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Article

Any role for the nucleophosmin (NPM1) gene in myelodysplastic syndromes and acute myeloid leukemia with chromosome 5 abnormalities?

Leukemia & lymphoma - 1 Nov 2007

Falini Brunangelo

Abstract excerpt

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Topics

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Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 5
Share to Karyotyping
Share to Leukemia, Myeloid, Acute

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Myelodysplastic Syndromes

Share to Nuclear Proteins

Share to Nucleophosmin

Source

Identifiers

PMID: 17990174
DOI: 10.1080/10428190701684534

Genes

NPM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Any role for the nucleophosmin (NPM1) gene in myelodysplastic syndromes and acute myeloid leukemia with chromosome 5 abnormalities?PMID 17990174Read ↗

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Acute myeloid leukemia with mutated nucleophosmin (NPM1): any hope for a targeted therapy?Semantic proximity Read ↗

Acute myeloid leukemia with mutated nucleophosmin (NPM1): molecular, pathological, and clinical features.Semantic proximity Read ↗

Characteristics and clinical behavior of acute myeloid leukemia harboring rare non-A/B/D nucleophosmin (NPM1) gene mutation subtypes: a single-center experience and review of the literature.Semantic proximity Read ↗

Nucleophosmin 1 (NPM1) mutations in chronic myelomonocytic leukemia and their prognostic relevanceSemantic proximity Read ↗

Nucleophosmin: A versatile molecule associated with hematological malignanciesSemantic proximity Read ↗

[Nucleophosmin mutations in hematological malignancies - review].Semantic proximity Read ↗

The potential role of nucleophosmin (NPM1) in the development of cancer.Semantic proximity Read ↗

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