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Immunity, ISSN 1074-7613, 03/2015, Volume 42, Issue 3, pp. 419 - 430
Macrophage polarization involves a coordinated metabolic and transcriptional rewiring that is only partially understood. By using an integrated high-throughput... 
IMMUNITY | CELLS | ACTIVATION | INFLAMMATION | NITRIC-OXIDE | INNATE | GLYCOSYLATION | IMMUNOLOGY | Glutamine - deficiency | Aspartic Acid - immunology | Argininosuccinic Acid - immunology | Mitochondria - immunology | Chemokine CCL22 - immunology | Metabolic Networks and Pathways - immunology | Mitochondria - genetics | Argininosuccinic Acid - metabolism | Gene Regulatory Networks - immunology | Isocitrate Dehydrogenase - immunology | Macrophages - immunology | Uridine Diphosphate N-Acetylglucosamine - metabolism | Nitric Oxide - immunology | Macrophages - classification | Aspartate Aminotransferase, Mitochondrial - immunology | Interleukin-6 - genetics | Signal Transduction | Gene Expression Regulation | Isocitrate Dehydrogenase - genetics | Glycosylation | Mitochondria - metabolism | Macrophages - cytology | Immunity, Innate | Citric Acid Cycle | Uridine Diphosphate N-Acetylglucosamine - immunology | Chemokine CCL22 - genetics | Macrophages - metabolism | Metabolic Networks and Pathways - genetics | Animals | Interleukin-6 - immunology | Transcription, Genetic - immunology | Aspartic Acid - metabolism | Mice | Aspartate Aminotransferase, Mitochondrial - genetics | Nitric Oxide - metabolism | Enzymes | Tracers (Biology) | Analysis | Nitric oxide | Physiological aspects | Aspartate | Genetic aspects | Genetic transcription | Macrophages | Glutamine | Metabolites | Rodents | Scientific imaging | Metabolism | Labeling | Mass spectrometry
Journal Article
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 11/2017, Volume 18, Issue 11, p. 2306
Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS). It affects more than two million people worldwide,... 
Multiple sclerosis | CCL22 | Cns autoimmunity | Dendritic cells | Migration | Experimental autoimmune encephalomyelitis | Neuroinflammation | CCL17 | CCR4 | Chemokines | ENCEPHALOMYELITIS | HUMAN MICROGLIA | MACROPHAGE-DERIVED CHEMOKINE | multiple sclerosis | BIOCHEMISTRY & MOLECULAR BIOLOGY | chemokines | CEREBROSPINAL-FLUID | CHEMISTRY, MULTIDISCIPLINARY | CUTTING EDGE | CNS autoimmunity | experimental autoimmune encephalomyelitis | dendritic cells | MULTIPLE-SCLEROSIS | neuroinflammation | migration | REGULATORY T-CELLS | CENTRAL-NERVOUS-SYSTEM | EXPRESSION | Receptors, CCR4 - immunology | Dendritic Cells - immunology | Humans | Central Nervous System - pathology | Dendritic Cells - pathology | Encephalomyelitis, Autoimmune, Experimental - immunology | Autoimmune Diseases of the Nervous System - pathology | Central Nervous System - immunology | Receptors, CCR4 - analysis | Chemokine CCL22 - analysis | Chemokine CCL22 - immunology | Autoimmunity - immunology | Chemokine CCL17 - immunology | Dendritic Cells - drug effects | Molecular Targeted Therapy - methods | Encephalomyelitis, Autoimmune, Experimental - pathology | Encephalomyelitis, Autoimmune, Experimental - drug therapy | Autoimmune Diseases of the Nervous System - drug therapy | Autoimmune Diseases of the Nervous System - immunology | Chemokine CCL17 - analysis | Animals | Central Nervous System - drug effects | Multiple Sclerosis - immunology | Multiple Sclerosis - pathology | Multiple Sclerosis - drug therapy | Encephalomyelitis | Pathogenesis | Central nervous system | Homeostasis | Nervous system | Antagonists | Lymphocytes T | CC chemokines | Proteins | CCL22 protein | Receptors | Demyelination | Lymphocytes | Protein transport | CCL17 protein | Carbon-carbon composites | Cellular manufacture | Antigen presentation | Immunization | Myelin | Experimental allergic encephalomyelitis | CD4 antigen | White blood cells | Neurological complications | Ligands | Adults | Autoimmune diseases
Journal Article
Anticancer Research, ISSN 0250-7005, 07/2017, Volume 37, Issue 7, pp. 3461 - 3471
Journal Article
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 5, pp. 7384 - 7390
Journal Article
International Journal of Cancer, ISSN 0020-7136, 03/2013, Volume 132, Issue 5, pp. 1070 - 1079
The type of immune cells that are present within the tumor microenvironment can play a crucial role in the survival of patients. However, little is known about... 
CCL22 | epithelial ovarian cancer | recruitment | Th17 | Treg | SURVIVAL | PERIPHERAL-BLOOD | TUMOR SURVEILLANCE | T(H)17 CELLS | ONCOLOGY | RELEVANCE | GROWTH | GENERATION | CARCINOMA | LYMPHOCYTES | Cell Growth Processes - immunology | T-Lymphocytes, Regulatory - metabolism | CD8-Positive T-Lymphocytes - pathology | Receptors, CCR4 - immunology | Dendritic Cells - immunology | Humans | Middle Aged | Ovarian Neoplasms - pathology | Monocytes - metabolism | Monocytes - immunology | Interferon-gamma - metabolism | Chemokine CCL22 - metabolism | T-Lymphocytes, Regulatory - immunology | Receptors, CCR4 - metabolism | Chemokine CCL22 - immunology | Th17 Cells - metabolism | Aged, 80 and over | CD8-Positive T-Lymphocytes - metabolism | Adult | Female | Lymphocytes, Tumor-Infiltrating - metabolism | Ovarian Neoplasms - metabolism | Dendritic Cells - metabolism | Macrophages - immunology | Disease Progression | Tumor Microenvironment - immunology | Macrophages - metabolism | Lymphocytes, Tumor-Infiltrating - pathology | Interferon-gamma - immunology | Cell Line, Tumor | Th17 Cells - immunology | Aged | CD8-Positive T-Lymphocytes - immunology | Lymphocytes, Tumor-Infiltrating - immunology | Ovarian Neoplasms - immunology | Development and progression | Universities and colleges | Dendritic cells | T cells | Macrophages | Ovarian cancer | Medical research | T cell receptors | Immunotherapy | Immune system | Tumors | CCL22 protein
Journal Article
Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, 05/2017, Volume 102, Issue 5, pp. 1468 - 1477
Context: Increasing evidences suggest a correlation between gut and type 1 diabetes (T1D). Objective: The objective of this study is to evaluate the gut... 
INCREASED INTESTINAL PERMEABILITY | HEALTHY-CHILDREN | DIFFERS | FECAL MICROBIOTA | DISEASE | ENDOCRINOLOGY & METABOLISM | CELL AUTOIMMUNITY | GUT MICROBIOTA | MELLITUS | ONSET | Receptors, CCR2 - genetics | Serum Amyloid P-Component - immunology | Receptors, CCR2 - immunology | Humans | Middle Aged | Tumor Necrosis Factor-alpha - genetics | Transcriptome | Child, Preschool | Male | Monocyte Chemoattractant Proteins - immunology | Vascular Endothelial Growth Factor A - genetics | Antigens, CD - genetics | Interleukin-4 Receptor alpha Subunit - genetics | Young Adult | Celiac Disease - microbiology | Cyclooxygenase 2 - genetics | Intestinal Mucosa - immunology | Diabetes Mellitus, Type 1 - microbiology | Tumor Necrosis Factor-alpha - immunology | Child | Real-Time Polymerase Chain Reaction | Duodenum - immunology | Vascular Endothelial Growth Factor A - immunology | C-Reactive Protein - genetics | Intestinal Mucosa - microbiology | Reverse Transcriptase Polymerase Chain Reaction | Monocyte Chemoattractant Proteins - genetics | Chemokine CCL22 - genetics | Chemokine CCL19 - genetics | Adolescent | RNA, Ribosomal, 16S - genetics | C-Reactive Protein - immunology | Antigens, CD - immunology | Infant | Case-Control Studies | Duodenum - microbiology | Chemokine CCL22 - immunology | Celiac Disease - immunology | Adult | Female | Diabetes Mellitus, Type 1 - immunology | Chemokine CCL19 - immunology | Cyclooxygenase 2 - immunology | Antigens, Differentiation, Myelomonocytic - immunology | Diabetes Mellitus, Type 1 - genetics | Gastrointestinal Microbiome - genetics | Interleukin-4 Receptor alpha Subunit - immunology | Antigens, Differentiation, Myelomonocytic - genetics | Serum Amyloid P-Component - genetics | Aged | Immunohistochemistry | CC chemokine receptors | rRNA 16S | CCL19 protein | Pathogenesis | Mucosa | Microbiomes | Diabetes mellitus (insulin dependent) | Macrophages | Small intestine | Gene sequencing | CCL22 protein | Microbiota | CCR2 protein | Intestine | Interleukin 4 receptors | Digestive tract | Duodenum | Digestive system | Abnormalities | Diabetes mellitus | Inflammation | Tumor necrosis factor-α | Gene expression | Ribonucleic acid--RNA | Disease control | Patients | Celiac disease | Biopsy | Infiltration | Diabetes | Cyclooxygenase-2 | Autoimmune diseases | Monocyte chemoattractant protein 1
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2014, Volume 111, Issue 11, pp. 4215 - 4220
Journal Article