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Gastroenterology, ISSN 0016-5085, 2010, Volume 139, Issue 3, pp. 882 - 892.e3
Journal Article
American journal of physiology: Gastrointestinal and liver physiology, ISSN 1522-1547, 2013, Volume 305, Issue 5, pp. G341 - G347
Colon has been shown to have a two-layered mucus system where the inner layer is devoid of bacteria. However, a complete overview of the mouse gastrointestinal... 
Bacteria | Mucus thickness | Goblet cells | Mucin | Mucus adhesiveness | mucus adhesiveness | PHYSIOLOGY | bacteria | HOST | MICROBIOTA | M-CELLS | mucus thickness | goblet cells | EPITHELIUM | mucin | IN-VIVO | BACTERIAL OVERGROWTH | CYSTIC-FIBROSIS | SECRETION | ACCUMULATION | GASTROENTEROLOGY & HEPATOLOGY | Gastric Mucosa - microbiology | Intestinal Mucosa - metabolism | Peyer's Patches - metabolism | Colon - drug effects | Fluorescent Dyes - metabolism | Male | Microscopy, Video | Peyer's Patches - drug effects | Gastric Mucosa - metabolism | Intestinal Absorption | Intestinal Mucosa - drug effects | Time Factors | Gastric Mucosa - drug effects | Female | Mucus - metabolism | Dinoprostone - pharmacology | Adhesiveness | Intestine, Small - microbiology | Mice, Inbred C57BL | Intestinal Mucosa - microbiology | Permeability | Colon - metabolism | Mucus - microbiology | Carbachol - pharmacology | Microscopy, Confocal | Animals | Intestine, Small - drug effects | Colon - microbiology | Mice | Intestine, Small - metabolism | Physiological aspects | Mucus | Health aspects | Gastrointestinal system | Mucosal Biology | Dinoprostone | Confocal | Gastric Mucosa | Intestine | pharmacology | Peyer's Patches | Colon | Intestinal Mucosa | Small | Cell and Molecular Biology | microbiology | drug effects | Inbred C57BL | Carbachol | Microscopy | Video | metabolism | Cell- och molekylärbiologi | Fluorescent Dyes
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2012, Volume 109, Issue 41, pp. E2784 - E2793
Journal Article
Gastroenterology, ISSN 0016-5085, 2015, Volume 149, Issue 6, pp. 1564 - 1574.e3
.... Activated matrix metalloproteinase 3 (MMP3) and MMP12, which are increased in inflamed mucosa of patients with IBD, have a wide range of substrates, including IgG1... 
Gastroenterology and Hepatology | Therapy | Inflammation | EFFECTOR FUNCTIONS | CROHNS-DISEASE | VIVO | ULCERATIVE-COLITIS | MATRIX METALLOPROTEINASES | IN-VITRO | HINGE | MONOCLONAL-ANTIBODIES | INFLIXIMAB | ETANERCEPT | GASTROENTEROLOGY & HEPATOLOGY | Tumor Necrosis Factor-alpha - metabolism | Intestinal Mucosa - metabolism | Epitopes - metabolism | Humans | Inflammatory Bowel Diseases - immunology | Middle Aged | Crohn Disease - metabolism | Etanercept - metabolism | Colon - immunology | Male | Colitis, Ulcerative - immunology | Inflammatory Bowel Diseases - metabolism | Case-Control Studies | Intestinal Mucosa - drug effects | Immunoblotting - methods | Infliximab - metabolism | Proteolysis - drug effects | Intestinal Mucosa - immunology | Female | Colitis, Ulcerative - drug therapy | Biological Factors - metabolism | Inflammatory Bowel Diseases - drug therapy | Colon - pathology | Colitis, Ulcerative - metabolism | Antibodies, Monoclonal, Humanized - metabolism | Matrix Metalloproteinase 3 - metabolism | Matrix Metalloproteinase 12 - metabolism | Adalimumab - metabolism | Crohn Disease - immunology | Colon - metabolism | Biopsy | Crohn Disease - drug therapy | Biological Factors - pharmacology | Immunoglobulin G - metabolism | Medical colleges | Tumor necrosis factor | Gastrointestinal diseases | Tumors | Necrosis
Journal Article
Journal Article
Journal Article
Immunity (Cambridge, Mass.), ISSN 1074-7613, 2013, Volume 38, Issue 5, pp. 970 - 983
Journal Article