Drug lipid metabolism inborn errors. Medical search. Frequent questions

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Anatomy17

Liver Adipose Tissue Cells, Cultured Adipocytes Muscle, Skeletal Brain Hepatocytes Fibroblasts Membrane Microdomains Microsomes, Liver Adipose Tissue, White Cell Line Cell Membrane Mitochondria 3T3-L1 Cells Erythrocytes Hep G2 Cells

Organisms7

Mice, Knockout Mice, Inbred C57BL Rats, Wistar Rats, Sprague-Dawley Rats, Inbred Strains Cattle Mice, Transgenic

Diseases52

Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Lipid Metabolism Disorders Carbohydrate Metabolism, Inborn Errors Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Phenylketonurias Smith-Lemli-Opitz Syndrome Refractive Errors Metabolic Diseases Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Brain Diseases, Metabolic Body Weight Metal Metabolism, Inborn Errors Fructose Metabolism, Inborn Errors Insulin Resistance Maple Syrup Urine Disease Porphyria, Erythropoietic Hyperargininemia Iron Metabolism Disorders Hyperlipidemias Failure to Thrive Obesity Fatty Liver Alkaptonuria Rare Diseases Citrullinemia Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Lysosomal Storage Diseases Pyruvate Dehydrogenase Complex Deficiency Disease Neuroaxonal Dystrophies Disease Models, Animal Hyperoxaluria, Primary Genetic Diseases, Inborn Renal Tubular Transport, Inborn Errors Diabetes Mellitus, Type 2 Liver Diseases Intellectual Disability Inflammation Nervous System Diseases Atherosclerosis

Chemicals and Drugs103

Lipids Lipid A Fatty Acids Lipid Bilayers Triglycerides Cholesterol Glucose Phospholipids Carnitine Homogentisate 1,2-Dioxygenase Lipid Peroxides alpha-Galactosidase Fatty Acids, Nonesterified Argininosuccinic Acid Insulin Isovaleryl-CoA Dehydrogenase Blood Glucose Dietary Fats Methylmalonic Acid PPAR alpha Lipoproteins Pentanoic Acids Oxidoreductases Acting on CH-CH Group Donors Hydroxocobalamin Methylmalonyl-CoA Mutase Sterol Regulatory Element Binding Protein 1 Glutarates Phosphatidylcholines Amidinotransferases Glutaryl-CoA Dehydrogenase Receptors, Cytoplasmic and Nuclear RNA, Messenger Acyl-CoA Dehydrogenase Bile Acids and Salts Lipoprotein Lipase Orphan Nuclear Receptors Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Acetates Lipase Cholesterol, HDL Oxidoreductases Adenylosuccinate Lyase Glycerol Peroxisome Proliferator-Activated Receptors Ornithine-Oxo-Acid Transaminase Sterol Regulatory Element Binding Proteins Fatty Acids, Unsaturated Oleic Acid Cytochrome P-450 Enzyme System Cholesterol, LDL Carbon Radioisotopes Hypolipidemic Agents Lipoproteins, VLDL Apolipoproteins E Carbon Isotopes Apolipoproteins B Transcription Factors Ornithine Argininosuccinate Lyase PPAR gamma Carrier Proteins Urea Oleic Acids Sterols Lipoproteins, LDL Uroporphyrinogen III Synthetase Ammonia Apolipoproteins Membrane Proteins Carnitine O-Palmitoyltransferase Sphingolipids Acyl-CoA Oxidase Acyl Coenzyme A Sterol Esterase Diglycerides Amino Acids Apolipoprotein A-I Fatty Acid Synthases Liposomes Phenylalanine Hydroxylase Glycerides Lactic Acid Fatty Acid-Binding Proteins Acyl-CoA Dehydrogenases Lipoproteins, HDL Phosphatidylinositols Leptin DNA Primers Carbon Coenzyme A Ligases Plant Oils Vitamin B 12 Fats Proteins Sterol Regulatory Element Binding Protein 2 Phosphatidate Phosphatase Sphingomyelins Palmitic Acids Biological Markers Fenofibrate Lactates Receptors, LDL DNA

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

Neonatal Screening Models, Biological Diagnostic Errors Magnetic Resonance Spectroscopy Body Weight Mass Spectrometry Gene Expression Profiling Obesity Gas Chromatography-Mass Spectrometry Reference Values Chromatography, Thin Layer Tandem Mass Spectrometry Chromatography, High Pressure Liquid Pedigree Disease Models, Animal Diet, Protein-Restricted Reproducibility of Results Oligonucleotide Array Sequence Analysis Organ Size Reverse Transcriptase Polymerase Chain Reaction Phlebotomy Blood Specimen Collection Polymerase Chain Reaction Glucose Tolerance Test Analysis of Variance Chromatography, Gas

Psychiatry and Psychology2

Fasting Intellectual Disability

Phenomena and Processes48

Lipid Metabolism Energy Metabolism Lipid Peroxidation Mutation Metabolic Networks and Pathways Metabolism Oxidation-Reduction Time Factors Lipolysis Body Weight Gene Expression Regulation Lipogenesis Phenotype Insulin Resistance Base Sequence Obesity Kinetics Diet Amino Acid Sequence Signal Transduction Homeostasis Homozygote Diet, High-Fat Genotype Fasting Glycolysis Eating Biological Transport Diet, Protein-Restricted Biotransformation Carbohydrate Metabolism Oxygen Consumption Organ Size Gene Expression Oxidative Stress Alleles Pregnancy Dose-Response Relationship, Drug Heterozygote Lipid Mobilization Metabolome Consanguinity Mutation, Missense Algorithms Body Composition Postprandial Period Protein Binding Citric Acid Cycle

Technology, Industry, Agriculture3

Lipid Bilayers Dietary Fats Liposomes

Information Science5

Molecular Sequence Data Base Sequence Amino Acid Sequence Algorithms Computer Simulation

Named Groups1

Infant, Newborn

Health Care6

Neonatal Screening Diagnostic Errors Reproducibility of Results Critical Pathways Technology Assessment, Biomedical Analysis of Variance

Geographicals1

Australian Capital Territory

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 Health Care Geographicals

Metabolism, Inborn Errors Lipid Metabolism Lipids Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Lipid A Steroid Metabolism, Inborn Errors Neonatal Screening Purine-Pyrimidine Metabolism, Inborn Errors Lipid Metabolism Disorders Liver Carbohydrate Metabolism, Inborn Errors Energy Metabolism Fatty Acids Lipid Bilayers Triglycerides Urea Cycle Disorders, Inborn Cholesterol Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Lipid Peroxidation Phenylketonurias Smith-Lemli-Opitz Syndrome Glucose Phospholipids Mutation Infant, Newborn Carnitine Refractive Errors Homogentisate 1,2-Dioxygenase Adipose Tissue Lipid Peroxides Metabolic Diseases Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors alpha-Galactosidase Molecular Sequence Data Fabry Disease Fatty Acids, Nonesterified Metabolic Networks and Pathways Metabolism Australian Capital Territory Ornithine Carbamoyltransferase Deficiency Disease Models, Biological Argininosuccinic Acid Oxidation-Reduction Insulin Isovaleryl-CoA Dehydrogenase Hypophosphatasia Blood Glucose Dietary Fats Methylmalonic Acid PPAR alpha Lipoproteins Time Factors Diagnostic Errors Brain Diseases, Metabolic Pentanoic Acids Magnetic Resonance Spectroscopy Oxidoreductases Acting on CH-CH Group Donors Lipolysis Hydroxocobalamin Methylmalonyl-CoA Mutase Body Weight Metal Metabolism, Inborn Errors Gene Expression Regulation Sterol Regulatory Element Binding Protein 1 Fructose Metabolism, Inborn Errors Lipogenesis Glutarates Phenotype Insulin Resistance Mice, Knockout Maple Syrup Urine Disease Phosphatidylcholines Mass Spectrometry Mice, Inbred C57BL Amidinotransferases Gene Expression Profiling Porphyria, Erythropoietic Glutaryl-CoA Dehydrogenase Receptors, Cytoplasmic and Nuclear RNA, Messenger Hyperargininemia Iron Metabolism Disorders Hyperlipidemias Base Sequence Acyl-CoA Dehydrogenase Bile Acids and Salts Lipoprotein Lipase Failure to Thrive Cells, Cultured Obesity Orphan Nuclear Receptors Adipocytes Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Fatty Liver Gas Chromatography-Mass Spectrometry

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