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Article

Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation.

Annals of hematology - 1 Dec 2010

De Braekeleer Etienne, Douet-Guilbert Nathalie, Basinko Audrey, Le Bris Marie-Josée, Morel Frédéric, Berthou Christian, Férec Claude, De Braekeleer Marc

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Share to Bone Marrow Transplantation
Share to Chromosome Banding
Share to Chromosomes, Human, Pair 21

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Core Binding Factor Alpha 2 Subunit

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Share to Leukemia, Myeloid, Acute

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Source

Identifiers

PMID: 20352434
DOI: 10.1007/s00277-010-0937-x

Genes

RUNX1

Provenance

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

Related research

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Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation.PMID 20352434Read ↗

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Clinico-pathologic characteristics and outcomes of the World Health Organization (WHO) provisional entity de novo acute myeloid leukemia with mutated RUNX1.Semantic proximity Read ↗

Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia.Semantic proximity Read ↗

RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features.Semantic proximity Read ↗

Acute Leukemias of Ambiguous Lineage With RUNX1 Mutations Show Similar Prognosis Compared to Acute Myeloid Leukemia With RUNX1 Mutations: A Study From the Bone Marrow Pathology Group.Semantic proximity Read ↗

RUNX1 Mutations in the Leukemic Progression of Severe Congenital Neutropenia.Semantic proximity Read ↗

Acute myeloid leukemia with GATA2 and WT1 mutations mimicking acute promyelocytic leukemia.Semantic proximity Read ↗

Molecular Basis of Hematological Disease Caused by Inherited or Acquired RUNX1 Mutations.Semantic proximity Read ↗

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