These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

596 related items for PubMed ID: 3469675

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
    Poll-The BT, Roels F, Ogier H, Scotto J, Vamecq J, Schutgens RB, Wanders RJ, van Roermund CW, van Wijland MJ, Schram AW.
    Am J Hum Genet; 1988 Mar 30; 42(3):422-34. PubMed ID: 2894756
    [Abstract] [Full Text] [Related]

  • 5. X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.
    Wanders RJ, van Roermund CW, van Wijland MJ, Nijenhuis AA, Tromp A, Schutgens RB, Brouwer-Kelder EM, Schram AW, Tager JM, van den Bosch H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):321-9. PubMed ID: 3652454
    [Abstract] [Full Text] [Related]

  • 6. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy.
    Lazo O, Contreras M, Hashmi M, Stanley W, Irazu C, Singh I.
    Proc Natl Acad Sci U S A; 1988 Oct 15; 85(20):7647-51. PubMed ID: 3174658
    [Abstract] [Full Text] [Related]

  • 7. 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.
    Christensen E, Grønn M, Hagve TA, Kase BF, Christophersen BO.
    Biochim Biophys Acta; 1989 Mar 14; 1002(1):79-83. PubMed ID: 2538146
    [Abstract] [Full Text] [Related]

  • 8. Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome.
    Suzuki Y, Orii T, Mori M, Tatibana M, Hashimoto T.
    Clin Chim Acta; 1986 Apr 30; 156(2):191-6. PubMed ID: 3519003
    [Abstract] [Full Text] [Related]

  • 9. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
    Reubsaet FA, Veerkamp JH, Brückwilder ML, Trijbels JM, Hashimoto T, Monnens LA.
    Biochim Biophys Acta; 1991 Jun 03; 1083(3):305-9. PubMed ID: 2049396
    [Abstract] [Full Text] [Related]

  • 10. Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome.
    Tager JM, Van der Beek WA, Wanders RJ, Hashimoto T, Heymans HS, Van den Bosch H, Schutgens RB, Schram AW.
    Biochem Biophys Res Commun; 1985 Feb 15; 126(3):1269-75. PubMed ID: 3977916
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy.
    Sandhir R, Khan M, Chahal A, Singh I.
    J Lipid Res; 1998 Nov 15; 39(11):2161-71. PubMed ID: 9799802
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.
    Naidu S, Hoefler G, Watkins PA, Chen WW, Moser AB, Hoefler S, Rance NE, Powers JM, Beard M, Green WR.
    Neurology; 1988 Jul 15; 38(7):1100-7. PubMed ID: 3386829
    [Abstract] [Full Text] [Related]

  • 15. Molecular cloning of the cDNAs for the subunits of rat mitochondrial fatty acid beta-oxidation multienzyme complex. Structural and functional relationships to other mitochondrial and peroxisomal beta-oxidation enzymes.
    Kamijo T, Aoyama T, Miyazaki J, Hashimoto T.
    J Biol Chem; 1993 Dec 15; 268(35):26452-60. PubMed ID: 8253773
    [Abstract] [Full Text] [Related]

  • 16. [Genes of peroxisomal enzymes].
    Osumi T, Hashimoto T.
    Tanpakushitsu Kakusan Koso; 1990 Jun 15; 35(8):1439-46. PubMed ID: 2374815
    [No Abstract] [Full Text] [Related]

  • 17. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
    Aubourg P, Kremser K, Roland MO, Rocchiccioli F, Singh I.
    Pediatr Res; 1993 Sep 15; 34(3):270-6. PubMed ID: 7510868
    [Abstract] [Full Text] [Related]

  • 18. Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.
    Wiesinger C, Kunze M, Regelsberger G, Forss-Petter S, Berger J.
    J Biol Chem; 2013 Jun 28; 288(26):19269-79. PubMed ID: 23671276
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.
    Singh I, Moser AE, Goldfischer S, Moser HW.
    Proc Natl Acad Sci U S A; 1984 Jul 28; 81(13):4203-7. PubMed ID: 6588384
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 30.