Induction of Fetal Globin in β-Thalassemia: Cellular Obstacles and Molecular Progress

Author:

PERRINE SUSAN P.,CASTANEDA SERGUEI A.,BOOSALIS MICHAEL S.,WHITE GARY L.,JONES BRANDON M.,BOHACEK REGINE

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Reference40 articles.

1. Pharmacologic modulation of fetal hemoglobin;Steinberg;Medicine,2001

2. The importance of the genetic picture and globin synthesis in determining the clinical and haematological features of thalassaemia intermedia;Gallo;Br. J. Haematol.,1979

3. The changing profile of homozygous β-thalassemia: demography, ethnicity, and age distribution of current North American patients and changes in two decades;Pearson;Pediatrics,1996

4. 4Rachmilewitz, E.A. & S.L. Schrier. 2001. Pathophysiology of β-thalassemia. In Disorders of Hemoglobin. M.H. Steinberg, B.G. Forget, D.R. Higgs & R.L. Nagel, Eds.: 233-251. Cambridge University Press. Cambridge.

5. Serum erythropoietin and erythropoiesis in high and low fetal hemoglobin beta-thalassemia intermedia patients;Galanello;Blood,1994

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