Dysfunction amino acid metabolism inborn errors. Medical search. Frequent questions

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Anatomy13

Liver Brain Cells, Cultured Muscle, Skeletal Cell Line Muscles Mitochondria Myocardium Fibroblasts Kidney Microsomes, Liver Hepatic Veins Endothelium, Vascular

Organisms13

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

Diseases40

Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Lipid Metabolism, Inborn Errors Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Carbohydrate Metabolism, Inborn Errors Urea Cycle Disorders, Inborn Brain Diseases, Metabolic, Inborn Argininosuccinic Aciduria Hyperammonemia Maple Syrup Urine Disease Phenylketonurias Ventricular Dysfunction, Left Erectile Dysfunction Smith-Lemli-Opitz Syndrome Refractive Errors Homocystinuria Disease Models, Animal Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Brain Diseases, Metabolic Metabolic Diseases Hypophosphatasia Starvation Body Weight Metal Metabolism, Inborn Errors Fructose Metabolism, Inborn Errors Hyperargininemia Porphyria, Erythropoietic Failure to Thrive Iron Metabolism Disorders Uremia Citrullinemia Alkaptonuria Rare Diseases Multiple Acyl Coenzyme A Dehydrogenase Deficiency Mucopolysaccharidoses Lysosomal Storage Diseases

Chemicals and Drugs95

Amino Acids Amino Acids, Sulfur Amino Acids, Branched-Chain Amino Acids, Essential Amino Acids, Aromatic Fatty Acids Leucine Nitrogen Glutamine Methionine Alanine Glucose Ammonia Urea Phenylalanine Carbon Isotopes Transaminases Bacterial Proteins Keto Acids Dietary Proteins Arginine RNA, Messenger Isoleucine Glycine Carbon Amino Acid Transport Systems Proteins Aspartic Acid Proteome Ornithine Insulin Carbon Radioisotopes Carnitine Aminoisobutyric Acids DNA, Complementary DNA Glutamates Valine Recombinant Proteins Arachidonic Acid Lysine Homogentisate 1,2-Dioxygenase alpha-Galactosidase Bile Acids and Salts Cysteine Plant Proteins Methylmalonyl-CoA Mutase Peptide Fragments Glutamic Acid Transcription Factors Methylmalonic Acid Argininosuccinic Acid 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)Arachidonic Acids Isovaleryl-CoA Dehydrogenase Glutarates Oxidoreductases Acting on CH-CH Group Donors DNA Primers Culture Media Sulfur Pentanoic Acids Muscle Proteins Blood Glucose Cystathionine gamma-Lyase Peptides Carbon Dioxide Lactates Carrier Proteins Hydroxocobalamin Threonine Cytochrome P-450 Enzyme System Oxidoreductases Betaine-Homocysteine S-Methyltransferase Fungal Proteins Cholesterol DNA-Binding Proteins Tyrosine Amidinotransferases Acyl-CoA Dehydrogenase Glutathione Recombinant Fusion Proteins Glutaryl-CoA Dehydrogenase Homocysteine Oxygen Iodobenzenes Quaternary Ammonium Compounds Membrane Proteins Saccharomyces cerevisiae Proteins Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Triglycerides Amino Acid Transport Systems, Basic Isoenzymes Glucagon Ornithine-Oxo-Acid Transaminase Adenylosuccinate Lyase

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

Neonatal Screening Amino Acid Substitution Cloning, Molecular Sequence Alignment Gene Expression Profiling Gas Chromatography-Mass Spectrometry Models, Biological Chromatography, High Pressure Liquid Mass Spectrometry Magnetic Resonance Spectroscopy Oligonucleotide Array Sequence Analysis Disease Models, Animal Models, Molecular Mutagenesis, Site-Directed Electrophoresis, Gel, Two-Dimensional Sequence Analysis, DNA Culture Media Body Weight Diagnostic Errors Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction Restriction Mapping Electrophoresis, Polyacrylamide Gel DNA Mutational Analysis Blood Urea Nitrogen Reference Values Pedigree Tandem Mass Spectrometry Reproducibility of Results

Psychiatry and Psychology2

Erectile Dysfunction Fasting

Phenomena and Processes60

Sequence Homology, Amino Acid Amino Acid Sequence Lipid Metabolism Mutation Energy Metabolism Metabolome Amino Acid Substitution Metabolic Networks and Pathways Base Sequence Kinetics Oxidation-Reduction Time Factors Phenotype Carbohydrate Metabolism Gene Expression Regulation, Bacterial Biological Transport Citric Acid Cycle Amino Acid Motifs Binding Sites Phylogeny Protein Biosynthesis Transcription, Genetic Transcriptome Nutritional Requirements Gene Expression Genes, Bacterial Glycolysis Signal Transduction Metabolism Substrate Specificity Gene Expression Regulation, Plant Gene Expression Regulation Sequence Homology, Nucleic Acid Protein Conformation Protein Binding Structure-Activity Relationship Diet Oxygen Consumption Protein Structure, Tertiary Oxidative Stress Gene Expression Regulation, Fungal Fasting Body Weight Multigene Family Species Specificity Homeostasis Stress, Physiological Molecular Weight Pregnancy Point Mutation Adaptation, Physiological Plasmids Mutation, Missense Dose-Response Relationship, Drug Fermentation Conserved Sequence Gluconeogenesis Protein Structure, Secondary Genotype Homozygote

Disciplines and Occupations3

Metabolomics Proteomics Computational Biology

Technology, Industry, Agriculture1

Dietary Proteins

Information Science4

Amino Acid Sequence Molecular Sequence Data Base Sequence Phylogeny

Named Groups1

Infant, Newborn

Health Care3

Neonatal Screening Diagnostic Errors Reproducibility of Results

Geographicals1

Australian Capital Territory

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

Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Amino Acids Amino Acids, Sulfur Amino Acids, Branched-Chain Sequence Homology, Amino Acid Amino Acid Sequence Lipid Metabolism, Inborn Errors Liver Amino Acids, Essential Lipid Metabolism Mutation Neonatal Screening Amino Acids, Aromatic Energy Metabolism Metabolome Purine-Pyrimidine Metabolism, Inborn Errors Steroid Metabolism, Inborn Errors Fatty Acids Leucine Molecular Sequence Data Carbohydrate Metabolism, Inborn Errors Amino Acid Substitution Metabolic Networks and Pathways Nitrogen Cloning, Molecular Metabolomics Glutamine Base Sequence Methionine Alanine Urea Cycle Disorders, Inborn Glucose Ammonia Brain Diseases, Metabolic, Inborn Kinetics Argininosuccinic Aciduria Hyperammonemia Urea Sequence Alignment Phenylalanine Carbon Isotopes Transaminases Maple Syrup Urine Disease Oxidation-Reduction Bacterial Proteins Gene Expression Profiling Keto Acids Phenylketonurias Gas Chromatography-Mass Spectrometry Escherichia coli Time Factors Dietary Proteins Arginine Models, Biological Chromatography, High Pressure Liquid RNA, Messenger Isoleucine Glycine Ventricular Dysfunction, Left Carbon Erectile Dysfunction Phenotype Amino Acid Transport Systems Proteins Aspartic Acid Proteome Carbohydrate Metabolism Smith-Lemli-Opitz Syndrome Ornithine Gene Expression Regulation, Bacterial Mass Spectrometry Infant, Newborn Magnetic Resonance Spectroscopy Insulin Carbon Radioisotopes Biological Transport Carnitine Aminoisobutyric Acids Citric Acid Cycle Brain Cells, Cultured Amino Acid Motifs Binding Sites Phylogeny Protein Biosynthesis DNA, Complementary DNA Glutamates Valine Recombinant Proteins Arachidonic Acid Refractive Errors Oligonucleotide Array Sequence Analysis Lysine Homogentisate 1,2-Dioxygenase Transcription, Genetic alpha-Galactosidase Bile Acids and Salts Saccharomyces cerevisiae

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