• 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

Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain.

作者信息

García-Sanz R, Alaejos I, Orfão A, Rasillo A, Chillón M C, Tabernero M D, Mateos M V, López-Pérez R, González D, Balanzategui A, González M, San Miguel J F, Bortolucci A

机构信息

Haematology Service, University Hospital of Salamanca, Instituto de Biología Molecular y Celular del Cáncer, Universidad de Salamanca, Salamanca, Spain.

出版信息

Br J Haematol. 1999 Dec;107(3):667-9. doi: 10.1046/j.1365-2141.1999.01747.x.

DOI:10.1046/j.1365-2141.1999.01747.x
PMID:10583273
Abstract

We report on a series of Spanish patients with acute lymphoblastic leukaemia in whom the t(12;21) [TEL/AML1] translocation could not be identified with two sensitive techniques: reverse transcript-polymerase chain reaction (RT-PCR) and fluorescence in-situ hybridization (FISH). 101 cases were analysed: 38 children (29 B-cell precursor; nine T-cell precursor) and 63 adults (48 B-cell precursor; 15 T-cell precursor). Specific RT-PCR to amplify the TEL/AML1 fusion transcript was negative in all 101 cases. Moreover, all 38 paediatric samples were also negative by interphase FISH analysis for the presence of the TEL/AML1 fusion. These results suggest the existence of geographic/race variations in the genotype of acute lymphoblastic leukaemia (ALL).

摘要

相似文献

1
Low frequency of the TEL/AML1 fusion gene in acute lymphoblastic leukaemia in Spain.
Br J Haematol. 1999 Dec;107(3):667-9. doi: 10.1046/j.1365-2141.1999.01747.x.
2
TEL-AML1 translocations with TEL and CDKN2 inactivation in acute lymphoblastic leukemia cell lines.急性淋巴细胞白血病细胞系中伴有TEL和CDKN2失活的TEL-AML1易位
Blood. 1996 Aug 1;88(3):785-94.
3
Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines.人类早期B系白血病细胞系中因(12;21)易位导致的TEL-AML1融合的发生情况。
Leukemia. 1997 Mar;11(3):441-7. doi: 10.1038/sj.leu.2400571.
4
Interphase FISH on TEL/AML1 positive acute lymphoblastic leukemia relapses--analysis of clinical relevance of additional TEL and AML1 copy number changes.TEL/AML1阳性急性淋巴细胞白血病复发时的间期荧光原位杂交——额外的TEL和AML1拷贝数变化的临床相关性分析
Eur J Haematol. 2009 Nov;83(5):420-32. doi: 10.1111/j.1600-0609.2009.01315.x. Epub 2009 Jul 6.
5
Molecular genetic studies on 167 pediatric ALL patients from different areas of Pakistan confirm a low frequency of the favorable prognosis fusion oncogene TEL-AML1 (t 12; 21) in underdeveloped countries of the region.对来自巴基斯坦不同地区的167名儿童急性淋巴细胞白血病患者进行的分子遗传学研究证实,该地区不发达国家中预后良好的融合致癌基因TEL-AML1(t(12;21))的频率较低。
Asian Pac J Cancer Prev. 2014;15(8):3541-6. doi: 10.7314/apjcp.2014.15.8.3541.
6
Expression levels of TEL, AML1, and the fusion products TEL-AML1 and AML1-TEL versus drug sensitivity and clinical outcome in t(12;21)-positive pediatric acute lymphoblastic leukemia.TEL、AML1以及融合产物TEL-AML1和AML1-TEL的表达水平与t(12;21)阳性儿童急性淋巴细胞白血病的药物敏感性及临床结局的关系
Clin Cancer Res. 2005 Apr 15;11(8):2974-80. doi: 10.1158/1078-0432.CCR-04-1829.
7
Correlation between the ETV6/CBFA2 (TEL/AML1) fusion gene and karyotypic abnormalities in children with B-cell precursor acute lymphoblastic leukemia.B 细胞前体急性淋巴细胞白血病患儿中 ETV6/CBFA2(TEL/AML1)融合基因与核型异常的相关性
Genes Chromosomes Cancer. 1996 Oct;17(2):127-35. doi: 10.1002/(SICI)1098-2264(199610)17:2<127::AID-GCC8>3.0.CO;2-7.
8
Rapid quantitative detection of TEL-AML1 fusion transcripts in pediatric acute lymphoblastic leukemia by real-time reverse transcription polymerase chain reaction using fluorescently labeled probes.使用荧光标记探针通过实时逆转录聚合酶链反应快速定量检测儿童急性淋巴细胞白血病中的TEL-AML1融合转录本
Haematologica. 2002 Jan;87(1):23-32.
9
TEL-AML1 fusion transcript in relapsed childhood acute lymphoblastic leukemia. The Berlin-Frankfurt-Münster Study Group.复发性儿童急性淋巴细胞白血病中的TEL-AML1融合转录本。柏林-法兰克福-明斯特研究小组。
Blood. 1998 Mar 1;91(5):1716-22.
10
ETV6/AML1 fusion by FISH in adult acute lymphoblastic leukemia.荧光原位杂交检测成人急性淋巴细胞白血病中的ETV6/AML1融合基因
Leukemia. 2002 Apr;16(4):669-74. doi: 10.1038/sj.leu.2402435.

引用本文的文献

1
High frequency and poor prognosis of late childhood BCR-ABL-positive and MLL-AF4-positive ALL define the need for advanced molecular diagnostics and improved therapeutic strategies in pediatric B-ALL in Pakistan.巴基斯坦儿童晚期BCR-ABL阳性和MLL-AF4阳性B淋巴细胞白血病的高频率及不良预后表明,该国小儿B淋巴细胞白血病需要先进的分子诊断方法及改进的治疗策略。
Mol Diagn Ther. 2015 Oct;19(5):277-87. doi: 10.1007/s40291-015-0149-0.
2
ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia.突尼斯儿童B系急性淋巴细胞白血病中的ETV6-RUNX1重排
Adv Hematol. 2009;2009:924301. doi: 10.1155/2009/924301. Epub 2009 Dec 22.
3
Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia.
儿童急性淋巴细胞白血病中最常见融合基因的临床特征。
Med Oncol. 2010 Jun;27(2):449-53. doi: 10.1007/s12032-009-9232-x. Epub 2009 Jun 2.
4
Molecular cytogenetic analysis of gene rearrangements in childhood acute lymphoblastic leukemia.儿童急性淋巴细胞白血病基因重排的分子细胞遗传学分析
J Korean Med Sci. 2005 Feb;20(1):36-41. doi: 10.3346/jkms.2005.20.1.36.