Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference29 articles.
1. Epidemiologic data of primary glomerular diseases in western France;Simon;Kidney Int,2004
2. The incidence of biopsy-proven glomerulonephritis in Australia;Briganti;Nephrol Dial Transplant,2001
3. Increasing incidence of focal-segmental glomerulosclerosis among adult nephropathies: a 20-year renal biopsy study;Haas;Am J Kidney Dis,1995
4. Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States;Kitiyakara;Am J Kidney Dis,2004
5. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis;Kaplan;Nat Genet,2000
Cited by 106 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. INF2 formin variants linked to human inherited kidney disease reprogram the transcriptome, causing mitotic chaos and cell death;Cellular and Molecular Life Sciences;2024-06-25
2. Missense Mutant Gain-of-Function Causes Inverted Formin 2 (INF2)-Related Focal Segmental Glomerulosclerosis (FSGS);2024-06-10
3. A Review of Focal Segmental Glomerulosclerosis Classification With a Focus on Genetic Associations;Kidney Medicine;2024-06
4. Prevalence of kidney health genetic variants in adults with sickle cell nephropathy;British Journal of Haematology;2024-05-12
5. Significance of genetic analysis in adult patients with inherited chronic kidney disease;BMJ Case Reports;2024-03
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