| scholarly article | Q13442814 |
| P50 | author | Jeffrey N Weiser | Q37378150 |
| P2093 | author name string | Kimberly M Davis | |
| P2860 | cites work | Nod1, an Apaf-1-like activator of caspase-9 and nuclear factor-kappaB | Q22010046 |
| Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB | Q24290546 | ||
| Genetic evidence that antibacterial activity of lysozyme is independent of its catalytic function | Q24291768 | ||
| RICK/Rip2/CARDIAK mediates signalling for receptors of the innate and adaptive immune systems | Q24292468 | ||
| Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection | Q24292675 | ||
| Lipoteichoic acid (LTA) of Streptococcus pneumoniae and Staphylococcus aureus activates immune cells via Toll-like receptor (TLR)-2, lipopolysaccharide-binding protein (LBP), and CD14, whereas TLR-4 and MD-2 are not involved | Q24295020 | ||
| Ultrastructural localization of lysozyme in human neutrophils by immunogold | Q24298836 | ||
| Distribution of Lysosomal Enzymes, Cationic Proteins, and Bactericidal Substances in Subcellular Fractions of Human Polymorphonuclear Leukocytes | Q24300614 | ||
| RIP2 is a novel NF-kappaB-activating and cell death-inducing kinase | Q24310179 | ||
| Murine Nod1 but not its human orthologue mediates innate immune detection of tracheal cytotoxin | Q24539124 | ||
| NOD2 and toll-like receptors are nonredundant recognition systems of Mycobacterium tuberculosis | Q24811631 | ||
| Human Peptidoglycan Recognition Protein-L Is an N-Acetylmuramoyl-L-alanine Amidase | Q28115452 | ||
| Host recognition of bacterial muramyl dipeptide mediated through NOD2. Implications for Crohn's disease | Q28201834 | ||
| Functional characterization of the peptide transporter PEPT2 in primary cultures of human upper airway epithelium | Q28300707 | ||
| Increased inflammation in lysozyme M-deficient mice in response to Micrococcus luteus and its peptidoglycan | Q28511228 | ||
| PGLYRP-2 and Nod2 are both required for peptidoglycan-induced arthritis and local inflammation | Q28587573 | ||
| A NOD2-NALP1 complex mediates caspase-1-dependent IL-1beta secretion in response to Bacillus anthracis infection and muramyl dipeptide | Q28589654 | ||
| Critical role of NOD2 in regulating the immune response to Staphylococcus aureus | Q28593011 | ||
| Peptidoglycan- and lipoteichoic acid-induced cell activation is mediated by toll-like receptor 2 | Q28646106 | ||
| Nod1 detects a unique muropeptide from gram-negative bacterial peptidoglycan | Q29618544 | ||
| An essential role for NOD1 in host recognition of bacterial peptidoglycan containing diaminopimelic acid | Q29620015 | ||
| Peptidoglycan recognition proteins are a new class of human bactericidal proteins | Q29871532 | ||
| A mammalian peptidoglycan recognition protein with N-acetylmuramoyl-L-alanine amidase activity | Q31147483 | ||
| A critical role for peptidoglycan N-deacetylation in Listeria evasion from the host innate immune system | Q33268810 | ||
| Resistance to mucosal lysozyme compensates for the fitness deficit of peptidoglycan modifications by Streptococcus pneumoniae | Q33392682 | ||
| Oxidative stress-induced peptidoglycan deacetylase in Helicobacter pylori | Q33400222 | ||
| The NOD/RIP2 pathway is essential for host defenses against Chlamydophila pneumoniae lung infection | Q33429029 | ||
| In vivo transcriptional profiling of Listeria monocytogenes and mutagenesis identify new virulence factors involved in infection | Q33455499 | ||
| NOD2, RIP2 and IRF5 play a critical role in the type I interferon response to Mycobacterium tuberculosis | Q33478396 | ||
| Staphylococcus aureus evades lysozyme-based peptidoglycan digestion that links phagocytosis, inflammasome activation, and IL-1beta secretion | Q33640502 | ||
| Specificity of the autolysin of Streptococcus (Diplococcus) pneumoniae | Q33793950 | ||
| Requirement for capsule in colonization by Streptococcus pneumoniae | Q34007742 | ||
| Toll-like receptor 2-dependent bacterial sensing does not occur via peptidoglycan recognition | Q34166263 | ||
| Peptidoglycan molecular requirements allowing detection by Nod1 and Nod2. | Q34215657 | ||
| Peptidoglycan N-acetylglucosamine deacetylase, a putative virulence factor in Streptococcus pneumoniae | Q34261872 | ||
| Nod1 responds to peptidoglycan delivered by the Helicobacter pylori cag pathogenicity island | Q34359740 | ||
| Primary structure of the peptidoglycan-derived tracheal cytotoxin of Bordetella pertussis | Q34449142 | ||
| Cross-linked peptidoglycan mediates lysostaphin binding to the cell wall envelope of Staphylococcus aureus | Q34514398 | ||
| Significant contribution of the pgdA gene to the virulence of Streptococcus suis | Q34874722 | ||
| The presence of peptidoglycan O-acetyltransferase in various staphylococcal species correlates with lysozyme resistance and pathogenicity | Q34975810 | ||
| Mechanism of action of penicillin: triggering of the pneumococcal autolytic enzyme by inhibitors of cell wall synthesis | Q35092585 | ||
| Two bactericidal targets for penicillin in pneumococci: autolysis-dependent and autolysis-independent killing mechanisms | Q35245445 | ||
| Modification of the structure of peptidoglycan is a strategy to avoid detection by nucleotide-binding oligomerization domain protein 1. | Q35689331 | ||
| Strain-related differences in lysozyme sensitivity and extent of O-acetylation of gonococcal peptidoglycan | Q36332054 | ||
| Membrane location of a deoxyribonuclease implicated in the genetic transformation of Diplococcus pneumoniae | Q36611400 | ||
| Peptidoglycan recognition proteins: pleiotropic sensors and effectors of antimicrobial defences | Q36761177 | ||
| Neisseria gonorrhoeae uses two lytic transglycosylases to produce cytotoxic peptidoglycan monomers | Q36845577 | ||
| Structural variation in the glycan strands of bacterial peptidoglycan | Q37028275 | ||
| Arthropathic properties of gonococcal peptidoglycan fragments: implications for the pathogenesis of disseminated gonococcal disease | Q37029625 | ||
| Cell envelope stress response in Gram-positive bacteria | Q37049377 | ||
| Strain distribution in extents of lysozyme resistance and O-acetylation of gonococcal peptidoglycan determined by high-performance liquid chromatography | Q37101759 | ||
| The TLR2-MyD88-NOD2-RIPK2 signalling axis regulates a balanced pro-inflammatory and IL-10-mediated anti-inflammatory cytokine response to Gram-positive cell walls | Q37139051 | ||
| Increased NOD2-mediated recognition of N-glycolyl muramyl dipeptide | Q37292790 | ||
| pH-dependent internalization of muramyl peptides from early endosomes enables Nod1 and Nod2 signaling | Q37358204 | ||
| Helicobacter pylori-mediated transcriptional regulation of the human beta-defensin 2 gene requires NF-kappaB. | Q39567005 | ||
| Clathrin- and dynamin-dependent endocytic pathway regulates muramyl dipeptide internalization and NOD2 activation | Q39870668 | ||
| The linkage between teichoic acid and peptidoglycan in bacterial cell walls | Q39876706 | ||
| Binding and Cellular Activation Studies Reveal That Toll-like Receptor 2 Can Differentially Recognize Peptidoglycan from Gram-positive and Gram-negative Bacteria | Q39891823 | ||
| Structure of the linkage units between ribitol teichoic acids and peptidoglycan | Q39966380 | ||
| Nod1 mediates cytoplasmic sensing of combinations of extracellular bacteria | Q40138263 | ||
| Contribution of phagocytosis and intracellular sensing for cytokine production by Staphylococcus aureus-activated macrophages | Q40205815 | ||
| hPepT1 transports muramyl dipeptide, activating NF-kappaB and stimulating IL-8 secretion in human colonic Caco2/bbe cells | Q40497021 | ||
| Nucleotide-binding oligomerization domain proteins are innate immune receptors for internalized Streptococcus pneumoniae | Q40542030 | ||
| Enterococcus faecalis constitutes an unusual bacterial model in lysozyme resistance | Q41904091 | ||
| Influence of wall teichoic acid on lysozyme resistance in Staphylococcus aureus. | Q41905397 | ||
| Mutations affecting peptidoglycan acetylation in Neisseria gonorrhoeae and Neisseria meningitidis | Q42949822 | ||
| A helix-loop-helix peptide at the upper lip of the active site cleft of lysozyme confers potent antimicrobial activity with membrane permeabilization action | Q43740251 | ||
| Mucosal clearance of capsule-expressing bacteria requires both TLR and nucleotide-binding oligomerization domain 1 signaling | Q44289699 | ||
| Penicillin enhances the toll-like receptor 2-mediated proinflammatory activity of Streptococcus pneumoniae. | Q44598925 | ||
| Mouse Lysozyme M Is Important in Pulmonary Host Defense againstKlebsiella pneumoniaeInfection | Q44655799 | ||
| Capsular expression in Streptococcus pneumoniae negatively affects spontaneous and antibiotic-induced lysis and contributes to antibiotic tolerance | Q44727665 | ||
| The glycopeptide vancomycin does not enhance toll-like receptor 2 (TLR2) activation by Streptococcus pneumoniae. | Q44931231 | ||
| Identification of the namH gene, encoding the hydroxylase responsible for the N-glycolylation of the mycobacterial peptidoglycan | Q45136861 | ||
| Why are pathogenic staphylococci so lysozyme resistant? The peptidoglycan O-acetyltransferase OatA is the major determinant for lysozyme resistance of Staphylococcus aureus | Q45231397 | ||
| Cationic polypeptides are required for antibacterial activity of human airway fluid. | Q45946168 | ||
| The pgdA gene encodes for a peptidoglycan N-acetylglucosamine deacetylase in Streptococcus pneumoniae | Q47865657 | ||
| Covalent linkage between the capsular polysaccharide and the cell wall peptidoglycan of Streptococcus pneumoniae revealed by immunochemical methods. | Q52241543 | ||
| The wall peptidoglycans of Neisseria perflava, Moraxella glucidolytica, Pseudomonas alcaligenes and Proteus vulgaris strain P18. | Q54014930 | ||
| Muramylpeptide shedding modulates cell sensing of Shigella flexneri. | Q54430471 | ||
| Glucosamine substitution and muramidase susceptibility in Bacillus anthracis. | Q54475192 | ||
| Multiple antibiotic resistance in a bacterium with suppressed autolytic system. | Q54677814 | ||
| Attenuation of penicillin resistance in a peptidoglycan O-acetyl transferase mutant of Streptococcus pneumoniae | Q57077244 | ||
| Bacterial membrane vesicles deliver peptidoglycan to NOD1 in epithelial cells | Q57272367 | ||
| RICK/RIP2 Mediates Innate Immune Responses Induced through Nod1 and Nod2 but Not TLRs | Q57275903 | ||
| Induction of Nod2 in Myelomonocytic and Intestinal Epithelial Cells via Nuclear Factor-κB Activation | Q59383486 | ||
| SpxB RegulatesO-Acetylation-dependent Resistance ofLactococcus lactisPeptidoglycan to Hydrolysis | Q60181267 | ||
| Serotypic variations among virulent pneumococci in deposition and degradation of covalently bound C3b: implications for phagocytosis and antibody production | Q70018803 | ||
| Identification of 2-amino-2-deoxyglucose residues in the peptidoglucan of Streptococcus pneumoniae | Q70508178 | ||
| Digestion of Streptococcus pneumoniae cell walls with its major peptidoglycan hydrolase releases branched stem peptides carrying proinflammatory activity | Q77353720 | ||
| The peptidoglycan-degrading property of lysozyme is not required for bactericidal activity in vivo | Q79755027 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 562-570 | |
| P577 | publication date | 2010-11-01 | |
| P1433 | published in | Infection and Immunity | Q6029193 |
| P1476 | title | Modifications to the peptidoglycan backbone help bacteria to establish infection | |
| P478 | volume | 79 |
| Q36696350 | (D)-Amino acid chemical reporters reveal peptidoglycan dynamics of an intracellular pathogen |
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