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MeSH Review

Vitamin E Deficiency

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Disease relevance of Vitamin E Deficiency


High impact information on Vitamin E Deficiency


Biological context of Vitamin E Deficiency


  1. Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. Doerflinger, N., Linder, C., Ouahchi, K., Gyapay, G., Weissenbach, J., Le Paslier, D., Rigault, P., Belal, S., Ben Hamida, C., Hentati, F. Am. J. Hum. Genet. (1995) [Pubmed]
  2. 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) [Pubmed]
  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) [Pubmed]
  4. The effect of vitamin E deficiency on some platelet membrane properties. Whitin, J.C., Gordon, R.K., Corwin, L.M., Simons, E.R. J. Lipid Res. (1982) [Pubmed]
  5. Effect of alpha tocopherol (vitamin E) deficiency on intestinal transport of passively absorbed drugs. Meshali, M.M., Nightingale, C.H. Journal of pharmaceutical sciences. (1976) [Pubmed]
  6. Vitamin E deficiency reduced lumbar bone calcium content in female rats. Norazlina, M., Chua, C.W., Ima-Nirwana, S. Med. J. Malaysia (2004) [Pubmed]
  7. Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization. Arita, M., Sato, Y., Miyata, A., Tanabe, T., Takahashi, E., Kayden, H.J., Arai, H., Inoue, K. Biochem. J. (1995) [Pubmed]
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