NEIL3 contributes to the Fanconi anemia/BRCA pathway by promoting the downstream double-strand break repair step
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference61 articles.
1. Preventing nonhomologous end joining suppresses DNA repair defects of Fanconi anemia;Adamo;Mol. Cell,2010
2. A genome-wide homologous recombination screen identifies the RNA-binding protein RBMX as a component of the DNA-damage response;Adamson;Nat. Cell Biol.,2012
3. Fanconi anemia and its diagnosis;Auerbach;Mutat. Res.,2009
4. Cooperation of the ATM and Fanconi anemia/BRCA pathways in double-strand break end resection;Cai;Cell Rep.,2020
5. Homologous-recombination-deficient tumours are dependent on Poltheta-mediated repair;Ceccaldi;Nature,2015
Cited by 5 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. NEIL3: A unique DNA glycosylase involved in interstrand DNA crosslink repair;DNA Repair;2024-07
2. Novel Processes Associated with the Repair of Interstrand Cross-Links Derived from Abasic Sites in Duplex DNA: Roles for the Base Excision Repair Glycosylase NEIL3 and the SRAP Protein HMCES;Chemical Research in Toxicology;2024-01-10
3. Fance deficiency inhibits primordial germ cell proliferation associated with transcription–replication conflicts accumulate and DNA repair defects;Journal of Ovarian Research;2023-08-10
4. Rev1-Rev7 Complex Inhibitor JH-RE-06 Enhances Mitomycin C Chemosensitivity in HCT116 Colorectal Cancer Cells;2023-06-27
5. An acquired BMF with FANCL gene heterozygous mutation: Case report;Medicine;2023-06-16
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