Monitoring of minimal residual disease in acute myeloid leukemia with frequent and rare patient‐specific NPM1 mutations
暂无分享,去创建一个
J. Mayer | Z. Ráčil | M. Lengerova | F. Rázga | M. Protivánková | I. Jeziskova | I. Palásek | D. Dvorakova
[1] J. Gribben,et al. Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fraction. , 2010, Blood.
[2] S. Schnittger,et al. Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemias. , 2010, Blood.
[3] B. Falini,et al. Acute myeloid leukemia with mutated NPM1: diagnosis, prognosis and therapeutic perspectives , 2009, Current opinion in oncology.
[4] T. Haferlach,et al. Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. , 2009, Blood.
[5] Martin Klabusay,et al. Detection and treatment of molecular relapse in acute myeloid leukemia with RUNX1 (AML1), CBFB, or MLL gene translocations: frequent quantitative monitoring of molecular markers in different compartments and correlation with WT1 gene expression. , 2009, Experimental hematology.
[6] D. Dvořáková,et al. A novel quantitative assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPM1 (nucleophosmin) exon 12 mutations , 2009, Leukemia.
[7] W. Hiddemann,et al. Monitoring minimal residual disease in acute myeloid leukaemia with NPM1 mutations by quantitative PCR: clonal evolution is a limiting factor , 2009, British journal of haematology.
[8] P. Bolufer,et al. Minimal residual disease detection in acute myeloid leukemia by mutant nucleophosmin (NPM1): comparison with WT1 gene expression. , 2008, Clinica chimica acta; international journal of clinical chemistry.
[9] F. Lo‐Coco,et al. An allele-specific rt-PCR assay to detect type A mutation of the nucleophosmin-1 gene in acute myeloid leukemia. , 2008, The Journal of molecular diagnostics : JMD.
[10] M. Yao,et al. Clinical implications of minimal residual disease monitoring by quantitative polymerase chain reaction in acute myeloid leukemia patients bearing nucleophosmin (NPM1) mutations , 2007, Leukemia.
[11] B. Falini,et al. Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations , 2006, Leukemia.
[12] J. Cayuela,et al. Prevalence, clinical profile, and prognosis of NPM mutations in AML with normal karyotype. , 2005, Blood.
[13] T. Naoe,et al. Clinical characteristics and prognostic implications of NPM1 mutations in acute myeloid leukemia. , 2005, Blood.
[14] R. Chiu,et al. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. , 2001, Clinical chemistry.
[15] N. Kröger,et al. Quantitative monitoring of NPM1 mutations provides a valid minimal residual disease parameter following allogeneic stem cell transplantation. , 2009, Experimental hematology.