(Q77596072)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

review article

1 reference

title

Lipid metabolism in peroxisomes in relation to human disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

author name string

R J Wanders

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

J M Tager

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

publication date

1 April 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

Molecular Aspects of Medicine

6 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

volume

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

page(s)

69-154

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

The occurrence of diastereomers of phytanic and pristanic acids and their determination by gas-liquid chromatography

6 December 2019

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The 17 beta-oestradiol dehydrogenase of pig endometrial cells is localized in specialized vesicles

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7 January 2021

Molecular cloning of a novel widely expressed human 80 kDa 17 beta-hydroxysteroid dehydrogenase IV

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7 January 2021

The presence of acyl-CoA hydrolase in rat brown-adipose-tissue peroxisomes

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7 January 2021

Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

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7 January 2021

Substrate specificities of 3-oxoacyl-CoA thiolase A and sterol carrier protein 2/3-oxoacyl-CoA thiolase purified from normal rat liver peroxisomes. Sterol carrier protein 2/3-oxoacyl-CoA thiolase is involved in the metabolism of 2-methyl-branched fa

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7 January 2021

Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase

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7 January 2021

Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor alpha (PPARalpha)

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7 January 2021

In vitro labeling of peroxisomal cholesterol with radioactive precursors

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7 January 2021

Biosynthesis of dolichol by rat liver peroxisomes.

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7 January 2021

Signs of testicular insufficiency in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy: a retrospective study

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7 January 2021

Brain MRI and electrophysiologic abnormalities in preclinical and clinical adrenomyeloneuropathy.

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7 January 2021

Alpha-decarboxylation, an important pathway for degradation of phytanic acid in animals

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7 January 2021

Molecular cloning and further characterization of rat peroxisomal trihydroxycoprostanoyl-CoA oxidase

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7 January 2021

Enhancement of long-chain acyl-CoA hydrolase activity in peroxisomes and mitochondria of rat liver by peroxisomal proliferators

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7 January 2021

Compartmentalization of cholesterol biosynthesis. Conversion of mevalonate to farnesyl diphosphate occurs in the peroxisomes

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7 January 2021

Evidence for biosynthesis of plasmenylcholine from plasmenylethanolamine in HL-60 cells

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7 January 2021

Purification and properties of carnitine acetyltransferase from human liver

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7 January 2021

The yeast YKL741 gene situated on the left arm of chromosome XI codes for a homologue of the human ALD protein.

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7 January 2021

Nucleotide sequence of human peroxisomal 3-oxoacyl-CoA thiolase

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7 January 2021

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

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7 January 2021

Carnitine acyltransferase and acyl-coenzyme A hydrolase activities in human liver. Quantitative analysis of their subcellular localization

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7 January 2021

Thiolase involved in bile acid formation

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7 January 2021

Alkylacyl glycerophosphoinositol in human and bovine erythrocytes. Molecular species composition and comparison with glycosyl-inositolphospholipid anchors of erythrocyte acetylcholinesterases

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7 January 2021

Molecular cloning of human phosphomevalonate kinase and identification of a consensus peroxisomal targeting sequence

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7 January 2021

Nerve conduction studies in adrenomyeloneuropathy

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7 January 2021

Purification and mechanism of delta 3,delta 5-t-2,t-4-dienoyl-CoA isomerase from rat liver.

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7 January 2021

Molecular cloning and sequence analysis of the rat liver carnitine octanoyltransferase cDNA, its natural gene and the gene promoter

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7 January 2021

Adrenoleukodystrophy. The chain shortening of erucic acid (22:1(n-9)) and adrenic acid (22:4(n-6)) is deficient in neonatal adrenoleukodystrophy and normal in X-linked adrenoleukodistrophy skin fibroblasts

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7 January 2021

Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay.

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7 January 2021

Divergent sequences in the 5' region of cDNA suggest alternative splicing as a mechanism for the generation of carnitine acetyltransferases with different subcellular localizations

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7 January 2021

alpha-Oxidation of 3-methyl-substituted fatty acids in rat liver. Production of formic acid instead of CO2, cofactor requirements, subcellular localization and formation of a 2-hydroxy-3-methylacyl-CoA intermediate

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7 January 2021

Formation of a 2-methyl-branched fatty aldehyde during peroxisomal α-oxidation

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7 January 2021

Production of formyl-CoA during peroxisomal alpha-oxidation of 3-methyl-branched fatty acids

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7 January 2021

cDNA cloning, recombinant expression, and site-directed mutagenesis of bovine liver carnitine octanoyltransferase--Arg505 binds the carboxylate group of carnitine

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7 January 2021

Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes.

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7 January 2021

Peroxisomes (microbodies and related particles)

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7 January 2021

Nucleotide sequence of human alkyl-dihydroxyacetonephosphate synthase cDNA reveals the presence of a peroxisomal targeting signal 2.

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7 January 2021

Polymerase chain reaction-based cloning of alkyl-dihydroxyacetonephosphate synthase complementary DNA from guinea pig liver

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7 January 2021

Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiency

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7 January 2021

Studies on the urinary excretion of thromboxane B2 in Zellweger patients and control subjects: evidence for a major role for peroxisomes in the beta-oxidative chain-shortening of thromboxane B2.

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7 January 2021

Metabolism of prostaglandin F2 alpha in Zellweger syndrome. Peroxisomal beta-oxidation is a major importance for in vivo degradation of prostaglandins in humans

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7 January 2021

Further characterization of the peroxisomal 3-hydroxyacyl-CoA dehydrogenases from rat liver. Relationship between the different dehydrogenases and evidence that fatty acids and the C27 bile acids di- and tri-hydroxycoprostanic acids are metabolized

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7 January 2021

Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal beta-oxidation of pristanic acid

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7 January 2021

Identification and characterization of the 2-enoyl-CoA hydratases involved in peroxisomal beta-oxidation in rat liver

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7 January 2021

Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single gene.

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7 January 2021

Cytochemical localization of peroxidatic activity of catalase in rat hepatic microbodies (peroxisomes).

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7 January 2021

Δ3,5-Δ2,4-Dienoyl-CoA Isomerase from Rat Liver

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7 January 2021

Accumulation of phytanic acid alpha-oxidation intermediates in Zellweger fibroblasts

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7 January 2021

Isolation and characterization of rat and human cDNAs encoding a novel putative peroxisomal enoyl-CoA hydratase

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7 January 2021

Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy

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7 January 2021

Properties of mitochondria and peroxisomal enoyl-CoA hydratases from rat liver

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7 January 2021

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

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7 January 2021

Pyrene dodecanoic acid coenzyme A ester: peroxisomal oxidation and chain shortening

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7 January 2021

Subcellular distribution and properties of acyl/alkyl dihydroxyacetone phosphate reductase in rodent livers

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7 January 2021

A growing interest in bacterial ether lipids

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7 January 2021

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome.

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7 January 2021

Regulation of the mevalonate pathway

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7 January 2021

The Saccharomyces cerevisiae peroxisomal 2,4-dienoyl-CoA reductase is encoded by the oleate-inducible gene SPS19.

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7 January 2021

Biosynthesis of phosphatidic acid in rat brain via acyl dihydroxyacetone phosphate

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7 January 2021

Lipid biosynthesis in peroxisomes

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7 January 2021

The existence of two mitochondrial isoforms of 2,4-dienoyl-CoA reductase in the rat.

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7 January 2021

Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies.

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7 January 2021

Peroxisomal beta-oxidation: enzymology and molecular biology

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7 January 2021

Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy

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7 January 2021

Peroxisomes contain delta 3,5,delta 2,4-dienoyl-CoA isomerase and thus possess all enzymes required for the beta-oxidation of unsaturated fatty acids by a novel reductase-dependent pathway

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7 January 2021

IDP3 encodes a peroxisomal NADP-dependent isocitrate dehydrogenase required for the beta-oxidation of unsaturated fatty acids

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7 January 2021

Refsum's disease: characterization of the enzyme defect in cell culture

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7 January 2021

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).

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7 January 2021

Primary hyperparathyroidism associated with pancytosis

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7 January 2021

ABC Transporters: From Microorganisms to Man

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7 January 2021

Peroxisomal beta-oxidation and polyunsaturated fatty acids

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7 January 2021

cDNA cloning of rat liver 2,4-dienoyl-CoA reductase

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7 January 2021

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

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7 January 2021

cDNA cloning of the human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase bifunctional enzyme and localization to chromosome 3q26.3-3q28: a free left Alu Arm is inserted in the 3' noncoding region

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7 January 2021

Alkyldihydroxyacetonephosphate synthase from guinea pig liver peroxisomes

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7 January 2021

α-Oxidation of 3-methyl-substituted fatty acids in rat liver

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7 January 2021

Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondria

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7 January 2021

Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans

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7 January 2021

Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctata

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7 January 2021

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene

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7 January 2021

Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's disease

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7 January 2021

Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase

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7 January 2021

Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein

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7 January 2021

REFSUM'S DISEASE (HERECOPATHIA ATACTICA POLYNEURITIFORMIS): AN INBORN ERROR OF LIPID METABOLISM WITH STORAGE OF 3,7,11,15-TETRAMETHYL HEXADECANOIC ACID. II. ISOLATION AND IDENTIFICATION OF THE STORAGE PRODUCT

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7 January 2021

Membrane topology of the 22 kDa integral peroxisomal membrane protein

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7 January 2021

3-Hydroxy-3-methylglutaryl coenzyme A reductase localization in rat liver peroxisomes and microsomes of control and cholestyramine-treated animals: quantitative biochemical and immunoelectron microscopical analyses

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7 January 2021

Assembly and function of the two ABC transporter proteins encoded in the human major histocompatibility complex

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7 January 2021

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy

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7 January 2021

X-linked adrenoleukodystrophy with non-diagnostic plasma very long chain fatty acids

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7 January 2021

[ON THE PRESENCE OF 3,7,11,15-TETRAMETHYLHEXADECANOIC ACID (PHYTANIC ACID) IN THE CHOLESTEROL ESTERS AND OTHER LIPOID FRACTIONS OF THE ORGANS IN A CASE OF A DISEASE OF UNKNOWN ORIGIN (POSSIBLY HEREDOPATHIA ATACTICA POLYNEURITIFORMIS, REFSUM'S SYNDR

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7 January 2021

Isolation and characterization of cDNA for human 120 kDa mitochondrial 2,4-dienoyl-coenzyme A reductase

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7 January 2021

Cell compartmentalization of cholesterol biosynthesis

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7 January 2021

beta-oxidation of fatty acids in mitochondria, peroxisomes, and bacteria: a century of continued progress

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7 January 2021

Degradation of unsaturated fatty acids. Identification of intermediates in the degradation of cis-4-decenoly-CoA by extracts of beef-liver mitochondria

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7 January 2021

Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver

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7 January 2021

Biosynthesis of choline plasmalogens in neonatal rat myocytes

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7 January 2021

Porcine 80-kDa protein reveals intrinsic 17 beta-hydroxysteroid dehydrogenase, fatty acyl-CoA-hydratase/dehydrogenase, and sterol transfer activities

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7 January 2021

Single-channel analysis of a large conductance channel in peroxisomes from rat liver.

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7 January 2021

Biochemical mechanisms of induction of hepatic peroxisome proliferation

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7 January 2021

Double bond removal from odd-numbered carbons during peroxisomal beta-oxidation of arachidonic acid requires both 2,4-dienoyl-CoA reductase and delta 3,5,delta 2,4-dienoyl-CoA isomerase

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7 January 2021

The 'ins' and 'outs' of mitochondrial membrane channels

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7 January 2021

Comparison of the carnitine acyltransferase activites from rat liver peroxisomes and microsomes

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7 January 2021

Severe deficiency of docosahexaenoic acid in peroxisomal disorders: a defect of delta 4 desaturation?

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7 January 2021

Blood polyunsaturated fatty acids in patients with peroxisomal disorders. A multicenter study

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7 January 2021

PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes

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7 January 2021

Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders

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7 January 2021

The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis

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7 January 2021

Phytanic acid alpha-oxidation in rat liver peroxisomes. Production of alpha-hydroxyphytanoyl-CoA and formate is enhanced by dioxygenase cofactors

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identification of PAHX, a Refsum disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Properties of Peroxisomal 3-Ketoacyl-CoA Thiolase from Rat Liver1

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification and properties of carnitine octanoyltransferase and carnitine palmitoyltransferase from rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identity of long-chain acyl-coenzyme A synthetase of microsomes, mitochondria, and peroxisomes in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Localization of the oxidative defect in phytanic acid degradation in patients with Refsum's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Clinical Aspects of Adrenoleukodystrophy and Adrenomyeloneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

A 31P NMR study of the internal pH of yeast peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Visualization of peroxisomes (microbodies) and mitochondria with diaminobenzidine

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification of peroxisomal acyl-CoA: dihydroxyacetonephosphate acyltransferase from human placenta

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The structure of the human sterol carrier protein X/sterol carrier protein 2 gene (SCP2).

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Human sterol carrier protein x/sterol carrier protein 2 gene has two promoters

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Fatty acid products of peroxisomal β-oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identification of the cDNA clone which encodes the 58-kDa protein containing the amino acid sequence of rat liver non-specific lipid-transfer protein (sterol-carrier protein 2). Homology with rat peroxisomal and mitochondrial 3-oxoacyl-CoA thiolases

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification and properties of acyl-CoA oxidase from rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Nucleotide sequence of the ERG12 gene of Saccharomyces cerevisiae encoding mevalonate kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Mitochondrial metabolite transporters.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Substrate stereospecificity in oxidation of (25S)-3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoyl-CoA by peroxisomal trihydroxy-5 beta-cholestanoyl-CoA oxidase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Detection of a homologous series of C26-C38 polyenoic fatty acids in the brain of patients without peroxisomes (Zellweger's syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The occurrence of polyenoic very long chain fatty acids with greater than 32 carbon atoms in molecular species of phosphatidylcholine in normal and peroxisome-deficient (Zellweger's syndrome) brain

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Formic acid is a product of the alpha-oxidation of fatty acids by human skin fibroblasts: deficiency of formic acid production in peroxisome-deficient fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Very long chain fatty acids in higher animals--a review

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Recombinant 2-enoyl-CoA hydratase derived from rat peroxisomal multifunctional enzyme 2: role of the hydratase reaction in bile acid synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peroxisomal multifunctional enzyme of beta-oxidation metabolizing D-3-hydroxyacyl-CoA esters in rat liver: molecular cloning, expression and characterization

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peroxisomal lipid metabolism.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The Membrane of Leaf Peroxisomes Contains a Porin-like Channel

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

A specific porin is involved in the malate shuttle of leaf peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Permeability properties of the porin of spinach leaf peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Isolation and characterization of a cDNA encoding Arabidopsis thaliana mevalonate kinase by genetic complementation in yeast.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Alkylacylglycerol molecular species in the glycosylinositol phospholipid membrane anchor of bovine erythrocyte acetylcholinesterase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Subcellular distribution and characteristics of trihydroxycoprostanoyl-CoA synthetase in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification and properties of an alpha-methylacyl-CoA racemase from rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification and characterization of an alpha-methylacyl-CoA racemase from human liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Molecular cloning of cDNA species for rat and mouse liver alpha-methylacyl-CoA racemases

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Stereochemistry of peroxisomal and mitochondrial beta-oxidation of alpha-methylacyl-CoAs

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identification of a fourth half ABC transporter in the human peroxisomal membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Structure and lipid distribution of polyenoic very-long-chain fatty acids in the brain of peroxisome-deficient patients (Zellweger syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Distinct long chain and very long chain fatty acyl CoA synthetases in rat liver peroxisomes and microsomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The subcellular localization of phytanic acid oxidase in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Conversion of U-C14-phytol to phytanic acid and its oxidation in heredopathia atactica polyneuritiformis

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Studies on the metabolic error in Refsum's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Metabolism of saturated and polyunsaturated fatty acids by normal and Zellweger syndrome skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The in vitro permeability of yeast peroxisomal membranes is caused by a 31 kDa integral membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Compartmentation of dicarboxylic acid beta-oxidation in rat liver: importance of peroxisomes in the metabolism of dicarboxylic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Contribution of peroxisomal beta-oxidation system to the chain-shortening of N-(alpha-methylbenzyl)azelaamic acid in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The PAL1 gene product is a peroxisomal ATP-binding cassette transporter in the yeast Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The formation of alpha-hydroxy phytanic acid from phytanic acid in mammalian tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification and properties of rat liver peroxisomal very-long-chain acyl-CoA synthetase.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Molecular cloning of cDNA encoding rat very long-chain acyl-CoA synthetase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Immunogold studies on peroxisomes: review of the localization of specific proteins in vertebrate peroxisomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The microsomal dicarboxylyl-CoA synthetase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Delay in diagnosis of X-linked adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindreds

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peripheral nerve abnormalities in adrenomyeloneuropathy: a clinical and electrodiagnostic study

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peroxisomal beta-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peroxisomal beta-oxidation of 2-methyl-branched acyl-CoA esters: stereospecific recognition of the 2S-methyl compounds by trihydroxycoprostanoyl-CoA oxidase and pristanoyl-CoA oxidase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Rat pristanoyl-CoA oxidase. cDNA cloning and recognition of its C-terminal (SQL) by the peroxisomal-targeting signal 1 receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Resolution of the phytanic acid alpha-oxidation pathway: identification of pristanal as product of the decarboxylation of 2-hydroxyphytanoyl-CoA

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell system

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Subcellular Compartmentation of Glycolytic Intermediates in Trypanosoma brucei

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

First prenatal diagnosis of acyl-CoA oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: Implications for Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Studies on phytanic acid alpha-oxidation in rat liver and cultured human skin fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Sterol carrier protein X (SCPx) is a peroxisomal branched-chain beta-ketothiolase specifically reacting with 3-oxo-pristanoyl-CoA: a new, unique role for SCPx in branched-chain fatty acid metabolism in peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Immunocytochemical evidence for the acidic nature of peroxisomes in methylotrophic yeasts

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Peroxisomal bifunctional enzyme deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Phytanic acid must be activated to phytanoyl-CoA prior to its alpha-oxidation in rat liver peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Mitochondrial oxidation of phytanic acid in human and monkey liver: Implication that Refsum's disease is not a peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Purification of dihydroxyacetone phosphate acyltransferase from guinea pig liver peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Transgenic mouse model of kidney disease: Insertional inactivation of ubiquitously expressed gene leads to nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Characterization of acyl-CoA thioesterase activity in isolated rat liver peroxisomes. Partial purification and characterization of a long-chain acyl-CoA thioesterase

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Phospholipid transfer proteins revisited

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The reactions catalyzed by the inducible bifunctional enzyme of rat liver peroxisomes cannot lead to the formation of bile acids

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Participation of peroxisomal beta-oxidation system in the chain-shortening of a xenobiotic acyl compound

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Participation of the peroxisomal beta-oxidation system in the chain-shortening of PCA16, a metabolite of the cytosine arabinoside prodrug, YNKO1, in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

Ether lipid synthesis: purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

The glomerulosclerosis gene Mpv17 encodes a peroxisomal protein producing reactive oxygen species

1 reference

https://api.crossref.org/works/10.1016%2FS0098-2997%2898%2900003-X

7 January 2021

10.1016/S0098-2997(98)00003-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9827430%20AND%20SRC:MED&resulttype=core&format=json

6 December 2019

1 reference