메뉴 건너뛰기




Volumn 127, Issue 16, 2006, Pages 601-604

Evaluation of V617F mutation of JAK2 in negative chromosome Philadelphia chronic myeloproliferative disorders;Valoración de la mutación V617F del gen JAK2 en síndromes mieloproliferativos crónicos con cromosoma Filadelfia negativo

Author keywords

BFU E; Essential thrombocytemia; JAK2; Myelofibrosis; Polycythemia vera

Indexed keywords

JANUS KINASE 2;

EID: 33845436783     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1157/13094416     Document Type: Article
Times cited : (4)

References (26)
  • 1
    • 27244452986 scopus 로고    scopus 로고
    • Genetics of myeloid malignancies: Pathogenetic and clinical implications
    • Frohling S, Scholl C, Gilliland DG, Levine RL. Genetics of myeloid malignancies: pathogenetic and clinical implications. J Clin Oncol. 2005;23:6285-95.
    • (2005) J Clin Oncol , vol.23 , pp. 6285-6295
    • Frohling, S.1    Scholl, C.2    Gilliland, D.G.3    Levine, R.L.4
  • 2
    • 11144235822 scopus 로고    scopus 로고
    • After chronic myelogenous leukemia: Tyrosine kinase inhibitors in other hematologic malignancies
    • Wadleigh M, DeAngelo DJ, Griffin JD, Stone RM. After chronic myelogenous leukemia: tyrosine kinase inhibitors in other hematologic malignancies. Blood. 2005;105:22-30.
    • (2005) Blood , vol.105 , pp. 22-30
    • Wadleigh, M.1    DeAngelo, D.J.2    Griffin, J.D.3    Stone, R.M.4
  • 3
    • 21344467318 scopus 로고    scopus 로고
    • Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
    • Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L, et al. Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood. 2005;106:2162-8.
    • (2005) Blood , vol.106 , pp. 2162-2168
    • Jones, A.V.1    Kreil, S.2    Zoi, K.3    Waghorn, K.4    Curtis, C.5    Zhang, L.6
  • 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, Staerk J, Delhommeau F, Lacout C, et al. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature. 2005;434:1144-8.
    • (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
  • 6
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Cancer Genome Project
    • Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, et al; Cancer Genome Project. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet. 2005;365:1054-61.
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scott, L.M.2    Campbell, P.J.3    East, C.4    Fourouclas, N.5    Swanton, S.6
  • 7
    • 20244369569 scopus 로고    scopus 로고
    • Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
    • Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005;7:387-97.
    • (2005) Cancer Cell , vol.7 , pp. 387-397
    • Levine, R.L.1    Wadleigh, M.2    Cools, J.3    Ebert, B.L.4    Wernig, G.5    Huntly, B.J.6
  • 8
    • 22544481483 scopus 로고    scopus 로고
    • Gain of function, loss of control - A molecular basis for chronic myeloproliferative disorders
    • Cazzola M, Skoda R. Gain of function, loss of control - a molecular basis for chronic myeloproliferative disorders. Haematologica. 2005;90:871-4.
    • (2005) Haematologica , vol.90 , pp. 871-874
    • Cazzola, M.1    Skoda, R.2
  • 9
    • 33644499189 scopus 로고    scopus 로고
    • Not just clonal expansion of hematopoietic cells, but also activation of their progeny in the pathogenesis of myeloproliferative disorders
    • Cazzola M, Passamonti F. Not just clonal expansion of hematopoietic cells, but also activation of their progeny in the pathogenesis of myeloproliferative disorders. Haematologica. 2006;91:159-61.
    • (2006) Haematologica , vol.91 , pp. 159-161
    • Cazzola, M.1    Passamonti, F.2
  • 10
    • 0001639195 scopus 로고
    • Some speculations on the myeloproliferative syndromes
    • Dameshek W. Some speculations on the myeloproliferative syndromes. Blood. 1951;6:372-5.
    • (1951) Blood , vol.6 , pp. 372-375
    • Dameshek, W.1
  • 11
    • 25844461158 scopus 로고    scopus 로고
    • The Jak2 V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patients
    • Goerttler PS, Steimle C, Marz E, Johansson PL, Andreasson B, Griesshammer M, et al. The Jak2 V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patients. Blood. 2005;106:2862-4.
    • (2005) Blood , vol.106 , pp. 2862-2864
    • Goerttler, P.S.1    Steimle, C.2    Marz, E.3    Johansson, P.L.4    Andreasson, B.5    Griesshammer, M.6
  • 12
    • 27144466017 scopus 로고    scopus 로고
    • The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders
    • Scott LM, Campbell PJ, Baxter EJ, Todd T, Stephens P, Edkins S, et al. The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders. Blood. 2005;106:2920-1.
    • (2005) Blood , vol.106 , pp. 2920-2921
    • Scott, L.M.1    Campbell, P.J.2    Baxter, E.J.3    Todd, T.4    Stephens, P.5    Edkins, S.6
  • 13
    • 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. The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both «atypical» myeloproliferative disorders and myelodysplastic syndromes. Blood. 2005;106:1207-9.
    • (2005) Blood , vol.106 , pp. 1207-1209
    • Steensma, D.P.1
  • 16
    • 27744606173 scopus 로고    scopus 로고
    • JAK2 mutation in essential thrombocythaemia: Clinical associations and long-term prognostic relevance
    • Wolanskyj AP, Lasho TL, Schwager SM, McClure RF, Wadleigh M, Lee SJ, et al. JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance. Br J Haematol. 2005;131:208-13.
    • (2005) Br J Haematol , vol.131 , pp. 208-213
    • Wolanskyj, A.P.1    Lasho, T.L.2    Schwager, S.M.3    McClure, R.F.4    Wadleigh, M.5    Lee, S.J.6
  • 18
    • 32944477304 scopus 로고    scopus 로고
    • Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia
    • Tefferi A, Sirhan S, Lasho TL, Schwager SM, Li CY, Dingli D, et al. Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia. Br J Haematol. 2005;131:166-71.
    • (2005) Br J Haematol , vol.131 , pp. 166-171
    • Tefferi, A.1    Sirhan, S.2    Lasho, T.L.3    Schwager, S.M.4    Li, C.Y.5    Dingli, D.6
  • 19
    • 29644439240 scopus 로고    scopus 로고
    • JAK1 and Tyk2 activation by the homologous polycythemia vera JAK2 V617F mutation: Cross-talk with IGF1 receptor
    • Staerk J, Kallin A, Demoulin JB, Vainchenker W, Constantinescu SN. JAK1 and Tyk2 activation by the homologous polycythemia vera JAK2 V617F mutation: cross-talk with IGF1 receptor. J Biol Chem. 2005;280:41893-9.
    • (2005) J Biol Chem , vol.280 , pp. 41893-41899
    • Staerk, J.1    Kallin, A.2    Demoulin, J.B.3    Vainchenker, W.4    Constantinescu, S.N.5
  • 20
    • 28244442441 scopus 로고    scopus 로고
    • Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: A prospective study
    • United Kingdom Myeloproliferative Disorders Study Group; Medical Research Council Adult Leukaemia Working Party; Australasian Leukaemia and Lymphoma Group
    • Campbell PJ, Scott LM, Buck G, Wheatley K, East CL, Marsden JT, et al; United Kingdom Myeloproliferative Disorders Study Group; Medical Research Council Adult Leukaemia Working Party; Australasian Leukaemia and Lymphoma Group. Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. Lancet. 2005;366:1945-53.
    • (2005) Lancet , vol.366 , pp. 1945-1953
    • Campbell, P.J.1    Scott, L.M.2    Buck, G.3    Wheatley, K.4    East, C.L.5    Marsden, J.T.6
  • 21
    • 33646470398 scopus 로고    scopus 로고
    • 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. A unique activating mutation in JAK2 (V617F) is at the origin of polycythemia vera and allows a new classification of myeloproliferative diseases. Hematology (Am Soc Hematol Educ Program). 2005;195-200.
    • (2005) Hematology (Am Soc Hematol Educ Program) , pp. 195-200
    • Vainchenker, W.1    Constantinescu, S.N.2
  • 22
    • 23844552419 scopus 로고    scopus 로고
    • Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis
    • General Haematology Task Force of the British Committee for Standards in Haematology
    • McMullin MF, Bareford D, Campbell P, Green AR, Harrison C, Hunt B, et al; General Haematology Task Force of the British Committee for Standards in Haematology. Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis. Br J Haematol. 2005;130:174-95.
    • (2005) Br J Haematol , vol.130 , pp. 174-195
    • McMullin, M.F.1    Bareford, D.2    Campbell, P.3    Green, A.R.4    Harrison, C.5    Hunt, B.6
  • 23
    • 0141574207 scopus 로고    scopus 로고
    • The rate of progression to polycythemia vera or essential thrombocythemia in patients with erythrocytosis or thrombocytosis
    • Ruggeri M, Tosetto A, Frezzato M, Rodeghiero F. The rate of progression to polycythemia vera or essential thrombocythemia in patients with erythrocytosis or thrombocytosis. Ann Intern Med. 2003;139:470-5.
    • (2003) Ann Intern Med , vol.139 , pp. 470-475
    • Ruggeri, M.1    Tosetto, A.2    Frezzato, M.3    Rodeghiero, F.4
  • 24
    • 0030731923 scopus 로고    scopus 로고
    • Spontaneous erythroid colony formation as the clue to an underlying myeloproliferative disorder in patients with Budd-Chiari syndrome or portal vein thrombosis
    • De Stefano V, Teofili L, Leone G, Michiels JJ. Spontaneous erythroid colony formation as the clue to an underlying myeloproliferative disorder in patients with Budd-Chiari syndrome or portal vein thrombosis. Semin Thromb Hemost. 1997;23:411-8.
    • (1997) Semin Thromb Hemost , vol.23 , pp. 411-418
    • De Stefano, V.1    Teofili, L.2    Leone, G.3    Michiels, J.J.4
  • 25
    • 0034839931 scopus 로고    scopus 로고
    • Genetic heterogeneity of primary familial and congenital polycythemia
    • Kralovics R, Prchal JT. Genetic heterogeneity of primary familial and congenital polycythemia. Am J Hematol. 2001;68:115-21.
    • (2001) Am J Hematol , vol.68 , pp. 115-121
    • Kralovics, R.1    Prchal, J.T.2
  • 26
    • 33644501833 scopus 로고    scopus 로고
    • Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status
    • Arellano-Rodrigo E, Álvarez-Larrán A, Reverter JC, Villamor N, Colomer D, Cervantes F. Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status. Haematologica. 2006;91:169-75.
    • (2006) Haematologica , vol.91 , pp. 169-175
    • Arellano-Rodrigo, E.1    Álvarez-Larrán, A.2    Reverter, J.C.3    Villamor, N.4    Colomer, D.5    Cervantes, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.