| PUBMED REFERENCES |
ORGANISMS |
| Characterization of Arabidopsis 6-phosphogluconolactonase T-DNA insertion mutants reveals an essential role for the oxidative section of the plastidic pentose phosphate pathway in plant growth and development.[Pubmed]
|
|
| Molecular characterization of the first two enzymes of the pentose-phosphate pathway of Trypanosoma brucei. Glucose-6-phosphate dehydrogenase and 6-phosphogluconolactonase.[Pubmed]
|
|
| Mutations in the Arabidopsis peroxisomal ABC transporter COMATOSE allow differentiation between multiple functions in planta: insights from an allelic series.[Pubmed]
|
|
| The Arabidopsis ALDP protein homologue COMATOSE is instrumental in peroxisomal acetate metabolism.[Pubmed]
|
|
| Plant ATP-binding cassette transporters.[Pubmed]
|
|
| Metabolite transport across the peroxisomal membrane.[Pubmed]
|
|
| The peroxisomal ABC transporter family.[Pubmed]
|
|
| Sucrose rescues seedling establishment but not germination of Arabidopsis mutants disrupted in peroxisomal fatty acid catabolism.[Pubmed]
|
|
| Peroxisomal Acyl-CoA synthetase activity is essential for seedling development in Arabidopsis thaliana.[Pubmed]
|
|
| Control of germination and lipid mobilization by COMATOSE, the Arabidopsis homologue of human ALDP.[Pubmed]
|
|
| Ped3p is a peroxisomal ATP-binding cassette transporter that might supply substrates for fatty acid beta-oxidation.[Pubmed]
|
|
| The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage.[Pubmed]
|
|
| X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.[Pubmed]
|
|
| Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.[Pubmed]
|
|
| Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model.[Pubmed]
|
|
| Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed]
|
|
| ABC transporters in lipid transport.[Pubmed]
|
|
| The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.[Pubmed]
|
|
| A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.[Pubmed]
|
|
| RNAi-mediated silencing of ABCD3 gene expression in rat C6 glial cells: a model system to study PMP70 function.[Pubmed]
|
|
| The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters.[Pubmed]
|
|
| Mitochondrial ATP-binding cassette proteins.[Pubmed]
|
|
| The peroxisomal lumen in Saccharomyces cerevisiae is alkaline.[Pubmed]
|
|
| Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motif.[Pubmed]
|
|
| Saccharomyces cerevisiae Adr1p governs fatty acid beta-oxidation and peroxisome proliferation by regulating POX1 and PEX11.[Pubmed]
|
|
| Adr1p-dependent regulation of the oleic acid-inducible yeast gene SPS19 encoding the peroxisomal beta-oxidation auxiliary enzyme 2,4-dienoyl-CoA reductase.[Pubmed]
|
|
| Peroxisomal degradation of trans-unsaturated fatty acids in the yeast Saccharomyces cerevisiae.[Pubmed]
|
|
| Predicting the function and subcellular location of Caenorhabditis elegans proteins similar to Saccharomyces cerevisiae beta-oxidation enzymes.[Pubmed]
|
|
| Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance.[Pubmed]
|
|
| Primary structure of human PMP69, a putative peroxisomal ABC-transporter.[Pubmed]
|
|
| A Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters.[Pubmed]
|
|
| The ABC transporter proteins Pat1 and Pat2 are required for import of long-chain fatty acids into peroxisomes of Saccharomyces cerevisiae.[Pubmed]
|
|
| Characterization and analysis of conserved motifs in a peroxisomal ATP-binding cassette transporter.[Pubmed]
|
|
| PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.[Pubmed]
|
|
| Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.[Pubmed]
|
|
| Characterization of Yarrowia lipolytica mutants affected in hydrophobic substrate utilization.[Pubmed]
|
|
| Cholesterol-deprivation increases mono-unsaturated very long-chain fatty acids in skin fibroblasts from patients with X-linked adrenoleukodystrophy.[Pubmed]
|
|
| ATP-binding and -hydrolysis activities of ALDP (ABCD1) and ALDRP (ABCD2), human peroxisomal ABC proteins, overexpressed in Sf21 cells.[Pubmed]
|
|
| Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis.[Pubmed]
|
|
| Novel insertion 496_497insG creating a stop codon D194X in a Chinese family with X-Linked adrenoleukodystrophy.[Pubmed]
|
|
| Overexpression of a human and a fungal ABC transporter similarly suppresses the differentiation defects of a fungal peroxisomal mutant but introduces pleiotropic cellular effects.[Pubmed]
|
|
| Functional characterization of the adrenoleukodystrophy protein (ALDP) and disease pathogenesis.[Pubmed]
|
|
| Two splice variants of human PEX19 exhibit distinct functions in peroxisomal assembly.[Pubmed]
|
|
| ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.[Pubmed]
|
|
| Targeting elements in the amino-terminal part direct the human 70-kDa peroxisomal integral membrane protein (PMP70) to peroxisomes.[Pubmed]
|
|
| Characterization and functional analysis of the nucleotide binding fold in human peroxisomal ATP binding cassette transporters.[Pubmed]
|
|
| Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins.[Pubmed]
|
|
| Identification of a fourth half ABC transporter in the human peroxisomal membrane.[Pubmed]
|
|
| Trypanosoma brucei glycosomal ABC transporters: identification and membrane targeting.[Pubmed]
|
|
| Peroxisome proliferation, wound-activated responses and expression of peroxisome-associated genes are cross-regulated but uncoupled in Arabidopsis thaliana.[Pubmed]
|
|
| The crystal structure of a plant 3-ketoacyl-CoA thiolase reveals the potential for redox control of peroxisomal fatty acid beta-oxidation.[Pubmed]
|
|
| An Arabidopsis mutant disrupted in valine catabolism is also compromised in peroxisomal fatty acid beta-oxidation.[Pubmed]
|
|
| Direct interaction between glyoxysomes and lipid bodies in cotyledons of the Arabidopsis thaliana ped1 mutant.[Pubmed]
|
|
| Requirement for 3-ketoacyl-CoA thiolase-2 in peroxisome development, fatty acid beta-oxidation and breakdown of triacylglycerol in lipid bodies of Arabidopsis seedlings.[Pubmed]
|
|
| Transport of peroxisomal proteins synthesized as large precursors in plants.[Pubmed]
|
|
| The multifunctional protein AtMFP2 is co-ordinately expressed with other genes of fatty acid beta-oxidation during seed germination in Arabidopsis thaliana (L.) Heynh.[Pubmed]
|
|
| A novel acyl-CoA oxidase that can oxidize short-chain acyl-CoA in plant peroxisomes.[Pubmed]
|
|
| Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid.[Pubmed]
|
|
| Peroxisomal beta-oxidation enzyme gene expression in the developing mouse brain.[Pubmed]
|
|
| Morphological heterogeneity of peroxisomes in cultured mouse Leydig cells.[Pubmed]
|
|
| Immunocytochemical demonstration of peroxisomes in cultured Leydig cells: a decrease in testosterone secretion precedes reduction of peroxisomes.[Pubmed]
|
|
| Different accumulations of 3-ketoacyl-CoA thiolase precursor in peroxisomes of Chinese hamster ovary cells harboring a dysfunction in the PEX2 protein.[Pubmed]
|
|
| Immunofluorescence technique for 100-nm-thick semithin sections of Epon-embedded tissues.[Pubmed]
|
|
| Sesamin, a sesame lignan, is a potent inducer of hepatic fatty acid oxidation in the rat.[Pubmed]
|
|
| Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.[Pubmed]
|
|
| Sterol carrier protein X is peroxisomal 3-oxoacyl coenzyme A thiolase with intrinsic sterol carrier and lipid transfer activity.[Pubmed]
|
|
| Impairment of peroxisomal beta-oxidation system by endotoxin treatment.[Pubmed]
|
|
| Post-translational import of 3-ketoacyl-CoA thiolase into rat liver peroxisomes in vitro.[Pubmed]
|
|
| The impact of aging on enzyme proteins of rat liver peroxisomes: quantitative analysis by immunoblotting and immunoelectron microscopy.[Pubmed]
|
|
| Signal peptide for peroxisomal targeting: replacement of an essential histidine residue by certain amino acids converts the amino-terminal presequence of peroxisomal 3-ketoacyl-CoA thiolase to a mitochondrial signal peptide.[Pubmed]
|
|
| A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase.[Pubmed]
|
|
| Mitochondrial metabolism of valproic acid.[Pubmed]
|
|
| Immunoelectron microscopic study of a new D-amino acid oxidase-immunoreactive subcompartment in rat liver peroxisomes.[Pubmed]
|
|
| Cloning and sequence determination of cDNA encoding a second rat liver peroxisomal 3-ketoacyl-CoA thiolase.[Pubmed]
|
|
| Immunogold localization of peroxisomal enzymes in Epon-embedded liver tissue. Enhancement of sensitivity by etching with ethanolic sodium hydroxide.[Pubmed]
|
|
| Immunocytochemical localization of peroxisomal enzymes in human liver biopsies.[Pubmed]
|
|
| Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate.[Pubmed]
|
|
| Biosynthesis and intracellular transport of enzymes of peroxisomal beta-oxidation.[Pubmed]
|
|
| Innermembrane association of three mitochondrial beta-oxidation enzymes revealed by immunoelectron microscopic technique.[Pubmed]
|
|
| Immunocytochemical localization of two peroxisomal enzymes of lipid beta-oxidation in specific granules of rat eosinophils.[Pubmed]
|
|
| Antifungal activity of Saccharomyces cerevisiae peroxisomal 3-ketoacyl-CoA thiolase.[Pubmed]
|
|
| Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids.[Pubmed]
|
|
| An n-alkane-responsive promoter element found in the gene encoding the peroxisomal protein of Candida tropicalis does not contain a C(6) zinc cluster DNA-binding motif.[Pubmed]
|
|
| The 2.8 A crystal structure of peroxisomal 3-ketoacyl-CoA thiolase of Saccharomyces cerevisiae: a five-layered alpha beta alpha beta alpha structure constructed from two core domains of identical topology.[Pubmed]
|
|
| Mutagenesis of the amino targeting signal of Saccharomyces cerevisiae 3-ketoacyl-CoA thiolase reveals conserved amino acids required for import into peroxisomes in vivo.[Pubmed]
|
|
| PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae.[Pubmed]
|
|
| Up-regulation of the peroxisomal beta-oxidation system occurs in butyrate-grown Candida tropicalis following disruption of the gene encoding peroxisomal 3-ketoacyl-CoA thiolase.[Pubmed]
|
|
| Genetic evaluation of physiological functions of thiolase isoenzymes in the n-alkalane-assimilating yeast Candida tropicalis.[Pubmed]
|
|
| Immunoelectron microscopic observation of the behaviors of peroxisomal enzymes inducibly synthesized in an n-alkane-utilizable yeast cell, Candida tropicalis.[Pubmed]
|
|
| Physiological roles of acetoacetyl-CoA thiolase in n-alkane-utilizable yeast, Candida tropicalis: possible contribution to alkane degradation and sterol biosynthesis.[Pubmed]
|
|
| Genes encoding peroxisomal enzymes are not necessarily assigned on the same chromosome of an n-alkane-utilizable yeast Candida tropicalis.[Pubmed]
|
|
| Peroxisomal acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase from an n-alkane-utilizing yeast, Candida tropicalis: purification and characterization.[Pubmed]
|
|
| Occurrence and possible roles of acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase in peroxisomes of an n-alkane-grown yeast, Candida tropicalis.[Pubmed]
|
|
| Cloning and expression in phospholipid containing cultures of the gene encoding the specific phosphatidylglycerol/phosphatidylinositol transfer protein from Aspergillus oryzae: evidence that the pg/pi-tp is tandemly arranged with the putative 3-ketoacyl-CoA thiolase gene.[Pubmed]
|
|
| Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes.[Pubmed]
|
|
| Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.[Pubmed]
|
|
| Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 gene.[Pubmed]
|
|
| Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder.[Pubmed]
|
|
| Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.[Pubmed]
|
|
| Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.[Pubmed]
|
|
| Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.[Pubmed]
|
|
| Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata.[Pubmed]
|
|
| Immunohistochemical expression of peroxisomal enzymes in developing human brain.[Pubmed]
|
|
| Peroxisomal disorders in children: immunohistochemistry and neuropathology.[Pubmed]
|
|
| Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata.[Pubmed]
|
|
| Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly.[Pubmed]
|
|
| Rhizomelic chondrodysplasia punctata: biochemical studies of peroxisomes isolated from cultured skin fibroblasts.[Pubmed]
|
|
| Aberrant subcellular localization of peroxisomal 3-ketoacyl-CoA thiolase in the Zellweger syndrome and rhizomelic chondrodysplasia punctata.[Pubmed]
|
|
| Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.[Pubmed]
|
|
| Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy.[Pubmed]
|
|
| Detection of peroxisomes in human liver and kidney fixed with formalin and embedded in paraffin: the use of catalase and lipid beta-oxidation enzymes as immunocytochemical markers.[Pubmed]
|
|
| Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.[Pubmed]
|
|
| Immunocytochemical demonstration of peroxisomal enzymes in human kidney biopsies.[Pubmed]
|
|
| Characterization of Aspergillus nidulans peroxisomes by immunoelectron microscopy.[Pubmed]
|
|
| Function of N-terminal import signals in trypanosome microbodies.[Pubmed]
|
|
| Induction and subcellular localization of enzymes participating in propionate metabolism in Candida tropicalis.[Pubmed]
|
|
| Identification and characterization of Arabidopsis indole-3-butyric acid response mutants defective in novel peroxisomal enzymes.[Pubmed]
|
|
| IBR3, a novel peroxisomal acyl-CoA dehydrogenase-like protein required for indole-3-butyric acid response.[Pubmed]
|
|
| Functional diversification of acyl-coenzyme A oxidases in jasmonic acid biosynthesis and action.[Pubmed]
|
|
| Peroxisomal beta-oxidation--a metabolic pathway with multiple functions.[Pubmed]
|
|
| Expression, purification and crystallization of two peroxisomal acyl-CoA oxidases from Arabidopsis thaliana.[Pubmed]
|
|
| Arabidopsis mutants in short- and medium-chain acyl-CoA oxidase activities accumulate acyl-CoAs and reveal that fatty acid beta-oxidation is essential for embryo development.[Pubmed]
|
|
| The Arabidopsis acyl-CoA oxidase gene family.[Pubmed]
|
|
| Importance of sequences adjacent to the terminal tripeptide in the import of a peroxisomal Candida tropicalis protein in plant peroxisomes.[Pubmed]
|
|
| Activity of peroxisomal enzymes, and levels of polyamines in LPA-transgenic mice on two different diets.[Pubmed]
|
|
| Targeted disruption of the peroxisomal thiolase B gene in mouse: a new model to study disorders related to peroxisomal lipid metabolism.[Pubmed]
|
|
| Sequential ordered fatty acid alpha oxidation and Delta9 desaturation are major determinants of lipid storage and utilization in differentiating adipocytes.[Pubmed]
|
|
| Expression of peroxisomal proteins provides clear evidence for the presence of peroxisomes in the male germ cell line GC1spg.[Pubmed]
|
|
| Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.[Pubmed]
|
|
| Lessons from knockout mice II: Mouse models for peroxisomal disorders with single protein deficiency.[Pubmed]
|
|
| Studies on the metabolic fate of n-3 polyunsaturated fatty acids.[Pubmed]
|
|
| Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.[Pubmed]
|
|
| Detection of peroxisomal proteins and their mRNAs in serial sections of fetal and newborn mouse organs.[Pubmed]
|
|
| Caloric restriction prevents oxidative damage induced by the carcinogen clofibrate in mouse liver.[Pubmed]
|
|
| Evidence for the involvement of the fatty acid and peroxisomal beta-oxidation pathways in the inhibition by dehydroepiandrosterone (DHEA) and induction by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and benz(a)anthracene (BA) of cytochrome P4501B1 (CYP1B1) in mouse embryo fibroblasts (C3H10T1/2 cells).[Pubmed]
|
|
| Peroxisomal impairment in Niemann-Pick type C disease.[Pubmed]
|
|
| Aging-related decrease in liver peroxisomal fatty acid oxidation in control and clofibrate-treated mice. A biochemical study and mechanistic approach.[Pubmed]
|
|
| Hepatic peroxisome proliferation in vitamin A-deficient mice without a simultaneous increase in peroxisomal acyl-CoA oxidase activity.[Pubmed]
|
|
| Liver peroxisomal fatty acid oxidizing system during aging in control and clofibrate-treated mice.[Pubmed]
|
|
| Eicosapentaenoic acid at hypotriglyceridemic dose enhances the hepatic antioxidant defense in mice.[Pubmed]
|
|
| Perfluorooctanoic acid has persistent effects on peroxisome proliferation and related parameters in mouse liver.[Pubmed]
|
|
| Reduced levels of peroxisomal enzymes in the kidney of the genetically obese (ob/ob) mouse. Contrast with liver.[Pubmed]
|
|
| Localization of carnitine acyltransferases and acyl-CoA beta-oxidation enzymes in small intestinal microperoxisomes (peroxisomes) of normal and clofibrate treated mice.[Pubmed]
|
|
| Detection of acyl-CoA beta-oxidation enzymes in peroxisomes (microperoxisomes) of mouse heart.[Pubmed]
|
|
| Rats selectively bred for low aerobic capacity have reduced hepatic mitochondrial oxidative capacity and susceptibility to hepatic steatosis and injury.[Pubmed]
|
|
| Effect of dietary n-6/n-3 ratio on liver n-6/n-3 ratio and peroxisomal beta-oxidation activity in rats.[Pubmed]
|
|
| Oct-2-en-4-ynoyl-CoA as a specific inhibitor of acyl-CoA oxidase.[Pubmed]
|
|
| Contribution of peroxisome-specific isoform of Lon protease in sorting PTS1 proteins to peroxisomes.[Pubmed]
|
|
| Metabolism and short-term metabolic effects of conjugated linoleic acids in rat hepatocytes.[Pubmed]
|
|
| Concerted action of leptin in regulation of fatty acid oxidation in skeletal muscle and liver.[Pubmed]
|
|
| Intrinsic enoyl-CoA isomerase activity of rat acyl-CoA oxidase I.[Pubmed]
|
|
| Impaired peroxisomal function in the central nervous system with inflammatory disease of experimental autoimmune encephalomyelitis animals and protection by lovastatin treatment.[Pubmed]
|
|
| Antioxidants attenuate diabetes-induced activation of peroxisomal functions in the rat kidney.[Pubmed]
|
|
| Immunohistochemical localization of peroxisomal enzymes during rat embryonic development.[Pubmed]
|
|
| Acyl-CoA dehydrogenases and acyl-CoA oxidases. Structural basis for mechanistic similarities and differences.[Pubmed]
|
|
| The hypotriglyceridemic effect of dietary n-3 FA is associated with increased beta-oxidation and reduced leptin expression.[Pubmed]
|
|
| Identification and cloning of two forms of liver peroxisomal fatty Acyl CoA Oxidase from the koala (Phascolarctos cinereus).[Pubmed]
|
|
| Modulation of the peroxisomal gene expression pattern by dehydroepiandrosterone and vitamin D: therapeutic implications.[Pubmed]
|
|
| Analyses in transfected cells and in vitro of a putative peroxisomal targeting signal of rat liver serine:pyruvate aminotransferase.[Pubmed]
|
|
| Three-dimensional structure of the flavoenzyme acyl-CoA oxidase-II from rat liver, the peroxisomal counterpart of mitochondrial acyl-CoA dehydrogenase.[Pubmed]
|
|
| Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.[Pubmed]
|
|
| Localization of mRNAs encoding peroxisomal proteins in cell culture by non-radioactive in situ hybridization. Comparison of rat and human hepatoma cells and their responses to two divergent hypolipidemic drugs.[Pubmed]
|
|
| Effect of sesamin on mitochondrial and peroxisomal beta-oxidation of arachidonic and eicosapentaenoic acids in rat liver.[Pubmed]
|
|
| Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1.[Pubmed]
|
|
| Insulin inhibits peroxisomal fatty acid oxidation in isolated rat hepatocytes.[Pubmed]
|
|
| Peroxisomal lipid degradation via beta- and alpha-oxidation in mammals.[Pubmed]
|
|
| Growth reduction in glioma cells after treatment with tetradecylthioacetic acid: changes in fatty acid metabolism and oxidative status.[Pubmed]
|
|
| Differential induction of stearoyl-CoA desaturase and acyl-CoA oxidase genes by fibrates in HepG2 cells.[Pubmed]
|
|
| Proliferation of mitochondria and gene expression of carnitine palmitoyltransferase and fatty acyl-CoA oxidase in rat skeletal muscle, heart and liver by hypolipidemic fatty acids.[Pubmed]
|
|
| Role and organization of peroxisomal beta-oxidation.[Pubmed]
|
|
| Induction by perfluorinated fatty acids with different carbon chain length of peroxisomal beta-oxidation in the liver of rats.[Pubmed]
|
|
| Gene expression of peroxisomal beta-oxidation enzymes in rat brain.[Pubmed]
|
|
| Cytochrome P450, peroxisome proliferation, and cytoplasmic fatty acid-binding protein content in liver, heart and kidney of the diabetic rat.[Pubmed]
|
|
| New insights in peroxisomal beta-oxidation. Implications for human peroxisomal disorders.[Pubmed]
|
|
| Impairment of peroxisomal structure and function in rat liver allograft rejection: prevention by cyclosporine.[Pubmed]
|
|
| Comparative effects of alpha- and gamma-linolenic acids on rat liver fatty acid oxidation.[Pubmed]
|
|
| Biogenesis of peroxisomes in fetal liver.[Pubmed]
|
|
| Molecular cloning and expression of cDNA encoding 3alpha,7alpha,12alpha-trihydroxy-5beta-chole stanoyl-CoA oxidase from rabbit liver.[Pubmed]
|
|
| Effect of gemfibrozil on centrifugal behavior of rat peroxisomes and activities of peroxisomal enzymes involved in lipid metabolism.[Pubmed]
|
|
| Up-regulated delta 9-desaturase gene expression by hypolipidemic peroxisome-proliferating fatty acids results in increased oleic acid content in liver and VLDL: accumulation of a delta 9-desaturated metabolite of tetradecylthioacetic acid.[Pubmed]
|
|
| Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome.[Pubmed]
|
|
| In vitro association with peroxisomes and conformational change of peroxisomal serine:pyruvate/alanine:glyoxylate aminotransferase in rat and human livers.[Pubmed]
|
|
| Stereoisomeric inversion of (25R)- and (25S)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acids in rat liver peroxisome.[Pubmed]
|
|
| Novel peroxisomal populations in subcellular fractions from rat liver. Implications for peroxisome structure and biogenesis.[Pubmed]
|
|
| Activity measurements of acyl-CoA oxidases in human liver.[Pubmed]
|
|
| Peroxisomal beta-oxidation. Purification of four novel 3-hydroxyacyl-CoA dehydrogenases from rat liver peroxisomes.[Pubmed]
|
|
| Estimation of peroxisomal beta-oxidation in rat heart by a direct assay of acyl-CoA oxidase.[Pubmed]
|
|
| Zonal heterogeneity of peroxisomal enzymes in rat liver: differential induction by three divergent hypolipidemic drugs.[Pubmed]
|
|
| Urate oxidase is imported into peroxisomes recognizing the C-terminal SKL motif of proteins.[Pubmed]
|
|
| Peroxisomal acyl-coenzyme A oxidase is a rate-limiting enzyme in a very-long-chain fatty acid beta-oxidation system.[Pubmed]
|
|
| Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase.[Pubmed]
|
|
| Alterations of peroxisomal function in ischemia-reperfusion injury of rat kidney.[Pubmed]
|
|
| An intimate collaboration between peroxisomes and lipid bodies.[Pubmed]
|
|
| Functional similarity between the peroxisomal PTS2 receptor binding protein Pex18p and the N-terminal half of the PTS1 receptor Pex5p.[Pubmed]
|
|
| Alpha-Ketoglutarate dehydrogenase and lipoic acid synthase are important for the functioning of peroxisomes of Saccharomyces cerevisiae.[Pubmed]
|
|
| Futile cycling of intermediates of fatty acid biosynthesis toward peroxisomal beta-oxidation in Saccharomyces cerevisiae.[Pubmed]
|
|
| Saccharomyces cerevisiae acyl-CoA oxidase follows a novel, non-PTS1, import pathway into peroxisomes that is dependent on Pex5p.[Pubmed]
|
|
| Pex11p plays a primary role in medium-chain fatty acid oxidation, a process that affects peroxisome number and size in Saccharomyces cerevisiae.[Pubmed]
|
|
| Oxygen and haem regulate the synthesis of peroxisomal proteins: catalase A, acyl-CoA oxidase and Pex1p in the yeast Saccharomyces cerevisiae; the regulation of these proteins by oxygen is not mediated by haem.[Pubmed]
|
|
| Analysis of the peroxisomal acyl-CoA oxidase gene product from Pichia pastoris and determination of its targeting signal.[Pubmed]
|
|
| Pex18p and Pex21p, a novel pair of related peroxins essential for peroxisomal targeting by the PTS2 pathway.[Pubmed]
|
|
| Regulation of peroxisomal fatty acyl-CoA oxidase in the yeast. Saccharomyces cerevisiae.[Pubmed]
|
|
| A complex containing two transcription factors regulates peroxisome proliferation and the coordinate induction of beta-oxidation enzymes in Saccharomyces cerevisiae.[Pubmed]
|
|
| Mutants of Saccharomyces cerevisiae with defects in acetate metabolism: isolation and characterization of Acn- mutants.[Pubmed]
|
|
| Identification of a yeast peroxisomal member of the family of AMP-binding proteins.[Pubmed]
|
|
| Purification, identification, and properties of a Saccharomyces cerevisiae oleate-activated upstream activating sequence-binding protein that is involved in the activation of POX1.[Pubmed]
|
|
| Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.[Pubmed]
|
|
| Maintenance of the peroxisomal compartment in glucose-repressed and anaerobically grown Saccharomyces cerevisiae cells.[Pubmed]
|
|
| Expression of the FOX1 gene of Saccharomyces cerevisiae is regulated by carbon source, but not by the known glucose repression genes.[Pubmed]
|
|
| PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes.[Pubmed]
|
|
| Three peroxisome protein packaging pathways suggested by selective permeabilization of yeast mutants defective in peroxisome biogenesis.[Pubmed]
|
|
| Peroxisomal disorders. Neurodevelopmental and biochemical aspects.[Pubmed]
|
|
| A negative regulating element controlling transcription of the gene encoding acyl-CoA oxidase in Saccharomyces cerevisiae.[Pubmed]
|
|
| Study on stereospecificity of enzyme reaction related to peroxisomal bile acid synthesis in rat liver.[Pubmed]
|
|
| Regulation of transcription of the gene coding for peroxisomal 3-oxoacyl-CoA thiolase of Saccharomyces cerevisiae.[Pubmed]
|
|
| Peroxisomes in Saccharomyces cerevisiae: immunofluorescence analysis and import of catalase A into isolated peroxisomes.[Pubmed]
|
|
| Participation of the peroxisomal beta-oxidation system in the chain-shortening of PCA16, a metabolite of the cytosine arabinoside prodrug, YNKO1, in rat liver.[Pubmed]
|
|
| Acyl-CoA synthetase and the peroxisomal enzymes of beta-oxidation in human liver. Quantitative analysis of their subcellular localization.[Pubmed]
|
|
| Regulation of peroxisomal proteins and organelle proliferation by multiple carbon sources in the methylotrophic yeast, Candida boidinii.[Pubmed]
|
|
| Acyl-CoA oxidase contains two targeting sequences each of which can mediate protein import into peroxisomes.[Pubmed]
|
|
| Import of the carboxy-terminal portion of acyl-CoA oxidase into peroxisomes of Candida tropicalis.[Pubmed]
|
|
| Efficient association of in vitro translation products with purified stable Candida tropicalis peroxisomes.[Pubmed]
|
|
| Peroxisomal acyl-coenzyme A oxidase multigene family of the yeast Candida tropicalis; nucleotide sequence of a third gene and its protein product.[Pubmed]
|
|
| Induction, identification, and cell-free translation of mRNAs coding for peroxisomal proteins in Candida tropicalis.[Pubmed]
|
|
| Two acyl-coenzyme A oxidases in peroxisomes of the yeast Candida tropicalis: primary structures deduced from genomic DNA sequence.[Pubmed]
|
|
| Cloning of cDNA coding for peroxisomal acyl-CoA oxidase from the yeast Candida tropicalis pK233.[Pubmed]
|
|
| Stereochemistry of dehydrogenation catalyzed by Acyl-CoA oxidase.[Pubmed]
|
|
| The effect of clofibrate on amphibian hepatic peroxisomes.[Pubmed]
|
|
| Effect of acyl-CoA oxidase activity on the accumulation of gamma-decalactone by the yeast Yarrowia lipolytica: a factorial approach.[Pubmed]
|
|
| A signal from inside the peroxisome initiates its division by promoting the remodeling of the peroxisomal membrane.[Pubmed]
|
|
| Observation of the Yarrowia lipolytica peroxisome-vacuole dynamics by fluorescence microscopy with a single filter set.[Pubmed]
|
|
| Peroxisome division in the yeast Yarrowia lipolytica is regulated by a signal from inside the peroxisome.[Pubmed]
|
|
| Acyl-CoA oxidase is imported as a heteropentameric, cofactor-containing complex into peroxisomes of Yarrowia lipolytica.[Pubmed]
|
|
| Cloning, sequencing, and characterization of five genes coding for acyl-CoA oxidase isozymes in the yeast Yarrowia lipolytica.[Pubmed]
|
|
| Pex20p of the yeast Yarrowia lipolytica is required for the oligomerization of thiolase in the cytosol and for its targeting to the peroxisome.[Pubmed]
|
|
| Effects of WY-14643 on peroxisomal enzyme activity and hormone secretion in immortalized human trophoblast cells.[Pubmed]
|
|
| Peroxisomal acyl-CoA-oxidase deficiency: two new cases.[Pubmed]
|
|
| PTS1-independent sorting of peroxisomal matrix proteins by Pex5p.[Pubmed]
|
|
| Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.[Pubmed]
|
|
| Peroxisomal branched chain fatty acid beta-oxidation pathway is upregulated in prostate cancer.[Pubmed]
|
|
| Peroxisomes, lipid metabolism, and peroxisomal disorders.[Pubmed]
|
|
| Carnitine prevents cyclic GMP-induced inhibition of peroxisomal enzyme activities.[Pubmed]
|
|
| Hyperpipecolic acidaemia: a diagnostic tool for peroxisomal disorders.[Pubmed]
|
|
| PPARalpha agonists clofibrate and gemfibrozil inhibit cell growth, down-regulate hCG and up-regulate progesterone secretions in immortalized human trophoblast cells.[Pubmed]
|
|
| Pex5p binding affinities for canonical and noncanonical PTS1 peptides.[Pubmed]
|
|
| Genetic-dependency of peroxisomal cell functions - emerging aspects.[Pubmed]
|
|
| Evidence for increased oxidative stress in peroxisomal D-bifunctional protein deficiency.[Pubmed]
|
|
| Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.[Pubmed]
|
|
| Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders.[Pubmed]
|
|
| Hitchhiking fads en route to peroxisomes.[Pubmed]
|
|
| Peroxisomal acyl CoA oxidase deficiency.[Pubmed]
|
|
| Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders.[Pubmed]
|
|
| Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis.[Pubmed]
|
|
| Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency.[Pubmed]
|
|
| Clinical consequences of defects in peroxisomal beta-oxidation.[Pubmed]
|
|
| Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.[Pubmed]
|
|
| Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.[Pubmed]
|
|
| Immunocytochemical investigation of catalase and peroxisomal lipid beta-oxidation enzymes in human hepatocellular tumors and liver cirrhosis.[Pubmed]
|
|
| Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.[Pubmed]
|
|
| Metabolic control of peroxisome abundance.[Pubmed]
|
|
| Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression.[Pubmed]
|
|
| Human long chain, very long chain and medium chain acyl-CoA dehydrogenases are specific for the S-enantiomer of 2- methylpentadecanoyl-CoA.[Pubmed]
|
|
| Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.[Pubmed]
|
|
| Incidence of peroxisomal disorders in Japan.[Pubmed]
|
|
| Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies.[Pubmed]
|
|
| Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients.[Pubmed]
|
|
| Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.[Pubmed]
|
|
| Mitochondrial short-chain acyl-CoA dehydrogenase of human liver and kidney can function as an oxidase.[Pubmed]
|
|
| Peroxisomal oxidation of the steroid side chain in bile acid formation.[Pubmed]
|
|
| Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders.[Pubmed]
|
|
| The activity and subcellular distribution of the peroxisomal enzyme acyl-CoA oxidase in human blood platelets.[Pubmed]
|
|
| Peroxisomal enzymes in normal and tumoral human breast.[Pubmed]
|
|
| Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation.[Pubmed]
|
|
| Peroxisomes in human colon carcinomas. A cytochemical and biochemical study.[Pubmed]
|
|
| Induction of beta-oxidation enzymes and microbody proliferation in Aspergillus nidulans.[Pubmed]
|
|
| The beta-oxidation system in catalase-free microbodies of the filamentous fungus Neurospora crassa. Purification of a multifunctional protein possessing 2-enoyl-CoA hydratase, L-3-hydroxyacyl-CoA dehydrogenase, and 3-hydroxyacyl-CoA epimerase activities.[Pubmed]
|
|
| How proteins get into microbodies (peroxisomes, glyoxysomes, glycosomes).[Pubmed]
|
|
| The regulation of peroxisomal enzyme systems of Tetrahymena pyriformis by fatty acid composition, glucose and oxygen in the medium.[Pubmed]
|
|
| RNA interference of peroxisome-related genes in C. elegans: a new model for human peroxisomal disorders.[Pubmed]
|
|
| Plasmalogen assembly: a key flavoenzyme.[Pubmed]
|
|
| Immunological localization and tissue distribution of alkyldihydroxyacetonephosphate synthase and deficiency of the enzyme in peroxisomal disorders.[Pubmed]
|
|
| Impaired membrane traffic in defective ether lipid biosynthesis.[Pubmed]
|
|
| Synthesis of plasmalogens in eye lens epithelial cells.[Pubmed]
|
|
| Peroxisomes and ether lipid biosynthesis in rat testis and epididymis.[Pubmed]
|
|
| Exclusive localization in peroxisomes of dihydroxyacetone phosphate acyltransferase and alkyl-dihydroxyacetone phosphate synthase in rat liver.[Pubmed]
|
|
| Kinetic studies of alkyl-dihydroxyacetone-phosphate (alkyl-glycerone-phosphate) synthase in peroxisomes of rat liver.[Pubmed]
|
|
| Topography of ether phospholipid biosynthesis.[Pubmed]
|
|
| Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts.[Pubmed]
|
|
| Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies.[Pubmed]
|
|
| Distribution of alkylglycerone-phosphate synthase in subcellular fractions of rat liver.[Pubmed]
|
|
| Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway.[Pubmed]
|
|
| Subcellular distribution of alkyl dihydroxyacetone phosphate synthase in rat liver.[Pubmed]
|
|
| Alkyl-dihydroxyacetonephosphate synthase.[Pubmed]
|
|
| Caenorhabditis elegans has a single pathway to target matrix proteins to peroxisomes.[Pubmed]
|
|
| Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.[Pubmed]
|
|
| Stability of alkyl-dihydroxyacetonephosphate synthase in human control and peroxisomal disorder fibroblasts.[Pubmed]
|
|
| Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities.[Pubmed]
|
|
| In vitro processing of the human alkyl-dihydroxyacetonephosphate synthase precursor.[Pubmed]
|
|
| Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes.[Pubmed]
|
|
| Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency.[Pubmed]
|
|
| Alkyl-dihydroxyacetonephosphate synthase.[Pubmed]
|
|
| Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation group.[Pubmed]
|
|
| Ether lipid synthesis: purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver.[Pubmed]
|
|
| Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation study.[Pubmed]
|
|
| Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls.[Pubmed]
|
|
| Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins.[Pubmed]
|
|
| Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.[Pubmed]
|
|
| Alkyl dihydroxyacetone phosphate synthase in glycosomes of Trypanosoma brucei.[Pubmed]
|
|
| Control of oxalate formation from L-hydroxyproline in liver mitochondria.[Pubmed]
|
|
| Mitochondrial targeting signal-induced conformational change and repression of the peroxisomal targeting signal of the precursor for rat liver serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Flux of the L-serine metabolism in rabbit, human, and dog livers. Substantial contributions of both mitochondrial and peroxisomal serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Fidelity of translation initiation of mRNA for the precursor of rat mitochondrial serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Immunocytochemical demonstration of serine: pyruvate amino-transferase in peroxisomes and mitochondria of rat kidney.[Pubmed]
|
|
| Fine localization of serine:pyruvate aminotransferase in rat hepatocytes revealed by a post-embedding immunocytochemical technique.[Pubmed]
|
|
| Peroxisomal localization of serine:pyruvate aminotransferase in human liver.[Pubmed]
|
|
| ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 case.[Pubmed]
|
|
| Immunocytochemical localization of serine: pyruvate aminotransferase in peroxisomes of the human liver parenchymal cells.[Pubmed]
|
|
| Identification of photorespiratory glutamate:glyoxylate aminotransferase (GGAT) gene in Arabidopsis.[Pubmed]
|
|
| Proteomic analysis of leaf peroxisomal proteins in greening cotyledons of Arabidopsis thaliana.[Pubmed]
|
|
| Peroxisomal alanine : glyoxylate aminotransferase (AGT1) is a photorespiratory enzyme with multiple substrates in Arabidopsis thaliana.[Pubmed]
|
|
| Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.[Pubmed]
|
|
| Peroxisomal and mitochondrial targeting of serine:pyruvate/alanine:glyoxylate aminotransferase in rat liver.[Pubmed]
|
|
| Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the feline gene.[Pubmed]
|
|
| Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the marmoset and rabbit genes.[Pubmed]
|
|
| Dimethylarginine:pyruvate aminotransferase in rats. Purification, properties, and identity with alanine:glyoxylate aminotransferase 2.[Pubmed]
|
|
| Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon.[Pubmed]
|
|
| Alanine: glyoxylate aminotransferase 1 is present in the peroxisomes of guinea pig kidney.[Pubmed]
|
|
| The effect of vitamin B6 deficiency on alanine: glyoxylate aminotransferase isoenzymes in rat liver.[Pubmed]
|
|
| Purification and properties of peroxisomal pyruvate (glyoxylate) aminotransferase from rat liver.[Pubmed]
|
|
| Subcellular distribution of pyruvate (glyoxylate) aminotransferases in rat liver.[Pubmed]
|
|
| The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis.[Pubmed]
|
|
| Peroxisomal import of human alanine:glyoxylate aminotransferase requires ancillary targeting information remote from its C terminus.[Pubmed]
|
|
| Molecular basis for the dual mitochondrial and cytosolic localization of alanine:glyoxylate aminotransferase in amphibian liver cells.[Pubmed]
|
|
| Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation.[Pubmed]
|
|
| Reactions of human liver peroxisomal alanine:glyoxylate aminotransferase with beta-chloro-L-alanine and L-cysteine: spectroscopic and kinetic analysis.[Pubmed]
|
|
| Construction, purification and characterization of untagged human liver alanine-glyoxylate aminotransferase expressed in Escherichia coli.[Pubmed]
|
|
| Characterization of peroxisomal targeting signals on alanine: glyoxylate aminotransferase.[Pubmed]
|
|
| Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways.[Pubmed]
|
|
| High incidence of hyperoxaluria in generalized peroxisomal disorders.[Pubmed]
|
|
| Cellular transfection to deliver alanine-glyoxylate aminotransferase to hepatocytes: a rational gene therapy for primary hyperoxaluria-1 (PH-1).[Pubmed]
|
|
| Molecular aetiology of primary hyperoxaluria type 1.[Pubmed]
|
|
| Diet and the frequency of the alanine:glyoxylate aminotransferase Pro11Leu polymorphism in different human populations.[Pubmed]
|
|
| Glycolate and glyoxylate metabolism in HepG2 cells.[Pubmed]
|
|
| Molecular aetiology of primary hyperoxaluria and its implications for clinical management.[Pubmed]
|
|
| Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1.[Pubmed]
|
|
| Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro.[Pubmed]
|
|
| Alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting in human hereditary kidney stone disease.[Pubmed]
|
|
| Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations.[Pubmed]
|
|
| Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1.[Pubmed]
|
|
| Evolution of alanine:glyoxylate aminotransferase intracellular targeting: structural and functional analysis of the guinea pig gene.[Pubmed]
|
|
| A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.[Pubmed]
|
|
| Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease.[Pubmed]
|
|
| Context dependency of the PTS1 motif in human alanine: glyoxylate aminotransferase 1.[Pubmed]
|
|
| Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine: glyoxylate aminotransferase.[Pubmed]
|
|
| Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.[Pubmed]
|
|
| Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.[Pubmed]
|
|
| Molecular basis of the variable mitochondrial and peroxisomal localisation of alanine-glyoxylate aminotransferase.[Pubmed]
|
|
| Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1.[Pubmed]
|
|
| Immunocytochemical localization of peroxisomal proteins in human liver and kidney.[Pubmed]
|
|
| Advances in the enzymology and molecular genetics of primary hyperoxaluria type 1. Prospects for gene therapy.[Pubmed]
|
|
| A new type of peroxisomal disorder with variable expression in liver and fibroblasts.[Pubmed]
|
|
| Heterogeneity of peroxisomes in human hepatoblastoma cell line HepG2. Evidence of distinct subpopulations.[Pubmed]
|
|
| Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.[Pubmed]
|
|
| Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.[Pubmed]
|
|
| Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation.[Pubmed]
|
|
| Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.[Pubmed]
|
|
| Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity.[Pubmed]
|
|
| Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.[Pubmed]
|
|
| Structure-function relationships in the peroxisome: implications for human disease.[Pubmed]
|
|
| An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.[Pubmed]
|
|
| Molecular and clinical heterogeneity in primary hyperoxaluria type 1.[Pubmed]
|
|
| Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian species.[Pubmed]
|
|
| Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.[Pubmed]
|
|
| Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.[Pubmed]
|
|
| Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.[Pubmed]
|
|
| Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.[Pubmed]
|
|
| Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.[Pubmed]
|
|
| Subcellular distribution, and physical and immunological properties of hepatic alanine: glyoxylate aminotransferase isoenzymes in different mammalian species.[Pubmed]
|
|
| Subcellular localization of superoxide dismutase in rat liver.[Pubmed]
|
|
| Mitochondria and peroxisomes from the cellular slime mould Dictyostelium discoideum. Isolation techniques and urate oxidase association with peroxisomes.[Pubmed]
|
|
| Intracellular positioning of isoforms explains an unusually large adenylate kinase gene family in the parasite Trypanosoma brucei.[Pubmed]
|
|
| The occurrence of glycosomes (microbodies) in the promastigote stage of four major Leishmania species.[Pubmed]
|
|
| Subcellular localization and physiological role of alpha-methylacyl-CoA racemase.[Pubmed]
|
|
| Mitochondrial and peroxisomal targeting of 2-methylacyl-CoA racemase in humans.[Pubmed]
|
|
| Purification and characterization of an alpha-methylacyl-CoA racemase from human liver.[Pubmed]
|
|
| Peroxisomal disorders affecting phytanic acid alpha-oxidation: a review.[Pubmed]
|
|
| Expression profiling identifies a novel alpha-methylacyl-CoA racemase exon with fumarate hydratase homology.[Pubmed]
|
|
| Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy.[Pubmed]
|
|
| Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.[Pubmed]
|
|
| Peroxisomal ATP import is essential for seedling development in Arabidopsis thaliana.[Pubmed]
|
|
| Proteomic identification and characterization of a novel peroxisomal adenine nucleotide transporter supplying ATP for fatty acid beta-oxidation in soybean and Arabidopsis.[Pubmed]
|
|
| The yeast peroxisomal adenine nucleotide transporter: characterization of two transport modes and involvement in DeltapH formation across peroxisomal membranes.[Pubmed]
|
|
| Identification of human PMP34 as a peroxisomal ATP transporter.[Pubmed]
|
|
| The peroxisomal transporter gene ANT1 is regulated by a deviant oleate response element (ORE): characterization of the signal for fatty acid induction.[Pubmed]
|
|
| Identification and functional reconstitution of the yeast peroxisomal adenine nucleotide transporter.[Pubmed]
|
|
| Developmental analysis of a putative ATP/ADP carrier protein localized on glyoxysomal membranes during the peroxisome transition in pumpkin cotyledons.[Pubmed]
|
|
| Identification of a peroxisomal ATP carrier required for medium-chain fatty acid beta-oxidation and normal peroxisome proliferation in Saccharomyces cerevisiae.[Pubmed]
|
|
| Peroxisomal membrane protein Pmp47 is essential in the metabolism of middle-chain fatty acid in yeast peroxisomes and Is associated with peroxisome proliferation.[Pubmed]
|
|
| Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34.[Pubmed]
|
|
| Identification and characterization of human PMP34, a protein closely related to the peroxisomal integral membrane protein PMP47 of Candida boidinii.[Pubmed]
|
|
| Multiple distinct targeting signals in integral peroxisomal membrane proteins.[Pubmed]
|
|
| MONODEHYROASCORBATE REDUCTASE4 is required for seed storage oil hydrolysis and postgerminative growth in Arabidopsis.[Pubmed]
|
|
| Arabidopsis peroxin 16 trafficks through the ER and an intermediate compartment to pre-existing peroxisomes via overlapping molecular targeting signals.[Pubmed]
|
|
| Senescence-specific regulation of catalases in Arabidopsis thaliana (L.) Heynh.[Pubmed]
|
|
| The Arabidopsis ascorbate peroxidase 3 is a peroxisomal membrane-bound antioxidant enzyme and is dispensable for Arabidopsis growth and development.[Pubmed]
|
|
| Arabidopsis peroxisomes possess functionally redundant membrane and matrix isoforms of monodehydroascorbate reductase.[Pubmed]
|
|
| Arabidopsis thaliana plants overexpressing thylakoidal ascorbate peroxidase show increased resistance to Paraquat-induced photooxidative stress and to nitric oxide-induced cell death.[Pubmed]
|
|
| Characterization of the targeting signal of the Arabidopsis 22-kD integral peroxisomal membrane protein.[Pubmed]
|
|
| Peroxisomal ascorbate peroxidase resides within a subdomain of rough endoplasmic reticulum in wild-type Arabidopsis cells.[Pubmed]
|
|
| Cloning of peroxisomal ascorbate peroxidase gene from barley and enhanced thermotolerance by overexpressing in Arabidopsis thaliana.[Pubmed]
|
|
| How are peroxisomes formed? The role of the endoplasmic reticulum and peroxins.[Pubmed]
|
|
| Pumpkin peroxisomal ascorbate peroxidase is localized on peroxisomal membranes and unknown membranous structures.[Pubmed]
|
|
| Are diverse signalling pathways integrated in the regulation of arabidopsis antioxidant defence gene expression in response to excess excitation energy?[Pubmed]
|
|
| Overexpression of an Arabidopsis peroxisomal ascorbate peroxidase gene in tobacco increases protection against oxidative stress.[Pubmed]
|
|
| ATG genes involved in non-selective autophagy are conserved from yeast to man, but the selective Cvt and pexophagy pathways also require organism-specific genes.[Pubmed]
|
|
| Autophagy-related pathways and specific role of sterol glucoside in yeasts.[Pubmed]
|
|
| Atg26 is not involved in autophagy-related pathways in Saccharomyces cerevisiae.[Pubmed]
|
|
| Topogenesis of peroxisomal proteins does not require a functional cytoplasm-to-vacuole transport.[Pubmed]
|
|
| Trs85 (Gsg1), a component of the TRAPP complexes, is required for the organization of the preautophagosomal structure during selective autophagy via the Cvt pathway.[Pubmed]
|
|
| Autophagy in yeast: a review of the molecular machinery.[Pubmed]
|
|
| Cvt18/Gsa12 is required for cytoplasm-to-vacuole transport, pexophagy, and autophagy in Saccharomyces cerevisiae and Pichia pastoris.[Pubmed]
|
|
| Apg2 is a novel protein required for the cytoplasm to vacuole targeting, autophagy, and pexophagy pathways.[Pubmed]
|
|
| Cvt9/Gsa9 functions in sequestering selective cytosolic cargo destined for the vacuole.[Pubmed]
|
|
| Structure and function of the yeast vacuole and its role in autophagy.[Pubmed]
|
|
| The reversible modification regulates the membrane-binding state of Apg8/Aut7 essential for autophagy and the cytoplasm to vacuole targeting pathway.[Pubmed]
|
|
| Peroxisome degradation in Saccharomyces cerevisiae is dependent on machinery of macroautophagy and the Cvt pathway.[Pubmed]
|
|
| Apg7p/Cvt2p is required for the cytoplasm-to-vacuole targeting, macroautophagy, and peroxisome degradation pathways.[Pubmed]
|
|
| Quantification and regulation of the subcellular distribution of bile acid coenzyme A:amino acid N-acyltransferase activity in rat liver.[Pubmed]
|
|
| Human and rat bile acid-CoA:amino acid N-acyltransferase are liver-specific peroxisomal enzymes: implications for intracellular bile salt transport.[Pubmed]
|
|
| Subcellular organization of bile acid amidation in human liver: a key issue in regulating the biosynthesis of bile salts.[Pubmed]
|
|
| Plant catalase is imported into peroxisomes by Pex5p but is distinct from typical PTS1 import.[Pubmed]
|
|
| Conditional oxidative stress responses in the Arabidopsis photorespiratory mutant cat2 demonstrate that redox state is a key modulator of daylength-dependent gene expression, and define photoperiod as a crucial factor in the regulation of H2O2-induced cell death.[Pubmed]
|
|
| Significance of plant sulfite oxidase.[Pubmed]
|
|
| Identification and characterization of a stress-inducible and a constitutive small heat-shock protein targeted to the matrix of plant peroxisomes.[Pubmed]
|
|
| Plant sulfite oxidase as novel producer of H2O2: combination of enzyme catalysis with a subsequent non-enzymatic reaction step.[Pubmed]
|
|
| Catalase deficiency drastically affects gene expression induced by high light in Arabidopsis thaliana.[Pubmed]
|
|
| Identification of peroxisomal targeting signal of pumpkin catalase and the binding analysis with PTS1 receptor.[Pubmed]
|
|
| Distribution and characterization of peroxisomes in Arabidopsis by visualization with GFP: dynamic morphology and actin-dependent movement.[Pubmed]
|
|
| Hydrogen peroxide homeostasis: activation of plant catalase by calcium/calmodulin.[Pubmed]
|
|
| Integrated temporal regulation of the photorespiratory pathway. Circadian regulation of two Arabidopsis genes encoding serine hydroxymethyltransferase.[Pubmed]
|
|
| Psychosine-induced alterations in peroxisomes of twitcher mouse liver.[Pubmed]
|
|
| Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration.[Pubmed]
|
|
| Characterization and regulation of monocarboxylate cotransporters Slc16a7 and Slc16a3 in preimplantation mouse embryos.[Pubmed]
|
|
| Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy.[Pubmed]
|
|
| Short- and medium-chain carnitine acyltransferases and acyl-CoA thioesterases in mouse provide complementary systems for transport of beta-oxidation products out of peroxisomes.[Pubmed]
|
|
| Peroxisomes in human and mouse testis: differential expression of peroxisomal proteins in germ cells and distinct somatic cell types of the testis.[Pubmed]
|
|
| Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain.[Pubmed]
|
|
| Relationship between reactive oxygen species and heme metabolism during the differentiation of Neuro2a cells.[Pubmed]
|
|
| Immunolocalization of hypochlorite-induced, catalase-bound free radical formation in mouse hepatocytes.[Pubmed]
|
|
| Cardiac overexpression of antioxidant catalase attenuates aging-induced cardiomyocyte relaxation dysfunction.[Pubmed]
|
|
| Human Mpv17-like protein is localized in peroxisomes and regulates expression of antioxidant enzymes.[Pubmed]
|
|
| Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system.[Pubmed]
|
|
| Functional domains and dynamic assembly of the peroxin Pex14p, the entry site of matrix proteins.[Pubmed]
|
|
| OCTN3 is a mammalian peroxisomal membrane carnitine transporter.[Pubmed]
|
|
| Extension of murine life span by overexpression of catalase targeted to mitochondria.[Pubmed]
|
|
| Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis.[Pubmed]
|
|
| Catalase transgenic mice: characterization and sensitivity to oxidative stress.[Pubmed]
|
|
| Involvement of the endoplasmic reticulum in peroxisome formation.[Pubmed]
|
|
| Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.[Pubmed]
|
|
| Cardiac-specific overexpression of catalase rescues ventricular myocytes from ethanol-induced cardiac contractile defect.[Pubmed]
|
|
| Molecular immunolabeling with recombinant single-chain variable fragment (scFv) antibodies designed with metal-binding domains.[Pubmed]
|
|
| Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase.[Pubmed]
|
|
| Suppressive effect of curcumin on trichloroethylene-induced oxidative stress.[Pubmed]
|
|
| Levels of DNA damage are unaltered in mice overexpressing human catalase in nuclei.[Pubmed]
|
|
| Cellular and subcellular localization of catalase in the heart of transgenic mice.[Pubmed]
|
|
| Induction of the peroxisomal glycerolipid-synthesizing enzymes during differentiation of 3T3-L1 adipocytes. Role in triacylglycerol synthesis.[Pubmed]
|
|
| Effects of vitamin A deficiency on selected xenobiotic-metabolizing enzymes and defenses against oxidative stress in mouse liver.[Pubmed]
|
|
| Hepatic histopathology of a vitamin A overdose in mouse liver.[Pubmed]
|
|
| Influence of dietary fat on the effect of endotoxin on murine hepatic peroxisomes.[Pubmed]
|
|
| Elevated catalase activity in red and white muscles of MyoD gene-inactivated mice.[Pubmed]
|
|
| Hepatotumorigenicity and peroxisome proliferation induced by the hypolipidemic CI-924 in a two-year study in male and female B6C3F1 mice.[Pubmed]
|
|
| Modification of lipoperoxidative effects of dichloroacetate and trichloroacetate is associated with peroxisome proliferation.[Pubmed]
|
|
| The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species.[Pubmed]
|
|
| Effects of acetylsalicylic acid on parameters related to peroxisome proliferation in mouse liver.[Pubmed]
|
|
| X-linked dominant ichthyosis with peroxisomal deficiency. An ultrastructural and ultracytochemical study of the Conradi-Hünermann syndrome and its murine homologue, the bare patches mouse.[Pubmed]
|
|
| Comparison of the potencies of (+)- and (-)-2-ethylhexanoic acid in causing peroxisome proliferation and related biological effects in mouse liver.[Pubmed]
|
|
| Effects of clofibrate withdrawal on peroxisomes in mouse hepatocytes.[Pubmed]
|
|
| Peroxisomes in liver, kidney and duodenum of nude mice bearing xenografts of human pancreatic adenocarcinomas.[Pubmed]
|
|
| Peroxisomes and reactive oxygen species, a lasting challenge.[Pubmed]
|
|
| Integrated fluorescence and transmission electron microscopy.[Pubmed]
|
|
| Kinetics of hydrogen peroxide elimination by astrocytes and C6 glioma cells analysis based on a mathematical model.[Pubmed]
|
|
| Purification of a crude mitochondrial fraction by density-gradient centrifugation.[Pubmed]
|
|
| Role of peroxisomes in the swift increase in alcohol metabolism.[Pubmed]
|
|
| Loss of peroxisomes causes oxygen insensitivity of the histochemical assay of glucose-6-phosphate dehydrogenase activity to detect cancer cells.[Pubmed]
|
|
| Treatment of surgically induced acute liver failure by transplantation of HNF4-overexpressing embryonic stem cells.[Pubmed]
|
|
| The behavior of peroxisomes in vitro: mammalian peroxisomes are osmotically sensitive particles.[Pubmed]
|
|
| Detailed analytical subcellular fractionation of non-pregnant porcine corpus luteum reveals peroxisomes of normal size and significant UDP-glucuronosyltransferase activity in the high-speed supernatant.[Pubmed]
|
|
| Modified peroxisomes in primary hepatocyte cultures.[Pubmed]
|
|
| Regulation of peroxisomal genes by DHEA and vitamin D.[Pubmed]
|
|
| Effects of dibromoacetonitrile on rats following 13-week drinking water exposure.[Pubmed]
|
|
| A simple method of rat renal brush border membrane preparation using polyethylene glycol precipitation.[Pubmed]
|
|
| Expression of catalase mRNA and protein in adult rat brain: detection by nonradioactive in situ hybridization with signal amplification by catalyzed reporter deposition (ISH-CARD) and immunohistochemistry (IHC)/immunofluorescence (IF).[Pubmed]
|
|
| Characterization of the expression of inducible nitric oxide synthase in rat and human liver during hemorrhagic shock.[Pubmed]
|
|
| Hepatocyte polarity and the peroxisomal compartment: a comparative study.[Pubmed]
|
|
| Damage to subcellular structures evoked by lipid peroxidation.[Pubmed]
|
|
| A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import.[Pubmed]
|
|
| A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.[Pubmed]
|
|
| Endogenous and endobiotic induced reactive oxygen species formation by isolated hepatocytes.[Pubmed]
|
|
| Catalase contents in cells determine sensitivity to the apoptosis inducer gallic acid.[Pubmed]
|
|
| Localization of cytosolic NADP-dependent isocitrate dehydrogenase in the peroxisomes of rat liver cells: biochemical and immunocytochemical studies.[Pubmed]
|
|
| Catalase immunocytochemistry allows automatic detection of lung type II alveolar cells.[Pubmed]
|
|
| Aging lowers steady-state antioxidant enzyme and stress protein expression in primary hepatocytes.[Pubmed]
|
|
| Peroxisomal proteins in rat gametes.[Pubmed]
|
|
| The role of 15-lipoxygenase in disruption of the peroxisomal membrane and in programmed degradation of peroxisomes in normal rat liver.[Pubmed]
|
|
| Oxidative stress, microsomal and peroxisomal fatty acid oxidation in the liver of rats treated with acetone.[Pubmed]
|
|
| Identification of the pathway of alpha-oxidation of cerebronic acid in peroxisomes.[Pubmed]
|
|
| High dietary levels of a conjugated linoleic acid mixture alter hepatic glycerophospholipid class profile and cholesterol-carrying serum lipoproteins of rats.[Pubmed]
|
|
| Isolation and biochemical characterization of peroxisomes from cultured rat glial cells.[Pubmed]
|
|
| Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant.[Pubmed]
|
|
| Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures.[Pubmed]
|
|
| Endotoxin induces structure-function alterations of rat liver peroxisomes: Kupffer cells released factors as possible modulators.[Pubmed]
|
|
| Current cytochemical techniques for the investigation of peroxisomes. A review.[Pubmed]
|
|
| Overexpression of human catalase inhibits proliferation and promotes apoptosis in vascular smooth muscle cells.[Pubmed]
|
|
| Differential binding of proteins to peroxisomes in rat hepatoma cells: unique association of enzymes involved in isoprenoid metabolism.[Pubmed]
|
|
| Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.[Pubmed]
|
|
| Maturation of the liver-specific peroxisome versus laminin, collagen IV and integrin expression.[Pubmed]
|
|
| 3-Hydroxy-3-methylglutaryl coenzyme A lyase: targeting and processing in peroxisomes and mitochondria.[Pubmed]
|
|
| Peroxisomes are involved in the swift increase in alcohol metabolism.[Pubmed]
|
|
| Some characteristics of peroxisomes in the slime mold, Dictyostelium discoideum.[Pubmed]
|
|
| The involvement of the plasma membrane in the development of Dictyostelium discoideum. I. Purification of the plasma membrane.[Pubmed]
|
|
| Dibutylphthalate and Tween 80 alter ultrastructure in Candida albicans: implications for peroxisome proliferation.[Pubmed]
|
|
| Catalase modifies yeast Saccharomyces cerevisiae response towards S-nitrosoglutathione-induced stress.[Pubmed]
|
|
| Sodium nitroprusside induces mild oxidative stress in Saccharomyces cerevisiae.[Pubmed]
|
|
| Catalases protect cellular proteins from oxidative modification in Saccharomyces cerevisiae.[Pubmed]
|
|
| Dual targeting of yeast catalase A to peroxisomes and mitochondria.[Pubmed]
|
|
| Overexpression of peroxisomal malate dehydrogenase MDH3 gene enhances cell death on H2O2 stress in the ald5 mutant of Saccharomyces cerevisiae.[Pubmed]
|
|
| Effect of yeast CTA1 gene expression on response of tobacco plants to tobacco mosaic virus infection.[Pubmed]
|
|
| Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy.[Pubmed]
|
|
| Synthesis of polyhydroxyalkanoate in the peroxisome of Saccharomyces cerevisiae by using intermediates of fatty acid beta-oxidation.[Pubmed]
|
|
| A mutation in the yeast mitochondrial ribosomal protein Rml2p is associated with a defect in catalase gene expression.[Pubmed]
|
|
| Overproduction of Pex5p stimulates import of alcohol oxidase and dihydroxyacetone synthase in a Hansenula polymorpha Pex14 null mutant.[Pubmed]
|
|
| Targeting and subcellular localization of Toxoplasma gondii catalase. Identification of peroxisomes in an apicomplexan parasite.[Pubmed]
|
|
| Identification and characterization of the human orthologue of yeast Pex14p.[Pubmed]
|
|
| Deviant Pex3p levels affect normal peroxisome formation in Hansenula polymorpha: a sharp increase of the protein level induces the proliferation of numerous, small protein-import competent peroxisomes.[Pubmed]
|
|
| The Hansenula polymorpha PEX14 gene encodes a novel peroxisomal membrane protein essential for peroxisome biogenesis.[Pubmed]
|
|
| A branched pathway for peroxisomal protein import: S. cerevisiae ghosts and an intraperoxisomal PTS2 receptor.[Pubmed]
|
|
| Localization and targeting of isocitrate lyases in Saccharomyces cerevisiae.[Pubmed]
|
|
| Identification of Pex13p a peroxisomal membrane receptor for the PTS1 recognition factor.[Pubmed]
|
|
| The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import PTS1-containing proteins.[Pubmed]
|
|
| Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence.[Pubmed]
|
|
| Pip2p: a transcriptional regulator of peroxisome proliferation in the yeast Saccharomyces cerevisiae.[Pubmed]
|
|
| A C-terminal region of the Saccharomyces cerevisiae transcription factor ADR1 plays an important role in the regulation of peroxisome proliferation by fatty acids.[Pubmed]
|
|
| Expression of genes encoding peroxisomal proteins in Saccharomyces cerevisiae is regulated by different circuits of transcriptional control.[Pubmed]
|
|
| Novel peroxisome clustering mutants and peroxisome biogenesis mutants of Saccharomyces cerevisiae.[Pubmed]
|
|
| A Saccharomyces cerevisiae upstream activating sequence mediates induction of peroxisome proliferation by fatty acids.[Pubmed]
|
|
| Two independent peroxisomal targeting signals in catalase A of Saccharomyces cerevisiae.[Pubmed]
|
|
| Human catalase is imported and assembled in peroxisomes of Saccharomyces cerevisiae.[Pubmed]
|
|
| Inhibitory action of palmitic acid on the growth of Saccharomyces cerevisiae.[Pubmed]
|
|
| Isolation of peroxisome assembly mutants from Saccharomyces cerevisiae with different morphologies using a novel positive selection procedure.[Pubmed]
|
|
| Peroxisome biogenesis in Saccharomyces cerevisiae.[Pubmed]
|
|
| Control of peroxisome proliferation in Saccharomyces cerevisiae by ADR1, SNF1 (CAT1, CCR1) and SNF4 (CAT3).[Pubmed]
|
|
| Cu,Zn superoxide dismutase is a peroxisomal enzyme in human fibroblasts and hepatoma cells.[Pubmed]
|
|
| Vector-mediated overexpression of catalase A in the yeast Saccharomyces cerevisiae induces inclusion body formation.[Pubmed]
|
|
| The Saccharomyces cerevisiae ADR1 gene is a positive regulator of transcription of genes encoding peroxisomal proteins.[Pubmed]
|
|
| Association of glyoxylate and beta-oxidation enzymes with peroxisomes of Saccharomyces cerevisiae.[Pubmed]
|
|
| Fate of highly expressed proteins destined to peroxisomes in Saccharomyces cerevisiae.[Pubmed]
|
|
| Functional complementation of catalase-defective peroxisomes in a methylotrophic yeast by import of the catalase A from Saccharomyces cerevisiae.[Pubmed]
|
|
| Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.[Pubmed]
|
|
| Functional expression and peroxisomal targeting of rat urate oxidase in monkey kidney cells.[Pubmed]
|
|
| Ectopic expression of catalase in Drosophila mitochondria increases stress resistance but not longevity.[Pubmed]
|
|
| Inducible expression and cellular localization of insulin-degrading enzyme in a stably transfected cell line.[Pubmed]
|
|
| Endosomal proteolysis of insulin by an acidic thiol metalloprotease unrelated to insulin degrading enzyme.[Pubmed]
|
|
| Cytochemical localization of a D-amino acid oxidizing enzyme in peroxisomes of Drosophila melanogaster.[Pubmed]
|
|
| Peroxisomes in wild-type and rosy mutant Drosophila melanogaster.[Pubmed]
|
|
| Studies by the National Toxicology Program on di(2-ethylhexyl)phthalate.[Pubmed]
|
|
| Effect of catalase-specific inhibitor 3-amino-1,2,4-triazole on yeast peroxisomal catalase in vivo.[Pubmed]
|
|
| Peroxisomal catalase in the methylotrophic yeast Candida boidinii: transport efficiency and metabolic significance.[Pubmed]
|
|
| Isolation, purification, and characterization of catalase from the methylotrophic yeast Pichia pastoris.[Pubmed]
|
|
| Antioxidant system within yeast peroxisome. Biochemical and physiological characterization of CbPmp20 in the methylotrophic yeast Candida boidinii.[Pubmed]
|
|
| Detection and substrate selectivity of new microbial D-amino acid oxidases.[Pubmed]
|
|
| Evaluation of peroxisomal heme in yeast.[Pubmed]
|
|
| The absence of Pmp47, a putative yeast peroxisomal transporter, causes a defect in transport and folding of a specific matrix enzyme.[Pubmed]
|
|
| Induction of peroxisome proliferation and increase of catalase activity in yeast, Candida albicans, by cadmium.[Pubmed]
|
|
| Beta-oxidation of butyrate, the short-chain-length fatty acid, occurs in peroxisomes in the yeast Candida tropicalis.[Pubmed]
|
|
| Development of multipurpose peroxisomes in Candida boidinii grown in oleic acid-methanol limited continuous cultures.[Pubmed]
|
|
| Effect of increasing methanol concentrations on physiology and cytology of Candida boidinii.[Pubmed]
|
|
| Evidence of peroxisomes and peroxisomal enzyme activities in the oleaginous yeast Apiotrichum curvatum.[Pubmed]
|
|
| Peroxisomal assembly: membrane proliferation precedes the induction of the abundant matrix proteins in the methylotrophic yeast Candida boidinii.[Pubmed]
|
|
| Lipid metabolism and cell composition of the oleaginous yeast Apiotrichum curvatum grown at different carbon to nitrogen ratios.[Pubmed]
|
|
| Proliferation and metabolic significance of peroxisomes in Candida boidinii during growth on D-alanine or oleic acid as the sole carbon source.[Pubmed]
|
|
| Enzyme activities in oleaginous yeasts accumulating and utilizing exogenous or endogenous lipids.[Pubmed]
|
|
| Production of Formaldehyde by Detergent-Treated Cells of a Methanol Yeast, Candida boidinii S2 Mutant Strain AOU-1.[Pubmed]
|
|
| Isolation of cDNA clones coding for peroxisomal proteins of Candida tropicalis: identification and sequence of a clone for catalase.[Pubmed]
|
|
| A proton-translocating adenosine triphosphatase is associated with the peroxisomal membrane of yeasts.[Pubmed]
|
|
| Properties of catalase purified from a methanol-grown yeast, Kloeckera sp. 2201.[Pubmed]
|
|
| Dihydroxyacetone synthase is an abundant constituent of the methanol-induced peroxisome of Candida boidinii.[Pubmed]
|
|
| Peroxisomal beta-oxidation system of Candida tropicalis. Purification of a multifunctional protein possessing enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase and 3-hydroxyacyl-CoA epimerase activities.[Pubmed]
|
|
| Biogenesis and metabolic significance of microbodies in urate-utilizing yeasts.[Pubmed]
|
|
| Significance of yeast peroxisomes in the metabolism of choline and ethanolamine.[Pubmed]
|
|
| Cell-free translation and regulation of Candida tropicalis catalase messenger RNA.[Pubmed]
|
|
| Properties of catalase purified from whole cells and peroxisomes of n-alkane-grown Candida tropicalis.[Pubmed]
|
|
| Peroxisomes of alkane-grown yeast: fundamental and practical aspects.[Pubmed]
|
|
| Development of amine oxidase-containing peroxisomes in yeasts during growth on glucose in the presence of methylamine as the sole source of nitrogen.[Pubmed]
|
|
| Localization of carnitine acetyltransferase in peroxisomes and in mitochondria of n-alkane-grown Candida tropicalis.[Pubmed]
|
|
| The effects of miconazole on the ultrastructure of Candida albicans.[Pubmed]
|
|
| Alcohol oxidase and catalase in peroxisomes of methanol-grown Candida boidinii.[Pubmed]
|
|
| Enzyme cytochemistry of Candida albicans.[Pubmed]
|
|
| Peroxisomal localization of D-aspartate oxidase and development of peroxisomes in the yeast Cryptococcus humicolus UJ1 grown on D-aspartate.[Pubmed]
|
|
| Lack of peroxisomal catalase causes a progeric phenotype in Caenorhabditis elegans.[Pubmed]
|
|
| Peroxisomes of the nematode Caenorhabditis elegans: distribution and morphological characteristics.[Pubmed]
|
|
| Immunological detection of alkaline-diaminobenzidine-negativeperoxisomes of the nematode Caenorhabditis elegans purification and unique pH optima of peroxisomal catalase.[Pubmed]
|
|
| Peroxisome biogenesis occurs in late dorsal-anterior structures in the development of Xenopus laevis.[Pubmed]
|
|
| Peroxisomes in pigment epithelium and Müller cells of amphibian retina possess D-amino acid oxidase as well as catalase.[Pubmed]
|
|
| Development of peroxisomes in amphibians. II. Cytochemical and biochemical studies on the liver, kidney, and pancreas.[Pubmed]
|
|
| Methods of plate pexophagy monitoring and positive selection for ATG gene cloning in yeasts.[Pubmed]
|
|
| The Yarrowia lipolytica gene PAY2 encodes a 42-kDa peroxisomal integral membrane protein essential for matrix protein import and peroxisome enlargement but not for peroxisome membrane proliferation.[Pubmed]
|
|
| Renal cell carcinoma and oxidative stress: The lack of peroxisomes.[Pubmed]
|
|
| Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.[Pubmed]
|
|
| Progeric effects of catalase inactivation in human cells.[Pubmed]
|
|
| Restoration of peroxisomal catalase import in a model of human cellular aging.[Pubmed]
|
|
| Drug delivery to peroxisomes: employing unique trafficking mechanisms to target protein therapeutics.[Pubmed]
|
|
| A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C.[Pubmed]
|
|
| Peroxisomes and aging.[Pubmed]
|
|
| Hypocatalasemic fibroblasts accumulate hydrogen peroxide and display age-associated pathologies.[Pubmed]
|
|
| Use of the land snail Helix aspersa as sentinel organism for monitoring ecotoxicologic effects of urban pollution: an integrated approach.[Pubmed]
|
|
| Very-long-chain fatty acids activate lysosomal hydrolases in neonatal human skin tissue.[Pubmed]
|
|
| Catalase regulates cell growth in HL60 human promyelocytic cells: evidence for growth regulation by H(2)O(2).[Pubmed]
|
|
| Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patients.[Pubmed]
|
|
| A metabolic model describing the H2O2 elimination by mammalian cells including H2O2 permeation through cytoplasmic and peroxisomal membranes: comparison with experimental data.[Pubmed]
|
|
| Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism.[Pubmed]
|
|
| Reinvestigation of trihydroxycholestanoic acidemia reveals a peroxisome biogenesis disorder.[Pubmed]
|
|
| Overexpression of human peroxiredoxin 5 in subcellular compartments of Chinese hamster ovary cells: effects on cytotoxicity and DNA damage caused by peroxides.[Pubmed]
|
|
| Existence of catalase-less peroxisomes in Sf21 insect cells.[Pubmed]
|
|
| Peroxisome senescence in human fibroblasts.[Pubmed]
|
|
| A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.[Pubmed]
|
|
| Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import.[Pubmed]
|
|
| In situ measurements of the pH of mammalian peroxisomes using the fluorescent protein pHluorin.[Pubmed]
|
|
| Peroxisomes in the apocrine sweat glands of the human axilla and their putative role in pheromone production.[Pubmed]
|
|
| Three-dimensional ultrastructural analysis of peroxisomes in HepG2 cells. Absence of peroxisomal reticulum but evidence of close spatial association with the endoplasmic reticulum.[Pubmed]
|
|
| Temperature sensitivity in peroxisome assembly processes characterizes milder forms of peroxisome biogenesis disorders.[Pubmed]
|
|
| Expression and prognostic significance of catalase in malignant mesothelioma.[Pubmed]
|
|
| Overexpression of wild-type and nuclear-targeted catalase modulates resistance to oxidative stress but does not alter spontaneous mutant frequencies at APRT.[Pubmed]
|
|
| Estimation of H2O2 gradients across biomembranes.[Pubmed]
|
|
| Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins.[Pubmed]
|
|
| Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome.[Pubmed]
|
|
| Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.[Pubmed]
|
|
| L-Pipecolic acid oxidase, a human enzyme essential for the degradation of L-pipecolic acid, is most similar to the monomeric sarcosine oxidases.[Pubmed]
|
|
| Atypical refsum disease with pipecolic acidemia and abnormal catalase distribution.[Pubmed]
|
|
| Oxidation of human catalase by singlet oxygen in myeloid leukemia cells.[Pubmed]
|
|
| Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.[Pubmed]
|
|
| Overexpression of human catalase gene decreases oxidized lipid-induced cytotoxicity in vascular smooth muscle cells.[Pubmed]
|
|
| Disorders of peroxisome biogenesis: complementation analysis shows genetic heterogeneity with strong overrepresentation of one group (PEX1 deficiency).[Pubmed]
|
|
| Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.[Pubmed]
|
|
| Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.[Pubmed]
|
|
| Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70.[Pubmed]
|
|
| Immunocytochemical localization of L-alpha-hydroxyacid oxidase in dense bar of dumb-bell-shaped peroxisomes of monkey kidney.[Pubmed]
|
|
| Effects of clofibric and beclobric acid in rat and monkey hepatocyte primary culture: influence on peroxisomal and mitochondrial beta-oxidation and the activity of catalase, glutathione S-transferase and glutathione peroxidase.[Pubmed]
|
|
| Hepatic peroxisomal changes induced by a tetrazole-substituted alkoxyacetophenone in rats and comparison with other species.[Pubmed]
|
|
| Induction of fatty acid beta-oxidation and peroxisome proliferation in the liver of rhesus monkeys by DL-040, a new hypolipidemic agent.[Pubmed]
|
|
| Induction of hepatic peroxisome proliferation in nonrodent species, including primates.[Pubmed]
|
|
| Peroxisomes (microbodies) in the myocardium of rodents and primates. A comparative Ultrastructural cytochemical study.[Pubmed]
|
|
| Microperoxisomes in retinal pigment epithelium.[Pubmed]
|
|
| Fundamental contribution of beta-oxidation to polyketide mycotoxin production in planta.[Pubmed]
|
|
| Multiple catalase genes are differentially regulated in Aspergillus nidulans.[Pubmed]
|
|
| Characterization of oleate-nonutilizing mutants of Aspergillus nidulans isolated by the 3-amino-1,2,4-triazole positive selection method.[Pubmed]
|
|
| Expression of active spinach glycolate oxidase in Aspergillus nidulans.[Pubmed]
|
|
| A eukaryote without catalase-containing microbodies: Neurospora crassa exhibits a unique cellular distribution of its four catalases.[Pubmed]
|
|
| Hex-1, a gene unique to filamentous fungi, encodes the major protein of the Woronin body and functions as a plug for septal pores.[Pubmed]
|
|
| The function and specificity of the C-terminal tripeptide glyoxysomal targeting signal in Neurospora crassa.[Pubmed]
|
|
| Cytoplasmic organelles of trypanosomatids: a cytochemical and stereological study.[Pubmed]
|
|
| Host peroxisomal properties are not restored to normal after treatment of visceral leishmaniasis with sodium antimony gluconate.[Pubmed]
|
|
| Peroxisomal function is altered during leishmania infection.[Pubmed]
|
|
| Histopathologic analysis of hamster hepatocytes submitted to experimental infection with Leishmania donovani.[Pubmed]
|
|
| Cytochemical localization of peroxisomes in Tetrahymena pyriformis.[Pubmed]
|
|
| Synthesis of glycolytic and peroxisomal enzymes in Tetrahymena following a change in culture conditions.[Pubmed]
|
|
| Localization of some enzymes of beta-oxidation of fatty acids in the peroxisomes of Tetrahymena.[Pubmed]
|
|
| Peroxisomes and hydrogenosomes in protozoa.[Pubmed]
|
|
| Distribution of tricarboxylic acid cycle enzymes and glyoxylate cycle enzymes between mitochondria and peroxisomes in Tetrahymena pyriformis.[Pubmed]
|
|
| chy1, an Arabidopsis mutant with impaired beta-oxidation, is defective in a peroxisomal beta-hydroxyisobutyryl-CoA hydrolase.[Pubmed]
|
|
| Subcellular targeting of nine calcium-dependent protein kinase isoforms from Arabidopsis.[Pubmed]
|
|
| Characterization of the induction of cytosolic and microsomal epoxide hydrolases by 2-ethylhexanoic acid in mouse liver.[Pubmed]
|
|
| The hepatic effects of hypolipidemic drugs (clofibrate, nafenopin, tibric acid, and Wy-14,643) on hepatic peroxisomes and peroxisome-associated enzymes.[Pubmed]
|
|
| Effects of oral administration of bezafibrate on peroxisomes and carnitine acetyltransferase in rat hepatocytes.[Pubmed]
|
|
| Peroxisomal fatty acid oxidation and inhibitors of the mitochondrial carnitine palmitoyltransferase I in isolated rat hepatocytes.[Pubmed]
|
|
| Purification of heart and liver mitochondrial carnitine acetyltransferase.[Pubmed]
|
|
| Induction of hepatic peroxisomes by a new, non-carboxylate-containing drug, bifonazole.[Pubmed]
|
|
| Response to thyroxine of lamellar bodies, peroxisomes and peroxisomal enzymes in the adult rat lung.[Pubmed]
|
|
| Effects of thia-substituted fatty acids on mitochondrial and peroxisomal beta-oxidation. Studies in vivo and in vitro.[Pubmed]
|
|
| Proliferation of peroxisomes without simultaneous induction of the peroxisomal fatty acid beta-oxidation.[Pubmed]
|
|
| Participation of peroxisomes in lipid biosynthesis in the harderian gland of guinea pig.[Pubmed]
|
|
| Rat liver metabolism of dicarboxylic acids.[Pubmed]
|
|
| Suppression of clofibrate-induced peroxisome proliferation in rat liver by nicardipine, a calcium antagonist.[Pubmed]
|
|
| Effects of prolonged administration of phthalate ester on the liver.[Pubmed]
|
|
| Valproic acid-induced increase in carnitine acetyltransferase in rat hepatocytes is not due to an induction of peroxisomes.[Pubmed]
|
|
| Di-n-octyl phthalate (DOP), a relatively ineffective peroxisome inducing straight chain isomer of the environmental contaminant di(2-ethylhexyl)phthalate (DEHP), enhances the development of putative preneoplastic lesions in rat liver.[Pubmed]
|
|
| Concentration-dependent inhibition of development of GGT positive foci in rat liver by the environmental contaminant di(2-ethylhexyl) phthalate.[Pubmed]
|
|
| Peroxisome-associated enzymes and serum lipids in tumour-bearing rats treated with peroxisome-proliferating agents.[Pubmed]
|
|
| Hypolipidemia and peroxisome proliferation induced by phenoxyacetic acid herbicides in rats.[Pubmed]
|
|
| Peroxisomal effects of phthalate esters in primary cultures of rat hepatocytes.[Pubmed]
|
|
| Carnitine acetyltransferase. Effect of malonyl-CoA, fasting and clofibrate feeding in mitochondria from different tissues.[Pubmed]
|
|
| Comparison of clofibrate and ethyl-5-(p-chlorophenoxy)-3-hydroxy-3-methylpentanoate induced changes in serum lipoprotein cholesterol and hepatic peroxisome proliferation in the normal rat.[Pubmed]
|
|
| Peroxisome proliferation in cultured rat hepatocytes produced by clofibrate and phthalate ester metabolites.[Pubmed]
|
|
| The short- and long-term effects of bezafibrate in the rat.[Pubmed]
|
|
| Effects of some hypolipidemic drugs on biochemical values and on hepatic peroxisomal enzymes of normolipemic rat.[Pubmed]
|
|
| Induction of peroxisomes and mitochondria by di(2-ethylhexyl)phthalate.[Pubmed]
|
|
| Physiological role of peroxisomal beta-oxidation in liver of fasted rats.[Pubmed]
|
|
| Effects of fat content in the diet on hepatic peroxisomes of the rat.[Pubmed]
|
|
| Carnitine acetyltransferase in developing mammals.[Pubmed]
|
|
| Hepatic peroxisome (microbody) proliferation in rats fed plasticizers and related compounds.[Pubmed]
|
|
| Hepatic peroxisome proliferation: induction by BR-931, a hypolipidemic analog of WY-14,643.[Pubmed]
|
|
| Alterations in peroxisomes of hepatomas.[Pubmed]
|
|
| Enzymic and morphological studies on catalase positive particles from brown fat of cold adapted rats.[Pubmed]
|
|
| Comparison of the carnitine acyltransferase activites from rat liver peroxisomes and microsomes.[Pubmed]
|
|
| Effect of clofibrate application on morphology and enzyme content of liver peroxisomes.[Pubmed]
|
|
| Carnitine-dependent transport of acetyl coenzyme A in Candida albicans is essential for growth on nonfermentable carbon sources and contributes to biofilm formation.[Pubmed]
|
|
| Carnitine acetyltransferases are required for growth on non-fermentable carbon sources but not for pathogenesis in Candida albicans.[Pubmed]
|
|
| Sorting of peroxisomal and mitochondrial carnitine acetyltransferase isozymes in the diploid yeast, Candida tropicalis.[Pubmed]
|
|
| Carnitine-dependent metabolic activities in Saccharomyces cerevisiae: three carnitine acetyltransferases are essential in a carnitine-dependent strain.[Pubmed]
|
|
| Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carnitine transporter, Agp2p.[Pubmed]
|
|
| Peroxisomal and mitochondrial carnitine acetyltransferase isozymes of the n-alkane-assimilating yeast, Candida tropicalis, occurred by alternative initiation of translation from the transcripts of a single gene.[Pubmed]
|
|
| Individual expression of Candida tropicalis peroxisomal and mitochondrial carnitine acetyltransferase-encoding genes and subcellular localization of the products in Saccharomyces cerevisiae.[Pubmed]
|
|
| Peroxisomal and mitochondrial carnitine acetyltransferases of the n-alkane-assimilating yeast Candida Tropicalis. Analysis of gene structure and translation products.[Pubmed]
|
|
| Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single gene.[Pubmed]
|
|
| Presence of carnitine acetyltransferase in peroxisomes and in mitochondria of oleic acid-grown Saccharomyces cerevisiae.[Pubmed]
|
|
| Candida albicans CTN gene family is induced during macrophage infection: homology, disruption and phenotypic analysis of CTN3 gene.[Pubmed]
|
|
| Changes in cell morphology and carnitine acetyltransferase activity in Candida albicans following growth on lipids and serum and after in vivo incubation in mice.[Pubmed]
|
|
| Enhancement of carnitine acetyltransferase synthesis in alkane-grown cells and propionate-grown cells of Candida tropicalis.[Pubmed]
|
|
| Peroxisomal and mitochondrial carnitine acetyltransferases in alkane-grown yeast Candida tropicalis.[Pubmed]
|
|
| Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1.[Pubmed]
|
|
| Modulation of metabolism in HepG2 cells upon treatment with cyclosporin A and Nva2-cyclosporin.[Pubmed]
|
|
| Carnitine--metabolism and functions.[Pubmed]
|
|
| Difference between species in response to a 3,5-dichloropyridyloxyphenoxy compound: induction of cytochrome P-450 and/or peroxisome proliferation.[Pubmed]
|
|
| The facC gene of Aspergillus nidulans encodes an acetate-inducible carnitine acetyltransferase.[Pubmed]
|
|
| The effect of structurally divergent herbicides on mouse liver xenobiotic-metabolizing enzymes (P-450-dependent mono-oxygenases, epoxide hydrolases and glutathione S-transferases) and carnitine acetyltransferase.[Pubmed]
|
|
| Carnitine octanoyltransferase of mouse liver peroxisomes: properties and effect of hypolipidemic drugs.[Pubmed]
|
|
| Hepatic effects of some [4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio] acetic acid (WY-14,643) analogs in the mouse.[Pubmed]
|
|
| Effects of ertiprotafib on hepatic cytochrome P450 and peroxisomal enzymes in rats and dogs, and in rat and human primary hepatocytes.[Pubmed]
|
|
| Inhibition of carnitine acyltransferase activities by bile acids in rat liver peroxisomes.[Pubmed]
|
|
| Differences in the response of Sprague-Dawley and Lewis rats to bezafibrate: the hypolipidemic effect and the induction of peroxisomal enzymes.[Pubmed]
|
|
| Co-suppression by nicardipine, a calcium antagonist, of induction of microsomal lauric acid hydroxylation with peroxisome proliferation in clofibrate-treated rat liver.[Pubmed]
|
|
| Characteristics of induction of peroxisomal fatty acid oxidation-related enzymes in rat liver by drugs. Relationships between structure and inducing activity.[Pubmed]
|
|
| Comparative induction of cytochrome P450IVA1 and peroxisome proliferation by ciprofibrate in the rat and marmoset.[Pubmed]
|
|
| Differential action of thyroid hormones and chemically related compounds on the activity of UDP-glucuronosyltransferases and cytochrome P-450 isozymes in rat liver.[Pubmed]
|
|
| Biochemical and morphological studies of ammonium perfluorooctanoate-induced hepatomegaly and peroxisome proliferation.[Pubmed]
|
|
| Structure-activity relationships for induction of peroxisomal enzyme activities by phthalate monoesters in primary rat hepatocyte cultures.[Pubmed]
|
|
| Proliferation of peroxisomes in pericentral hepatocytes of rat liver after administration of a new hypocholesterolemic agent (BM 15766). Sex-dependent ultrastructural differences.[Pubmed]
|
|
| Effects of some hypolipidemic agents on biochemical values and hepatic peroxisomal enzymes in rats: comparison of probucol, CGA, KCD-232, MLM-160, AL-369 and clinofibrate with clofibrate.[Pubmed]
|
|
| Hepatic peroxisome proliferation and hypolipidemic effects of di(2-ethylhexyl)phthalate in neonatal and adult rats.[Pubmed]
|
|
| Studies on the genetic effects of phthalic acid esters on cells in culture.[Pubmed]
|
|
| Effects of some anti-inflammatory drugs on biochemical values and on hepatic peroxisomal enzymes of rat.[Pubmed]
|
|
| Effect of the antilipolytic compound acipimox on peroxisome marker enzymes, lipid pattern and biotransformation related functions in rat liver.[Pubmed]
|
|
| Effects of long-term vitamin E deficiency and restoration on rat hepatic peroxisomes.[Pubmed]
|
|
| The effect of hypolipidaemic agents on peroxisomal beta-oxidation and mixed-function oxidase activities in primary cultures of rat hepatocytes. Relationship between induction of palmitoyl-CoA oxidation and lauric acid hydroxylation.[Pubmed]
|
|
| Comparative studies on di-(2-ethylhexyl) phthalate-induced hepatic peroxisome proliferation in the rat and hamster.[Pubmed]
|
|
| Induction of peroxisomal enzymes in livers of neonatal rats exposed to lactating mothers treated with hypolipidaemic drugs. Role of drug metabolite transfer in milk.[Pubmed]
|
|
| Changes in peroxisomal fatty acid oxidation in the diabetic rat liver.[Pubmed]
|
|
| Studies on peroxisomes. IX. Biochemical effects of simfibrate on precursor incorporation into polypeptide associated with peroxisome proliferation in rat liver.[Pubmed]
|
|
| Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids.[Pubmed]
|
|
| The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditions.[Pubmed]
|
|
| Activity and mRNA levels of enzymes involved in hepatic fatty acid oxidation in mice fed citrus flavonoids.[Pubmed]
|
|
| Developmental changes in carnitine octanoyltransferase gene expression in intestine and liver of suckling rats.[Pubmed]
|
|
| Natural trans-splicing in carnitine octanoyltransferase pre-mRNAs in rat liver.[Pubmed]
|
|
| Evidence of two catalytically active carnitine medium/long chain acyltransferases in rat liver peroxisomes.[Pubmed]
|
|
| Some properties of the malonyl-CoA sensitive carnitine long/medium chain acyltransferase activities of peroxisomes and microsomes of rat liver.[Pubmed]
|
|
| Cloning, sequencing, and regulation of rat liver carnitine octanoyltransferase: transcriptional stimulation of the enzyme during peroxisome proliferation.[Pubmed]
|
|
| Carnitine acyltransferase and acyl-coenzyme A hydrolase activities in human liver. Quantitative analysis of their subcellular localization.[Pubmed]
|
|
| Purification and properties of carnitine octanoyltransferase and carnitine palmitoyltransferase from rat liver.[Pubmed]
|
|
| Inhibition by etomoxir of rat liver carnitine octanoyltransferase is produced through the co-ordinate interaction with two histidine residues.[Pubmed]
|
|
| Identification of the two histidine residues responsible for the inhibition by malonyl-CoA in peroxisomal carnitine octanoyltransferase from rat liver.[Pubmed]
|
|
| Selective modulation of carnitine long-chain acyltransferase activities. Kinetics, inhibitors, and active sites of COT and CPT-II.[Pubmed]
|
|
| Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts.[Pubmed]
|
|
| Regulation of the long-chain carnitine acyltransferases.[Pubmed]
|
|
| Processing of carnitine octanoyltransferase pre-mRNAs by cis and trans-splicing.[Pubmed]
|
|
| Arabidopsis peroxisomal citrate synthase is required for fatty acid respiration and seed germination.[Pubmed]
|
|
| Proteomic analysis of the Arabidopsis cell wall reveals unexpected proteins with new cellular locations.[Pubmed]
|
|
| Oligomeric proteins containing N-terminal targeting signals are imported into peroxisomes in transgenic Arabidopsis.[Pubmed]
|
|
| Glyoxysomal malate dehydrogenase in pumpkin: cloning of a cDNA and functional analysis of its presequence.[Pubmed]
|
|
| Targeting and processing of a chimeric protein with the N-terminal presequence of the precursor to glyoxysomal citrate synthase.[Pubmed]
|
|
| Contribution of mitochondria and peroxisomes to palmitate oxidation in rat and bovine tissues.[Pubmed]
|
|
| The effect of dehydroepiandrosterone acetate on liver peroxisomal enzyme activities of male and female rats.[Pubmed]
|
|
| Glucagon and fasting do not activate peroxisomal fatty acid beta-oxidation in rat liver.[Pubmed]
|
|
| Disruption of the peroxisomal citrate synthase CshA affects cell growth and multicellular development in Dictyostelium discoideum.[Pubmed]
|
|
| Functional comparison of citrate synthase isoforms from S. cerevisiae.[Pubmed]
|
|
| Mutational and functional analysis of the cryptic N-terminal targeting signal for both mitochondria and peroxisomes in yeast peroxisomal citrate synthase Cit2p.[Pubmed]
|
|
| Mitochondrial transporters involved in oleic acid utilization and glutamate metabolism in yeast.[Pubmed]
|
|
| Identification of a cryptic N-terminal signal in Saccharomyces cerevisiae peroxisomal citrate synthase that functions in both peroxisomal and mitochondrial targeting.[Pubmed]
|
|
| Metabolic effects of mislocalized mitochondrial and peroxisomal citrate synthases in yeast Saccharomyces cerevisiae.[Pubmed]
|
|
| RTG genes in yeast that function in communication between mitochondria and the nucleus are also required for expression of genes encoding peroxisomal proteins.[Pubmed]
|
|
| RTG1 and RTG2: two yeast genes required for a novel path of communication from mitochondria to the nucleus.[Pubmed]
|
|
| Alternative topogenic signals in peroxisomal citrate synthase of Saccharomyces cerevisiae.[Pubmed]
|
|
| Citrate synthase encoded by the CIT2 gene of Saccharomyces cerevisiae is peroxisomal.[Pubmed]
|
|
| Presence of a bacterial-like citrate synthase gene in Tetrahymena thermophila: recent lateral gene transfers (LGT) or multiple gene losses subsequent to a single ancient LGT?[Pubmed]
|
|
| Presence of D-amino-acid oxidase protein in mutant mice lacking D-amino-acid oxidase activity.[Pubmed]
|
|
| Peroxisome development in the metanephric kidney of mouse.[Pubmed]
|
|
| Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice.[Pubmed]
|
|
| D-Serine exposure resulted in gene expression changes indicative of activation of fibrogenic pathways and down-regulation of energy metabolism and oxidative stress response.[Pubmed]
|
|
| Sodium benzoate attenuates D-serine induced nephrotoxicity in the rat.[Pubmed]
|
|
| Immunocytochemical localization of D-amino acid oxidase in rat brain.[Pubmed]
|
|
| Presence of heterogeneous peroxisomal populations in the rat nervous tissue.[Pubmed]
|
|
| Immunohistochemical localization of peroxisomal enzymes in developing rat kidney tissues.[Pubmed]
|
|
| In situ heterogeneity of peroxisomal oxidase activities: an update.[Pubmed]
|
|
| Extinction coefficient of polymerized diaminobenzidine complexed with cobalt as final reaction product of histochemical oxidase reactions.[Pubmed]
|
|
| Effects of Di-(2-ethylhexyl)phthalate on peroxisomes of liver, kidney and brain of lactating rats and their pups.[Pubmed]
|
|
| Differentiation of kidney cortex peroxisomes in fetal and newborn rats.[Pubmed]
|
|
| Permeability properties of peroxisomes in digitonin-permeabilized rat hepatocytes. Evidence for free permeability towards a variety of substrates.[Pubmed]
|
|
| Peroxisomes and peroxisomal enzymes along the crypt-villus axis of the rat intestine.[Pubmed]
|
|
| In situ kinetic measurements of D-amino acid oxidase in rat liver with respect to its substrate specificity.[Pubmed]
|
|
| Peroxisome through cell differentiation and neoplasia.[Pubmed]
|
|
| Ultrastructural aspects of the biogenesis of peroxisomes in rat liver.[Pubmed]
|
|
| The use of unfixed cryostat sections for electron microscopic study of D-amino acid oxidase activity in rat liver.[Pubmed]
|
|
| Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomes.[Pubmed]
|
|
| Frog cones as well as Müller cells have peroxisomes.[Pubmed]
|
|
| Postnatal development and isolation of peroxisomes from brain.[Pubmed]
|
|
| Peroxisomal oxidases and catalase in liver and kidney homogenates of normal and di(ethylhexyl)phthalate-fed rats.[Pubmed]
|
|
| Cytochemical and immunocytochemical study on the peroxisomes of rat liver after administration of a hypolipidemic drug, MLM-160.[Pubmed]
|
|
| D-aspartate oxidation by rat and bovine renal peroxisomes: an electron microscopic cytochemical study.[Pubmed]
|
|
| Altered acyl-CoA metabolism in riboflavin deficiency.[Pubmed]
|
|
| L-pipecolate oxidase: a distinct peroxisomal enzyme in man.[Pubmed]
|
|
| D-aspartate oxidase in rat, bovine and sheep kidney cortex is localized in peroxisomes.[Pubmed]
|
|
| Peroxisomal oxidases: cytochemical localization and biological relevance.[Pubmed]
|
|
| Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins.[Pubmed]
|
|
| Heterogenous staining of D-amino acid oxidase in peroxisomes of rat liver and kidney. A light and electron microscopic study.[Pubmed]
|
|
| Three-dimensional reconstruction of a peroxisomal reticulum in regenerating rat liver: evidence of interconnections between heterogeneous segments.[Pubmed]
|
|
| Immunoelectron microscopic localization of D-amino acid oxidase in rat kidney and liver.[Pubmed]
|
|
| Immunocytochemical localization of D-amino acid oxidase in the central clear matrix of rat kidney peroxisomes.[Pubmed]
|
|
| Effect of suloctidil on rat liver.[Pubmed]
|
|
| L-pipecolaturia in Zellweger syndrome.[Pubmed]
|
|
| Differentiation of liver peroxisomes in the foetal and newborn rat. Cytochemistry of catalase and D-aminoacid oxidase.[Pubmed]
|
|
| Effects of antilipolytic agents on rat liver peroxisomes and peroxisomal oxidative activities.[Pubmed]
|
|
| Kinetic properties of rat kidney D-amino acid oxidase associated with peroxisomes.[Pubmed]
|
|
| Rat liver peroxisomes. I. New peroxisome population induced by thyroid hormones in the liver of male rats.[Pubmed]
|
|
| Determination of the cross-points of rat liver peroxisomes, peroxisomal core and the core components by cross-partition.[Pubmed]
|
|
| Ultrastructural localization of D-amino acid oxidase in microperoxisomes of the rat nervous system.[Pubmed]
|
|
| Molecular cloning of TvDAO1, a gene encoding a D-amino acid oxidase from Trigonopsis variabilis and its expression in Saccharomyces cerevisiae and Kluyveromyces lactis.[Pubmed]
|
|
| Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver.[Pubmed]
|
|
| Peroxisomal oxidation of thiazolidine carboxylates in firefly fat body, frog retina, and rat liver and kidney.[Pubmed]
|
|
| Peroxisomes in the head of Drosophila melanogaster.[Pubmed]
|
|
| Physiological role of the D-amino acid oxidase gene, DAO1, in carbon and nitrogen metabolism in the methylotrophic yeast Candida boidinii.[Pubmed]
|
|
| Peroxisomes induced in Candida boidinii by methanol, oleic acid and D-alanine vary in metabolic function but share common integral membrane proteins.[Pubmed]
|
|
| The human L-pipecolic acid oxidase is similar to bacterial monomeric sarcosine oxidases rather than D-amino acid oxidases.[Pubmed]
|
|
| Contributions of the immunogold technique to investigation of the biology of peroxisomes.[Pubmed]
|
|
| Peroxisomes and peroxisomal enzymes in the human fetal small intestine.[Pubmed]
|
|
| Histochemistry of peroxisomal enzyme activities: a tool in the diagnosis of Zellweger syndrome.[Pubmed]
|
|
| Molecular cloning and chromosomal localization of a human gene encoding D-amino-acid oxidase.[Pubmed]
|
|
| Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy.[Pubmed]
|
|
| Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities.[Pubmed]
|
|
| Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate.[Pubmed]
|
|
| Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.[Pubmed]
|
|
| Peroxisomes (microbodies) in human glial tumors. a cytochemical ultrastructural study.[Pubmed]
|
|
| C-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signal.[Pubmed]
|
|
| Cellular and subcellular distribution of D-aspartate oxidase in human and rat brain.[Pubmed]
|
|
| D-aspartate oxidase, a peroxisomal enzyme in liver of rat and man.[Pubmed]
|
|
| A 27.368 kDa retinal reductase in New Zealand white rabbit liver cytosol encoded by the peroxisomal retinol dehydrogenase-reductase cDNA: purification and characterization of the enzyme.[Pubmed]
|
|
| An outer segment localization signal at the C terminus of the photoreceptor-specific retinol dehydrogenase.[Pubmed]
|
|
| Binary structure of the two-domain (3R)-hydroxyacyl-CoA dehydrogenase from rat peroxisomal multifunctional enzyme type 2 at 2.38 A resolution.[Pubmed]
|
|
| Yeast peroxisomal multifunctional enzyme: (3R)-hydroxyacyl-CoA dehydrogenase domains A and B are required for optimal growth on oleic acid.[Pubmed]
|
|
| Substrate specificities of peroxisomal members of short-chain alcohol dehydrogenase superfamily: expression and characterization of dehydrogenase part of Candida tropicalis multifunctional enzyme.[Pubmed]
|
|
| The cytosolic DnaJ-like protein djp1p is involved specifically in peroxisomal protein import.[Pubmed]
|
|
| Peroxisome elongation and constriction but not fission can occur independently of dynamin-like protein 1.[Pubmed]
|
|
| Dynamin-like protein-dependent formation of Woronin bodies in Saccharomyces cerevisiae upon heterologous expression of a single protein.[Pubmed]
|
|
| The dynamin-like protein Vps1p of the yeast Saccharomyces cerevisiae associates with peroxisomes in a Pex19p-dependent manner.[Pubmed]
|
|
| Assay and functional analysis of dynamin-like protein 1 in peroxisome division.[Pubmed]
|
|
| The dynamin-like GTPase DLP1 is essential for peroxisome division and is recruited to peroxisomes in part by PEX11.[Pubmed]
|
|
| A role for Vps1p, actin, and the Myo2p motor in peroxisome abundance and inheritance in Saccharomyces cerevisiae.[Pubmed]
|
|
| A lethal defect of mitochondrial and peroxisomal fission.[Pubmed]
|
|
| Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis.[Pubmed]
|
|
| Elongation of peroxisomes as an indicator for efficient dynamin-like protein 1 knock down in mammalian cells.[Pubmed]
|
|
| The 3-hydroxyacyl-CoA epimerase activity of rat liver peroxisomes is due to the combined actions of two enoyl-CoA hydratases: a revision of the epimerase-dependent pathway of unsaturated fatty acid oxidation.[Pubmed]
|
|
| Evidence for a novel pathway for the targeting of a Saccharomyces cerevisiae peroxisomal protein belonging to the isomerase/hydratase family.[Pubmed]
|
|
| Peroxisomal beta-oxidation enzymes.[Pubmed]
|
|
| Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency.[Pubmed]
|
|
| Studies on the intracellular distributions of soluble epoxide hydrolase and of catalase by digitonin-permeabilization of hepatocytes isolated from control and clofibrate-treated mice.[Pubmed]
|
|
| Purification and characterization of an epoxide hydrolase from the peroxisomal fraction of mouse liver.[Pubmed]
|
|
| In vitro translation of cytosolic and peroxisomal epoxide hydrolase and catalase on liver polyribosomes from untreated and clofibrate-treated C57B1/6 mice.[Pubmed]
|
|
| Distribution and nature of epoxide hydrolase activity in subcellular organelles of mouse liver.[Pubmed]
|
|
| Subcellular localization of epoxide hydrolase in mouse liver and kidney.[Pubmed]
|
|
| Epoxide hydrolase activity in isolated peroxisomes of mouse liver.[Pubmed]
|
|
| An impaired peroxisomal targeting sequence leading to an unusual bicompartmental distribution of cytosolic epoxide hydrolase.[Pubmed]
|
|
| Microsomal and cytosolic epoxide hydrolases, the peroxisomal fatty acid beta-oxidation system and catalase. Activities, distribution and induction in rat liver parenchymal and non-parenchymal cells.[Pubmed]
|
|
| Induction of xenobiotic-metabolizing enzymes and peroxisome proliferation in rat liver caused by dietary exposure to di(2-ethylhexyl)phosphate.[Pubmed]
|
|
| Rat cytosolic epoxide hydrolase.[Pubmed]
|
|
| Immuno-electron-microscopic studies on the subcellular distribution of rat liver epoxide hydrolase and the effect of phenobarbitone and 2-acetamidofluorene treatment.[Pubmed]
|
|
| Protein quaternary structure and expression levels contribute to peroxisomal-targeting-sequence-1-mediated peroxisomal import of human soluble epoxide hydrolase.[Pubmed]
|
|
| Identification of two Arabidopsis genes encoding a peroxisomal oxidoreductase-like protein and an acyl-CoA synthetase-like protein that are required for responses to pro-auxins.[Pubmed]
|
|
| Genome-wide analysis of a land plant-specific acyl:coenzyme A synthetase (ACS) gene family in Arabidopsis, poplar, rice and Physcomitrella.[Pubmed]
|
|
| Jasmonates meet fatty acids: functional analysis of a new acyl-coenzyme A synthetase family from Arabidopsis thaliana.[Pubmed]
|
|
| Characterization of Arabidopsis fluoroacetate-resistant mutants reveals the principal mechanism of acetate activation for entry into the glyoxylate cycle.[Pubmed]
|
|
| Two long-chain acyl-CoA synthetases from Arabidopsis thaliana involved in peroxisomal fatty acid beta-oxidation.[Pubmed]
|
|
| Fatty acid transport protein 4 is the principal very long chain fatty acyl-CoA synthetase in skin fibroblasts.[Pubmed]
|
|
| X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases.[Pubmed]
|
|
| Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient mice.[Pubmed]
|
|
| Hepatic enzymatic synthesis and hydrolysis of CoA esters of solvent-derived oxa acids.[Pubmed]
|
|
| Human very-long-chain acyl-CoA synthetase: cloning, topography, and relevance to branched-chain fatty acid metabolism.[Pubmed]
|
|
| Phytanic acid activation in rat liver peroxisomes is catalyzed by long-chain acyl-CoA synthetase.[Pubmed]
|
|
| Paradoxical increase in peroxisomal cyanide-insensitive respiration following dietary exposure to WY-14,643 in the perfused liver.[Pubmed]
|
|
| Purification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetase.[Pubmed]
|
|
| Peroxisomal beta-oxidation of branched chain fatty acids in rat liver. Evidence that carnitine palmitoyltransferase I prevents transport of branched chain fatty acids into mitochondria.[Pubmed]
|
|
| Influence of chronic administration of valproate on ultrastructure and enzyme content of peroxisomes in rat liver and kidney. Oxidation of valproate by liver peroxisomes.[Pubmed]
|
|
| Mitochondrial and peroxisomal beta-oxidation of stearic and lignoceric acids by rat brain.[Pubmed]
|
|
| Pathway of alpha-linolenic acid through the mitochondrial outer membrane in the rat liver and influence on the rate of oxidation. Comparison with linoleic and oleic acids.[Pubmed]
|
|
| Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.[Pubmed]
|
|
| Integral membrane polypeptides of rat liver peroxisomes: topology and response to different metabolic states.[Pubmed]
|
|
| Identity of long-chain acyl-coenzyme A synthetase of microsomes, mitochondria, and peroxisomes in rat liver.[Pubmed]
|
|
| Participation of peroxisomal beta-oxidation system in the chain-shortening of a xenobiotic acyl compound.[Pubmed]
|
|
| Acyl-CoA synthetase in rat liver peroxisomes. Computer-assisted analysis of cell fractionation experiments.[Pubmed]
|
|
| Acyl-Coenzyme A synthetase and fatty acid oxidation in rat liver peroxisomes.[Pubmed]
|
|
| Intracellular Localization of Enzymes of Fatty Acid-beta-Oxidation in the Alga Cyanidium caldarium.[Pubmed]
|
|
| Murine bubblegum orthologue is a microsomal very long-chain acyl-CoA synthetase.[Pubmed]
|
|
| A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.[Pubmed]
|
|
| Disruption of a yeast very-long-chain acyl-CoA synthetase gene simulates the cellular phenotype of X-linked adrenoleukodystrophy.[Pubmed]
|
|
| Intraperoxisomal localization of very-long-chain fatty acyl-CoA synthetase: implication in X-adrenoleukodystrophy.[Pubmed]
|
|
| Human liver-specific very-long-chain acyl-coenzyme A synthetase: cDNA cloning and characterization of a second enzymatically active protein.[Pubmed]
|
|
| Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations.[Pubmed]
|
|
| Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell system.[Pubmed]
|
|
| Molecular cloning of cDNA encoding rat very long-chain acyl-CoA synthetase.[Pubmed]
|
|
| Long-chain fatty Acyl-CoA synthetase enzymatic activity in rat liver cell nuclei.[Pubmed]
|
|
| Peroxisomal activation of long- and very long-chain fatty acids in the yeast Pichia pastoris.[Pubmed]
|
|
| Phytanic acid must be activated to phytanoyl-CoA prior to its alpha-oxidation in rat liver peroxisomes.[Pubmed]
|
|
| Subcellular distribution and characteristics of ciprofibroyl-CoA synthetase in rat liver. Its possible identity with long-chain acyl-CoA synthetase.[Pubmed]
|
|
| Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liver.[Pubmed]
|
|
| Long-chain-acyl-CoA synthetase and very-long-chain-acyl-CoA synthetase activities in peroxisomes and microsomes from rat liver. An enzymological study.[Pubmed]
|
|
| Evidence that peroxisomal acyl-CoA synthetase is located at the cytoplasmic side of the peroxisomal membrane.[Pubmed]
|
|
| Triacylglycerol synthesis in the oleaginous yeast Candida curvata D.[Pubmed]
|
|
| Subcellular localization of long-chain alcohol dehydrogenase and aldehyde dehydrogenase in n-alkane-grown Candida tropicalis.[Pubmed]
|
|
| Overexpression of a modified human malonyl-CoA decarboxylase blocks the glucose-induced increase in malonyl-CoA level but has no impact on insulin secretion in INS-1-derived (832/13) beta-cells.[Pubmed]
|
|
| Cerebral inflammation in X-linked adrenoleukodystrophy.[Pubmed]
|
|
| Peroxisomal beta-oxidation of branched chain fatty acids in human skin fibroblasts.[Pubmed]
|
|
| X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts.[Pubmed]
|
|
| Very long chain fatty acid beta-oxidation by subcellular fractions of normal and Zellweger syndrome skin fibroblasts.[Pubmed]
|
|
| Beta-oxidation of very-long-chain fatty acids and their coenzyme A derivatives by human skin fibroblasts.[Pubmed]
|
|
| Mammalian wax biosynthesis. I. Identification of two fatty acyl-Coenzyme A reductases with different substrate specificities and tissue distributions.[Pubmed]
|
|
| Plant-like traits associated with metabolism of Trypanosoma parasites.[Pubmed]
|
|
| Structures of type 2 peroxisomal targeting signals in two trypanosomatid aldolases.[Pubmed]
|
|
| Import of fructose bisphosphate aldolase into the glycosomes of Trypanosoma brucei.[Pubmed]
|
|
| Interaction of Leishmania PTS2 receptor peroxin 7 with the glycosomal protein import machinery.[Pubmed]
|
|
| Cloning and characterization of Leishmania mexicana fructose-1,6-bisphosphate aldolase.[Pubmed]
|
|
| Nematode biochemistry. XIII. Peroxisomes in the free-living nematode, Turbatrix aceti.[Pubmed]
|
|
| Cytochemical changes in hepatocytes of rats with endotoxemia or sepsis: localization of fibronectin, calcium, and enzymes.[Pubmed]
|
|
| Succinate secreted by Trypanosoma brucei is produced by a novel and unique glycosomal enzyme, NADH-dependent fumarate reductase.[Pubmed]
|
|
| A mitochondrial NADH-dependent fumarate reductase involved in the production of succinate excreted by procyclic Trypanosoma brucei.[Pubmed]
|
|
| The crystal structure of glucose-6-phosphate isomerase from Leishmania mexicana reveals novel active site features.[Pubmed]
|
|
| Detection of mRNAs encoding peroxisomal proteins by non-radioactive in situ hybridization with digoxigenin-labelled cRNAs.[Pubmed]
|
|
| L-lactate dehydrogenase A4- and A3B isoforms are bona fide peroxisomal enzymes in rat liver. Evidence for involvement in intraperoxisomal NADH reoxidation.[Pubmed]
|
|
| Tomato bushy stunt virus co-opts the RNA-binding function of a host metabolic enzyme for viral genomic RNA synthesis.[Pubmed]
|
|
| Alanine aminotransferase homologs catalyze the glutamate:glyoxylate aminotransferase reaction in peroxisomes of Arabidopsis.[Pubmed]
|
|
| Purification and Characterization of Hydroxypyruvate Reductase from Cucumber Cotyledons.[Pubmed]
|
|
| Glyoxylate aminotransferase in peroxisomes from rat liver and kidney.[Pubmed]
|
|
| Targeted disruption of glycerol kinase gene in mice: expression analysis in liver shows alterations in network partners related to glycerol kinase activity.[Pubmed]
|
|
| Peroxisomal localization of glucose-6-phosphate dehydrogenase and pyrophosphate-stimulated dihydroxyacetone-phosphate acyltransferase in mouse kidney.[Pubmed]
|
|
| Predominant localization of dihydroxyacetone-phosphate acyltransferase activity in renal peroxisomes of male and female mice.[Pubmed]
|
|
| Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method.[Pubmed]
|
|
| Comparison of the activities of some peroxisomal and extraperoxisomal lipid-metabolizing enzymes in liver and extrahepatic tissues of the rat.[Pubmed]
|
|
| Glycerolipid synthetic capacity of rat liver peroxisomes.[Pubmed]
|
|
| Rat liver dihydroxyacetone-phosphate acyltransferases and their contribution to glycerolipid synthesis.[Pubmed]
|
|
| Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies).[Pubmed]
|
|
| Leishmania major expresses a single dihydroxyacetone phosphate acyltransferase localized in the glycosome, important for rapid growth and survival at high cell density and essential for virulence.[Pubmed]
|
|
| Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.[Pubmed]
|
|
| Etherphospholipid biosynthesis and dihydroxyactetone-phosphate acyltransferase: resolution of the genomic organization of the human gnpat gene and its use in the identification of novel mutations.[Pubmed]
|
|
| Zellweger syndrome in Saudi Arabia and its distinct features.[Pubmed]
|
|
| Isolation of a Chinese hamster fibroblast variant defective in dihydroxyacetonephosphate acyltransferase activity and plasmalogen biosynthesis: use of a novel two-step selection protocol.[Pubmed]
|
|
| Late-onset generalized disorder of peroxisomes.[Pubmed]
|
|
| Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells.[Pubmed]
|
|
| Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease.[Pubmed]
|
|
| Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly.[Pubmed]
|
|
| HMG-CoA reductase inhibitors perturb fatty acid metabolism and induce peroxisomes in keratinocytes.[Pubmed]
|
|
| Zellweger syndrome in a preterm, small for gestational age infant.[Pubmed]
|
|
| Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.[Pubmed]
|
|
| Factors influencing the latency of the peroxisomal enzyme dihydroxyacetone-phosphate acyltransferase (DHAP-AT) in permeabilized human skin fibroblasts.[Pubmed]
|
|
| Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.[Pubmed]
|
|
| Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction.[Pubmed]
|
|
| Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.[Pubmed]
|
|
| A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).[Pubmed]
|
|
| A sibship with a mild variant of Zellweger syndrome.[Pubmed]
|
|
| Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.[Pubmed]
|
|
| Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.[Pubmed]
|
|
| A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells.[Pubmed]
|
|
| A milder variant of Zellweger syndrome.[Pubmed]
|
|
| Targeted disruption of ether lipid synthesis in mice.[Pubmed]
|
|
| Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.[Pubmed]
|
|
| Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.[Pubmed]
|
|
| Lipid biosynthesis in peroxisomes.[Pubmed]
|
|
| Biosynthesis of glycerolipid precursors in rat liver peroxisomes and their transport and conversion to phosphatidate in the endoplasmic reticulum.[Pubmed]
|
|
| Latency of the peroxisomal enzyme acyl-CoA:dihydroxyacetonephosphate acyltransferase in digitonin-permeabilized fibroblasts: the effect of ATP and ATPase inhibitors.[Pubmed]
|
|
| Changes in the activities of dihydroxyacetone phosphate and glycerol-3-phosphate acyltransferases in rat liver under various conditions.[Pubmed]
|
|
| A rapid method for the isolation of peroxisomes from rat liver.[Pubmed]
|
|
| Biochemical markers predicting survival in peroxisome biogenesis disorders.[Pubmed]
|
|
| Biochemical markers predicting survival in peroxisome biogenesis disorders.[Pubmed]
|
|
| A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.[Pubmed]
|
|
| Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase.[Pubmed]
|
|
| Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.[Pubmed]
|
|
| Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.[Pubmed]
|
|
| Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group.[Pubmed]
|
|
| Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome.[Pubmed]
|
|
| Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case report.[Pubmed]
|
|
| Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.[Pubmed]
|
|
| Identification of L-pipecolate oxidase in human liver and its deficiency in the Zellweger syndrome.[Pubmed]
|
|
| Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.[Pubmed]
|
|
| Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.[Pubmed]
|
|
| Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.[Pubmed]
|
|
| Arabidopsis mutants define an in vivo role for isoenzymes of aspartate aminotransferase in plant nitrogen assimilation.[Pubmed]
|
|
| Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiae.[Pubmed]
|
|
| The noninvolvement of MDH as NAD-oxidoreductase shuttle in rat liver peroxisomes.[Pubmed]
|
|
| Postnatal development of peroxisomal and mitochondrial enzymes in rat liver.[Pubmed]
|
|
| Molecular characterization of glycosomal NAD(+)-dependent glycerol 3-phosphate dehydrogenase from Trypanosoma brucei rhodesiense.[Pubmed]
|
|
| Arabidopsis PEX19 is a dimeric protein that binds the peroxin PEX10.[Pubmed]
|
|
| Chloroplast unusual positioning1 is essential for proper chloroplast positioning.[Pubmed]
|
|
| Rapid hepatocyte nuclear translocation of the Forkhead Box M1B (FoxM1B) transcription factor caused a transient increase in size of regenerating transgenic hepatocytes.[Pubmed]
|
|
| Insights into the membrane proteome of rat liver peroxisomes: microsomal glutathione-S-transferase is shared by both subcellular compartments.[Pubmed]
|
|
| Principal component analysis of mass spectra of peptides generated from the tryptic digestion of protein mixtures.[Pubmed]
|
|
| The relationship between decrease in Cx32 and induction of P450 isozymes in the early phase of clofibrate hepatocarcinogenesis in the rat.[Pubmed]
|
|
| Juxtaposition of peroxisomes and chromosomes in mitotic hepatocytes following methyl clofenapate administration to rats.[Pubmed]
|
|
| Characterizations of and interactions between bile ductule cells and hepatocytes in early stages of rat hepatocarcinogenesis induced by ethionine.[Pubmed]
|
|
| Subcellular distribution of N-ethylmaleimide-stimulatable glutathione S-transferase activity in rat liver. Evidence of localization of glutathione S-transferase in peroxisomal membrane.[Pubmed]
|
|
| Quantitative stereological evaluation of four histochemical markers of altered foci in multistage hepatocarcinogenesis in the rat.[Pubmed]
|
|
| Identifying Pex21p as a protein that specifically interacts with yeast seryl-tRNA synthetase.[Pubmed]
|
|
| The PAL1 gene product is a peroxisomal ATP-binding cassette transporter in the yeast Saccharomyces cerevisiae.[Pubmed]
|
|
| Peroxisomal targeting of mammalian hydroxyacid oxidase 1 requires the C-terminal tripeptide SKI.[Pubmed]
|
|
| Oxidative stress-mediated down-regulation of rat hydroxyacid oxidase 1, a liver-specific peroxisomal enzyme.[Pubmed]
|
|
| Immunoelectron microscopic localization of the isozymes of L-alpha-hydroxyacid oxidase in renal peroxisomes of beef and sheep: evidence of distinct intraorganellar subcompartmentation.[Pubmed]
|
|
| Electron microscopic cytochemical localization of alpha-hydroxyacid oxidase in rat kidney cortex. Heterogeneous staining of peroxisomes.[Pubmed]
|
|
| Electron microscopic cytochemical localization of alpha-hydroxyacid oxidase in rat liver. Association with the crystalline core and matrix of peroxisomes.[Pubmed]
|
|
| Light and electron microscopic localization of L-alpha-hydroxyacid oxidase in rat kidney revealed by immunocytochemical techniques.[Pubmed]
|
|
| Influence of subtotal hepatectomy on peroxisomes and peroxisomal enzymes of rat liver and isolated liver cell fractions.[Pubmed]
|
|
| Low-density particles (W-particles) containing catalase in Zellweger syndrome and normal fibroblasts.[Pubmed]
|
|
| Effect of x-irradiation on the permeability of L-alpha hydroxy acid oxidase from mouse liver peroxisomes.[Pubmed]
|
|
| Selective induction of peroxisomal enzymes by the hypolipidemic drug bezafibrate. Detection of modulations by automatic image analysis in conjunction with immunoelectron microscopy and immunoblotting.[Pubmed]
|
|
| Catalase in guinea pig hepatocytes is localized in cytoplasm, nuclear matrix and peroxisomes.[Pubmed]
|
|
| Cytochemical localization of catalase and several hydrogen peroxide-producing oxidases in the nucleoids and matrix of rat liver peroxisomes.[Pubmed]
|
|
| Unusual responses of rat hepatic and renal peroxisomes to RMI 14, 514, a new hypolipidemic agent.[Pubmed]
|
|
| Studies on peroxisomes. VI. Relationship between the peroxisomal core and urate oxidase.[Pubmed]
|
|
| Structure, composition, physical properties, and turnover of proliferated peroxisomes. A study of the trophic effects of Su-13437 on rat liver.[Pubmed]
|
|
| Studies on peroxisomes. V. Effect of ethyl p-chlorophenoxyisobutyrate on the centrifugal behavior of rat liver peroxisomes.[Pubmed]
|
|
| Ultrastructural localization of L-alpha-hydroxy acid oxidase in rat liver perioxisomes.[Pubmed]
|
|
| Cytochemical localization by ferricyanide reduction of -hydroxy acid oxidase activity in peroxisomes of rat kidney.[Pubmed]
|
|
| Mevalonate pyrophosphate decarboxylase is predominantly located in the cytosol of rat hepatocytes.[Pubmed]
|
|
| Molecular and biochemical characterization of hexokinase from Trypanosoma cruzi.[Pubmed]
|
|
| Peroxisome function regulates growth on glucose in the basidiomycete fungus Cryptococcus neoformans.[Pubmed]
|
|
| Molecular and biochemical characterization of novel glucokinases from Trypanosoma cruzi and Leishmania spp.[Pubmed]
|
|
| The crystal structure of Trypanosoma cruzi glucokinase reveals features determining oligomerization and anomer specificity of hexose-phosphorylating enzymes.[Pubmed]
|
|
| Bisphosphonates as inhibitors of Trypanosoma cruzi hexokinase: kinetic and metabolic studies.[Pubmed]
|
|
| Experimental and in silico analyses of glycolytic flux control in bloodstream form Trypanosoma brucei.[Pubmed]
|
|
| Probing the role of compartmentation of glycolysis in procyclic form Trypanosoma brucei: RNA interference studies of PEX14, hexokinase, and phosphofructokinase.[Pubmed]
|
|
| Molecular characterization of the hexokinase gene from Leishmania major.[Pubmed]
|
|
| 3-Hydroxy-3-methylglutaryl-CoA lyase is present in mouse and human liver peroxisomes.[Pubmed]
|
|
| Investigation of the oligomeric status of the peroxisomal isoform of human 3-hydroxy-3-methylglutaryl-CoA lyase.[Pubmed]
|
|
| Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes.[Pubmed]
|
|
| Phytanic acid alpha-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomes.[Pubmed]
|
|
| Purification, molecular cloning, and expression of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal thiamine pyrophosphate-dependent enzyme that catalyzes the carbon-carbon bond cleavage during alpha-oxidation of 3-methyl-branched fatty acids.[Pubmed]
|
|
| The role of 2-hydroxyacyl-CoA lyase, a thiamin pyrophosphate-dependent enzyme, in the peroxisomal metabolism of 3-methyl-branched fatty acids and 2-hydroxy straight-chain fatty acids.[Pubmed]
|
|
| Phytanic acid alpha-oxidation in man: identification of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal enzyme with normal activity in Zellweger syndrome.[Pubmed]
|
|
| A cytosolic pathway for the conversion of hydroxypyruvate to glycerate during photorespiration in Arabidopsis.[Pubmed]
|
|
| Peroxisomal malate dehydrogenase is not essential for photorespiration in Arabidopsis but its absence causes an increase in the stoichiometry of photorespiratory CO2 release.[Pubmed]
|
|
| A leaf-peroxisomal protein, hydroxypyruvate reductase, is produced by light-regulated alternative splicing.[Pubmed]
|
|
| Light regulates alternative splicing of hydroxypyruvate reductase in pumpkin.[Pubmed]
|
|
| Hydroxypyruvate reductase with a carboxy-terminal targeting signal to microbodies is expressed in Arabidopsis.[Pubmed]
|
|
| Plants express a lipid transfer protein with high similarity to mammalian sterol carrier protein-2.[Pubmed]
|
|
| Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.[Pubmed]
|
|
| Inactivation of the peroxisomal multifunctional protein-2 in mice impedes the degradation of not only 2-methyl-branched fatty acids and bile acid intermediates but also of very long chain fatty acids.[Pubmed]
|
|
| MFE1, a member of the peroxisomal hydroxyacyl coenzyme A dehydrogenase family, affects fatty acid metabolism necessary for morphogenesis in Dictyostelium spp.[Pubmed]
|
|
| A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency.[Pubmed]
|
|
| Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed method.[Pubmed]
|
|
| Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency.[Pubmed]
|
|
| Role of an ancestral d-bifunctional protein containing two sterol-carrier protein-2 domains in lipid uptake and trafficking in Toxoplasma.[Pubmed]
|
|
| Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency.[Pubmed]
|
|
| Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfall.[Pubmed]
|
|
| Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency.[Pubmed]
|
|
| Characteristic acylcarnitine profiles in inherited defects of peroxisome biogenesis: a novel tool for screening diagnosis using tandem mass spectrometry.[Pubmed]
|
|
| Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency.[Pubmed]
|
|
| Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.[Pubmed]
|
|
| A common ancestor for Candida tropicalis and dehydrogenases that synthesize antibiotics and steroids.[Pubmed]
|
|
| Insulin-degrading enzyme exists inside of rat liver peroxisomes and degrades oxidized proteins.[Pubmed]
|
|
| The rat insulin-degrading enzyme. Molecular cloning and characterization of tissue-specific transcripts.[Pubmed]
|
|
| Insulin degrading enzyme is expressed in the human cerebrovascular endothelium and in cultured human cerebrovascular endothelial cells.[Pubmed]
|
|
| Insulin-degrading enzyme does not require peroxisomal localization for insulin degradation.[Pubmed]
|
|
| Insulin-degrading enzyme.[Pubmed]
|
|
| Regulation of isocitrate metabolism in peroxisomes in Tetrahymena pyriformis.[Pubmed]
|
|
| Isolation of peroxisomes from rat liver using sucrose and Percoll gradients.[Pubmed]
|
|
| Liver peroxisomes, cytology and function.[Pubmed]
|
|
| The synthesis and turnover of rat liver peroxisomes. I. Fractionation of peroxisome proteins.[Pubmed]
|
|
| Dual compartmental localization and function of mammalian NADP+-specific isocitrate dehydrogenase in yeast.[Pubmed]
|
|
| Cloning and expression of Aspergillus niger icdA gene encoding mitochondrial NADP+-specific isocitrate dehydrogenase.[Pubmed]
|
|
| Influence of compartmental localization on the function of yeast NADP+-specific isocitrate dehydrogenases.[Pubmed]
|
|
| A single gene produces mitochondrial, cytoplasmic, and peroxisomal NADP-dependent isocitrate dehydrogenase in Aspergillus nidulans.[Pubmed]
|
|
| The human PICD gene encodes a cytoplasmic and peroxisomal NADP(+)-dependent isocitrate dehydrogenase.[Pubmed]
|
|
| Sources of NADPH and expression of mammalian NADP+-specific isocitrate dehydrogenases in Saccharomyces cerevisiae.[Pubmed]
|
|
| Peroxisomal beta-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions.[Pubmed]
|
|
| IDP3 encodes a peroxisomal NADP-dependent isocitrate dehydrogenase required for the beta-oxidation of unsaturated fatty acids.[Pubmed]
|
|
| Gene analysis of an NADP-linked isocitrate dehydrogenase localized in peroxisomes of the n-alkane-assimilating yeast Candida tropicalis.[Pubmed]
|
|
| Immunochemically distinct NADP-linked isocitrate dehydrogenase isozymes in mitochondria and peroxisomes of Candida tropicalis.[Pubmed]
|
|
| Novel NADP-linked isocitrate dehydrogenase present in peroxisomes of n-alkane-utilizing yeast, Candida tropicalis: comparison with mitochondrial NAD-linked isocitrate dehydrogenase.[Pubmed]
|
|
| Sequence-based discovery of the human and rodent peroxisomal proteome.[Pubmed]
|
|
| Cloning and subcellular localization of hamster and rat isopentenyl diphosphate dimethylallyl diphosphate isomerase. A PTS1 motif targets the enzyme to peroxisomes.[Pubmed]
|
|
| Vesicle membrane association of nitric oxide synthase in primary mouse macrophages.[Pubmed]
|
|
| Monomeric inducible nitric oxide synthase localizes to peroxisomes in hepatocytes.[Pubmed]
|
|
</