Deficiency are long chain fatty acid oxidation. Medical search. Frequent questions

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Anatomy22

Microbodies Liver Peroxisomes Mitochondria, Liver Myocardium Mitochondria Adipose Tissue Muscle, Skeletal Cells, Cultured Fibroblasts Mitochondria, Muscle Cell Line Skin Gastrointestinal Contents Cell Membrane Vernix Caseosa X Chromosome Hepatocytes Mitochondria, Heart Adipocytes Colon Heart

Organisms9

Mice, Knockout Mice, Inbred C57BL Rats, Sprague-Dawley Rats, Inbred Strains Saccharomyces cerevisiae Escherichia coli Rats, Wistar Swine Cattle

Diseases24

Adrenoleukodystrophy Diffuse Cerebral Sclerosis of Schilder Biotinidase Deficiency Lipid Metabolism, Inborn Errors Peroxisomal Disorders Protein C Deficiency alpha 1-Antitrypsin Deficiency Deficiency Diseases Vitamin B 12 Deficiency Glucosephosphate Dehydrogenase Deficiency Fatty Liver Folic Acid Deficiency IgA Deficiency Anemia, Iron-Deficiency Vitamin D Deficiency Zellweger Syndrome Body Weight Obesity Starvation Metabolism, Inborn Errors Insulin Resistance Riboflavin Deficiency Refsum Disease Chondrodysplasia Punctata

Chemicals and Drugs140

Fatty Acids Coenzyme A Ligases Fatty Acid Transport Proteins Palmitic Acid Malonyl Coenzyme A Carnitine O-Palmitoyltransferase Caprylates Acyl Coenzyme A Palmitates Fatty Acids, Unsaturated Palmitic Acids Oleic Acids Oleic Acid Fatty Acids, Nonesterified 3-Hydroxyacyl CoA Dehydrogenases Carnitine Fatty Acid-Binding Proteins Acyl-CoA Dehydrogenase, Long-Chain Fatty Acids, Volatile Fatty Acid Desaturases Phytanic Acid Enoyl-CoA Hydratase Erucic Acids Stearic Acids Fatty Acid Synthases Acetyl-CoA Carboxylase Palmitoyl Coenzyme A Mitochondrial Trifunctional Protein Triglycerides Coenzyme A Sphingolipids Fatty Acids, Omega-3 Epoxy Compounds Methylmalonate-Semialdehyde Dehydrogenase (Acylating)Glucose Butyrates Antigens, CD36 Triazenes Acyl-CoA Dehydrogenase Phospholipids Lipids Myelin P2 Protein Triolein Acetyltransferases Acetyl-CoA C-Acyltransferase Ketone Bodies Dietary Fats Fatty Acids, Essential Carrier Proteins PPAR alpha Acetates Fatty Acids, Omega-6 Acyl-CoA Oxidase Vitamin B 12 Multienzyme Complexes Palmitoylcarnitine Acetyl Coenzyme A 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase Propionates RNA, Messenger Ceramides Acyltransferases AMP-Activated Protein Kinases Esters Membrane Proteins Acyl-CoA Dehydrogenases Lauric Acids Iron Phytol Thiolester Hydrolases Fatty Acids, Monounsaturated Carbon-Carbon Double Bond Isomerases Insulin Racemases and Epimerases Carnitine Acyltransferases Transcription Factors Recombinant Proteins Fish Oils Carbon Isotopes 3-Hydroxybutyric Acid Eicosapentaenoic Acid Zinc DNA, Complementary Cholesterol Docosahexaenoic Acids Aminoimidazole Carboxamide Linoleic Acid Glycerides Trimetazidine Neoplasm Proteins Caproates Butyric Acid Dicarboxylic Acids Saccharomyces cerevisiae Proteins Adenylate Kinase Fats Oxidoreductases Lanolin Plant Oils Carboxy-Lyases Dietary Fats, Unsaturated Ketones Blood Glucose Receptors, Cytoplasmic and Nuclear Dodecenoyl-CoA Isomerase Mitochondrial Proteins Waxes Laurates Citrate (si)-Synthase Carbon Radioisotopes Ribonucleotides Acetic Acid Trans Fatty Acids Diacylglycerol O-Acyltransferase Nerve Tissue Proteins Vitamin D alpha-Linolenic Acid Pentanoic Acids Palmitoyl-CoA Hydrolase PPAR delta Linoleic Acids Fatty Alcohols Carbon Dioxide Hydroxymethylglutaryl-CoA Synthase Glycogen ATP-Binding Cassette Transporters Lactic Acid Citrates Stearoyl-CoA Desaturase Acetyl-CoA C-Acetyltransferase Fatty Acid Synthase, Type I Enzyme Inhibitors Serum Albumin Glycerol Oxygen Myristic Acid Hydroxybutyrates Diglycerides Lipase Glycerol-3-Phosphate O-Acyltransferase

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Chromatography, Gas Chromatography, Thin Layer Gas Chromatography-Mass Spectrometry Cloning, Molecular Chromatography, High Pressure Liquid Models, Biological Mass Spectrometry Body Weight Polymerase Chain Reaction Obesity Blotting, Western Pedigree Calorimetry, Indirect Magnetic Resonance Spectroscopy Reverse Transcriptase Polymerase Chain Reaction

Psychiatry and Psychology1

Phenomena and Processes44

Oxidation-Reduction Lipid Metabolism Kinetics Mutation Substrate Specificity Energy Metabolism Amino Acid Sequence Biological Transport Phenotype Base Sequence Esterification Structure-Activity Relationship Time Factors Oxygen Consumption Acylation Diet Intestinal Absorption Protein Binding Hydrogen-Ion Concentration Glycolysis X Chromosome Sequence Homology, Amino Acid Lipolysis Binding Sites Fasting Body Weight Gene Expression Regulation Lipogenesis Obesity Molecular Structure Genotype Citric Acid Cycle Dose-Response Relationship, Drug Insulin Resistance Temperature Gene Expression Regulation, Enzymologic Tissue Distribution Carbohydrate Metabolism Transcription, Genetic Diet, High-Fat Gluconeogenesis Signal Transduction Fermentation Phylogeny

Technology, Industry, Agriculture3

Dietary Fats Dietary Fats, Unsaturated Animal Feed

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Phylogeny

Named Groups1

Infant, Newborn

Health Care1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Technology, Industry, Agriculture Information Science Named Groups

Fatty Acids Adrenoleukodystrophy Molecular Sequence Data Oxidation-Reduction Coenzyme A Ligases Fatty Acid Transport Proteins Palmitic Acid Malonyl Coenzyme A Carnitine O-Palmitoyltransferase Caprylates Acyl Coenzyme A Palmitates Fatty Acids, Unsaturated Palmitic Acids Oleic Acids Oleic Acid Fatty Acids, Nonesterified 3-Hydroxyacyl CoA Dehydrogenases Carnitine Fatty Acid-Binding Proteins Acyl-CoA Dehydrogenase, Long-Chain Microbodies Liver Fatty Acids, Volatile Fatty Acid Desaturases Lipid Metabolism Phytanic Acid Enoyl-CoA Hydratase Erucic Acids Stearic Acids Fatty Acid Synthases Acetyl-CoA Carboxylase Diffuse Cerebral Sclerosis of Schilder Biotinidase Deficiency Palmitoyl Coenzyme A Lipid Metabolism, Inborn Errors Mitochondrial Trifunctional Protein Triglycerides Coenzyme A Sphingolipids Fatty Acids, Omega-3 Peroxisomes Epoxy Compounds Methylmalonate-Semialdehyde Dehydrogenase (Acylating)Glucose Peroxisomal Disorders Protein C Deficiency Butyrates alpha 1-Antitrypsin Deficiency Deficiency Diseases Vitamin B 12 Deficiency Antigens, CD36 Triazenes Acyl-CoA Dehydrogenase Kinetics Phospholipids Mice, Knockout Lipids Chromatography, Gas Glucosephosphate Dehydrogenase Deficiency Chromatography, Thin Layer Myelin P2 Protein Triolein Acetyltransferases Mitochondria, Liver Mutation Acetyl-CoA C-Acyltransferase Ketone Bodies Substrate Specificity Myocardium Mitochondria Gas Chromatography-Mass Spectrometry Dietary Fats Fatty Liver Energy Metabolism Amino Acid Sequence Biological Transport Fatty Acids, Essential Carrier Proteins Folic Acid Deficiency IgA Deficiency Adipose Tissue Mice, Inbred C57BL PPAR alpha Phenotype Muscle, Skeletal Acetates Fatty Acids, Omega-6 Acyl-CoA Oxidase Vitamin B 12 Cells, Cultured Multienzyme Complexes Palmitoylcarnitine Anemia, Iron-Deficiency Base Sequence Acetyl Coenzyme A 3-Oxoacyl-(Acyl-Carrier-Protein) Synthase Propionates RNA, Messenger Ceramides

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