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Scientific Reports, ISSN 2045-2322, 03/2017, Volume 7, Issue 1, p. 43412
This study was conducted to investigate impacts of dietary protein levels on gut bacterial community and gut barrier. The intestinal microbiota of finishing... 
POSTWEANING DIARRHEA | HOST METABOLISM | CELLS | FINISHING PIGS | HOMEOSTASIS | PIGLETS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | MODULATING INTESTINAL PERMEABILITY | BUTYRATE | PROMOTES | Dietary Proteins - administration & dosage | Peptostreptococcus - drug effects | Tight Junction Proteins - genetics | Receptors, G-Protein-Coupled - metabolism | Colon - drug effects | Ileum - metabolism | Escherichia - metabolism | Escherichia - classification | Fatty Acids, Volatile - metabolism | Intestinal Mucosa - drug effects | Occludin - metabolism | Genetic Variation | Polycomb Repressive Complex 1 - genetics | Dietary Proteins - metabolism | Ileum - drug effects | Swine | Shigella - metabolism | Tight Junction Proteins - metabolism | Firmicutes - isolation & purification | Intestinal Mucosa - microbiology | Peptostreptococcus - isolation & purification | Colon - metabolism | Gastrointestinal Microbiome - drug effects | Claudin-1 - genetics | Escherichia - drug effects | Receptors, G-Protein-Coupled - genetics | Escherichia - isolation & purification | Firmicutes - drug effects | Animal Feed | Peptostreptococcus - classification | Intestinal Mucosa - metabolism | Polycomb Repressive Complex 1 - metabolism | Shigella - classification | Gastrointestinal Microbiome - physiology | Clostridium - isolation & purification | Shigella - drug effects | Clostridium - classification | Occludin - genetics | Claudin-1 - metabolism | Biogenic Amines - metabolism | Diet, Protein-Restricted - methods | Firmicutes - metabolism | Digestion - drug effects | Firmicutes - classification | Shigella - isolation & purification | Peptostreptococcus - metabolism | Digestion - physiology | Gene Expression Regulation - drug effects | Animals | Clostridium - metabolism | Colon - microbiology | Ileum - microbiology | Clostridium - drug effects | Amines | Digestive system | Mucosa | Ileum | Studies | Proteins | Protein composition | Metabolites | Intestine | Fish | Intestinal microflora | Colon | Digestive tract | Biogenic amines | Colonization
Journal Article
2012, 3rd ed., ISBN 0470661518, xxi, 456
Amino Acid Metabolism, 3rdEditioncovers all aspects of the biochemistry and nutritional biochemistry of the amino acids. Starting with an overview of nitrogen... 
Amino acids | Acides aminés | Metabolism | Métabolisme | Amino Acids - metabolism
Book
Nature, ISSN 0028-0836, 10/2017, Volume 550, Issue 7674, pp. 119 - 123
Catecholamine-induced lipolysis, the first step in the generation of energy substrates by the hydrolysis of triglycerides(1), declines with age(2,3). The... 
MONOAMINE-OXIDASE | CELLS | OBESITY | ACTIVATION | MULTIDISCIPLINARY SCIENCES | ACCUMULATION | IDENTIFICATION | GENE ONTOLOGY | DEFICIENCY | ADIPOSE-TISSUE | AGE | Inflammasomes - metabolism | Lipolysis - drug effects | Catecholamines - metabolism | Growth Differentiation Factor 3 - metabolism | Sterol Esterase - metabolism | Aging - drug effects | Adipose Tissue - cytology | Caspase 1 - metabolism | Gene Expression Profiling | Growth Differentiation Factor 3 - deficiency | Lipolysis - genetics | Adipose Tissue - metabolism | Aging - genetics | Monoamine Oxidase Inhibitors - pharmacology | NLR Family, Pyrin Domain-Containing 3 Protein - metabolism | Lipase - metabolism | NLR Family, Pyrin Domain-Containing 3 Protein - deficiency | Gene Expression Regulation - drug effects | Macrophages - metabolism | Animals | Norepinephrine - metabolism | Growth Differentiation Factor 3 - genetics | Adipocytes - metabolism | Mice | Adipose Tissue - drug effects | Catecholamines - pharmacology | Aging - metabolism | Monoamine Oxidase - metabolism | Aging | Observations | Catecholamine metabolism | Health aspects | Elderly people | Adipose tissue | Oxidase | Genomes | Adipocytes | Kinases | Macrophages | Lipase | Caspase-1 | Reduction | Energy resources | Clonal deletion | Deletion | Noradrenaline | Age | Enzymes | Starvation | Fasting | Body temperature | Aging (artificial) | Glycerol | Caspase | Principal components analysis | Triglycerides | Inflammation | Bioavailability | Metabolism | Gene expression | Sympathetic nervous system | Catecholamine | Fatty acids | Substrates | Lipolysis | Amine oxidase (flavin-containing) | Signaling | Catabolism | Norepinephrine | Elderly | Geriatrics
Journal Article
Science, ISSN 0036-8075, 1/2009, Volume 323, Issue 5910, pp. 101 - 106
Journal Article
2006, 2nd ed., ISBN 9780521824552, xxii, 688 p., [1] leaf of plates
Neonatal nutrition has a pivotal role in normal child development and is of even greater importance in the sick or premature neonate. This 2006 edition... 
Infants (Newborn) -- Nutrition | Infants (Newborn) -- Diseases | Infants (Newborn) -- Growth | Infants (Newborn) -- Metabolism | Inclusive education | Cross-cultural studies | Education and state | Infants (Newborn)
Book
Nature Medicine, ISSN 1078-8956, 06/2017, Volume 23, Issue 6, pp. 733 - 741
Blood vessels in the central nervous system (CNS) are controlled by neuronal activity. For example, widespread vessel constriction (vessel tone) is induced by... 
MEDICINE, RESEARCH & EXPERIMENTAL | PIAL VESSELS | RAT | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRACE AMINES | SYNAPTIC-TRANSMISSION | HYPOXIA | CELL BIOLOGY | CENTRAL-NERVOUS-SYSTEM | LOCOMOTOR FUNCTION | CEREBRAL-ARTERIES | RECEPTORS | BRAIN | Capillaries - pathology | Serotonin 5-HT1 Receptor Antagonists - pharmacology | Receptors, Adrenergic, alpha-2 - metabolism | Transcriptome | Capillaries - drug effects | RNA, Messenger - metabolism | Oxygen - metabolism | Hypoxia - metabolism | Receptors, Serotonin, 5-HT1 - metabolism | Spinal Cord Injuries - pathology | Receptor, Serotonin, 5-HT1B - metabolism | Aromatic-L-Amino-Acid Decarboxylases - metabolism | Tyramine - metabolism | Capillaries - metabolism | Locomotion - drug effects | Injections, Spinal | Capillaries - physiopathology | Spinal Cord Injuries - metabolism | Pericytes - metabolism | Vasoconstriction | Rats | Microscopy, Interference | Oxygen Inhalation Therapy | Microscopy, Confocal | Animals | Norepinephrine - metabolism | Tryptamines - metabolism | Serotonin - metabolism | Spinal Cord Injuries - physiopathology | Biogenic Monoamines - metabolism | Locomotion - physiology | Enzymes | Care and treatment | Analysis | Tryptophan | Spinal cord injuries | Dosage and administration | Drug therapy | Health aspects | Noradrenaline | Blood flow | spinal cord injury | AADC | hypoxia | pericyte | capillary | locomotion | Trace amines | neurovascular coupling | 5-HT1B receptor | motoneurons | ischemia
Journal Article
Analytical Chemistry, ISSN 0003-2700, 03/2005, Volume 77, Issue 5, pp. 1282 - 1289
Journal Article
Diabetes, Obesity and Metabolism, ISSN 1462-8902, 07/2018, Volume 20, Issue 7, pp. 1623 - 1631
Aims Sevelamer, a non‐absorbable amine‐based resin used for treatment of hyperphosphataemia, has been demonstrated to have a marked bile acid‐binding potential... 
antidiabetic drug | drug mechanism | type 2 diabetes | GLP‐1 | glucose metabolism | GLP-1 | PROTEIN | RELEASE | INSULIN | SEQUESTRATION | METABOLISM | COLESEVELAM | DISEASE | ENDOCRINOLOGY & METABOLISM | FARNESOID-X-RECEPTOR | TYPE-2 DIABETES-MELLITUS | BINDING | Gastric Inhibitory Polypeptide - metabolism | Area Under Curve | Humans | Middle Aged | Male | Sequestering Agents - therapeutic use | Diabetes Mellitus, Type 2 - metabolism | Sevelamer - therapeutic use | Fibroblast Growth Factors - metabolism | Cholecystokinin - metabolism | Female | C-Peptide - metabolism | Chelating Agents - therapeutic use | Double-Blind Method | Glucagon-Like Peptide 1 - metabolism | Cholesterol, HDL - metabolism | Bile Acids and Salts - metabolism | Cholesterol - metabolism | Gastric Emptying | Gastrointestinal Microbiome - genetics | Triglycerides - metabolism | Energy Metabolism | Cholesterol, LDL - metabolism | RNA, Ribosomal, 16S - genetics | Glucagon - metabolism | Aged | Blood Glucose - metabolism | Diabetes Mellitus, Type 2 - drug therapy | Type 2 diabetes | Amines | Glucagon | Microbiota (Symbiotic organisms) | Lipids | Glucose | Insulin | Dextrose | Deoxycholic acid | Glucose metabolism | Physiological aspects | Fibroblast growth factors | Cholecystokinin | Fibroblast growth factor | Peptides | Liver | Microbiota | Intestine | Fibroblasts | Lipid metabolism | Lipogenesis | Diabetes mellitus (non-insulin dependent) | Digestive tract | Growth factors | Bile acids | Digestive system | Diabetes mellitus | Energy expenditure | Gastric emptying | Patients | Acids | Diabetes | Receptor mechanisms | Bile | colesevelam | disease | insulin | farnesoid-x-receptor | release | binding | type-2 diabetes-mellitus | Endokrinologi och diabetes | sequestration | protein | Endocrinology & Metabolism | metabolism | Endocrinology and Diabetes
Journal Article
European Journal of Pharmacology, ISSN 0014-2999, 08/2014, Volume 736, pp. 26 - 34
Thiazole derivatives are attractive candidates for drug development because they can be efficiently synthesized and are active against a number of diseases and... 
Oxidative stress | Inflammation | Diabetes | Antioxidant | Thiazole derivative | LIPID-PEROXIDATION | ESSENTIAL OIL | ANTIOXIDANT ENZYMES | 2-CYCLOPROPYLIMINO-3-METHYL-1,3-THIAZOLINE HYDROCHLORIDE | INFLAMMATORY DISEASE | BETA-CELL DAMAGE | KEY ENZYMES | HEPG2 CELLS | PHARMACOLOGY & PHARMACY | NF-KAPPA-B | CARBOHYDRATE-METABOLISM | Tumor Necrosis Factor-alpha - metabolism | Diabetes Mellitus, Experimental - drug therapy | Glutathione - metabolism | Male | NF-kappa B - metabolism | Thiazoles - therapeutic use | Insulin - blood | Hyperglycemia - drug therapy | Ascorbic Acid - metabolism | Liver - drug effects | Interleukin-1beta - metabolism | Lipid Peroxidation - drug effects | Adamantane - therapeutic use | Anti-Inflammatory Agents - therapeutic use | Diabetes Mellitus, Experimental - metabolism | Superoxide Dismutase - metabolism | Adamantane - analogs & derivatives | Hypoglycemic Agents - therapeutic use | Malondialdehyde - metabolism | Adamantane - pharmacology | Blood Glucose - analysis | Hyperlipidemias - metabolism | Anti-Inflammatory Agents - pharmacology | Hyperlipidemias - drug therapy | Liver - metabolism | Antioxidants - pharmacology | Hypolipidemic Agents - pharmacology | Rats, Sprague-Dawley | Hypoglycemic Agents - pharmacology | Catalase - metabolism | Hyperglycemia - metabolism | Antioxidants - therapeutic use | Animals | Lipid Metabolism - drug effects | Vitamin E - metabolism | Hypolipidemic Agents - therapeutic use | Thiazoles - pharmacology | Oxidative Stress - drug effects | Nitric Oxide - metabolism | Amines | Glycogen | Isoenzymes | Blood sugar | Streptozocin | Superoxide | Triglycerides | Fructose | Antioxidants | Glucose metabolism | Hyperglycemia | Synthesis | Nitric oxide
Journal Article