메뉴 건너뛰기




Volumn 22, Issue 4, 2008, Pages 870-873

Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patients

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYUREA; JANUS KINASE 2; STEROID; WARFARIN;

EID: 42349112583     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/sj.leu.2404971     Document Type: Letter
Times cited : (61)

References (8)
  • 1
    • 33847176174 scopus 로고    scopus 로고
    • The chronic myeloproliferative disorders and mutation of JAK2: Dameshek's 54-year-old speculation comes of age
    • Kaushansky K. The chronic myeloproliferative disorders and mutation of JAK2: Dameshek's 54-year-old speculation comes of age. Best Pract Res Clin Haematol 2007; 20: 5-12.
    • (2007) Best Pract Res Clin Haematol , vol.20 , pp. 5-12
    • Kaushansky, K.1
  • 2
    • 33646546386 scopus 로고    scopus 로고
    • The JAK2V617F mutation occurs in hematopoietic stem cells in polycythemia vera and predisposes toward erythroid differentiation
    • Jamieson CH, Gotlib J, Durocher JA, Chao MP, Mariappan MR, Lay M et al. The JAK2V617F mutation occurs in hematopoietic stem cells in polycythemia vera and predisposes toward erythroid differentiation. PNAS 2006; 103: 6224-6229.
    • (2006) PNAS , vol.103 , pp. 6224-6229
    • Jamieson, C.H.1    Gotlib, J.2    Durocher, J.A.3    Chao, M.P.4    Mariappan, M.R.5    Lay, M.6
  • 3
    • 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
  • 4
    • 33846660947 scopus 로고    scopus 로고
    • JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis
    • Scott LM, Tong W, Levine M, Scott MA, Beer PA, Stratton MR et al. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis. NEJM 2007; 356: 459-468.
    • (2007) NEJM , vol.356 , pp. 459-468
    • Scott, L.M.1    Tong, W.2    Levine, M.3    Scott, M.A.4    Beer, P.A.5    Stratton, M.R.6
  • 5
    • 34548128326 scopus 로고    scopus 로고
    • Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2 617F-negative polycythemia vera
    • Epub ahead of print June 28
    • Pardanani A, Lasho TL, Finke C, Hanson CA, Tefferi A. Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2 617F-negative polycythemia vera. Leukemia 2007; Epub ahead of print (June 28): 1-4.
    • (2007) Leukemia , pp. 1-4
    • Pardanani, A.1    Lasho, T.L.2    Finke, C.3    Hanson, C.A.4    Tefferi, A.5
  • 6
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myelo-proliferative disorders
    • Baxter E, Scott L, Campbell P, East C, Fourouclas N, Swanton S et al Acquired mutation of the tyrosine kinase JAK2 in human myelo-proliferative disorders. Lancet 2005; 365: 1054-1061.
    • (2005) Lancet , vol.365 , pp. 1054-1061
    • Baxter, E.1    Scott, L.2    Campbell, P.3    East, C.4    Fourouclas, N.5    Swanton, S.6
  • 7
    • 34548042964 scopus 로고    scopus 로고
    • Proposals and rationale for revision of the World Health Organisation diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel
    • Tefferi A, Thiele J, Orazi A, Kvasnicka HM, Barbui T, Hanson CA et al Proposals and rationale for revision of the World Health Organisation diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: Recommendations from an ad hoc international expert panel. Blood 2007; 110: 1092-1097.
    • (2007) Blood , vol.110 , pp. 1092-1097
    • Tefferi, A.1    Thiele, J.2    Orazi, A.3    Kvasnicka, H.M.4    Barbui, T.5    Hanson, C.A.6
  • 8
    • 33846976182 scopus 로고    scopus 로고
    • The JAK2V617F mutation involves B- and T-lymphocyte lineages in a subgroup of patients with Philadelphia-chromosome negative chronic myeloproliferative disorders
    • Larsen TS, Christensen JH, Hasselbalch HC, Pallisgaard N. The JAK2V617F mutation involves B- and T-lymphocyte lineages in a subgroup of patients with Philadelphia-chromosome negative chronic myeloproliferative disorders. BJH 2007; 136: 745-751.
    • (2007) BJH , vol.136 , pp. 745-751
    • Larsen, T.S.1    Christensen, J.H.2    Hasselbalch, H.C.3    Pallisgaard, N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.