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2. The JAK2V617F allele burden and STAT3- and STAT5 phosphorylation in myeloproliferative neoplasms: early prefibrotic myelofibrosis compared with essential thrombocythemia, polycythemia vera and myelofibrosis. Risum M; Madelung A; Bondo H; Bzorek M; Kristensen MH; Stamp IM; Hasselbalch HC APMIS; 2011 Aug; 119(8):498-504. PubMed ID: 21749449 [TBL] [Abstract][Full Text] [Related]
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4. The presence of JAK2V617F in primary myelofibrosis or its allele burden in polycythemia vera predicts chemosensitivity to hydroxyurea. Sirhan S; Lasho TL; Hanson CA; Mesa RA; Pardanani A; Tefferi A Am J Hematol; 2008 May; 83(5):363-5. PubMed ID: 18266209 [TBL] [Abstract][Full Text] [Related]
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6. JAK2V617F mutational frequency in polycythemia vera: 100%, >90%, less? Verstovsek S; Silver RT; Cross NC; Tefferi A Leukemia; 2006 Nov; 20(11):2067. PubMed ID: 16990780 [No Abstract] [Full Text] [Related]
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8. JAK2V617F mutation in a 9-year-old girl with polycythemia vera and Budd-Chiari syndrome: a case report. Benedik-Dolničar M; Homan M; Brecelj J J Pediatr Hematol Oncol; 2012 Apr; 34(3):243-4. PubMed ID: 21552144 [No Abstract] [Full Text] [Related]
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10. [Correlations of JAK2V617F point mutation with clinical and laboratory features in patients with polycythemia vera]. Shen YF; Xia J; Lu MZ; Jiang YQ Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Feb; 17(1):121-4. PubMed ID: 19236761 [TBL] [Abstract][Full Text] [Related]
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16. Frequent reduction or absence of detection of the JAK2-mutated clone in JAK2V617F-positive patients within the first years of hydroxyurea therapy. Girodon F; Schaeffer C; Cleyrat C; Mounier M; Lafont I; Santos FD; Duval A; Maynadié M; Hermouet S Haematologica; 2008 Nov; 93(11):1723-7. PubMed ID: 18728027 [TBL] [Abstract][Full Text] [Related]
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20. Bone marrow morphologic features in polycythemia vera with JAK2 exon 12 mutations. Lakey MA; Pardanani A; Hoyer JD; Nguyen PL; Lasho TL; Tefferi A; Hanson CA Am J Clin Pathol; 2010 Jun; 133(6):942-8. PubMed ID: 20472853 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]