Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway

Author:

Yehia Lamis1ORCID,Jindal Supriya2,Komar Anton A123,Eng Charis1345ORCID

Affiliation:

1. Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA

2. Center for Gene Regulation in Health and Disease, Department of Biological, Geological and Environmental Sciences, Cleveland State University, Cleveland, OH, USA

3. Germline High Risk Cancer Focus Group, CASE Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA

4. Taussig Cancer Institute, Cleveland Clinic, OH, USA

5. Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH, USA

Funder

Ambrose Monell Foundation

Breast Cancer Research Foundation

National Cancer Institute

American Cancer Society

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference43 articles.

1. Rare-disease genetics in the era of next-generation sequencing: discovery to translation;Boycott;Nat. Rev. Genet,2013

2. Germline heterozygous variants in SEC23B are associated with cowden syndrome and enriched in apparently sporadic thyroid cancer;Yehia;Am. J. Hum. Genet,2015

3. Lifetime cancer risks in individuals with germline PTEN mutations;Tan;Clin. Cancer Res,2012

4. COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum;Barlowe;Cell,1994

5. Coordination of COPII vesicle trafficking by Sec23;Fromme;Trends Cell Biol,2008

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