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Journal Abstract Search

390 related items for PubMed ID: 12509471

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  • 3. [Adrenoleukodystrophy: molecular pathogenesis and development of therapeutic agents].
    Morita M.
    Yakugaku Zasshi; 2007 Jul; 127(7):1059-64. PubMed ID: 17603264
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  • 7. 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 Jul; 9(9):e108655. PubMed ID: 25255441
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  • 10. Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy.
    Heinzer AK, Kemp S, Lu JF, Watkins PA, Smith KD.
    J Biol Chem; 2002 Aug 09; 277(32):28765-73. PubMed ID: 12048192
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  • 11. Biochemical aspects of X-linked adrenoleukodystrophy.
    Kemp S, Wanders R.
    Brain Pathol; 2010 Jul 09; 20(4):831-7. PubMed ID: 20626744
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  • 12. A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.
    Heinzer AK, Watkins PA, Lu JF, Kemp S, Moser AB, Li YY, Mihalik S, Powers JM, Smith KD.
    Hum Mol Genet; 2003 May 15; 12(10):1145-54. PubMed ID: 12719378
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  • 13. [Adrenoleukodystrophy: structure and function of ALDP, and intracellular behavior of mutant ALDP with naturally occurring missense mutations].
    Takahashi N, Morita M, Imanaka T.
    Yakugaku Zasshi; 2007 Jan 15; 127(1):163-72. PubMed ID: 17202797
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  • 14. ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy.
    Baarine M, Beeson C, Singh A, Singh I.
    J Neurochem; 2015 May 15; 133(3):380-96. PubMed ID: 25393703
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  • 15. Caffeic acid phenethyl ester induces adrenoleukodystrophy (Abcd2) gene in human X-ALD fibroblasts and inhibits the proinflammatory response in Abcd1/2 silenced mouse primary astrocytes.
    Singh J, Khan M, Singh I.
    Biochim Biophys Acta; 2013 Apr 15; 1831(4):747-58. PubMed ID: 23318275
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  • 16. The role of ELOVL1 in very long-chain fatty acid homeostasis and X-linked adrenoleukodystrophy.
    Ofman R, Dijkstra IM, van Roermund CW, Burger N, Turkenburg M, van Cruchten A, van Engen CE, Wanders RJ, Kemp S.
    EMBO Mol Med; 2010 Mar 15; 2(3):90-7. PubMed ID: 20166112
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  • 17. 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 15; 7(2):239-47. PubMed ID: 9425230
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  • 18. Astrocytes and mitochondria from adrenoleukodystrophy protein (ABCD1)-deficient mice reveal that the adrenoleukodystrophy-associated very long-chain fatty acids target several cellular energy-dependent functions.
    Kruska N, Schönfeld P, Pujol A, Reiser G.
    Biochim Biophys Acta; 2015 May 15; 1852(5):925-36. PubMed ID: 25583114
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  • 19. 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
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  • 20. Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy.
    López-Erauskin J, Galino J, Ruiz M, Cuezva JM, Fabregat I, Cacabelos D, Boada J, Martínez J, Ferrer I, Pamplona R, Villarroya F, Portero-Otín M, Fourcade S, Pujol A.
    Hum Mol Genet; 2013 Aug 15; 22(16):3296-305. PubMed ID: 23604518
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