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Journal of Neuroscience, ISSN 0270-6474, 05/2011, Volume 31, Issue 20, pp. 7563 - 7567
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2012, Volume 32, Issue 38, pp. 13244 - 13254
Journal Article
Handbook of experimental pharmacology, ISSN 0171-2004, 2017, Volume 241, p. 121
Mast cells and basophils represent the most relevant source of histamine in the immune system. Histamine is stored in cytoplasmic granules along with other... 
Histamine - metabolism | Animals | Cytokines - metabolism | Hypersensitivity - metabolism | Receptors, G-Protein-Coupled - metabolism | Immune System - metabolism | Humans | Histamine Release - physiology | Mast Cells - metabolism | Basophils - metabolism
Journal Article
British Journal of Pharmacology, ISSN 0007-1188, 09/2013, Volume 170, Issue 1, pp. 38 - 45
Journal Article
European Journal of Immunology, ISSN 0014-2980, 03/2008, Volume 38, Issue 3, pp. 855 - 863
Mediator release from mast cells (MC) is a crucial step in allergic and non‐allergic inflammatory disorders. However, the final events in response to... 
Allergology | Cellular immunology | Mast cells | Mucosal immunity | FUSION | INVOLVEMENT | IMMUNOLOGY | mast cells | COMPOUND EXOCYTOSIS | IDENTIFICATION | cellular immunology | MEDIATOR RELEASE | HUMAN EOSINOPHILS | allergology | SNARE COMPLEXES | SNAP-23 | RECEPTORS | EXPRESSION | mucosal immunity | Gene Expression - drug effects | SNARE Proteins - genetics | Humans | Qb-SNARE Proteins - metabolism | R-SNARE Proteins - metabolism | Qb-SNARE Proteins - genetics | Cytoplasm - metabolism | Qc-SNARE Proteins - immunology | Vesicle-Associated Membrane Protein 2 - physiology | Vesicle-Associated Membrane Protein 2 - genetics | Vesicle-Associated Membrane Protein 3 - physiology | Qc-SNARE Proteins - metabolism | Mast Cells - metabolism | Qa-SNARE Proteins - genetics | Cell Membrane - metabolism | Histamine Release - drug effects | Vesicle-Associated Membrane Protein 3 - genetics | R-SNARE Proteins - genetics | Vesicle-Associated Membrane Protein 3 - metabolism | Histamine Release - physiology | Mast Cells - physiology | Tetanus Toxin - pharmacology | Qa-SNARE Proteins - immunology | Reverse Transcriptase Polymerase Chain Reaction | Mast Cells - drug effects | Blotting, Western | Antibodies - pharmacology | R-SNARE Proteins - physiology | Metalloendopeptidases - pharmacology | Qa-SNARE Proteins - metabolism | Fluorescent Antibody Technique | Qb-SNARE Proteins - immunology | Qc-SNARE Proteins - genetics | Vesicle-Associated Membrane Protein 2 - metabolism | SNARE Proteins - metabolism | Cell Degranulation - physiology | Cell Degranulation - drug effects | Index Medicus | Qb-SNARE Proteins | Cell Membrane | Vesicle-Associated Membrane Protein 2 | Gene Expression | Vesicle-Associated Membrane Protein 3 | Cell Degranulation | Tetanus Toxin | R-SNARE Proteins | Antibodies | Metalloendopeptidases | Life Sciences | Immunology | Qa-SNARE Proteins | Qc-SNARE Proteins | Histamine Release | SNARE Proteins | Cytoplasm | Mast Cells
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 06/2010, Volume 30, Issue 23, pp. 7845 - 7852
Journal Article
The Journal of Immunology, ISSN 0022-1767, 07/2003, Volume 171, Issue 1, pp. 338 - 345
Journal Article
Gut, ISSN 0017-5749, 12/2014, Volume 63, Issue 12, pp. 1873 - 1882
Objectives Substantial evidence implicates mast cells and their main constituent histamine in the pathogenesis of visceral hypersensitivity. We explored the... 
VISCERAL NOCICEPTION | MAST CELLS | VISCERAL HYPERSENSITIVITY | HISTAMINE | PAIN | ANTAGONIST | EXPERIMENTAL COLITIS | SENSITIZATION | INFLAMMATION | MAST-CELLS | NEURONS | H-4 RECEPTOR | MODEL | GASTROENTEROLOGY & HEPATOLOGY | COLORECTAL DISTENSION | Intestinal Mucosa - metabolism | Cetirizine - pharmacology | Receptors, G-Protein-Coupled - metabolism | Colitis - complications | Male | Histamine - metabolism | Receptors, Histamine H1 - metabolism | Hypersensitivity - metabolism | Hypersensitivity - etiology | Colitis - diagnosis | Mast Cells - metabolism | Indoles - pharmacology | Receptors, Histamine H4 | Disease Models, Animal | Histamine H1 Antagonists, Non-Sedating - pharmacology | Hypersensitivity - therapy | Histamine Release - physiology | Rats | Regeneration - physiology | Mast Cells - drug effects | Piperazines - pharmacology | Rats, Sprague-Dawley | Colonoscopy - methods | Colitis - etiology | Receptors, Histamine - metabolism | Regeneration - drug effects | Animals | Colitis - physiopathology | Convalescence | Hypersensitivity - physiopathology | Colitis - metabolism | Receptors, G-Protein-Coupled - antagonists & inhibitors | Intestinal Mucosa - pathology | Trinitrobenzenesulfonic Acid - pharmacology | Allergy | Histamine | Inflammation | Allergic reaction | Analysis | Risk factors | Studies | Psychological aspects | Inflammatory bowel disease | Pain | Serotonin | Rodents | Irritable bowel syndrome | Clinical trials | Colon | Abdomen | Asthma
Journal Article