Genetic and epigenetic determinants mediate proneness of oncogene breakpoint sites for involvement in TCR translocations-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Genetic and epigenetic determinants mediate proneness of oncogene breakpoint sites for involvement in TCR translocations

Published:2013-12-05 Issue:2 Volume:15 Page:72-81
ISSN:1466-4879
Container-title:Genes & Immunity
language:en
Short-container-title:Genes Immun

Author:

Larmonie N S D,van der Spek A,Bogers A J J C,van Dongen J J M,Langerak A W

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Immunology

Link

http://www.nature.com/articles/gene201363.pdf

Reference61 articles.

1. Chiaretti S, Foa R . T-cell acute lymphoblastic leukemia. Haematologica 2009; 94: 160–162.

2. Van Vlierberghe P, Pieters R, Beverloo HB, Meijerink JP . Molecular-genetic insights in paediatric T-cell acute lymphoblastic leukaemia. Br J Haematol 2008; 143: 153–168.

3. Marculescu R, Vanura K, Montpellier B, Roulland S, Le T, Navarro JM et al. Recombinase, chromosomal translocations and lymphoid neoplasia: targeting mistakes and repair failures. DNA Repair (Amst) 2006; 5: 1246–1258.

4. Dik WA, Nadel B, Przybylski GK, Asnafi V, Grabarczyk P, Navarro JM et al. Different chromosomal breakpoints impact the level of LMO2 expression in T-ALL. Blood 2007; 110: 388–392.

5. Ferrando AA, Neuberg DS, Staunton J, Loh ML, Huard C, Raimondi SC et al. Gene expression signatures define novel oncogenic pathways in T cell acute lymphoblastic leukemia. Cancer Cell 2002; 1: 75–87.

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An integrated transcriptome analysis in T-cell acute lymphoblastic leukemia links DNA methylation subgroups to dysregulated TAL1 and ANTP homeobox gene expression;Cancer Medicine;2018-12-21

2. MN1 overexpression is driven by loss of DNMT3B methylation activity in inv(16) pediatric AML;Oncogene;2017-09-11

3. Chromosomal Translocations and Gene Rearrangements in Acute Lymphoblastic Leukaemia;Chromosomal Translocations and Genome Rearrangements in Cancer;2015

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3