Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution.

Cancer research - 15 Mar 2006

Chou Wen-Chien, Tang Jih-Luh, Lin Liang-In, Yao Ming, Tsay Woei, Chen Chien-Yuan, Wu Shang-Ju, Huang Chi-Fei, Chiou Rong-Jing, Tseng Mei-Hsuan, Lin Dong-Tsamn, Lin Kai-Hsin, Chen Yao-Chang, Tien Hwei-Fang

Abstract excerpt

Nucleophosmin (NPM) mutations have been found in a significant proportion of adults with de novo acute myeloid leukemia (AML), especially in those of a normal karyotype. These results provide a basis for studies of the pathogenesis in this specific subgroup of AML. In this study, NPM mutations we...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acute Disease
Share to Age Factors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Disease Progression

Share to Immunophenotyping

Share to Leukemia, Myeloid

Share to Nuclear Proteins

Share to Nucleophosmin

Source

Identifiers

PMID: 16540685
DOI: 10.1158/0008-5472.CAN-05-4316

Genes

FLT3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16540685-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution.PMID 16540685Read ↗

Nucleophosmin mutation in de-novo acute myeloid leukemia.Semantic proximity Read ↗

Non-A type nucleophosmin 1 gene mutation predicts poor clinical outcome in de novo adult acute myeloid leukemia: differential clinical importance of NPM1 mutation according to subtype.Semantic proximity Read ↗

Genetic, Phenotypic, and Clinical Heterogeneity of NPM1-Mutant Acute Myeloid LeukemiasSemantic proximity Read ↗

Analysis of NPM1 gene mutations in Chinese adults with acute myeloid leukemia.Semantic proximity Read ↗

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.Semantic proximity Read ↗

Acute myeloid leukemia with mutated nucleophosmin (NPM1): is it a distinct entity?Semantic proximity Read ↗

Genetic. Phenotypic and Clinical Heterogeneity of NPM1-Mutant Acute Myeloid LeukemiasSemantic 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 mutations in Chinese adults with acute myelogenous leukemia.Semantic proximity Read ↗

Nucleophosmin1 (NPM1) abnormality in hematologic malignancies, and therapeutic targeting of mutant NPM1 in acute myeloid leukemiaSemantic proximity Read ↗

Clinical prognostic value of different NPM1 mutations in acute myeloid leukemia patients.Semantic proximity Read ↗

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.