scholarly article | Q13442814 |
P50 | author | Satish Keshav | Q39185485 |
P2093 | author name string | S Gordon | |
M Stein | |||
N Harris | |||
P2860 | cites work | Cloning and expression in Escherichia coli of the cDNA for murine tumor necrosis factor | Q28507398 |
Mouse lysozyme M gene: isolation, characterization, and expression studies | Q33642637 | ||
Monomeric IgG2a promotes maturation of bone-marrow macrophages and expression of the mannose receptor | Q37411181 | ||
The macrophage mannose receptor: current status | Q37912609 | ||
Recombinant interleukin-4 enhances the chemiluminescent oxidative burst of murine peritoneal macrophages | Q41680999 | ||
Priming the macrophage respiratory burst with IL-4: enhancement with TNF-alpha but inhibition by IFN-gamma. | Q44491658 | ||
Differential regulation of class II MHC determinants on macrophages by IFN-gamma and IL-4. | Q44938035 | ||
Influences of interleukins 2 and 4 on tumor necrosis factor production by murine mononuclear phagocytes. | Q46263029 | ||
Augmentation of glucocorticoid action on human monocytes by interleukin-4 | Q67290338 | ||
IL-4 and granulocyte-macrophage colony-stimulating factor selectively increase HLA-DR and HLA-DP antigens but not HLA-DQ antigens on human monocytes | Q67296179 | ||
Interleukin 4 down-regulates the expression of CD14 in normal human monocytes | Q67676596 | ||
Modulation of phenotypic and functional properties of human peripheral blood monocytes by IL-4 | Q68128479 | ||
Differential regulation of IL-1 production in human monocytes by IFN-gamma and IL-4 | Q68340490 | ||
IL-4 inhibits superoxide production by human mononuclear phagocytes | Q68447056 | ||
IL-4 inhibits the expression of IL-8 from stimulated human monocytes | Q68533598 | ||
Maintenance of granuloma macrophages in serum-free medium | Q70325516 | ||
Interferon-gamma and B cell stimulatory factor-1 reciprocally regulate Ig isotype production | Q70338857 | ||
B cell stimulatory factor-1 (interleukin 4) activates macrophages for increased tumoricidal activity and expression of Ia antigens | Q70341808 | ||
Receptor-mediated pinocytosis of mannose glycoconjugates by macrophages: characterization and evidence for receptor recycling | Q71494370 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | macrophage | Q184204 |
P304 | page(s) | 287-292 | |
P577 | publication date | 1992-07-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | Interleukin 4 potently enhances murine macrophage mannose receptor activity: a marker of alternative immunologic macrophage activation | |
P478 | volume | 176 |
Q36283368 | A Novel Peroxisome Proliferator-activated Receptor (PPAR)γ Agonist 2-Hydroxyethyl 5-chloro-4,5-didehydrojasmonate Exerts Anti-Inflammatory Effects in Colitis |
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Q35652512 | A Systematic Approach to Identify Markers of Distinctly Activated Human Macrophages |
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Q42463233 | A comparison between isolated blood dendritic cells and monocyte-derived dendritic cells in pigs |
Q28281103 | A functional soluble form of the murine mannose receptor is produced by macrophages in vitro and is present in mouse serum |
Q37624601 | A lipidomic perspective on inflammatory macrophage eicosanoid signaling |
Q40471121 | A perspective on single cell behavior during infection |
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Q43195252 | ANG II receptor blockade enhances anti-inflammatory macrophages in anti-glomerular basement membrane glomerulonephritis |
Q35626060 | ASK1 modulates the expression of microRNA Let7A in microglia under high glucose in vitro condition. |
Q34677978 | Abandoning M1/M2 for a Network Model of Macrophage Function |
Q38690367 | Abdominal surgery induced gastric ileus and activation of M1 like macrophages in the gastric myenteric plexus: prevention by central vagal activation in rats |
Q36376247 | Absence of the Macrophage Mannose Receptor in Mice Does Not Increase Susceptibility toPneumocystis cariniiInfection In Vivo |
Q57464886 | Abundant a proliferation-inducing ligand (APRIL)-producing macrophages contribute to plasma cell accumulation in immunoglobulin G4-related disease |
Q35570465 | Accelerated wound closure in mice deficient for interleukin-10. |
Q24305842 | Acetylation of snail modulates the cytokinome of cancer cells to enhance the recruitment of macrophages |
Q39271657 | Activation of Macrophages in Response to Biomaterials |
Q24309152 | Activation of a TGF-beta-specific multistep gene expression program in mature macrophages requires glucocorticoid-mediated surface expression of TGF-beta receptor II |
Q37098588 | Activation of alveolar macrophages via the alternative pathway in herpesvirus-induced lung fibrosis |
Q42085711 | Activation of murine macrophages |
Q33816747 | Activation state of stromal inflammatory cells in murine metastatic pancreatic adenocarcinoma |
Q34150591 | Adiponectin primes human monocytes into alternative anti-inflammatory M2 macrophages |
Q34146922 | Adoptive transfer of IL-4Rα+ macrophages is sufficient to enhance eosinophilic inflammation in a mouse model of allergic lung inflammation |
Q36339559 | Adoptive transfer of immunomodulatory M2 macrophages prevents type 1 diabetes in NOD mice |
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Q37234908 | Age-related increases in ozone-induced injury and altered pulmonary mechanics in mice with progressive lung inflammation |
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Q33621624 | Alternatively activated macrophages derived from monocytes and tissue macrophages are phenotypically and functionally distinct. |
Q37438259 | Alternatively activated macrophages in infection and autoimmunity |
Q89554255 | Alternatively activated macrophages; a double-edged sword in allergic asthma |
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Q34298792 | Antiretroviral therapy in macrophages: implication for HIV eradication |
Q33929735 | Apolipoprotein A-I mimetic 4F alters the function of human monocyte-derived macrophages |
Q38283533 | Are "resting" microglia more "m2"? |
Q36252619 | Arginase 1+ microglia reduce Aβ plaque deposition during IL-1β-dependent neuroinflammation |
Q37474041 | Arginase in parasitic infections: macrophage activation, immunosuppression, and intracellular signals |
Q30275232 | Arteriogenesis in murine adipose tissue is contingent on CD68+ /CD206+ macrophages. |
Q36568996 | Astrocyte and macrophage regulation of YKL-40 expression and cellular response in neuroinflammation |
Q33754812 | Augmentation of human macrophage candidacidal capacity by recombinant human myeloperoxidase and granulocyte-macrophage colony-stimulating factor. |
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Q57801756 | Azithromycin promotes alternatively activated macrophage phenotype in systematic lupus erythematosus via PI3K/Akt signaling pathway |
Q36729660 | B cells promote inflammation in obesity and type 2 diabetes through regulation of T-cell function and an inflammatory cytokine profile |
Q33903923 | BCAT1 controls metabolic reprogramming in activated human macrophages and is associated with inflammatory diseases |
Q40505080 | BCG-induced granuloma formation in murine tissues |
Q93074166 | BNCT induced immunomodulatory effects contribute to mammary tumor inhibition |
Q35747364 | Beta1 and beta2 integrins mediate adhesion during macrophage fusion and multinucleated foreign body giant cell formation |
Q34556828 | Biochemical and functional characterization of three activated macrophage populations. |
Q37832678 | Biocompatibility of implants: lymphocyte/macrophage interactions |
Q57151173 | Black, White, and Gray: Macrophages in Skin Repair and Disease |
Q34218604 | Blockade of IL-6 Trans signaling attenuates pulmonary fibrosis |
Q38983052 | Blockade of the T cell immunoglobulin and mucin domain protein 3 pathway exacerbates sepsis-induced immune deviation and immunosuppression |
Q37129845 | Blood monocytes: distinct subsets, how they relate to dendritic cells, and their possible roles in the regulation of T-cell responses |
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Q47831738 | Bone marrow-derived mesenchymal stem cells propagate immunosuppressive/anti-inflammatory macrophages in cell-to-cell contact-independent and -dependent manners under hypoxic culture. |
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Q39148044 | Brain inflammation is accompanied by peripheral inflammation in Cstb (-/-) mice, a model for progressive myoclonus epilepsy. |
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Q36292623 | CD11c(+) monocyte/macrophages promote chronic Helicobacter hepaticus-induced intestinal inflammation through the production of IL-23. |
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Q30433527 | CXCL4 downregulates the atheroprotective hemoglobin receptor CD163 in human macrophages |
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Q42773865 | Classically and alternatively activated bone marrow derived macrophages differ in cytoskeletal functions and migration towards specific CNS cell types |
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Q48546230 | Glutamate metabolism in HIV-infected macrophages: implications for the CNS. |
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Q35942660 | High and low molecular weight hyaluronic acid differentially influence macrophage activation |
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Q37038993 | Identification and characterization of infiltrating macrophages in acetaminophen-induced liver injury |
Q37325176 | Identification of a CD11b(+)/Gr-1(+)/CD31(+) myeloid progenitor capable of activating or suppressing CD8(+) T cells. |
Q47998941 | Identification of compounds that decrease numbers of Mycobacteria in human macrophages in the presence of serum amyloid P. |
Q38719578 | Identification of different macrophage subpopulations with distinct activities in a mouse model of oxygen-induced retinopathy. |
Q46328983 | Identifying exposition to low oxygen environment in human macrophages using secondary ion mass spectrometry and multivariate analysis. |
Q36052406 | Identifying functional microRNAs in macrophages with polarized phenotypes |
Q37150998 | Immobilized heavy chain-hyaluronic acid polarizes lipopolysaccharide-activated macrophages toward M2 phenotype |
Q38492631 | Immune attack: the role of inflammation in Alzheimer disease. |
Q64979483 | Immune cell census in murine atherosclerosis: cytometry by time of flight illuminates vascular myeloid cell diversity. |
Q64946812 | Immune cell subset differentiation and tissue inflammation. |
Q35985907 | Immune modulation as a therapeutic strategy in bone regeneration |
Q38755567 | Immune polarization by hookworms: taking cues from T helper type 2, type 2 innate lymphoid cells and alternatively activated macrophages. |
Q37386324 | Immune regulation by non-lymphoid cells in transplantation. |
Q26829220 | Immune vulnerability of infants to tuberculosis |
Q44185283 | Immunocompetence of macrophages in rats exposed to Candida albicans infection and stress |
Q71848361 | Immunohistochemical identification of type II alternatively activated dendritic macrophages (RM 3/1+3, MS-1+/-, 25F9-) in psoriatic dermis |
Q39653247 | Immunologic environment influences macrophage response to Porphyromonas gingivalis. |
Q26827675 | Immunological cells and functions in Gaucher disease |
Q37974937 | Immunology in the clinic review series; focus on cancer: tumour-associated macrophages: undisputed stars of the inflammatory tumour microenvironment |
Q92513187 | Immunopathology of Airway Surface Liquid Dehydration Disease |
Q35470983 | Immunopathology of tuberculosis: roles of macrophages and monocytes |
Q41727507 | Immunoproteasome dysfunction augments alternative polarization of alveolar macrophages |
Q41480089 | Immunoregulation by Taenia crassiceps and its antigens |
Q24532069 | Immunosenescence and macrophage functional plasticity: dysregulation of macrophage function by age-associated microenvironmental changes |
Q33557388 | Impact of endobronchial allergen provocation on macrophage phenotype in asthmatics |
Q49890355 | Implications of macrophage polarization in autoimmunity. |
Q33713080 | Improvement of spinal non-viral IL-10 gene delivery by D-mannose as a transgene adjuvant to control chronic neuropathic pain |
Q35133965 | In vitro comparison of the effects of probiotic, commensal and pathogenic strains on macrophage polarization. |
Q36103380 | In vivo downregulation of innate and adaptive immune responses in corneal allograft rejection by HC-HA/PTX3 complex purified from amniotic membrane |
Q34302328 | Increased percentages of T helper cells producing IL-17 and monocytes expressing markers of alternative activation in patients with sepsis |
Q58612977 | Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models |
Q34157473 | Induction of M2 regulatory macrophages through the β2-adrenergic receptor with protection during endotoxemia and acute lung injury |
Q36414300 | Induction of alternatively activated macrophages enhances pathogenesis during severe acute respiratory syndrome coronavirus infection |
Q22253372 | Induction of functional IL-8 receptors by IL-4 and IL-13 in human monocytes |
Q37965038 | Induction of protective immunity against cryptococcosis |
Q92461599 | Infection drives meningeal engraftment by inflammatory monocytes that impairs CNS immunity |
Q57477502 | Infection, modulation and responses of antigen-presenting cells to African swine fever viruses |
Q37148129 | Infiltration of m2 tumor-associated macrophages in oral squamous cell carcinoma correlates with tumor malignancy. |
Q36679987 | Inflammation and wound healing: the role of the macrophage |
Q55397625 | Inflammation-Induced Adverse Pregnancy and Neonatal Outcomes Can Be Improved by the Immunomodulatory Peptide Exendin-4. |
Q29622851 | Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis |
Q81163080 | Influence of pathological progression on the balance between cellular and humoral immune responses in bovine tuberculosis |
Q33831146 | Influences of age-related changes in mesenchymal stem cells on macrophages during in-vitro culture. |
Q35422948 | Ingestion of acapsular Cryptococcus neoformans occurs via mannose and beta-glucan receptors, resulting in cytokine production and increased phagocytosis of the encapsulated form |
Q34055968 | Innate immune regulation by STAT-mediated transcriptional mechanisms. |
Q35073787 | Innate immune responses to lung-stage helminth infection induce alternatively activated alveolar macrophages |
Q64970090 | Integrated Functional Analysis of the Nuclear Proteome of Classically and Alternatively Activated Macrophages. |
Q53646506 | Interaction between pancreatic cancer cells and tumor-associated macrophages promotes the invasion of pancreatic cancer cells and the differentiation and migration of macrophages. |
Q77329375 | Interactions between Mycobacterium tuberculosis and host cells: are mycobacterial sugars the key? |
Q33649222 | Interferon and alternative activation of monocyte/macrophages in systemic sclerosis-associated pulmonary arterial hypertension. |
Q86049622 | Interferon regulatory factor 7 participates in the M1-like microglial polarization switch |
Q52731929 | Interleukin 4 modulates microglia homeostasis and attenuates the early slowly progressive phase of amyotrophic lateral sclerosis. |
Q56943358 | Interleukin-10 increases mannose receptor expression and endocytic activity in monocyte-derived dendritic cells |
Q34505654 | Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype |
Q72680200 | Interleukin-13 alters the activation state of murine macrophages in vitro: comparison with interleukin-4 and interferon-gamma |
Q36846054 | Interleukin-19 in breast cancer |
Q33722773 | Interleukin-33 contributes to both M1 and M2 chemokine marker expression in human macrophages |
Q33678403 | Interleukin-33 regulates intestinal inflammation by modulating macrophages in inflammatory bowel disease |
Q58085764 | Interleukin-4 Induces Expression of the Integrin αvβ3via Transactivation of the β3Gene |
Q54685581 | Interleukin-4 and dexamethasone counterregulate extracellular matrix remodelling and phagocytosis in type-2 macrophages. |
Q33761762 | Interleukin-4 enhances pulmonary clearance of Pseudomonas aeruginosa. |
Q36711467 | Interleukin-4- and interleukin-13-mediated alternatively activated macrophages: roles in homeostasis and disease. |
Q35782114 | Interleukin-4-induced macrophage fusion is prevented by inhibitors of mannose receptor activity |
Q37295266 | Interstitial cells of Cajal, macrophages and mast cells in the gut musculature: morphology, distribution, spatial and possible functional interactions |
Q36245798 | Intimal lining layer macrophages but not synovial sublining macrophages display an IL-10 polarized-like phenotype in chronic synovitis |
Q34962285 | Intracellular survival and persistence of Chlamydia muridarum is determined by macrophage polarization |
Q37058442 | Investigation of macrophage polarization using bone marrow derived macrophages |
Q40891697 | Involvement of IGF-1 and Akt in M1/M2 activation state in bone marrow-derived macrophages. |
Q35544447 | Involvement of mannose receptor in cytokine interleukin-1beta (IL-1beta), IL-6, and granulocyte-macrophage colony-stimulating factor responses, but not in chemokine macrophage inflammatory protein 1beta (MIP-1beta), MIP-2, and KC responses, caused b |
Q91638697 | Iron nanoparticle-labeled murine mesenchymal stromal cells in an osteoarthritic model persists and suggests anti-inflammatory mechanism of action |
Q38898354 | Is Synovial Macrophage Activation the Inflammatory Link Between Obesity and Osteoarthritis? |
Q52921513 | Isolation and Differentiation of Murine Macrophages. |
Q92418418 | JAK/STAT inhibition in macrophages promotes therapeutic resistance by inducing expression of protumorigenic factors |
Q37401084 | Key role of macrophages in the pathogenesis of CD18 hypomorphic murine model of psoriasis |
Q30276711 | Knowledge gaps to understanding cardiac macrophage polarization following myocardial infarction |
Q94402057 | Kupffer Cell Metabolism and Function |
Q57025342 | LC3-Associated Phagocytosis in Myeloid Cells Promotes Tumor Immune Tolerance |
Q77675906 | Langerhans cells do not express alternative macrophage activation-associated CC chemokine (AMAC)-1 |
Q45880966 | Lentiviral-mediated administration of IL-25 in the CNS induces alternative activation of microglia |
Q37052936 | Lipocalin 2 deactivates macrophages and worsens pneumococcal pneumonia outcomes |
Q89624108 | Liver fibrosis and CD206+ macrophage accumulation are suppressed by anti-GM-CSF therapy |
Q61941964 | Location or origin? What is critical for macrophage propagation of lung fibrosis? |
Q42623032 | Long-term culture of multibacillary leprosy macrophages isolated from skin lesions: a new model to study Mycobacterium leprae-human cell interaction |
Q37583613 | Low molecular weight hyaluronan activates cytosolic phospholipase A2α and eicosanoid production in monocytes and macrophages. |
Q38021705 | Lymphocytes in obesity-related adipose tissue inflammation |
Q42948860 | Lymphocytes modulate innate immune responses and neuronal damage in experimental meningitis |
Q36200878 | Lymphocytic Microparticles Modulate Angiogenic Properties of Macrophages in Laser-induced Choroidal Neovascularization |
Q48327546 | M1 Means Kill; M2 Means Heal. |
Q35600855 | M1 and M2 macrophages: the chicken and the egg of immunity |
Q87712013 | M1- and M2-macrophage polarization in rat liver cirrhosis induced by thioacetamide (TAA), focusing on Iba1 and galectin-3 |
Q64120737 | M2 Macrophages as a Potential Target for Antiatherosclerosis Treatment |
Q51008909 | M2 macrophages induce EMT through the TGF-β/Smad2 signaling pathway. |
Q35473223 | M2-polarized tumor-associated macrophages are associated with poor prognoses resulting from accelerated lymphangiogenesis in lung adenocarcinoma |
Q52718712 | MK2 contributes to tumor progression by promoting M2 macrophage polarization and tumor angiogenesis. |
Q38450486 | MR detection of LPS-induced neutrophil activation using mannan-coated superparamagnetic iron oxide nanoparticles |
Q90601875 | Macrophage Activation and Functions during Helminth Infection: Recent Advances from the Laboratory Mouse |
Q37978620 | Macrophage Phenotype Modulation by CXCL4 in Atherosclerosis |
Q38615856 | Macrophage Polarization and Bone Formation: A review. |
Q63740086 | Macrophage Polarization in Physiological and Pathological Pregnancy |
Q38816403 | Macrophage Polarization: Decisions That Affect Health |
Q92617815 | Macrophage Polarization: Different Gene Signatures in M1(LPS+) vs. Classically and M2(LPS-) vs. Alternatively Activated Macrophages |
Q30354651 | Macrophage Recruitment and Polarization During Collateral Vessel Remodeling in Murine Adipose Tissue. |
Q45418471 | Macrophage activation and human immunodeficiency virus infection: HIV replication directs macrophages towards a pro-inflammatory phenotype while previous activation modulates macrophage susceptibility to infection and viral production |
Q29620642 | Macrophage activation and polarization: nomenclature and experimental guidelines |
Q39565014 | Macrophage activation and skeletal muscle healing following traumatic injury |
Q46811059 | Macrophage activation switching: an asset for the resolution of inflammation |
Q33999220 | Macrophage control of phagocytosed mycobacteria is increased by factors secreted by alveolar epithelial cells through nitric oxide independent mechanisms |
Q34937306 | Macrophage diversity in cardiac inflammation: a review |
Q33537990 | Macrophage dysfunction impairs resolution of inflammation in the wounds of diabetic mice |
Q38893448 | Macrophage form, function, and phenotype in mycobacterial infection: lessons from tuberculosis and other diseases |
Q36692041 | Macrophage heterogeneity in respiratory diseases |
Q44899038 | Macrophage mannose receptor in chronic sinus disease |
Q41228225 | Macrophage membrane molecules: markers of tissue differentiation and heterogeneity |
Q36850453 | Macrophage phenotypes during tissue repair |
Q38260570 | Macrophage phenotypes in atherosclerosis. |
Q29614349 | Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm |
Q33527405 | Macrophage plasticity in experimental atherosclerosis |
Q33716370 | Macrophage polarization in inflammatory diseases |
Q42920879 | Macrophage polarization in response to wear particles in vitro. |
Q28084850 | Macrophage responses to implants: prospects for personalized medicine |
Q33802153 | Macrophage roles following myocardial infarction |
Q37728093 | Macrophage signaling in HIV-1 infection |
Q28392242 | Macrophage silica nanoparticle response is phenotypically dependent |
Q28731852 | Macrophage sub-populations and the lipoxin A4 receptor implicate active inflammation during equine tendon repair |
Q89463384 | Macrophage subsets in atherosclerosis as defined by single-cell technologies |
Q37364177 | Macrophage-derived MCPIP1 mediates silica-induced pulmonary fibrosis via autophagy |
Q38056128 | Macrophage-targeted therapy: CD64-based immunotoxins for treatment of chronic inflammatory diseases. |
Q27027100 | Macrophage: SHIP of Immunity |
Q99551345 | Macrophages and the maintenance of homeostasis |
Q59880046 | Macrophages are exploited from an innate wound healing response to facilitate cancer metastasis |
Q33694114 | Macrophages are necessary for epimorphic regeneration in African spiny mice. |
Q89454243 | Macrophages directly contribute collagen to scar formation during zebrafish heart regeneration and mouse heart repair |
Q34983474 | Macrophages from patients with cirrhotic ascites showed function alteration of host defense receptor |
Q40610652 | Macrophages in chronic type 2 inflammation have a novel phenotype characterized by the abundant expression of Ym1 and Fizz1 that can be partly replicated in vitro. |
Q30525251 | Macrophages in collateral arteriogenesis. |
Q35535915 | Macrophages in diabetic gastroparesis--the missing link? |
Q37289610 | Macrophages in hepatitis B and hepatitis C virus infections |
Q35595537 | Macrophages in immunopathology of atherosclerosis: a target for diagnostics and therapy. |
Q36722852 | Macrophages in inflammatory multiple sclerosis lesions have an intermediate activation status |
Q38965333 | Macrophages in neuroinflammation: role of the renin-angiotensin-system. |
Q38194688 | Macrophages in solid organ transplantation |
Q47368141 | Macrophages under pressure: the role of macrophage polarization in hypertension. |
Q37179242 | Macrophages-Key cells in the response to wear debris from joint replacements. |
Q49609112 | Macrophages: Key orchestrators of a tumor microenvironment defined by therapeutic resistance. |
Q34076279 | Macrophages: master regulators of inflammation and fibrosis |
Q33617258 | Macrophagic and microglial responses after focal traumatic brain injury in the female rat. |
Q37628185 | Mammary Gland Involution Provides a Unique Model to Study the TGF-β Cancer Paradox |
Q28137872 | Mannose receptor and its putative ligands in normal murine lymphoid and nonlymphoid organs: In situ expression of mannose receptor by selected macrophages, endothelial cells, perivascular microglia, and mesangial cells, but not dendritic cells |
Q40665049 | Mannose receptor determination by an ELISA-like method |
Q48107825 | Mannose receptor high, M2 dermal macrophages mediate nonhealing Leishmania major infection in a Th1 immune environment. |
Q36118366 | Mannose receptor regulates myoblast motility and muscle growth |
Q38680574 | Mannosylated liposomes improve therapeutic effects of paclitaxel in colon cancer models |
Q45005983 | Markers of macrophage differentiation in experimental silicosis |
Q35980874 | Mast cell TLR2 signaling is crucial for effective killing of Francisella tularensis |
Q34579554 | Mast cell/IL-4 control of Francisella tularensis replication and host cell death is associated with increased ATP production and phagosomal acidification |
Q41757918 | Mast cells aggravate sepsis by inhibiting peritoneal macrophage phagocytosis |
Q47593606 | Mechanical ventilation induces IL-4 secretion in lungs and reduces the phagocytic capacity of lung macrophages |
Q41722140 | Membrane molecules as differentiation antigens of murine macrophages. |
Q26800098 | Mesenchymal Stromal Cells Affect Disease Outcomes via Macrophage Polarization |
Q34502380 | Mesenchymal stem cells ameliorate rhabdomyolysis-induced acute kidney injury via the activation of M2 macrophages |
Q48469192 | Mesenchymal stem cells enhance α-synuclein clearance via M2 microglia polarization in experimental and human parkinsonian disorder. |
Q47579457 | Mesenchymal stromal cells mediate a switch to alternatively activated monocytes/macrophages after acute myocardial infarction |
Q64062371 | Metabolic Targets for Improvement of Allogeneic Hematopoietic Stem Cell Transplantation and Graft-vs.-Host Disease |
Q47804954 | Metabolic characterization and RNA profiling reveal glycolytic dependence of profibrotic phenotype of alveolar macrophages in lung fibrosis |
Q92664771 | Metabolic influence on macrophage polarization and pathogenesis |
Q34117016 | Metabolic reprograming in macrophage polarization. |
Q28080815 | Metabolic reprogramming in macrophages and dendritic cells in innate immunity |
Q90214418 | Metformin induces CD11b+-cell-mediated growth inhibition of an osteosarcoma: implications for metabolic reprogramming of myeloid cells and anti-tumor effects |
Q64074554 | MicroRNA Post-transcriptional Regulation of the NLRP3 Inflammasome in Immunopathologies |
Q98726639 | MicroRNA sequences modulating inflammation and lipid accumulation in macrophage "foam" cells: Implications for atherosclerosis |
Q36266476 | MicroRNA-223 is a crucial mediator of PPARγ-regulated alternative macrophage activation |
Q47749757 | Microarray and bioinformatics analyses of gene expression profiles in BALB/c murine macrophage polarization |
Q43169264 | Microenvironmental regulation of the progression of oral potentially malignant disorders towards malignancy |
Q47106944 | Microglia and Monocytes/Macrophages Polarization Reveal Novel Therapeutic Mechanism against Stroke. |
Q46445039 | Microglia in normal appearing white matter of multiple sclerosis are alerted but immunosuppressed |
Q36547001 | Microglial M1/M2 polarization and metabolic states |
Q36000073 | Mineralocorticoid receptor blockade prevents Western diet-induced diastolic dysfunction in female mice |
Q36087549 | Model-Based Characterization of Inflammatory Gene Expression Patterns of Activated Macrophages. |
Q37256953 | Modeling the immune rheostat of macrophages in the lung in response to infection |
Q51336724 | Modulation of Immune Responses by Particulate Materials. |
Q46368288 | Modulation of chitotriosidase during macrophage differentiation. |
Q40841572 | Modulation of macrophage function by transforming growth factor beta, interleukin-4, and interleukin-10. |
Q38890797 | Modulation of murine macrophage behavior in vivo and in vitro. |
Q43235609 | Mono(2-ethylhexyl) phthalate induces both pro- and anti-inflammatory responses in rat alveolar macrophages through crosstalk between p38, the lipoxygenase pathway and PPARalpha |
Q39271596 | Monocyte/Macrophage: NK Cell Cooperation-Old Tools for New Functions |
Q36166316 | Monocytes/Macrophages Upregulate the Hyaluronidase HYAL1 and Adapt Its Subcellular Trafficking to Promote Extracellular Residency upon Differentiation into Osteoclasts |
Q60958205 | More Than Just a Removal Service: Scavenger Receptors in Leukocyte Trafficking |
Q38640912 | Morphologic, phenotypic, and transcriptomic characterization of classically and alternatively activated canine blood-derived macrophages in vitro |
Q35646486 | Much More than M1 and M2 Macrophages, There are also CD169(+) and TCR(+) Macrophages |
Q38105045 | Mucopolysaccharide diseases: a complex interplay between neuroinflammation, microglial activation and adaptive immunity. |
Q46657854 | Multinucleated giant cell formation exhibits features of phagocytosis with participation of the endoplasmic reticulum |
Q38721005 | Multinucleated giant cells in the implant bed of bone substitutes are foreign body giant cells-New insights into the material-mediated healing process. |
Q71120130 | Multiple cutaneous B-cell pseudolymphomas after allergen injections |
Q57073314 | Multivalent nanosystems: targeting monocytes/macrophages |
Q33848355 | Mycobacteria induce TPL-2 mediated IL-10 in IL-4-generated alternatively activated macrophages |
Q80171702 | Myelin-phagocytosing macrophages in isolated sciatic and optic nerves reveal a unique reactive phenotype |
Q47761139 | Myeloid cell plasticity in the evolution of central nervous system autoimmunity |
Q47123928 | Myeloid cell recruitment versus local proliferation differentiates susceptibility from resistance to filarial infection. |
Q41106752 | Myeloid expression of the AP-1 transcription factor JUNB modulates outcomes of type 1 and type 2 parasitic infections. |
Q33708751 | Myeloperoxidase-targeted imaging of active inflammatory lesions in murine experimental autoimmune encephalomyelitis |
Q35722787 | NRF2 Signaling Negatively Regulates Phorbol-12-Myristate-13-Acetate (PMA)-Induced Differentiation of Human Monocytic U937 Cells into Pro-Inflammatory Macrophages |
Q90327575 | Nanostructured titanium regulates osseointegration via influencing macrophage polarization in the osteogenic environment |
Q40538969 | Neither classical nor alternative macrophage activation is required for Pneumocystis clearance during immune reconstitution inflammatory syndrome |
Q26798236 | Nerve injury and neuropathic pain - A question of age |
Q33768246 | Neuroinflammation and M2 microglia: the good, the bad, and the inflamed. |
Q27014919 | Neuroinflammation in Alzheimer's disease; A source of heterogeneity and target for personalized therapy |
Q38779873 | Neuroinflammation: the devil is in the details |
Q41581503 | Neuropathic pain is constitutively suppressed in early life by anti-inflammatory neuroimmune regulation |
Q54551338 | Neurotrophins modulate monocyte chemotaxis without affecting macrophage function. |
Q93052075 | New Insights on the Role of Lipid Metabolism in the Metabolic Reprogramming of Macrophages |
Q40866271 | New insights into the multidimensional concept of macrophage ontogeny, activation and function. |
Q35825965 | Non-canonical alternatives: what a macrophage is 4 |
Q30252830 | Non-classical monocytes are biased progenitors of wound healing macrophages during soft tissue injury. |
Q39243680 | Norepinephrine suppresses wound macrophage phagocytic efficiency through alpha- and beta-adrenoreceptor dependent pathways |
Q38183358 | Novel biological strategies for treatment of wear particle-induced periprosthetic osteolysis of orthopaedic implants for joint replacement |
Q38415235 | Novel grooved substrata stimulate macrophage fusion, CCL2 and MMP-9 secretion |
Q91497015 | Obesity: a neuroimmunometabolic perspective |
Q30601730 | Omega-1 knockdown in Schistosoma mansoni eggs by lentivirus transduction reduces granuloma size in vivo |
Q39011826 | One microenvironment does not fit all: heterogeneity beyond cancer cells |
Q90629499 | Optimization of T-cell receptor-modified T cells for cancer therapy |
Q90282347 | Oral squamous carcinoma cells promote macrophage polarization in an MIF-dependent manner |
Q50190677 | Orchestrating liver repair - a newly discovered function of hepatic iNKT cells. |
Q41910192 | Origin and Functions of Tumor-Associated Myeloid Cells (TAMCs). |
Q36632387 | Origin of monocytes and their differentiation to macrophages and dendritic cells |
Q38963160 | Osseointegration of Zirconia in the Presence of Multinucleated Giant Cells. |
Q39738927 | Osteopontin affects macrophage polarization promoting endocytic but not inflammatory properties. |
Q33540045 | Other functions, other genes: alternative activation of antigen-presenting cells |
Q42378990 | Overexpression of OSM and IL-6 impacts the polarization of pro-fibrotic macrophages and the development of bleomycin-induced lung fibrosis |
Q24682128 | Oxidative metabolism and PGC-1beta attenuate macrophage-mediated inflammation |
Q91739144 | PAM3 protects against DSS-induced colitis by altering the M2:M1 ratio |
Q40944312 | Paracrine effects of IL-4 transfection on TS/A adenocarcinoma cells mediate reduced in vivo growth |
Q38550186 | Parasites: what are they good for? |
Q37349951 | Parasitic helminths: a pharmacopeia of anti-inflammatory molecules. |
Q92760428 | Peptide-based targeting of immunosuppressive cells in cancer |
Q92421234 | Pericytes in Cutaneous Wound Healing |
Q37209286 | Peritoneal macrophages from patients with cirrhotic ascites show impaired phagocytosis and vigorous respiratory burst |
Q91048642 | Perivascular macrophages in health and disease |
Q41730593 | Phagocyte-bacteria interactions |
Q91706849 | Pharmacological Targeting of Microglial Activation: New Therapeutic Approach |
Q46728072 | Phenotypic Characterization of Human Monocytes following Macronutrient Intake in Healthy Humans |
Q37998021 | Phenotypic and functional heterogeneity of macrophages and dendritic cell subsets in the healthy and atherosclerosis-prone aorta |
Q37246771 | Phenotypic characterization of lung macrophages in asthmatic patients: overexpression of CCL17. |
Q45830978 | Phenotypic correlations between monocytes and CD4+ T cells in allergic patients. |
Q36470642 | Phenotypic dichotomies in the foreign body reaction |
Q34978459 | Phenotypic expression in human monocyte-derived interleukin-4-induced foreign body giant cells and macrophages in vitro: dependence on material surface properties |
Q53546016 | Phenotypic, functional, and plasticity features of classical and alternatively activated human macrophages. |
Q38272127 | Pleiotropic role of PPARγ in intracerebral hemorrhage: an intricate system involving Nrf2, RXR, and NF-κB. |
Q88929744 | Polymer-augmented liposomes enhancing antibiotic delivery against intracellular infections |
Q46546679 | Polysaccharide-rich fraction of Agaricus brasiliensis enhances the candidacidal activity of murine macrophages |
Q38444555 | Porous implants modulate healing and induce shifts in local macrophage polarization in the foreign body reaction. |
Q34298543 | Porphyromonas gingivalis lipopolysaccharide weakly activates M1 and M2 polarized mouse macrophages but induces inflammatory cytokines. |
Q35116475 | Possible role of arginase-1 in concomitant tumor immunity |
Q92856462 | Potential Immunotherapeutic Targets on Myeloid Cells for Neurovascular Repair After Ischemic Stroke |
Q35627060 | Potential role for alternatively activated macrophages in the secondary bacterial infection during recovery from influenza |
Q36508642 | Preterm birth and single nucleotide polymorphisms in cytokine genes |
Q40717214 | Primary Heligmosomoides polygyrus bakeri infection induces myeloid-derived suppressor cells that suppress CD4+ Th2 responses and promote chronic infection |
Q34139938 | Progressive visceral leishmaniasis is driven by dominant parasite-induced STAT6 activation and STAT6-dependent host arginase 1 expression |
Q36862833 | Properties of human blood monocytes. II. Monocytes from healthy adults are highly heterogeneous within and among individuals |
Q36303538 | Protective immunity against pulmonary cryptococcosis is associated with STAT1-mediated classical macrophage activation |
Q47831410 | Proteomic Signature Reveals Modulation of Human Macrophage Polarization and Functions Under Differing Environmental Oxygen Conditions. |
Q33597147 | Pulmonary infection with an interferon-gamma-producing Cryptococcus neoformans strain results in classical macrophage activation and protection |
Q42436985 | Pulmonary surfactant protein A regulates TLR expression and activity in human macrophages |
Q46667650 | Purinergic signaling during macrophage differentiation results in M2 alternative activated macrophages |
Q47169463 | RANKL-induced M1 macrophages are involved in bone formation |
Q33831780 | RBP4 activates antigen-presenting cells, leading to adipose tissue inflammation and systemic insulin resistance |
Q33796715 | Rapid host defense against Aspergillus fumigatus involves alveolar macrophages with a predominance of alternatively activated phenotype |
Q90426278 | Recombinant Listeria promotes tumor rejection by CD8+ T cell-dependent remodeling of the tumor microenvironment |
Q51698784 | Recombinant Trichinella spiralis 53-kDa protein activates M2 macrophages and attenuates the LPS-induced damage of endotoxemia. |
Q38785193 | Recruited Monocytes and Type 2 Immunity Promote Lung Regeneration following Pneumonectomy |
Q38250319 | Recruiting specialized macrophages across the borders to restore brain functions |
Q37032282 | Redox control of inflammation in macrophages |
Q88298734 | Reduced substrate stiffness promotes M2-like macrophage activation and enhances peroxisome proliferator-activated receptor γ expression |
Q37440504 | Reduction of eotaxin production and eosinophil recruitment by pulmonary autologous macrophage transfer in a cockroach allergen-induced asthma model |
Q58692657 | Regulation of Energy Expenditure and Brown/Beige Thermogenic Activity by Interleukins: New Roles for Old Actors |
Q38979320 | Regulation of IL-4 Expression in Immunity and Diseases |
Q61807003 | Regulation of Type 2 Immunity in Myocardial Infarction |
Q36040842 | Regulation of alternative macrophage activation in the liver following acetaminophen intoxication by stem cell-derived tyrosine kinase |
Q26773786 | Regulation of epithelial-mesenchymal transition by tumor-associated macrophages in cancer |
Q36472048 | Regulation of fibrosis by the immune system |
Q38411808 | Regulation of immunity by Taeniids: lessons from animal models and in vitro studies |
Q36232198 | Regulation of inflammation by interleukin-4: a review of "alternatives" |
Q35125229 | Regulation of macrophage motility by the water channel aquaporin-1: crucial role of M0/M2 phenotype switch |
Q37313634 | Regulation of metabolic health and adipose tissue function by group 2 innate lymphoid cells |
Q54587789 | Regulators of macrophage activation. |
Q34219837 | Regulatory macrophages: setting the threshold for therapy |
Q36934619 | Repair of astrocytes, blood vessels, and myelin in the injured brain: possible roles of blood monocytes |
Q37889633 | Repertoire of microglial and macrophage responses after spinal cord injury |
Q90521533 | Resolution of Deep Venous Thrombosis: Proposed Immune Paradigms |
Q92715753 | Resolution of inflammation in periodontitis: a review |
Q38068503 | Review: activation patterns of microglia and their identification in the human brain. |
Q37657853 | Rheb1 deletion in myeloid cells aggravates OVA-induced allergic inflammation in mice |
Q35207665 | Rhinovirus infection induces interleukin-13 production from CD11b-positive, M2-polarized exudative macrophages |
Q35524932 | Rhinovirus infection of allergen-sensitized and -challenged mice induces eotaxin release from functionally polarized macrophages. |
Q33799737 | Rhinovirus-induced macrophage cytokine expression does not require endocytosis or replication |
Q36277715 | Role for microglia in sex differences after ischemic stroke: importance of M2 |
Q34309028 | Role of IL-4 gene polymorphisms in HBV-related hepatocellular carcinoma in a Chinese population |
Q37273123 | Role of breast regression protein 39 (BRP-39)/chitinase 3-like-1 in Th2 and IL-13-induced tissue responses and apoptosis |
Q64111310 | Role of macrophages in experimental liver injury and repair in mice |
Q33902198 | Role of macrophages in the progression of acute pancreatitis |
Q37960792 | Role of tumor-associated macrophages in the progression of hepatocellular carcinoma |
Q38396105 | Roles of microglia in brain development, tissue maintenance and repair. |
Q24598566 | S100A7 enhances mammary tumorigenesis through upregulation of inflammatory pathways |
Q34346340 | SPI-1 encoded genes of Salmonella Typhimurium influence differential polarization of porcine alveolar macrophages in vitro |
Q34641231 | STAT6 transcription factor is a facilitator of the nuclear receptor PPARγ-regulated gene expression in macrophages and dendritic cells |
Q34776805 | STAT6⁻/⁻ mice exhibit decreased cells with alternatively activated macrophage phenotypes and enhanced disease severity in murine neurocysticercosis |
Q42726211 | Selective inhibition and augmentation of alternative macrophage activation by progesterone. |
Q35173433 | Selenium levels affect the IL-4-induced expression of alternative activation markers in murine macrophages |
Q44240692 | Sequential expression of macrophage anti-microbial/inflammatory and wound healing markers following innate, alternative and classical activation. |
Q49921149 | Sex Differences in Abdominal Aortic Aneurysms. |
Q37312771 | Shaping the murine macrophage phenotype: IL-4 and cyclic AMP synergistically activate the arginase I promoter |
Q37618669 | Shared signaling systems in myeloid cell-mediated muscle regeneration |
Q54530046 | Shift toward an alternatively activated macrophage response in lungs of NO2-exposed rats. |
Q37959949 | Signal Transducers and Activators of Transcription (STAT) family members in helminth infections |
Q38204175 | Signaling pathways involved in MDSC regulation |
Q33633305 | Similarity and diversity in macrophage activation by nematodes, trematodes, and cestodes. |
Q93125442 | Single cell transcriptomics based-MacSpectrum reveals novel macrophage activation signatures in diseases |
Q87376871 | Soluble CD163 serum levels are elevated and correlated with IL-12 and CXCL10 in patients with long-standing rheumatoid arthritis |
Q34259885 | Soluble immune complexes shift the TLR-induced cytokine production of distinct polarized human macrophage subsets towards IL-10 |
Q39348940 | Some aspects of the host response to methacrylic acid containing beads in a mouse air pouch |
Q36255054 | Susceptibility of bone marrow-derived macrophages to influenza virus infection is dependent on macrophage phenotype. |
Q39658224 | Synergistic activation by p38MAPK and glucocorticoid signaling mediates induction of M2-like tumor-associated macrophages expressing the novel CD20 homolog MS4A8A. |
Q34544517 | Synthetic cationic peptide IDR-1018 modulates human macrophage differentiation |
Q92292838 | Systemic Immuno-metabolic alterations in chronic obstructive pulmonary disease (COPD) |
Q37588446 | TGF-β induces M2-like macrophage polarization via SNAIL-mediated suppression of a pro-inflammatory phenotype |
Q34306291 | TGFβ signaling plays a critical role in promoting alternative macrophage activation |
Q35145474 | TGR5 reduces macrophage migration through mTOR-induced C/EBPβ differential translation |
Q27693193 | TH1/TH2 paradigm extended: macrophage polarization as an unappreciated pathogen-driven escape mechanism? |
Q81245724 | TLR9 activation is a key event for the maintenance of a mycobacterial antigen-elicited pulmonary granulomatous response |
Q37342405 | TNF-Mediated Restriction of Arginase 1 Expression in Myeloid Cells Triggers Type 2 NO Synthase Activity at the Site of Infection |
Q48276186 | TREM-1 regulates macrophage polarization in ureteral obstruction |
Q57911908 | Targeted IL-4 therapy synergizes with dexamethasone to induce a state of tolerance by promoting Treg cells and macrophages in mice with arthritis |
Q33695357 | Targeting resolution of neuroinflammation after ischemic stroke with a lipoxin A4 analog: Protective mechanisms and long-term effects on neurological recovery. |
Q34803221 | Targeting tumor-associated macrophages as a novel strategy against breast cancer |
Q41854447 | Temporal Characterization of Microglia/Macrophage Phenotypes in a Mouse Model of Neonatal Hypoxic-Ischemic Brain Injury |
Q36377797 | Temporal phenotypic features distinguish polarized macrophages in vitro |
Q35567138 | Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis. |
Q35565153 | Th2-associated alternative Kupffer cell activation promotes liver fibrosis without inducing local inflammation |
Q88811523 | The ABP Dendrimer, a Drug-Candidate against Inflammatory Diseases That Triggers the Activation of Interleukin-10 Producing Immune Cells |
Q39265394 | The Contribution of Immune Infiltrates to Ototoxicity and Cochlear Hair Cell Loss |
Q39188002 | The Dr. Jekyll and Mr. Hyde complexity of the macrophage response in disease |
Q47620705 | The Effects of Intestinal Nematode L4 Stage on Mouse Experimental Autoimmune Encephalomyelitis. |
Q36005808 | The Interleukin-13 Receptor-α1 Chain Is Essential for Induction of the Alternative Macrophage Activation Pathway by IL-13 but Not IL-4. |
Q57062755 | The Jmjd3-Irf4 axis regulates M2 macrophage polarization and host responses against helminth infection |
Q29615845 | The M1 and M2 paradigm of macrophage activation: time for reassessment |
Q46241798 | The Mannose Receptor in Regulation of Helminth-Mediated Host Immunity |
Q90705241 | The Metabolic Requirements of Th2 Cell Differentiation |
Q92106730 | The Metabolic Signature of Macrophage Responses |
Q38646389 | The Mononuclear Phagocyte System in Organ Transplantation. |
Q92857858 | The Mononuclear Phagocytic System. Generation of Diversity |
Q38691715 | The Role of Decidual Macrophages During Normal and Pathological Pregnancy |
Q26852646 | The Role of Different Monocyte Subsets in the Pathogenesis of Atherosclerosis and Acute Coronary Syndromes |
Q38315987 | The Role of Macrophages in Promoting and Maintaining Homeostasis at the Fetal-Maternal Interface. |
Q35222060 | The Schistosoma mansoni hepatic egg granuloma provides a favorable microenvironment for sustained growth of Leishmania donovani |
Q34072227 | The absence of MyD88 has no effect on the induction of alternatively activated macrophage during Fasciola hepatica infection |
Q42234391 | The adenosine-dependent angiogenic switch of macrophages to an M2-like phenotype is independent of interleukin-4 receptor alpha (IL-4Rα) signaling |
Q97092161 | The apparition macrophage and Döderlein bacillus is negatively correlated in class I Papanicolaou smear: A morphological examination |
Q24606039 | The chemokine CCL18 causes maturation of cultured monocytes to macrophages in the M2 spectrum |
Q38097660 | The complexity of arterial classical monocyte recruitment. |
Q38195893 | The dynamic lives of macrophage and dendritic cell subsets in atherosclerosis |
Q58701739 | The effects of insulin on the inflammatory activity of BV2 microglia |
Q37400831 | The effects on weight loss and gene expression in adipose and hepatic tissues of very-low carbohydrate and low-fat isoenergetic diets in diet-induced obese mice |
Q35338729 | The emerging understanding of myeloid cells as partners and targets in tumor rejection |
Q42929951 | The expression of tumor-associated macrophages in papillary thyroid carcinoma. |
Q40971693 | The extracellular matrix of eggshell displays anti-inflammatory activities through NF-κB in LPS-triggered human immune cells |
Q35970492 | The generation of macrophages with anti-inflammatory activity in the absence of STAT6 signaling |
Q34620962 | The heterogenic properties of monocytes/macrophages and neutrophils in inflammatory response in diabetes. |
Q24646191 | The human macrophage mannose receptor directs Mycobacterium tuberculosis lipoarabinomannan-mediated phagosome biogenesis |
Q34164767 | The human tissue-biomaterial interface: a role for PPARγ-dependent glucocorticoid receptor activation in regulating the CD163+ M2 macrophage phenotype |
Q33525044 | The identification of markers of macrophage differentiation in PMA-stimulated THP-1 cells and monocyte-derived macrophages |
Q37672033 | The immunomodulatory roles of macrophages at the maternal-fetal interface |
Q61844835 | The immunophenotype of decidual macrophages in acute atherosis |
Q38123243 | The impact of neuroimmune changes on development of amyloid pathology; relevance to Alzheimer's disease. |
Q35565148 | The increase in mannose receptor recycling favors arginase induction and Trypanosoma cruzi survival in macrophages |
Q28086874 | The ischemic environment drives microglia and macrophage function |
Q46485632 | The mannose receptor binds Trichuris muris excretory/secretory proteins but is not essential for protective immunity |
Q35200863 | The mannose receptor in the brain |
Q28266161 | The mannose receptor is a pattern recognition receptor involved in host defense |
Q38312058 | The mannose receptor is expressed by olfactory ensheathing cells in the rat olfactory bulb. |
Q21090526 | The mannose receptor mediates dengue virus infection of macrophages |
Q38008966 | The molecular profile of microglia under the influence of glioma |
Q58582556 | The monocyte-macrophage-mast cell axis in dengue pathogenesis |
Q58786407 | The plasticity of primary microglia and their multifaceted effects on endogenous neural stem cells in vitro and in vivo |
Q43865526 | The polarization of T(h)1/T(h)2 balance is dependent on the intracellular thiol redox status of macrophages due to the distinctive cytokine production |
Q55325629 | The puzzling mechanism of compensatory lung growth. |
Q43873599 | The regulatory peptide pidotimod facilitates M2 macrophage polarization and its function |
Q38975948 | The role of macrophage phenotype in vascularization of tissue engineering scaffolds |
Q36913752 | The role of peritoneal alternatively activated macrophages in the process of peritoneal fibrosis related to peritoneal dialysis |
Q38083804 | The role of pregnancy-specific glycoprotein 1a (PSG1a) in regulating the innate and adaptive immune response |
Q58544871 | The signaling protein Wnt5a promotes TGFβ1-mediated macrophage polarization and kidney fibrosis by inducing the transcriptional regulators Yap/Taz |
Q43995521 | The skewing to Th1 induced by lentinan is directed through the distinctive cytokine production by macrophages with elevated intracellular glutathione content |
Q44045459 | The skin fungus-induced Th1- and Th2-related cytokine, chemokine and prostaglandin E2 production in peripheral blood mononuclear cells from patients with atopic dermatitis and psoriasis vulgaris |
Q34343645 | The tumor microenvironment in colorectal carcinogenesis |
Q36389337 | Therapeutic T cells induce tumor-directed chemotaxis of innate immune cells through tumor-specific secretion of chemokines and stimulation of B16BL6 melanoma to secrete chemokines |
Q33556819 | Thioredoxin peroxidase secreted by Fasciola hepatica induces the alternative activation of macrophages |
Q40109019 | Thymic Stromal Lymphopoietin Is Critical for Regulation of Proinflammatory Cytokine Response and Resistance to Experimental Trypanosoma congolense Infection |
Q36545986 | Thymic stromal lymphopoietin amplifies the differentiation of alternatively activated macrophages |
Q35201949 | Tissue-resident macrophages: then and now. |
Q37690485 | Tissues in different anatomical sites can sculpt and vary the tumor microenvironment to affect responses to therapy |
Q34264020 | Toll-like receptor 3 ligand polyinosinic:polycytidylic acid promotes wound healing in human and murine skin |
Q91935631 | Toxoplasma ROP16I/III ameliorated inflammatory bowel diseases via inducing M2 phenotype of macrophages |
Q37040044 | Transcriptome analysis reveals human cytomegalovirus reprograms monocyte differentiation toward an M1 macrophage |
Q34011343 | Transcriptome profiles associated to VHSV infection or DNA vaccination in turbot (Scophthalmus maximus) |
Q98303052 | Transcriptome sequencing supports a conservation of macrophage polarization in fish |
Q28068273 | Transition from inflammation to proliferation: a critical step during wound healing |
Q35894863 | Transmembrane protein 106a activates mouse peritoneal macrophages via the MAPK and NF-κB signaling pathways |
Q89093850 | Tribbles homolog 1 deficiency modulates function and polarization of murine bone marrow-derived macrophages |
Q46080947 | Truncated thioredoxin (Trx-80) promotes pro-inflammatory macrophages of the M1 phenotype and enhances atherosclerosis |
Q49544289 | Tumor Associated Macrophages as Therapeutic Targets for Breast Cancer. |
Q28071990 | Tumor Associated Macrophages in Kidney Cancer |
Q39155704 | Tumor associated macrophage expressing CD204 is associated with tumor aggressiveness of esophageal squamous cell carcinoma. |
Q37148134 | Tumor-associated macrophages as incessant builders and destroyers of the cancer stroma |
Q96303449 | Tumor-associated macrophages in classical Hodgkin lymphoma: hormetic relationship to outcome |
Q35737704 | Tumor-associated macrophages in oral premalignant lesions coexpress CD163 and STAT1 in a Th1-dominated microenvironment. |
Q36849038 | Tumor-associated macrophages subvert T-cell function and correlate with reduced survival in clear cell renal cell carcinoma |
Q99551899 | Tumor-associated macrophages: Role in the pathological process of tumorigenesis and prospective therapeutic use (Review) |
Q38105286 | Tumor-associated macrophages: functional diversity, clinical significance, and open questions |
Q38883475 | Tumour cell derived effects on monocyte/macrophage polarization and function and modulatory potential of Viscum album lipophilic extract in vitro |
Q37238286 | Type 2 innate lymphoid cells constitutively express arginase-I in the naive and inflamed lung |
Q83068118 | Type II-activated macrophages suppress the development of experimental autoimmune encephalomyelitis |
Q37056347 | Understanding the multiple functions of Gr-1(+) cell subpopulations during microbial infection |
Q37308827 | Unfolding the relationship between secreted molecular chaperones and macrophage activation states |
Q88640276 | Unified nexus of macrophages and maresins in cardiac reparative mechanisms |
Q89719700 | Unique Pro-Inflammatory Response of Macrophages during Apoptotic Cancer Cell Clearance |
Q48505385 | Vascular niche IL-6 induces alternative macrophage activation in glioblastoma through HIF-2α. |
Q45864348 | Vessel-associated myogenic precursors control macrophage activation and clearance of apoptotic cells |
Q50099553 | Wandering pathways in the regulation of innate immunity and inflammation. |
Q47826206 | When Immune Cells Turn Bad-Tumor-Associated Microglia/Macrophages in Glioma. |
Q37622424 | mTORC2 signalling regulates M2 macrophage differentiation in response to helminth infection and adaptive thermogenesis |
Q37162763 | miR-155 Deletion in Mice Overcomes Neuron-Intrinsic and Neuron-Extrinsic Barriers to Spinal Cord Repair. |
Q52655307 | miR-21 depletion in macrophages promotes tumoricidal polarization and enhances PD-1 immunotherapy. |
Q34509678 | γ-Interferon-inducible lysosomal thiol reductase (GILT) maintains phagosomal proteolysis in alternatively activated macrophages |
Q28397640 | γδ T Cells Are Required for M2 Macrophage Polarization and Resolution of Ozone-Induced Pulmonary Inflammation in Mice |
Q36477914 | γδ T cells protect against LPS-induced lung injury |
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