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

Mutation of the WT1 gene in myelodysplastic syndrome and acute myeloid leukaemia post myelodysplastic syndrome.

British journal of haematology - 1 Jun 1999

Mori N, Okada M, Motoji T, Mizoguchi H

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 Acute Disease
Share to Leukemia, Myeloid
Share to Mutation
Share to Myelodysplastic Syndromes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10354161
DOI: 10.1046/j.1365-2141.1999.01497.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation of the WT1 gene in myelodysplastic syndrome and acute myeloid leukaemia post myelodysplastic syndrome.PMID 10354161Read ↗

Mutation analysis of the WT1 gene in myelodysplastic syndromes.Semantic proximity Read ↗

[Comparison of genetic mutations in myelodysplastic syndrome and acute myeloid leukemia].Semantic proximity Read ↗

The Impact of Somatic and Germline Mutations in Myelodysplastic Syndromes and Related Disorders.Semantic proximity Read ↗

WT1 and GATA1 expression in myelodysplastic syndrome and acute leukemiaSemantic proximity Read ↗

Genetic abnormalities in myelodysplastic syndrome.Semantic proximity Read ↗

AML1 mutation and FLT3-internal tandem duplication in leukemia transformed from myelodysplastic syndrome.Semantic proximity Read ↗

Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.Semantic proximity Read ↗

Impaired mitochondrial gene transcription in myelodysplastic syndromes and acute myeloid leukemia with myelodysplasia-related changesSemantic proximity Read ↗

[Genetic abnormalities in myelodysplastic syndrome].Semantic proximity Read ↗

Splicing factor mutations in myelodysplasia.Semantic proximity Read ↗

TET2 mutations in myelodysplasia and myeloid malignancies.Semantic proximity Read ↗

Clinical associations of CSNK1A1 mutation in myelodysplastic syndrome.Semantic proximity Read ↗

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