AML1/RUNX1 mutations in 470 adult patients with de novo acute myeloid leukemia: prognostic implication and interaction with other gene alterations

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder

(2009) C. Preudhomme et al.   BLOOD

Molecular pathways mediating MDS/AML with focus on AML1/RUNX1 point mutations

(2009) Yuka Harada et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Cell cycle and developmental control of hematopoiesis by Runx1

(2009) Alan D. Friedman   JOURNAL OF CELLULAR PHYSIOLOGY

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

(2008) C. J. Owen et al.   BLOOD

A novel RUNX1 mutation in familial platelet disorder with propensity to develop myeloid malignancies

(2008) K. Kirito et al.   HAEMATOLOGICA

Wilms’ Tumor 1 Gene Mutations Independently Predict Poor Outcome in Adults With Cytogenetically Normal Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study

(2008) Peter Paschka et al.   JOURNAL OF CLINICAL ONCOLOGY

Cooperating gene mutations in acute myeloid leukemia: a review of the literature

(2008) A Renneville et al.   LEUKEMIA

Mutations and Treatment Outcome in Cytogenetically Normal Acute Myeloid Leukemia

(2008) Richard F. Schlenk et al.   NEW ENGLAND JOURNAL OF MEDICINE

Review: genetic models of acute myeloid leukaemia

(2008) E McCormack et al.   ONCOGENE

Prognostic Implications of Gene Mutations in Acute Myeloid Leukemia With Normal Cytogenetics

(2008) Verena Gaidzik et al.   SEMINARS IN ONCOLOGY

Gatekeeper function of the RUNX1 transcription factor in acute leukemia

(2007) Birte Niebuhr et al.   BLOOD CELLS MOLECULES AND DISEASES