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Volumn 20, Issue 8, 2006, Pages 1453-1454

JAK2 mutation in a boy with polycythemia vera, but not in other pediatric hematologic disorders [8]

Author keywords

[No Author keywords available]

Indexed keywords

JANUS KINASE 2;

EID: 33746109984     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/sj.leu.2404259     Document Type: Letter
Times cited : (9)

References (8)
  • 1
    • 20144363192 scopus 로고    scopus 로고
    • Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
    • Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S 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    East, C.4    Fourouclas, N.5    Swanton, S.6
  • 3
    • 17844383458 scopus 로고    scopus 로고
    • A unique clonal JAK2 mutation leading to constitutive signaling 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 signaling 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
  • 4
    • 27144432878 scopus 로고    scopus 로고
    • JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia
    • Tono C, Xu G, Toki T, Takahashi Y, Sasaki S, Terui K et al. JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia. Leukemia 2005; 19: 1843-1844.
    • (2005) Leukemia , vol.19 , pp. 1843-1844
    • Tono, C.1    Xu, G.2    Toki, T.3    Takahashi, Y.4    Sasaki, S.5    Terui, K.6
  • 5
    • 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: 2920-2921.
    • (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
  • 6
    • 33344471932 scopus 로고    scopus 로고
    • KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): A study of the Japanese Childhood AML Cooperative Study Group
    • Shimada A, Taki T, Tabuchi K, Tawa A, Horibe K, Tsuchida M et al. KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): A study of the Japanese Childhood AML Cooperative Study Group. Blood 2006; 107: 1806-1809.
    • (2006) Blood , vol.107 , pp. 1806-1809
    • Shimada, A.1    Taki, T.2    Tabuchi, K.3    Tawa, A.4    Horibe, K.5    Tsuchida, M.6
  • 8
    • 25844518265 scopus 로고    scopus 로고
    • The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
    • Levine RL, Loriaux M, Huntly BJ, Loh ML, Beran M, Stoffregen E et al. The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia. Blood 2005; 106: 3377-3379.
    • (2005) Blood , vol.106 , pp. 3377-3379
    • Levine, R.L.1    Loriaux, M.2    Huntly, B.J.3    Loh, M.L.4    Beran, M.5    Stoffregen, E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.