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

Home page Questions and answers Statistics Donations Contact

Anatomy9

Liver Cells, Cultured Brain Muscle, Skeletal Cell Line Muscles Fibroblasts Microsomes, Liver Hepatic Veins

Organisms12

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

Diseases39

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 Smith-Lemli-Opitz Syndrome Refractive Errors Homocystinuria Candidiasis, Chronic Mucocutaneous Pyruvate Metabolism, Inborn Errors Fabry Disease Ornithine Carbamoyltransferase Deficiency Disease Hypophosphatasia Brain Diseases, Metabolic Starvation Metabolic Diseases Metal Metabolism, Inborn Errors Fructose Metabolism, Inborn Errors Body Weight Hyperargininemia Porphyria, Erythropoietic Iron Metabolism Disorders Failure to Thrive Citrullinemia Alkaptonuria Disease Models, Animal Rare Diseases Multiple Acyl Coenzyme A Dehydrogenase Deficiency Uremia Mucopolysaccharidoses Lysosomal Storage Diseases Pyruvate Dehydrogenase Complex Deficiency Disease

Chemicals and Drugs100

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment29

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

Psychiatry and Psychology1

Phenomena and Processes62

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

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 Care2

Neonatal Screening Diagnostic Errors

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

No FAQ available that match "physiological amino acid metabolism inborn errors"