| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.JBIOR.2013.09.009 |
| P8608 | Fatcat ID | release_jftxdxmogvdj7hc5xefeybhswe |
| P932 | PMC publication ID | 3946543 |
| P698 | PubMed publication ID | 24113376 |
| P5875 | ResearchGate publication ID | 257647296 |
| P50 | author | Edward A. Dennis | Q54261384 |
| P2093 | author name string | Paul C Norris | |
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| Foam cells in atherosclerosis | Q38115664 | ||
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| Identification of a key pathway required for the sterile inflammatory response triggered by dying cells | Q40119160 | ||
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| Monoclonal antibody to the murine type 3 complement receptor inhibits adhesion of myelomonocytic cells in vitro and inflammatory cell recruitment in vivo | Q41905685 | ||
| Regulation of TNFalpha and interleukin-10 production by prostaglandins I(2) and E(2): studies with prostaglandin receptor-deficient mice and prostaglandin E-receptor subtype-selective synthetic agonists | Q43574326 | ||
| Conditional knockout mouse for tissue-specific disruption of the cyclooxygenase-2 (Cox-2) gene | Q46051063 | ||
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| Differential roles of macrophages in diverse phases of skin repair. | Q54440277 | ||
| Conditional macrophage ablation demonstrates that resident macrophages initiate acute peritoneal inflammation | Q81377946 | ||
| Macrophages sequentially change their functional phenotype in response to changes in microenvironmental influences | Q81880357 | ||
| Structure of human chitotriosidase. Implications for specific inhibitor design and function of mammalian chitinase-like lectins | Q27638875 | ||
| Obesity is associated with macrophage accumulation in adipose tissue | Q27860976 | ||
| Spinal 12-lipoxygenase-derived hepoxilin A3 contributes to inflammatory hyperalgesia via activation of TRPV1 and TRPA1 receptors | Q28264127 | ||
| Macrophage plasticity and polarization: in vivo veritas | Q29547620 | ||
| Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes | Q29547633 | ||
| Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm | Q29614349 | ||
| Alternative activation of macrophages: mechanism and functions | Q29614350 | ||
| Macrophages, inflammation, and insulin resistance | Q29614351 | ||
| IDO expression by dendritic cells: tolerance and tryptophan catabolism | Q29614752 | ||
| How dying cells alert the immune system to danger | Q29615501 | ||
| Fate mapping analysis reveals that adult microglia derive from primitive macrophages | Q29616177 | ||
| Macrophage activation and polarization | Q29616353 | ||
| Monocyte recruitment during infection and inflammation | Q29620067 | ||
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| Pharmacological correction of a defect in PPAR-gamma signaling ameliorates disease severity in Cftr-deficient mice | Q33712428 | ||
| Macrophage scavenger receptors and foam cell formation. | Q33782030 | ||
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| Mammalian chitinase-like proteins. | Q33976447 | ||
| Monocyte-mediated defense against microbial pathogens. | Q34065898 | ||
| The role of the P2X₇ receptor in infectious diseases | Q34079146 | ||
| Molecular physiology of P2X receptors and ATP signalling at synapses | Q34188163 | ||
| Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation | Q34326460 | ||
| Class A scavenger receptors, macrophages, and atherosclerosis | Q34372269 | ||
| A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-kappaB and enhanced IRF-3/STAT1 activation). | Q34465280 | ||
| Biochemical and functional characterization of three activated macrophage populations. | Q34556828 | ||
| Macrophages regulate the angiogenic switch in a mouse model of breast cancer | Q34582812 | ||
| Cox-2 deletion in myeloid and endothelial cells, but not in epithelial cells, exacerbates murine colitis | Q34617230 | ||
| Enzymes and receptors of prostaglandin pathways with arachidonic acid-derived versus eicosapentaenoic acid-derived substrates and products | Q34630820 | ||
| Thematic Review Series: Proteomics. An integrated omics analysis of eicosanoid biology | Q34952213 | ||
| The macrophage foam cell as a target for therapeutic intervention | Q34986351 | ||
| A potential role of macrophage activation in the treatment of cancer | Q34987424 | ||
| Specificity of eicosanoid production depends on the TLR-4-stimulated macrophage phenotype | Q35170002 | ||
| High-throughput lipidomic analysis of fatty acid derived eicosanoids and N-acylethanolamines | Q35490988 | ||
| Recent advances in molecular biology and physiology of the prostaglandin E2-biosynthetic pathway | Q35592569 | ||
| Immunological consequences of apoptotic cell phagocytosis | Q35928204 | ||
| Omega-3 fatty acids cause dramatic changes in TLR4 and purinergic eicosanoid signaling | Q36001468 | ||
| P921 | main subject | inflammation | Q101991 |
| macrophage | Q184204 | ||
| P304 | page(s) | 99-110 | |
| P577 | publication date | 2013-09-25 | |
| P1433 | published in | Advances in Biological Regulation | Q26854003 |
| P1476 | title | A lipidomic perspective on inflammatory macrophage eicosanoid signaling | |
| P478 | volume | 54 |
| Q52708939 | APOL1 renal risk variants induce aberrant THP-1 monocyte differentiation and increase eicosanoid production via enhanced expression of cyclooxygenase 2. |
| Q38782571 | An analysis on the suppression of NO and PGE2 by diphenylheptane A and its effect on glycerophospholipids of lipopolysaccharide-induced RAW264.7 cells with UPLC/ESI-QTOF-MS. |
| Q36815776 | Arachidonic acid-derived signaling lipids and functions in impaired healing |
| Q55007448 | Development and application of a UHPLC-MS/MS metabolomics based comprehensive systemic and tissue-specific screening method for inflammatory, oxidative and nitrosative stress. |
| Q53637723 | Down-regulation of NF-κB expression by n-3 fatty acid-rich linseed oil is modulated by PPARγ activation, eicosanoid cascade and secretion of cytokines by macrophages in rats fed partially hydrogenated vegetable fat. |
| Q90193544 | ER-Mitochondria Communication in Cells of the Innate Immune System |
| Q36122730 | Fatty acid-related modulations of membrane fluidity in cells: detection and implications. |
| Q38207743 | Fatty acids and cardiac disease: fuel carrying a message |
| Q90294479 | Fatty acids and selected endocannabinoids content in cerebrospinal fluids from patients with neuroinfections |
| Q46395772 | Global assessment of oxidized free fatty acids in brain reveals an enzymatic predominance to oxidative signaling after trauma |
| Q28608553 | Integrated metabolic modelling reveals cell-type specific epigenetic control points of the macrophage metabolic network |
| Q34835482 | Lipidome of atherosclerotic plaques from hypercholesterolemic rabbits |
| Q50062519 | Metabolic regulation of macrophage phenotype and function. |
| Q35561091 | Opposite cross-talk by oleate and palmitate on insulin signaling in hepatocytes through macrophage activation |
| Q46250023 | Oxidized LDL triggers changes in oxidative stress and inflammatory biomarkers in human macrophages |
| Q42725788 | Polarization of Macrophages toward M2 Phenotype Is Favored by Reduction in iPLA2β (Group VIA Phospholipase A2) |
| Q99711505 | Requisite Omega-3 HUFA Biomarker Thresholds for Preventing Murine Lupus Flaring |
| Q57177488 | Role of oxylipins in cardiovascular diseases |
| Q47696134 | Specific plasma oxylipins increase the odds of cardiovascular and cerebrovascular events in patients with peripheral artery disease. |
| Q90612384 | Stereotactic Body Radiation and Interleukin-12 Combination Therapy Eradicates Pancreatic Tumors by Repolarizing the Immune Microenvironment |
| Q36847053 | UPLC-MS/MS-Based Profiling of Eicosanoids in RAW264.7 Cells Treated with Lipopolysaccharide |
| Q35674290 | Understanding the Mysterious M2 Macrophage through Activation Markers and Effector Mechanisms |
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