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Nature Medicine  1, 307 - 308 (1995)
doi:10.1038/nm0495-307

Sickle cell paths converge on hydroxyurea

Orah S. Platt1

1Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA

The realization that a mutation in a haemoglobin gene is at the root of sickle cell anaemia and the discovery of an effective treatment are separated by years. But sickle cell research is a model for how different paths of inquiry can come together with good result.

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  9. Letvin, N.L., Linch, D.C., Beardsley, G.P., Mcln-tyre, K.W. & Nathan, D.G. Augmentation of fetal hemoglobin production in anemic monkeys by hydroxyurea. New Engl. J. Med. 310, 869−873 (1984). | PubMed  | ISI | ChemPort |
  10. Platt, O.S., Orkin, S.H., Dover, G., Beardsley, G.P., Miller, B. & Nathan, D.G. Hydroxyurea en-hancess fetal hemoglobin production in sickle cell anemia. J. clin. Invest. 74, 652−656 (1987).
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  12. Charache, S. et al. Hydroxyurea: Effects on hemoglobin F production in patients with sickle cell anemia. Blood 79, 2555−2565 (1992). | PubMed  | ISI | ChemPort |
  13. Goldberg, M.A. et al. Treatment of sickle cell anemia with hydroxyurea and erythropoietin. New Engl. J. Med. 323, 366−372 (1990). | PubMed  | ISI | ChemPort |
  14. Bridges, K. et al. Hydroxyurea changes SS RBC biochemical/biophysical profile to that of SC RBCs. Blood 84 (suppl. 1), 413a (1994).
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ISSN: 1078-8956
EISSN: 1546-170X
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