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Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells.

作者信息

Prigojin H, Brusel M, Fuchs O, Shomrat R, Legum C, Nudel U, Yaffe D

机构信息

Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

FEBS Lett. 1993 Dec 6;335(2):223-30. doi: 10.1016/0014-5793(93)80734-c.

DOI:10.1016/0014-5793(93)80734-c
PMID:8253201
Abstract

We have examined the expression of several Duchenne muscular dystrophy (DMD) gene products in amniotic fluid (AF) and chorionic villus sampling (CVS) cells. Variable amounts of dystrophin could be detected in most CVS and AF samples by immunoprecipitation followed by Western blot analysis. PCR analysis demonstrated the presence of the muscle type dystrophin mRNA in all AF cell cultures. The brain type dystrophin mRNA was also detected in some of these cultures. These DMD gene transcripts are of fetal origin and are produced by most or all clonable AF cells. The results may facilitate the development of a method for prenatal diagnosis of DMD, based on the expression of the gene in AF and CVS cells.

摘要

相似文献

1
Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells.
FEBS Lett. 1993 Dec 6;335(2):223-30. doi: 10.1016/0014-5793(93)80734-c.
2
Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy.羊膜细胞、绒毛膜绒毛细胞和成纤维细胞中肌生成激活后肌营养不良蛋白表达的分析。一种诊断杜氏肌营养不良症的新方法。
N Engl J Med. 1993 Sep 23;329(13):915-20. doi: 10.1056/NEJM199309233291303.
3
Dystrophin protein and RFLP analysis for fetal diagnosis and carrier confirmation of Duchenne muscular dystrophy.
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Zhonghua Fu Chan Ke Za Zhi. 2013 Mar;48(3):161-4.
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Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.在缺乏患病男孩DNA的情况下,利用构象多态性对杜氏肌营养不良进行分子诊断。
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