||
Children with invasive Staphylococcus aureus disease exhibit a potently neutralizing antibody response to the cytotoxin LukAB. | Q37643858 | ||
Caveolin-1: a critical regulator of lung injury | Q37811611 | ||
Invited review: Mastitis in dairy heifers: nature of the disease, potential impact, prevention, and control. | Q37988105 | ||
Pathogenic pore-forming proteins: function and host response. | Q38043620 | ||
The role of the Panton-Valentine leucocidin toxin in staphylococcal disease: a systematic review and meta-analysis | Q38055963 | ||
Staphylococcus aureus: a pathogen with still unresolved issues. | Q38133206 | ||
The structural role of receptor tyrosine sulfation in chemokine recognition. | Q38151741 | ||
Transcription profiling-based identification of Staphylococcus aureus genes regulated by the agr and/or sarA loci. | Q38294549 | ||
TspanC8 Tetraspanins and A Disintegrin and Metalloprotease 10 (ADAM10) Interact via Their Extracellular Regions: EVIDENCE FOR DISTINCT BINDING MECHANISMS FOR DIFFERENT TspanC8 PROTEINS. | Q38377767 | ||
Pore-forming toxins: ancient, but never really out of fashion | Q38660364 | ||
Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individuals. | Q48025275 | ||
Panton-valentine leukocidin genes in a phage-like particle isolated from mitomycin C-treated Staphylococcus aureus V8 (ATCC 49775). | Q48041560 | ||
Molecular characteristics and virulence factors in methicillin-susceptible, resistant, and heterogeneous vancomycin-intermediate Staphylococcus aureus from central-southern China. | Q54211543 | ||
Fimbrial proteins of porphyromonas gingivalis mediate in vivo virulence and exploit TLR2 and complement receptor 3 to persist in macrophages. | Q54476982 | ||
Internalization of staphylococcal leukotoxins that bind and divert the C5a receptor is required for intracellular Ca2+mobilization by human neutrophils | Q57823983 | ||
p-Sulfonato-calix[n]arenes inhibit staphylococcal bicomponent leukotoxins by supramolecular interactions | Q57824011 | ||
α-Hemolysin, not Panton-Valentine leukocidin, impacts rabbit mortality from severe sepsis with methicillin-resistant Staphylococcus aureus osteomyelitis | Q58441120 | ||
Listeriolysin O allows Listeria monocytogenes replication in macrophage vacuoles | Q59069113 | ||
Staphylococcal alpha-toxin-induced PGI2 production in endothelial cells: role of calcium | Q60364680 | ||
Membrane-damaging action of staphylococcal alpha-toxin on phospholipid-cholesterol liposomes | Q68983785 | ||
Pore formation by a two-component leukocidin from Staphylococcus aureus within the membrane of human polymorphonuclear leukocytes | Q70480981 | ||
Effect of staphylococcal leukocidin on mouse leukocyte system | Q70673026 | ||
Crystallization and properties of staphylococcal leukocidin | Q71527948 | ||
Rabbit erythrocyte band 3: a receptor for staphylococcal alpha toxin | Q72135626 | ||
Sequential binding of Staphylococcal gamma-hemolysin to human erythrocytes and complex formation of the hemolysin on the cell surface | Q73403710 | ||
The sae locus of Staphylococcus aureus controls exoprotein synthesis at the transcriptional level | Q73485644 | ||
Contribution of Panton-Valentine leukocidin in community-associated methicillin-resistant Staphylococcus aureus pathogenesis | Q33369089 | ||
Panton-valentine leukocidin enhances the severity of community-associated methicillin-resistant Staphylococcus aureus rabbit osteomyelitis | Q33506628 | ||
Staphylococcus aureus alpha-hemolysin activates the NLRP3-inflammasome in human and mouse monocytic cells | Q33510340 | ||
IL-1beta processing in host defense: beyond the inflammasomes | Q33535878 | ||
Identification of a novel Staphylococcus aureus two-component leukotoxin using cell surface proteomics | Q33641315 | ||
Antibody-mediated enhancement of community-acquired methicillin-resistant Staphylococcus aureus infection. | Q33719836 | ||
The bicomponent pore-forming leucocidins of Staphylococcus aureus | Q33743499 | ||
Virulence gene expression in human community-acquired Staphylococcus aureus infection. | Q33744296 | ||
Cytotoxin and pyrogenic toxin superantigen gene profiles of Staphylococcus aureus associated with subclinical mastitis in dairy cows and relationships with macrorestriction genomic profiles. | Q33752928 | ||
Importance of the global regulators Agr and SaeRS in the pathogenesis of CA-MRSA USA300 infection | Q33769704 | ||
ADAM10 mediates E-cadherin shedding and regulates epithelial cell-cell adhesion, migration, and beta-catenin translocation. | Q33878896 | ||
Global changes in Staphylococcus aureus gene expression in human blood | Q33883340 | ||
Insights into alpha-hemolysin (Hla) evolution and expression among Staphylococcus aureus clones with hospital and community origin | Q33916217 | ||
Staphylococcus aureus Panton-Valentine leukocidin causes necrotizing pneumonia | Q34002030 | ||
Flow cytometric determination of Panton-Valentine leucocidin S component binding | Q34006878 | ||
Association between Staphylococcus aureus strains carrying gene for Panton-Valentine leukocidin and highly lethal necrotising pneumonia in young immunocompetent patients | Q34117822 | ||
Cross-talk between Staphylococcus aureus leukocidins-intoxicated macrophages and lung epithelial cells triggers chemokine secretion in an inflammasome-dependent manner. | Q34157497 | ||
Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy–negative individuals | Q34304229 | ||
Genomic organization of the glycoprotein D gene: Duffy blood group Fya/Fyb alloantigen system is associated with a polymorphism at the 44-amino acid residue. | Q34316948 | ||
Role of pore-forming toxins in bacterial infectious diseases | Q34346202 | ||
ADAM10 mediates ectodomain shedding of the betacellulin precursor activated by p-aminophenylmercuric acetate and extracellular calcium influx | Q34362287 | ||
Staphylococcus aureus infections: epidemiology, pathophysiology, clinical manifestations, and management. | Q34478074 | ||
The staphylococcal toxins γ-haemolysin AB and CB differentially target phagocytes by employing specific chemokine receptors | Q34495209 | ||
Neutrophil-derived IL-1β is sufficient for abscess formation in immunity against Staphylococcus aureus in mice | Q34499405 | ||
Sequencing of leucocidin R from Staphylococcus aureus P83 suggests that staphylococcal leucocidins and gamma-hemolysin are members of a single, two-component family of toxins. | Q34524072 | ||
Distinct Bacteriophages Encoding Panton-Valentine Leukocidin (PVL) among International Methicillin-Resistant Staphylococcus aureus Clones Harboring PVL | Q34596685 | ||
Leucotoxic activities of Staphylococcus aureus strains isolated from cows, ewes, and goats with mastitis: importance of LukM/LukF'-PV leukotoxin. | Q34779287 | ||
Structure-function analysis of heterodimer formation, oligomerization, and receptor binding of the Staphylococcus aureus bi-component toxin LukGH. | Q34801327 | ||
Staphylococcus aureus alpha toxin suppresses effective innate and adaptive immune responses in a murine dermonecrosis model | Q35009064 | ||
Symmetry requirements for effective blocking of pore-forming toxins: comparative study with alpha-, beta-, and gamma-cyclodextrin derivatives | Q35065917 | ||
Roles of alpha-toxin and beta-toxin in virulence of Staphylococcus aureus for the mouse mammary gland | Q35100591 | ||
Control of the oxidative burst of human neutrophils by staphylococcal leukotoxins | Q35105922 | ||
Molecular features of the cytolytic pore-forming bacterial protein toxins | Q35126280 | ||
Deletion of Adam10 in endothelial cells leads to defects in organ-specific vascular structures | Q35140965 | ||
Comparative analysis of USA300 virulence determinants in a rabbit model of skin and soft tissue infection | Q35167140 | ||
A Staphylococcus aureus pore-forming toxin subverts the activity of ADAM10 to cause lethal infection in mice | Q35332249 | ||
Panton-Valentine leucocidin and gamma-hemolysin from Staphylococcus aureus ATCC 49775 are encoded by distinct genetic loci and have different biological activities | Q35445793 | ||
Toxin-induced necroptosis is a major mechanism of Staphylococcus aureus lung damage. | Q35447430 | ||
Molecular differentiation of historic phage-type 80/81 and contemporary epidemic Staphylococcus aureus | Q35518683 | ||
Five birds, one stone: neutralization of α-hemolysin and 4 bi-component leukocidins of Staphylococcus aureus with a single human monoclonal antibody | Q35530119 | ||
Specific roles of alpha-toxin and beta-toxin during Staphylococcus aureus corneal infection. | Q35546006 | ||
Atypical chemokine receptor 1 deficiency reduces atherogenesis in ApoE-knockout mice | Q35661830 | ||
Staphylococcus aureus Leukocidin A/B (LukAB) Kills Human Monocytes via Host NLRP3 and ASC when Extracellular, but Not Intracellular | Q35662239 | ||
Staphylococcus aureus leucocidin ED contributes to systemic infection by targeting neutrophils and promoting bacterial growth in vivo. | Q35673338 | ||
Surface proteins and exotoxins are required for the pathogenesis of Staphylococcus aureus pneumonia | Q35689313 | ||
Bovine Staphylococcus aureus Secretes the Leukocidin LukMF' To Kill Migrating Neutrophils through CCR1. | Q35715328 | ||
Tissue-specific patterning of host innate immune responses by Staphylococcus aureus α-toxin | Q35730332 | ||
Characterization of a new cytotoxin that contributes to Staphylococcus aureus pathogenesis. | Q35851869 | ||
Increased Susceptibility of Humanized NSG Mice to Panton-Valentine Leukocidin and Staphylococcus aureus Skin Infection. | Q35855538 | ||
Differential Interaction of the Staphylococcal Toxins Panton-Valentine Leukocidin and γ-Hemolysin CB with Human C5a Receptors | Q35864500 | ||
Pore-Forming Toxins Induce Macrophage Necroptosis during Acute Bacterial Pneumonia | Q35867134 | ||
Genetic requirement for ADAM10 in severe Staphylococcus aureus skin infection | Q35888551 | ||
The Staphylococcus aureus alpha-toxin perturbs the barrier function in Caco-2 epithelial cell monolayers by altering junctional integrity | Q35944103 | ||
CD36 Is Essential for Regulation of the Host Innate Response to Staphylococcus aureus α-Toxin-Mediated Dermonecrosis. | Q35988737 | ||
Subunit stoichiometry of staphylococcal alpha-hemolysin in crystals and on membranes: a heptameric transmembrane pore | Q36006598 | ||
Staphylococcus aureus Targets the Duffy Antigen Receptor for Chemokines (DARC) to Lyse Erythrocytes | Q36081594 | ||
ADAM10 mediates vascular injury induced by Staphylococcus aureus α-hemolysin | Q36083334 | ||
Context matters: The importance of dimerization-induced conformation of the LukGH leukocidin of Staphylococcus aureus for the generation of neutralizing antibodies. | Q36088381 | ||
Sublytic concentrations of Staphylococcus aureus Panton-Valentine leukocidin alter human PMN gene expression and enhance bactericidal capacity | Q36091286 | ||
Leukocidin genes lukF-P83 and lukM are associated with Taphylococcus aureus clonal complexes 151, 479 and 133 isolated from bovine udder infections in Thuringia, Germany | Q36156519 | ||
Immune-activating properties of Panton-Valentine leukocidin improve the outcome in a model of methicillin-resistant Staphylococcus aureus pneumonia. | Q36211152 | ||
Modelling staphylococcal pneumonia in a human 3D lung tissue model system delineates toxin-mediated pathology | Q36245190 | ||
Defining immunological dysfunction in sepsis: A requisite tool for precision medicine | Q38724457 | ||
Staphylococcus aureus α-toxin-mediated cation entry depolarizes membrane potential and activates p38 MAP kinase in airway epithelial cells. | Q38753520 | ||
The interplay between regulated necrosis and bacterial infection | Q38799157 | ||
Staphylococcus aureus Infection in Humanized Mice: A New Model to Study Pathogenicity Associated With Human Immune Response | Q39042514 | ||
Production and Purification of the Gamma Haemolysin of Staphylococcus aureus 'Smith 5R' | Q39068592 | ||
Panton-Valentine leukocidin facilitates the escape of Staphylococcus aureus from human keratinocyte endosomes and induces apoptosis | Q39108475 | ||
The staphylococcal toxin Panton-Valentine Leukocidin targets human C5a receptors. | Q39416905 | ||
Variable expressions of Staphylococcus aureus bicomponent leucotoxins semiquantified by competitive reverse transcription-PCR. | Q39487418 | ||
Alpha-toxin and gamma-toxin jointly promote Staphylococcus aureus virulence in murine septic arthritis. | Q39509909 | ||
Alpha-toxin damages the air-blood barrier of the lung in a rat model of Staphylococcus aureus-induced pneumonia. | Q39512487 | ||
Staphylococcus aureus evades the extracellular antimicrobial activity of mast cells by promoting its own uptake | Q39528464 | ||
Macrophage receptors for Mycobacterium tuberculosis | Q39570480 | ||
Virulent combinations of adhesin and toxin genes in natural populations of Staphylococcus aureus | Q39656261 | ||
Prevention and treatment of Staphylococcus aureus pneumonia with a beta-cyclodextrin derivative | Q39791076 | ||
Novel path to apoptosis: small transmembrane pores created by staphylococcal alpha-toxin in T lymphocytes evoke internucleosomal DNA degradation. | Q39859690 | ||
Virulence factors of Staphylococcus aureus induce Erk-MAP kinase activation and c-Fos expression in S9 and 16HBE14o- human airway epithelial cells | Q39903246 | ||
The expression of alpha-haemolysin is required for Staphylococcus aureus phagosomal escape after internalization in CFT-1 cells | Q39984249 | ||
Release of interleukin-1 beta associated with potent cytocidal action of staphylococcal alpha-toxin on human monocytes | Q40160139 | ||
α-Hemolysin enhances Staphylococcus aureus internalization and survival within mast cells by modulating the expression of β1 integrin | Q40287757 | ||
The gamma-hemolysin locus of Staphylococcus aureus comprises three linked genes, two of which are identical to the genes for the F and S components of leukocidin. | Q40374096 | ||
GTP-binding proteins are involved in the modulated activity of human neutrophils treated with the Panton-Valentine leukocidin from Staphylococcus aureus | Q40376413 | ||
Humanized Mice Exhibit Increased Susceptibility to Staphylococcus aureus Pneumonia. | Q40537073 | ||
Mode of action of staphylococcal leukocidin: effects of the S and F components on the activities of membrane-associated enzymes of rabbit polymorphonuclear leukocytes | Q40612632 | ||
Dissecting the role of ADAM10 as a mediator of Staphylococcus aureus α-toxin action | Q40686973 | ||
Staphylococcus aureus α toxin potentiates opportunistic bacterial lung infections | Q40761003 | ||
Influence of Sae-regulated and Agr-regulated factors on the escape of Staphylococcus aureus from human macrophages | Q40784729 | ||
Separation of Gamma Hemolysin from Staphylococcus aureus Smith 5R. | Q40885562 | ||
ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and beta-catenin nuclear signalling | Q41107179 | ||
Prevalence and molecular characteristics of methicillin-resistant Staphylococcus aureus among skin and soft tissue infections in an emergency department in Guyana. | Q41568939 | ||
The disintegrin/metalloproteinase Adam10 is essential for epidermal integrity and Notch-mediated signaling | Q41602986 | ||
Engineered covalent leucotoxin heterodimers form functional pores: insights into S-F interactions | Q41816275 | ||
ADAM10 regulates endothelial permeability and T-Cell transmigration by proteolysis of vascular endothelial cadherin. | Q41840639 | ||
Diversity of prophages in dominant Staphylococcus aureus clonal lineages. | Q41910627 | ||
Studies on the binding of staphylococcal 125I-labeled α-toxin to rabbit erythrocytes | Q42015587 | ||
Virulence Genes and Genotypic Associations in Nasal Carriage, Community-Associated Methicillin-Susceptible and Methicillin-Resistant USA400 Staphylococcus aureus Isolates | Q42088460 | ||
Fractionation of a leucocidin from Staphylococcus aureus | Q42245754 | ||
ADAM10-Dependent Signaling Through Notch1 and Notch4 Controls Development of Organ-Specific Vascular Beds. | Q42377492 | ||
Purification, cloning and characterization of variant LukE-LukD with strong leukocidal activity of staphylococcal bi-component leukotoxin family | Q42594991 | ||
The agr P2 operon: an autocatalytic sensory transduction system in Staphylococcus aureus. | Q42676857 | ||
Complete nucleotide sequence and molecular characterization of the temperate staphylococcal bacteriophage phiPVL carrying Panton-Valentine leukocidin genes | Q42680997 | ||
SarA level is a determinant of agr activation in Staphylococcus aureus | Q42692133 | ||
Leukotoxin family genes in Staphylococcus aureus isolated from domestic animals and prevalence of lukM-lukF-PV genes by bacteriophages in bovine isolates | Q43824436 | ||
Properties of the gamma haemolysin of Staphylococcus aureus 'Smith 5R' | Q44202155 | ||
Tyrosine sulfation of human antibodies contributes to recognition of the CCR5 binding region of HIV-1 gp120. | Q44530442 | ||
MyD88 mediates neutrophil recruitment initiated by IL-1R but not TLR2 activation in immunity against Staphylococcus aureus | Q44537222 | ||
Comparison of community- and health care-associated methicillin-resistant Staphylococcus aureus infection | Q44686515 | ||
Sulphated tyrosines mediate association of chemokines and Plasmodium vivax Duffy binding protein with the Duffy antigen/receptor for chemokines (DARC). | Q45273570 | ||
Staphylococcus aureus alpha-toxin. Dual mechanism of binding to target cells | Q46384886 | ||
Comparison of virulence in community-associated methicillin-resistant Staphylococcus aureus pulsotypes USA300 and USA400 in a rat model of pneumonia | Q46504308 | ||
Virulence genes of bovine Staphylococcus aureus from persistent and nonpersistent intramammary infections with different clinical characteristics | Q46980823 | ||
P921 | main subject | Staphylococcus aureus | Q188121 |
P577 | publication date | 2017-04-23 | |
P1433 | published in | Seminars in Cell & Developmental Biology | Q14330411 |
P1476 | title | Staphylococcus aureus pore-forming toxins: The interface of pathogen and host complexity |
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