Clonal expansion of a new MLL rearrangement in the absence of leukemia
Open Access
- 15 May 2005
- journal article
- Published by American Society of Hematology in Blood
- Vol. 105 (10) , 4151-4152
- https://doi.org/10.1182/blood-2005-01-0286
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Diagnostic tool for the identification of MLL rearrangements including unknown partner genesProceedings of the National Academy of Sciences, 2004
- Extending the repertoire of the mixed-lineage leukemia gene MLL in leukemogenesisGenes & Development, 2004
- Combined analysis of morphology and fluorescence in situ hybridization in follow-up of minimal residual disease in a child with Philadelphia-positive acute lymphoblastic leukemiaCancer Genetics and Cytogenetics, 2002
- A mammalian Rho-specific guanine-nucleotide exchange factor (p164-RhoGEF) without a pleckstrin homology domainBiochemical Journal, 2002
- Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet™) combined morphological and cytogenetical analysisLeukemia, 2002
- Molecular mechanisms of leukemogenesis mediated by MLL fusion proteinsOncogene, 2001
- MLL rearrangements in haematological malignancies: lessons from clinical and biological studiesBritish Journal of Haematology, 1999
- A trithorax–like gene is interrupted by chromosome 11q23 translocations in acute leukaemiasNature Genetics, 1992
- Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.Proceedings of the National Academy of Sciences, 1991