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Gut, ISSN 0017-5749, 09/2013, Volume 62, Issue 9, pp. 1306 - 1314
Objective Proper interactions between the intestinal mucosa, gut microbiota and nutrient flow are required to establish homoeostasis of the host. Since the... 
microbiota | SURGERY | GASTRIC BYPASS | gastrointestinal tract | transcriptome | lipid metabolism | INTESTINE | mucins | gut immunology | BL 6J ex-germ-free mice | immune response | GLUTAMATE | inherited metabolic disease | MICE | gut inflammation | energy metabolism | mucosal immunology | HOMEOSTASIS | C57 | colonic microflora | anti-bacterial mucosal immunity | Campylobacter jejuni | bacterial interactions | intestinal bacteria | AMINO-ACID | INFLAMMATORY-BOWEL-DISEASE | gene regulation | BIOSYNTHESIS | liver metabolism | jejunum | glucose metabolism | EXPRESSION | gene expression | metabonome | probiotics | crohn's disease | GASTROENTEROLOGY & HEPATOLOGY | Metabolomics | Bacteria - metabolism | Intestinal Mucosa - metabolism | Microbiota - physiology | Jejunum - pathology | Humans | Jejunum - microbiology | Transcriptome | Homeostasis | Intestinal Mucosa - microbiology | Phylogeny | Jejunum - metabolism | Host-Pathogen Interactions | Feces - microbiology | Animals | Energy Metabolism | Jejunum - physiopathology | Time Factors | Models, Animal | Mice | Intestinal Absorption - physiology | Heart surgery | Small intestine | Experiments | Insulin | Studies | Nutrition research | Metabolites | Diet | Rodents | Insulin resistance | Gastrointestinal surgery | Diabetes | Laboratory animals | Metabolic disorders | Life Sciences | Agricultural sciences | homeostasis | intestine | expression | inflammatory-bowel-disease | biosynthesis | amino-acid | mice | gastric bypass | glutamate | surgery
Journal Article
The American journal of gastroenterology, ISSN 0002-9270, 07/2011, Volume 106, Issue 7, pp. 1290 - 1298
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2019, Volume 116, Issue 21, pp. 10333 - 10338
High ambient temperature has multiple potential effects on the organism such as hyperthermia, endotoxemia, and/or systemic inflammation. However, it is often... 
BARRIER DYSFUNCTION | EXPRESSION ANALYSIS | CROHNS-DISEASE | ALKALINE-PHOSPHATASE | MACROPHAGES | MULTIDISCIPLINARY SCIENCES | PATTERNS | IRON | laser capture microdissection | RNAseq | infiltrating immune cells | heat stress | jejunal mucosa | INFLAMMATION | RECEPTORS | Lactation - immunology | Intestinal Mucosa - metabolism | Jejunum - physiology | Inflammation - immunology | Jejunum - immunology | Hot Temperature | Heat-Shock Response - physiology | Heat Stress Disorders - physiopathology | Jejunum - metabolism | Intestinal Mucosa - physiology | Heat Stress Disorders - immunology | Inflammation - metabolism | Animals | Tight Junction Proteins - immunology | Cattle | Intestinal Mucosa - immunology | Lactation - metabolism | Female | Heat-Shock Response - immunology | Lactation - physiology | Tight Junction Proteins - metabolism | Inflammation - physiopathology | Heat stress disorders | Complications and side effects | Intestines | Immune response | Physiological aspects | Genetic aspects | Health aspects | Diseases | Regulators | Temperature | Dairy products | Mucosa | Homeostasis | Macrophages | Gene sequencing | Lipopolysaccharides | Jejunum | Ambient temperature | Intestine | Heat stress | Endotoxemia | Immune system | Phenotypes | Cytokines | Intensive farming | Ribonucleic acid--RNA | Gene expression | Heat | Food intake | Heat tolerance | Infiltration | Hyperthermia | Phagocytosis | Index Medicus | Biological Sciences
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 7, p. e69014
Broiler chickens are rather resistant to deoxynivalenol and thus, clinical signs are rarely seen. However, effects of subclinical concentrations of... 
MYCOTOXIN DEOXYNIVALENOL | XANTHINE OXIDOREDUCTASE | LIPID-PEROXIDATION | EPITHELIAL-CELLS | PERFORMANCE | MULTIDISCIPLINARY SCIENCES | DNA-DAMAGE | IN-VIVO | T-2 TOXIN | ANIMAL FEED | ABSORPTION | Ileum - pathology | Liver - pathology | Jejunum - pathology | Intestine, Small - pathology | Ileum - metabolism | RNA, Messenger - metabolism | Jejunum - metabolism | Jejunum - drug effects | Ileum - drug effects | Chickens - genetics | Tight Junctions - drug effects | Biomarkers - metabolism | Tight Junctions - metabolism | Liver - metabolism | RNA, Messenger - genetics | Oxidative Stress - genetics | Genes, Essential | Gene Expression Regulation - drug effects | Trichothecenes - toxicity | Animals | Adsorption | Intestine, Small - drug effects | Inflammation - genetics | Intestine, Small - metabolism | Oxidative Stress - drug effects | Oxidative stress | Inflammation | RNA | Gene expression | Analysis | Genes | Poultry | Oxidoreductase | Liver | DNA damage | Lipid peroxidation | Lipids | Biochemistry | Veterinary medicine | Small intestine | Proteins | Toxicology | Jejunum | Heme | Toll-like receptors | Digestive tract | Deoxyribonucleic acid--DNA | Immune system | Hypoxia-inducible factors | Enzymes | Clay | Food contamination & poisoning | Cytokines | Duodenum | Digestive system | Agricultural commodities | Pharmacology | TLR4 protein | Deoxynivalenol | Xanthine | Ileum | Bacteriology | Feeding | Protein synthesis | Chickens | Morphology | Xanthine oxidoreductase | Reagents | Hypoxia | Feeds | Deoxyribonucleic acid | DNA
Journal Article
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2011, Volume 141, Issue 4, pp. 1314 - 1322.e5
Background & Aims Proton pump inhibitors (PPIs) and nonsteroidal anti-inflammatory drugs (NSAIDs) are among the most commonly used classes of drugs, with the... 
Gastroenterology and Hepatology | Ulcer | Microflora | Bleeding | Acid Secretion | ULCERS | NONSTEROIDAL ANTIINFLAMMATORY DRUG | PERMEABILITY | RATS | INDOMETHACIN | LEUKOCYTE ADHERENCE | INDUCED GASTRIC DAMAGE | PATHOGENESIS | NITRIC-OXIDE | BACTERIAL OVERGROWTH | GASTROENTEROLOGY & HEPATOLOGY | Jejunum - pathology | Rats, Wistar | Colon - drug effects | Hematocrit | Peptic Ulcer - prevention & control | Male | Omeprazole - toxicity | Bifidobacterium - isolation & purification | Bifidobacterium - growth & development | Actinobacteria - drug effects | Jejunum - drug effects | Drug Interactions | Peptic Ulcer - microbiology | Time Factors | Actinobacteria - genetics | Actinobacteria - isolation & purification | Disease Models, Animal | Bifidobacterium - genetics | Jejunum - microbiology | Rats | Celecoxib | Probiotics - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Proton Pump Inhibitors - toxicity | Anti-Inflammatory Agents, Non-Steroidal - toxicity | Peptic Ulcer - pathology | Denaturing Gradient Gel Electrophoresis | 2-Pyridinylmethylsulfinylbenzimidazoles - toxicity | Gastrointestinal Hemorrhage - chemically induced | Gastrointestinal Hemorrhage - prevention & control | Bifidobacterium - drug effects | Animals | Gastrointestinal Hemorrhage - microbiology | Actinobacteria - growth & development | Pyrazoles - toxicity | Anti-Inflammatory Agents, Non-Steroidal - pharmacokinetics | Naproxen - toxicity | Sulfonamides - toxicity | Colon - microbiology | Peptic Ulcer - chemically induced | Gastrointestinal Hemorrhage - pathology | Lansoprazole | Proton pump inhibitors | Messenger RNA | Nonsteroidal anti-inflammatory drugs
Journal Article
BMC gastroenterology, ISSN 1471-230X, 2016, Volume 16, Issue 1, p. 40
Background: Breastfeeding is associated with a variety of positive health outcomes in children and is recommended exclusively for the first 6 months of life;... 
Peyer's patches | GALT | Jejunum | Nutrition | Ileum | PIGS | EARLY INFANCY | PERMEABILITY | BARRIER | ENVIRONMENT | COLONIZATION | GUT MICROBIOTA | HUMAN-MILK | IMMUNE-RESPONSES | GASTROENTEROLOGY & HEPATOLOGY | Interleukin-8 - genetics | Up-Regulation | Jejunum - pathology | Cadherins - metabolism | Calcium - metabolism | Humans | Ileum - metabolism | Interleukin-8 - drug effects | Leukemia Inhibitory Factor - genetics | Vascular Endothelial Growth Factor A - metabolism | Peyer's Patches - drug effects | RNA, Messenger - metabolism | Vascular Endothelial Growth Factor A - genetics | Antigens, CD - genetics | Antigens, CD - metabolism | Jejunum - metabolism | Leukemia Inhibitory Factor - metabolism | Jejunum - drug effects | Fas Ligand Protein - drug effects | Ileum - drug effects | Swine | Interleukin-8 - metabolism | Cadherins - genetics | Soy Foods | Cytokines - genetics | Interleukin-6 - metabolism | Infant, Newborn | Milk | Animals, Newborn | Interleukin-6 - genetics | Down-Regulation | Interleukin-27 - genetics | Gastrointestinal Microbiome - drug effects | Diet | Interleukin-10 - genetics | Interleukin-15 - metabolism | Intestine, Small - metabolism | Peyer's Patches - immunology | Fas Ligand Protein - genetics | Fas Ligand Protein - metabolism | Ileum - pathology | Interferon-alpha - drug effects | Intestine, Small - pathology | Interferon-alpha - genetics | Interleukin-10 - metabolism | Interleukin-9 - metabolism | Vascular Endothelial Growth Factor A - drug effects | Interleukin-27 - metabolism | RNA, Messenger - drug effects | Interferon-alpha - metabolism | Cytokines - metabolism | Intestine, Small - microbiology | Jejunum - microbiology | Infant Formula - pharmacology | Animals | Interleukin-15 - genetics | Cytokines - drug effects | Interleukin-9 - genetics | Intestine, Small - drug effects | Leukemia Inhibitory Factor - drug effects | Ileum - microbiology | Interleukin-10 | Analysis | Influence | Research | Gene expression | Breast feeding | Health aspects
Journal Article
American journal of physiology: Gastrointestinal and liver physiology, ISSN 1522-1547, 2008, Volume 294, Issue 1, pp. G217 - G225
Celiac disease is a gluten intolerance caused by a T-cell response against human leukocyte antigen (HLA)-DQ2 and DQ8-bound gluten peptides. Some subjects... 
Muscle contractility | Food sensitivity | Intestinal ion transport | IMMUNE-RESPONSE | PHYSIOLOGY | ION-TRANSPORT | MACROPHAGES | food sensitivity | CELIAC-DISEASE | intestinal ion transport | MURINE MODEL | INFLAMMATION | POSTINFECTIVE GUT DYSFUNCTION | muscle contractility | GASTROENTEROLOGY & HEPATOLOGY | IRRITABLE-BOWEL-SYNDROME | INTRAEPITHELIAL LYMPHOCYTES | INTESTINAL PERMEABILITY | HLA-DQ Antigens - metabolism | Intestinal Mucosa - metabolism | Intestinal Mucosa - physiopathology | Neuromuscular Junction - drug effects | Neuromuscular Junction - metabolism | Acetylcholine - metabolism | Intestinal Mucosa - drug effects | Jejunum - metabolism | Neuromuscular Junction - immunology | Jejunum - drug effects | Lymphocytes - immunology | Jejunum - physiopathology | Celiac Disease - immunology | Forkhead Transcription Factors - metabolism | Intestinal Mucosa - immunology | Cholinergic Agonists - pharmacology | Macrophages - immunology | Disease Models, Animal | Celiac Disease - chemically induced | Gliadin - immunology | Celiac Disease - physiopathology | Mice, Transgenic | Jejunum - immunology | Immunity, Innate | Neuromuscular Junction - physiopathology | Carbachol - pharmacology | Animals | Muscle Contraction | Membrane Potentials | HLA-DQ Antigens - genetics | Antibodies - blood | Intestinal Secretions - metabolism | Mice | Celiac Disease - metabolism | Jejunum - innervation
Journal Article
Stem cells (Dayton, Ohio), ISSN 1066-5099, 2014, Volume 32, Issue 5, pp. 1083 - 1091
Journal Article
Gut, ISSN 0017-5749, 08/2013, Volume 62, Issue 8, pp. 1160 - 1168
Objective Recently, the authors demonstrated altered gene expression in the jejunal mucosa of diarrhoea-predominant irritable bowel syndrome patients (IBS-D);... 
small bowel disease | ACTIVATION | anorectal function | intestinal barrier function | visceral sensitivity | PHOSPHORYLATION | enteric bacterial microflora | MAST-CELLS | intestinal mast cells | PARACELLULAR PERMEABILITY | gut immunology | TIGHT JUNCTIONS | intestinal permeability | serotonin | OCCLUDIN | gut inflammation | functional bowel disorder | gas physiology | IBS PATIENTS | neurogastroenterology | gastrointestinal motility | stress | neural-immune interactions | INVOLVEMENT | brain-gut interaction | IBS-D | antibacterial mucosal immunity | mucosal mast cells | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | gene expression | motility disorders | tight junction signalling | Intestinal Mucosa - metabolism | Phosphorylation | Jejunum - pathology | Prospective Studies | Humans | Middle Aged | Male | Diarrhea - pathology | Jejunum - metabolism | Jejunum - ultrastructure | Young Adult | Adult | Female | Tight Junction Proteins - metabolism | Irritable Bowel Syndrome - metabolism | Intestinal Mucosa - ultrastructure | Irritable Bowel Syndrome - complications | Biopsy | Mast Cells - pathology | Adolescent | Irritable Bowel Syndrome - pathology | Sex Factors | Diarrhea - etiology | Diarrhea - metabolism | Myosin Light Chains - metabolism | Intercellular Junctions - ultrastructure | Stress, Psychological - complications | Intestinal Mucosa - pathology | Disease | Gastrointestinal tract diseases | Mucosa | Confocal microscopy | Kinases | Small intestine | Proteins | Cell activation | Pain | Intestine | Ultrastructure | Rodents | Gastroenterology | Myosin | Diarrhea | Inflammation | Permeability | Gene expression | Abdomen | Studies | Hypotheses | Transmission electron microscopy | Lymphocytes B | Cell number | Irritable bowel syndrome | Tryptase | Cytoskeleton | Mast cells | Cytoplasm
Journal Article