Autosomal Dominant Mutation in the Signal Peptide of Renin in a Kindred With Anemia, Hyperuricemia, and CKD
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference24 articles.
1. Cloning and sequence analysis of cDNA for human renin precursor;Imai;Proc Natl Acad Sci U S A,1983
2. The effect of high perfusion pressures on the granulation of juxtaglomerular cells in an isolated kidney;Tobian;J Clin Invest,1959
3. Renin release from isolated juxtaglomerular apparatus depends on macula densa chloride transport;Lorenz;Am J Physiol,1991
4. Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis;Gribouval;Nat Genet,2005
5. Renin-angiotensin system in kidney development: renal tubular dysgenesis;Gubler;Kidney Int,2010
Cited by 25 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. Identification of novel prognostic targets in acute kidney injury using bioinformatics and next generation sequencing data analysis;2024-03-17
2. Mechanism of anti-hyperuricemia of isobavachin based on network pharmacology and molecular docking;Computers in Biology and Medicine;2023-03
3. Btg2 mutation induces renal injury and impairs blood pressure control in female rats;Physiological Genomics;2022-07-01
4. Phenylbutyrate rescues the transport defect of the Sec61α mutations V67G and T185A for renin;Life Science Alliance;2022-01-21
5. Autosomal Dominant Tubulointerstitial Kidney Disease;Pediatric Nephrology;2022
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