| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2009 | Janet Ebberink | Hum. Mutat. | Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.[Pubmed] |
| 2006 | Rachel Zufferey | J. Biol. Chem. | 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] |
| 2004 | Inderjit Singh | Brain Res. | Impaired peroxisomal function in the central nervous system with inflammatory disease of experimental autoimmune encephalomyelitis animals and protection by lovastatin treatment.[Pubmed] |
| 2003 | Claus Rodemer | Adv. Exp. Med. Biol. | Targeted disruption of ether lipid synthesis in mice.[Pubmed] |
| 2003 | Jeannette Gootjes | Adv. Exp. Med. Biol. | Biochemical markers predicting survival in peroxisome biogenesis disorders.[Pubmed] |
| 2003 | Johannes Berger | Adv. Exp. Med. Biol. | Lessons from knockout mice II: Mouse models for peroxisomal disorders with single protein deficiency.[Pubmed] |
| 2003 | Bikramjit Raychaudhury | Med. Sci. Monit. | Peroxisomal function is altered during leishmania infection.[Pubmed] |
| 2002 | J Gootjes | Neurology | Biochemical markers predicting survival in peroxisome biogenesis disorders.[Pubmed] |
| 2001 | R Ofman | Biochem. Biophys. Res. Commun. | 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] |
| 2001 | C Thai | Hum. Mol. Genet. | Impaired membrane traffic in defective ether lipid biosynthesis.[Pubmed] |
| 2001 | S Reisse | Biol. Reprod. | Peroxisomes and ether lipid biosynthesis in rat testis and epididymis.[Pubmed] |
| 2001 | S Farioli-Vecchioli | Histochem. Cell Biol. | Catalase immunocytochemistry allows automatic detection of lung type II alveolar cells.[Pubmed] |
| 2000 | N Hajra | J. Biol. Chem. | Induction of the peroxisomal glycerolipid-synthesizing enzymes during differentiation of 3T3-L1 adipocytes. Role in triacylglycerol synthesis.[Pubmed] |
| 1999 | N Shimozawa | J. Med. Genet. | Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.[Pubmed] |
| 1999 | J Biermann | Eur. J. Biochem. | Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes.[Pubmed] |
| 1999 | L Ijlst | J. Lipid Res. | Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities.[Pubmed] |
| 1999 | M al-Essa | Zellweger syndrome in Saudi Arabia and its distinct features.[Pubmed] | |
| 1999 | C Thai | FEBS Lett. | Synthesis of plasmalogens in eye lens epithelial cells.[Pubmed] |
| 1998 | N Nagan | Biochem. J. | Isolation of a Chinese hamster fibroblast variant defective in dihydroxyacetonephosphate acyltransferase activity and plasmalogen biosynthesis: use of a novel two-step selection protocol.[Pubmed] |
| 1997 | H Thai | FEBS Lett. | Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase.[Pubmed] |
| 1997 | I Singh | Biochem. Mol. Med. | 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] |
| 1997 | M Purdue | Nat. Genet. | Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor.[Pubmed] |
| 1996 | H Hebestreit | Eur. J. Pediatr. | Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.[Pubmed] |
| 1996 | K Burdette | Neurology | Late-onset generalized disorder of peroxisomes.[Pubmed] |
| 1996 | N Shimozawa | Pediatr. Res. | Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.[Pubmed] |
| 1996 | Motley Motley | Biochim. Biophys. Acta | Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation group.[Pubmed] |
| 1996 | Hajra Hajra | Ann. N. Y. Acad. Sci. | Lipid biosynthesis in peroxisomes.[Pubmed] |
| 1995 | R Wanders | J. Inherit. Metab. Dis. | Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells.[Pubmed] |
| 1995 | H Zomer | Biochim. Biophys. Acta | Alkyl dihydroxyacetone phosphate synthase in glycosomes of Trypanosoma brucei.[Pubmed] |
| 1994 | S Emami | Arch Dermatol | 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] |
| 1994 | A Cimini | Cell. Mol. Biol. (Noisy-le-grand) | Effects of Di-(2-ethylhexyl)phthalate on peroxisomes of liver, kidney and brain of lactating rats and their pups.[Pubmed] |
| 1994 | S Stefanini | Biol. Cell | Differentiation of kidney cortex peroxisomes in fetal and newborn rats.[Pubmed] |
| 1993 | H Singh | J. Lipid Res. | Exclusive localization in peroxisomes of dihydroxyacetone phosphate acyltransferase and alkyl-dihydroxyacetone phosphate synthase in rat liver.[Pubmed] |
| 1993 | J Zomer | Biochim. Biophys. Acta | Ether lipid synthesis: purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver.[Pubmed] |
| 1992 | S Zoeller | J. Biol. Chem. | Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomes.[Pubmed] |
| 1992 | S Emami | Arch Dermatol | Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease.[Pubmed] |
| 1992 | H Okamoto | Exp. Cell Res. | Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly.[Pubmed] |
| 1992 | A Heikoop | Hum. Genet. | Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation study.[Pubmed] |
| 1992 | Williams Williams | J. Lipid Res. | HMG-CoA reductase inhibitors perturb fatty acid metabolism and induce peroxisomes in keratinocytes.[Pubmed] |
| 1992 | S Das | J. Biol. Chem. | Biosynthesis of glycerolipid precursors in rat liver peroxisomes and their transport and conversion to phosphatidate in the endoplasmic reticulum.[Pubmed] |
| 1992 | C Samsom | J. Inherit. Metab. Dis. | Zellweger syndrome in a preterm, small for gestational age infant.[Pubmed] |
| 1992 | H Stanczak | Hum. Hered. | Complementation in Zellweger syndrome: biochemical analysis of newly generated peroxisomes.[Pubmed] |
| 1991 | S Brul | J. Inherit. Metab. Dis. | Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome.[Pubmed] |
| 1991 | O Lazo | J. Neurochem. | Postnatal development and isolation of peroxisomes from brain.[Pubmed] |
| 1991 | M Wiemer | Biochim. Biophys. Acta | Phenotypic heterogeneity in cultured skin fibroblasts from patients with disorders of peroxisome biogenesis belonging to the same complementation group.[Pubmed] |
| 1991 | W Lageweg | Biochem. J. | Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver.[Pubmed] |
| 1991 | Wolvetang Wolvetang | Biochim. Biophys. Acta | Factors influencing the latency of the peroxisomal enzyme dihydroxyacetone-phosphate acyltransferase (DHAP-AT) in permeabilized human skin fibroblasts.[Pubmed] |
| 1991 | I Singh | Arch. Biochem. Biophys. | Rhizomelic chondrodysplasia punctata: biochemical studies of peroxisomes isolated from cultured skin fibroblasts.[Pubmed] |
| 1990 | H Pike | J. Pediatr. | Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction.[Pubmed] |
| 1990 | Stevens Stevens | J. Biol. Chem. | Class F Thy-1-negative murine lymphoma cells are deficient in ether lipid biosynthesis.[Pubmed] |
| 1990 | C Wanders | Biochem. Biophys. Res. Commun. | Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome.[Pubmed] |
| 1990 | E Wanders | J. Neurol. Sci. | Infantile phytanic acid storage disease, a disorder of peroxisome biogenesis: a case report.[Pubmed] |
| 1990 | Wolvetang Wolvetang | Biochem. Biophys. Res. Commun. | Latency of the peroxisomal enzyme acyl-CoA:dihydroxyacetonephosphate acyltransferase in digitonin-permeabilized fibroblasts: the effect of ATP and ATPase inhibitors.[Pubmed] |
| 1990 | S Horie | Biochim. Biophys. Acta | Changes in the activities of dihydroxyacetone phosphate and glycerol-3-phosphate acyltransferases in rat liver under various conditions.[Pubmed] |
| 1989 | D Hardeman | Biochim. Biophys. Acta | Topography of ether phospholipid biosynthesis.[Pubmed] |
| 1989 | S Horie | Biochem. J. | Participation of peroxisomes in lipid biosynthesis in the harderian gland of guinea pig.[Pubmed] |
| 1989 | H Singh | Arch. Biochem. Biophys. | Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts.[Pubmed] |
| 1989 | T Zoeller | J. Biol. Chem. | Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome.[Pubmed] |
| 1988 | N Shimozawa | Pediatr. Res. | Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy.[Pubmed] |
| 1988 | Y Suzuki | J. Pediatr. | Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.[Pubmed] |
| 1988 | F Poll-The | Am. J. Hum. Genet. | A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).[Pubmed] |
| 1988 | D Hardeman | Biochim. Biophys. Acta | Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies.[Pubmed] |
| 1988 | H Wanders | Biochem. Biophys. Res. Commun. | Identification of L-pipecolate oxidase in human liver and its deficiency in the Zellweger syndrome.[Pubmed] |
| 1988 | S Brul | J. Clin. Invest. | Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.[Pubmed] |
| 1988 | H Wanders | J. Inherit. Metab. Dis. | Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia.[Pubmed] |
| 1987 | Webber Webber | Arch. Biochem. Biophys. | Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls.[Pubmed] |
| 1987 | K Barth | J. Inherit. Metab. Dis. | A sibship with a mild variant of Zellweger syndrome.[Pubmed] |
| 1987 | G Schutgens | J. Inherit. Metab. Dis. | Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.[Pubmed] |
| 1987 | Patel Patel | Biochem. J. | Peroxisomal localization of glucose-6-phosphate dehydrogenase and pyrophosphate-stimulated dihydroxyacetone-phosphate acyltransferase in mouse kidney.[Pubmed] |
| 1986 | J Vamecq | Am. J. Pathol. | Multiple peroxisomal enzymatic deficiency disorders. A comparative biochemical and morphologic study of Zellweger cerebrohepatorenal syndrome and neonatal adrenoleukodystrophy.[Pubmed] |
| 1986 | R Schutgens | Biochim. Biophys. Acta | Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method.[Pubmed] |
| 1986 | J Wilson | Am. J. Med. Genet. | Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.[Pubmed] |
| 1986 | G Wanders | Eur. J. Pediatr. | 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] |
| 1986 | Ghosh Ghosh | Anal. Biochem. | A rapid method for the isolation of peroxisomes from rat liver.[Pubmed] |
| 1985 | P Mannaerts | Biochem. J. | Comparison of the activities of some peroxisomal and extraperoxisomal lipid-metabolizing enzymes in liver and extrahepatic tissues of the rat.[Pubmed] |
| 1985 | V Lazarow | Pediatr. Res. | Zellweger syndrome: biochemical and morphological studies on two patients treated with clofibrate.[Pubmed] |
| 1985 | Barth Barth | Eur. J. Pediatr. | A milder variant of Zellweger syndrome.[Pubmed] |
| 1985 | Mackness Mackness | Comp. Biochem. Physiol., B | Predominant localization of dihydroxyacetone-phosphate acyltransferase activity in renal peroxisomes of male and female mice.[Pubmed] |
| 1985 | G Schrakamp | J. Lipid Res. | Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.[Pubmed] |
| 1984 | Datta Datta | N. Engl. J. Med. | 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] |
| 1984 | Ballas Ballas | Biochim. Biophys. Acta | Glycerolipid synthetic capacity of rat liver peroxisomes.[Pubmed] |
| 1984 | P Declercq | J. Biol. Chem. | Rat liver dihydroxyacetone-phosphate acyltransferases and their contribution to glycerolipid synthesis.[Pubmed] |
| 1984 | M Wanders | Biochem. Biophys. Res. Commun. | Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome.[Pubmed] |
| 1984 | Hart Hart | Mol. Biochem. Parasitol. | The occurrence of glycosomes (microbodies) in the promastigote stage of four major Leishmania species.[Pubmed] |
| 1982 | Hajra Hajra | Ann. N. Y. Acad. Sci. | Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway.[Pubmed] |
| 1979 | Hajra Hajra | J. Biol. Chem. | Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies).[Pubmed] |
| 0 | Hum. Genet. | A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.[Pubmed] | |
| 0 | J. Biomed. Sci. | Antioxidants attenuate diabetes-induced activation of peroxisomal functions in the rat kidney.[Pubmed] | |
| 0 | Cell Biochem. Funct. | Carnitine prevents cyclic GMP-induced inhibition of peroxisomal enzyme activities.[Pubmed] |