메뉴 건너뛰기




Volumn 109, Issue 11, 2007, Pages 2279-2284

Clinical correlates of JAK2V617F allele burden in essential thrombocythemia

Author keywords

Allele burden; Essential thrombocythemia; JAK2V617F

Indexed keywords

GENOMIC DNA;

EID: 34249071097     PISSN: 0008543X     EISSN: 10970142     Source Type: Journal    
DOI: 10.1002/cncr.22663     Document Type: Article
Times cited : (140)

References (22)
  • 1
    • 17644424955 scopus 로고    scopus 로고
    • A gain-of-function mutation of JAK2 in myeloproliferative disorders
    • Kralovics R, Passamonti F, Buser AS, et al. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med. 2005;352:1779-1790.
    • (2005) N Engl J Med , vol.352 , pp. 1779-1790
    • Kralovics, R.1    Passamonti, F.2    Buser, A.S.3
  • 2
    • 33748684367 scopus 로고    scopus 로고
    • The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera
    • 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. 2006;108:1865-1867.
    • (2006) Blood , vol.108 , pp. 1865-1867
    • Lippert, E.1    Boissinot, M.2    Kralovics, R.3
  • 3
    • 27744606173 scopus 로고    scopus 로고
    • JAK2 mutation in essential thrombocythaemia: Clinical associations and long-term prognostic relevance
    • Wolanskyj AP, Lasho TL, Schwager SM, et al. JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance. Br J Haematol. 2005;131:208-213.
    • (2005) Br J Haematol , vol.131 , pp. 208-213
    • Wolanskyj, A.P.1    Lasho, T.L.2    Schwager, S.M.3
  • 4
    • 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
    • Campbell PJ, Scott LM, Buck G, et al. Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study. Lancet. 2005;366:1945-1953.
    • (2005) Lancet , vol.366 , pp. 1945-1953
    • Campbell, P.J.1    Scott, L.M.2    Buck, G.3
  • 5
    • 33746858555 scopus 로고    scopus 로고
    • JAK2V617F mutation in platelets from essential thrombocythemia patients: Correlation with clinical features and analysis of STAT5 phosphorylation status
    • Heller PG, Lev PR, Salim JP, et al. JAK2V617F mutation in platelets from essential thrombocythemia patients: correlation with clinical features and analysis of STAT5 phosphorylation status. Eur J Haematol. 2006;77:210-216.
    • (2006) Eur J Haematol , vol.77 , pp. 210-216
    • Heller, P.G.1    Lev, P.R.2    Salim, J.P.3
  • 6
    • 27144443646 scopus 로고    scopus 로고
    • Clinical implications of the JAK2 V617F mutation in essential thrombocythemia
    • Antonioli E, Guglielmelli P, Pancrazzi A, et al. Clinical implications of the JAK2 V617F mutation in essential thrombocythemia. Leukemia. 2005;19:1847-1849.
    • (2005) Leukemia , vol.19 , pp. 1847-1849
    • Antonioli, E.1    Guglielmelli, P.2    Pancrazzi, A.3
  • 7
    • 33644826144 scopus 로고    scopus 로고
    • The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia
    • Cheung B, Radia D, Pantelidis P, Yadegarfar G, Harrison C. The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia. Br J Haematol. 2006;132:244-245.
    • (2006) Br J Haematol , vol.132 , pp. 244-245
    • Cheung, B.1    Radia, D.2    Pantelidis, P.3    Yadegarfar, G.4    Harrison, C.5
  • 8
    • 33947262701 scopus 로고    scopus 로고
    • Leukocytosis is a risk factor for thrombosis in essential thrombocythemia: Interaction with treatment, standard risk factors and Jak2 mutation status
    • Carobbio A, Finazzi G, Guerini V et al. Leukocytosis is a risk factor for thrombosis in essential thrombocythemia: interaction with treatment, standard risk factors and Jak2 mutation status. Blood. 2007;109:2310-2313.
    • (2007) Blood , vol.109 , pp. 2310-2313
    • Carobbio, A.1    Finazzi, G.2    Guerini, V.3
  • 9
    • 33645400695 scopus 로고    scopus 로고
    • X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and MMM patients with clonal hematopoiesis
    • Levine RL, Belisle C, Wadleigh M, et al. X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and MMM patients with clonal hematopoiesis. Blood. 2006;107:4139-4141.
    • (2006) Blood , vol.107 , pp. 4139-4141
    • Levine, R.L.1    Belisle, C.2    Wadleigh, M.3
  • 10
    • 30844456807 scopus 로고    scopus 로고
    • WHO histological classification of chronic myeloproliferative diseases
    • Jaffe ES, Harris NL, Stein H, Vardiman JW, editors, Lyon, France: International Agency for Research on Cancer (IARC) Press;
    • Vardiman JW, Brunning RD, Harris NL. WHO histological classification of chronic myeloproliferative diseases. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, editors. World Health Organization Classification of Tumours: Tumours of the Haematopoietic and Lymphoid Tissues. Lyon, France: International Agency for Research on Cancer (IARC) Press; 2001:17-44.
    • (2001) World Health Organization Classification of Tumours: Tumours of the Haematopoietic and Lymphoid Tissues , pp. 17-44
    • Vardiman, J.W.1    Brunning, R.D.2    Harris, N.L.3
  • 11
    • 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, et al. Concomitant neutrophil JAK2 mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia. Br J Haematol. 2005;131:166-171.
    • (2005) Br J Haematol , vol.131 , pp. 166-171
    • Tefferi, A.1    Sirhan, S.2    Lasho, T.L.3
  • 12
    • 33744505451 scopus 로고    scopus 로고
    • Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome
    • Patel RK, Lea NC, Heneghan MA, et al. Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome. Gastroenterology. 2006;130:2031-2038.
    • (2006) Gastroenterology , vol.130 , pp. 2031-2038
    • Patel, R.K.1    Lea, N.C.2    Heneghan, M.A.3
  • 13
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Baxter EJ, Scott LM, Campbell PJ, et al. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet. 2005;365:1054-1061.
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.J.1    Scott, L.M.2    Campbell, P.J.3
  • 14
    • 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, et al. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005;7:387-397.
    • (2005) Cancer Cell , vol.7 , pp. 387-397
    • Levine, R.L.1    Wadleigh, M.2    Cools, J.3
  • 15
    • 31444439623 scopus 로고    scopus 로고
    • Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis
    • James C, Delhommeau F, Marzac C, et al. Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis. Leukemia. 2006;20:350-353.
    • (2006) Leukemia , vol.20 , pp. 350-353
    • James, C.1    Delhommeau, F.2    Marzac, C.3
  • 16
    • 33645740979 scopus 로고    scopus 로고
    • Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha
    • Jones AV Silver RT, Waghorn K, et al. Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha. Blood. 2006;107:3339-3341.
    • (2006) Blood , vol.107 , pp. 3339-3341
    • Jones, A.V.1    Silver, R.T.2    Waghorn, K.3
  • 17
    • 32144461605 scopus 로고    scopus 로고
    • Essential thrombocythemia beyond the first decade: Life expectancy, long-term complication rates, and prognostic factors
    • Wolanskyj AR Schwager SM, McClure RF, Larson DR, Tefferi A. Essential thrombocythemia beyond the first decade: life expectancy, long-term complication rates, and prognostic factors. Mayo Clin Proc. 2006;81:159-166.
    • (2006) Mayo Clin Proc , vol.81 , pp. 159-166
    • Wolanskyj, A.R.1    Schwager, S.M.2    McClure, R.F.3    Larson, D.R.4    Tefferi, A.5
  • 18
    • 33947208087 scopus 로고    scopus 로고
    • Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera
    • Landolfi R, Di Gennaro L, Barbui T, et al. Leukocytosis as a major thrombotic risk factor in patients with polycythemia vera. Blood. 2007;109:2446-2452.
    • (2007) Blood , vol.109 , pp. 2446-2452
    • Landolfi, R.1    Di Gennaro, L.2    Barbui, T.3
  • 19
    • 34249007698 scopus 로고    scopus 로고
    • Influence of the Jak2V617F mutational load at diagnosis on major clinical aspects in patients with polycythemia vera
    • Abstract 5
    • Vannucchi AM, Antonioli E, Guglielmelli P, et al. Influence of the Jak2V617F mutational load at diagnosis on major clinical aspects in patients with polycythemia vera. Blood. 2006;108. Abstract 5.
    • (2006) Blood , pp. 108
    • Vannucchi, A.M.1    Antonioli, E.2    Guglielmelli, P.3
  • 20
    • 31544477194 scopus 로고    scopus 로고
    • The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera
    • Tefferi A, Lasho TL, Schwager SM, et al. The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera. Cancer. 2006;106:631-635.
    • (2006) Cancer , vol.106 , pp. 631-635
    • Tefferi, A.1    Lasho, T.L.2    Schwager, S.M.3
  • 21
    • 33846883073 scopus 로고    scopus 로고
    • Long-term serial analysis of X-chromosome inactivation patterns and JAK2 V617F mutant levels in patients with essential thrombocythemia show that minor mutant-positive clones can remain stable for many years
    • Gale RE, Allen AJ, Nash MJ, Linch DC. Long-term serial analysis of X-chromosome inactivation patterns and JAK2 V617F mutant levels in patients with essential thrombocythemia show that minor mutant-positive clones can remain stable for many years. Blood. 2007;109:1241-1243.
    • (2007) Blood , vol.109 , pp. 1241-1243
    • Gale, R.E.1    Allen, A.J.2    Nash, M.J.3    Linch, D.C.4
  • 22
    • 27244432586 scopus 로고    scopus 로고
    • Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes
    • Lasho TL, Mesa R, Gilliland DG, Tefferi A. Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes. Br J Haematol. 2005;130:797-799.
    • (2005) Br J Haematol , vol.130 , pp. 797-799
    • Lasho, T.L.1    Mesa, R.2    Gilliland, D.G.3    Tefferi, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.