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Cancer Genet Cytogenet ; 160(2): 184-7, 2005 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-15993277

RESUMO

Deletions of the 5'ABL region adjacent to the t(9;22)(q34;q11) have recently been reported in 8-32.7% of patients with chronic myeloid leukemia (CML). The deletions were visualized with fluorescence in situ hybridization using, in the majority of the cases, the Vysis LSI BCR/ABL ES (extra signal) probe. In our series, 10 of 99 CML patients (10.1%) were characterized by a 5'ABL deletion. We show that 3'BCR losses are observed in nearly all the cases with 5'ABL deletions. Moreover, the different genetic events (Philadelphia chromosome formation; 5'ABL and 3'BCR deletions) occur simultaneously in a one-step process without any evidence for genetic instability in the target bone marrow cells.


Assuntos
Proteínas de Fusão bcr-abl/genética , Instabilidade Genômica/genética , Leucemia Mielogênica Crônica BCR-ABL Positiva/genética , Deleção de Sequência/genética , Feminino , Humanos , Hibridização in Situ Fluorescente , Masculino , Pessoa de Meia-Idade
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