A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference22 articles.
1. Nonsyndromic hearing impairment is associated with a mutation in DFNA5;Van Laer;Nat. Genet.,1998
2. Characterization of a gene that is inversely correlated with estrogen receptor expression (ICERE-1) in breast carcinomas;Thompson;Eur. J. Biochem.,1998
3. DFNA5 (ICERE-1) contributes to acquired etoposide resistance in melanoma cells;Lage;FEBS Lett.,2001
4. Genetic and molecular analysis of DNA43 and DNA52: two new cell-cycle genes in Saccharomyces cerevisiae;Solomon;Yeast,1992
5. A lesion in the DNA replication initiation factor Mcm10 induces pausing of elongation forks through chromosomal replication origins in Saccharomyces cerevisiae;Merchant;Mol. Cell. Biol.,1997
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. Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss;PLOS ONE;2022-11-09
2. A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family;BMC Medical Genomics;2022-07-21
3. Gasdermin E: A Prospective Target for Therapy of Diseases;Frontiers in Pharmacology;2022-04-06
4. Blocking GSDME-mediated pyroptosis in renal tubular epithelial cells alleviates disease activity in lupus mice;Cell Death Discovery;2022-03-12
5. Mini-Review: GSDME-Mediated Pyroptosis in Diabetic Nephropathy;Frontiers in Pharmacology;2021-11-16
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