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Cancer Genet ; 260-261: 37-40, 2022 01.
Artigo em Inglês | MEDLINE | ID: mdl-34915342

RESUMO

Pediatric acute myeloid leukemia (AML) is genetically heterogenous (Olsson et al., 2016). t(X;6)(p11;q23) is a rare but recurrent chromosomal translocation in infant AML thought to be associated with male sex and basophilic differentiation (Dastugue et al., 1997). Here we report molecular characterization of AML with t(X;6)(p11;q23);MYB-GATA1 in two female infants and demonstrate preserved GATA1 expression in the sample tested. These findings further debunk a concept that this fusion was restricted to males, in whom it disrupts the only copy of the X-linked GATA1 gene, causing presumable complete loss of GATA1 function. Our data also demonstrate the power and efficiency of RNA sequencing for subclassification of leukemia on a clinically relevant timeline.


Assuntos
Fator de Transcrição GATA1/genética , Leucemia Mieloide Aguda/genética , Proteínas Proto-Oncogênicas c-myb/genética , Translocação Genética , Cromossomos Humanos Par 6/genética , Cromossomos Humanos Par 9/genética , Cromossomos Humanos X/genética , Feminino , Humanos , Lactente , Proteínas de Fusão Oncogênica/genética , Análise de Sequência de RNA
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