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卵巢肿瘤中11p13威尔姆斯肿瘤抑制基因(WT1)的分析。

Analysis of the 11p13 Wilms' tumor suppressor gene (WT1) in ovarian tumors.

作者信息

Bruening W, Gros P, Sato T, Stanimir J, Nakamura Y, Housman D, Pelletier J

机构信息

Department of Biochemistry, McGill University, Montreal, Quebec, Canada.

出版信息

Cancer Invest. 1993;11(4):393-9. doi: 10.3109/07357909309018871.

Abstract

We have examined the status of the Wilms' tumor suppressor gene (WT1), residing at chromosome 11 band p13, in a total of 40 cancers of the female reproductive tract. Northern blot analysis revealed that the WT1 gene is expressed in a large percentage of ovarian tumors (75%) analyzed. Single-strand conformation polymorphism analysis was performed on all the tumors in this study in an attempt to detect mutations within the WT1 gene. Only silent mutations were detected within intron 7 of WT1 using this method. Loss of heterozygosity studies were performed at the WT1 locus in several ovarian tumors and revealed that in the informative cases, heterozygosity was retained.

摘要

我们检测了位于11号染色体p13带的威尔姆斯瘤抑癌基因(WT1)在40例女性生殖道癌症中的状态。Northern印迹分析显示,在所分析的大部分卵巢肿瘤(75%)中WT1基因有表达。本研究对所有肿瘤进行了单链构象多态性分析,试图检测WT1基因内的突变。用此方法仅在WT1的第7内含子中检测到沉默突变。在几例卵巢肿瘤中对WT1基因座进行了杂合性缺失研究,结果显示,在信息充分的病例中,杂合性得以保留。

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