• 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

Conventional cytogenetics for myeloid neoplasms in the era of next-generation-sequencing.

作者信息

Kuo Frank C, Steensma David P, Dal Cin Paola

机构信息

Brigham and Women's Hospital, Boston, Massachusetts, USA.

Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Am J Hematol. 2017 Mar;92(3):227-229. doi: 10.1002/ajh.24642.

DOI:10.1002/ajh.24642
PMID:28054397
Abstract
摘要

相似文献

1
Conventional cytogenetics for myeloid neoplasms in the era of next-generation-sequencing.下一代测序时代髓系肿瘤的传统细胞遗传学
Am J Hematol. 2017 Mar;92(3):227-229. doi: 10.1002/ajh.24642.
2
Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms.靶向下一代测序可作为骨髓增生性肿瘤中常规检测的替代方法。
PLoS One. 2019 Mar 6;14(3):e0212228. doi: 10.1371/journal.pone.0212228. eCollection 2019.
3
Addition of chromosomal microarray and next generation sequencing to FISH and classical cytogenetics enhances genomic profiling of myeloid malignancies.将染色体微阵列和下一代测序技术添加到荧光原位杂交（FISH）和经典细胞遗传学中，可增强髓系恶性肿瘤的基因组分析。
Cancer Genet. 2017 Oct;216-217:128-141. doi: 10.1016/j.cancergen.2017.07.010. Epub 2017 Aug 14.
4
Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification.巴西正常核型急性髓系白血病患者的突变谱分析：二代测序在基因组分类中的价值
J Investig Med. 2017 Dec;65(8):1155-1158. doi: 10.1136/jim-2017-000566. Epub 2017 Sep 18.
5
The Value of Next-Generation Sequencing in the Screening and Evaluation of Hematologic Neoplasms in Clinical Practice.在临床实践中，下一代测序在血液系统肿瘤的筛查和评估中的价值。
Am J Clin Pathol. 2020 Apr 15;153(5):639-645. doi: 10.1093/ajcp/aqz203.
6
Next-generation sequencing-based panel testing for myeloid neoplasms.基于二代测序的髓系肿瘤基因检测 panel 检测
Curr Hematol Malig Rep. 2015 Jun;10(2):104-11. doi: 10.1007/s11899-015-0256-3.
7
Close correlation of copy number aberrations detected by next-generation sequencing with results from routine cytogenetics in acute myeloid leukemia.下一代测序检测到的急性髓系白血病拷贝数畸变与常规细胞遗传学结果的密切相关性。
Genes Chromosomes Cancer. 2016 Jul;55(7):553-67. doi: 10.1002/gcc.22359. Epub 2016 May 2.
8
Detecting the "undetectable" alterations: Use of NGS to uncover high-risk alterations.检测“难以检测”的改变：使用 NGS 揭示高危改变。
Cancer Genet. 2022 Jun;264-265:5-7. doi: 10.1016/j.cancergen.2022.02.005. Epub 2022 Feb 22.
9
Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.急性髓系白血病中因1号、8号和12号染色体重排导致的ETV6-LYN融合的新一代测序及分子细胞遗传学特征分析
Cancer Genet. 2017 Dec;218-219:15-19. doi: 10.1016/j.cancergen.2017.09.001. Epub 2017 Sep 13.
10
Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia.骨髓增生异常综合征和慢性粒单核细胞白血病中的靶向新一代测序有助于疑难病例的诊断并鉴定转化型急性髓系白血病中常见的剪接体突变。
Am J Clin Pathol. 2016 Apr;145(4):497-506. doi: 10.1093/ajcp/aqw016. Epub 2016 Apr 22.

引用本文的文献

1
The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies.靶向新一代测序在细胞遗传学正常的髓系恶性肿瘤中的应用重要性
Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021013. doi: 10.4084/MJHID.2021.013. eCollection 2021.
2
Techniques for detecting chromosomal aberrations in myelodysplastic syndromes.检测骨髓增生异常综合征中染色体畸变的技术。
Oncotarget. 2017 May 9;8(37):62716-62729. doi: 10.18632/oncotarget.17698. eCollection 2017 Sep 22.