• 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

On the mechanism of NPM1 mutations in acute myeloid leukemia.

作者信息

Lieber Michael R, Hsieh Chih-Lin

机构信息

USC Norris Comprehensive Cancer Center and Departments of Pathology, Molecular Microbiology & Immunology, Cancer Biology, and Section of Molecular & Computational Biology (Department of Biological Sciences), Los Angeles, CA, USA.

USC Norris Comprehensive Cancer Center and Department of Urology, University of Southern California, Los Angeles, CA, USA.

出版信息

Leukemia. 2025 Jul 28. doi: 10.1038/s41375-025-02722-3.

DOI:10.1038/s41375-025-02722-3
PMID:40721647
Abstract
摘要

相似文献

1
On the mechanism of NPM1 mutations in acute myeloid leukemia.急性髓系白血病中NPM1突变的机制
Leukemia. 2025 Jul 28. doi: 10.1038/s41375-025-02722-3.
2
Clinical Characteristics and Outcomes of Acute Myeloid Leukemia Patients Harboring Triple Mutations and the Potential Prognostic Value of .携带三重突变的急性髓系白血病患者的临床特征与预后及……的潜在预后价值
Cancer Control. 2025 Jan-Dec;32:10732748251359836. doi: 10.1177/10732748251359836. Epub 2025 Jul 17.
3
NRF2 maintains redox balance via ME1 and NRF2 inhibitor synergizes with venetoclax in NPM1-mutated acute myeloid leukemia.NRF2通过ME1维持氧化还原平衡,且NRF2抑制剂与维奈托克在NPM1突变的急性髓系白血病中具有协同作用。
Cancer Metab. 2025 Jun 18;13(1):32. doi: 10.1186/s40170-025-00401-6.
4
Impact of secondary-type mutations on the prognosis of AML patients with NPM1 mutation: a systematic review and meta-analysis.继发性类型突变对伴有NPM1突变的急性髓系白血病患者预后的影响:一项系统评价和荟萃分析
Ann Hematol. 2025 May 28. doi: 10.1007/s00277-025-06431-w.
5
-Mutated AML: Deciphering the Molecular and Clinical Puzzle in the Era of Novel Treatment Strategies.- 突变型急性髓系白血病:在新型治疗策略时代破解分子与临床谜题
Cancers (Basel). 2025 Jun 23;17(13):2095. doi: 10.3390/cancers17132095.
6
Molecular, Clinical Features, and Prognostic Implications of PTPN11 Mutation in Adult Patients with Acute Myeloid Leukemia in China.中国成年急性髓系白血病患者中PTPN11突变的分子特征、临床特点及预后意义
Clin Lab. 2025 Jul 1;71(7). doi: 10.7754/Clin.Lab.2025.241242.
7
Prognostic significance of FLT3 internal tandem duplication, nucleophosmin 1, and CEBPA gene mutations for acute myeloid leukemia patients with normal karyotype and younger than 60 years: a systematic review and meta-analysis.核磷酸蛋白 1、CEBPA 基因突变和 FLT3 内部串联重复对核型正常且年龄小于 60 岁的急性髓系白血病患者的预后意义:系统评价和荟萃分析。
Ann Hematol. 2014 Aug;93(8):1279-86. doi: 10.1007/s00277-014-2072-6. Epub 2014 May 7.
8
[Gene Mutation Characteristics, Prognosis and Survival Analysis of Patients with Acute Myeloid Leukemia].急性髓系白血病患者的基因突变特征、预后及生存分析
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2025 Jun;33(3):691-697. doi: 10.19746/j.cnki.issn.1009-2137.2025.03.010.
9
Protective effects for HLA-B*40:01 and C*03:04 in NPM1-mutated AML: result of a large HLA association study.HLA-B*40:01和C*03:04对NPM1突变型急性髓系白血病的保护作用:一项大型HLA关联研究的结果
Front Immunol. 2025 Jun 10;16:1571508. doi: 10.3389/fimmu.2025.1571508. eCollection 2025.
10
Real-World Outcomes in -ITD Mutated Acute Myeloid Leukemia: Impact of NPM1 Mutations and Allogeneic Transplantation in a Retrospective Unicentric Cohort.伴有内部串联重复(ITD)突变的急性髓系白血病的真实世界结局:回顾性单中心队列中核磷蛋白(NPM1)突变和异基因移植的影响
J Clin Med. 2025 Jul 18;14(14):5110. doi: 10.3390/jcm14145110.

本文引用的文献

1
Molecular mechanism for regulating APOBEC3G DNA editing function by the non-catalytic domain.非催化结构域调控 APOBEC3G DNA 编辑功能的分子机制
Nat Commun. 2024 Oct 10;15(1):8773. doi: 10.1038/s41467-024-52671-1.
2
The RNA tether model for human chromosomal translocation fragile zones.人类染色体易位脆性区的 RNA 系绳模型。
Trends Biochem Sci. 2024 May;49(5):391-400. doi: 10.1016/j.tibs.2024.02.003. Epub 2024 Mar 14.
3
The Identification of APOBEC3G as a Potential Prognostic Biomarker in Acute Myeloid Leukemia and a Possible Drug Target for Crotonoside.
APOBEC3G 作为急性髓系白血病潜在预后生物标志物的鉴定及巴豆苷的可能药物靶点
Molecules. 2022 Sep 7;27(18):5804. doi: 10.3390/molecules27185804.
4
International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data.国际髓系肿瘤和急性白血病分类:整合形态学、临床和基因组数据。
Blood. 2022 Sep 15;140(11):1200-1228. doi: 10.1182/blood.2022015850.
5
The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms.《世界卫生组织造血与淋巴组织肿瘤分类》第五版:淋巴肿瘤。
Leukemia. 2022 Jul;36(7):1720-1748. doi: 10.1038/s41375-022-01620-2. Epub 2022 Jun 22.
6
The mRNA tether model for activation-induced deaminase and its relevance for Ig somatic hypermutation and class switch recombination.激活诱导脱氨酶的mRNA系留模型及其与Ig体细胞高频突变和类别转换重组的相关性。
DNA Repair (Amst). 2022 Feb;110:103271. doi: 10.1016/j.dnarep.2021.103271. Epub 2021 Dec 30.
7
The mechanisms of human lymphoid chromosomal translocations and their medical relevance.人类淋巴染色体易位的机制及其医学相关性。
Crit Rev Biochem Mol Biol. 2022 Jun;57(3):227-243. doi: 10.1080/10409238.2021.2004576. Epub 2021 Dec 7.
8
Deamination hotspots among APOBEC3 family members are defined by both target site sequence context and ssDNA secondary structure.APOBEC3 家族成员中的脱氨酶热点由靶序列上下文和单链 DNA 二级结构共同定义。
Nucleic Acids Res. 2020 Feb 20;48(3):1353-1371. doi: 10.1093/nar/gkz1164.
9
The curious incident of TdT-mediated mutations in AML.急性髓系白血病中末端脱氧核苷酸转移酶介导的突变这一奇特事件。
Blood. 2019 Dec 19;134(25):2229-2231. doi: 10.1182/blood.2019003619.
10
Terminal deoxynucleotidyl transferase promotes acute myeloid leukemia by priming FLT3-ITD replication slippage.端粒酶通过引发 FLT3-ITD 复制滑动促进急性髓细胞白血病。
Blood. 2019 Dec 19;134(25):2281-2290. doi: 10.1182/blood.2019001238.