• 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

What's germane in the germline? Finding clinically relevant germline variants in myeloid neoplasms from tumor only screening.

作者信息

Brown Anna L, Hiwase Devendra K

机构信息

Department of Genetics and Molecular Pathology, SA Pathology, Adelaide, South Australia, Australia; Centre for Cancer Biology, SA Pathology & University of South Australia, Adelaide, South Australia, Australia; School of Medicine, University of Adelaide, Adelaide, South Australia, Australia.

School of Medicine, University of Adelaide, Adelaide, South Australia, Australia; Department of Haematology, Royal Adelaide Hospital, Central Adelaide Local Health Network, Adelaide, Australia; Cancer Theme, South Australian Health and Medical Research Institute, Adelaide, Australia.

出版信息

Leuk Res. 2020 Sep;96:106431. doi: 10.1016/j.leukres.2020.106431. Epub 2020 Jul 31.

DOI:10.1016/j.leukres.2020.106431
PMID:32771235
Abstract
摘要

相似文献

1
What's germane in the germline? Finding clinically relevant germline variants in myeloid neoplasms from tumor only screening.生殖系中什么是相关的？仅通过肿瘤筛查在髓系肿瘤中寻找临床相关的生殖系变异。
Leuk Res. 2020 Sep;96:106431. doi: 10.1016/j.leukres.2020.106431. Epub 2020 Jul 31.
2
Strategy for identification of a potential inherited leukemia predisposition in a 299 patient's cohort with tumor-only sequencing data.仅对肿瘤进行测序的 299 例患者队列中潜在遗传性白血病易感性的鉴定策略。
Leuk Res. 2020 Aug;95:106386. doi: 10.1016/j.leukres.2020.106386. Epub 2020 May 24.
3
An analysis of the variant in a cohort of individuals with myeloid neoplasms; suggests it is a benign germline variant.
Leuk Lymphoma. 2021 May;62(5):1255-1258. doi: 10.1080/10428194.2020.1861272. Epub 2020 Dec 21.
4
Identifying patients with genetic predisposition to acute myeloid leukemia.识别急性髓系白血病的遗传易感性患者。
Best Pract Res Clin Haematol. 2018 Dec;31(4):373-378. doi: 10.1016/j.beha.2018.09.014. Epub 2018 Sep 25.
5
Investigation of clinically relevant germline variants detected by next-generation sequencing in patients with childhood cancer: a review of the literature.通过下一代测序检测到的儿童癌症患者中具有临床意义的种系变异的研究：文献综述。
J Med Genet. 2018 Dec;55(12):785-793. doi: 10.1136/jmedgenet-2018-105488. Epub 2018 Oct 4.
6
Clinical and immunophenotypic characteristics of familial leukemia predisposition caused by PAX5 germline variants.PAX5种系变异导致的家族性白血病易感性的临床和免疫表型特征
Leukemia. 2022 Sep;36(9):2338-2342. doi: 10.1038/s41375-022-01661-7. Epub 2022 Jul 28.
7
Myeloid neoplasms with germline DDX41 mutation.伴有种系DDX41突变的髓系肿瘤
Int J Hematol. 2017 Aug;106(2):163-174. doi: 10.1007/s12185-017-2260-y. Epub 2017 May 25.
8
[Genetic predisposition to pediatric myeloid malignancies].[儿童髓系恶性肿瘤的遗传易感性]
Rinsho Ketsueki. 2016 Jun;57(6):730-5. doi: 10.11406/rinketsu.57.730.
9
Germline ETV6 mutations and predisposition to hematological malignancies.胚系ETV6突变与血液系统恶性肿瘤易感性
Int J Hematol. 2017 Aug;106(2):189-195. doi: 10.1007/s12185-017-2259-4. Epub 2017 May 29.
10
Myeloid Neoplasms with Germline Predisposition: A New Provisional Entity Within the World Health Organization Classification.具有种系易感性的髓系肿瘤：世界卫生组织分类中的一个新暂定实体。
Surg Pathol Clin. 2016 Mar;9(1):165-76. doi: 10.1016/j.path.2015.09.010.

引用本文的文献

1
Inherited Predispositions to Myeloid Neoplasms: Pathogenesis and Clinical Implications.髓系肿瘤的遗传易感性：发病机制与临床意义
Annu Rev Pathol. 2025 Jan;20(1):87-114. doi: 10.1146/annurev-pathmechdis-111523-023420. Epub 2025 Jan 2.
2
Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26.与 RUNX1、ETV6 和 ANKRD26 种系变异相关的遗传性血小板疾病。
Blood. 2023 Mar 30;141(13):1533-1543. doi: 10.1182/blood.2022017735.