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215 related items for PubMed ID: 10329405

  • 1. Full length cDNA cloning, promoter sequence, and genomic organization of the human adrenoleukodystrophy related (ALDR) gene functionally redundant to the gene responsible for X-linked adrenoleukodystrophy.
    Holzinger A, Mayerhofer P, Berger J, Lichtner P, Kammerer S, Roscher AA.
    Biochem Biophys Res Commun; 1999 May 10; 258(2):436-42. PubMed ID: 10329405
    [Abstract] [Full Text] [Related]

  • 2. Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP).
    Broccardo C, Troffer-Charlier N, Savary S, Mandel JL, Chimini G.
    Eur J Hum Genet; 1998 May 10; 6(6):638-41. PubMed ID: 9887385
    [Abstract] [Full Text] [Related]

  • 3. 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 10; 8(5):907-13. PubMed ID: 10196381
    [Abstract] [Full Text] [Related]

  • 4. cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.
    Holzinger A, Kammerer S, Berger J, Roscher AA.
    Biochem Biophys Res Commun; 1997 Oct 09; 239(1):261-4. PubMed ID: 9345306
    [Abstract] [Full Text] [Related]

  • 5. Rat adrenoleukodystrophy-related (ALDR) gene: full-length cDNA sequence and new insight in expression.
    Albet S, Bentejac M, Savary S, Gondcaille C, Netik A, Berger J, Szpirer C, Troffer-Charlier N, Bugaut M.
    Biochim Biophys Acta; 2001 Jan 26; 1517(2):257-69. PubMed ID: 11342107
    [Abstract] [Full Text] [Related]

  • 6. Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.
    Kemp S, Wei HM, Lu JF, Braiterman LT, McGuinness MC, Moser AB, Watkins PA, Smith KD.
    Nat Med; 1998 Nov 26; 4(11):1261-8. PubMed ID: 9809549
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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 06; 265(2):719-27. PubMed ID: 10504404
    [Abstract] [Full Text] [Related]

  • 9. Evaluation of pharmacological induction of fatty acid beta-oxidation in X-linked adrenoleukodystrophy.
    McGuinness MC, Zhang HP, Smith KD.
    Mol Genet Metab; 2001 Oct 06; 74(1-2):256-63. PubMed ID: 11592822
    [Abstract] [Full Text] [Related]

  • 10. X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment.
    Kemp S, Wanders RJ.
    Mol Genet Metab; 2007 Mar 06; 90(3):268-76. PubMed ID: 17092750
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolin.
    Pujol A, Troffer-Charlier N, Metzger E, Chimini G, Mandel JL.
    Genomics; 2000 Nov 15; 70(1):131-9. PubMed ID: 11087670
    [Abstract] [Full Text] [Related]

  • 13. Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters.
    Mosser J, Douar AM, Sarde CO, Kioschis P, Feil R, Moser H, Poustka AM, Mandel JL, Aubourg P.
    Nature; 1993 Feb 25; 361(6414):726-30. PubMed ID: 8441467
    [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 25; 58(6):1135-44. PubMed ID: 8651290
    [Abstract] [Full Text] [Related]

  • 15. Substrate specificity overlap and interaction between adrenoleukodystrophy protein (ALDP/ABCD1) and adrenoleukodystrophy-related protein (ALDRP/ABCD2).
    Genin EC, Geillon F, Gondcaille C, Athias A, Gambert P, Trompier D, Savary S.
    J Biol Chem; 2011 Mar 11; 286(10):8075-8084. PubMed ID: 21209459
    [Abstract] [Full Text] [Related]

  • 16. Mutational analysis of patients with X-linked adrenoleukodystrophy.
    Kok F, Neumann S, Sarde CO, Zheng S, Wu KH, Wei HM, Bergin J, Watkins PA, Gould S, Sack G.
    Hum Mutat; 1995 Mar 11; 6(2):104-15. PubMed ID: 7581394
    [Abstract] [Full Text] [Related]

  • 17. Fibrate induction of the adrenoleukodystrophy-related gene (ABCD2): promoter analysis and role of the peroxisome proliferator-activated receptor PPARalpha.
    Fourcade S, Savary S, Albet S, Gauthé D, Gondcaille C, Pineau T, Bellenger J, Bentejac M, Holzinger A, Berger J, Bugaut M.
    Eur J Biochem; 2001 Jun 11; 268(12):3490-500. PubMed ID: 11422379
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 01; 7(2):239-47. PubMed ID: 9425230
    [Abstract] [Full Text] [Related]

  • 20. Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.
    Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA.
    J Neurosci Res; 1997 Dec 01; 50(5):829-43. PubMed ID: 9418970
    [Abstract] [Full Text] [Related]

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