Aggregates are the biologically active units of endotoxin.
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Co-operation of TLR4 and raft proteins in LPS-induced pro-inflammatory signalingSequence context induced antimicrobial activity: insight into lipopolysaccharide permeabilizationEthanolic Echinacea purpurea Extracts Contain a Mixture of Cytokine-Suppressive and Cytokine-Inducing Compounds, Including Some That Originate from Endophytic BacteriaInnate immunity in Arabidopsis thaliana: lipopolysaccharides activate nitric oxide synthase (NOS) and induce defense genes.Structure of the lipid A-inner core region and biological activity of Plesiomonas shigelloides O54 (strain CNCTC 113/92) lipopolysaccharide.Morphology, size distribution, and aggregate structure of lipopolysaccharide and lipid A dispersions from enterobacterial origin.Mapping residue-specific contacts of polymyxin B with lipopolysaccharide by saturation transfer difference NMR: insights into outer-membrane disruption and endotoxin neutralization.Modeling the electrostatic potential of asymmetric lipopolysaccharide membranes: the MEMPOT algorithm implemented in DelPhi.Differential induction of the toll-like receptor 4-MyD88-dependent and -independent signaling pathways by endotoxins.The role of Toll-like receptors in the regulation of neutrophil migration, activation, and apoptosis.Lipopolysaccharides with acylation defects potentiate TLR4 signaling and shape T cell responses.Wood dust exposure and risk of lung cancerIn-Field Implementation of a Recombinant Factor C Assay for the Detection of Lipopolysaccharide as a Biomarker of Extant Life within Glacial Environments.Targeting glioblastoma via intranasal administration of Ff bacteriophages.Endotoxin deactivation by transient acidification.Functional Roles of Aromatic Residues and Helices of Papiliocin in its Antimicrobial and Anti-inflammatory Activities.Structure and function of papiliocin with antimicrobial and anti-inflammatory activities isolated from the swallowtail butterfly, Papilio xuthus.Adjuvants for Leishmania vaccines: from models to clinical application.A potent anti-inflammatory peptide from the salivary glands of horsefly.Characterization of the apoLp-III/LPS complex: insight into the mode of binding interactionMechanisms of endotoxin neutralization by synthetic cationic compounds.Aggregation behavior of an ultra-pure lipopolysaccharide that stimulates TLR-4 receptors.Apolipoprotein A-II augments monocyte responses to LPS by suppressing the inhibitory activity of LPS-binding protein.A novel fluorescent probe that senses the physical state of lipid bilayers.CD14 mediates binding of high doses of LPS but is dispensable for TNF-α productionAdjuvants containing natural and synthetic Toll-like receptor 4 ligands.Antimicrobial peptides and endotoxin inhibit cytokine and nitric oxide release but amplify respiratory burst response in human and murine macrophages.Anti-inflammatory activities of cecropin A and its mechanism of action.Comparison of anti-endotoxin activity of apoE and apoA mimetic derivatives of a model amphipathic peptide 18A.Intact rough- and smooth-form lipopolysaccharides from Escherichia coli separated by preparative gel electrophoresis exhibit differential biologic activity in human macrophages.Enantiomeric 9-mer peptide analogs of protaetiamycine with bacterial cell selectivities and anti-inflammatory activities.Perturbation of Lipopolysaccharide (LPS) Micelles by Sushi 3 (S3) antimicrobial peptide. The importance of an intermolecular disulfide bond in S3 dimer for binding, disruption, and neutralization of LPS.Differential inductions of TNF-alpha and IGTP, IIGP by structurally diverse classic and non-classic lipopolysaccharides.Biophysical analysis of the interaction of granulysin-derived peptides with enterobacterial endotoxinsDesigned beta-boomerang antiendotoxic and antimicrobial peptides: structures and activities in lipopolysaccharide.Mechanism of interaction of optimized Limulus-derived cyclic peptides with endotoxins: thermodynamic, biophysical and microbiological analysis.Tryptophan end-tagging for promoted lipopolysaccharide interactions and anti-inflammatory effects.Lipopolysaccharide enters the rat brain by a lipoprotein-mediated transport mechanism in physiological conditions.QMix® irrigant reduces lipopolysacharide (LPS) levels in an in vitro model.Pulmonary surfactant protein A-induced changes in the molecular conformation of bacterial deep-rough LPS lead to reduced activity on human macrophages.
P2860
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P2860
Aggregates are the biologically active units of endotoxin.
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Aggregates are the biologically active units of endotoxin.
@ast
Aggregates are the biologically active units of endotoxin.
@en
type
label
Aggregates are the biologically active units of endotoxin.
@ast
Aggregates are the biologically active units of endotoxin.
@en
prefLabel
Aggregates are the biologically active units of endotoxin.
@ast
Aggregates are the biologically active units of endotoxin.
@en
P2093
P356
P1476
Aggregates are the biologically active units of endotoxin.
@en
P2093
Andra B Schromm
Buko Lindner
Koichi Fukase
Mareike Mueller
Shoichi Kusumoto
Ulrich Seydel
P304
26307-26313
P356
10.1074/JBC.M401231200
P407
P577
2004-04-19T00:00:00Z