Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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Rare Cytogenetic Abnormalities and Alteration of microRNAs in Acute Myeloid Leukemia and Response to Therapy Identification of novel diagnostic biomarkers for thyroid carcinoma.Acute myeloid leukemia

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P2860

Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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Acute myeloid leukemia with translocation t(3;5): new molecular insights.

@en

P1476

Acute myeloid leukemia with translocation t(3;5): new molecular insights

@en

P2093

Aline Renneville

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Caroline Mayeur-Rousse

http://www.w3.org/2001/XMLSchema#string

Elise Labis

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P2860

The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes

Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype.

The t(3;5)(q25.1;q34) of myelodysplastic syndrome and acute myeloid leukemia produces a novel fusion gene, NPM-MLF1.

Prognostic significance of DNA methyltransferase 3A mutations in cytogenetically normal acute myeloid leukemia: a study by the Acute Leukemia French Association.

Detection of t(3;5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature.

Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): association with other gene abnormalities and previously established gene expression signatures and their favorable prognostic significance.

Clinicopathologic manifestations and breakpoints of the t(3;5) in patients with acute nonlymphocytic leukemia.

Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.

NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia.

Loss of the NPM1 gene in myeloid disorders with chromosome 5 rearrangements.

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e52-4

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scholarly article

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10.3324/HAEMATOL.2012.082149

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P478

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Claude Preudhomme

O Nibourel

Florent Dumézy

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2013-02-12T00:00:00Z

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235603584

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23403313

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3660006

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Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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P2860

P2860

Acute myeloid leukemia with translocation t(3;5): new molecular insights.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932