• 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

结构异常Y染色体的聚合酶链反应检测

PCR detection of structurally abnormal Y chromosomes.

作者信息

Nagafuchi S, Seki S, Nakahori Y, Tamura T, Numabe H, Nakagome Y

机构信息

Department of Congenital Abnormalities Research, National Children's Medical Research Center, Tokyo, Japan.

出版信息

Jpn J Hum Genet. 1992 Sep;37(3):187-93. doi: 10.1007/BF01900712.

DOI:10.1007/BF01900712
PMID:1472700
Abstract

Three probes each detecting a locus on the proximal long arm of the Y chromosome were partially sequenced. Thus, 3 sets of novel primers were developed which enable PCR detection of these 3 loci. Five previously reported primer sets, 3 on the short arm and each one on the centromere and the distal long arm, were mapped along with the novel three using a mapping panel consisted of 8 patients each with different structural abnormality of the Y chromosome. Now, PCR detection of these 8 loci covering an entire length of the Y chromosome has become possible enabling rapid screening of patients with Y chromosome aberrations.

摘要

对三个分别检测Y染色体近端长臂上一个位点的探针进行了部分测序。因此,开发了3组新型引物,可用于对这3个位点进行PCR检测。使用由8名Y染色体结构异常各异的患者组成的定位板,将5组先前报道的引物(3组位于短臂,每组分别位于着丝粒和远端长臂)与新的3组引物一起进行了定位。现在,已能够对覆盖Y染色体全长的这8个位点进行PCR检测,从而能够快速筛查Y染色体畸变患者。

相似文献

1
PCR detection of structurally abnormal Y chromosomes.结构异常Y染色体的聚合酶链反应检测
Jpn J Hum Genet. 1992 Sep;37(3):187-93. doi: 10.1007/BF01900712.
2
[Screening for Y chromosome sequences in patients with Turner syndrome].[特纳综合征患者Y染色体序列筛查]
Acta Med Port. 2002 Mar-Apr;15(2):89-100.
3
Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
Prenat Diagn. 2001 Jun;21(6):484-7. doi: 10.1002/pd.79.
4
Normal and abnormal interchanges between the human X and Y chromosomes.人类X和Y染色体之间的正常与异常互换。
Development. 1987;101 Suppl:67-74.
5
[The Y chromosome and sex determination].[Y染色体与性别决定]
Reprod Nutr Dev. 1990;Suppl 1:27s-38s.
6
The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes.
Hum Genet. 1992 Aug;89(6):590-2. doi: 10.1007/BF00221943.
7
A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.一种解释具有非荧光Y染色体的45,X/46,XY嵌合体异常现象的理论。三例病例报告。
Ann Genet. 1978 Mar;21(1):5-11.
8
Giemsa-11 technique elucidating three structurally altered nonfluorescent Y chromosomes: r (Y), idic (Yp), dir tan dup (Yp).
Ann Genet. 1988;31(4):235-40.
9
Mapping of testis-determining locus on Yp by the molecular genetic analysis of XX males and XY females.通过对XX男性和XY女性的分子遗传学分析定位Y染色体短臂上的睾丸决定位点。
Development. 1987;101 Suppl:51-8.
10
Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.二核苷酸重复位点为人类2号染色体连锁图谱提供了信息丰富的遗传标记。
Genomics. 1993 Jun;16(3):612-8. doi: 10.1006/geno.1993.1238.

引用本文的文献

1
Reprogramming human cancer cells in the mouse mammary gland.在小鼠乳腺中重编程人类癌细胞。
Cancer Res. 2010 Aug 1;70(15):6336-43. doi: 10.1158/0008-5472.CAN-10-0591. Epub 2010 Jul 20.
2
Sex identification by polymerase chain reaction using a Y-autosome homologous primer set.
Jpn J Hum Genet. 1993 Dec;38(4):429-31. doi: 10.1007/BF01907990.
3
The majority of the marker chromosomes in Japanese patients with stigmata of Turner syndrome are derived from Y chromosomes.
Hum Genet. 1992 Aug;89(6):590-2. doi: 10.1007/BF00221943.