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Journal Abstract Search

390 related items for PubMed ID: 12509471

  • 21. Evidence of oxidative stress in very long chain fatty acid--treated oligodendrocytes and potentialization of ROS production using RNA interference-directed knockdown of ABCD1 and ACOX1 peroxisomal proteins.
    Baarine M, Andréoletti P, Athias A, Nury T, Zarrouk A, Ragot K, Vejux A, Riedinger JM, Kattan Z, Bessede G, Trompier D, Savary S, Cherkaoui-Malki M, Lizard G.
    Neuroscience; 2012 Jun 28; 213():1-18. PubMed ID: 22521832
    [Abstract] [Full Text] [Related]

  • 22. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters.
    van Roermund CW, Visser WF, Ijlst L, van Cruchten A, Boek M, Kulik W, Waterham HR, Wanders RJ.
    FASEB J; 2008 Dec 28; 22(12):4201-8. PubMed ID: 18757502
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  • 23. X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes.
    Weber FD, Wiesinger C, Forss-Petter S, Regelsberger G, Einwich A, Weber WH, Köhler W, Stockinger H, Berger J.
    Hum Mol Genet; 2014 May 15; 23(10):2542-50. PubMed ID: 24363066
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  • 24. ABC subfamily D proteins and very long chain fatty acid metabolism as novel targets in adrenoleukodystrophy.
    Morita M, Shimozawa N, Kashiwayama Y, Suzuki Y, Imanaka T.
    Curr Drug Targets; 2011 May 15; 12(5):694-706. PubMed ID: 21039332
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  • 25. 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
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  • 31. 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 15; 90(3):268-76. PubMed ID: 17092750
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  • 33. 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
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  • 34. Profiling and Imaging of Phospholipids in Brains of Abcd1-Deficient Mice.
    Hama K, Fujiwara Y, Morita M, Yamazaki F, Nakashima Y, Takei S, Takashima S, Setou M, Shimozawa N, Imanaka T, Yokoyama K.
    Lipids; 2018 Jan 15; 53(1):85-102. PubMed ID: 29469952
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  • 35. Metformin-induced mitochondrial function and ABCD2 up-regulation in X-linked adrenoleukodystrophy involves AMP-activated protein kinase.
    Singh J, Olle B, Suhail H, Felicella MM, Giri S.
    J Neurochem; 2016 Jul 15; 138(1):86-100. PubMed ID: 26849413
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  • 37. ABCD1 Transporter Deficiency Results in Altered Cholesterol Homeostasis.
    Buda A, Forss-Petter S, Hua R, Jaspers Y, Lassnig M, Waidhofer-Söllner P, Kemp S, Kim P, Weinhofer I, Berger J.
    Biomolecules; 2023 Aug 31; 13(9):. PubMed ID: 37759733
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  • 38. ABCD1 translation-initiator mutation demonstrates genotype-phenotype correlation for AMN.
    O'Neill GN, Aoki M, Brown RH.
    Neurology; 2001 Dec 11; 57(11):1956-62. PubMed ID: 11739809
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  • 39. X-linked adrenoleukodystrophy: clinical, metabolic, genetic and pathophysiological aspects.
    Kemp S, Berger J, Aubourg P.
    Biochim Biophys Acta; 2012 Sep 11; 1822(9):1465-74. PubMed ID: 22483867
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  • 40. 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
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