• 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

荧光聚合酶链反应:第一部分。一种实现单细胞基因诊断和DNA指纹识别的新方法。

Fluorescent polymerase chain reaction: Part I. A new method allowing genetic diagnosis and DNA fingerprinting of single cells.

作者信息

Findlay I, Quirke P

机构信息

Centre for Reproduction, Growth and Development, University of Leeds, Leeds General Infirmary, UK.

出版信息

Hum Reprod Update. 1996 Mar-Apr;2(2):137-52. doi: 10.1093/humupd/2.2.137.

DOI:10.1093/humupd/2.2.137
PMID:9079409
Abstract

The analysis of genetic material is fundamental to many medical and scientific applications. One method that has been used extensively for detection or diagnosis of genetic material, especially for single-gene defects or sex, is the polymerase chain reaction (PCR). It is particularly useful when the amount of genetic material is very limited, or samples have been degraded or fixed. In recent years, sensitivity has increased so that even single copies of genes within a single cell can be detected. This article discusses some of the difficulties involved with single-cell PCR and introduces single-cell fluorescent PCR and its potential applications. The use of fluorescent PCR to reduce misdiagnosis is discussed in detail.

摘要

遗传物质分析是许多医学和科学应用的基础。一种被广泛用于检测或诊断遗传物质,尤其是单基因缺陷或性别的方法是聚合酶链反应(PCR)。当遗传物质的量非常有限,或者样本已经降解或固定时,它特别有用。近年来,灵敏度有所提高,以至于单个细胞内的单拷贝基因都能被检测到。本文讨论了单细胞PCR所涉及的一些困难,并介绍了单细胞荧光PCR及其潜在应用。详细讨论了使用荧光PCR减少误诊的问题。

相似文献

1
Fluorescent polymerase chain reaction: Part I. A new method allowing genetic diagnosis and DNA fingerprinting of single cells.荧光聚合酶链反应:第一部分。一种实现单细胞基因诊断和DNA指纹识别的新方法。
Hum Reprod Update. 1996 Mar-Apr;2(2):137-52. doi: 10.1093/humupd/2.2.137.
2
Using MF-PCR to diagnose multiple defects from single cells: implications for PGD.使用多重荧光定量聚合酶链反应(MF-PCR)诊断单细胞中的多种缺陷:对植入前基因诊断(PGD)的意义。
Mol Cell Endocrinol. 2001 Oct 22;183 Suppl 1:S5-12. doi: 10.1016/s0303-7207(01)00567-6.
3
Simultaneous DNA 'fingerprinting', diagnosis of sex and single-gene defect status from single cells.
Hum Reprod. 1995 Apr;10(4):1005-13.
4
Fluorescent PCR: a new technique for PGD of sex and single-gene defects.荧光聚合酶链反应:一种用于性连锁疾病和单基因缺陷植入前基因诊断的新技术。
J Assist Reprod Genet. 1996 Feb;13(2):96-103. doi: 10.1007/BF02072528.
5
Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells.
Ann Hum Genet. 1998 Jan;62(Pt 1):9-23. doi: 10.1046/j.1469-1809.1998.6210009.x.
6
Rapid genetic diagnosis at 7-9 weeks gestation: diagnosis of sex, single gene defects and DNA fingerprint from coelomic samples.孕7 - 9周时的快速基因诊断:从体腔样本中诊断性别、单基因缺陷和DNA指纹。
Hum Reprod. 1996 Nov;11(11):2548-53. doi: 10.1093/oxfordjournals.humrep.a019158.
7
Diagnosis of sex and cystic fibrosis status in fetal erythroblasts isolated from cord blood.
Prenat Diagn. 1999 Feb;19(2):172-4.
8
Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508).用于囊性纤维化(ΔF508)植入前诊断的最佳聚合酶链反应扩增
BMJ. 1995 Aug 26;311(7004):536-40. doi: 10.1136/bmj.311.7004.536.
9
[The polymerase chain reaction PCR and its use in genetic diagnosis].
Kinderarztl Prax. 1991 May;59(5):135-8.
10
Allelic drop-out and preferential amplification in single cells and human blastomeres: implications for preimplantation diagnosis of sex and cystic fibrosis.单细胞和人类卵裂球中的等位基因脱扣与优先扩增:对性别和囊性纤维化植入前诊断的影响。
Hum Reprod. 1995 Jun;10(6):1609-18. doi: 10.1093/humrep/10.6.1609.

引用本文的文献

1
Characteristics of X- and Y-chromosome specific regions of the amelogenin gene and a PCR-based method for sex identification in red deer (Cervus elaphus).X 和 Y 染色体特异性区域的牙本质基质蛋白基因特征及基于 PCR 的赤鹿( Cervus elaphus )性别鉴定方法。
Mol Biol Rep. 2010 Jul;37(6):2915-8. doi: 10.1007/s11033-009-9852-4. Epub 2009 Oct 7.
2
A highly polymorphic insertion in the Y-chromosome amelogenin gene can be used for evolutionary biology, population genetics and sexing in Cetacea and Artiodactyla.Y染色体牙釉蛋白基因中的一个高度多态性插入可用于鲸目和偶蹄目动物的进化生物学、群体遗传学及性别鉴定。
BMC Genet. 2008 Oct 16;9:64. doi: 10.1186/1471-2156-9-64.
3
Preimplantation genetic diagnosis using fluorescent polymerase chain reaction: results and future developments.
使用荧光聚合酶链反应的植入前基因诊断:结果与未来发展
J Assist Reprod Genet. 1999 Apr;16(4):199-206. doi: 10.1023/a:1020364807226.
4
Accuracy of preimplantation diagnosis of single-gene disorders by polar body analysis of oocytes.通过卵母细胞极体分析对单基因疾病进行植入前诊断的准确性。
J Assist Reprod Genet. 1999 Apr;16(4):192-8. doi: 10.1023/a:1020312823155.
5
Same day diagnosis of Down's syndrome and sex in single cells using multiplex fluorescent PCR.使用多重荧光聚合酶链反应在单细胞中同日诊断唐氏综合征和性别。
Mol Pathol. 1998 Jun;51(3):164-7. doi: 10.1136/mp.51.3.164.
6
Comparison of FISH PRINS, and conventional and fluorescent PCR for single-cell sexing: suitability for preimplantation genetic diagnosis.用于单细胞性别鉴定的荧光原位杂交、引物原位标记以及传统和荧光聚合酶链反应的比较:对植入前基因诊断的适用性
J Assist Reprod Genet. 1998 May;15(5):258-65. doi: 10.1023/a:1022584225311.
7
Allele dropout in polar bodies and blastomeres.极体和卵裂球中的等位基因脱扣。
J Assist Reprod Genet. 1998 May;15(5):253-7. doi: 10.1023/a:1022532108472.
8
Prenatal detection of trisomy 21 and 18 from amniotic fluid by quantitative fluorescent polymerase chain reaction.通过定量荧光聚合酶链反应对羊水进行产前检测21三体和18三体。
J Med Genet. 1998 Feb;35(2):126-9. doi: 10.1136/jmg.35.2.126.