Induction of γ-globin gene expression by tallimustine analogs in human erythroid cells
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826 haematologica/journal of hematology vol. 88(07):july 2003 common mutation in hemochromastosis type 4. Blood 2002;100:733-4. 8. Camaschella C, Roetto A, De Gobbi M. Genetic haemochromatosis: genes and mutations associated with iron loading Best Pract Res Clin Haematol 2002;15:261-76. 9. Cazzola M, Cremonesi L, Papaioannou M, Soriani N, Kioumi A, Charalambidou A, et al. Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3). Br J Haematol 2002;119:539-46. 10. Wallace DF, Pedersen P, Dixon JL, Stephenson P, Searle JW, Powell LW, et al. Novel mutation in ferroportin 1 gene is associated with autosomal dominant hemochromatosis. Blood 2002;100:692-4. 11. Vulpe CD, Kuo YM, Murphy TL, Cowley L, Askwith C, Libina N, et al. Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse. Nat Genet 1999;21:195-9.
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تاریخ انتشار 2003