Suppr超能文献

Allelic deletion mapping of putative tumor suppressor genes on 17q in sporadic ovarian cancer.

作者信息

Chen K C, Hsieh T T, Schwartz P E, Yang-Feng T L

机构信息

Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Taipei, Taiwan.

出版信息

J Obstet Gynaecol (Tokyo 1995). 1995 Dec;21(6):619-24. doi: 10.1111/j.1447-0756.1995.tb00921.x.

Abstract

OBJECTIVES

  1. To study whether the same or different chromosome 17q genes may be involved in the oncogenesis of familial and sporadic ovarian malignancies. 2) To localize the candidate gene in the sporadic ovarian cancers.

METHODS (STUDY DESIGN): Using DNA extracted from ovarian tumors and corresponding peripheral leukocyte, we examined the status of loss of heterozygosity (LOH) at 12 loci spanning chromosome 17q12-q25 by Southern hybridization and polymerase chain reaction.

RESULTS

Comparison of the extent of LOH among 25 epithelial ovarian tumors showing allele loss at one or more loci on 17q, the smallest overlapping region of allelic deletion is between D17S579 and GIP, with a genetic distance of approximate 2 cM.

CONCLUSIONS

From our allelic deletion analysis of chromosome 17q loci, it indicates that there are more than one ovarian cancer candidate genes on chromosome 17q.

摘要

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验