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Journal Abstract Search


547 related items for PubMed ID: 16304380

  • 1. A unique activating mutation in JAK2 (V617F) is at the origin of polycythemia vera and allows a new classification of myeloproliferative diseases.
    Vainchenker W, Constantinescu SN.
    Hematology Am Soc Hematol Educ Program; 2005; ():195-200. PubMed ID: 16304380
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  • 3. The 2001 World Health Organization and updated European clinical and pathological criteria for the diagnosis, classification, and staging of the Philadelphia chromosome-negative chronic myeloproliferative disorders.
    Michiels JJ, De Raeve H, Berneman Z, Van Bockstaele D, Hebeda K, Lam K, Schroyens W.
    Semin Thromb Hemost; 2006 Jun; 32(4 Pt 2):307-40. PubMed ID: 16810609
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  • 7. The JAK2V617F mutation in polycythemia vera and other myeloproliferative disorders: one mutation for three diseases?
    James C.
    Hematology Am Soc Hematol Educ Program; 2008 Jun; ():69-75. PubMed ID: 19074061
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  • 8. [Myeloproliferative diseases caused by JAK2 mutation].
    Nagata K, Shimoda K.
    Rinsho Byori; 2009 Apr; 57(4):357-64. PubMed ID: 19489438
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  • 9. New insights into the pathogenesis of JAK2 V617F-positive myeloproliferative disorders and consequences for the management of patients.
    Villeval JL, James C, Pisani DF, Casadevall N, Vainchenker W.
    Semin Thromb Hemost; 2006 Jun; 32(4 Pt 2):341-51. PubMed ID: 16810610
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  • 10. [Advance of study on JAK2 V617F in myeloproliferative disorders -- review].
    Xu YY, Li HM.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2009 Feb; 17(1):238-42. PubMed ID: 19236788
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  • 11. Polycythemia vera: scientific advances and current practice.
    Tefferi A, Spivak JL.
    Semin Hematol; 2005 Oct; 42(4):206-20. PubMed ID: 16210034
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  • 12. Molecular pathogenesis and therapy of polycythemia induced in mice by JAK2 V617F.
    Zaleskas VM, Krause DS, Lazarides K, Patel N, Hu Y, Li S, Van Etten RA.
    PLoS One; 2006 Dec 20; 1(1):e18. PubMed ID: 17183644
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  • 14. JAK2-V617F mutation in Moroccan patients with myeloproliferative disorders: contribution, diagnosis and therapeutic prospects.
    Benmoussa A, Dehbi H, Fehri S, Quessar A, Nadifi S.
    Pathol Biol (Paris); 2011 Aug 20; 59(4):e89-92. PubMed ID: 19939582
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  • 16. [Significance of the JAK2V617F mutation in patients with chronic myeloproliferative neoplasia].
    Iványi JL, Marton E, Plander M.
    Orv Hetil; 2011 Nov 06; 152(45):1795-803. PubMed ID: 22011365
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  • 18. The role of Janus Kinase 2 V617F mutation in extramedullary hematopoiesis of the spleen in neoplastic myeloid disorders.
    Hsieh PP, Olsen RJ, O'Malley DP, Konoplev SN, Hussong JW, Dunphy CH, Perkins SL, Cheng L, Lin P, Chang CC.
    Mod Pathol; 2007 Sep 06; 20(9):929-35. PubMed ID: 17643100
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  • 19. [Evaluation of V617F mutation of JAK2 in negative chromosome Philadelphia chronic myeloproliferative disorders].
    Remacha AF, Puget G, Nomdedéu JF, Estivill C, Sardà MP, Canals C.
    Med Clin (Barc); 2006 Oct 28; 127(16):601-4. PubMed ID: 17145024
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