Absence of the JAK2 mutation V617F in CD34+ hematopoietic stem and progenitor cells from patients with BCR-ABL-positive CML in chronic phase and blast crisis
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference10 articles.
1. A unique activating mutation in JAK2 (V617F) is at the origin of polycythemia vera and allows a new classification of myeloproliferative diseases;Vainchenker;Hematology (Am Soc Hematol Educ Program),2005
2. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders;Jones;Blood,2005
3. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia;Jelinek;Blood,2005
4. The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia;Levine;Blood,2005
5. The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders;Scott;Blood,2005
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Emergence of BCR-ABL1 Chronic Myeloid Leukemia in a JAK2-V617F Polycythemia Vera;Journal of Hematology;2020
2. Simultaneous occurrence of the JAK2V617F mutation and BCR-ABL gene rearrangement in patients with chronic myeloproliferative disorders;Leukemia Research;2008-06
3. Analysis of the exon 12 and 14 mutations of the JAK2 gene in Philadelphia chromosome-positive leukemia;Leukemia;2007-09-13
4. Marrow fibrosis and its relevance during imatinib treatment of chronic myeloid leukemia;Leukemia;2007-09-06
5. Reply to ‘Myeloproliferative disorders with coexisting BCR-ABL translocation and JAK2V617F mutation’ by Dr Ronald S Go;Leukemia;2007-06-28
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