Molecular heterogeneity of the NUP98/HOXA9 fusion transcript in myelodysplastic syndromes associated with t(7;11)(p15;p15)
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01754.x/fullpdf
Reference12 articles.
1. Proposals for the classification of the myelodysplastic syndromes;Bennett;British Journal of Haematology,1982
2. The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class 1 homeoprotein HOXA9;Borrow;Nature Genetics,1996
3. Clinical, haematological and molecular studies in patients with chromosome translocation t(7;11): a study of four Chinese patients in Taiwan;Huang;British Journal of Haematology,1997
4. ISCN 1995 An International System for Human Cytogenetic Nomenclature Cytogenetics and Cell Genetics
5. Ecotropic murine leukemia virus DNA content of normal and lymphomatous tissues of BXH-2 recombinant inbred mice;Jenkins;Journal of Virology,1982
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3. HOXA9 Regulome and Pharmacological Interventions in Leukemia;Advances in Experimental Medicine and Biology;2024
4. Inherited heterozygous Fanconi anemia gene mutations in a therapy-related CMML patient with a rare NUP98-HOXC11 fusion: A case report;Frontiers in Oncology;2022-10-19
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