A Locus for an Autosomal Dominant Form of Progressive Renal Failure and Hypertension at Chromosome 1q21
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference20 articles.
1. Familial nephritis associated with the nephrotic syndrome in a family with severe involvement in females;Albert;Am J Dis Child,1969
2. Familial nephritis;Ben-Ishay;Israel J Med Sci,1967
3. Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease (ADMCKD);Christodoulou;Hum Mol Genet,1998
4. Hereditary nephropathy without deafness;Dockhorn;Am J Dis Child,1967
5. The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16;European Polycystic Kidney Disease Consortium;Cell,1994
Cited by 37 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. Interactions between the intrarenal dopaminergic and the renin–angiotensin systems in the control of systemic arterial pressure;Clinical Science;2022-08
2. Dopamine D5 receptor-mediated decreases in mitochondrial reactive oxygen species production are cAMP and autophagy dependent;Hypertension Research;2021-04-05
3. Reversible Treatment of Pressure Overload‐Induced Left Ventricular Hypertrophy through Drd5 Nucleic Acid Delivery Mediated by Functional Polyaminoglycoside;Advanced Science;2021-01-06
4. Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin;Kidney International;2014-09
5. D5 dopamine receptor decreases NADPH oxidase, reactive oxygen species and blood pressure via heme oxygenase-1;Hypertension Research;2013-02-21
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