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Items: 1 to 20 of 268

1.

The alpha-tocopherol transfer protein.

Manor D, Morley S.

Vitam Horm. 2007;76:45-65. Review.

PMID:
17628171
2.

Biochemical consequences of heritable mutations in the alpha-tocopherol transfer protein.

Qian J, Atkinson J, Manor D.

Biochemistry. 2006 Jul 11;45(27):8236-42.

PMID:
16819822
3.

Molecular determinants of heritable vitamin E deficiency.

Morley S, Panagabko C, Shineman D, Mani B, Stocker A, Atkinson J, Manor D.

Biochemistry. 2004 Apr 13;43(14):4143-9.

PMID:
15065857
4.

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.

PMID:
12899840
5.
6.

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;1031:109-26.

PMID:
15753139
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.

8.

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;9(2):141-5.

PMID:
7719340
9.

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;25(3):130-7.

PMID:
15300460
10.

Prolonged alpha-tocopherol deficiency decreases oxidative stress and unmasks alpha-tocopherol-dependent regulation of mitochondrial function in the brain.

Cuddihy SL, Ali SS, Musiek ES, Lucero J, Kopp SJ, Morrow JD, Dugan LL.

J Biol Chem. 2008 Mar 14;283(11):6915-24. doi: 10.1074/jbc.M702572200. Epub 2008 Jan 7.

12.

Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families.

Cavalier L, Ouahchi K, Kayden HJ, Di Donato S, Reutenauer L, Mandel JL, Koenig M.

Am J Hum Genet. 1998 Feb;62(2):301-10.

13.

Molecular mechanisms of vitamin E transport.

Stocker A.

Ann N Y Acad Sci. 2004 Dec;1031:44-59. Review.

PMID:
15753133
14.

Intracellular trafficking of vitamin E in hepatocytes: the role of tocopherol transfer protein.

Qian J, Morley S, Wilson K, Nava P, Atkinson J, Manor D.

J Lipid Res. 2005 Oct;46(10):2072-82. Epub 2005 Jul 16.

15.

The α-tocopherol transfer protein is essential for vertebrate embryogenesis.

Miller GW, Ulatowski L, Labut EM, Lebold KM, Manor D, Atkinson J, Barton CL, Tanguay RL, Traber MG.

PLoS One. 2012;7(10):e47402. doi: 10.1371/journal.pone.0047402. Epub 2012 Oct 15.

16.

[Physiological function of alpha-tocopherol transfer protein].

Arita M, Arai H, Inoue K.

Tanpakushitsu Kakusan Koso. 1999 Jun;44(8 Suppl):1219-26. Review. Japanese. No abstract available.

PMID:
10397007
17.

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 Jan-Feb;116(1-2):31-6.

PMID:
12592926
18.

Vitamin E trafficking.

Traber MG, Burton GW, Hamilton RL.

Ann N Y Acad Sci. 2004 Dec;1031:1-12. Review.

PMID:
15753129
19.
20.

Cerebellar ataxia due to isolated vitamin E deficiency.

Jayaram S, Soman A, Tarvade S, Londhe V.

Indian J Med Sci. 2005 Jan;59(1):20-3.

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