On the molecular origins of the chronic myeloproliferative disorders: it all makes sense
Author:
Affiliation:
1. From the Department of Medicine, Division of Hematology/Oncology, University of California San Diego, San Diego, CA.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/105/11/4187/1708551/zh801105004187.pdf
Reference45 articles.
1. Dameshek W. Some speculations on the myeloproliferative syndromes. Blood. 1951;6: 372-375.
2. Deininger MWN, Goldman JM, Melo JV. The molecular biology of chronic myeloid leukemia. Blood. 2000;96: 3343-3356.
3. Tefferi A, Pardanani A. Clinical, genetic, and therapeutic insights into systemic mast cell disease. Curr Opin Hematol. 2004;11: 58-64.
4. Baxter EJ, Scott LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative diseases. Lancet. 2005;365: 1054-1061.
5. Levine RL, Wadleigh M, Cools J, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. Prepublished on March 24, 2005, as DOI 10.1016/..2005.03.023.
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