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Volumn 108, Issue 5, 2006, Pages 1781-1782

The JAK2-V617F mutation and essential thrombocythemia features in a subset of patients with refractory anemia with ring sideroblasts (RARS) [9]

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2;

EID: 33748177825     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2006-03-008227     Document Type: Letter
Times cited : (52)

References (8)
  • 2
    • 0036220061 scopus 로고    scopus 로고
    • Essential thrombocythemia with ringed sideroblasts: A heterogenous spectrum of diseases, but not a distinct entity
    • Schmitt-Graeff A, Thiele J, Zuk I, Kvasnicka HM. Essential thrombocythemia with ringed sideroblasts: a heterogenous spectrum of diseases, but not a distinct entity. Haematologica. 2002;87:392-399.
    • (2002) Haematologica , vol.87 , pp. 392-399
    • Schmitt-Graeff, A.1    Thiele, J.2    Zuk, I.3    Kvasnicka, H.M.4
  • 3
    • 32944465625 scopus 로고    scopus 로고
    • Ringed sideroblasts with thrombocytosis: An uncommon mixed myelodysplastic/myeloproliferative disease of older adults
    • Shaw GR. Ringed sideroblasts with thrombocytosis: an uncommon mixed myelodysplastic/myeloproliferative disease of older adults. Br J Haematol. 2005;131:180-184.
    • (2005) Br J Haematol , vol.131 , pp. 180-184
    • Shaw, G.R.1
  • 4
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    • James C, Ugo V, Le Couedic JP, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature. 2005;434:1144-1148.
    • (2005) Nature , vol.434 , pp. 1144-1148
    • James, C.1    Ugo, V.2    Le Couedic, J.P.3
  • 5
    • 21344440357 scopus 로고    scopus 로고
    • The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes
    • Steensma DP, Dewald GW, Lasho TL, et al. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes. Blood. 2005;106:1207-1209.
    • (2005) Blood , vol.106 , pp. 1207-1209
    • Steensma, D.P.1    Dewald, G.W.2    Lasho, T.L.3
  • 6
    • 33748684367 scopus 로고    scopus 로고
    • The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera
    • Prepublished on May 25, 2006, as DOI 10.1182/blood-2006-01-013540
    • Lippert E, Boissinot M, Kralovics R, et al. The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera. Blood. Prepublished on May 25, 2006, as DOI 10.1182/blood-2006-01-013540.
    • Blood
    • Lippert, E.1    Boissinot, M.2    Kralovics, R.3
  • 7
    • 28544431813 scopus 로고    scopus 로고
    • The JAK2 V617F tyrosine kinase mutation in myelodysplastic syndromes (MDS) developing myelofibrosis indicates the myeloproliferative nature in a subset of MDS patients
    • Ohyashiki K, Aota Y, Akahane D, et al. The JAK2 V617F tyrosine kinase mutation in myelodysplastic syndromes (MDS) developing myelofibrosis indicates the myeloproliferative nature in a subset of MDS patients. Leukemia. 2005;19:2359-2360.
    • (2005) Leukemia , vol.19 , pp. 2359-2360
    • Ohyashiki, K.1    Aota, Y.2    Akahane, D.3
  • 8
    • 6344277580 scopus 로고    scopus 로고
    • A standardized endogenous megakaryocytic/erythroid (EMC/EEC) colony assay for the diagnosis of essential thrombocythemia
    • Dobo I, Boiret N, Lippert E, et al. A standardized endogenous megakaryocytic/erythroid (EMC/EEC) colony assay for the diagnosis of essential thrombocythemia. Haematologica. 2004;89:1203-1208.
    • (2004) Haematologica , vol.89 , pp. 1203-1208
    • Dobo, I.1    Boiret, N.2    Lippert, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.