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PLoS ONE, ISSN 1932-6203, 04/2018, Volume 13, Issue 4, p. e0196433
The neurodegenerative disease multiple sclerosis (MS) is pathologically characterized by the massive influx of immune cells into the central nervous system.... 
MIGRATION | CELLS | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | ACTIVATION | INFLAMMATION | CHEMOKINES | INTEGRIN | MULTIDISCIPLINARY SCIENCES | FIBRONECTIN | TISSUE TRANSGLUTAMINASE | Spinal Cord - drug effects | Spinal Cord - metabolism | GTP-Binding Proteins - antagonists & inhibitors | Humans | Quinolines - pharmacology | Pyrrolidines - pharmacology | Pyrrolidines - therapeutic use | Benzamides - therapeutic use | Piperidines - pharmacology | Spinal Cord - pathology | Enzyme Inhibitors - chemistry | Protein Binding - drug effects | Monocytes - pathology | Anti-Inflammatory Agents - therapeutic use | Benzamides - pharmacology | Transglutaminases - antagonists & inhibitors | Benzamides - chemistry | Disease Models, Animal | Naphthalenes - chemistry | Piperidines - chemistry | Encephalomyelitis, Autoimmune, Experimental - pathology | Anti-Inflammatory Agents - pharmacology | Encephalomyelitis, Autoimmune, Experimental - drug therapy | Mice, Inbred C57BL | Quinolines - chemistry | Cells, Cultured | Enzyme Inhibitors - pharmacology | Isoxazoles - chemistry | Enzyme Inhibitors - therapeutic use | Pyrrolidines - chemistry | Fibronectins - metabolism | Naphthalenes - pharmacology | Isoxazoles - pharmacology | Monocytes - drug effects | Animals | Anti-Inflammatory Agents - chemistry | Piperidines - therapeutic use | Transglutaminases - metabolism | Multiple Sclerosis - pathology | Mice | Quinolines - therapeutic use | Isoxazoles - therapeutic use | Naphthalenes - therapeutic use | GTP-Binding Proteins - metabolism | Multiple Sclerosis - drug therapy | Multiple sclerosis | Care and treatment | Enzyme inhibitors | Physiological aspects | Development and progression | Transglutaminases | Research | Drug therapy | Neurological research | Health aspects | Spinal cord | Neurosciences | Enzyme activity | Encephalomyelitis | Leukocyte migration | Central nervous system | Cognitive ability | Leukocytes | Cell surface | Fibronectin | Enzymatic activity | Demyelination | Rodents | Extracellular matrix | Recombinant | Immune system | Enzymes | Blood vessels | Crosslinking | Pharmacology | Bioavailability | Adhesion | Transglutaminase 2 | Experimental allergic encephalomyelitis | Substrates | White blood cells | Pathology | Monocytes | Inhibitors | Infiltration | Cell migration
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, p. e83631
Autoantibodies are believed to be maintained by either the continuous generation of short-lived plasma cells in secondary lymphoid tissues or by long-lived... 
DERMAL-EPIDERMAL SEPARATION | MEMORY B-CELLS | CD154 EXPRESSION | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | PASSIVE TRANSFER | HUMORAL IMMUNITY | VII COLLAGEN | T-CELLS | NZB/W MICE | MAJOR SITE | T-Lymphocyte Subsets - immunology | Epidermolysis Bullosa Acquisita - immunology | Bone Marrow - immunology | Spleen - immunology | Epidermolysis Bullosa Acquisita - blood | Autoantibodies - blood | Collagen Type VII - immunology | Lymph Nodes - metabolism | Epitopes, B-Lymphocyte - immunology | Lymph Nodes - immunology | Autoantibodies - biosynthesis | Epidermolysis Bullosa Acquisita - metabolism | Autoantibodies - immunology | Animals | Spleen - metabolism | T-Lymphocyte Subsets - metabolism | Bone Marrow - metabolism | Plasma Cells - metabolism | Mice | Disease Models, Animal | Plasma Cells - immunology | Autoimmunity | Antigens | Autoantibodies | Epidermolysis bullosa | Analysis | B cells | T cells | Plasma | Disease | Lymphocytes T | Epidermolysis bullosa acquisita | Arthritis | Tissues | Lymph nodes | Lymphocytes | Bone marrow | Skin diseases | Localization | Fusion protein | Half life | Spleen | Immunization | Lymphatic system | Dermatology | Inflammation | T cell receptors | Lymphoid tissue | CD4 antigen | Intermediates | Drainage | Collagen | Plasma cells | Blistering | Skin | Bone | Position (location) | Autoimmune diseases | Lymph
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 06/2019, Volume 78, Issue 6, pp. 492 - 500
Leukocyte infiltration is an important pathological hallmark of multiple sclerosis (MS) and is therefore targeted by current MS therapies. The enzyme tissue... 
CELLS | IMMUNITY | Multiple sclerosis | ACTIVATION | DIFFERENTIAL EXPRESSION | SUBSETS | Leukocytes | PATHOLOGY | Macrophages | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOGENESIS | Monocytes | CXCR1 | MICROGLIA | DISEASE | Tissue transglutaminase | Original
Journal Article
Amino Acids, ISSN 0939-4451, 3/2017, Volume 49, Issue 3, pp. 643 - 658
Leukocyte infiltration into the central nervous system (CNS) is a key pathological feature in multiple sclerosis (MS) and the MS animal model experimental... 
Life Sciences | Biochemistry, general | Intravital microscopy | Immunohistochemistry | Analytical Chemistry | Multiple sclerosis | Life Sciences, general | Biochemical Engineering | Proteomics | Neurobiology | Cell crawling | Original
Journal Article
Nature immunology, ISSN 1529-2908, 8/2013, Volume 14, Issue 8, pp. 785 - 792
Using intravital imaging of the liver, we unveil a collaborative role for platelets with Kupffer cells (KCs) in eradicating bloodborne bacterial infections.... 
imaging | Immune surveillance | platelet aggregation
Journal Article
Amino Acids, ISSN 0939-4451, 03/2017, Volume 49, Issue 3, p. 643
  Leukocyte infiltration into the central nervous system (CNS) is a key pathological feature in multiple sclerosis (MS) and the MS animal model experimental... 
Journal Article
Amino Acids, ISSN 0939-4451, 03/2017, Volume 49, Issue 3, pp. 643 - 658
Leukocyte infiltration into the central nervous system (CNS) is a key pathological feature in multiple sclerosis (MS) and the MS animal model experimental... 
Journal Article
Amino Acids, ISSN 0939-4451, 03/2017, Volume 49, Issue 3, p. 643
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s00726-016-2359-0 
Immunohistochemistry | Neurosciences | Multiple sclerosis | Encephalomyelitis | Genetic engineering | Medical imaging equipment
Journal Article
Journal Article
Journal Article
Brain, Behavior, and Immunity, ISSN 0889-1591, 2015, Volume 50, pp. 141 - 154
Highlights • TG2 is present in MHCII+ infiltrating cells in active MS lesions. • Inhibition of TG2 activity dramatically reduces clinical symptoms of EAE. •... 
Psychiatry | Allergy and Immunology | Immunohistochemistry | Experimental autoimmune encephalomyelitis | Multiple sclerosis | Demyelination | Migration | encephalomyelitis | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | DIFFERENTIAL EXPRESSION | TRANSENDOTHELIAL MIGRATION | ALZHEIMERS-DISEASE | EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS | CROSS-LINKING | IMMUNOLOGY | NEUROSCIENCES | LESIONS | NITRIC-OXIDE | SELECTIVE INHIBITORS | Experimental autoimmune | CENTRAL-NERVOUS-SYSTEM | GTP-Binding Proteins - antagonists & inhibitors | Humans | Cerebral Cortex - pathology | Transglutaminases - genetics | Male | RNA, Messenger - metabolism | GTP-Binding Proteins - genetics | T-Lymphocytes - metabolism | Spinal Cord - pathology | Inflammation Mediators - metabolism | Aged, 80 and over | Female | Myelin Sheath - enzymology | Transglutaminases - antagonists & inhibitors | Cerebral Cortex - enzymology | Multiple Sclerosis - enzymology | Encephalomyelitis, Autoimmune, Experimental - pathology | Mice, Inbred C57BL | Spinal Cord - enzymology | Rats | Macrophages - enzymology | Mice, Knockout | Isoxazoles - pharmacology | Cell Movement - drug effects | Animals | Encephalomyelitis, Autoimmune, Experimental - enzymology | Spleen - metabolism | Transglutaminases - metabolism | Multiple Sclerosis - pathology | Aged | Mice | Endothelial Cells - pathology | Endothelial Cells - enzymology | GTP-Binding Proteins - metabolism | T cells | Macrophages | Patient outcomes
Journal Article
PLoS ONE, 12/2013, Volume 8, Issue 12
Autoantibodies are believed to be maintained by either the continuous generation of short-lived plasma cells in secondary lymphoid tissues or by long-lived... 
Journal Article
Amino Acids, ISSN 0939-4451, 3/2017, Volume 49, Issue 3, pp. 441 - 452
Monocytes and macrophages are key players in inflammatory processes following an infection or tissue damage. Monocytes adhere and extravasate into the inflamed... 
Life Sciences | Biochemistry, general | Analytical Chemistry | Multiple sclerosis | Life Sciences, general | Biochemical Engineering | Proteomics | Neurobiology | Efferocytosis | Inflammation | Differentiation | Adhesion | KAPPA-B ACTIVATION | TGF-BETA | TRANSENDOTHELIAL MIGRATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HUMAN-BLOOD MONOCYTES | PROINFLAMMATORY CYTOKINE PRODUCTION | MULTIPLE-SCLEROSIS | SIGNALING PATHWAY | APOPTOTIC CELLS | ENDOTHELIAL-CELLS | ALTERNATIVE ACTIVATION | Cytoskeletal Proteins - genetics | Atherosclerosis - genetics | Humans | Transglutaminases - genetics | Monocytes - immunology | GTP-Binding Proteins - genetics | Transglutaminases - immunology | Cell Movement - immunology | Sepsis - pathology | Monocytes - pathology | Cytokines - genetics | Macrophages - immunology | Cytokines - immunology | Atherosclerosis - pathology | Sepsis - immunology | Atherosclerosis - immunology | GTP-Binding Proteins - immunology | Macrophages - pathology | Signal Transduction | Extracellular Matrix Proteins - genetics | Toll-Like Receptors - immunology | Gene Expression Regulation | Multiple Sclerosis - genetics | Sepsis - genetics | Cell Adhesion - immunology | Cytoskeletal Proteins - immunology | Extracellular Matrix Proteins - immunology | Toll-Like Receptors - genetics | Multiple Sclerosis - immunology | Multiple Sclerosis - pathology | Phagocytosis | Enzymes | Neurosciences | Macrophages | Analysis | Atherosclerosis | Invited Review
Journal Article
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