GNPAT by Pubmed references

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 Bikramjit Raychaudhury Med. Sci. Monit. Peroxisomal function is altered during leishmania infection.[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]
2002 J Gootjes Neurology Biochemical markers predicting survival in peroxisome biogenesis disorders.[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]
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]
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 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]
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]
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-H√ľnermann 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 J Zomer Biochim. Biophys. Acta Ether lipid synthesis: purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver.[Pubmed]
1993 H Singh J. Lipid Res. Exclusive localization in peroxisomes of dihydroxyacetone phosphate acyltransferase and alkyl-dihydroxyacetone phosphate synthase in rat 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 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]
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]
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]
1990 H Pike J. Pediatr. Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction.[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 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]
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]
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 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]
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]
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]