• 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

实体瘤细胞遗传学:当前观点

Solid tumor cytogenetics: current perspectives.

作者信息

Nanjangud Gouri, Amarillo Ina, Rao P Nagesh

机构信息

Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, 2-226 Rehab Center, 1000 Veteran Avenue, Los Angeles, CA 90024, USA.

出版信息

Clin Lab Med. 2011 Dec;31(4):785-811, xi. doi: 10.1016/j.cll.2011.07.007. Epub 2011 Oct 21.

DOI:10.1016/j.cll.2011.07.007
PMID:22118748
Abstract

Conventional cytogenetics in conjunction with Fluorescence in Situ Hybridization (FISH) continues to remain an important and integral component in the diagnosis and management of solid tumors. The ability to effectively detect the vast majority of clinically relevant chromosomal aberrations with a rapid-to-acceptable turnaround time makes them the most cost-effective screening/detection tool currently available in modern pathology. In this review, we describe a representative set of solid tumors in which chromosomal analysis and/or FISH plays a significant role in the routine clinical management of solid tumors.

摘要

传统细胞遗传学与荧光原位杂交(FISH)相结合,仍然是实体瘤诊断和管理中的重要组成部分。能够在快速到可接受的周转时间内有效检测绝大多数临床相关染色体畸变,使其成为现代病理学中目前最具成本效益的筛查/检测工具。在本综述中,我们描述了一组具有代表性的实体瘤,其中染色体分析和/或FISH在实体瘤的常规临床管理中发挥着重要作用。

相似文献

1
Solid tumor cytogenetics: current perspectives.实体瘤细胞遗传学:当前观点
Clin Lab Med. 2011 Dec;31(4):785-811, xi. doi: 10.1016/j.cll.2011.07.007. Epub 2011 Oct 21.
2
Efficacy of current molecular cytogenetic protocols for the diagnosis of chromosome aberrations in tumor specimens.当前分子细胞遗传学方案在肿瘤标本染色体畸变诊断中的效能
Cytokines Mol Ther. 1996 Sep;2(3):163-9.
3
Toward the validation of aneusomy detection by fluorescence in situ hybridization in bladder cancer: comparative analysis with cytology, cytogenetics, and clinical features predicts recurrence and defines clinical testing limitations.膀胱癌荧光原位杂交检测非整倍体的验证:与细胞学、细胞遗传学及临床特征的比较分析可预测复发并界定临床检测局限性
Clin Cancer Res. 1997 Dec;3(12 Pt 1):2317-28.
4
Fluorescent in situ hybridization as an adjunct to conventional cytogenetics.荧光原位杂交作为传统细胞遗传学的辅助手段。
Ann Clin Lab Sci. 1994 Mar-Apr;24(2):153-63.
5
Fluorescent in-situ hybridization--some of its applications in clinical cytogenetics.荧光原位杂交——其在临床细胞遗传学中的一些应用
Singapore Med J. 1997 Nov;38(11):497-503.
6
Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).使用荧光原位杂交技术(FISH)检测染色体异常。
Natl Med J India. 1998 Nov-Dec;11(6):259-63.
7
Cytogenetics, in situ hybridization and molecular approaches in the diagnosis of cancer.细胞遗传学、原位杂交及分子方法在癌症诊断中的应用
Ann Clin Lab Sci. 1998 Nov-Dec;28(6):324-30.
8
[Chromosomal in situ hybridization and interphase cytogenetics in single cell and tissue section preparations: new methods in tumor diagnosis and clinical cytogenetics].[单细胞及组织切片标本中的染色体原位杂交与间期细胞遗传学:肿瘤诊断及临床细胞遗传学新方法]
Verh Dtsch Ges Pathol. 1994;78:111-23.
9
Fluorescence in situ hybridization (FISH) in cytogenetics of leukemia.白血病细胞遗传学中的荧光原位杂交(FISH)技术。
Folia Biol (Praha). 1996;42(6):311-4.
10
[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].[荧光原位杂交(FISH)诊断非整倍体;在染色体畸变风险增加的妊娠中的价值]
Z Geburtshilfe Neonatol. 2000 Jan-Feb;204(1):1-7. doi: 10.1055/s-2000-10188.

引用本文的文献

1
Analysis of chromosome translocation frequency after a single CT scan in adults.成人单次CT扫描后染色体易位频率分析。
J Radiat Res. 2016 Jun;57(3):220-6. doi: 10.1093/jrr/rrv090. Epub 2016 Feb 13.
2
Increase in dicentric chromosome formation after a single CT scan in adults.成人单次CT扫描后双着丝粒染色体形成增加。
Sci Rep. 2015 Sep 9;5:13882. doi: 10.1038/srep13882.