## Abstract The translocation t(9;11)(p22;q23) is a recurring chromosomal abnormality in acute myeloid leukemia (AML) fusing two genes designated as __MLL__ and __AF9.__ Within __MLL,__ almost all rearrangements cluster in an 8.3βkb restricted region and fuse 5β² portions of __MLL__ to a variety of
Cloning and sequence analysis of four t(9;11) therapy-related leukemia breakpoints
β Scribed by Atlas, M; Head, D; Behm, F; Schmidt, E; Zeleznik-Le, N J; Roe, B A; Burian, D; Domer, P H
- Book ID
- 110054028
- Publisher
- Nature Publishing Group
- Year
- 1998
- Tongue
- English
- Weight
- 241 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0887-6924
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## Abstract Thirteen cosmid probes were mapped on the long arm of chromosome 11 between 11q22 and 11q24 by nonradioactive in situ hybridization. Starting with these localizations and those of other probes mapped to 11q23, four acute leukemias with translocations involving 11q23 were studied with th
## Abstract We compared genomic breakpoints at the __PML__ and __RARA__ loci in 23 patients with therapyβrelated acute promyelocytic leukemia (tβAPL) and 25 de novo APL cases.Eighteen of 23 tβAPL cases received the topoisomerase II poison mitoxantrone for their primary disorder. DNA breaks were clu
The t(6;9) associated with a subtype of acute myeloid leukemia (AML) was shown t o generate a fusion between the 3' part of the CAN gene on chromosome 9 and the 5' part of the DEK gene on chromosome 6. The same part of the CAN gene appeared t o be involved in a case of acute undifferentiated leukemi