Metabolism, Inborn ErrorsLipid MetabolismLipid BilayersMembrane LipidsLipidsAmino Acid Metabolism, Inborn ErrorsLiposomesPhosphatidylcholinesLipid Metabolism, Inborn ErrorsLipid ASteroid Metabolism, Inborn ErrorsNeonatal ScreeningPurine-Pyrimidine Metabolism, Inborn ErrorsLipid Metabolism DisordersLiverCarbohydrate Metabolism, Inborn ErrorsEnergy MetabolismFatty AcidsTriglyceridesUrea Cycle Disorders, InbornCholesterolBrain Diseases, Metabolic, InbornArgininosuccinic AciduriaHyperammonemiaLipid PeroxidationPhenylketonuriasSmith-Lemli-Opitz SyndromeGlucosePhospholipidsMutationInfant, NewbornCarnitineRefractive ErrorsHomogentisate 1,2-DioxygenaseAdipose TissueLipid PeroxidesMetabolic DiseasesHomocystinuriaCandidiasis, Chronic MucocutaneousPyruvate Metabolism, Inborn Errorsalpha-GalactosidaseMolecular Sequence DataFabry DiseaseFatty Acids, NonesterifiedMetabolic Networks and PathwaysMetabolismAustralian Capital TerritoryOrnithine Carbamoyltransferase Deficiency DiseaseModels, BiologicalArgininosuccinic AcidOxidation-ReductionInsulinIsovaleryl-CoA DehydrogenaseHypophosphatasiaBlood GlucoseDietary FatsMethylmalonic AcidPPAR alphaLipoproteinsTime FactorsDiagnostic ErrorsBrain Diseases, MetabolicPentanoic AcidsMagnetic Resonance SpectroscopyOxidoreductases Acting on CH-CH Group DonorsLipolysisHydroxocobalaminMethylmalonyl-CoA MutaseBody WeightMetal Metabolism, Inborn ErrorsGene Expression RegulationSterol Regulatory Element Binding Protein 1Fructose Metabolism, Inborn ErrorsLipogenesisGlutaratesPhenotypeInsulin ResistanceMice, KnockoutMaple Syrup Urine DiseaseMass SpectrometryMice, Inbred C57BLAmidinotransferasesGene Expression ProfilingPorphyria, ErythropoieticGlutaryl-CoA DehydrogenaseReceptors, Cytoplasmic and NuclearRNA, MessengerHyperargininemiaIron Metabolism DisordersHyperlipidemiasBase SequenceAcyl-CoA DehydrogenaseBile Acids and SaltsLipoprotein LipaseFailure to ThriveCells, CulturedObesityOrphan Nuclear ReceptorsAdipocytesLong-Chain-3-Hydroxyacyl-CoA Dehydrogenase