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The Journal of Physiology, ISSN 0022-3751, 2004, Volume 556, Issue 3, pp. 983 - 1000
Muscular adaptation to physical exercise has previously been described as a repair process following tissue damage. Recently, evidence has been published to... 
INDUCED INJURY | PHYSIOLOGY | IMMUNOREACTIVITY | ECCENTRIC EXERCISE | REGENERATION | LEUKEMIA INHIBITORY FACTOR | DENERVATED HUMAN MUSCLE | SATELLITE CELLS | STRENGTH | FACTOR-I | EXPRESSION | NEUROSCIENCES | Immunohistochemistry | Granulocytes - cytology | Cytokines - analysis | Humans | Middle Aged | DNA-Binding Proteins - analysis | Ki-67 Antigen - metabolism | Male | Muscle, Skeletal - metabolism | Proteins - analysis | Pain - metabolism | fas Receptor - metabolism | Fascia - chemistry | Oxygen Consumption - physiology | fas Receptor - analysis | Antigens, CD - metabolism | Antigens, CD - analysis | Running - physiology | C-Reactive Protein - metabolism | Aryl Hydrocarbon Receptor Nuclear Translocator | CD11b Antigen - analysis | Receptors, Cytokine - metabolism | Testosterone - blood | C-Reactive Protein - analysis | Hormones - blood | Leukocytes - chemistry | Interleukin-6 - metabolism | Lymphocytes - metabolism | CD56 Antigen - analysis | Lymphocytes - cytology | Insulin-Like Growth Factor I - analysis | Muscle, Skeletal - physiology | CD3 Complex - metabolism | Leukemia Inhibitory Factor Receptor alpha Subunit | Regression Analysis | Pain - physiopathology | Receptors, Cytokine - analysis | Adolescent | Antigens, Differentiation, Myelomonocytic - analysis | Creatine Kinase - metabolism | Transcription Factors - analysis | Leukocytes - metabolism | Insulin-Like Growth Factor I - metabolism | Receptors, OSM-LIF | Interleukin-6 - analysis | Monocytes - cytology | Receptors, Cell Surface - analysis | Monocytes - metabolism | Receptors, Aryl Hydrocarbon - analysis | DNA-Binding Proteins - metabolism | Testosterone - metabolism | Flow Cytometry | Interleukin-6 - blood | Exercise Test - methods | Muscle, Skeletal - chemistry | Fascia - metabolism | Heart Rate - physiology | Receptors, Aryl Hydrocarbon - metabolism | Adult | Female | Leukocyte Count | Leukemia Inhibitory Factor | Isometric Contraction - physiology | Cytokines - blood | Leukocytes - cytology | CD56 Antigen - metabolism | Creatine Kinase - blood | Cytokines - metabolism | Receptors, Cell Surface - metabolism | Transcription Factors - metabolism | CD3 Complex - analysis | Ki-67 Antigen - analysis | Proteins - metabolism | Hormones - metabolism | Antigens, Differentiation, Myelomonocytic - metabolism | CD11b Antigen - metabolism | Growth Substances - metabolism | Pain - diagnosis | Research Papers
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 6/2011, Volume 108, Issue 24, pp. 9927 - 9932
.... Consequently, in the absence of FcRn, Fcγ receptor (FcγR)-mediated antigen uptake fails to initiate cross-presentation... 
T lymphocytes | Antigens | Fc receptors | Cross priming | Dendritic cells | Internalization | Phagosomes | Inflammation | Oxidation | MHC CLASS-I | GAMMA-RECEPTOR | CD8(+) | VIVO | MULTIDISCIPLINARY SCIENCES | DISEASE | MONOCYTES | ANTIGEN PRESENTATION | MYASTHENIA-GRAVIS | T-CELLS | CUTTING EDGE | Dextran Sulfate | Membrane Glycoproteins - metabolism | Cytosol - immunology | Dendritic Cells - immunology | Receptors, Fc - metabolism | NADPH Oxidases - metabolism | NADPH Oxidases - immunology | Vacuolar Proton-Translocating ATPases - metabolism | Receptors, IgG - metabolism | Histocompatibility Antigens Class I - metabolism | Vacuolar Proton-Translocating ATPases - immunology | Phagosomes - immunology | Flow Cytometry | Immunoglobulin G - immunology | Colitis - chemically induced | Membrane Glycoproteins - immunology | Colitis - immunology | Dendritic Cells - metabolism | rab GTP-Binding Proteins - metabolism | CD11b Antigen - immunology | Mice, Inbred C57BL | Phagosomes - metabolism | Histocompatibility Antigens Class I - immunology | Mice, Transgenic | Histocompatibility Antigens Class I - genetics | Receptors, IgG - immunology | NADPH Oxidase 2 | Blotting, Western | CD8 Antigens - immunology | Mice, Knockout | CD8 Antigens - metabolism | Animals | Immunoglobulin G - genetics | Receptors, Fc - immunology | Cross-Priming - immunology | rab GTP-Binding Proteins - immunology | Colitis - metabolism | Protein Binding | rab27 GTP-Binding Proteins | Antigens - immunology | Cytosol - metabolism | Receptors, Fc - genetics | Mice | CD11b Antigen - metabolism | Mutation | Hydrogen-Ion Concentration | Immunoglobulin G - metabolism | Biological Sciences
Journal Article
The Journal of Immunology, ISSN 0022-1767, 07/2006, Volume 177, Issue 2, pp. 1250 - 1256
Langerhans cells have been thought to play a major role as APCs for induction of specific immune responses to Leishmania major. Although their requirement for... 
IMMUNITY | SUSCEPTIBILITY | LANGERIN/CD207 | POPULATIONS | MULTIPLE LOCI | MICE | CD8-ALPHA(+) | IMMUNOLOGY | IDENTIFICATION | LANGERHANS CELLS | ANTIGEN | T-Lymphocyte Subsets - immunology | Leishmania major - immunology | Antigens, Protozoan - immunology | Lymph Nodes - pathology | Coculture Techniques | Dendritic Cells - immunology | Leishmaniasis, Cutaneous - immunology | Antigens, Protozoan - metabolism | Antigen Presentation | Langerhans Cells - immunology | Epitopes, T-Lymphocyte - immunology | CD11c Antigen - biosynthesis | Dendritic Cells - metabolism | Antigen-Presenting Cells - metabolism | Mice, Inbred C57BL | Receptors, Chemokine - metabolism | Cells, Cultured | Leishmaniasis, Cutaneous - pathology | Lymph Nodes - metabolism | Mice, Transgenic | Leishmaniasis, Cutaneous - metabolism | Lymph Nodes - immunology | Antigen-Presenting Cells - immunology | CD8 Antigens - metabolism | Animals | T-Lymphocyte Subsets - parasitology | T-Lymphocyte Subsets - metabolism | Mice | Mice, Inbred BALB C | Langerhans Cells - metabolism | Epitopes, T-Lymphocyte - metabolism | CD11b Antigen - biosynthesis | T-Lymphocyte Subsets | Antigens, CD8 | Leishmaniasis, Cutaneous | Dendritic Cells | Langerhans Cells | Epitopes, T-Lymphocyte | Lymph Nodes | Antigens, CD11c | Antigens, CD11b | Antigens, Protozoan | Life Sciences | Antigen-Presenting Cells | Immunology | Receptors, Chemokine | Leishmania major
Journal Article
Science, ISSN 0036-8075, 09/2017, Volume 357, Issue 6355, pp. 1014 - 1021
Journal Article
Nature immunology, ISSN 1529-2916, 2014, Volume 15, Issue 10, pp. 929 - 937
The paradigm that macrophages that reside in steady-state tissues are derived from embryonic precursors has never been investigated in the intestine, which... 
RESPONSES | DENDRITIC CELLS | MICROGLIA | BONE-MARROW | GUT | TISSUE MACROPHAGES | RECEPTOR | STEADY-STATE | DIFFERENTIATION | IMMUNOLOGY | REVEALS | Receptors, CCR2 - genetics | Intestinal Mucosa - metabolism | Cell Proliferation | Receptors, CCR2 - immunology | Monocytes - metabolism | Intestines - metabolism | Monocytes - immunology | Intestines - immunology | Parabiosis | Intestinal Mucosa - cytology | CD11b Antigen - genetics | Flow Cytometry | Time Factors | Intestinal Mucosa - immunology | Bone Marrow Transplantation | Gene Expression - immunology | Antigens, Differentiation - metabolism | Antigens, Ly - metabolism | Receptors, Chemokine - genetics | Macrophages - immunology | Animals, Newborn | CD11b Antigen - immunology | Mice, Inbred C57BL | Receptors, Chemokine - metabolism | Mice, Transgenic | Receptors, Chemokine - immunology | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Cell Differentiation - immunology | Macrophages - metabolism | Models, Immunological | Receptors, CCR2 - metabolism | Animals | Antigens, Ly - immunology | Antigens, Differentiation - genetics | CD11b Antigen - metabolism | CX3C Chemokine Receptor 1 | Antigens, Differentiation - immunology | Intestines - cytology | Physiological aspects | Regulation | Immune response | Microbiota (Symbiotic organisms) | Macrophages | Properties
Journal Article
PLoS pathogens, ISSN 1553-7374, 2010, Volume 6, Issue 10, p. e1001159
The species-specific phenolic glycolipid 1 (PGL-1) is suspected to play a critical role in the pathogenesis of leprosy, a chronic disease of the skin and... 
ACTIVATION | DENDRITIC CELLS | MICROBIOLOGY | HUMAN MONOCYTES | PHENOLIC GLYCOLIPID-1 | PHTHIOCEROL DIESTER | CD11B/CD18 | VIROLOGY | VIRULENCE FACTORS | BIOSYNTHESIS | TUBERCULOSIS COMPLEX | RECEPTORS | PARASITOLOGY | Cricetulus | Protein Engineering - methods | Humans | Immunity, Innate - genetics | Antigens, Bacterial - genetics | Time Factors | Immunity, Innate - physiology | Immune Evasion - genetics | Mycobacterium bovis - genetics | CHO Cells | Recombinant Proteins - metabolism | Cricetinae | Cells, Cultured | Recombinant Proteins - chemistry | Antigen Presentation - genetics | Mycobacterium leprae - genetics | Recombinant Proteins - genetics | Phagocytes - metabolism | Glycolipids - metabolism | Phagocytes - immunology | Glycolipids - genetics | Animals | Mycobacterium bovis - metabolism | Models, Biological | Glycolipids - physiology | Antigens, Bacterial - physiology | Antigens, Bacterial - metabolism | Immune Evasion - immunology | Antigen Presentation - physiology | Enzymes | Medical research | Immune response | Genetically modified organisms | Physiological aspects | Medicine, Experimental | Leprosy | Lipids | Genetic aspects | Genetic engineering | Macrophages | Health aspects | Life Sciences | Microbiology and Parasitology | Immunology | Cellular Biology | Infections | Pathogenesis | Experiments | Binding sites | Chronic illnesses
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 4/2012, Volume 109, Issue 16, pp. 6175 - 6180
Dendritic cells (DC) are antigen-presenting cells found in both lymphoid and nonlymphoid organs, including the brain (bDC... 
T lymphocytes | Antigens | Brain | Phenotypes | Dendritic cells | Memory interference | Neurons | Antigen presenting cells | Infections | Ova | Antigen presentation | Neuroinflammation | MOUSE-BRAIN | antigen presentation | MULTIDISCIPLINARY SCIENCES | MICROGLIAL CELLS | INTERFERON | neuroinflammation | IN-VIVO | CENTRAL-NERVOUS-SYSTEM | CHOROID-PLEXUS | STEADY-STATE | MICE | VESICULAR STOMATITIS-VIRUS | MIXED LEUKOCYTE REACTION | Antigens, CD - immunology | Receptor, Macrophage Colony-Stimulating Factor - immunology | Encephalitis, Viral - genetics | Leukocyte Common Antigens - metabolism | Ovalbumin - immunology | Dendritic Cells - immunology | Brain - virology | Olfactory Bulb - metabolism | Olfactory Bulb - immunology | Receptor, Macrophage Colony-Stimulating Factor - metabolism | Antigens, CD - metabolism | Brain - metabolism | Leukocyte Common Antigens - immunology | Flow Cytometry | T-Lymphocytes - metabolism | Integrin alpha Chains - immunology | Antigens, Ly - metabolism | Encephalitis, Viral - metabolism | Dendritic Cells - metabolism | Rhabdoviridae Infections - metabolism | CD11b Antigen - immunology | Mice, Inbred C57BL | Receptors, Chemokine - metabolism | Cells, Cultured | Mice, Transgenic | Integrin alpha Chains - metabolism | Receptors, Chemokine - immunology | Antigen Presentation - immunology | Microscopy, Confocal | Animals | Antigens, Ly - immunology | Rhabdoviridae Infections - immunology | Rhabdoviridae Infections - genetics | Luminescent Proteins - genetics | T-Lymphocytes - immunology | Mice | CD11b Antigen - metabolism | Brain - immunology | Encephalitis, Viral - immunology | Vesicular stomatitis Indiana virus - immunology | Luminescent Proteins - metabolism | Biological Sciences
Journal Article
Journal Article
The Journal of Immunology, ISSN 0022-1767, 03/2008, Volume 180, Issue 5, pp. 3019 - 3027
Journal Article
Leukemia, ISSN 1476-5551, 2018, Volume 32, Issue 9, pp. 1932 - 1947
...) expression on tumor and dendritic cells. We further evaluated the effect of ACY241 on antigen-specific cytotoxic T lymphocytes (CTL... 
MHC CLASS-I | SURVIVAL | DEXAMETHASONE | METHYLATION | ONCOLOGY | PHOSPHORYLATION | POTENTIAL THERAPEUTIC APPLICATION | CELL DIFFERENTIATION | RICOLINOSTAT | HEMATOLOGY | CANCER | EXPRESSION | Neoplasms - metabolism | T-Lymphocyte Subsets - immunology | Humans | Epitopes, T-Lymphocyte - genetics | Multiple Myeloma - immunology | X-Box Binding Protein 1 - chemistry | T-Lymphocytes, Cytotoxic - drug effects | Lymphocyte Activation - immunology | Multiple Myeloma - drug therapy | Neoplasms - genetics | T-Lymphocyte Subsets - drug effects | Epitopes, T-Lymphocyte - immunology | Gene Expression Regulation, Neoplastic - drug effects | Cytotoxicity, Immunologic - drug effects | T-Lymphocytes, Cytotoxic - immunology | Antigens, Neoplasm - genetics | X-Box Binding Protein 1 - immunology | Antigens, Neoplasm - immunology | Peptides - immunology | Histone Deacetylases - metabolism | Multiple Myeloma - metabolism | Neoplasms - drug therapy | Signal Transduction - drug effects | T-Lymphocytes, Cytotoxic - metabolism | Lymphocyte Activation - drug effects | Neoplasms - immunology | T-Lymphocyte Subsets - metabolism | Biomarkers | Cell Line, Tumor | Histone Deacetylase Inhibitors - pharmacology | Immunologic Memory | X-Box Binding Protein 1 - genetics | Multiple Myeloma - genetics | Enzymes | Care and treatment | Multiple myeloma | Hydrolases | Development and progression | Genetic aspects | Regulation | Health aspects | Regulators | Transcription | CD86 antigen | Peptides | CD8 antigen | Cytotoxicity | AKT protein | Activation | Lymphocytes T | Drug development | CD28 antigen | B7 antigen | Immunity | CD40L protein | Anticancer properties | Time dependence | Cell activation | Antitumor agents | Interleukin 2 | Lymphocytes | CD38 antigen | Bone marrow | CD25 antigen | Foxp3 protein | Perforin | Immune system | Antigens | Immunological memory | CD11b antigen | Immune response | Dendritic cells | CD80 antigen | CD4 antigen | Inhibitors | Immune checkpoint | γ-Interferon | Tumors | Bcl-6 protein
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 5, p. e36814
Cardiac tissue macrophages (cTMs) are a previously uncharacterised cell type that we have identified and characterise here as an abundant GFP(+) population... 
GROWTH FACTOR-I | GENE SIGNATURE | STEM-CELLS | MUSCLE REGENERATION | FRACTALKINE RECEPTOR | MONOCYTE | DENDRITIC CELLS | VIVO | MULTIDISCIPLINARY SCIENCES | DIET-INDUCED OBESITY | ADIPOSE-TISSUE | Antigens, CD - biosynthesis | Leukocyte Common Antigens - biosynthesis | Brain - metabolism | Myocardium - metabolism | Receptors, Cell Surface - biosynthesis | Macrophage Activation - physiology | Antigens, Differentiation, Myelomonocytic - biosynthesis | Brain - cytology | Insulin-Like Growth Factor I - biosynthesis | Myocytes, Cardiac - cytology | Endothelial Cells - metabolism | Mice, Transgenic | Spleen - cytology | Macrophages - cytology | Myocardium - cytology | Glycoproteins - biosynthesis | Antigens, Differentiation - biosynthesis | Macrophages - metabolism | Animals | Spleen - metabolism | Endothelial Cells - cytology | Homeostasis - physiology | Myocytes, Cardiac - metabolism | Mice | CD11b Antigen - biosynthesis | Macrophages | Gene expression | Analysis | Heart | Brain | Flow cytometry | Heart attacks | Laboratories | Insulin-like growth factor I | Homeostasis | Insulin-like growth factors | Blood | CD45 antigen | Ethics | Immunology | Transgenic animals | Bone marrow | Trends | Heart diseases | Spleen | Antigens | Enzymes | CD11b antigen | Immunomodulation | Markers | Cardiomyocytes | Inflammation | Endothelial cells | Medicine | CD163 antigen | Cytometry | Stem cells | Myocardium | Molecular biology
Journal Article
Blood, ISSN 0006-4971, 04/2013, Volume 121, Issue 15, pp. 2975 - 2987
Myeloid-derived suppressor cells (MDSCs) are a heterogeneous, immature myeloid cell population with the ability to suppress immune responses. MDSCs have been... 
CANCER-PATIENTS | SUBPOPULATIONS | DENDRITIC CELLS | T-REGULATORY CELLS | IMMUNOSUPPRESSION | MACROPHAGES | PERIPHERAL-BLOOD | DIFFERENTIATION | IDENTIFICATION | HEMATOLOGY | PROGRESSION | Cell Proliferation | Reactive Oxygen Species - metabolism | Coculture Techniques | Humans | Sialic Acid Binding Ig-like Lectin 3 - immunology | Multiple Myeloma - immunology | Thalidomide - pharmacology | Lewis X Antigen - metabolism | Lipopolysaccharides - immunology | Thalidomide - analogs & derivatives | Flow Cytometry | T-Lymphocytes - metabolism | Myeloid Cells - immunology | Reactive Oxygen Species - immunology | Myeloid Cells - drug effects | Antineoplastic Agents - pharmacology | HLA-DR Antigens - metabolism | Sialic Acid Binding Ig-like Lectin 3 - metabolism | Cytokines - immunology | Tumor Microenvironment - drug effects | Bortezomib | CD11b Antigen - immunology | Cytokines - metabolism | Cells, Cultured | Lewis X Antigen - immunology | Multiple Myeloma - metabolism | Tumor Microenvironment - immunology | Multiple Myeloma - pathology | Lipopolysaccharides - pharmacology | Cell Line, Tumor | Myeloid Cells - metabolism | T-Lymphocytes - immunology | HLA-DR Antigens - immunology | CD11b Antigen - metabolism | Pyrazines - pharmacology | Immunologic Factors - pharmacology | Boronic Acids - pharmacology | Tumor Burden - immunology | Lymphoid Neoplasia
Journal Article