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

A unique acute myeloid leukemia patient with cryptic NUP98-NSD1 gene and ASXL1 mutation.

Leukemia & lymphoma - 1 Jan 2016

Cui Jiangxia, Xie Jundan, Qin Lili, Chen Suning, Zhao Yun, Wu Deipei

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers
Share to Comparative Genomic Hybridization
Share to DNA Mutational Analysis
Share to Immunophenotyping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

Share to Mutation

Share to Oncogene Proteins, Fusion

Share to Repressor Proteins

Source

Identifiers

PMID: 25860235
DOI: 10.3109/10428194.2015.1037755

Genes

ASXL1
NSD1
NUP98

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A unique acute myeloid leukemia patient with cryptic NUP98-NSD1 gene and ASXL1 mutation.PMID 25860235Read ↗

Clinical implications of NUP98::NSD1 fusion at diagnosis in adult FLT3-ITD positive AML.Semantic proximity Read ↗

Comprehensive mutational profiling and clinical outcome of adult acute myeloid leukemia patients with NUP98 rearrangement.Semantic proximity Read ↗

Identification of novel NUP98 fusion partners and comutations in acute myeloid leukemia: an adult cohort study.Semantic proximity Read ↗

Adult acute myeloid leukemia patients with NUP98 rearrangement have frequent cryptic translocations and unfavorable outcomeSemantic proximity Read ↗

An atypical chronic neutrophilic leukemia patient harboring ASXL1 and NRAS mutations associated with monoclonal plasma cell dyscrasia presenting as hemopericardium.Semantic proximity Read ↗

Analysis of NUP98/NSD1 translocations in adult AML and MDS patientsSemantic proximity Read ↗

Mixed phenotype acute leukemia in a child associated with a NUP98-NSD1 fusion and NRAS p.Gly61Arg mutation.Semantic proximity Read ↗

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression patternSemantic 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 ↗

NUP98::NSD1 and FLT3-ITD collaborate to generate acute myeloid leukemiaSemantic proximity Read ↗

NUP98-fusion transcripts characterize different biological entities within acute myeloid leukemia: a report from the AIEOP-AML group.Semantic proximity Read ↗

Frequent ASXL1 mutations in children and young adults with chronic myeloid leukemia.Semantic proximity Read ↗

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