Suppr超能文献

应用胎儿卵巢基质细胞培养进行细胞遗传学诊断。卵巢基质培养的细胞遗传学诊断。

The use of foetal ovarian stromal cell culture for cytogenetic diagnosis. Stromal ovarian culture cytogenetic diagnosis.

机构信息

Unitat de Biologia, Facultat de Medicina, Universitat Autònoma de Barcelona, Barcelona, 08193, Spain.

出版信息

Cytotechnology. 2003 Jan;41(1):45-9. doi: 10.1023/A:1024228932488.

Abstract

Some studies have been carried out to analyze human female first meiotic prophase. Most of them use samples from foetuses collected after legal interruption of pregnancy. In some cases, a control population is needed and foetuses aborted for non-chromosomal reasons are used. The assumption of these samples as being euploids could perhaps represent an error. In this article, we describe an easy methodology to certify the euploidy of foetal ovarian tissue using an one-week somatic culture. Using this protocol, we have obtained a primary culture in 88.2% of the studied cases, material usable for being karyotyped in 93.3% of the cases, and a cytogenetic diagnosis was performed in 100% of these cases. Finding the same karyotype in cultured cells in cases in which we had a prenatal cytogenetic diagnosis has validated the technique, and in applying this protocol we have been able to check our prophase meiotic-study control population.

摘要

一些研究旨在分析人类女性第一次减数分裂前期。这些研究大多使用从合法终止妊娠后收集的胎儿样本。在某些情况下,需要一个对照组,并且使用因非染色体原因而流产的胎儿。这些样本被假设为整倍体,这可能是一个错误。在本文中,我们描述了一种使用一周体细培养来鉴定胎儿卵巢组织整倍体的简单方法。使用该方案,我们在 88.2%的研究病例中获得了原代培养,在 93.3%的病例中获得了可用于核型分析的材料,并对这些病例中的 100%进行了细胞遗传学诊断。在我们进行产前细胞遗传学诊断的病例中,在培养细胞中发现相同的核型验证了该技术,并且通过应用该方案,我们能够检查我们的减数分裂前期研究对照人群。

相似文献

本文引用的文献

2
Patterns of meiotic recombination in human fetal oocytes.人类胎儿卵母细胞减数分裂重组模式。
Am J Hum Genet. 2002 Jun;70(6):1469-79. doi: 10.1086/340734. Epub 2002 May 1.
5
Crossing over analysis at pachytene in man.人类粗线期的交叉分析。
Eur J Hum Genet. 1998 Jul-Aug;6(4):350-8. doi: 10.1038/sj.ejhg.5200200.
6
An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization.
Cytogenet Cell Genet. 1998;80(1-4):48-53. doi: 10.1159/000014956.
9
Non-disjunction of chromosome 18.18号染色体不分离
Hum Mol Genet. 1998 Apr;7(4):661-9. doi: 10.1093/hmg/7.4.661.

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