JAK2V617F mutation in essential thrombocythaemia: clinical associations and long‐term prognostic relevance
暂无分享,去创建一个
M. Wadleigh | A. Tefferi | Stephanie J. Lee | T. Lasho | A. Wolanskyj | R. McClure | S. Schwager | D. Gary Gilliland | R. Mcclure
[1] E. Estey,et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia. , 2005, Blood.
[2] D. Steensma,et al. The JAK2V617F tyrosine kinase mutation in myelofibrosis with myeloid metaplasia: lineage specificity and clinical correlates , 2005 .
[3] H. Heimpel,et al. The Jak2V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patients. , 2005, Blood.
[4] D. Gilliland,et al. Concomitant neutrophil JAK2V617F mutation screening and PRV‐1 expression analysis in myeloproliferative disorders and secondary polycythaemia , 2005, British journal of haematology.
[5] D. Oscier,et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. , 2005, Blood.
[6] David P Steensma,et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. , 2005, Blood.
[7] C. Harrison. Essential thrombocythaemia: challenges and evidence‐based management , 2005, British journal of haematology.
[8] Qingshan Li,et al. Identification of an Acquired JAK2 Mutation in Polycythemia Vera* , 2005, Journal of Biological Chemistry.
[9] Stefan N. Constantinescu,et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera , 2005, Nature.
[10] Mario Cazzola,et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. , 2005, The New England journal of medicine.
[11] Sandra A. Moore,et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. , 2005, Cancer cell.
[12] P. Campbell,et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders , 2005, The Lancet.
[13] A. Tefferi,et al. Thrombosis and haemorrhage in polycythaemia vera and essential thrombocythaemia , 2005, British journal of haematology.
[14] 松山 智洋. What's going on 造血器腫瘍 A gain-of-function mutation of JAK2 in myeloproliferative disorders. Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR, Tichelli A, Cazzola M, Skoda RC. N Engl J Med. 2005; 352: 1779-90. PMID:15858187.--慢性骨髄増殖性疾患においてJAK2遺伝子の変異が高頻度にみられることを示した論文 , 2005 .
[15] D. Oscier,et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. , 2005, Blood.
[16] M. Cazzola,et al. Life expectancy and prognostic factors for survival in patients with polycythemia vera and essential thrombocythemia. , 2004, The American journal of medicine.
[17] A. Tefferi,et al. Platelet‐rich plasma serotonin levels in chronic myeloproliferative disorders: evaluation of diagnostic use and comparison with the neutrophil PRV‐1 assay , 2004, British journal of haematology.
[18] M. Cazzola,et al. Clinical significance of neutrophil CD177 mRNA expression in Ph‐negative chronic myeloproliferative disorders , 2004, British journal of haematology.
[19] R. Mesa,et al. Neutrophil PRV-1 expression across the chronic myeloproliferative disorders and in secondary or spurious polycythemia. , 2004, Blood.
[20] A. Dispenzieri,et al. FIP1L1-PDGFRA and c-kit D816V mutation-based clonality studies in systemic mast cell disease associated with eosinophilia. , 2004, Haematologica.
[21] T. Barbui,et al. Practice guidelines for the therapy of essential thrombocythemia. A statement from the Italian Society of Hematology, the Italian Society of Experimental Hematology and the Italian Group for Bone Marrow Transplantation. , 2004, Haematologica.
[22] A. Tefferi,et al. Both B and T lymphocytes may be clonally involved in myelofibrosis with myeloid metaplasia. , 2003, Blood.
[23] Juergen Thiele,et al. Clinical and Pathological Criteria for the Diagnosis of Essential Thrombocythemia, Polycythemia Vera, and Idiopathic Myelofibrosis (Agnogenic Myeloid Metaplasia) , 2002, International journal of hematology.
[24] J. Marsden,et al. Serum erythropoietin values in erythrocytoses and in primary thrombocythaemia , 2002, British journal of haematology.
[25] R. Fonseca,et al. A long-term retrospective study of young women with essential thrombocythemia. , 2001, Mayo Clinic proceedings.
[26] Paulo N. Correa,et al. Hypersensitivity of circulating progenitor cells to megakaryocyte growth and development factor (PEG-rHu MGDF) in essential thrombocythemia. , 2000, Blood.
[27] A. Tefferi,et al. Megakaryocyte c‐Mpl expression inchronic myeloproliferative disorders and the myelodysplastic syndrome: immunoperoxidase staining patterns and clinical correlates , 2000, European journal of haematology.
[28] A. Mire-Sluis,et al. Platelet c‐mpl expression is dysregulated in patients with essential thrombocythaemia but this is not of diagnostic value , 1999, British journal of haematology.
[29] C. Harrison,et al. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications. , 1999, Blood.
[30] E. Ikkala,et al. Megakaryocyte and erythroid colony formation in essential thrombocythaemia and reactive thrombocytosis: diagnostic value and correlation to complications , 1993, British journal of haematology.
[31] G. Faguet,et al. Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell. , 1981, Blood.