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Journal Abstract Search

220 related items for PubMed ID: 17628170

  • 1. Structure and function of alpha-tocopherol transfer protein: implications for vitamin E metabolism and AVED.
    Christopher Min K.
    Vitam Horm; 2007; 76():23-43. PubMed ID: 17628170
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  • 5. The alpha-tocopherol transfer protein.
    Manor D, Morley S.
    Vitam Horm; 2007; 76():45-65. PubMed ID: 17628171
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  • 6. Crystal structure of human alpha-tocopherol transfer protein bound to its ligand: implications for ataxia with vitamin E deficiency.
    Min KC, Kovall RA, Hendrickson WA.
    Proc Natl Acad Sci U S A; 2003 Dec 09; 100(25):14713-8. PubMed ID: 14657365
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  • 7. Delayed-onset ataxia in mice lacking alpha -tocopherol transfer protein: model for neuronal degeneration caused by chronic oxidative stress.
    Yokota T, Igarashi K, Uchihara T, Jishage K, Tomita H, Inaba A, Li Y, Arita M, Suzuki H, Mizusawa H, Arai H.
    Proc Natl Acad Sci U S A; 2001 Dec 18; 98(26):15185-90. PubMed ID: 11752462
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  • 8. Alpha-tocopherol transfer protein deficiency in mice causes multi-organ deregulation of gene networks and behavioral deficits with age.
    Gohil K, Godzdanker R, O'Roark E, Schock BC, Kaini RR, Packer L, Cross CE, Traber MG.
    Ann N Y Acad Sci; 2004 Dec 18; 1031():109-26. PubMed ID: 15753139
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  • 9. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.
    Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M.
    Nat Genet; 1995 Feb 18; 9(2):141-5. PubMed ID: 7719340
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  • 10. Vitamin E.
    Mustacich DJ, Bruno RS, Traber MG.
    Vitam Horm; 2007 Feb 18; 76():1-21. PubMed ID: 17628169
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  • 11. Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency.
    Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed.
    Ann Neurol; 1996 Mar 18; 39(3):295-300. PubMed ID: 8602747
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  • 12. The molecular basis of vitamin E retention: structure of human alpha-tocopherol transfer protein.
    Meier R, Tomizaki T, Schulze-Briese C, Baumann U, Stocker A.
    J Mol Biol; 2003 Aug 15; 331(3):725-34. PubMed ID: 12899840
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  • 14. Preparation of fluorescent tocopherols for use in protein binding and localization with the alpha-tocopherol transfer protein.
    Nava P, Cecchini M, Chirico S, Gordon H, Morley S, Manor D, Atkinson J.
    Bioorg Med Chem; 2006 Jun 01; 14(11):3721-36. PubMed ID: 16481173
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  • 15. Molecular genetic and expression analysis of alpha-tocopherol transfer protein mRNA in German shepherd dogs with degenerative myelopathy.
    Fechner H, Johnston PE, Sharp NJ, Montague P, Griffiths IR, Wang X, Olby N, Looman AC, Poller W, Flegel T.
    Berl Munch Tierarztl Wochenschr; 2003 Jun 01; 116(1-2):31-6. PubMed ID: 12592926
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  • 16. Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.
    Mariotti C, Gellera C, Rimoldi M, Mineri R, Uziel G, Zorzi G, Pareyson D, Piccolo G, Gambi D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S.
    Neurol Sci; 2004 Jul 01; 25(3):130-7. PubMed ID: 15300460
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  • 18. Vitamin E: an overview of major research directions.
    Zingg JM.
    Mol Aspects Med; 2007 Jul 01; 28(5-6):400-22. PubMed ID: 17624418
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  • 20. [Friedreich's ataxia and hereditary vitamin E deficiency. Case study].
    Labauge P, Cavalier L, Ichalalène L, Castelnovo G.
    Rev Neurol (Paris); 1998 May 01; 154(4):339-41. PubMed ID: 9773063
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