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Volumn 92, Issue 12, 2007, Pages 1585-1589

Somatic mutations of JAK2 exon 12 as a molecular basis of erythrocytosis

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROPOIETIN; HYPOXIA INDUCIBLE FACTOR 1; JANUS KINASE 2;

EID: 37049036160     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: 10.3324/haematol.11506     Document Type: Editorial
Times cited : (19)

References (24)
  • 1
    • 37049020486 scopus 로고
    • Hillman RS, Finch CA. Red, 5 ed. Philadelphia: F.A. Davis;
    • Hillman RS, Finch CA. Red Cell Manual. 5 ed. Philadelphia: F.A. Davis; 1985.
    • (1985) Cell Manual
  • 2
    • 0033568576 scopus 로고    scopus 로고
    • Regulation of the erythropoietin gene
    • Ebert BL, Bunn HF. Regulation of the erythropoietin gene. Blood 1999;94:1864-77.
    • (1999) Blood , vol.94 , pp. 1864-1877
    • Ebert, B.L.1    Bunn, H.F.2
  • 4
    • 35148888161 scopus 로고    scopus 로고
    • Life with oxygen
    • Semenza GL. Life with oxygen. Science 2007;318:62-4.
    • (2007) Science , vol.318 , pp. 62-64
    • Semenza, G.L.1
  • 5
    • 35148828429 scopus 로고    scopus 로고
    • Hypoxia-inducible factor 1 (HIF-1) pathway
    • Semenza GL. Hypoxia-inducible factor 1 (HIF-1) pathway. Sci STKE 2007;2007:cm8.
    • (2007) Sci STKE 2007
    • Semenza, G.L.1
  • 6
    • 0025123918 scopus 로고
    • Erythropoietin receptor. Subunit structure and activation
    • D'Andrea AD, Zon LI. Erythropoietin receptor. Subunit structure and activation. J Clin Invest 1990;86:681-7.
    • (1990) J Clin Invest , vol.86 , pp. 681-687
    • D'Andrea, A.D.1    Zon, L.I.2
  • 7
    • 0025908919 scopus 로고
    • Erythropoietin receptor characteristics on primary human erythroid cells
    • Broudy VC, Lin N, Brice M, Nakamoto B, Papayannopoulou T. Erythropoietin receptor characteristics on primary human erythroid cells. Blood 1991; 77:2583-90.
    • (1991) Blood , vol.77 , pp. 2583-2590
    • Broudy, V.C.1    Lin, N.2    Brice, M.3    Nakamoto, B.4    Papayannopoulou, T.5
  • 8
    • 34548042964 scopus 로고    scopus 로고
    • Proposals and rationale for revision of the World Health Organization 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 Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel. Blood 2007;110:1092-7.
    • (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
  • 10
    • 13244272302 scopus 로고    scopus 로고
    • Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: Five new Caucasian patients
    • Bento MC, Chang KT, Guan Y, Liu E, Caldas G, Gatti RA, et al. Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients. Haematologica 2005;90:128-9.
    • (2005) Haematologica , vol.90 , pp. 128-129
    • Bento, M.C.1    Chang, K.T.2    Guan, Y.3    Liu, E.4    Caldas, G.5    Gatti, R.A.6
  • 11
    • 13244281831 scopus 로고    scopus 로고
    • Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis
    • Cario H, Schwarz K, Jorch N, Kyank U, Petrides PE, Schneider DT, et al. Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis. Haematologica 2005;90:19-24.
    • (2005) Haematologica , vol.90 , pp. 19-24
    • Cario, H.1    Schwarz, K.2    Jorch, N.3    Kyank, U.4    Petrides, P.E.5    Schneider, D.T.6
  • 12
    • 20344370255 scopus 로고    scopus 로고
    • Low frequency of VHL gene mutations in young individuals with polycythemia and high serum erythropoietin
    • Randi ML, Murgia A, Putti MC, Martella M, Casarin A, Opocher G, et al. Low frequency of VHL gene mutations in young individuals with polycythemia and high serum erythropoietin. Haematologica 2005;90:689-91.
    • (2005) Haematologica , vol.90 , pp. 689-691
    • Randi, M.L.1    Murgia, A.2    Putti, M.C.3    Martella, M.4    Casarin, A.5    Opocher, G.6
  • 13
    • 33646406275 scopus 로고    scopus 로고
    • Relation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders
    • Passamonti F, Rumi E, Pietra D, Della Porta MG, Boveri E, Pascutto C, et al. Relation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders. Blood 2006;107:3676-82.
    • (2006) Blood , vol.107 , pp. 3676-3682
    • Passamonti, F.1    Rumi, E.2    Pietra, D.3    Della Porta, M.G.4    Boveri, E.5    Pascutto, C.6
  • 14
    • 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.
    • (2006) Haematologica , vol.91 , pp. 159
    • Cazzola, M.1    Passamonti, F.2
  • 15
    • 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
  • 16
    • 37049034302 scopus 로고    scopus 로고
    • Familial chronic myeloproliferative disorders: Clinical phenotype and evidence of disease anticipation
    • in press
    • Rumi E, Passamonti F, Della Porta MG, Elena C, Arcaini L, Vanelli L, et al. Familial chronic myeloproliferative disorders: clinical phenotype and evidence of disease anticipation. J Clin Oncol 2007, in press.
    • (2007) J Clin Oncol
    • Rumi, E.1    Passamonti, F.2    Della Porta, M.G.3    Elena, C.4    Arcaini, L.5    Vanelli, L.6
  • 17
    • 33645461067 scopus 로고    scopus 로고
    • The incidence of the JAK2 V617F mutation in patients with idiopathic erythrocytosis
    • Percy MJ, Jones FG, Green AR, Reilly JT, McMullin MF. The incidence of the JAK2 V617F mutation in patients with idiopathic erythrocytosis. Haematologica 2006;91:413-4.
    • (2006) Haematologica , vol.91 , pp. 413-414
    • Percy, M.J.1    Jones, F.G.2    Green, A.R.3    Reilly, J.T.4    McMullin, M.F.5
  • 19
    • 34548128326 scopus 로고    scopus 로고
    • Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera
    • Pardanani A, Lasho TL, Finke C, Hanson CA, Tefferi A. Prevalence and clinicopathologic correlates of JAK2 exon 12 mutations in JAK2V617F-negative polycythemia vera. Leukemia 2007;21:1960-3.
    • (2007) Leukemia , vol.21 , pp. 1960-1963
    • Pardanani, A.1    Lasho, T.L.2    Finke, C.3    Hanson, C.A.4    Tefferi, A.5
  • 20
    • 35448963775 scopus 로고    scopus 로고
    • Phenotypic variations and new mutations in JAK2 V617F-negative polycythemia vera, erythrocytosis, and idiopathic myelofibrosis
    • Williams DM, Kim AH, Rogers O, Spivak JL, Moliterno AR. Phenotypic variations and new mutations in JAK2 V617F-negative polycythemia vera, erythrocytosis, and idiopathic myelofibrosis. Exp Hematol 2007; 35:1641-6.
    • (2007) Exp Hematol , vol.35 , pp. 1641-1646
    • Williams, D.M.1    Kim, A.H.2    Rogers, O.3    Spivak, J.L.4    Moliterno, A.R.5
  • 22
    • 37049013530 scopus 로고    scopus 로고
    • JAK2 exon 12 mutations occurr frequently in idiopathic erythrocytosis patients widi low serum erythropoietin levels
    • Percy MJ, Scott LM, Erber WN, Harrison CN, Jones FCG, Green AR, et al. JAK2 exon 12 mutations occurr frequently in idiopathic erythrocytosis patients widi low serum erythropoietin levels. Haematologica 2007;92:1607-14.
    • (2007) Haematologica , vol.92 , pp. 1607-1614
    • Percy, M.J.1    Scott, L.M.2    Erber, W.N.3    Harrison, C.N.4    Jones, F.C.G.5    Green, A.R.6
  • 24
    • 37049009113 scopus 로고    scopus 로고
    • Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, et al. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 2007 Nov 6; [Epub ahead of print].
    • Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, et al. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 2007 Nov 6; [Epub ahead of print].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.