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Journal Article
Gastroenterology, ISSN 0016-5085, 2010, Volume 139, Issue 3, pp. 1008 - 1018.e1
Journal Article
Journal Article
Journal of Pharmacology and Experimental Therapeutics, ISSN 0022-3565, 07/2010, Volume 334, Issue 1, pp. 310 - 317
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 06/2004, Volume 22, Issue 11, pp. 2108 - 2121
Journal Article
Clinica Chimica Acta, ISSN 0009-8981, 2008, Volume 388, Issue 1, pp. 51 - 58
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/2008, Volume 143, Issue 1, pp. 60 - 70
Journal Article
Cancer Letters, ISSN 0304-3835, 2009, Volume 284, Issue 2, pp. 216 - 221
Abstract Autotaxin, also known as NPP2 (nucleotide pyrophosphatase/phosphodiesterase 2), is a secreted lysophospholipase-D that generates lysophosphatidic acid... 
Hematology, Oncology and Palliative Medicine | Scavenger receptor | Liver sinusoidal endothelial cells | Metastasis | Lysophospholipase-D | Autotaxin | ANGIOGENIC FACTOR | CANCER CELLS | BONE METASTASES | BREAST-CARCINOMA CELLS | SECRETED LYSOPHOSPHOLIPASE-D | THERAPY | LYSOPHOSPHATIDIC ACID | ONCOLOGY | EXPRESSION | PROMOTES | MOTILITY | Phosphodiesterase I - blood | Multienzyme Complexes - blood | Injections, Intravenous | Neoplasm Proteins - administration & dosage | Rats, Wistar | Humans | Neoplasm Proteins - physiology | Multienzyme Complexes - administration & dosage | Male | Metabolic Clearance Rate | Receptors, Scavenger - antagonists & inhibitors | Phosphoric Diester Hydrolases - pharmacokinetics | Phosphodiesterase I - administration & dosage | Multienzyme Complexes - pharmacokinetics | Neoplasm Metastasis - prevention & control | Phosphoric Diester Hydrolases - blood | Pyrophosphatases - administration & dosage | Phosphodiesterase I - pharmacokinetics | Receptors, Scavenger - metabolism | Serum Albumin, Bovine - pharmacology | Endothelial Cells - metabolism | Pyrophosphatases - blood | Formaldehyde - pharmacology | Rats | Pyrophosphatases - pharmacokinetics | Liver - blood supply | Animals | Neoplasm Metastasis - physiopathology | Neoplasm Proteins - blood | Cells, Cultured - metabolism | Mice | Neoplasm Proteins - pharmacokinetics | Phosphoric Diester Hydrolases - administration & dosage | Liver | Endothelium | Proteins | Angiogenesis | Motility | Rodents | Radioactivity | Index Medicus
Journal Article
Journal Article
American Journal of Physiology - Endocrinology and Metabolism, ISSN 0193-1849, 06/2016, Volume 310, Issue 11, pp. E947 - E957
Glucagon-like peptide-1 (GLP-1) may have direct favorable effects on cardiovascular system. The aim of this study was to investigate the effects of the GLP-1... 
Endothelial nitric oxide synthase | Glucagon-like peptide-1 | Human umbilical vein endothelial cells | Coronary flow velocity reserve | Type 2 diabetes mellitus | AMP-activated protein kinase | Exenatide | CORONARY FLOW VELOCITY | PHYSIOLOGY | coronary flow velocity reserve | NITRIC-OXIDE SYNTHASE | glucagon-like peptide-1 | DIABETES-MELLITUS | RESERVE | human umbilical vein endothelial cells | ENDOCRINOLOGY & METABOLISM | type 2 diabetes mellitus | endothelial nitric oxide synthase | TETRAHYDROBIOPTERIN | ARTERY | exenatide | DOPPLER-ECHOCARDIOGRAPHY | NONINVASIVE ASSESSMENT | AGONIST | Multienzyme Complexes - blood | AMP-Activated Protein Kinases - metabolism | Echocardiography | Humans | Middle Aged | Endothelium, Vascular - physiopathology | Endothelium, Vascular - drug effects | Male | Diabetic Angiopathies - drug therapy | Diabetic Angiopathies - diagnostic imaging | Peptides - administration & dosage | Dose-Response Relationship, Drug | Nitric Oxide Synthase Type III - blood | Diabetic Angiopathies - physiopathology | Glucagon-Like Peptide-1 Receptor - metabolism | Cardiotonic Agents - administration & dosage | Hypoglycemic Agents - administration & dosage | Signal Transduction - drug effects | Endothelium, Vascular - diagnostic imaging | Oncogene Protein v-akt - blood | Venoms - administration & dosage | Adult | Female | Type 2 diabetes | Physiological aspects | Dosage and administration | Endothelium | Cardiovascular system | Phosphorylation | Oxygen | Peptides | Hemoglobin | Diabetes | Cell adhesion & migration | Index Medicus
Journal Article
Pediatrics, ISSN 0031-4005, 06/2002, Volume 109, Issue 6, pp. 999 - 1008
Objective. To evaluate an approach to the diagnosis and treatment of maple syrup disease (MSD). Methods. Family histories and molecular testing for the Y393N... 
Metabolic disease | Isoleucine valine | Maple syrup disease | Branched-chain ketoacid dehydrogenase | Newborn screening | Dystonia | Essential amino acid deficiencies | Leucine | Blood brain barrier | Mennonite | Neutral amino acid transporter | leucine | Guthrie bacterial inhibition assay | URINE-DISEASE | neutral amino acid transporter | metabolic disease | LOCUS | branched-chain ketoacid dehydrogenase | isoleucine valine | CHILDREN | maple syrup disease | blood brain barrier | essential amino acid deficiencies | tandem mass spectrometry | dystonia | PEDIATRICS | NUTRITION | MUTATIONS | newborn screening | Multienzyme Complexes - blood | Follow-Up Studies | Amino Acids, Branched-Chain - metabolism | Humans | Clinical Protocols | Neonatal Screening | Maple Syrup Urine Disease - diagnosis | Furosemide - therapeutic use | Osmolar Concentration | Polymerase Chain Reaction | Maple Syrup Urine Disease - blood | Adult | Female | Saline Solution, Hypertonic - therapeutic use | Infant, Newborn | Alanine - blood | Hydrazines | Isoleucine - blood | Leucine - metabolism | 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide) | Valine - blood | Maple Syrup Urine Disease - therapy | Leucine - blood | Mannitol - therapeutic use | Alanine - metabolism | Treatment Outcome | Multienzyme Complexes - genetics | Ketone Oxidoreductases - genetics | Sodium - blood | Isoleucine - metabolism | Ketone Oxidoreductases - blood | Valine - metabolism | Mutation | Amino Acids, Branched-Chain - blood | Maple syrup urine disease | Care and treatment | Studies | Medical research | Pediatrics | Disease | Medical diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
Blood, ISSN 0006-4971, 11/2008, Volume 112, Issue 9, pp. 3900 - 3906
Previous research has shown that glycolytic enzymes (GEs) exist as multienzyme complexes on the inner surface of human erythrocyte membranes. Because GE... 
HEMOGLOBIN | TARGETED DISRUPTION | TRANSPORT | DOMAIN | BAND-3 | METABOLISM | BINDING-SITE | CELL-MEMBRANES | HEMATOLOGY | SPHEROCYTOSIS | SKELETON |