t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia
Open Access
- 1 June 2000
- journal article
- case report
- Published by Wiley in British Journal of Haematology
- Vol. 109 (4) , 788-793
- https://doi.org/10.1046/j.1365-2141.2000.02106.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- CREB Binding Protein Interacts with Nucleoporin-Specific FG Repeats That Activate Transcription and Mediate NUP98-HOXA9 OncogenicityMolecular and Cellular Biology, 1999
- Sequential molecular monitoring of chimerism in chronic myeloid leukemia patients receiving donor lymphocyte transfusion for relapse after bone marrow transplantationBone Marrow Transplantation, 1997
- The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9Nature Genetics, 1996
- Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemiaNature Genetics, 1996
- ALL-1 gene at chromosome 11q23 is consistently altered in acute leukemia of early infancyBlood, 1993
- Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector.Proceedings of the National Academy of Sciences, 1992
- Can, a putative oncogene associated with myeloid leukemogenesis, may be activated by fusion of its 3' half to different genes: characterization of the set gene.Molecular and Cellular Biology, 1992
- The translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNA.Molecular and Cellular Biology, 1992
- A rare translocation (4;11)(q21;p14–15) in an acute lymphoblastic leukemia expressing T-cell and myeloid markersCancer Genetics and Cytogenetics, 1991
- The (4;11) translocation in acute leukaemia of childhood: the importance of additional chromosomal aberrationsBritish Journal of Haematology, 1985