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American Journal of Surgical Pathology, ISSN 0147-5185, 12/2006, Volume 30, Issue 12, pp. 1502 - 1512
Inflammatory myofibroblastic tumor (IMT) of the urinary tract, also termed postoperative spindle cell nodule, inflammatory pseudotumor, and pseudosarcomatous... 
ALK | Sarcoma | Pseudosarcoma | Bladder | FISH | Urinary tract | Inflammatory myofibroblastic tumor | SURGERY | PSEUDOSARCOMATOUS FIBROMYXOID TUMOR | DIFFERENTIAL-DIAGNOSIS | sarcoma | PLASMA-CELL GRANULOMA | FUSION | ALK EXPRESSION | inflammatory myofibroblastic tumor | urinary tract | PSEUDOTUMOR | PATHOLOGY | LESIONS | ANAPLASTIC LYMPHOMA KINASE | pseudosarcoma | bladder | OF-THE-LITERATURE | Inflammation - pathology | Urologic Diseases - enzymology | Urologic Diseases - genetics | Protein-Tyrosine Kinases - metabolism | Carcinoma, Transitional Cell - enzymology | Humans | Middle Aged | Ureter - enzymology | Child, Preschool | Male | Urinary Bladder - pathology | Urothelium - pathology | Prostate - pathology | Protein-Tyrosine Kinases - genetics | Fibrosarcoma - pathology | Urothelium - enzymology | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Urinary Bladder - enzymology | Child | Carcinoma, Transitional Cell - genetics | Granuloma, Plasma Cell - enzymology | Granuloma, Plasma Cell - genetics | In Situ Hybridization, Fluorescence | Receptor Protein-Tyrosine Kinases | Granuloma, Plasma Cell - pathology | Fibrosarcoma - genetics | Carcinoma, Transitional Cell - pathology | Urologic Diseases - pathology | Adolescent | Aged | Prostate - enzymology | Fibrosarcoma - enzymology | Ureter - pathology
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2011, Volume 108, Issue 17, pp. 7086 - 7090
Journal Article
Endocrinology, ISSN 0013-7227, 12/2017, Volume 158, Issue 12, pp. 4165 - 4173
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 09/2011, Volume 301, Issue 3, pp. H813 - H823
Gelinas R, Thompson-Legault J, Bouchard B, Daneault C, Mansour A, Gillis MA, Charron G, Gavino V, Labarthe F, Des Rosiers C. Prolonged QT interval and lipid... 
Triglycerides | Metabolic fluxes | Docosahexaenoic acid | Isolated working mouse heart perfusion | DEFECTS | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | SUDDEN-DEATH | CIRRHOTIC CARDIOMYOPATHY | CARDIAC MYOCYTES | isolated working mouse heart perfusion | COENZYME-A DEHYDROGENASE | triglycerides | DEFICIENT MICE | METABOLISM | FATTY-ACID OXIDATION | docosahexaenoic acid | PERIPHERAL VASCULAR DISEASE | FISH-OIL | metabolic fluxes | Palmitic Acid - metabolism | Age Factors | Muscular Diseases - enzymology | Long QT Syndrome - enzymology | Male | Metabolism, Inborn Errors - enzymology | Mice, 129 Strain | Long QT Syndrome - physiopathology | Mitochondrial Diseases - complications | Muscular Diseases - physiopathology | Aging | Fish Oils - administration & dosage | Lipid Metabolism - genetics | Disease Models, Animal | Mitochondrial Diseases - genetics | Myocardial Contraction | Long QT Syndrome - prevention & control | Oxidation-Reduction | Liver - metabolism | Mice, Inbred C57BL | Acyl-CoA Dehydrogenase, Long-Chain - genetics | Telemetry | Metabolism, Inborn Errors - genetics | Mice, Knockout | Triglycerides - metabolism | Mitochondrial Diseases - enzymology | Myocardium - enzymology | Animals | Analysis of Variance | Heart Conduction System - physiopathology | Perfusion | Lipid Metabolism, Inborn Errors | Fish Oils - metabolism | Long QT Syndrome - genetics | Muscular Diseases - complications | Mice | Muscular Diseases - genetics | Mitochondrial Diseases - physiopathology | Metabolism, Inborn Errors - complications | Metabolism, Inborn Errors - physiopathology | Acyl-CoA Dehydrogenase, Long-Chain - deficiency | Docosahexaenoic Acids - metabolism | Electrocardiography, Ambulatory | Energetics and Metabolism
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 2, pp. 636 - 641
Journal Article
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 1/2018, Volume 41, Issue 1, pp. 117 - 127
Classic galactosemia is a genetic disorder of galactose metabolism, caused by severe deficiency of galactose-1-phosphate uridylyltransferase (GALT) enzyme... 
Human Genetics | Biochemistry, general | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | DANIO-RERIO | MEDICINE, RESEARCH & EXPERIMENTAL | METABOLITES | DISORDERS | OUTCOME SEVERITY | DROSOPHILA-MELANOGASTER MODEL | CHILDREN | MOUSE MODEL | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | MOVEMENT | STRESS | PHOSPHATE URIDYLYLTRANSFERASE GALT | Nervous System Diseases - enzymology | Genetic Predisposition to Disease | Galactosemias - enzymology | UTP-Hexose-1-Phosphate Uridylyltransferase - genetics | Animals, Genetically Modified | Nervous System Diseases - genetics | Zebrafish - genetics | Infertility - genetics | Motor Activity - genetics | Fertility - genetics | Galactosemias - genetics | Infertility - enzymology | Phenotype | Zebrafish Proteins - deficiency | Animals | UTP-Hexose-1-Phosphate Uridylyltransferase - deficiency | Zebrafish - metabolism | Nervous System Diseases - etiology | Infertility - physiopathology | Nervous System Diseases - physiopathology | Zebrafish Proteins - genetics | Infertility - etiology | Disease Models, Animal | Galactosemias - complications | Genetically modified animals | Phosphates | Enzymes | Medical colleges | Medical research | Developmental biology | Analysis | Medical genetics | Physiological aspects | Medicine, Experimental | Homozygotes | Phenotypes | Fertility | Motor activity | Neurological complications | GALT gene | High-throughput screening | Mutation | Galactose | Galactosemia | Original
Journal Article