• 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

A crude lysate of cells immobilized on solid support can serve as a matrix for enzymatic DNA amplification.

作者信息

Skryabin B V, Khalchitsky S E, Kuzjmin A I, Kaboev O K, Kalinin V N, Schwartz E I

机构信息

Riga Medical Institute, Ministry of Health, USSR.

出版信息

Nucleic Acids Res. 1990 Jul 25;18(14):4289. doi: 10.1093/nar/18.14.4289.

DOI:10.1093/nar/18.14.4289
PMID:2377487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC331227/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae4d/331227/06bc15213a9d/nar00198-0240-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae4d/331227/06bc15213a9d/nar00198-0240-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae4d/331227/06bc15213a9d/nar00198-0240-a.jpg

相似文献

1
A crude lysate of cells immobilized on solid support can serve as a matrix for enzymatic DNA amplification.固定在固体支持物上的细胞粗裂解物可作为酶促DNA扩增的基质。
Nucleic Acids Res. 1990 Jul 25;18(14):4289. doi: 10.1093/nar/18.14.4289.
2
Identification of exonic deletions in the PAH gene causing phenylketonuria by MLPA analysis.通过多重连接依赖探针扩增(MLPA)分析鉴定导致苯丙酮尿症的PAH基因外显子缺失。
Clin Chim Acta. 2006 Nov;373(1-2):164-7. doi: 10.1016/j.cca.2006.05.003. Epub 2006 May 12.
3
A novel mutation in exon 8 of the phenylalanine hydroxylase gene in the Polish population.
Hum Mutat. 1993;2(1):74-6. doi: 10.1002/humu.1380020114.
4
Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuria.
Hum Mutat. 1992;1(2):154-8. doi: 10.1002/humu.1380010211.
5
[Identification of a nature of mutation in the 12th exon of phenylalanine hydroxylase gene in patients with phenylketonuria].
Bioorg Khim. 1989 Dec;15(12):1690-2.
6
Distribution of some point mutations in the phenylalanine hydroxylase gene of phenylketonuria patients from the Moscow region.莫斯科地区苯丙酮尿症患者苯丙氨酸羟化酶基因中某些点突变的分布情况。
Hum Hered. 1993 Jul-Aug;43(4):244-9. doi: 10.1159/000154138.
7
[Mutation analysis of phenylalanine hydroxylase gene in patients w ith phenylketonuria in Henan province].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):142-6. doi: 10.3760/cma.j.issn.1003-9406.2011.02.005.
8
A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family.
Hum Mutat. 1992;1(4):344-6. doi: 10.1002/humu.1380010414.
9
Structure of the phenylalanine hydroxylase gene in Drosophila melanogaster and evidence of alternative promoter usage.
Biochem Biophys Res Commun. 1996 Aug 5;225(1):238-42. doi: 10.1006/bbrc.1996.1160.
10
Screening for base mutations in the PAH and HPRT loci using the polymerase chain reaction (PCR) in combination with denaturing gradient gel electrophoresis (DGGE).使用聚合酶链反应(PCR)结合变性梯度凝胶电泳(DGGE)对PAH和HPRT基因座中的碱基突变进行筛查。
Prog Clin Biol Res. 1990;340A:389-98.

引用本文的文献

1
Molecular diagnosis of some common genetic diseases in Russia and the former USSR: present and future.俄罗斯及前苏联一些常见遗传病的分子诊断:现状与未来
J Med Genet. 1993 Feb;30(2):141-6. doi: 10.1136/jmg.30.2.141.

本文引用的文献

1
Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction.通过聚合酶链反应进行DNA扩增来筛查苯丙酮尿症突变。
Lancet. 1988 Mar 5;1(8584):497-9. doi: 10.1016/s0140-6736(88)91295-0.
2
The polymerase chain reaction: an improved method for the analysis of nucleic acids.聚合酶链反应:一种用于核酸分析的改进方法。
Hum Genet. 1989 Aug;83(1):1-15. doi: 10.1007/BF00274139.