Metabolic aspects of peroxisomal β-oxidation

[1]  H. Schulz,et al.  Beta oxidation of fatty acids. , 1991, Biochimica et biophysica acta.

[2]  T. Hagve,et al.  Omega-oxidation of fatty acids studied in isolated liver cells. , 1991, Biochimica et biophysica acta.

[3]  I. Issemann,et al.  Activation of a member of the steroid hormone receptor superfamily by peroxisome proliferators , 1990, Nature.

[4]  A. O. Farrants,et al.  Differential induction of peroxisomal oxidation of palmitic acid and 3α, 7α, 12α-trihydroxy-5β-cholestanoic acid in rat liver , 1990 .

[5]  J. Lowenstein,et al.  The involvement of carnitine intermediates in peroxisomal fatty acid oxidation: a study with 2-bromofatty acids. , 1990, Archives of biochemistry and biophysics.

[6]  R. Berge,et al.  Effects of thia-substituted fatty acids on mitochondrial and peroxisomal beta-oxidation. Studies in vivo and in vitro. , 1990, The Biochemical journal.

[7]  S. Eaton,et al.  Intermediates of peroxisomal β-oxidation. A study of the fatty acyl-CoA esters which accumulate during peroxisomal β-oxidation of [U-14C]hexadecanoate , 1990 .

[8]  A. Poulos,et al.  Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation. , 1990, The Biochemical journal.

[9]  J. Veerkamp,et al.  The involvement of fatty acid binding protein in peroxisomal fatty acid oxidation , 1990, FEBS letters.

[10]  S. Skrede,et al.  The effect of adaptation on the metabolism of dodecylthioacetic acid (a 3-thia fatty acid) in rat tissues. , 1990, Biochimica et biophysica acta.

[11]  J. Bremer,et al.  Alkylthioacetic acids (3-thia fatty acids) are metabolized and excreted as shortened dicarboxylic acids in vivo. , 1990, Biochimica et biophysica acta.

[12]  T. Hagve,et al.  The Zellweger syndrome: deficient conversion of docosahexaenoic acid (22:6(n-3)) to eicosapentaenoic acid (20:5(n-3)) and normal delta 4-desaturase activity in cultured skin fibroblasts. , 1990, Biochimica et biophysica acta.

[13]  I. Singh,et al.  Topographical localization of peroxisomal acyl-CoA ligases: differential localization of palmitoyl-CoA and lignoceroyl-CoA ligases. , 1990 .

[14]  I. Björkhem,et al.  Identification of intermediates in the peroxisomal β-oxidation of linoleic acid , 1990 .

[15]  P. Clayton,et al.  Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. , 1990, The Journal of clinical investigation.

[16]  G. Mannaerts,et al.  Presence of three acyl-CoA oxidases in rat liver peroxisomes. An inducible fatty acyl-CoA oxidase, a noninducible fatty acyl-CoA oxidase, and a noninducible trihydroxycoprostanoyl-CoA oxidase. , 1990, The Journal of biological chemistry.

[17]  P. Watkins,et al.  Mitochondrial oxidation of phytanic acid in human and monkey liver: implication that Refsum's disease is not a peroxisomal disorder. , 1990, Biochemical and biophysical research communications.

[18]  J. Hiltunen,et al.  Peroxisomal bifunctional protein from rat liver is a trifunctional enzyme possessing 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities. , 1990, The Journal of biological chemistry.

[19]  J. Bremer,et al.  Metabolism of dicarboxylic acids in rat hepatocytes. , 1990, Biochimica et biophysica acta.

[20]  D. Johnson,et al.  A comparative study of straight chain and branched chain fatty acid oxidation in skin fibroblasts from patients with peroxisomal disorders. , 1990, Journal of lipid research.

[21]  T. Suga,et al.  Different regulation of hepatic peroxisomal beta-oxidation activity in rats treated with clofibrate and partially hydrogenated marine oil. , 1990, Biochemical and biophysical research communications.

[22]  Russell K Yamazaki,et al.  The oxidation of dicarboxylic acid CoA esters via peroxisomal fatty acyl-CoA oxidase. , 1989, Biochimica et biophysica acta.

[23]  J. Hiltunen,et al.  The known purified mammalian 2,4-dienoyl-CoA reductases are mitochondrial isoenzymes. , 1989, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[24]  R. Berge,et al.  Alkylthio acetic acids (3-thia fatty acids)--a new group of non-beta-oxidizable peroxisome-inducing fatty acid analogues--II. Dose-response studies on hepatic peroxisomal- and mitochondrial changes and long-chain fatty acid metabolizing enzymes in rats. , 1989, Biochemical pharmacology.

[25]  H. Hayashi,et al.  The role of peroxisomal fatty acyl-CoA β-oxidation in bile acid biosynthesis , 1989 .

[26]  A. Deangelo,et al.  Species and strain sensitivity to the induction of peroxisome proliferation by chloroacetic acids. , 1989, Toxicology and applied pharmacology.

[27]  J. Hiltunen,et al.  Epimerization of 3-hydroxyacyl-CoA esters in rat liver. Involvement of two 2-enoyl-CoA hydratases. , 1989, The Journal of biological chemistry.

[28]  R. Berge,et al.  The presence of acyl-CoA hydrolase in rat brown-adipose-tissue peroxisomes. , 1989, The Biochemical journal.

[29]  J. Vamecq,et al.  Peroxisomal and mitochondrial beta-oxidation of monocarboxylyl-CoA, omega-hydroxymonocarboxylyl-CoA and dicarboxylyl-CoA esters in tissues from untreated and clofibrate-treated rats. , 1989, Journal of biochemistry.

[30]  H. Kawashima,et al.  Isolation of a new form of cytochrome P-450 with prostaglandin A and fatty acid omega-hydroxylase activities from rabbit kidney cortex microsomes. , 1989, Journal of biochemistry.

[31]  F. Leighton,et al.  Free acetate production by rat hepatocytes during peroxisomal fatty acid and dicarboxylic acid oxidation. , 1989, The Journal of biological chemistry.

[32]  I. Björkhem,et al.  Peroxisomal bile acid-CoA:amino-acid N-acyltransferase in rat liver. , 1989, The Journal of biological chemistry.

[33]  L. Brady,et al.  Co-ordinate induction of hepatic mitochondrial and peroxisomal carnitine acyltransferase synthesis by diet and drugs. , 1989, The Biochemical journal.

[34]  H. Schulz,et al.  The 3-hydroxyacyl-CoA epimerase activity of rat liver peroxisomes is due to the combined actions of two enoyl-CoA hydratases: a revision of the epimerase-dependent pathway of unsaturated fatty acid oxidation. , 1989, Biochemical and biophysical research communications.

[35]  D. Tweedie,et al.  Induction of microsomal NADPH-cytochrome P-450 reductase and cytochrome P-450IVA1 (P-450LA omega) by dehydroepiandrosterone in rats: a possible peroxisomal proliferator. , 1989, Cancer research.

[36]  I. Singh,et al.  Adrenoleukodystrophy: impaired oxidation of fatty acids due to peroxisomal lignoceroyl-CoA ligase deficiency. , 1989, Archives of biochemistry and biophysics.

[37]  A. O. Farrants,et al.  Identification of 3α,7α,12α-trihydroxy-5β-cholest-24-enoic acid as an intermediate in the peroxisomal conversion of 3α,7α,12α-trihydroxy-5β-cholestanoic acid to cholic acid , 1989 .

[38]  T. Hagve,et al.  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. , 1989, Biochimica et biophysica acta.

[39]  A. Moser,et al.  Peroxisomal bifunctional enzyme deficiency. , 1989, The Journal of clinical investigation.

[40]  B. Crabtree,et al.  Evidence that the production of acetate in rat hepatocytes is a predominantly cytoplasmic process. , 1989, The Biochemical journal.

[41]  T. Watanabe,et al.  Compartmentation of dicarboxylic acid beta-oxidation in rat liver: importance of peroxisomes in the metabolism of dicarboxylic acids. , 1989, Biochimica et biophysica acta.

[42]  R. Wanders,et al.  Peroxisomal disorders in neurology , 1988, Journal of the Neurological Sciences.

[43]  J. Bar-Tana,et al.  Hypolipidemic, Antiobesity, and Hypoglycemic-Hypoinsulinemic Effects of β,β′-Methyl-Substituted Hexadecanedioic Acid in Sand Rats , 1988, Diabetes.

[44]  J. Vamecq,et al.  Comparison of the metabolism of dodecanedioic acid in vivo in control, riboflavin-deficient and clofibrate-treated rats. , 1988, European journal of biochemistry.

[45]  F. Leighton,et al.  Detection of an ATPase activity in rat liver peroxisomes. , 1988, Biochemical and biophysical research communications.

[46]  T. Suga,et al.  Induction of peroxisome proliferation in rat liver by dietary treatment with 2,2,4,4,6,8,8-heptamethylnonane. , 1988, Xenobiotica; the fate of foreign compounds in biological systems.

[47]  J. Bar-Tana,et al.  The induction of liver peroxisomal proliferation by β,β′-methyl-substituted hexadecanedioic acid (MEDICA 16) , 1988 .

[48]  T. Flatmark,et al.  On the mechanism of induction of the enzyme systems for peroxisomal beta-oxidation of fatty acids in rat liver by diets rich in partially hydrogenated fish oil. , 1988, Biochimica et biophysica acta.

[49]  R. Thurman,et al.  Catalase-dependent ethanol oxidation in perfused rat liver. Requirement for fatty-acid-stimulated H2O2 production by peroxisomes. , 1988, European journal of biochemistry.

[50]  B. Künnecke,et al.  In situ metabolism of 1,omega medium chain dicarboxylic acids in the liver of intact rats as detected by 13C and 1H NMR. , 1988, The Journal of biological chemistry.

[51]  J. I. Pedersen,et al.  Subcellular localization of 3 alpha, 7 alpha-dihydroxy- and 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoyl-coenzyme A ligase(s) in rat liver. , 1988, Journal of lipid research.

[52]  J. Bremer,et al.  Metabolism of dicarboxylic acids in vivo and in the perfused kidney of the rat. , 1988, Biochimica et biophysica acta.

[53]  G. Mannaerts,et al.  Inhibition of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid oxidation and of bile acid secretion in rat liver by fatty acids. , 1988, The Journal of biological chemistry.

[54]  B. Lake,et al.  Co-induction of microsomal cytochrome P-452 and the peroxisomal fatty acid beta-oxidation pathway in the rat by clofibrate and di-(2-ethylhexyl)phthalate. Dose-response studies. , 1988, Biochemical pharmacology.

[55]  T. Hagve,et al.  The Zellweger syndrome: deficient chain-shortening of erucic acid (22:1 (n-9)) and adrenic acid (22:4 (n-6)) in cultured skin fibroblasts. , 1988, Biochimica et biophysica acta.

[56]  R. Wanders,et al.  A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy). , 1988, American journal of human genetics.

[57]  S. Gatt,et al.  Pyrene dodecanoic acid coenzyme A ester: peroxisomal oxidation and chain shortening. , 1988, Biochimica et Biophysica Acta.

[58]  H. Osmundsen,et al.  Peroxisomal beta-oxidation of long-chain fatty acids possessing different extents of unsaturation. , 1987, The Biochemical journal.

[59]  J. Vamecq,et al.  Peroxisomal oxidation of L-2-hydroxyphytanic acid in rat kidney cortex. , 1987, European journal of biochemistry.

[60]  E. Newsholme,et al.  The effect of dehydroepiandrosterone acetate on liver peroxisomal enzyme activities of male and female rats. , 1987, The Journal of nutrition.

[61]  R. Wanders,et al.  Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome. , 1987, Clinica chimica acta; international journal of clinical chemistry.

[62]  U. Diczfalusy,et al.  Chain-shortening of prostaglandin F2α by rat liver peroxisomes , 1987 .

[63]  E. Lock,et al.  The induction of ω and β-oxidation of fatty acids and effect on α2u globulin content in the liver and kidney of rats administered 2, 2, 4-trimethylpentane , 1987 .

[64]  P. Veldhoven,et al.  Permeability of the peroxisomal membrane to cofactors of beta-oxidation. Evidence for the presence of a pore-forming protein. , 1987, The Journal of biological chemistry.

[65]  J. Hiltunen,et al.  beta-Oxidation of polyunsaturated fatty acids by rat liver peroxisomes. A role for 2,4-dienoyl-coenzyme A reductase in peroxisomal beta-oxidation. , 1986, The Journal of biological chemistry.

[66]  H. Schulz,et al.  Channeling of 3-hydroxy-4-trans-decenoyl coenzyme A on the bifunctional beta-oxidation enzyme from rat liver peroxisomes and on the large subunit of the fatty acid oxidation complex from Escherichia coli. , 1986, The Journal of biological chemistry.

[67]  A. Nilsson,et al.  The effect of high-fat diets on microsomal lauric acid hydroxylation in rat liver. , 1986, Biochimica et biophysica acta.

[68]  P. Veldhoven,et al.  Coenzyme A in purified peroxisomes is not freely soluble in the matrix but firmly bound to a matrix protein. , 1986, Biochemical and biophysical research communications.

[69]  J. Veerkamp,et al.  Effect of dietary fat on total and peroxisomal fatty acid oxidation in rat tissues. , 1986, Biochimica et biophysica acta.

[70]  J. I. Pedersen,et al.  Conjugation of cholic acid with taurine and glycine by rat liver peroxisomes. , 1986, Biochemical and biophysical research communications.

[71]  J. I. Pedersen,et al.  In vitro formation of bile acids from di- and trihydroxy-5 beta-cholestanoic acid in human liver peroxisomes. , 1986, Biochimica et biophysica acta.

[72]  M. Sugano,et al.  Strain dependence of the metabolism of cis- and trans-isomers of 9-octadecenoic acid in perfused liver and cell-free preparation in rats. , 1986, Biochimica et biophysica acta.

[73]  J. I. Pedersen,et al.  Formation of chenodeoxycholic acid from 3 alpha, 7 alpha-dihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes. , 1986, Journal of lipid research.

[74]  S. Kolvraa,et al.  In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liver. , 1986, Biochimica et biophysica acta.

[75]  H. Schulz,et al.  Effect of growth hormone on fatty acid oxidation: growth hormone increases the activity of 2,4-dienoyl-CoA reductase in mitochondria. , 1986, Archives of biochemistry and biophysics.

[76]  I. Singh,et al.  Lignoceroyl‐CoASH ligase: enzyme defect in fatty acid β‐oxidation system in X‐linked childhood adrenoleukodystrophy , 1986, FEBS letters.

[77]  J. Veerkamp,et al.  Peroxisomal fatty acid oxidation in rat and human tissues. Effect of nutritional state, clofibrate treatment and postnatal development in the rat. , 1986, Biochimica et biophysica acta.

[78]  T. Hagve,et al.  Evidence for peroxisomal retroconversion of adrenic acid (22:4(n-6)) and docosahexaenoic acids (22:6(n-3)) in isolated liver cells. , 1986, Biochimica et biophysica acta.

[79]  B. Strandvik,et al.  In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid. , 1985, The Journal of clinical investigation.

[80]  R. Berge,et al.  Correlation between the cellular level of long-chain acyl-CoA, peroxisomal beta-oxidation, and palmitoyl-CoA hydrolase activity in rat liver. Are the two enzyme systems regulated by a substrate-induced mechanism? , 1985, Biochimica et biophysica acta.

[81]  L. Peña,et al.  Bile acid synthesis in rat liver peroxisomes: metabolism of 26-hydroxycholesterol to 3 beta-hydroxy-5-cholenoic acid. , 1985, Journal of lipid research.

[82]  J. Vamecq,et al.  The microsomal dicarboxylyl-CoA synthetase. , 1985, The Biochemical journal.

[83]  M Tanaka,et al.  The induction of peroxisome proliferation in rat liver by perfluorinated fatty acids, metabolically inert derivatives of fatty acids. , 1985, Journal of biochemistry.

[84]  P. Lazarow,et al.  Flux of palmitate through the peroxisomal and mitochondrial beta-oxidation systems in isolated rat hepatocytes. , 1985, Biochimica et biophysica acta.

[85]  H. Schulz,et al.  3‐Hydroxyacyl‐CoA epimerase is a peroxisomal enzyme and therefore not involved in mitochondrial fatty acid oxidation , 1985, FEBS letters.

[86]  T. Suga,et al.  Enhancement of peroxisomal beta-oxidation in the liver of rats and mice treated with valproic acid. , 1985, Biochemical pharmacology.

[87]  J. Crabb,et al.  Peroxisomal β‐oxidation system of Candida tropicalis , 1985 .

[88]  H. Osmundsen Mitochondria, peroxisomes and hepatic fatty acid oxidation , 1985 .

[89]  J. I. Pedersen,et al.  Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger. , 1985, The Journal of clinical investigation.

[90]  H. Pownall,et al.  Pyrenedodecanoylcarnitine and pyrenedodecanoyl coenzyme A: kinetics and thermodynamics of their intermembrane transfer. , 1984, Biochemistry.

[91]  A. Poulos,et al.  Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome? , 1984, Clinical genetics.

[92]  T. Watanabe,et al.  Participation of peroxisomal beta-oxidation system in the chain-shortening of a xenobiotic acyl compound. , 1984, Biochemical and biophysical research communications.

[93]  J. I. Pedersen,et al.  Mechanism of peroxisomal 24-hydroxylation of 3α,7α,12α-trihydroxy-5β-cholestanoic acid in rat liver , 1984 .

[94]  S. Alexson,et al.  A direct comparison between peroxisomal and mitochondrial preferences for fatty-acyl beta-oxidation predicts channelling of medium-chain and very-long-chain unsaturated fatty acids to peroxisomes. , 1984, Biochimica et biophysica acta.

[95]  S. Skrede,et al.  Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome. , 1984, Scandinavian journal of clinical and laboratory investigation.

[96]  B. Strandvik,et al.  Urinary excretion of dicarboxylic acids from patients with the Zellweger syndrome. Importance of peroxisomes in beta-oxidation of dicarboxylic acids. , 1984, Biochimica et biophysica acta.

[97]  T. Flatmark,et al.  Enhancement of long-chain acyl-CoA hydrolase activity in peroxisomes and mitochondria of rat liver by peroxisomal proliferators. , 1984, European journal of biochemistry.

[98]  C. Clark The cellular distribution of steroid hormone receptors: have we got it right? , 1984 .

[99]  G. Dallner,et al.  Phthalate Esters and Their Effect on the Liver , 1984, Hepatology.

[100]  J. I. Pedersen,et al.  Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes. , 1983, Journal of lipid research.

[101]  S. Passi,et al.  Metabolism of straight saturated medium chain length (C9 to C12) dicarboxylic acids. , 1983, Journal of lipid research.

[102]  J. Hiltunen,et al.  β-Oxidation of polyunsaturated fatty acids having double bonds at even-numbered positions in isolated rat liver mitochondria , 1983 .

[103]  M. Thomassen,et al.  Stimulation of microperoxisomal β-oxidation in rat heart by high-fat diets , 1983 .

[104]  J. Červenka,et al.  A role for 2,4-enoyl-CoA reductase in mitochondrial beta-oxidation of polyunsaturated fatty acids. Effects of treatment with clofibrate on oxidation of polyunsaturated acylcarnitines by isolated rat liver mitochondria. , 1982, The Biochemical journal.

[105]  L. Hagey,et al.  Degradation of cholesterol to propionic acid by rat liver peroxisomes. , 1982, Biochemical and biophysical research communications.

[106]  M. Thomassen,et al.  Characterization of the stimulatory effect of high-fat diets on peroxisomal beta-oxidation in rat liver. , 1982, The Biochemical journal.

[107]  T. Hashimoto INDIVIDUAL PEROXISOMAL βT‐OXIDATION ENZYMES * , 1982 .

[108]  H. Osmundsen PEROXISOMAL βT‐OXIDATION OF LONG FATTY ACIDS: EFFECTS OF HIGH FAT DIETS * , 1982 .

[109]  G. Mannaerts,et al.  Evidence that peroxisomal acyl-CoA synthetase is located at the cytoplasmic side of the peroxisomal membrane. , 1982, The Biochemical journal.

[110]  J. Russo,et al.  Hormone-dependent changes in peroxisomal enzyme activity in guinea pig adrenal. , 1982, Journal of Biological Chemistry.

[111]  H. Shio,et al.  Polypeptide and phospholipid composition of the membrane of rat liver peroxisomes: comparison with endoplasmic reticulum and mitochondrial membranes , 1982, The Journal of cell biology.

[112]  G. Janssen,et al.  Structure of the side chain of the C29 dicarboxylic bile acid occurring in infants with coprostanic acidemia. , 1982, Journal of lipid research.

[113]  J. Bremer,et al.  Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet. , 1982, Journal of lipid research.

[114]  D. Turnbull,et al.  Increased activity of peroxisomal beta-oxidation in rat liver caused by ethyl 2(5(4-chlorophenyl)pentyl)-oxiran-2-carboxylate: an inhibitor of mitochondrial beta-oxidation. , 1982, Biochemical and biophysical research communications.

[115]  W. Kunau,et al.  Degradation of unsaturated fatty acids in peroxisomes. Existence of a 2,4-dienoyl-CoA reductase pathway. , 1981, The Journal of biological chemistry.

[116]  R. Holman,et al.  Beta-oxidation of the geometric and positional isomers of octadecenoic acid by rat heart and liver mitochondria. , 1981, Biochimica et biophysica acta.

[117]  E. Foerster,et al.  Peroxisomal fatty acid oxidation as detected by H2O2 production in intact perfused rat liver. , 1981, The Biochemical journal.

[118]  G. Mannaerts,et al.  Subcellular distribution of coenzyme A: evidence for a separate coenzyme A pool in peroxisomes. , 1981, Biochemical and biophysical research communications.

[119]  M. Thomassen,et al.  Effects of high-fat diets on hepatic fatty acid oxidation in the rat. Isolation of rat liver peroxisomes by vertical-rotor centrifugation by using a self-generated, iso-osmotic, Percoll gradient. , 1981, The Biochemical journal.

[120]  J. I. Pedersen,et al.  Conversion of 3α,7α,12α‐trihydroxy‐5β‐cholestanoic acid into cholic acid by rat liver peroxisomes , 1980 .

[121]  J. Bremer,et al.  Increased 4‐enoyl‐CoA reductase activity in liver mitochondria of rats fed high‐fat diets and its effect on fatty acid oxidation and the inhibitory action of pent‐4‐enoate , 1980, FEBS letters.

[122]  J. Russo,et al.  Stereological analysis of the guinea pig adrenal: effects of dexamethasone and ACTH treatment with emphasis on the inner cortex. , 1980, The American journal of anatomy.

[123]  M. Utter,et al.  Purification and characterization of an extramitochondrial acetyl coenzyme A hydrolase from rat liver. , 1980, The Journal of biological chemistry.

[124]  I. Björkhem,et al.  Cerebrotendinous xanthomatosis: a defect in mitochondrial 26-hydroxylation required for normal biosynthesis of cholic acid. , 1980, The Journal of clinical investigation.

[125]  J. Bremer,et al.  In vivo induction of 4-enoyl-CoA reductase by clofibrate in liver mitochondria and its effect on pent-4-enoate metabolism. , 1980, Biochemical and biophysical research communications.

[126]  J. Norseth Increased β-oxidation of erucic acid in perfused hearts from rats fed clofibrate , 1980 .

[127]  S. Lindstedt,et al.  3-hydroxydecanedioic acid and related homologues: urinary metabolites in ketoacidosis. , 1980, Clinical chemistry.

[128]  G. Dallner,et al.  Possible involvement of fatty acid binding protein in peroxisomal β-oxidation of fatty acids , 1980 .

[129]  M. Thomassen,et al.  Induction of peroxisomal beta-oxidation in rat liver by high-fat diets. , 1980, The Biochemical journal.

[130]  G. Janssen,et al.  C27 Bile Acids in Infants with Coprostanic Acidemia and Occurrence of a 3α,7α,12α‐Trihydroxy‐5β‐C29 Dicarboxylic Bile Acid as a Major Component in Their Serum , 1979 .

[131]  H. Osmundsen,et al.  Regulation of peroxisomal fatty acid oxidation , 1979, FEBS Letters.

[132]  J. Norseth The effect of feeding rats with partially hydrogenated marine oil or rapeseed oil on the chain shortening of erucic acid in perfused heart. , 1979, Biochimica et biophysica acta.

[133]  J. Bremer,et al.  The stimulation of erucate metabolism in isolated rat hepatocytes by rapeseed oil and hydrogenated marine oil-containing diets. , 1979, Biochimica et biophysica acta.

[134]  G. Mannaerts,et al.  Mitochondrial and peroxisomal fatty acid oxidation in liver homogenates and isolated hepatocytes from control and clofibrate-treated rats. , 1979, The Journal of biological chemistry.

[135]  R. Hanson,et al.  Defects of bile acid synthesis in Zellweger's syndrome. , 1979, Science.

[136]  K. Norum,et al.  Peroxisomal oxidation of long chain fatty acids , 1979, FEBS letters.

[137]  B. Landau,et al.  ω-Oxidation of fatty acids and the acetylation of p-aminobenzoic acid , 1979 .

[138]  W. Kunau,et al.  Degradation of Unsaturated Fatty Acids , 1978 .

[139]  J. Bremer,et al.  Comparative biochemistry of beta-oxidation. An investigation into the abilities of isolated heart mitochondria of various animal species to oxidize long-chain fatty acids, including the C22:1 monoenes. , 1978, The Biochemical journal.

[140]  I. Björkhem On the quantitative importance of omega-oxidation of fatty acids. , 1978, Journal of lipid research.

[141]  B. Landau,et al.  Contribution of omega-oxidation to fatty acid oxidation by liver of rat and monkey. , 1978, Journal of lipid research.

[142]  J. McGarry,et al.  Hepatic fatty acid oxidation and ketogenesis after clofibrate treatment. , 1978, Biochimica et biophysica acta.

[143]  P. Lazarow Rat liver peroxisomes catalyze the beta oxidation of fatty acids. , 1978, The Journal of biological chemistry.

[144]  D. Williamson,et al.  Origins of blood acetate in the rat. , 1977, Biochemical Journal.

[145]  P. Lazarow Three hypolipidemic drugs increase hepatic palmitoyl-coenzyme A oxidation in the rat. , 1977, Science.

[146]  B. Landau,et al.  Role of omega oxidation of fatty acids in formation of the acetyl unit for acetylation. , 1977, The Journal of biological chemistry.

[147]  F. Wada,et al.  Studies on fatty acid omega-oxidation. Antiketogenic effect and gluconeogenicity of dicarboxylic acids. , 1977, Biochimica et biophysica acta.

[148]  J. Bremer,et al.  Monoethlenic C20 and C22 fatty acids in marine oil and rapeseed oil. Studies on their oxidation and on their relative ability to inhibit palmitate oxidation in heart and liver mitochondria. , 1977, Biochimica et biophysica acta.

[149]  S. Lindstedt,et al.  Structure of some aliphatic dicarboxylic acids found in the urine of an infant with congenital lactic acidosis. , 1976, Clinical chemistry.

[150]  S. Lindstedt,et al.  5-Decynedioic acid, an acetylenic compound in human urine. , 1975, Clinical chemistry.

[151]  J. Gustafsson Biosynthesis of cholic acid in rat liver. 24-Hydroxylation of 3alpha, 7alpha, 12alpha-trihydroxy-5beta-cholestanoic acid. , 1975, The Journal of biological chemistry.

[152]  J. E. Pettersen In vivo studies on the metabolism of hexanedioic acid. , 1975, Clinica chimica acta; international journal of clinical chemistry.

[153]  S. Lindstedt,et al.  3,4-Methylene hexanedioic acid--a previously unknown compound in human urine. , 1974, Clinica chimica acta; international journal of clinical chemistry.

[154]  I. Rapin,et al.  Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome , 1973, Science.

[155]  R. Paoletti,et al.  The beta-oxidative cleavage of long-chain fatty acids in rat-liver cytoplasm. , 1973, European journal of biochemistry.

[156]  J. E. Pettersen In vitro studies on the metabolism of hexadecanedioic acid and its mono-L-carnitine ester. , 1973, Biochimica et biophysica acta.

[157]  I. Björkhem,et al.  On the role of alcohol dehydrogenase in omega-oxidation of fatty acids. , 1972, European journal of biochemistry.

[158]  J. E. Pettersen Formation of n-hexanedioic acid from hexadecanoic acid by an initial oxidation in ketotic rats. , 1972, Clinica chimica acta; international journal of clinical chemistry.

[159]  E. Eggermont,et al.  Trihydroxycoprostanic acid in the duodenal fluid of two children with intrahepatic bile duct anomalies. , 1972, Biochimica et biophysica acta.

[160]  E. Jellum,et al.  The occurrence of adipic and suberic acid in urine from ketotic patients. , 1972, Clinica chimica acta; international journal of clinical chemistry.

[161]  E. Granström On the metabolism of prostaglandin F2alpha in female subjects: structures of two C14 metabolites. , 1972 .

[162]  F. Wada,et al.  Studies on the physiological significance of fatty acid -oxidation. , 1971, Journal of biochemistry.

[163]  J. Mustard,et al.  Thromboembolism: A Manifestation of the Response of Blood to Injury , 1970, Circulation.

[164]  J. Williamson,et al.  Control of citric acid cycle activity in rat heart mitochondria. , 1970, The Journal of biological chemistry.

[165]  B. Wostmann,et al.  Fecal neutral steroids and bile acids from germfree rats. , 1969, Journal of lipid research.

[166]  O. Stokke α-Oxidation of a β-methyl-substituted fatty acid in guinea-pig liver mitochondria , 1968 .

[167]  O. Stokke,et al.  α-Oxidation as an alternative pathway for the degradation of branched-chain fatty acids in man, and its failure in patients with refsum's disease , 1967 .

[168]  E. Staple,et al.  The formation of cholic acid from 3α,7α, 12α,-24ξ-tetrahydroxycoprostanic acid by rat liver , 1965 .

[169]  N. Tryding,et al.  Intestinal absorption and metabolism of 2:2-dimethylstearic acid in the rat. , 1954, The Biochemical journal.

[170]  J. I. Pedersen,et al.  Importance of Peroxisomes in the Formation of Chenodeoxycholic Acid in Human Liver. Metabolism of 3α,7α-Dihydroxy-5β-cholestanoic Acid in Zellweger Syndrome , 1991, Pediatric Research.

[171]  Charles R.scriver The Metabolic basis of inherited disease , 1989 .

[172]  J. Vamecq,et al.  Pathophysiology of peroxisomal beta-oxidation. , 1989, Essays in biochemistry.

[173]  K. Verheyden,et al.  Subcellular distribution and characteristics of trihydroxycoprostanoyl-CoA synthetase in rat liver. , 1989, The Biochemical journal.

[174]  E. Lock,et al.  Biochemical mechanisms of induction of hepatic peroxisome proliferation. , 1989, Annual review of pharmacology and toxicology.

[175]  R. Ramsay The soluble carnitine palmitoyltransferase from bovine liver. A comparison with the enzymes from peroxisomes and from the mitochondrial inner membrane. , 1988, Biochemical Journal.

[176]  M. Healy,et al.  Enzymes of carnitine acylation. Is overt carnitine palmitoyltransferase of liver peroxisomal carnitine octanoyltransferase? , 1988, Biochemical Journal.

[177]  H. Schulz,et al.  Beta-oxidation of unsaturated fatty acids: a revised pathway , 1987 .

[178]  G. Krishna,et al.  Valproic acid-induced increase in carnitine acetyltransferase in rat hepatocytes is not due to an induction of peroxisomes. , 1987, Journal of toxicology and environmental health.

[179]  H. Moser New approaches in peroxisomal disorders. , 1987, Developmental neuroscience.

[180]  R. Wanders,et al.  Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies. , 1987, Enzyme.

[181]  M. Rao,et al.  Peroxisome proliterators and cancer: mechanisms and implications , 1986 .

[182]  P. Bougnères,et al.  Medium- and Long-Chain Dicarboxylic Aciduria in Patients with Zellweger Syndrome and Neonatal Adrenoleukodystrophy , 1986, Pediatric Research.

[183]  J. Svendsen,et al.  Absolute configuration of 3-hydroxyadipic acid in human urine. , 1985, Journal of chromatography.

[184]  N. Lalwani,et al.  Induction of hepatic peroxisome proliferation in nonrodent species, including primates. , 1984, The American journal of pathology.

[185]  F. Hartl,et al.  Rat liver peroxisomes, II. Stimulation of peroxisomal fatty-acid beta-oxidation by thyroid hormones. , 1983, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[186]  J. I. Pedersen,et al.  Role of the 26-hydroxylase in the biosynthesis of bile acids in the normal state and in cerebrotendinous xanthomatosis. An in vivo study. , 1983, The Journal of clinical investigation.

[187]  H. Osmundsen Factors which can influence beta-oxidation by peroxisomes isolated from livers of clofibrate treated rats. Some properties of peroxisomal fractions isolated in a self-generated Percoll gradient by vertical rotor centrifugation. , 1982, The International journal of biochemistry.

[188]  U. Houtsmuller Biochemical Aspects of Fatty Acids with trans Double Bonds , 1978 .

[189]  B. Chance,et al.  The role of H 2 O 2 generation in perfused rat liver and the reaction of catalase compound I and hydrogen donors. , 1973, Archives of biochemistry and biophysics.

[190]  E. Staple,et al.  The formation of bile acids from cholesterol. The conversion of 5-beta-cholestane-3-alpha,7-alpha-triol-26-oic acid to cholic acid via 5-beta-cholestane-3-alpha,7-alpha,12-alpha, 24-xi-tetraol-26-oic acid I by rat liver. , 1966, The Journal of biological chemistry.

[191]  G. Weitzel Biochemie verzweigter Carbonsäuren. VI. Mitteilung. Stoffwechselversuche mit alkylverzweigten höheren Fettsäuren , 1951 .

[192]  G. Weitzel Biochemie verzweigter Carbonsäuren. I. Mitteilung. Stoffwechselversuche mit alkylierten Adipinsäuren , 1950 .

[193]  K. Bernhard Methyloxydationen im Tierkörper. Der Abbau alkyl-substituierter Malonsäuren , 1941 .

[194]  R. Kuhn,et al.  Über Methyl-oxydationen im Tierkörper. , 1936 .

[195]  P. E. Verkade,et al.  Researches on fat metabolism. II. , 1934, The Biochemical journal.