Complementation of V(D)J recombination defect and X-ray sensitivity of scid mouse cells by human chromosome 8
Author:
Publisher
Elsevier BV
Subject
Genetics,Toxicology,Molecular Biology
Reference25 articles.
1. Integration of a dominant selectable marker into human chromosomes and transfer of marked chromosomes to mouse cells by microcell fusion;Athwal;Somat. Cell Mol. Genet.,1985
2. scid mutation in mice confers hypersensitivity to ionizing radiation and a deficiency in DNA double-strand break repair;Biedermann,1991
3. A severe combined immunodeficiency mutation in the mouse;Bosma;Nature,1983
4. The mouse mutation severe combined immune deficiency (scid) is on chromosome 16;Bosma;Immunogenetics,1989
5. V(D)J recombination coding junction formation without DNA homology: Processing of coding termini;Boubnov;Mol. Cell. Biol.,1993
Cited by 33 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. Monochromosomal Hybrids and Chromosome Transfer: A Functional Approach for Gene Identification;Cancer Genomics & Proteomics;2017-03-10
2. DNA repair gene XRCC7 G6721T variant and susceptibility to colorectal cancer;Egyptian Journal of Medical Human Genetics;2016-10
3. T-Cell Development;Fetal and Neonatal Physiology;2011
4. PHF10 Is Required for Cell Proliferation in Normal and SV40-Immortalized Human Fibroblast Cells;Cytogenetic and Genome Research;2009
5. V(D)J Recombination: Double-Strand Break Repair Gene Products Used in the Joining Mechanism;Annals of the New York Academy of Sciences;2008-06-28
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