BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference28 articles.
1. The allelic architecture of human disease genes: common disease-common variant.or not?;JK Pritchard;Hum Mol Genet,2002
2. Inherited susceptibility for pediatric cancer;SE Plon;Cancer J. Sudbury Mass,2005
3. De novo recurrent germline mutation of the BRCA2 gene in a patient with early onset breast cancer;RB Van der Luijt;J Med Genet,2001
4. A novel de novo BRCA2 mutation of paternal origin identified in a Spanish woman with early onset bilateral breast cancer;O Diez;Breast Cancer Res Treat,2010
5. Rate of de novo mutations and the importance of father's age to disease risk;A Kong;Nature,2012
Cited by 38 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synergistic antitumor effect of liposomal-based formulations of olaparib and topotecan in primary epithelial ovarian cancer cells;Cancer Cell International;2024-08-12
2. More evidence for widespread antagonistic pleiotropy in polymorphic disease alleles;Frontiers in Genetics;2024-06-17
3. Fertility Preservation in BRCA1/2 Germline Mutation Carriers: An Overview;Life;2024-05-10
4. BRCA1 protein dose-dependent risk for embryonic oxidative DNA damage, embryopathies and neurodevelopmental disorders with and without ethanol exposure;Redox Biology;2024-04
5. Brca2 (p.T1942fs/+) dissipates ovarian reserve in rats through oxidative stress in follicular granulosa cells;Free Radical Research;2024-02
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3