• 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

A functional polymorphism in the CEBPE gene promoter influences acute lymphoblastic leukemia risk through interaction with the hematopoietic transcription factor Ikaros.

作者信息

Wiemels J L, de Smith A J, Xiao J, Lee S-T, Muench M O, Fomin M E, Zhou M, Hansen H M, Termuhlen A, Metayer C, Walsh K M

机构信息

Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA.

Division of Neuroepidemiology, Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.

出版信息

Leukemia. 2016 May;30(5):1194-7. doi: 10.1038/leu.2015.251. Epub 2015 Sep 16.

DOI:10.1038/leu.2015.251
PMID:26437776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4794412/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff9/4794412/928d54fb601f/nihms-717029-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff9/4794412/39147d3f0f97/nihms-717029-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff9/4794412/928d54fb601f/nihms-717029-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff9/4794412/39147d3f0f97/nihms-717029-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ff9/4794412/928d54fb601f/nihms-717029-f0002.jpg

相似文献

1
A functional polymorphism in the CEBPE gene promoter influences acute lymphoblastic leukemia risk through interaction with the hematopoietic transcription factor Ikaros.CEBPE基因启动子中的功能性多态性通过与造血转录因子Ikaros相互作用影响急性淋巴细胞白血病风险。
Leukemia. 2016 May;30(5):1194-7. doi: 10.1038/leu.2015.251. Epub 2015 Sep 16.
2
Genetic polymorphisms in ARID5B, CEBPE, IKZF1 and CDKN2A in relation with risk of acute lymphoblastic leukaemia in adults: a Group for Research on Adult Acute Lymphoblastic Leukaemia (GRAALL) study.成人急性淋巴细胞白血病风险与ARID5B、CEBPE、IKZF1和CDKN2A基因多态性的关系:成人急性淋巴细胞白血病研究组(GRAALL)的一项研究
Br J Haematol. 2012 Dec;159(5):599-602. doi: 10.1111/bjh.12063. Epub 2012 Sep 27.
3
Association of Genetic Variants in ARID5B, IKZF1 and CEBPE with Risk of Childhood de novo B-Lineage Acute Lymphoblastic Leukemia in India.ARID5B、IKZF1和CEBPE基因变异与印度儿童原发性B淋巴细胞白血病风险的关联
Asian Pac J Cancer Prev. 2016;17(8):3989-95.
4
Childhood acute lymphoblastic leukemia-associated risk-loci IKZF1, ARID5B and CEBPE and risk of pediatric non-Hodgkin lymphoma: a report from the Berlin-Frankfurt-Münster Study Group.儿童急性淋巴细胞白血病相关风险基因座IKZF1、ARID5B和CEBPE与儿童非霍奇金淋巴瘤风险:来自柏林-法兰克福-明斯特研究小组的报告
Leuk Lymphoma. 2015 Mar;56(3):814-6. doi: 10.3109/10428194.2014.933479. Epub 2014 Aug 13.
5
Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence.IKZF1、ARID5B、CDKN2A和CEBPE基因变异与突尼斯儿童急性淋巴细胞白血病风险的关联及其对白血病发病率种族差异的影响。
Pediatr Hematol Oncol. 2016 Apr;33(3):157-67. doi: 10.3109/08880018.2016.1161685.
6
Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.IKZF1、ARID5B和CEBPE基因变异与生命早期感染替代指标与西班牙裔儿童急性淋巴细胞白血病风险的关联。
Cancer Causes Control. 2015 Apr;26(4):609-19. doi: 10.1007/s10552-015-0550-3. Epub 2015 Mar 12.
7
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.在不同种族人群中,10p12.31-12.2 上的新型易感性变异与儿童急性淋巴细胞白血病相关。
J Natl Cancer Inst. 2013 May 15;105(10):733-42. doi: 10.1093/jnci/djt042. Epub 2013 Mar 19.
8
Germline variants in IKZF1, ARID5B, and CEBPE as risk factors for adult-onset acute lymphoblastic leukemia: an analysis from the GMALL study group.IKZF1、ARID5B和CEBPE中的种系变异作为成人急性淋巴细胞白血病的危险因素:来自GMALL研究组的分析
Haematologica. 2014 Feb;99(2):e23-5. doi: 10.3324/haematol.2013.090720.
9
Contributions of IKZF1, DDC, CDKN2A, CEBPE, and LMO1 Gene Polymorphisms to Acute Lymphoblastic Leukemia in a Yemeni Population.IKZF1、DDC、CDKN2A、CEBPE和LMO1基因多态性对也门人群急性淋巴细胞白血病的影响
Genet Test Mol Biomarkers. 2017 Oct;21(10):592-599. doi: 10.1089/gtmb.2017.0084. Epub 2017 Aug 2.
10
Genetic variation and the risk of acute lymphoblastic leukemia.基因变异与急性淋巴细胞白血病风险
Leuk Res. 2010 Oct;34(10):1269-70. doi: 10.1016/j.leukres.2010.05.013. Epub 2010 Jun 9.

引用本文的文献

1
Overview on Aneuploidy in Childhood B-Cell Acute Lymphoblastic Leukemia.儿童 B 细胞急性淋巴细胞白血病非整倍体概述。
Int J Mol Sci. 2023 May 15;24(10):8764. doi: 10.3390/ijms24108764.
2
Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children.超二倍体:已知的最长、最普遍、最神秘的儿童急性淋巴细胞白血病形式。
Leukemia. 2022 Dec;36(12):2769-2783. doi: 10.1038/s41375-022-01720-z. Epub 2022 Oct 20.
3
An acquired phosphatidylinositol 4-phosphate transport initiates T-cell deterioration and leukemogenesis.

本文引用的文献

1
Stage-specific control of early B cell development by the transcription factor Ikaros.转录因子 Ikaros 对早期 B 细胞发育的阶段特异性控制。
Nat Immunol. 2014 Mar;15(3):283-93. doi: 10.1038/ni.2828. Epub 2014 Feb 9.
2
PTPRG inhibition by DNA methylation and cooperation with RAS gene activation in childhood acute lymphoblastic leukemia.DNA 甲基化抑制 PTPRG 与 RAS 基因激活在儿童急性淋巴细胞白血病中的合作。
Int J Cancer. 2014 Sep 1;135(5):1101-9. doi: 10.1002/ijc.28759. Epub 2014 Feb 19.
3
Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse.
一种获得性的磷脂酰肌醇 4-磷酸转运起始了 T 细胞恶化和白血病发生。
Nat Commun. 2022 Jul 29;13(1):4390. doi: 10.1038/s41467-022-32104-7.
4
Variant to function mapping at single-cell resolution through network propagation.通过网络传播实现单细胞分辨率下的变体功能映射。
Nat Biotechnol. 2022 Nov;40(11):1644-1653. doi: 10.1038/s41587-022-01341-y. Epub 2022 Jun 6.
5
Variant to function mapping at single-cell resolution through network propagation.通过网络传播实现单细胞分辨率下的变异到功能映射。
bioRxiv. 2022 Jan 24:2022.01.23.477426. doi: 10.1101/2022.01.23.477426.
6
Genome-wide trans-ethnic meta-analysis identifies novel susceptibility loci for childhood acute lymphoblastic leukemia.全基因组跨种族荟萃分析确定了儿童急性淋巴细胞白血病的新易感基因座。
Leukemia. 2022 Mar;36(3):865-868. doi: 10.1038/s41375-021-01465-1. Epub 2021 Nov 8.
7
Somatic Sex: On the Origin of Neoplasms With Chromosome Counts in Uneven Ploidy Ranges.体细胞性征:关于染色体数处于非整倍体范围的肿瘤的起源
Front Cell Dev Biol. 2021 Aug 4;9:631946. doi: 10.3389/fcell.2021.631946. eCollection 2021.
8
B-ALL Complexity: Is Targeted Therapy Still A Valuable Approach for Pediatric Patients?B淋巴细胞白血病的复杂性:靶向治疗对儿科患者来说仍然是一种有价值的方法吗?
Cancers (Basel). 2020 Nov 24;12(12):3498. doi: 10.3390/cancers12123498.
9
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children.儿童高倍体急性淋巴细胞白血病中的胚系易感性突变。
Genes Chromosomes Cancer. 2019 Oct;58(10):723-730. doi: 10.1002/gcc.22765. Epub 2019 May 27.
10
Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11.2 is mediated by a CEBPE promoter polymorphism.14q11.2 上的 B 细胞急性淋巴细胞白血病遗传易感性由 CEBPE 启动子多态性介导。
Leukemia. 2019 Jan;33(1):1-14. doi: 10.1038/s41375-018-0184-z. Epub 2018 Jul 6.
遗传 GATA3 变异与 Ph 样儿童急性淋巴细胞白血病和复发风险相关。
Nat Genet. 2013 Dec;45(12):1494-8. doi: 10.1038/ng.2803. Epub 2013 Oct 20.
4
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.10p12.2 和 10p14 上的变异影响儿童 B 细胞急性淋巴细胞白血病的风险和表型。
Blood. 2013 Nov 7;122(19):3298-307. doi: 10.1182/blood-2013-03-491316. Epub 2013 Aug 30.
5
The Genotype-Tissue Expression (GTEx) project.基因型-组织表达 (GTEx) 项目。
Nat Genet. 2013 Jun;45(6):580-5. doi: 10.1038/ng.2653.
6
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.在不同种族人群中,10p12.31-12.2 上的新型易感性变异与儿童急性淋巴细胞白血病相关。
J Natl Cancer Inst. 2013 May 15;105(10):733-42. doi: 10.1093/jnci/djt042. Epub 2013 Mar 19.
7
Annotation of functional variation in personal genomes using RegulomeDB.利用 RegulomeDB 注释个人基因组中的功能变异。
Genome Res. 2012 Sep;22(9):1790-7. doi: 10.1101/gr.137323.112.
8
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants.HaploReg:一个用于探索染色质状态、保守性以及一组遗传连锁变体中调控基序改变的资源。
Nucleic Acids Res. 2012 Jan;40(Database issue):D930-4. doi: 10.1093/nar/gkr917. Epub 2011 Nov 7.
9
Regulatory circuitries coordinated by transcription factors and microRNAs at the cornerstone of hematopoietic stem cell self-renewal and differentiation.转录因子和 microRNAs 协调调控的调控回路是造血干细胞自我更新和分化的基石。
Curr Stem Cell Res Ther. 2011 Jun;6(2):142-61. doi: 10.2174/157488811795495431.
10
Accurate inference of transcription factor binding from DNA sequence and chromatin accessibility data.从 DNA 序列和染色质可及性数据中准确推断转录因子结合。
Genome Res. 2011 Mar;21(3):447-55. doi: 10.1101/gr.112623.110. Epub 2010 Nov 24.