• 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

Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participants.

作者信息

Harrison C J, Cuneo A, Clark R, Johansson B, Lafage-Pochitaloff M, Mugneret F, Moorman A V, Secker-Walker L M

机构信息

Department of Haematology, Royal Free Hospital School of Medicine, London, UK.

出版信息

Leukemia. 1998 May;12(5):811-22. doi: 10.1038/sj.leu.2401017.

DOI:10.1038/sj.leu.2401017
PMID:9593286
Abstract

The MLL gene located at 11q23 has been described as a 'promiscuous' gene due its involvement with a large number of genetic partners. The EU Concerted Action Workshop on 11q23 provided 550 cases for study of which 82 showed abnormalities which did not involve the established translocations or deletion of 11q23. In these 'other' cases, which included inversions and duplications, 11q23 was found to be involved with 25 chromosome partners of which 10 had not been previously reported. These were 1q31, 4p11, 6q13, 8q21, 10q22, 10q25, 11q11, 11q21, 13q34 and 18q23. This study demonstrated the value of the Workshop, in confirming the diversity of chromosomal partner sites involved with 11q23 and in the identification of new partners.

摘要

相似文献

1
Ten novel 11q23 chromosomal partner sites. European 11q23 Workshop participants.
Leukemia. 1998 May;12(5):811-22. doi: 10.1038/sj.leu.2401017.
2
Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings.荧光原位杂交(FISH)分析揭示的隐匿性插入和易位或非分裂白血病细胞在分子和细胞遗传学结果不一致的婴儿急性白血病中
Leukemia. 2003 May;17(5):876-82. doi: 10.1038/sj.leu.2402900.
3
ALL-1 gene rearrangements in DNA topoisomerase II inhibitor-related leukemia in children.儿童DNA拓扑异构酶II抑制剂相关白血病中的ALL-1基因重排
Blood. 1995 Jun 1;85(11):3250-6.
4
The t(6;11)(q27;q23) translocation in acute leukemia: a laboratory and clinical study of 30 cases. EU Concerted Action 11q23 Workshop participants.
Leukemia. 1998 May;12(5):788-91. doi: 10.1038/sj.leu.2401013.
5
Acute lymphoblastic leukemias with deletion of 11q23 or a novel inversion (11)(p13q23) lack MLL gene rearrangements and have favorable clinical features.伴有11q23缺失或新的inv(11)(p13q23)的急性淋巴细胞白血病缺乏MLL基因重排,且具有良好的临床特征。
Blood. 1995 Sep 1;86(5):1881-6.
6
Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.急性白血病中t(9;11) MLL-AF9融合基因复杂基因组断点连接的鉴定
Genes Chromosomes Cancer. 1997 Oct;20(2):185-95.
7
Clinical and biological characteristics of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: confirmation of the existence of different entities with 11q23 breakpoint.与具有不平衡11q23异常的病例相比,伴有平衡的11q23染色体异常或MLL基因重排的成人初发和继发性急性髓系白血病的临床和生物学特征:证实存在具有11q23断点的不同实体。
Leukemia. 1998 Jan;12(1):25-33. doi: 10.1038/sj.leu.2400853.
8
Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities.比较细胞遗传学、Southern印迹法和荧光原位杂交作为检测急性白血病伴11q23异常儿童中MLL基因重排的方法。
Leukemia. 1999 Nov;13(11):1713-20. doi: 10.1038/sj.leu.2401512.
9
Two new translocations involving the 11q23 region map outside the MLL locus in myeloid leukemias.在髓系白血病中,两个涉及11q23区域的新易位定位于MLL基因座之外。
Haematologica. 2002 Oct;87(10):1014-20.
10
Molecular analysis of infant acute leukemia.
Leuk Lymphoma. 1997 Apr;25(3-4):191-9. doi: 10.3109/10428199709114159.

引用本文的文献

1
Co-existence of :: fusion and variant in a pediatric case with acute myeloid leukemia: a case report and literature review.一名急性髓系白血病儿科病例中融合基因与变异共存:病例报告及文献综述
Front Oncol. 2023 Dec 13;13:1308786. doi: 10.3389/fonc.2023.1308786. eCollection 2023.
2
Clinical profile in positive acute myeloid leukemia: Does it often co-occur with mutations?阳性急性髓系白血病的临床特征:它是否常与突变同时发生?
Front Med (Lausanne). 2022 Sep 21;9:890959. doi: 10.3389/fmed.2022.890959. eCollection 2022.
3
Establishment of a novel human lymphoblastic cell strain with the long arm of chromosome 11 aberration without MLL rearrangement.
建立一个新型的人淋巴母细胞株,其 11 号染色体长臂异常,但没有 MLL 重排。
Sci Rep. 2017 Apr 13;7(1):867. doi: 10.1038/s41598-017-00874-6.
4
DNMT3A and TET2 in the Pre-Leukemic Phase of Hematopoietic Disorders.造血系统疾病白血病前期阶段中的DNMT3A和TET2
Front Oncol. 2016 Aug 22;6:187. doi: 10.3389/fonc.2016.00187. eCollection 2016.
5
A rare case of pediatric T lymphoblastic leukemia with t(11;17)(q23;q21) involving mixed-lineage leukemia gene rearrangement.1例罕见的伴有t(11;17)(q23;q21)且涉及混合谱系白血病基因重排的儿童T淋巴细胞白血病。
Ann Lab Med. 2016 Jan;36(1):64-6. doi: 10.3343/alm.2016.36.1.64.
6
Molecular characterization and clinical impact of t(11;15)(q23;q14-15) MLL-CASC5 rearrangement.t(11;15)(q23;q14-15) MLL-CASC5重排的分子特征及临床影响
Haematologica. 2014 Jan;99(1):e11-3. doi: 10.3324/haematol.2013.095638.
7
First description of the t(10;11)(q22;q23)/MLL-TET1 translocation in a T-cell lymphoblastic lymphoma, with subsequent lineage switch to acute myelomonocytic myeloid leukemia.首次报道T细胞淋巴母细胞淋巴瘤中t(10;11)(q22;q23)/MLL-TET1易位,随后谱系转变为急性粒单核细胞白血病。
Haematologica. 2013 Dec;98(12):e166-8. doi: 10.3324/haematol.2013.096750.
8
Genomic breakpoints and clinical features of MLL-TET1 rearrangement in acute leukemias.急性白血病中MLL-TET1重排的基因组断点与临床特征
Haematologica. 2013 Apr;98(4):e55-7. doi: 10.3324/haematol.2012.076323. Epub 2012 Oct 25.
9
Therapy-related acute myeloid leukemia 6 years after clonal detection of inv(11)(q21q23) and MLL gene rearrangement.
Int J Hematol. 2006 Apr;83(3):247-51. doi: 10.1532/IJH97.05152.
10
Molecular pathogenesis of MLL-associated leukemias.MLL相关白血病的分子发病机制。
Int J Hematol. 2005 Jul;82(1):9-20. doi: 10.1532/IJH97.05042.