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

The clinical relevance of Wilms Tumour 1 (WT1) gene mutations in acute leukaemia.

Hematological oncology - 1 Mar 2010

Owen Carolyn, Fitzgibbon Jude, Paschka Peter

Abstract excerpt

Recurrent genetic aberrations are important predictors of outcome in acute myeloid leukaemia (AML). Numerous novel molecular abnormalities have been identified and investigated in recent years adding to the risk stratification and prognostication of conventional karyotyping. Mutations in the Wilm...

Read the complete abstract on PubMed

Topics

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

Share to Acute Lymphoblastic Leukemia research
Share to Acute Myeloid Leukemia Research
Share to Genes, Wilms Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

Share to Mutation

Share to Prognosis

Share to Renal and related cancers

Share to WT1 Proteins

Source

Identifiers

PMID: 20013787
DOI: 10.1002/hon.931

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20013787-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The clinical relevance of Wilms Tumour 1 (WT1) gene mutations in acute leukaemia.PMID 20013787Read ↗

Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia.Semantic proximity Read ↗

Wilms tumor 1 mutations in the pathogenesis of acute myeloid leukemia.Semantic proximity Read ↗

Prognostic impact of Wilms tumor gene mutations in Egyptian patients with acute myeloid leukemia with normal karyotype.Semantic proximity Read ↗

Wilms' tumor (WT1) gene mutations occur mainly in acute myeloid leukemia and may confer drug resistance.Semantic proximity Read ↗

Friend or foe? The case of Wilms' Tumor 1 (WT1) mutations in acute myeloid leukemia.Semantic proximity Read ↗

Prognostic Impact of Wilms' Tumour 1 Mutation in Patients with Acute Myeloid Leukaemia.Semantic proximity Read ↗

Wilms tumor 1 gene mutations are associated with a higher risk of recurrence in young adults with acute myeloid leukemia: a study from the Acute Leukemia French Association.Semantic proximity Read ↗

Wilms Tumor 1 Mutations are Independent Poor Prognostic Factors in Pediatric Acute Myeloid LeukemiaSemantic proximity Read ↗

Prognostic implications of mutations and expression of the Wilms tumor 1 (WT1) gene in adult acute T-lymphoblastic leukemia.Semantic proximity Read ↗

WT1 mutations are secondary events in AML, show varying frequencies and impact on prognosis between genetic subgroups.Semantic proximity Read ↗

Frequency and Clinical Impact of WT1 Mutations in the Context of CEBPA-Mutated Acute Myeloid LeukemiaSemantic proximity Read ↗

Prevalence and Prognostic Impact of Wilms' Tumor 1 (WT1) Gene, Including SNP rs16754 in Cytogenetically Normal Acute Myeloblastic Leukemia (CN-AML): An Iranian Experience.Semantic proximity Read ↗

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