Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 203

1.

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
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.

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
4.

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
5.
6.
7.

Ligand specificity in the CRAL-TRIO protein family.

Panagabko C, Morley S, Hernandez M, Cassolato P, Gordon H, Parsons R, Manor D, Atkinson J.

Biochemistry. 2003 Jun 3;42(21):6467-74.

PMID:
12767229
8.

The alpha-tocopherol transfer protein.

Manor D, Morley S.

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

PMID:
17628171
9.

Expression and refolding of recombinant human alpha-tocopherol transfer protein capable of specific alpha-tocopherol binding.

Panagabko C, Morley S, Neely S, Lei H, Manor D, Atkinson J.

Protein Expr Purif. 2002 Apr;24(3):395-403.

PMID:
11922755
10.

Impaired α-TTP-PIPs interaction underlies familial vitamin E deficiency.

Kono N, Ohto U, Hiramatsu T, Urabe M, Uchida Y, Satow Y, Arai H.

Science. 2013 May 31;340(6136):1106-10. doi: 10.1126/science.1233508. Epub 2013 Apr 18.

11.

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.

12.

pH-dependent translocation of alpha-tocopherol transfer protein (alpha-TTP) between hepatic cytosol and late endosomes.

Horiguchi M, Arita M, Kaempf-Rotzoll DE, Tsujimoto M, Inoue K, Arai H.

Genes Cells. 2003 Oct;8(10):789-800.

13.

Structural consequences of mutations to the α-tocopherol transfer protein associated with the neurodegenerative disease ataxia with vitamin E deficiency.

Bromley D, Anderson PC, Daggett V.

Biochemistry. 2013 Jun 18;52(24):4264-73. doi: 10.1021/bi4001084. Epub 2013 Jun 10.

14.

The contribution of surface residues to membrane binding and ligand transfer by the α-tocopherol transfer protein (α-TTP).

Zhang WX, Thakur V, Lomize A, Pogozheva I, Panagabko C, Cecchini M, Baptist M, Morley S, Manor D, Atkinson J.

J Mol Biol. 2011 Jan 28;405(4):972-88. doi: 10.1016/j.jmb.2010.11.028. Epub 2010 Nov 24.

15.

Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.

Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, Zaim A, Schmitt M, Belaidi H, Ouazzani R, Chkili T, Koenig M.

J Neurol Sci. 2002 Jun 15;198(1-2):25-9.

PMID:
12039660
16.

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
17.

Ataxia with isolated vitamin E deficiency: a Japanese family carrying a novel mutation in the alpha-tocopherol transfer protein gene.

Hoshino M, Masuda N, Ito Y, Murata M, Goto J, Sakurai M, Kanazawa I.

Ann Neurol. 1999 Jun;45(6):809-12.

PMID:
10360777
18.

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
19.

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;39(3):295-300.

PMID:
8602747
20.

Vitamin E trafficking.

Traber MG, Burton GW, Hamilton RL.

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

PMID:
15753129

Supplemental Content

Support Center