Peroxisomal DisordersZellweger SyndromeRefsum DiseaseAdrenoleukodystrophyMicrobodiesChondrodysplasia Punctata, RhizomelicPhytanic AcidPlasmalogensPeroxisomesChondrodysplasia PunctataAcetyl-CoA C-AcetyltransferasePeroxisomal Multifunctional Protein-2Fatty AcidsLipid Metabolism, Inborn ErrorsProtein TransportMitochondrial Membrane Transport ProteinsMitochondriaIntracellular MembranesMembrane ProteinsMolecular Sequence DataOxidation-ReductionGas Chromatography-Mass Spectrometryran GTP-Binding ProteinMembrane Transport ProteinsBiological TransportAmino Acid SequenceChloroplastsFibroblastsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsGeneticsAcyl-CoA OxidasePeasReceptors, Cytoplasmic and NuclearBiogenesisMitochondrial Proteinsbeta KaryopherinsAcetyl-CoA C-AcyltransferaseFungal ProteinsGlyoxysomesPichiaEnoyl-CoA HydrataseProtein PrecursorsMutationalpha KaryopherinsNuclear Localization SignalsKaryopherinsProtein Sorting SignalsChloroplast ProteinsPeroxisomal Bifunctional EnzymeCell NucleusCarrier ProteinsBase SequenceBipolar DisorderCytosolPlant ProteinsRecombinant Fusion ProteinsNuclear Pore Complex Proteins3-Hydroxyacyl CoA DehydrogenasesNuclear ProteinsSequence Homology, Amino AcidProtein BindingMitochondrial MembranesMolecular ChaperonesHSP70 Heat-Shock ProteinsArabidopsisArabidopsis ProteinsMental DisordersPlastidsCell CompartmentationClofibrateAnxiety DisordersPhenotypeModels, BiologicalMood DisordersNuclear EnvelopeGenes, FungalCatalaseCloning, MolecularLiverSequence AlignmentGenetics, PopulationGenetic Complementation TestNucleocytoplasmic Transport ProteinsCytoplasmNuclear Pore