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Volumn 22, Issue 1, 2008, Pages 195-198

Absence of nucleophosmin leukaemic mutants in B and T cells from AML with NPM1 mutations: Implications for the cell of origin of NPMc+ AML [4]

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOPHOSMIN;

EID: 38349075761     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/sj.leu.2404857     Document Type: Letter
Times cited : (19)

References (8)
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    • Falini B, Nicoletti I, Martelli MF, Mecucci C. Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+AML): Biologic and clinical features. Blood 2007; 109: 874-885.
    • (2007) Blood , vol.109 , pp. 874-885
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  • 3
    • 33748703838 scopus 로고    scopus 로고
    • Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia
    • Falini B, Martelli MP, Bolli N, Bonasso R, Ghia E, Pallotta MT et al Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia. Blood 2006; 108: 1999-2005.
    • (2006) Blood , vol.108 , pp. 1999-2005
    • Falini, B.1    Martelli, M.P.2    Bolli, N.3    Bonasso, R.4    Ghia, E.5    Pallotta, M.T.6
  • 4
    • 33845483445 scopus 로고    scopus 로고
    • Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification
    • Pasqualucci L, Liso A, Martelli MP, Bolli N, Pacini R, Tabarrini A et al. Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification. Blood 2006; 108: 4146-4155.
    • (2006) Blood , vol.108 , pp. 4146-4155
    • Pasqualucci, L.1    Liso, A.2    Martelli, M.P.3    Bolli, N.4    Pacini, R.5    Tabarrini, A.6
  • 5
    • 33846007215 scopus 로고    scopus 로고
    • Evidence that the JAK2 G1849T (V617F) mutation occurs in a lymphomyeloid progenitor in polycythemia vera and idiopathic myelofibrosis
    • Delhommeau F, Dupont S, Tonetti C, Masse A, Godin I, Le Couedic JP et al. Evidence that the JAK2 G1849T (V617F) mutation occurs in a lymphomyeloid progenitor in polycythemia vera and idiopathic myelofibrosis. Blood 2007; 109: 71-77.
    • (2007) Blood , vol.109 , pp. 71-77
    • Delhommeau, F.1    Dupont, S.2    Tonetti, C.3    Masse, A.4    Godin, I.5    Le Couedic, J.P.6
  • 6
    • 23044459136 scopus 로고    scopus 로고
    • Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+ AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance
    • Alcalay M, Tiacci E, Bergomas R, Bigerna B, Venturini E, Minardi SP et al. Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+ AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance. Blood 2005; 106: 899-902.
    • (2005) Blood , vol.106 , pp. 899-902
    • Alcalay, M.1    Tiacci, E.2    Bergomas, R.3    Bigerna, B.4    Venturini, E.5    Minardi, S.P.6
  • 7
    • 0037515610 scopus 로고    scopus 로고
    • Enforced granulocyte/macrophage colony-stimulating factor signals do not support lymphopoiesis, but instruct lymphoid to myelomonocytic lineage conversion
    • Iwasaki-Arai J, Iwasaki H, Miyamoto T, Watanabe S, Akashi K. Enforced granulocyte/macrophage colony-stimulating factor signals do not support lymphopoiesis, but instruct lymphoid to myelomonocytic lineage conversion. J Exp Med 2003; 197: 1311-1322.
    • (2003) J Exp Med , vol.197 , pp. 1311-1322
    • Iwasaki-Arai, J.1    Iwasaki, H.2    Miyamoto, T.3    Watanabe, S.4    Akashi, K.5
  • 8
    • 18244384493 scopus 로고    scopus 로고
    • Identification of a human B-cell/myeloid common progenitor by the absence of CXCR4
    • Hou YH, Srour EF, Ramsey H, Dahl R, Broxmeyer HE, Hromas R. Identification of a human B-cell/myeloid common progenitor by the absence of CXCR4. Blood 2005; 105: 3488-3492.
    • (2005) Blood , vol.105 , pp. 3488-3492
    • Hou, Y.H.1    Srour, E.F.2    Ramsey, H.3    Dahl, R.4    Broxmeyer, H.E.5    Hromas, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.