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The Journal of Immunology, ISSN 0022-1767, 01/2004, Volume 172, Issue 1, pp. 567 - 576
The signaling mechanism by which the anti-inflammatory cytokine IL-10 mediates suppression of proinflammatory cytokine synthesis remains largely unknown.... 
RHEUMATOID-ARTHRITIS | TUMOR-NECROSIS-FACTOR | DNA-BINDING | HUMAN NEUTROPHILS | TYROSINE PHOSPHORYLATION | INTERLEUKIN-10 RECEPTOR | GENE-EXPRESSION | KAPPA-B-ALPHA | IMMUNOLOGY | HUMAN MONOCYTES | MONONUCLEAR PHAGOCYTES | Protein Binding - genetics | Protein Biosynthesis | Interleukin-6 - antagonists & inhibitors | Humans | Tumor Necrosis Factor-alpha - genetics | Immunoglobulins - genetics | Lipopolysaccharides - antagonists & inhibitors | RNA, Messenger - metabolism | Suppressor of Cytokine Signaling Proteins | Repressor Proteins - antagonists & inhibitors | Antigens, CD - metabolism | Trans-Activators - physiology | Protein Tyrosine Phosphatases - antagonists & inhibitors | RNA, Messenger - biosynthesis | Protein Tyrosine Phosphatases - genetics | Inflammation Mediators - physiology | Glycoproteins - genetics | DNA-Binding Proteins - physiology | Protein Tyrosine Phosphatases - biosynthesis | DNA-Binding Proteins - antagonists & inhibitors | Signal Transduction - genetics | DNA - metabolism | Down-Regulation - genetics | Macrophages - metabolism | Protein Tyrosine Phosphatase, Non-Receptor Type 2 | Repressor Proteins - biosynthesis | Up-Regulation - immunology | Interleukin-10 - antagonists & inhibitors | Lipopolysaccharides - pharmacology | Adenoviruses, Human - genetics | Interleukin-10 - immunology | Tumor Necrosis Factor-alpha - biosynthesis | Phosphorylation | Tissue Inhibitor of Metalloproteinase-1 - biosynthesis | Antigens, CD - biosynthesis | Receptors, Cell Surface | Receptors, IgG - biosynthesis | Receptors, IgG - antagonists & inhibitors | Interleukin-10 - physiology | Signal Transduction - immunology | Tissue Inhibitor of Metalloproteinase-1 - metabolism | Signaling Lymphocytic Activation Molecule Family Member 1 | Receptors, Tumor Necrosis Factor - antagonists & inhibitors | RNA, Messenger - antagonists & inhibitors | Receptors, Tumor Necrosis Factor, Type II | Trans-Activators - genetics | Inflammation Mediators - antagonists & inhibitors | Trans-Activators - biosynthesis | Immunoglobulins - biosynthesis | Macrophages - immunology | Inflammation Mediators - immunology | Receptors, Tumor Necrosis Factor - metabolism | Immune Sera - pharmacology | Proteins - physiology | Cells, Cultured | Glycoproteins - antagonists & inhibitors | Histocompatibility Antigens Class II - biosynthesis | Tissue Inhibitor of Metalloproteinase-1 - antagonists & inhibitors | Transcription Factors - antagonists & inhibitors | Transcription Factors - biosynthesis | Up-Regulation - genetics | DNA-Binding Proteins - genetics | DNA - antagonists & inhibitors | Glycoproteins - biosynthesis | Suppressor of Cytokine Signaling 3 Protein | Down-Regulation - immunology | Interleukin-6 - biosynthesis | Receptors, Tumor Necrosis Factor - biosynthesis | STAT3 Transcription Factor | Trans-Activators - antagonists & inhibitors | Genetic Vectors | DNA-Binding Proteins - biosynthesis | Tumor Necrosis Factor-alpha - antagonists & inhibitors | SOCS-3 protein | Index Medicus | Abridged Index Medicus
Journal Article
Cancer Research, ISSN 0008-5472, 06/2010, Volume 70, Issue 11, pp. 4335 - 4345
Journal Article
Inflammation, ISSN 0360-3997, 8/2013, Volume 36, Issue 4, pp. 921 - 931
Murine macrophages are activated by interferon-γ (IFN-γ) and/or Toll-like receptor (TLR) agonists such as bacterial endotoxin (lipopolysaccharide [LPS]) to... 
Pathology | alternative activation | Medicine & Public Health | Rheumatology | adenosine receptor | Internal Medicine | macrophage | TLR | Pharmacology/Toxicology | IL-4Rα | ACTIVATION | A(2A) RECEPTORS | C/EBP-BETA | IL-10 PRODUCTION | INJURY | IL-4R alpha | IMMUNOLOGY | MURINE | CELL BIOLOGY | REPAIR | LIPOPOLYSACCHARIDE | TRANSCRIPTIONAL REGULATION | EXPRESSION | Vascular Endothelial Growth Factor A - biosynthesis | Nitric Oxide Synthase Type II - biosynthesis | Mannose-Binding Lectins - biosynthesis | Arginase - biosynthesis | Intercellular Signaling Peptides and Proteins - biosynthesis | Male | Lectins, C-Type - biosynthesis | Lectins - biosynthesis | Interleukin-4 Receptor alpha Subunit - genetics | Cell Differentiation | Receptors, Cell Surface - biosynthesis | Macrophages - immunology | Interleukin-12 - biosynthesis | Interleukin-4 Receptor alpha Subunit - metabolism | Signal Transduction | Purinergic P1 Receptor Agonists - pharmacology | Cells, Cultured | Mice, Transgenic | Adenosine - pharmacology | Receptor, Adenosine A2A - metabolism | beta-N-Acetylhexosaminidases - biosynthesis | Neovascularization, Physiologic - immunology | Macrophage Activation | Animals | Adenosine - metabolism | Interleukin-10 - biosynthesis | Macrophages - drug effects | Mice | Mice, Inbred BALB C | Tumor Necrosis Factor-alpha - biosynthesis | Physiological aspects | Cell receptors | Genetic aspects | Cellular signal transduction | Research | Macrophages | Index Medicus | IL4Rα | Alternative Activation | Adenosine Receptor | Macrophage
Journal Article
Journal Article
Journal of Immunology, ISSN 0022-1767, 04/2016, Volume 196, Issue 8, pp. 3421 - 3428
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2011, Volume 108, Issue 42, pp. 17408 - 17413
Contact of Mycobacterium tuberculosis (M.tb) with the immune system requires interactions between microbial surface molecules and host pattern recognition... 
Untranslated regions | RNA stability | Cell culture techniques | Messenger RNA | MicroRNA | Mycobacterium tuberculosis | Infections | Biosynthesis | Physiological regulation | Macrophages | Innate immunity | Intracellular pathogen | Cell signaling | Lipoglycans | CONTAINING MESSENGER-RNAS | IMMUNE-RESPONSE | STABILITY | MULTIDISCIPLINARY SCIENCES | P38 MAPK | lipoglycans | FACTOR-ALPHA | TUMOR-NECROSIS-FACTOR | RICH ELEMENT | innate immunity | intracellular pathogen | cell signaling | INFECTION | BINDING | EXPRESSION | Promoter Regions, Genetic | Phosphorylation | Humans | Tumor Necrosis Factor-alpha - genetics | Mycobacterium tuberculosis - immunology | MicroRNAs - metabolism | MAP Kinase Kinase 2 - metabolism | Toll-Like Receptor 2 - metabolism | RNA Stability | Lipopolysaccharides - immunology | MAP Kinase Signaling System - immunology | Mycobacterium tuberculosis - pathogenicity | Macrophages - metabolism | Virulence - immunology | Lipopolysaccharides - pharmacology | Macrophages - drug effects | MicroRNAs - genetics | p38 Mitogen-Activated Protein Kinases - metabolism | In Vitro Techniques | Proto-Oncogene Proteins c-akt - metabolism | Tumor Necrosis Factor-alpha - biosynthesis | Macrophages - immunology | Macrophages - microbiology | Tumor necrosis factor | Physiological aspects | Genetic aspects | Research | Mitogen-activated protein kinases | Gram-positive bacteria | Signal transduction | Kinases | Ribonucleic acid--RNA | Gene expression | Index Medicus | 1-Phosphatidylinositol 3-kinase | Biological Sciences
Journal Article
Cellular Immunology, ISSN 0008-8749, 01/2013, Volume 281, Issue 1, pp. 51 - 61
Journal Article
Journal of Leukocyte Biology, ISSN 0741-5400, 06/2006, Volume 79, Issue 6, pp. 1279 - 1285
Dendritic cells (DCs) play an important role in innate and adaptive immune responses. In addition to their phagocytic activity, DCs present foreign antigens to... 
human | cytokines | cell activation | Human | Cytokines | Cell activation | SIGNAL-TRANSDUCTION PATHWAYS | ACTIVATION | RECEPTOR | ANTIGEN PRESENTATION | IMMUNOLOGY | CUTTING EDGE | CELL BIOLOGY | B-CELLS | HUMAN NK | COMMON GAMMA-CHAIN | HEMATOLOGY | T-CELLS | IFN-ALPHA | Dendritic Cells - immunology | Humans | Membrane Glycoproteins - biosynthesis | Receptors, Interleukin-1 - genetics | Tumor Necrosis Factor-alpha - genetics | Suppressor of Cytokine Signaling 1 Protein | Gene Expression Profiling | Lipopolysaccharides - antagonists & inhibitors | RNA, Messenger - biosynthesis | Interleukins - physiology | T-Lymphocytes - metabolism | Chemokines, CC - biosynthesis | Cells, Cultured - immunology | Chemokines, CXC - biosynthesis | Cytokines - genetics | Intracellular Signaling Peptides and Proteins - genetics | Interleukin-12 - biosynthesis | Chemokine CCL5 | Cells, Cultured - drug effects | Receptors, Interleukin-21 | Lymphocyte Activation | Repressor Proteins - genetics | Suppressor of Cytokine Signaling Proteins - genetics | Toll-Like Receptor 4 - genetics | Receptors, Interleukin-1 - biosynthesis | Receptors, Interleukin - genetics | Dendritic Cells - secretion | Feedback, Physiological | Macrophages - metabolism | Repressor Proteins - biosynthesis | T-Lymphocytes - immunology | Cells, Cultured - metabolism | HLA-DR Antigens - biosynthesis | Suppressor of Cytokine Signaling Proteins - biosynthesis | Tumor Necrosis Factor-alpha - biosynthesis | Receptors, Interleukin - biosynthesis | Toll-Like Receptor 4 - biosynthesis | Interleukin-12 - genetics | Dendritic Cells - drug effects | Interleukins - pharmacology | Receptors, Interferon - genetics | Dendritic Cells - metabolism | RNA, Messenger - genetics | Cell Communication | Recombinant Proteins - pharmacology | Chemokines, CXC - genetics | Membrane Glycoproteins - genetics | Gene Expression Regulation - drug effects | Suppressor of Cytokine Signaling 3 Protein | Chemokines, CC - genetics | Macrophages - drug effects | Interleukin-21 Receptor alpha Subunit | Receptors, Interferon - biosynthesis | Cytokines - biosynthesis | Interferon-gamma - pharmacology | Index Medicus
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2011, Volume 6, Issue 10, pp. e25514 - e25514
Coxiella burnetii, the etiologic agent of human Q fever, is a Gram-negative and naturally obligate intracellular bacterium. The O-specific polysaccharide chain... 
PHOSPHOMANNOSE ISOMERASE | O-ANTIGENS | Q-FEVER | PSEUDOMONAS-AERUGINOSA | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | 9 MILE | STRAIN PRISCILLA | PHASE-I LIPOPOLYSACCHARIDE | POLYACRYLAMIDE GELS | PROTEINS | Biocatalysis | Guanosine Diphosphate Sugars - biosynthesis | Guanosine Diphosphate Sugars - chemistry | Guanosine Diphosphate Mannose - chemistry | Humans | Lipopolysaccharides - metabolism | Guanosine Diphosphate Mannose - biosynthesis | Biosynthetic Pathways | Mannose-6-Phosphate Isomerase - metabolism | Mutation - genetics | Coxiella burnetii - enzymology | Deoxy Sugars - chemistry | Coxiella burnetii - metabolism | Nucleotidyltransferases | Phosphotransferases (Phosphomutases) - metabolism | Escherichia coli - metabolism | Bacterial Proteins - metabolism | Kinetics | Bacterial Proteins - isolation & purification | Deoxy Sugars - biosynthesis | Phosphates | Salmonella | Laboratories | GDP-mannose | Escherichia coli | Lipids | Mannose | Biosynthesis | Dehydration | Lipopolysaccharides | Proteins | Biological effects | GDP-D-mannose | Enzymatic activity | E coli | Etiology | Pseudomonas aeruginosa | Bacteria | Complementation | Gram-negative bacteria | Chemical synthesis | Chromosomes | Sugars | Recombinant | Enzymes | Fructose-6-phosphate | Isomerization | Cloning | Chemical reactions | Phosphomannomutase | Physical properties | Fructose | Fever | Phosphoglucomutase | Medicine | Studies | Q fever | Open reading frames | GDP-mannose pyrophosphorylase | Methods | Index Medicus
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 06/2013, Volume 1832, Issue 6, pp. 848 - 863
Sepsis is characterized by systematic inflammation and contributes to cardiac dysfunction. This study was designed to examine the effect of protein kinase B... 
Heart | ER stress | Sepsis | Akt | Contractile function | Apoptosis | OXIDATIVE STRESS | CONTRACTILE DYSFUNCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEART-FAILURE | ENDOPLASMIC-RETICULUM STRESS | AUTOPHAGY | GROWTH-FACTOR I | SIGNAL-TRANSDUCTION | SYNTHASE | BIOPHYSICS | INFLAMMATORY RESPONSE | NF-KAPPA-B | Caspase 9 - genetics | Apoptosis - drug effects | Calcium - metabolism | Heat-Shock Proteins - biosynthesis | Myocardial Contraction - drug effects | bcl-2-Associated X Protein - biosynthesis | Apoptosis - genetics | Glycogen Synthase Kinase 3 beta | Heat-Shock Proteins - genetics | Phosphorylation - genetics | Caspase 3 - genetics | Phosphorylation - drug effects | Transcription Factor CHOP - biosynthesis | Proto-Oncogene Proteins c-akt - metabolism | Apoptosis Regulatory Proteins - biosynthesis | Lipopolysaccharides - toxicity | Endoplasmic Reticulum Stress - drug effects | Mice, Transgenic | Glycogen Synthase Kinase 3 - genetics | Eukaryotic Initiation Factor-2 - genetics | Mice | Enzyme Activation - genetics | Transcription Factor CHOP - genetics | Eukaryotic Initiation Factor-2 - biosynthesis | Microtubule-Associated Proteins - genetics | bcl-X Protein - genetics | Extracellular Signal-Regulated MAP Kinases - metabolism | Endoplasmic Reticulum Stress - genetics | Extracellular Signal-Regulated MAP Kinases - genetics | Proto-Oncogene Proteins c-akt - genetics | Myocardial Contraction - genetics | MAP Kinase Signaling System - genetics | Apoptosis Regulatory Proteins - genetics | Caspase 3 - biosynthesis | bcl-X Protein - biosynthesis | bcl-2-Associated X Protein - genetics | Beclin-1 | Gene Expression Regulation - genetics | Myocardium - pathology | Transcription Factors - biosynthesis | Transcription Factors - genetics | Enzyme Activation - drug effects | Glycogen Synthase Kinase 3 - metabolism | Microtubule-Associated Proteins - biosynthesis | Gene Expression Regulation - drug effects | Autophagy-Related Protein 7 | Myocardium - enzymology | Animals | MAP Kinase Signaling System - drug effects | Caspase 9 - biosynthesis
Journal Article
Journal Article