• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

[Cloning the region of chromosome 22 participating in translocation t(9,22) in human chronic myeloid leukemia].

作者信息

Pokrovskaia E S, Domninskiĭ D A, Babushkina E A, Krutov A A, Tagiev A F, Grineva N I

出版信息

Mol Biol (Mosk). 1993 Jan-Feb;27(1):185-91.

PMID:8483470
Abstract

Using oligonucleotide probes, sequences containing the Mbcr locus involved in chromosome translocation t(9:22) were cloned form the library of human genes in the Charon 4A vector. The recombinant clone lambda BCR 1.1 obtained contained Mbcr sequences, but the 3' region of the Mbcr locus in lambda BCR 1.1 clone was strongly altered. Subcloning of a fragment of the altered region and blot hybridization analysis using it as a DNA probe revealed recombination in the 3' region of the Mbcr locus in clone lambda BCR 1.1 which resulted in insertion of unknown sequences into the region. A modified system is suggested for chromosome 22 breakpoint identification using restriction analysis of genome DNA with four restriction endonucleases and one 5'-DNA probe.

摘要

相似文献

1
[Cloning the region of chromosome 22 participating in translocation t(9,22) in human chronic myeloid leukemia].
Mol Biol (Mosk). 1993 Jan-Feb;27(1):185-91.
2
BCR gene recombines with genomically distinct sites on band 11Q13 in complex BCR-ABL translocations of chronic myeloid leukemia.
Oncogene. 1996 Feb 1;12(3):677-85.
3
Fluorescence in situ hybridization characterization of different cryptic BCR-ABL rearrangements in chronic myeloid leukemia.慢性髓性白血病中不同隐匿性BCR-ABL重排的荧光原位杂交特征分析
Cancer Genet Cytogenet. 2004 Dec;155(2):132-7. doi: 10.1016/j.cancergencyto.2004.02.026.
4
Detailed mapping of methylcytosine positions at the CpG island surrounding the Pa promoter at the bcr-abl locus in CML patients and in two cell lines, K562 and BV173.对慢性粒细胞白血病(CML)患者以及两种细胞系K562和BV173中bcr-abl基因座处Pa启动子周围CpG岛的甲基胞嘧啶位置进行详细定位。
Blood Cells Mol Dis. 2000 Jun;26(3):193-204. doi: 10.1006/bcmd.2000.0296.
5
Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.慢性髓性白血病基因组断点处的微同源性和散布重复元件
Genes Chromosomes Cancer. 2008 Jul;47(7):625-32. doi: 10.1002/gcc.20568.
6
DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias.
Oncogene. 1993 Jun;8(6):1679-83.
7
"Home-brew" FISH assay shows higher efficiency than BCR-ABL dual color, dual fusion probe in detecting microdeletions and complex rearrangements associated with t(9;22) in chronic myeloid leukemia.“自制”荧光原位杂交(FISH)检测法在检测慢性髓性白血病中与t(9;22)相关的微缺失和复杂重排方面,比BCR-ABL双色双融合探针具有更高的效率。
Cancer Genet Cytogenet. 2007 Apr 15;174(2):121-6. doi: 10.1016/j.cancergencyto.2006.09.025.
8
Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).伴有罕见变异型BCR-ABL易位的慢性髓性白血病:t(9;22;21)(q34;q11.2;q11.2)
Cancer Genet Cytogenet. 2007 Nov;179(1):85-7. doi: 10.1016/j.cancergencyto.2007.08.010.
9
The first BCR gene intron contains breakpoints in Philadelphia chromosome positive leukemia.首个BCR基因内含子在费城染色体阳性白血病中存在断点。
Nucleic Acids Res. 1988 Nov 11;16(21):10069-81. doi: 10.1093/nar/16.21.10069.
10
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.ABL1-BCR转录缺失的异质性分子基础:BCR-ABL1阳性慢性髓性白血病中der(9)t(9;22)的缺失及标准t(9;22)的变体
Genes Chromosomes Cancer. 2002 Jun;34(2):193-200. doi: 10.1002/gcc.10056.