Transferrin therapy ameliorates disease in β-thalassemic mice-Reference-Cited by-同舟云学术

Transferrin therapy ameliorates disease in β-thalassemic mice

Published:2010-01-24 Issue:2 Volume:16 Page:177-182
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Li Huihui,Rybicki Anne C,Suzuka Sandra M,von Bonsdorff Leni,Breuer William,Hall Charles B,Cabantchik Z Ioav,Bouhassira Eric E,Fabry Mary E,Ginzburg Yelena Z

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2073.pdf

Reference45 articles.

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3. Centis, F. et al. The importance of erythroid expansion in determining the extent of apoptosis in erythroid precursors in patients with β-thalassemia major. Blood 96, 3624–3629 (2000).

4. Pippard, M.J., Callender, S.T., Warner, G.T. & Weatherall, D.J. Iron absorption and loading in β-thalassemia intermedia. Lancet 20, 819–821 (1979).

5. Park, C.H., Valore, E.V., Waring, A.J. & Ganz, T. Hepcidin, a urinary antimicrobial peptide synthesized in the liver. J. Biol. Chem. 276, 7806–7810 (2001).

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