Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia
- 5 May 2005
- journal article
- research article
- Published by Springer Nature in Leukemia
- Vol. 19 (7) , 1276-1278
- https://doi.org/10.1038/sj.leu.2403788
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Loci other than 21q22.12 (RUNX1) and 16q21–23.2 cause familial AMLLeukemia, 2005
- CEBPA point mutations in hematological malignanciesLeukemia, 2005
- Mutation ofCEBPAin Familial Acute Myeloid LeukemiaNew England Journal of Medicine, 2004
- A dominant-negative mutant of C/EBPα, associated with acute myeloid leukemias, inhibits differentiation of myeloid and erythroid progenitors of man but not mouseBlood, 2004
- CCAAT/Enhancer Binding Protein α Is a Regulatory Switch Sufficient for Induction of Granulocytic Development from Bipotential Myeloid ProgenitorsMolecular and Cellular Biology, 1998
- Familial acute myeloid leukaemia: four male members of a single family over three consecutive generations exhibiting anticipationBritish Journal of Haematology, 1998