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Journal Abstract Search


263 related items for PubMed ID: 9425230

  • 1. Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins.
    Braiterman LT, Zheng S, Watkins PA, Geraghty MT, Johnson G, McGuinness MC, Moser AB, Smith KD.
    Hum Mol Genet; 1998 Feb; 7(2):239-47. PubMed ID: 9425230
    [Abstract] [Full Text] [Related]

  • 2. Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy.
    Netik A, Forss-Petter S, Holzinger A, Molzer B, Unterrainer G, Berger J.
    Hum Mol Genet; 1999 May; 8(5):907-13. PubMed ID: 10196381
    [Abstract] [Full Text] [Related]

  • 3. Peroxisomal very long chain fatty acid beta-oxidation activity is determined by the level of adrenodeukodystrophy protein (ALDP) expression.
    Braiterman LT, Watkins PA, Moser AB, Smith KD.
    Mol Genet Metab; 1999 Feb; 66(2):91-9. PubMed ID: 10068511
    [Abstract] [Full Text] [Related]

  • 4. Co-expression of mutated and normal adrenoleukodystrophy protein reduces protein function: implications for gene therapy of X-linked adrenoleukodystrophy.
    Unterrainer G, Molzer B, Forss-Petter S, Berger J.
    Hum Mol Genet; 2000 Nov 01; 9(18):2609-16. PubMed ID: 11063720
    [Abstract] [Full Text] [Related]

  • 5. The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.
    Berger J, Albet S, Bentejac M, Netik A, Holzinger A, Roscher AA, Bugaut M, Forss-Petter S.
    Eur J Biochem; 1999 Oct 01; 265(2):719-27. PubMed ID: 10504404
    [Abstract] [Full Text] [Related]

  • 6. A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern.
    Lombard-Platet G, Savary S, Sarde CO, Mandel JL, Chimini G.
    Proc Natl Acad Sci U S A; 1996 Feb 06; 93(3):1265-9. PubMed ID: 8577752
    [Abstract] [Full Text] [Related]

  • 7. Homo- and heterodimerization of peroxisomal ATP-binding cassette half-transporters.
    Liu LX, Janvier K, Berteaux-Lecellier V, Cartier N, Benarous R, Aubourg P.
    J Biol Chem; 1999 Nov 12; 274(46):32738-43. PubMed ID: 10551832
    [Abstract] [Full Text] [Related]

  • 8. Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy.
    McGuinness MC, Lu JF, Zhang HP, Dong GX, Heinzer AK, Watkins PA, Powers J, Smith KD.
    Mol Cell Biol; 2003 Jan 12; 23(2):744-53. PubMed ID: 12509471
    [Abstract] [Full Text] [Related]

  • 9. Very-long-chain fatty acid metabolism in adrenoleukodystrophy protein-deficient mice.
    Yamada T, Shinnoh N, Kondo A, Uchiyama A, Shimozawa N, Kira J, Kobayashi T.
    Cell Biochem Biophys; 2000 Jan 12; 32 Spring():239-46. PubMed ID: 11330052
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Biochemical aspects of X-linked adrenoleukodystrophy.
    Kemp S, Wanders R.
    Brain Pathol; 2010 Jul 28; 20(4):831-7. PubMed ID: 20626744
    [Abstract] [Full Text] [Related]

  • 12. Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3).
    Hillebrand M, Verrier SE, Ohlenbusch A, Schäfer A, Söling HD, Wouters FS, Gärtner J.
    J Biol Chem; 2007 Sep 14; 282(37):26997-27005. PubMed ID: 17609205
    [Abstract] [Full Text] [Related]

  • 13. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
    Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, Steinberg SJ.
    Am J Hum Genet; 2002 Jun 14; 70(6):1520-31. PubMed ID: 11992258
    [Abstract] [Full Text] [Related]

  • 14. Mutational and protein analysis of patients and heterozygous women with X-linked adrenoleukodystrophy.
    Feigenbaum V, Lombard-Platet G, Guidoux S, Sarde CO, Mandel JL, Aubourg P.
    Am J Hum Genet; 1996 Jun 14; 58(6):1135-44. PubMed ID: 8651290
    [Abstract] [Full Text] [Related]

  • 15. Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expression.
    Zhang X, De Marcos Lousa C, Schutte-Lensink N, Ofman R, Wanders RJ, Baldwin SA, Baker A, Kemp S, Theodoulou FL.
    Biochem J; 2011 Jun 15; 436(3):547-57. PubMed ID: 21476988
    [Abstract] [Full Text] [Related]

  • 16. Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy.
    McGuinness MC, Zhang HP, Smith KD.
    Mol Genet Metab; 2001 Jun 15; 74(1-2):256-63. PubMed ID: 11592822
    [Abstract] [Full Text] [Related]

  • 17. HDAC inhibitor SAHA normalizes the levels of VLCFAs in human skin fibroblasts from X-ALD patients and downregulates the expression of proinflammatory cytokines in Abcd1/2-silenced mouse astrocytes.
    Singh J, Khan M, Singh I.
    J Lipid Res; 2011 Nov 15; 52(11):2056-69. PubMed ID: 21891797
    [Abstract] [Full Text] [Related]

  • 18. Topology of ATP-binding domain of adrenoleukodystrophy gene product in peroxisomes.
    Contreras M, Sengupta TK, Sheikh F, Aubourg P, Singh I.
    Arch Biochem Biophys; 1996 Oct 15; 334(2):369-79. PubMed ID: 8900413
    [Abstract] [Full Text] [Related]

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  • 20. Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA.
    Shinnoh N, Yamada T, Yoshimura T, Furuya H, Yoshida Y, Suzuki Y, Shimozawa N, Orii T, Kobayashi T.
    Biochem Biophys Res Commun; 1995 May 25; 210(3):830-6. PubMed ID: 7763255
    [Abstract] [Full Text] [Related]


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