Detection of RBM 15-MKL 1 Fusion Was Useful for Diagnosis and Monitoring of Minimal Residual Disease in Infant Acute Megakaryoblastic Leukemia
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Y. Fujii | T. Morishima | Yuko Yamamoto | M. Oda | K. Hamamoto | A. Shimada | Yoshimi Nakamura | T. Nagai | A. Takeda | Toshiyuki Watanabe | S. Yoshino | Kanae Sakakibara | Mutsuko Yamada | Yuki Watanabe
[1] Y. Hayashi,et al. High WT1 mRNA expression after induction chemotherapy and FLT3-ITD have prognostic impact in pediatric acute myeloid leukemia: a study of the Japanese Childhood AML Cooperative Study Group , 2012, International Journal of Hematology.
[2] I. Buño,et al. Evaluation of minimal residual disease by real-time quantitative PCR of Wilms' tumor 1 expression in patients with acute myelogenous leukemia after allogeneic stem cell transplantation: correlation with flow cytometry and chimerism. , 2012, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.
[3] Hirotoshi Sakaguchi,et al. Molecular lesions in childhood and adult acute megakaryoblastic leukaemia , 2012, British journal of haematology.
[4] M. Teixeira,et al. Acute megakaryoblastic leukemia with a four‐way variant translocation originating the RBM15–MKL1 fusion gene , 2011, Pediatric blood & cancer.
[5] C. Bloomfield,et al. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. , 2009, Blood.
[6] 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.
[7] A. Orazi. Histopathology in the Diagnosis and Classification of Acute Myeloid Leukemia, Myelodysplastic Syndromes, and Myelodysplastic/Myeloproliferative Diseases , 2007, Pathobiology.
[8] G. Schuurhuis,et al. MRD parameters using immunophenotypic detection methods are highly reliable in predicting survival in acute myeloid leukaemia , 2004, Leukemia.
[9] R. Berger,et al. A novel real-time RT-PCR assay for quantification of OTT-MAL fusion transcript reliable for diagnosis of t(1;22) and minimal residual disease (MRD) detection , 2003, Leukemia.
[10] G. Flandrin,et al. Acute Megakaryoblastic Leukaemia: A National Clinical and Biological Study of 53 Adult and Childhood Cases by the Groupe Français d'Hématologie Cellulaire (GFHC) , 2003, Leukemia & lymphoma.
[11] Dean Nizetic,et al. Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia , 2001, Nature Genetics.
[12] Nicole Dastugue,et al. Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[13] N. Heerema,et al. Nineteen cases of the t(1;22)(p13;q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group , 2000, Leukemia.
[14] A. Pappo,et al. The t(1;22) (p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group Study. , 1991, Blood.