融合基因
染色体易位
阿布勒
融合蛋白
癌症研究
聚合酶链反应
断点
融合
酪氨酸激酶
基因
生物
医学
分子生物学
遗传学
信号转导
重组DNA
哲学
语言学
作者
Thomas Ernst,Joannah Score,Michael W. Deininger,Claire Hidalgo-Curtis,Peter M. Lackie,William B. Ershler,John M. Goldman,Nicholas C.P. Cross,FrancisH. Grand
标识
DOI:10.1111/j.1365-2141.2010.08457.x
摘要
Summary We have identified two novel ABL1 fusion genes in two patients with B‐cell acute lymphoblastic leukaemia (ALL) associated with a t(3;9)(p12;q34) and a t(5;9)(q23;q34), respectively. Molecular analysis revealed a FOXP1‐ABL1 fusion for the t(3;9) and a SNX2‐ABL1 fusion for the t(5;9). The fusions were confirmed by specific amplification of the genomic breakpoints using reverse transcription polymerase chain reaction. The identification of ALL with rare ABL1 fusion partners is important because the leukaemia may respond to tyrosine kinase inhibitors in the same way as ALL patients with a classical BCR‐ABL1 fusion gene.
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