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Journal Abstract Search

212 related items for PubMed ID: 8279468

  • 1. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.
    Suzuki Y, Shimozawa N, Yajima S, Tomatsu S, Kondo N, Nakada Y, Akaboshi S, Lai M, Tanabe Y, Hashimoto T.
    Am J Hum Genet; 1994 Jan; 54(1):36-43. PubMed ID: 8279468
    [Abstract] [Full Text] [Related]

  • 2. Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.
    Wanders RJ, van Roermund CW, Brul S, Schutgens RB, Tager JM.
    J Inherit Metab Dis; 1992 Jan; 15(3):385-8. PubMed ID: 1357231
    [No Abstract] [Full Text] [Related]

  • 3. Peroxisomal bifunctional enzyme deficiency.
    Watkins PA, Chen WW, Harris CJ, Hoefler G, Hoefler S, Blake DC, Balfe A, Kelley RI, Moser AB, Beard ME.
    J Clin Invest; 1989 Mar; 83(3):771-7. PubMed ID: 2921319
    [Abstract] [Full Text] [Related]

  • 4. Peroxisomal disorders: overview.
    Moser HW, Moser AB.
    Ann N Y Acad Sci; 1996 Dec 27; 804():427-41. PubMed ID: 8993562
    [No Abstract] [Full Text] [Related]

  • 5. Transcription regulation of peroxisomal fatty acyl-CoA oxidase and enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase in rat liver by peroxisome proliferators.
    Reddy JK, Goel SK, Nemali MR, Carrino JJ, Laffler TG, Reddy MK, Sperbeck SJ, Osumi T, Hashimoto T, Lalwani ND.
    Proc Natl Acad Sci U S A; 1986 Mar 27; 83(6):1747-51. PubMed ID: 3456610
    [Abstract] [Full Text] [Related]

  • 6. Biochemical findings in a series of Australian patients with isolated defects in peroxisomal beta-oxidation.
    Paton BC, Sharp PC, Poulos A.
    Ann N Y Acad Sci; 1996 Dec 27; 804():750-1. PubMed ID: 8993614
    [No Abstract] [Full Text] [Related]

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  • 8. Induction of the three peroxisomal beta-oxidation enzymes is synergistically regulated by dexamethasone and fatty acids, and counteracted by insulin in Morris 7800C1 hepatoma cells in culture.
    Sørensen HN, Gautik KM, Bremer J, Spydevold O.
    Eur J Biochem; 1992 Sep 15; 208(3):705-11. PubMed ID: 1356767
    [Abstract] [Full Text] [Related]

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  • 10. Peroxisomal Delta3-cis-Delta2-trans-enoyl-CoA isomerase encoded by ECI1 is required for growth of the yeast Saccharomyces cerevisiae on unsaturated fatty acids.
    Gurvitz A, Mursula AM, Firzinger A, Hamilton B, Kilpeläinen SH, Hartig A, Ruis H, Hiltunen JK, Rottensteiner H.
    J Biol Chem; 1998 Nov 20; 273(47):31366-74. PubMed ID: 9813046
    [Abstract] [Full Text] [Related]

  • 11. Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect.
    Guerroui S, Aubourg P, Chen WW, Hashimoto T, Scotto J.
    Biochem Biophys Res Commun; 1989 May 30; 161(1):242-51. PubMed ID: 2471528
    [Abstract] [Full Text] [Related]

  • 12. [Peroxisomal D-bifunctional enzyme deficiency. A case report].
    Chávez-Torres R, Ruiz-Chávez J, Ruiz-Cruz E, Juárez-Naranjo E, Campos-Campos L, Villanueva-Padrón L, Horta-Martínez A, Montes-Castillo Mde L, Monroy-Hernández V, Hernández-Caballero E.
    Rev Med Inst Mex Seguro Soc; 2008 May 30; 46(4):445-8. PubMed ID: 19213219
    [Abstract] [Full Text] [Related]

  • 13. Impairment of peroxisomal beta-oxidation system by endotoxin treatment.
    Dhaunsi GS, Hanevold CD, Singh I.
    Mol Cell Biochem; 1994 Jun 29; 135(2):187-93. PubMed ID: 7838145
    [Abstract] [Full Text] [Related]

  • 14. A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities.
    Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Tager JM, Stephenson JB, Clayton PT.
    J Inherit Metab Dis; 1990 Jun 29; 13(3):375-9. PubMed ID: 2122104
    [No Abstract] [Full Text] [Related]

  • 15. Peroxisomal beta-oxidation: enzymology and molecular biology.
    Hashimoto T.
    Ann N Y Acad Sci; 1996 Dec 27; 804():86-98. PubMed ID: 8993538
    [No Abstract] [Full Text] [Related]

  • 16. Absence of spontaneous peroxisome proliferation in enoyl-CoA Hydratase/L-3-hydroxyacyl-CoA dehydrogenase-deficient mouse liver. Further support for the role of fatty acyl CoA oxidase in PPARalpha ligand metabolism.
    Qi C, Zhu Y, Pan J, Usuda N, Maeda N, Yeldandi AV, Rao MS, Hashimoto T, Reddy JK.
    J Biol Chem; 1999 May 28; 274(22):15775-80. PubMed ID: 10336479
    [Abstract] [Full Text] [Related]

  • 17. D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.
    Suzuki Y, Jiang LL, Souri M, Miyazawa S, Fukuda S, Zhang Z, Une M, Shimozawa N, Kondo N, Orii T, Hashimoto T.
    Am J Hum Genet; 1997 Nov 28; 61(5):1153-62. PubMed ID: 9345094
    [Abstract] [Full Text] [Related]

  • 18. The peroxisomal beta-oxidation enzyme system of rat heart. Basal level and effect of the peroxisome proliferator clofibrate.
    Kvannes J, Eikhom TS, Flatmark T.
    Biochim Biophys Acta; 1994 Nov 11; 1201(2):203-16. PubMed ID: 7947933
    [Abstract] [Full Text] [Related]

  • 19. D-hydroxyacyl-CoA dehydrogenase deficiency. Identification of a new peroxisomal disorder with implications for other disorders of beta-oxidation.
    van Grunsven EG, van Berkel E, Denis S, Mooijer PA, Wanders RJ.
    Adv Exp Med Biol; 1999 Nov 11; 466():365-9. PubMed ID: 10709664
    [Abstract] [Full Text] [Related]

  • 20. Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
    Fukuda S, Suzuki Y, Shimozawa N, Zhang Z, Orii T, Aoyama T, Hashimoto T, Kondo N.
    J Inherit Metab Dis; 1998 Feb 11; 21(1):23-8. PubMed ID: 9501266
    [Abstract] [Full Text] [Related]

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