The Molecular Genetics of Recurring Chromosome Abnormalities in Acute Myeloid Leukemia
- 31 October 2000
- journal article
- Published by Elsevier in Seminars in Hematology
- Vol. 37 (4) , 368-380
- https://doi.org/10.1016/s0037-1963(00)90017-9
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- 11p15 translocations involving theNUP98 gene in childhood therapy-related acute myeloid leukemia/myelodysplastic syndromeGenes, Chromosomes and Cancer, 1999
- The Transcriptional Coactivators p300 and CBP Are Histone AcetyltransferasesPublished by Elsevier ,1996
- The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding proteinNature Genetics, 1996
- An Mll–AF9 Fusion Gene Made by Homologous Recombination Causes Acute Leukemia in Chimeric Mice: A Method to Create Fusion OncogenesCell, 1996
- Altered Hox expression and segmental identity in Mll-mutant miceNature, 1995
- The t(4;11) chromosome translocation of human acute leukemias fuses the ALL-1 gene, related to Drosophila trithorax, to the AF-4 geneCell, 1992
- Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemiasCell, 1992
- A trithorax–like gene is interrupted by chromosome 11q23 translocations in acute leukaemiasNature Genetics, 1992
- The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locusNature, 1990
- Secondary Acute Myeloid Leukemia in Children Treated for Acute Lymphoid LeukemiaNew England Journal of Medicine, 1989