A. Poulos

发表

Monoenoic fatty acids in human brain lipids: Isomer identification and distribution

D. Johnson, K. Beckman, A. Fellenberg, 1992, Lipids.

The quantitation of plasma phytanic acid by mass fragmentography.

A. Poulos, G. Phillipou, 1976, Clinica chimica acta; international journal of clinical chemistry.

Simultaneous deficiency of sphingolipid activator proteins 1 and 2 is caused by a mutation in the initiation codon of their common gene.

A. Poulos, J. Weber, M. Schröder, 1992, The Journal of biological chemistry.

Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: Biochemical signs of combined sphingolipidoses

A. Poulos, M. Popp, T. Grisar, 1989, European Journal of Pediatrics.

Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase.

A. Poulos, K. Harzer, B. Kustermann-Kuhn, 1992, The Biochemical journal.

Activation of Mitogen-activated Protein Kinase by Arachidonic Acid in Rat Liver Epithelial WB Cells by a Protein Kinase C-dependent Mechanism (*)

A. Poulos, D. Rathjen, A. Ferrante, 1995, The Journal of Biological Chemistry.

Effects of β-oxa and β-thia polyunsaturated fatty acids on agonist-induced increase in endothelial cell adhesion molecules

B. S. Robinson, A. Poulos, A. Ferrante, 2007, Lipids.

Neutrophil oxygen radical generation. Synergistic responses to tumor necrosis factor and mono/polyunsaturated fatty acids.

D. P. Harvey, Yedan Li, A. Poulos, 1996, The Journal of clinical investigation.

Effect of fatty acid structure on neutrophil adhesion, degranulation and damage to endothelial cells.

B. S. Robinson, A. Poulos, A. Ferrante, 1995, Atherosclerosis.

Neutrophil migration inhibitory properties of polyunsaturated fatty acids. The role of fatty acid structure, metabolism, and possible second messenger systems.

D. P. Harvey, D. Johnson, B. S. Robinson, 1994, The Journal of clinical investigation.

The neutrophil respiratory burst. Responses to fatty acids, N-formylmethionylleucylphenylalanine and phorbol ester suggest divergent signalling mechanisms.

D. P. Harvey, B. S. Robinson, A. Poulos, 1991, European journal of biochemistry.

Carrageenan-Induced Paw Reaction and Delayed-Type Hypersensitivity , and Proliferation , Cytokine Production ,3 , Inhibits T Lymphocyte n-Oxa 21 : 3 β Acid , A Novel Long Chain Polyunsaturated Fatty

B. S. Robinson, A. Poulos, A. Ferrante, 2001 .

A Novel Long Chain Polyunsaturated Fatty Acid, β-Oxa 21:3n-3, Inhibits T Lymphocyte Proliferation, Cytokine Production, Delayed-Type Hypersensitivity, and Carrageenan-Induced Paw Reaction and Selectively Targets Intracellular Signals1

B. S. Robinson, A. Poulos, D. Rathjen, 2001, The Journal of Immunology.

Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders

J. Christodoulou, A. Poulos, C. Chow, 2005, Virchows Archiv A.

Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta): increase of very long chain fatty acids in brain discloses a peroxisomal disorder

H. Bernheimer, A. Poulos, B. Molzer, 2004, Acta Neuropathologica.

Molecular Species of Phosphatidylcholine Containing Very Long Chain Fatty Acids in Human Brain: Enrichment in X‐Linked Adrenoleukodystrophy Brain and Diseases of Peroxisome Biogenesis Brain

D. Johnson, A. Poulos, P. Sharp, 1991, Journal of neurochemistry.

Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts.

A. Poulos, H. Singh, S. Usher, 1989, Archives of biochemistry and biophysics.

Accumulation and defective β‐oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants

A. Poulos, H. Singh, B. Paton, 1986, Clinical genetics.

Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: Plasma changes and skin fibroblast phytanic acid oxidase

D. Danks, A. Fellenberg, A. Poulos, 1985, Human Genetics.

Adrenomyeloneuropathy--clinical and biochemical diagnosis.

S. Berkovic, A. Fellenberg, A. Poulos, 1983, Australian and New Zealand journal of medicine.

Docosahexanoic acid (22:6, n‐3) but not eicosapentaenoic acid (20:5, n‐3) can induce neutrophil‐mediated injury of cultured endothelial cells: involvement of neutrophil elastase

D. P. Harvey, A. Poulos, A. Ferrante, 1993, Journal of leukocyte biology.

Synthesis of polyunsaturated β-thia and γ-thia fatty acids from naturally derived polyunsaturated fatty alcohols and in vitro evaluation of their susceptibility to β-oxidation

A. Poulos, A. Ferrante, D. Rathjen, 1998 .

Partial synthesis of [1-14C]phytanic acid

D. Johnson, A. Poulos, E. Barone, 2006, Lipids.

Diagnosis of Refsum's disease using [1‐14C]phytanic acid as substrate

A. Poulos, 1981, Clinical genetics.

ENZYMOLOGICAL DIAGNOSIS OF A GROUP OF LYSOSOMAL STORAGE DISEASES: REVIEW OF 5‐YEAR EXPERIENCE OF 1600 PATIENT‐SAMPLE REFERRALS

A. Poulos, A. Pollard, G. Hill, 1980, The Medical journal of Australia.

The bile salt activation of leucocyte sphingolipid hydrolase activity and the modifying effects of triton X-100.

K. Beckman, A. Poulos, 1980, Clinica chimica acta; international journal of clinical chemistry.

The effect of the interdependence of protein and bile salt concentrations on the measurement of cerebroside sulphate sulphatase activity in human leucocyte and fibroblast extracts.

K. Beckman, A. Poulos, A. Pollard, 1980, Biochimica et biophysica acta.

Sphingomyelinase in cultured skin fibroblasts from normal and Niemann‐Pick type C patients

N. Hudson, A. Poulos, E. Ranieri, 1983, Clinical genetics.

Dolichol metabolism in cultured skin fibroblasts from patients with “neuronal” ceroid lipofuscinosis (Batten's disease)

A. Poulos, B. Paton, 1984, Journal of Inherited Metabolic Disease.

Diagnosis of Tay-Sachs disease using [3H]N-acetylneuraminic acid labelled GM2 ganglioside as substrate.

A. Poulos, W. Carey, J. Holding, 1982, Clinica chimica acta; international journal of clinical chemistry.

Studies on the activation of the enzymatic hydrolysis of sphingomyelin liposomes.

A. Poulos, J. Callahan, E. Ranieri, 1984, Biochimica et biophysica acta.

Identification of a catalase-negative sub-population of peroxisomes induced in mouse liver by clofibrate.

D. Crane, A. Poulos, C. Masters, 1991, Biochimica et biophysica acta.

Synthesis of hydroperoxide and perketal derivatives of polyunsaturated fatty acids as potential antimalarial agents

A. Poulos, A. Ferrante, L. Kumaratilake, 1998 .

Enhancement of neutrophil-mediated killing of Plasmodium falciparum asexual blood forms by fatty acids: importance of fatty acid structure

B. S. Robinson, A. Poulos, A. Ferrante, 1997, Infection and immunity.

Hepatic storage of bis(monoacylglycerol) phosphate without concomitant storage of sphingomyelin in a 72‐year‐old patient with a partial deficiency of sphingomyelinase

K. Beckman, A. Poulos, A. Pollard, 1982, Clinical genetics.

A rapid method for the estimation of β-galacto-cerebrosidase, β-glucocerebrosidase and sphingomyelinase activities in leukocytes

A. Poulos, A. Pollard, 1976 .

Establishment of a normal range of morphometric values for peroxisomes in paediatric liver

A. J. Bourne, A. Poulos, J. L. Hughes, 2005, Virchows Archiv A.

The misleading presence of glucose in lipid extracts from human liver.

K. Beckman, A. Poulos, 1978, Clinica chimica acta; international journal of clinical chemistry.

Plasmacis-dec-4-enoic acid measured by isotope dilution mass spectrometry; an improved assay to diagnose medium-chain acyl-CoA dehydrogenase deficiency

D. Johnson, A. Poulos, E. Robertson, 1994, Journal of Inherited Metabolic Disease.

X-linked adrenoleukodystrophy: the Australasian experience.

A. Poulos, E. Kirk, B. Carey, 1998, American journal of medical genetics.

Pitfalls in the prenatal diagnosis of peroxisomal β‐oxidation defects by chorionic villus sampling

A. Poulos, E. Robertson, W. Carey, 1994, Prenatal diagnosis.

Novel molecular species of sphingomyelin containing 2-hydroxylated polyenoic very-long-chain fatty acids in mammalian testes and spermatozoa.

D. Johnson, B. S. Robinson, A. Poulos, 1992, The Journal of biological chemistry.

Differences in the metabolism of eicosatetraenoic (20:4(n - 6)), tetracosatetraenoic (24:4(n - 6)) and triacontatetraenoic (30:4(n - 6)) acids in human neutrophils.

D. Johnson, B. S. Robinson, A. Poulos, 1994, Biochimica et biophysica acta.

Identification of 3α,7α,12α-trihydroxy-5β-cholestan-26-oic acid, an intermediate in cholic acid synthesis, in the plasma of patients with infantile Refsum's disease

A. Poulos, M. Whiting, 1985, Journal of Inherited Metabolic Disease.

Inhibition of gap junctional communication by polyunsaturated fatty acids in WB cells: evidence that connexin 43 is not hyperphosphorylated.

B. S. Robinson, A. Poulos, A. Ferrante, 1995, Carcinogenesis.

Exclusive localization in peroxisomes of dihydroxyacetone phosphate acyltransferase and alkyl-dihydroxyacetone phosphate synthase in rat liver.

K. Beckman, A. Poulos, H. Singh, 1993, Journal of lipid research.

Mitochondrial and Peroxisomal β‐Oxidation of Stearic and Lignoceric Acids by Rat Brain

A. Poulos, H. Singh, S. Usher, 1989, Journal of neurochemistry.

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

A. Poulos, H. Singh, 1988, Archives of biochemistry and biophysics.

Very long chain fatty acid β-oxidation by rat liver mitochondria and peroxisomes

A. Poulos, Harmeet Singh, N. Derwas, 1987 .

Very long chain fatty acid beta-oxidation by subcellular fractions of normal and Zellweger syndrome skin fibroblasts.

A. Poulos, H. Singh, N. Derwas, 1987, Archives of biochemistry and biophysics.

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.

D. Johnson, A. Poulos, C. Easton, 1988, The Biochemical journal.

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

D. Johnson, A. Fellenberg, A. Poulos, 1986, The Biochemical journal.

Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation.

A. Poulos, H. Singh, J. M. Street, 1990, The Biochemical journal.

Antimalarial properties of n-3 and n-6 polyunsaturated fatty acids: in vitro effects on Plasmodium falciparum and in vivo effects on P. berghei.

B. S. Robinson, A. Poulos, A. Ferrante, 1992, The Journal of clinical investigation.

Synthesis of very long chain fatty acid methyl esters

A. Poulos, C. Easton, M. Kling, 1993 .

Oxidation of oxa and thia fatty acids and related compounds catalysed by 5- and 15-lipoxygenase.

A. Poulos, A. Ferrante, D. Rathjen, 2001, Bioorganic & medicinal chemistry.

Activation of neutral sphingomyelinase in human neutrophils by polyunsaturated‘qc fatty acids

B. S. Robinson, A. Poulos, A. Ferrante, 1997, Immunology.

A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders.

D. Johnson, A. Poulos, H. Singh, 1990, Journal of lipid research.

Rhizomelic chondrodysplasia punctata: clinical, pathologic, and biochemical findings in two patients.

D. Johnson, K. Beckman, A. Fellenberg, 1988, The Journal of pediatrics.

Patterns of Refsum's disease. Phytanic acid oxidase deficiency.

A. Poulos, A. Pollard, J. Mitchell, 1984, Archives of disease in childhood.

Peroxisomal L-Pipecolic Acid Oxidation Is Deficient in Liver from Zellweger Syndrome Patients

H. Moser, D. Danks, A. Poulos, 1989, Pediatric Research.

Antenatal diagnosis of infantile Refsum's disease

B. Poll-The, A. Poulos, J. Saudubray, 1985, Clinical genetics.

Preparation and characterisation of tritiated derivates of galactosylceramide and glucosylceramide

A. Poulos, A. Pollard, 1978 .

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.

D. Johnson, A. Poulos, C. Easton, 1993, The Biochemical journal.

The rapid assay of cerebroside sulphate sulphatase (sulphatidase) using [3H]cerebroside sulphate as substrate.

K. Beckman, A. Poulos, 1978, Clinica chimica acta; international journal of clinical chemistry.

Trihexosylceramide α-galactosidase of human leucocytes

K. Beckman, A. Poulos, 1978 .

The estimation of sphingolipids by gas chromatography-chemical ionization mass spectrometry of their derived aldehydes with particular reference to the ceramides of children's plasma.

A. Poulos, G. Phillipou, A. Pollard, 1979, Analytical biochemistry.

Very long chain fatty acids in higher animals—A review

A. Poulos, 2006, Lipids.

Very long chain fatty acids in X‐linked adrenoleukodystrophy brain after treatment with Lorenzo's oil

K. Beckman, A. Poulos, R. Gibson, 1994, Annals of neurology.

Glyceryl ethers in peroxisomal disease

D. Johnson, K. Beckman, A. Poulos, 1991, Clinical genetics.

Lipid metabolism in Zellweger's syndrome.

A. Poulos, 1989, Progress in lipid research.

Gas chromatography-mass spectrometry of fatty aldehydes and their oxime derivatives

A. Poulos, G. Phillipou, 1978 .

Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction

H. Moser, R. Wanders, R. Schutgens, 1986, Journal of Inherited Metabolic Disease.

Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: studies in four children.

A. Poulos, R. Weleber, S. Budden, 1986, The Journal of pediatrics.

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

A. Poulos, M. Whiting, P. Sharp, 1984, Clinical genetics.

Effect of exogenous fatty acids with greater than 22 carbon atoms (very long chain fatty acids) on superoxide production by human neutrophils.

D. Johnson, B. S. Robinson, A. Poulos, 1994, Journal of immunology.

Effect of tumor necrosis factor-alpha on the metabolism of arachidonic acid in human neutrophils.

B. S. Robinson, A. Poulos, A. Ferrante, 1996, Journal of lipid research.

Phytanic acid oxidase deficiency

A. Poulos, A. Pollard, G. Mortimer, 1984 .

Partial deficiency of dihydroxyacetone phosphate acyltransferase activity in both classical and infantile Refsum's diseases

A. Poulos, B. Paton, J. V. Crugten, 1986, Journal of Inherited Metabolic Disease.

Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years

A. Poulos, E. Robertson, J. Manson, 1988, European Journal of Pediatrics.

Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders

A. Poulos, J. Saudubray, O. Skjeldal, 2004, Human Genetics.

Autopsy findings in two siblings with infantile Refsum disease

J. Christodoulou, D. Danks, A. Fellenberg, 2004, Acta Neuropathologica.

Identification of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid, an intermediate in cholic acid synthesis, in the plasma of patients with infantile Refsum's disease.

A. Poulos, M. Whiting, 1985, Journal of inherited metabolic disease.

Plasma and skin fibroblast C26 fatty acids in infantile Refsum's disease

A. Poulos, P. Sharp, 1984, Neurology.

Peroxisomal integral membrane proteins in livers of patients with Zellweger syndrome, infantile Refsum's disease and X-linked adrenoleukodystrophy

H. Moser, D. Danks, A. Poulos, 1988, Journal of Inherited Metabolic Disease.

Prenatal diagnosis of zellweger's syndrome by chorionic villus sampling‐and a caveat

A. Poulos, E. Robertson, W. Carey, 1986, Prenatal diagnosis.

Prenatal diagnosis of Zellweger syndrome and related disorders: Impaired degradation of phytanic acid

B. Poll-The, A. Poulos, E. Christensen, 1986, European Journal of Pediatrics.

Peroxisomal P-oxidation of branched chain fatty acids in human skin fibroblasts

A. Poulos, David W. Johnson, Harmeet Singh, 2002 .

Peroxisomal beta-oxidation of branched chain fatty acids in human skin fibroblasts.

D. Johnson, A. Poulos, H. Singh, 1992, Journal of lipid research.

Plasma polyenoic very‐long‐chain fatty acids in peroxisomal disease

D. Johnson, A. Poulos, P. Sharp, 1989, Neurology.

β-oxidation of very-long-chain fatty acids and their coenzyme A derivatives by human skin fibroblasts

A. Poulos, Harmeet Singh, N. Derwas, 1987 .

A comparative study of stearic and lignoceric acid oxidation by human skin fibroblasts.

A. Poulos, H. Singh, 1986, Archives of biochemistry and biophysics.

Morphometry of peroxisomes and immunolocalisation of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders

D. Crane, A. Poulos, E. Robertson, 2005, Virchows Archiv A.

Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects.

D. Crane, A. Poulos, B. Paton, 1996, The Journal of clinical investigation.

Inherited Peroxisomal Disorders: Defects in the Oxidation of Very Long Chain Fatty Acids and Phytanic Acid

A. Fellenberg, A. Poulos, David W. Johnson, 1987 .

Ultrastructure and immunocytochemistry of hepatic peroxisomes in rhizomelic chondrodysplasia punctata

D. Sillence, D. Crane, A. Poulos, 1992, European Journal of Pediatrics.

Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction

D. Johnson, A. Fellenberg, A. Poulos, 1988, European Journal of Pediatrics.

Isotope labelling of lipids using the Favorsky rearrangement

A. Poulos, David W. Johnson, 1989 .

Syntheses of deuterium-labelled pristanic and phytanic acids

A. Poulos, David W. Johnson, 1988 .

Beta-oxidation of very-long-chain fatty acids and their coenzyme A derivatives by human skin fibroblasts.

A. Poulos, H. Singh, N. Derwas, 1987, Archives of biochemistry and biophysics.

Very long-chain fatty acids in peroxisomal disease.

D. Johnson, K. Beckman, B. S. Robinson, 1992, Advances in experimental medicine and biology.

Polyunsaturated Nitroalkanes and Nitro‐Substituted Fatty Acids.

A. Poulos, A. Ferrante, D. Rathjen, 2001 .

Normal dolichol concentration in urine sediments from four patients with neuronal ceroid lipofuscinosis (Batten's disease)

A. Poulos, B. Paton, 1987, Journal of Inherited Metabolic Disease.

Determination of phospholipid base structure by CA MIKES mass spectrometry.

D. Johnson, A. Poulos, C. Easton, 1988, Journal of lipid research.

Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group.

J. Christodoulou, A. Poulos, Y. Suzuki, 1995, The Journal of pediatrics.

Studies on the Activation of Sphingomyelinase Activity in Niemann-Pick Type A, B, and C Fibroblasts: Enzymological Differentiation of Types A and B

A. Poulos, J. Callahan, E. Ranieri, 1984, Pediatric Research.

Unique molecular species of phosphatidylcholine containing very-long-chain (C24-C38) polyenoic fatty acids in rat brain.

D. Johnson, B. S. Robinson, A. Poulos, 1990, The Biochemical journal.

Long and very long chain polyunsaturated fatty acids of the n-6 series in rat seminiferous tubules. Active desaturation of 24:4n-6 to 24:5n-6 and concomitant formation of odd and even chain tetraenoic and pentaenoic fatty acids up to C32.

D. Johnson, B. S. Robinson, A. Poulos, 1993, The Journal of biological chemistry.

Occurrence of unusual molecular species of sphingomyelin containing 28-34-carbon polyenoic fatty acids in ram spermatozoa.

D. Johnson, K. Beckman, A. Poulos, 1987, The Biochemical journal.

Simple mass spectrometric differentiation of the n-3, n-6 and n-9 series of methylene interrupted polyenoic acids

A. Fellenberg, A. Poulos, David W. Johnson, 1987 .

The occurrence of polyenoic fatty acids with greater than 22 carbon atoms in mammalian spermatozoa.

D. Johnson, A. Fellenberg, A. Poulos, 1986, The Biochemical journal.

Ether-containing lipids of the slime mold,Physarum polycephalum: II. Rates of biosynthesis

G. A. Thompson, A. Poulos, 1971, Lipids.

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

D. Johnson, A. Fellenberg, A. Poulos, 1987, The Biochemical journal.

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.

K. Beckman, A. Poulos, H. Singh, 1994, The Journal of biological chemistry.

A case of combined Farber and Sandhoff disease

H. Moser, A. Sewell, A. Poulos, 1989, European Journal of Pediatrics.

Effect of 22-32 carbon n-3 polyunsaturated fatty acids on superoxide production in human neutrophils: synergism of docosahexaenoic acid with f-met-leu-phe and phorbol ester.

D. P. Harvey, B. S. Robinson, A. Poulos, 1991, Immunology.

Altered responses of human macrophages to lipopolysaccharide by hydroperoxy eicosatetraenoic acid, hydroxy eicosatetraenoic acid, and arachidonic acid. Inhibition of tumor necrosis factor production.

C. P. Morris, B. S. Robinson, A. Poulos, 1997, The Journal of clinical investigation.

Inhibition of stimulus-induced endothelial cell intercellular adhesion molecule-1, E-selectin, and vascular cellular adhesion molecule-1 expression by arachidonic acid and its hydroxy and hydroperoxy derivatives.

B. S. Robinson, A. Poulos, A. Ferrante, 1997, Circulation research.

Inhibitory effects of arachidonic acid (20:4,n-6) and its monohydroperoxy- and hydroxy-metabolites on procoagulant activity in endothelial cells.

B. S. Robinson, A. Poulos, A. Ferrante, 1995, Atherosclerosis.

In Vitro Activation of Rat Brain Protein Kinase C by Polyenoic Very‐Long‐Chain Fatty Acids

K. Clark, B. S. Robinson, A. Poulos, 1994, Journal of neurochemistry.

Deficiency of phospholipase C acting on phosphatidylglycerol in Niernann‐Pick disease

J. Wherrett, A. Poulos, J. Callahan, 1983, Neurology.

N-6 and n-3 polyunsaturated fatty acids stimulate translocation of protein kinase Calpha, -betaI, -betaII and -epsilon and enhance agonist-induced NADPH oxidase in macrophages.

A. Poulos, A. Ferrante, D. Rathjen, 1997, The Biochemical journal.

Immunocytochemical localization of sphingolipid activator protein 2 (SAP-2) in normal and SAP-deficient fibroblasts.

A. Poulos, K. Harzer, J. L. Hughes, 1990, European journal of cell biology.

Studies on the structure of sphingomyelinase. Amino acid composition and heterogeneity on isoelectric focusing.

D. Davidson, A. Poulos, J. Callahan, 1983, The Biochemical journal.

Excretion of 3,6-epoxydicarboxylic acids in peroxisomal disorders.

A. Poulos, J. Pitt, 1993, Clinica chimica acta; international journal of clinical chemistry.

A Case of Krabbe's Leukodystrophy Without Globoid Cells

A. Poulos, P. Mckelvie, I. Hopkins, 1990, Pathology.

Metabolism of hexacosatetraenoic acid (C26:4,n-6) in immature rat brain.

D. Johnson, B. S. Robinson, A. Poulos, 1990, Biochemical Journal.

Evidence of two catalytically active carnitine medium/long chain acyltransferases in rat liver peroxisomes.

K. Beckman, A. Poulos, H. Singh, 1996, Journal of lipid research.

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

C. P. Morris, A. Poulos, S. Heron, 1997, American journal of human genetics.

Enzymatic hydrolysis of sphingomyelin liposomes by normal tissues and tissues from patients with Niemann-Pick disease.

A. Poulos, J. Callahan, C. S. Jones, 1983, Biochimica et biophysica acta.

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

D. Johnson, A. Poulos, H. Singh, 1989, The Biochemical journal.

Phytanic acid oxidase deficiency . Patterns of Refsum ' s disease

A. Poulos, A. Pollard, J. Mitchell, 2006 .

Metabolism of trideuterated iso-lignoceric acid in rats in Vivo and in human fibroblasts in culture

K. Beckman, A. Poulos, David W. Johnson, 1999, Lipids.

Phospholipid changes in spermatozoa during passage through the genital tract of the bull.

A. Poulos, J. Voglmayr, I. White, 1973, Biochimica et biophysica acta.

Substrate specificity of rat liver mitochondrial carnitine palmitoyl transferase I: evidence against α‐oxidation of phytanic acid in rat liver mitochondria

A. Poulos, H. Singh, Alfred Poulos, 1995, FEBS letters.

A Novel β-Oxa Polyunsaturated Fatty Acid Downregulates the Activation of the I&kgr;B Kinase/Nuclear Factor &kgr;B Pathway, Inhibits Expression of Endothelial Cell Adhesion Molecules, and Depresses Inflammation

B. S. Robinson, A. Poulos, A. Ferrante, 2006 .

Ether-containing lipids of the slime mold,Physarum polycephalum: I. Characterization and quantification

G. A. Thompson, A. Poulos, W. M. Stourgeon, 1971, Lipids.

A comparison of the properties and bile salt specificities of galactosylceramide and lactosyl ceramide beta-galactosidase activities in human leucocytes and fibroblasts.

K. Beckman, A. Poulos, 1980, Clinica chimica acta; international journal of clinical chemistry.

A potential source of error in the enzymatic diagnosis of the neurolipidoses when radiolabelled sphinogolipids are used as substrates.

A. Poulos, A. Pollard, 1976, Clinica chimica acta; international journal of clinical chemistry.

Very long chain fatty acid beta-oxidation by rat liver mitochondria and peroxisomes.

A. Poulos, H. Singh, N. Derwas, 1987, Archives of biochemistry and biophysics.