메뉴 건너뛰기




Volumn 23, Issue 5, 2009, Pages 852-855

MPLW515L mutation in acute megakaryoblastic leukaemia

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2; THROMBOPOIETIN RECEPTOR; JAK2 PROTEIN, HUMAN; MPL PROTEIN, HUMAN;

EID: 66849103934     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/leu.2008.371     Document Type: Article
Times cited : (37)

References (14)
  • 1
    • 31544447448 scopus 로고    scopus 로고
    • Adult acute megakaryocytic leukemia: An analysis of 37 patients treated at MD Anderson Cancer Center
    • Oki Y, Kantarjian HM, Zhou X, Cortes J, Faderl S, Verstovsek S et al Adult acute megakaryocytic leukemia: An analysis of 37 patients treated at MD Anderson Cancer Center. Blood 2006; 107: 880-884.
    • (2006) Blood , vol.107 , pp. 880-884
    • Oki, Y.1    Kantarjian, H.M.2    Zhou, X.3    Cortes, J.4    Faderl, S.5    Verstovsek, S.6
  • 2
    • 34250863880 scopus 로고    scopus 로고
    • Histopathology in the diagnosis and classification of acute myeloid leukemia, myelodysplastic syndromes, and myelodysplastic/ myeloproliferative diseases
    • Orazi A. Histopathology in the diagnosis and classification of acute myeloid leukemia, myelodysplastic syndromes, and myelodysplastic/ myeloproliferative diseases. Pathobiology 2007; 74: 97-114.
    • (2007) Pathobiology , vol.74 , pp. 97-114
    • Orazi, A.1
  • 3
    • 33744500207 scopus 로고    scopus 로고
    • JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained
    • Steensma DP, McClure RF, Karp JE, Tefferi A, Lasho TL, Powell HL et al. JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained. Leukemia 2006; 20: 971-978.
    • (2006) Leukemia , vol.20 , pp. 971-978
    • Steensma, D.P.1    McClure, R.F.2    Karp, J.E.3    Tefferi, A.4    Lasho, T.L.5    Powell, H.L.6
  • 4
    • 0030465354 scopus 로고    scopus 로고
    • Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26
    • Schnittger S, de Sauvage FJ, Le Paslier D, Fonatsch C. Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26. Leukemia 1996; 10: 1891-1896.
    • (1996) Leukemia , vol.10 , pp. 1891-1896
    • Schnittger, S.1    de Sauvage, F.J.2    Le Paslier, D.3    Fonatsch, C.4
  • 5
    • 54049107944 scopus 로고    scopus 로고
    • Activating mutations in human acute megakaryoblastic leukemia
    • e-pub ahead of print
    • Malinge S, Ragu C, Delia-Valle V, Pisani D, Constantinescu SN, Perez C et al. Activating mutations in human acute megakaryoblastic leukemia. Blood 2008; 112: 4220-4226; [e-pub ahead of print].
    • (2008) Blood , vol.112 , pp. 4220-4226
    • Malinge, S.1    Ragu, C.2    Delia-Valle, V.3    Pisani, D.4    Constantinescu, S.N.5    Perez, C.6
  • 6
    • 33750534561 scopus 로고    scopus 로고
    • MPL515 mutations in myeloproliferative and other myeloid disorders: A study of 1182 patients
    • Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M et al MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood 2006; 108: 3472-3476.
    • (2006) Blood , vol.108 , pp. 3472-3476
    • Pardanani, A.D.1    Levine, R.L.2    Lasho, T.3    Pikman, Y.4    Mesa, R.A.5    Wadleigh, M.6
  • 7
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    • James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C 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    Staerk, J.4    Delhommeau, F.5    Lacout, C.6
  • 8
    • 25844447519 scopus 로고    scopus 로고
    • JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosomenegative CML, and megakaryocytic leukemia
    • Jelinek J, Oki Y, Charibyan V, Bueso-Ramos C, Prchal JT, Verstovsek S et al. JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia chromosomenegative CML, and megakaryocytic leukemia. Blood 2005; 106: 3370-3373.
    • (2005) Blood , vol.106 , pp. 3370-3373
    • Jelinek, J.1    Oki, Y.2    Charibyan, V.3    Bueso-Ramos, C.4    Prchal, J.T.5    Verstovsek, S.6
  • 9
    • 34249712934 scopus 로고    scopus 로고
    • Expression of the JAK2 V617F mutation is not found in de novo AML and MDS but is detected in MDS-derived leukemia of megakaryoblastic nature
    • Nishii K, Nanbu R, Lorenzo VF, Monma F, Kato K, Ryuu H et al. Expression of the JAK2 V617F mutation is not found in de novo AML and MDS but is detected in MDS-derived leukemia of megakaryoblastic nature. Leukemia 2007; 21: 1337-1338.
    • (2007) Leukemia , vol.21 , pp. 1337-1338
    • Nishii, K.1    Nanbu, R.2    Lorenzo, V.F.3    Monma, F.4    Kato, K.5    Ryuu, H.6
  • 10
    • 31544474025 scopus 로고    scopus 로고
    • Rare occurrence of the JAK2 V617F mutation in AML subtypes M5, M6, and M7
    • Fröhling S, Lipka DB, Kayser S, Scholl C, Schlenk RF, Döhner H et al. Rare occurrence of the JAK2 V617F mutation in AML subtypes M5, M6, and M7. Blood 2006; 107: 1242-1243.
    • (2006) Blood , vol.107 , pp. 1242-1243
    • Fröhling, S.1    Lipka, D.B.2    Kayser, S.3    Scholl, C.4    Schlenk, R.F.5    Döhner, H.6
  • 11
    • 0037322641 scopus 로고    scopus 로고
    • Quantitative intra-individual monitoring-of BCR-ABL transcript levels in archival bone marrow trephines of patients with chronic myeloid leukemia
    • Bock O, Lehmann U, Kreipe H. Quantitative intra-individual monitoring-of BCR-ABL transcript levels in archival bone marrow trephines of patients with chronic myeloid leukemia. J Mol Diagn 2003; 5: 54-60.
    • (2003) J Mol Diagn , vol.5 , pp. 54-60
    • Bock, O.1    Lehmann, U.2    Kreipe, H.3
  • 12
    • 34547946210 scopus 로고    scopus 로고
    • Analysis of JAK3, JAK2, and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome
    • Norton A, Fisher C, Liu H, Wen Q, Mundschau G, Fuster JL et al. Analysis of JAK3, JAK2, and C-MPL mutations in transient myeloproliferative disorder and myeloid leukemia of Down syndrome blasts in children with Down syndrome. Blood 2007; 110: 1077-1079.
    • (2007) Blood , vol.110 , pp. 1077-1079
    • Norton, A.1    Fisher, C.2    Liu, H.3    Wen, Q.4    Mundschau, G.5    Fuster, J.L.6
  • 14
    • 43749104715 scopus 로고    scopus 로고
    • Chronic myeloproliferative diseases with concurrent BCR-ABL junction and JAK2V617F mutation
    • Hussein K, Bock O, Theophile K, Seegers A, Arps H, Basten O et al. Chronic myeloproliferative diseases with concurrent BCR-ABL junction and JAK2V617F mutation. Leukemia 2008; 22: 1059-1062.
    • (2008) Leukemia , vol.22 , pp. 1059-1062
    • Hussein, K.1    Bock, O.2    Theophile, K.3    Seegers, A.4    Arps, H.5    Basten, O.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.