Lipids lipid metabolism inborn errors. Medical search. Frequent questions

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Anatomy16

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

Organisms6

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

Diseases50

Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Lipid Metabolism Disorders Steroid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors 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 Body Weight Hypophosphatasia Hyperlipidemias Insulin Resistance Brain Diseases, Metabolic Metal Metabolism, Inborn Errors Obesity Fructose Metabolism, Inborn Errors Maple Syrup Urine Disease Porphyria, Erythropoietic Iron Metabolism Disorders Hyperargininemia Failure to Thrive Fatty Liver Alkaptonuria Rare Diseases Citrullinemia Multiple Acyl Coenzyme A Dehydrogenase Deficiency Disease Models, Animal Mucopolysaccharidoses Lysosomal Storage Diseases Pyruvate Dehydrogenase Complex Deficiency Disease Neuroaxonal Dystrophies Hyperoxaluria, Primary Genetic Diseases, Inborn Diabetes Mellitus, Type 2 Renal Tubular Transport, Inborn Errors Atherosclerosis Inflammation Liver Diseases

Chemicals and Drugs112

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment23

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

Psychiatry and Psychology1

Phenomena and Processes49

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

Technology, Industry, Agriculture4

Lipid Bilayers Dietary Fats Liposomes Membranes, Artificial

Information Science4

Molecular Sequence Data Amino Acid Sequence Base Sequence Algorithms

Named Groups1

Infant, Newborn

Health Care4

Neonatal Screening Diagnostic Errors Reproducibility of Results Temperature

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

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