NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia-Reference-Cited by-同舟云学术

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

Published:2008-03-01 Issue:3 Volume:93 Page:439-442
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Falini B.,Mecucci C.,Saglio G.,Coco F. L.,Diverio D.,Brown P.,Pane F.,Mancini M.,Martelli M. P.,Pileri S.,Haferlach T.,Haferlach C.,Schnittger S.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 69 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Targeting Menin and CD47 to Address Unmet Needs in Acute Myeloid Leukemia;Cancers;2022-11-29

2. The Prognostic Effect Of The NPM1 Mutation And The FLT3-ITD Genes In Acute Promyelocytic Leukemia;Journal of Regenerative Biology and Medicine;2022-03-15

3. Novel NPM1 exon 5 mutations and gene fusions leading to aberrant cytoplasmic nucleophosmin in AML;Blood;2021-12-23

4. Chronic myeloid leukemia, BCR-ABL1-positive, carrying NPM1 mutation – First case series from a single institution;Leukemia Research;2021-12

5. References;Flow Cytometry of Hematological Malignancies;2021-04-06

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