PALB2 mutations in breast cancer patients from a multi-ethnic region in northwest China-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

PALB2 mutations in breast cancer patients from a multi-ethnic region in northwest China

Published:2015-10-21 Issue:1 Volume:20 Page:
ISSN:2047-783X
Container-title:European Journal of Medical Research
language:en
Short-container-title:Eur J Med Res

Author:

Li Yong Tao,Jiang Wei Hua,Wang Xiao Wen,Zhang Ming Shuai,Zhang Cheng Guang,Yi Li Na,WuwaliKhan Fulati,Ayoufu Aisikaer,Ou Jiang Hua

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s40001-015-0182-9

Reference27 articles.

1. Benson JR, Jatoi I. The global breast cancer burden. Future Oncol. 2012;8:697–702.

2. Stephens PJ, Tarpey PS, Davies H, Van Loo P, Greenman C, Wedge DC, et al. The landscape of cancer genes and mutational processes in breast cancer. Nature. 2012;486:400–4.

3. Turnbull C, Rahman N. Genetic predisposition to breast cancer: past, present, and future. Annu Rev Genomics Hum Genet. 2008;9:321–45.

4. Kurian AW. BRCA1 and BRCA2 mutations across race and ethnicity: distribution and clinical implications. Curr Opin Obstet Gynecol. 2010;22:72–8.

5. Tischkowitz M, Xia B. PALB2/FANCN: recombining Cancer and Fanconi anemia. Cancer Res. 2010;70:7353–9.

Cited by 11 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. Spectrum and characteristics of germline PALB2 pathogenic variants in 1556 early-onset breast cancer patients in China;Journal of Cancer Research and Clinical Oncology;2024-06-25

2. Türkiye’deki kanser hastalarında kalıtsal PALB2 gen varyantlarının yeni nesil dizileme yöntemiyle araştırılması;Adıyaman Üniversitesi Sağlık Bilimleri Dergisi;2023-12-31

3. Low prevalence of germline TP53 and PALB2 mutations in unselected cohort of breast cancer patients from Brunei Darussalam;F1000Research;2023-11-30

4. PALB2 Variants Extend the Mutational Profile of Hungarian Patients with Breast and Ovarian Cancer;Cancers;2023-08-31

5. Molecular genetic features of hereditary forms of breast cancer (systematic review);Pharmacogenetics and Pharmacogenomics;2023-07-19

同舟云学术

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