Suppr超能文献

一种可能的单核细胞白血病特异性染色体标志物:又有3例t(9;11)(p22;q24)患者及另1例t(11;17)(q24;q21)患者,均患有急性单核母细胞白血病。

A possible specific chromosome marker for monocytic leukemia: three more patients with t(9;11)(p22;q24) and another with t(11;17)(q24;q21), each with acute monoblastic leukemia.

作者信息

Dewald G W, Morrison-DeLap S J, Schuchard K A, Spurbeck J L, Pierre R V

出版信息

Cancer Genet Cytogenet. 1983 Mar;8(3):203-12. doi: 10.1016/0165-4608(83)90136-x.

Abstract

An apparently balanced 9;11 reciprocal translocation with break points most likely at 9p22 and 11q24 was found in 3 patients with acute monocytic leukemia [M5 in the French-American-British (FAB) classification schema]. This translocation was not observed in 6 other patients with M5 acute nonlymphocytic leukemia (ANLL) or in chromosome studies on 143 patients with other types of ANLL. This study supports the previously published suggestion that such 9;11 translocations may be associated with some patients with M5 ANLL. In this report, we have also included a patient with M5 ANLL who had an 11;17 translocation with break points apparently at 11q24 and 17q21. Perhaps this is a variant translocation of chromosome No. 11, which may also be associated with monocytic leukemia.

摘要

在3例急性单核细胞白血病患者(按照法美英(FAB)分类标准为M5型)中发现了一种明显平衡的9;11相互易位,断点最可能位于9p22和11q24。在其他6例M5型急性非淋巴细胞白血病(ANLL)患者中未观察到这种易位,在对143例其他类型ANLL患者的染色体研究中也未发现。这项研究支持了之前发表的观点,即这种9;11易位可能与部分M5型ANLL患者有关。在本报告中,我们还纳入了1例M5型ANLL患者,其存在11;17易位,断点明显位于11q24和17q21。这可能是11号染色体的一种变异易位,也可能与单核细胞白血病有关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验