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首页> 外文期刊>Annals of Clinical and Laboratory Science: Official Journal of the Association of Clinical Scientists >Detection of trisomy 8 in philadelphia chromosome-positive CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques and its relation to c-myc involvement.
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Detection of trisomy 8 in philadelphia chromosome-positive CML patients using conventional cytogenetic and interphase fluorescence in situ hybridization techniques and its relation to c-myc involvement.

机译:使用常规细胞遗传学和相间荧光原位杂交技术检测费城染色体阳性CML患者的三体性8及其与c-myc参与的关系。

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摘要

Trisomy 8 (+8) is a common clonal evolution marker for progression in chronic myelogenous leukemia. The relationship of +8 to various stages of t(9;22) leukemias is not firmly established. To explore this association we examined bone marrow (BM) cells from 10 Philadelphia chromosome positive (Ph+) chronic myeloid leukemia (CML) patients in different stages of the disease, using conventional cytogenetic technique(CCT) and interphase fluorescence in situ hybridization (FISH). FISH detection of chromosome 8 was accomplished using the D8Z2 (Oncor) probe specific for the centrometric region of chromosome 8. Five hundred interphase nuclei were counted for each patient. Three of the 10 patients were selected for detection of c-myc gene locus located in the 8q24.2-24.3 region using the L
机译:三体性8(+8)是慢性粒细胞性白血病进展中常见的克隆进化标记。 +8与t(9; 22)白血病各个阶段之间的关系尚不确定。为了探索这种关系,我们使用常规细胞遗传学技术(CCT)和相间荧光原位杂交(FISH)检查了该疾病不同阶段的10位费城染色体阳性(Ph +)慢性粒细胞白血病(CML)患者的骨髓(BM)细胞。使用特异于8号染色体中心区域的D8Z2(Oncor)探针完成8号染色体的FISH检测。每个患者计数500个相间核。使用L选择10例患者中的3例用于检测位于8q24.2-24.3区域的c-myc基因位点

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