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Journal Abstract Search

358 related items for PubMed ID: 10196381

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

  • 22. Cholesterol regulates ABCD2 expression: implications for the therapy of X-linked adrenoleukodystrophy.
    Weinhofer I, Forss-Petter S, Zigman M, Berger J.
    Hum Mol Genet; 2002 Oct 15; 11(22):2701-8. PubMed ID: 12374760
    [Abstract] [Full Text] [Related]

  • 23. Biochemical aspects of X-linked adrenoleukodystrophy.
    Kemp S, Wanders R.
    Brain Pathol; 2010 Jul 15; 20(4):831-7. PubMed ID: 20626744
    [Abstract] [Full Text] [Related]

  • 24. 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 15; 58(6):1135-44. PubMed ID: 8651290
    [Abstract] [Full Text] [Related]

  • 25. Bezafibrate lowers very long-chain fatty acids in X-linked adrenoleukodystrophy fibroblasts by inhibiting fatty acid elongation.
    Engelen M, Schackmann MJ, Ofman R, Sanders RJ, Dijkstra IM, Houten SM, Fourcade S, Pujol A, Poll-The BT, Wanders RJ, Kemp S.
    J Inherit Metab Dis; 2012 Nov 15; 35(6):1137-45. PubMed ID: 22447153
    [Abstract] [Full Text] [Related]

  • 26. ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.
    Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ.
    J Inherit Metab Dis; 1996 Nov 15; 19(5):667-74. PubMed ID: 8892025
    [Abstract] [Full Text] [Related]

  • 27. Adrenoleukodystrophy protein enhances association of very long-chain acyl-coenzyme A synthetase with the peroxisome.
    Yamada T, Taniwaki T, Shinnoh N, Uchiyama A, Shimozawa N, Ohyagi Y, Asahara H, Kira J.
    Neurology; 1999 Feb 15; 52(3):614-6. PubMed ID: 10025797
    [Abstract] [Full Text] [Related]

  • 28. PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene.
    Shani N, Watkins PA, Valle D.
    Proc Natl Acad Sci U S A; 1995 Jun 20; 92(13):6012-6. PubMed ID: 7597071
    [Abstract] [Full Text] [Related]

  • 29. Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation.
    van Roermund CW, Visser WF, Ijlst L, Waterham HR, Wanders RJ.
    Biochim Biophys Acta; 2011 Mar 20; 1811(3):148-52. PubMed ID: 21145416
    [Abstract] [Full Text] [Related]

  • 30. Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice.
    Muneer Z, Wiesinger C, Voigtländer T, Werner HB, Berger J, Forss-Petter S.
    PLoS One; 2014 Mar 20; 9(9):e108655. PubMed ID: 25255441
    [Abstract] [Full Text] [Related]

  • 31. Altered expression of ALDP in X-linked adrenoleukodystrophy.
    Watkins PA, Gould SJ, Smith MA, Braiterman LT, Wei HM, Kok F, Moser AB, Moser HW, Smith KD.
    Am J Hum Genet; 1995 Aug 20; 57(2):292-301. PubMed ID: 7668254
    [Abstract] [Full Text] [Related]

  • 32. 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 20; 268(12):3490-500. PubMed ID: 11422379
    [Abstract] [Full Text] [Related]

  • 33. A novel cell model to study the function of the adrenoleukodystrophy-related protein.
    Gueugnon F, Volodina N, Taouil JE, Lopez TE, Gondcaille C, Grand AS, Mooijer PA, Kemp S, Wanders RJ, Savary S.
    Biochem Biophys Res Commun; 2006 Mar 03; 341(1):150-7. PubMed ID: 16412981
    [Abstract] [Full Text] [Related]

  • 34. Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism.
    Kobayashi T, Shinnoh N, Kondo A, Yamada T.
    Biochem Biophys Res Commun; 1997 Mar 27; 232(3):631-6. PubMed ID: 9126326
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis.
    Guimarães CP, Sá-Miranda C, Azevedo JE.
    J Hum Genet; 2005 Jan 26; 50(2):99-105. PubMed ID: 15682271
    [Abstract] [Full Text] [Related]

  • 37. 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 26; 23(2):744-53. PubMed ID: 12509471
    [Abstract] [Full Text] [Related]

  • 38. Functional characterization of the adrenoleukodystrophy protein (ALDP) and disease pathogenesis.
    Gärtner J, Dehmel T, Klusmann A, Roerig P.
    Endocr Res; 2002 Nov 26; 28(4):741-8. PubMed ID: 12530690
    [Abstract] [Full Text] [Related]

  • 39. Peroxisomal ABC Transporters: An Update.
    Tawbeh A, Gondcaille C, Trompier D, Savary S.
    Int J Mol Sci; 2021 Jun 05; 22(11):. PubMed ID: 34198763
    [Abstract] [Full Text] [Related]

  • 40. 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 05; 70(6):1520-31. PubMed ID: 11992258
    [Abstract] [Full Text] [Related]

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