• 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

[应用毛细管技术建立无精子因子(AZF)微缺失筛查方法及临床试验]

[Establishment of a screening method for AZF microdeletions by capillary technology and a clinical trial].

作者信息

He Tianwen, Zhao Hui, Zhao Xin, Lu Jian, Zheng Yichun, Zhang Changbin, Yin Aihua

机构信息

Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Reproductive Center, Guangdong Women and Children' Hospital, Guangzhou, Guangdong 511442, China. Email:

出版信息

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):550-4. doi: 10.3760/cma.j.issn.1003-9406.2016.04.028.

DOI:10.3760/cma.j.issn.1003-9406.2016.04.028
PMID:27455019
Abstract

OBJECTIVE

To establish an accurate, fast and simple screening method for AZF microdeletions using capillary technology and use it for clinical testing.

METHODS

For each pair of primers, the 5' end of either forward or reverse primer was labeled with a FAM, JOE or TAMRA fluorescence dyes to establish multiplex quantitative fluorescence PCR systems for the establishment of a screening method of Y chromosome AZF microdeletions by capillary technology. The detection of Y chromosome AZF microdeletion was carried out on 725 cases of non-obstructive azoospermia, oligospermia or asthenospermia.

RESULTS

A screening method for Y chromosome AZF microdeletions using capillary technology was established. Thirty eight cases of AZF microdeletions were found among 725 cases of non-obstructive azoospermia, oligospermia or asthenospermia, which gave a deletion rate of 5.24%. Y chromosomal microdeletions were found in 8.62% of the azoospermia group, 6.75% of the oligozoospermic group, and 2.23% of the asthenospermia group.

CONCLUSION

An accurate, fast and simple screening method of Y chromosome AZF microdeletions by capillary technology has been established, which may have an important clinical value.

摘要

目的

建立一种利用毛细管技术准确、快速且简便的AZF微缺失筛查方法,并将其应用于临床检测。

方法

对每对引物,正向或反向引物的5′端用FAM、JOE或TAMRA荧光染料标记,建立多重定量荧光PCR系统,以确立用毛细管技术筛查Y染色体AZF微缺失的方法。对725例非梗阻性无精子症、少精子症或弱精子症患者进行Y染色体AZF微缺失检测。

结果

建立了利用毛细管技术筛查Y染色体AZF微缺失的方法。在725例非梗阻性无精子症、少精子症或弱精子症患者中发现38例AZF微缺失,缺失率为5.24%。无精子症组Y染色体微缺失率为8.62%,少精子症组为6.75%,弱精子症组为2.23%。

结论

已建立利用毛细管技术准确、快速且简便的Y染色体AZF微缺失筛查方法,可能具有重要临床价值。

相似文献

1
[Establishment of a screening method for AZF microdeletions by capillary technology and a clinical trial].[应用毛细管技术建立无精子因子(AZF)微缺失筛查方法及临床试验]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):550-4. doi: 10.3760/cma.j.issn.1003-9406.2016.04.028.
2
[Multiplex ligation-dependent probe amplification for detecting AZF microdeletions on the Y chromosome in infertile men with azoospermia or severe oligozoospermia].[多重连接依赖探针扩增技术检测无精子症或严重少精子症不育男性Y染色体上的AZF微缺失]
Zhonghua Nan Ke Xue. 2012 Feb;18(2):115-21.
3
Human Y chromosome microdeletion analysis by PCR multiplex protocols identifying only clinically relevant AZF microdeletions.采用仅鉴定临床相关的无精子因子(AZF)微缺失的聚合酶链反应多重方案进行人类Y染色体微缺失分析。
Methods Mol Biol. 2013;927:187-204. doi: 10.1007/978-1-62703-038-0_17.
4
First study of microdeletions in the Y chromosome of Algerian infertile men with idiopathic oligo- or azoospermia.对患有特发性少精子症或无精子症的阿尔及利亚不育男性Y染色体微缺失的首次研究。
Urol Int. 2013;90(4):455-9. doi: 10.1159/000347046. Epub 2013 Mar 16.
5
Rapid and simultaneous screening of 47,XXY and AZF microdeletions by quadruplex real-time polymerase chain reaction.通过四重实时聚合酶链反应快速同步筛查47,XXY和AZF微缺失
Reprod Biol. 2015 Jun;15(2):113-21. doi: 10.1016/j.repbio.2015.02.002. Epub 2015 Feb 20.
6
Y chromosome microdeletions screening in Tunisian infertile men.突尼斯不育男性的Y染色体微缺失筛查
Ann Biol Clin (Paris). 2019 Oct 1;77(5):517-523. doi: 10.1684/abc.2019.1478.
7
[Screening of azoospermia factor microdeletions on Y chromosome in infertile men by QF-PCR].[应用QF-PCR技术筛查男性不育患者Y染色体无精子因子微缺失]
Yi Chuan. 2014 Jun;36(6):552-7. doi: 10.3724/SP.J.1005.2014.0552.
8
Correlation between Y chromosome microdeletion and male infertility.Y染色体微缺失与男性不育之间的相关性。
Genet Mol Res. 2016 Jun 3;15(2):gmr8426. doi: 10.4238/gmr.15028426.
9
Karyotypic abnormalities and molecular analysis of Y chromosome microdeletion in Iranian Azeri Turkish population infertile men.伊朗阿塞拜疆土耳其人群不育男性的核型异常和 Y 染色体微缺失的分子分析。
Syst Biol Reprod Med. 2020 Apr;66(2):140-146. doi: 10.1080/19396368.2019.1682083. Epub 2019 Nov 5.
10
A new molecular diagnostic approach to assess Y chromosome microdeletions in infertile men.一种评估不育男性Y染色体微缺失的新型分子诊断方法。
J Int Med Res. 2012;40(1):237-48. doi: 10.1177/147323001204000124.