review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Michael Otto | Q37377631 |
P2860 | cites work | Insights on Evolution of Virulence and Resistance from the Complete Genome Analysis of an Early Methicillin-Resistant Staphylococcus aureus Strain and a Biofilm-Producing Methicillin-Resistant Staphylococcus epidermidis Strain | Q22065445 |
Microbial biofilms | Q22255624 | ||
A bacterial effector targets Mad2L2, an APC inhibitor, to modulate host cell cycling | Q24338298 | ||
Sortases and the art of anchoring proteins to the envelopes of gram-positive bacteria | Q24544133 | ||
Compartmentalized control of skin immunity by resident commensals | Q24603475 | ||
Corynebacterium diphtheriae employs specific minor pilins to target human pharyngeal epithelial cells | Q24614910 | ||
Housekeeping sortase facilitates the cell wall anchoring of pilus polymers in Corynebacterium diphtheriae | Q24621355 | ||
The skin microbiome | Q24634180 | ||
Helicobacter pylori SabA adhesin in persistent infection and chronic inflammation | Q24650188 | ||
Skin microbiota: a source of disease or defence? | Q24651518 | ||
The intercellular adhesin involved in biofilm accumulation of Staphylococcus epidermidis is a linear beta-1,6-linked glucosaminoglycan: purification and structural analysis | Q24684968 | ||
Dental caries from a molecular microbiological perspective | Q27013918 | ||
Defining the healthy"core microbiome" of oral microbial communities | Q27496627 | ||
Structural basis of the interaction of the pyelonephritic E. coli adhesin to its human kidney receptor | Q27633071 | ||
A “dock, lock, and latch” Structural Model for a Staphylococcal Adhesin Binding to Fibrinogen | Q27642376 | ||
Staphylococcus aureus infections | Q28131787 | ||
Virulence mechanisms and persistence strategies of the human gastric pathogen Helicobacter pylori | Q37610841 | ||
Listeria as an enteroinvasive gastrointestinal pathogen | Q37610844 | ||
Detection of virulence-associated genes not useful for discriminating between invasive and commensal Staphylococcus epidermidis strains from a bone marrow transplant unit | Q37703008 | ||
Acid stress response in enteropathogenic gammaproteobacteria: an aptitude for survival | Q37746998 | ||
Bacterial interactions with the host epithelium. | Q37773685 | ||
Intracellular lifestyles and immune evasion strategies of uropathogenic Escherichia coli. | Q37786336 | ||
Clinical practice. Streptococcal pharyngitis | Q37842495 | ||
Adhesion mechanisms of staphylococci | Q37873838 | ||
Acne sans P. acnes | Q37998152 | ||
Fimbriation and curliation in Escherichia coli O157:H7: a paradigm of intestinal and environmental colonization | Q38012016 | ||
Pneumococcal pneumonia: mechanisms of infection and resolution. | Q38032699 | ||
Bacterial adhesion to animal tissues: protein determinants for recognition of extracellular matrix components. | Q38033715 | ||
Staphylococcal infections: mechanisms of biofilm maturation and detachment as critical determinants of pathogenicity | Q38035969 | ||
Attachment of Helicobacter pylori to human gastric epithelium mediated by blood group antigens | Q38313312 | ||
The sialic acid binding SabA adhesin of Helicobacter pylori is essential for nonopsonic activation of human neutrophils | Q38331012 | ||
Clumping factor B, a fibrinogen-binding MSCRAMM (microbial surface components recognizing adhesive matrix molecules) adhesin of Staphylococcus aureus, also binds to the tail region of type I cytokeratin 10. | Q38336258 | ||
A novel Staphylococcus aureus biofilm phenotype mediated by the fibronectin-binding proteins, FnBPA and FnBPB. | Q38608812 | ||
Molecular basis of bacterial adhesion in the oral cavity. | Q39465209 | ||
The D-alanine residues of Staphylococcus aureus teichoic acids alter the susceptibility to vancomycin and the activity of autolytic enzymes | Q39475411 | ||
Key role of teichoic acid net charge in Staphylococcus aureus colonization of artificial surfaces | Q39520103 | ||
Exploring the 3D molecular architecture of Escherichia coli type 1 pili | Q64449467 | ||
Mannose-resistant haemagglutination and P antigen recognition are characteristic of Escherichia coli causing primary pyelonephritis | Q64452063 | ||
Protein A from Staphylococcus aureus: the biological significance of its reaction with IgG | Q68536231 | ||
Partial purification and characterization of lipase (EC 3.1.1.3) from Propionibacterium acnes | Q70214593 | ||
Structure and Stability of Protein H and the M1 Protein from Streptococcus pyogenes. Implications for Other Surface Proteins of Gram-Positive Bacteria | Q71786176 | ||
The Fbe (SdrG) protein of Staphylococcus epidermidis HB promotes bacterial adherence to fibrinogen | Q74459780 | ||
Identification and characterization of binding properties of Helicobacter pylori by glycoconjugate arrays | Q81411171 | ||
Biofilms of clinical strains of Staphylococcus that do not contain polysaccharide intercellular adhesin | Q82370085 | ||
Pathogenesis of Helicobacter pylori infection | Q84477773 | ||
Propionibacterium acnes as an etiological agent of arthroplastic and osteosynthetic infections--two cases with specific clinical presentation including formation of draining fistulae | Q84862793 | ||
The role of microbiota in infectious disease | Q37086530 | ||
Type IV pili: e pluribus unum? | Q37133352 | ||
Staphylococcal biofilms | Q37153224 | ||
Quorum sensing in staphylococci | Q37247099 | ||
Biofilms in skin infections: Propionibacterium acnes and acne vulgaris | Q37265033 | ||
Animal models of Streptococcus pneumoniae disease | Q37293669 | ||
Streptococcus adherence and colonization. | Q37333704 | ||
In vitro binding of type 1-fimbriated Escherichia coli to uroplakins Ia and Ib: relation to urinary tract infections | Q37358183 | ||
Coagulase-negative staphylococcal infections | Q37366080 | ||
The pgaABCD locus of Escherichia coli promotes the synthesis of a polysaccharide adhesin required for biofilm formation | Q37425741 | ||
The fibrinogen binding protein of Staphylococcus epidermidis is a target for opsonic antibodies | Q37427893 | ||
Molecular pathogenesis of necrotizing fasciitis | Q37593577 | ||
Gut flora in health and disease | Q28209082 | ||
Staphylococcus epidermidis--the 'accidental' pathogen | Q28252268 | ||
Functional adaptation of BabA, the H. pylori ABO blood group antigen binding adhesin | Q28273716 | ||
The gut microbiota--masters of host development and physiology | Q28286102 | ||
Streptococcus pneumoniae anchor to activated human cells by the receptor for platelet-activating factor | Q28289854 | ||
Microbial ecology of the skin | Q28291445 | ||
Pseudomonas aeruginosa biofilms in cystic fibrosis | Q28299966 | ||
Modulation of eDNA release and degradation affects Staphylococcus aureus biofilm maturation | Q28475591 | ||
Identification and characterization of an aliphatic amidase in Helicobacter pylori | Q28484790 | ||
Comparative genomics and transcriptomics of Propionibacterium acnes | Q28743188 | ||
Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration | Q29547429 | ||
Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms | Q29615294 | ||
Comparative genomics reveals distinct host-interacting traits of three major human-associated propionibacteria | Q30009551 | ||
Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group | Q31797996 | ||
Molecular analysis of the bacterial microbiota in the human stomach | Q33231429 | ||
SabA is the H. pylori hemagglutinin and is polymorphic in binding to sialylated glycans | Q33264403 | ||
SdrF, a Staphylococcus epidermidis surface protein, contributes to the initiation of ventricular assist device driveline-related infections | Q33438438 | ||
Molecular characterization of a novel Staphylococcus aureus surface protein (SasC) involved in cell aggregation and biofilm accumulation | Q33511984 | ||
Quorum sensing and virulence of Pseudomonas aeruginosa during lung infection of cystic fibrosis patients | Q33559774 | ||
The human nasal microbiota and Staphylococcus aureus carriage | Q33586161 | ||
Factors characterizing Staphylococcus epidermidis invasiveness determined by comparative genomics | Q33716049 | ||
Pili in Gram-positive bacteria: assembly, involvement in colonization and biofilm development | Q33739275 | ||
Analysis of protein expression regulated by the Helicobacter pylori ArsRS two-component signal transduction system | Q33769136 | ||
Longitudinal analysis of the group A Streptococcus transcriptome in experimental pharyngitis in cynomolgus macaques | Q33853470 | ||
Staphylococcus aureus sortase, an enzyme that anchors surface proteins to the cell wall | Q33869464 | ||
The serine-aspartate repeat (Sdr) protein family in Staphylococcus epidermidis | Q33908009 | ||
The multifunctional Staphylococcus aureus autolysin aaa mediates adherence to immobilized fibrinogen and fibronectin | Q33946932 | ||
SdrG, a fibrinogen-binding bacterial adhesin of the microbial surface components recognizing adhesive matrix molecules subfamily from Staphylococcus epidermidis, targets the thrombin cleavage site in the Bbeta chain | Q33948050 | ||
A crucial role for exopolysaccharide modification in bacterial biofilm formation, immune evasion, and virulence | Q33982558 | ||
The intercellular adhesion (ica) locus is present in Staphylococcus aureus and is required for biofilm formation | Q34002214 | ||
Staphylococcus caprae strains carry determinants known to be involved in pathogenicity: a gene encoding an autolysin-binding fibronectin and the ica operon involved in biofilm formation | Q34005871 | ||
Identification and characterization of hsa, the gene encoding the sialic acid-binding adhesin of Streptococcus gordonii DL1. | Q34120240 | ||
Sat, the secreted autotransporter toxin of uropathogenic Escherichia coli, is a vacuolating cytotoxin for bladder and kidney epithelial cells | Q34128314 | ||
Assembly of pili on the surface of Corynebacterium diphtheriae. | Q34277236 | ||
The role of nasal carriage in Staphylococcus aureus infections | Q34470454 | ||
Assembly and role of pili in group B streptococci. | Q34541449 | ||
Colonization resistance and microbial ecophysiology: using gnotobiotic mouse models and single-cell technology to explore the intestinal jungle. | Q34714359 | ||
Biology of Streptococcus mutans-derived glucosyltransferases: role in extracellular matrix formation of cariogenic biofilms | Q34746465 | ||
Pyrosequencing analysis of oral microbiota in children with severe early childhood dental caries | Q34762288 | ||
Role of the accessory gene regulator agr in community-associated methicillin-resistant Staphylococcus aureus pathogenesis. | Q34931778 | ||
Structural biology of the chaperone-usher pathway of pilus biogenesis | Q35007461 | ||
Bacterial skin commensals and their role as host guardians | Q35063389 | ||
Capsule enhances pneumococcal colonization by limiting mucus-mediated clearance. | Q35689073 | ||
Structures of the lectins from Pseudomonas aeruginosa: insight into the molecular basis for host glycan recognition | Q35719952 | ||
Phase variation in pneumococcal opacity: relationship between colonial morphology and nasopharyngeal colonization | Q35782997 | ||
Distribution and persistence of Staphylococcus and Micrococcus species and other aerobic bacteria on human skin | Q35800564 | ||
Pseudomonas aeruginosa pili and flagella mediate distinct binding and signaling events at the apical and basolateral surface of airway epithelium | Q35873580 | ||
The intracellular status of Streptococcus pyogenes: role of extracellular matrix-binding proteins and their regulation. | Q35922710 | ||
Bacterial evasion of innate host defenses--the Staphylococcus aureus lesson | Q35922712 | ||
MRSA epidemic linked to a quickly spreading colonization and virulence determinant. | Q36044499 | ||
Escherichia coli, fimbriae, bacterial persistence and host response induction in the human urinary tract | Q36291999 | ||
Interleukin 8 receptor deficiency confers susceptibility to acute experimental pyelonephritis and may have a human counterpart. | Q36368846 | ||
Bap: a family of surface proteins involved in biofilm formation. | Q36374369 | ||
Construction and expression of recombinant plasmids encoding type 1 or D-mannose-resistant pili from a urinary tract infection Escherichia coli isolate | Q36427678 | ||
Mutans streptococci and the development of dental plaque | Q36435484 | ||
Molecular basis of in vivo biofilm formation by bacterial pathogens | Q36488561 | ||
Mechanism of conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patients | Q36528781 | ||
Biofilms, a new approach to the microbiology of dental plaque | Q36602665 | ||
Molecular biology of microbial ureases | Q36669965 | ||
Type IV pili: paradoxes in form and function | Q36742465 | ||
Expression of Staphylococcus epidermidis SdrG increases following exposure to an in vivo environment | Q36747096 | ||
Microbial ecology of the cystic fibrosis lung | Q36767381 | ||
Molecular basis of intercellular adhesion in the biofilm-forming Staphylococcus epidermidis | Q36820016 | ||
Sticky fibers and uropathogenesis: bacterial adhesins in the urinary tract | Q36895740 | ||
The presence of icaADBC is detrimental to the colonization of human skin by Staphylococcus epidermidis | Q36933087 | ||
Severe infections caused by Propionibacterium acnes: an underestimated pathogen in late postoperative infections | Q36987675 | ||
Salivary-agglutinin-mediated adherence of Streptococcus mutans to early plaque bacteria. | Q36987697 | ||
A zinc-dependent adhesion module is responsible for intercellular adhesion in staphylococcal biofilms | Q36992464 | ||
To build a biofilm | Q39750137 | ||
Detection of the intercellular adhesion gene cluster (ica) and phase variation in Staphylococcus epidermidis blood culture strains and mucosal isolates | Q39829189 | ||
A 140-kilodalton extracellular protein is essential for the accumulation of Staphylococcus epidermidis strains on surfaces | Q39833176 | ||
Type 1 pilus-mediated bacterial invasion of bladder epithelial cells | Q39922793 | ||
A temporal signal, independent of agr, is required for hla but not spa transcription in Staphylococcus aureus | Q39945412 | ||
Scavenger receptor gp340 aggregates group A streptococci by binding pili. | Q39986003 | ||
Calcium-dependent salivary agglutinin with reactivity to various oral bacterial species. | Q40161320 | ||
Infections caused by nondiphtheria corynebacteria | Q40251630 | ||
The normal human anaerobic microflora. | Q40253482 | ||
Polysaccharide intercellular adhesin or protein factors in biofilm accumulation of Staphylococcus epidermidis and Staphylococcus aureus isolated from prosthetic hip and knee joint infections. | Q40257482 | ||
Fibrinogen-binding protein/clumping factor from Staphylococcus aureus | Q40427682 | ||
Increased colonization of indwelling medical devices by quorum-sensing mutants of Staphylococcus epidermidis in vivo | Q40513868 | ||
A review of the skin and its appendages. | Q40553048 | ||
MSCRAMM-mediated adherence of microorganisms to host tissues. | Q40572996 | ||
Pilus and nonpilus bacterial adhesins: assembly and function in cell recognition | Q40710188 | ||
Escherichia coli P fimbriae utilize the Toll-like receptor 4 pathway for cell activation | Q40813373 | ||
Two genetic loci produce distinct carbohydrate-rich structural components of the Pseudomonas aeruginosa biofilm matrix | Q40993746 | ||
Structural reevaluation of Streptococcus pneumoniae Lipoteichoic acid and new insights into its immunostimulatory potency | Q41278331 | ||
Structure, function and immunogenicity of streptococcal antigen I/II polypeptides | Q41357563 | ||
Localized tufts of fibrils on Staphylococcus epidermidis NCTC 11047 are comprised of the accumulation-associated protein | Q41948127 | ||
Role of surface protein SasG in biofilm formation by Staphylococcus aureus. | Q42067303 | ||
Requirement of histidine kinases HP0165 and HP1364 for acid resistance in Helicobacter pylori | Q42582000 | ||
Evidence for autolysin-mediated primary attachment of Staphylococcus epidermidis to a polystyrene surface | Q42660245 | ||
The agr P2 operon: an autocatalytic sensory transduction system in Staphylococcus aureus. | Q42676857 | ||
agr function in clinical Staphylococcus aureus isolates. | Q42732301 | ||
Group B streptococcal pilus proteins contribute to adherence to and invasion of brain microvascular endothelial cells | Q42957326 | ||
Protein A-mediated multicellular behavior in Staphylococcus aureus. | Q43192510 | ||
The giant extracellular matrix-binding protein of Staphylococcus epidermidis mediates biofilm accumulation and attachment to fibronectin | Q43234542 | ||
Experimental colonization of pigs with methicillin-resistant Staphylococcus aureus (MRSA): insights into the colonization and transmission of livestock-associated MRSA. | Q43533025 | ||
The AmiE aliphatic amidase and AmiF formamidase of Helicobacter pylori: natural evolution of two enzyme paralogues | Q43612698 | ||
Pyrosequencing analysis of the oral microflora of healthy adults | Q44095685 | ||
Genes in the accessory sec locus of Streptococcus gordonii have three functionally distinct effects on the expression of the platelet-binding protein GspB. | Q44405963 | ||
Formation of Propionibacterium acnes biofilms on orthopaedic biomaterials and their susceptibility to antimicrobials. | Q44451413 | ||
Fibronectin binding by Propionibacterium acnes | Q44560489 | ||
Identification and preliminary characterization of cell-wall-anchored proteins of Staphylococcus epidermidis | Q44570742 | ||
Identification and characterization of a novel autolysin (Aae) with adhesive properties from Staphylococcus epidermidis | Q44605325 | ||
Helicobacter pylori arginase inhibits T cell proliferation and reduces the expression of the TCR zeta-chain (CD3zeta). | Q44947169 | ||
Induction of Staphylococcus epidermidis biofilm formation via proteolytic processing of the accumulation-associated protein by staphylococcal and host proteases | Q45307990 | ||
Bacteria hijack integrin-linked kinase to stabilize focal adhesions and block cell detachment. | Q45986472 | ||
Deglycosylation of human glycoconjugates by the sequential activities of exoglycosidases expressed by Streptococcus pneumoniae | Q46899381 | ||
Characterization of the N-acetylglucosaminyltransferase activity involved in the biosynthesis of the Staphylococcus epidermidis polysaccharide intercellular adhesin | Q47859356 | ||
Biofilm-growing intestinal anaerobic bacteria | Q47987425 | ||
Clumping factor B (ClfB), a new surface-located fibrinogen-binding adhesin of Staphylococcus aureus | Q48012907 | ||
Molecular characterization of the clumping factor (fibrinogen receptor) of Staphylococcus aureus | Q48086155 | ||
Development of a skin colonization model in gnotobiotic piglets for the study of the microbial ecology of meticillin-resistant Staphylococcus aureus ST398. | Q51168770 | ||
Virulent aggregates of Streptococcus pyogenes are generated by homophilic protein-protein interactions. | Q54038136 | ||
Acne vulgaris | Q54139548 | ||
Bacterial insertion sequence IS256 as a potential molecular marker to discriminate invasive strains from commensal strains of Staphylococcus epidermidis. | Q54634844 | ||
Sequence Variation in Group AStreptococcusPili and Association of Pilus Backbone Types with Lancefield T Serotypes | Q57988261 | ||
Localization of the receptor-binding protein adhesin at the tip of the bacterial pilus | Q59071543 | ||
Polysaccharides serve as scaffold of biofilms formed by mucoidPseudomonas aeruginosa | Q59139058 | ||
BACTERIAL VIRULENCE IN URINARY TRACT INFECTION | Q62061199 | ||
Colonisation by Streptococcus pneumoniae and Staphylococcus aureus in healthy children | Q63916849 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1250-1270 | |
P577 | publication date | 2014-09-29 | |
P1433 | published in | FEMS Microbiology Reviews | Q15762226 |
P1476 | title | Physical stress and bacterial colonization | |
P478 | volume | 38 |
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